Montreal Children's Hospital is a children's hospital in Montreal, Quebec, Canada. Founded in 1904, it is affiliated with the McGill University Health Centre and McGill University, Faculty of Medicine. The hospital has 154 single-patient rooms, 52-bed neonatology unit, 6 operating rooms and 6 intervention rooms.
----
1: Cunan ET, Dudley RWR, Shemie SD. In reply: Withholding therapeutic
interventions in brain(stem) death: is it a self-fulfilling prophecy? Can J
Anaesth. 2022 Sep 12. doi: 10.1007/s12630-022-02326-w. Epub ahead of print.
PMID: 36097131.
2: Marefi A, Husein N, Dunbar M, Dewey D, Letourneau N, Oskoui M, Kirton A,
Shevell MI; Canadian Cerebral Palsy Registry (CCPR). Risk Factors for Term-Born
Periventricular White Matter Injury in Children With Cerebral Palsy: A Case-
Control Study. Neurology. 2022 Aug 30:10.1212/WNL.0000000000201274. doi:
10.1212/WNL.0000000000201274. Epub ahead of print. PMID: 36041870.
3: Ashour M, Minato E, Alawadhi A, Berrahmoune S, Simard-Tremblay E, Poulin C,
Myers KA. Diagnostic utility of specific abnormal EEG patterns in children for
determining epilepsy phenotype and presence of structural brain abnormalities.
Heliyon. 2022 Aug 10;8(8):e10172. doi: 10.1016/j.heliyon.2022.e10172. PMID:
36033323; PMCID: PMC9399955.
4: Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG,
Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A,
Abbondanza F, Rimfeld K, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates
TC, Bernard M, Blokland K, Bonte M, Børglum AD, Bourgeron T, Brandeis D, Ceroni
F, Csépe V, Dale PS, de Jong PF, DeFries JC, Démonet JF, Demontis D, Feng Y,
Gordon SD, Guger SL, Hayiou-Thomas ME, Hernández-Cabrera JA, Hottenga JJ, Hulme
C, Kere J, Kerr EN, Koomar T, Landerl K, Leonard GT, Lovett MW, Lyytinen H,
Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT,
Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus
F, Richer L, Simpson NH, Smith SD, Snowling MJ, Stein J, Strug LJ, Talcott JB,
Tiemeier H, van der Schroeff MP, Verhoef E, Watkins KE, Wilkinson M, Wright MJ,
Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-Myhsok
B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Reilly S, Schulte-Körne
G, Tomblin JB, van Bergen E, Whitehouse AJO, Willcutt EG, St Pourcain B, Francks
C, Fisher SE. Genome-wide analyses of individual differences in quantitatively
assessed reading- and language-related skills in up to 34,000 people. Proc Natl
Acad Sci U S A. 2022 Aug 30;119(35):e2202764119. doi: 10.1073/pnas.2202764119.
Epub 2022 Aug 23. PMID: 35998220; PMCID: PMC9436320.
5: Jia X, Zhang S, Tan S, Du B, He M, Qin H, Chen J, Duan X, Luo J, Chen F,
Ouyang L, Wang J, Chen G, Yu B, Zhang G, Zhang Z, Lyu Y, Huang Y, Jiao J, Chen
JYH, Swoboda KJ, Agolini E, Novelli A, Leoni C, Zampino G, Cappuccio G,
Brunetti-Pierri N, Gerard B, Ginglinger E, Richer J, McMillan H, White-Brown A,
Hoekzema K, Bernier RA, Kurtz-Nelson EC, Earl RK, Meddens C, Alders M, Fuchs M,
Caumes R, Brunelle P, Smol T, Kuehl R, Day-Salvatore DL, Monaghan KG, Morrow MM,
Eichler EE, Hu Z, Yuan L, Tan J, Xia K, Shen Y, Guo H. De novo variants in genes
regulating stress granule assembly associate with neurodevelopmental disorders.
Sci Adv. 2022 Aug 19;8(33):eabo7112. doi: 10.1126/sciadv.abo7112. Epub 2022 Aug
17. PMID: 35977029; PMCID: PMC9385150.
6: Hatoum R, Chen JS, Lavergne P, Shlobin NA, Wang A, Elkaim LM, Dodin P,
Couturier CP, Ibrahim GM, Fallah A, Venne D, Perreault S, Wang AC, Jabado N,
Dudley RWR, Weil AG. Extent of Tumor Resection and Survival in Pediatric
Patients With High-Grade Gliomas: A Systematic Review and Meta-analysis. JAMA
Netw Open. 2022 Aug 1;5(8):e2226551. doi: 10.1001/jamanetworkopen.2022.26551.
PMID: 35972743; PMCID: PMC9382445.
7: Botelho F, Gripp K, Yanchar N, Naus A, Poenaru D, Baird R, Reis E, Farias L,
Silva AG, Viana F, Neto JAP, Silva S, Ribeiro K, Gatto L, Faleiro MD, Fernandez
MG, Salgado LS, Sampaio NZ, Faleiro MD, Mendes AL, Ferreira RV, Marcião L, Canto
G, Borges J, Araújo V, Andrade G, Braga J, Bentes L, Pinto L, Ndasi HT, Amlani
LM, Aminake G, Penda X, Tima S, Lechtig A, Agarwal-Harding KJ, Whyte M, Fowler-
Woods M, Fowler-Woods A, Shingoose G, Hatala A, Daeninck F, Vergis A, Clouston
K, Hardy K, Djadje L, Djoutsop OM, Djabo AT, Kanmounye US, Youmbi VN, Kakobo P,
Djoutsop OM, Djabo AT, Kanmounye US, Tafesse S, Tamene B, Chimdesa Z, Alemayehu
E, Abera B, Yifru D, Belachew FK, Tirsit A, Deyassa N, Moen BE, Sundstrøm T,
Lund-Johansen M, Abebe M, Khan R, Mekasha A, Soklaridis S, Haji F, Asingei J,
O'Flynn EP, O'Donovan DT, Masuka SC, Mashava D, Akello FV, Ulisubisya MM, Franco
H, Njai A, Simister S, Joseph M, Woolley P, James D, Evans FM, Rai E, Roy N,
Bansal V, Kamble J, Aroke A, David S, Veetil D, Soni KD, Wärnberg MG, Zadey S,
Vissoci JRN, Iyer H, Zadey S, Shetty R, Zadey S, Jindal A, Iyer H, Ouma G, Shah
SSNH, Hinchman C, Rayel IM, Dworkin M, Agarwal-Harding KJ, Mlinde E, Amlani LM,
May CJ, Banza LN, Chokotho L, Agarwal-Harding KJ, Dworkin M, Mbomuwa F, Chidothi
P, Martin C Jr, Harrison WJ, Agarwal-Harding KJ, Chokotho L, Paek S, Amlani L,
Mbomuwa F, Chidothi P, Martin C Jr, Harrison WJ, Agarwal-Harding KJ, Chokotho L,
Adégné T, Abdoulmouinou P, Amadou T, Youssouf T, Madiassa K, Younoussa DM,
Moussa S, Amadou B, Hawa T, Laurent A, Jesuyajolu DA, Okeke CA, Obuh O,
Jesuyajolu DA, Ehizibue PE, Ikemefula NE, Ekennia-Ebeh JO, Ibraham AA, Ikegwuonu
OE, Diehl TM, Bunogerane GJ, Neal D, Ndibanje AJ, Petroze RT, Ntaganda E,
Milligan L, Cairncross L, Malherbe F, Roodt L, Kyengera DK, O'Hara NN, Stockton
D, Bedada A, Hsiao M, Chilisa U, Yarranton B, Chinyepi N, Azzie G, Moon J,
Rehany Z, Bakhshi M, Bergeron A, Boulanger N, Watt L, Wong EG, Pawlak N, Bierema
C, Ameh E, Bekele A, Jimenez MF, Lakhoo K, Roy N, Sacato H, Tefera G, Ozgediz D,
Jayaraman S, Peric I, Youngson G, Ameh E, Borgstein E, O'Flynn E; CROCODILE
study group, Simoes J, Kingsley PA, Sasson L, Dekel H, Sternfeld AR, Assa S,
Sarid RS, Mnong'one NJ, Sharau GG, Mongella SM, Caryl WG, Goldman B, Bola R,
Ngonzi J, Ujoh F, Kihumuro RB, Lett R, Torquato A, Tavares C, Lech G, Džunic A,
Ujoh F, Gusa V, Apeaii R, Noor R, Bola R, Guyan IO, Christilaw J, Hodgins S,
Lett R, Binda C, Heo K, Cheng S, Foggin H, Hu G, Lam S, Feng L, Labinaz A, Adams
J, Livergant R, Williams S, Vasanthakumaran T, Lounes Y, Mata J, Hache P,
Schamberg-Bahadori C, Monytuil A, Mayom E, Joharifard S, Joos É, Paterson A,
Maswime S, Hardy A, Pearse RM, Biccard BM; African Surgical Outcomes (ASOS)
group and International Surgical Outcomes (ISOS) group, Salehi M, Zivkovic I,
Jatana S, Joharifard S, Joos É, Flores MJ, Brown KE, Roberts HJ, Donnelley CA,
von Kaeppler EP, Eliezer E, Haonga B, Morshed S, Shearer DW. Decolonizing Global
Surgery: Bethune Round Table, 2022 Conference on Global Surgery (virtual), June
16-18, 2022. Can J Surg. 2022 Aug 12;65(4 Suppl 1):S1-S18. doi:
10.1503/cjs.007622. PMID: 35961679; PMCID: PMC9388215.
8: Bolduc ME, Rennick JE, Gagnon I, Sokol E, Brossard-Racine M, Majnemer A.
Identifying developmental challenges of youth with congenital heart defects: A
patient-oriented perspective. Child Care Health Dev. 2022 Aug 9. doi:
10.1111/cch.13037. Epub ahead of print. PMID: 35945137.
9: Pekeles H, Myers KA. Post-vaccination drug-resistant epileptic spasms
associated with homozygous IFNAR2 pathogenic variant: Case report✰.
Seizure. 2022 Jul 26;101:117-119. doi: 10.1016/j.seizure.2022.07.016. Epub ahead
of print. PMID: 35944424.
10: Sahly AN, Buhas D, Myers KA. MT-TA pathogenic variants may cause
developmental and epileptic encephalopathy without myopathy. Am J Med Genet A.
2022 Aug 3. doi: 10.1002/ajmg.a.62925. Epub ahead of print. PMID: 35920329.
11: Nolden KA, Egner JM, Collier JJ, Russell OM, Alston CL, Harwig MC, Widlansky
ME, Sasorith S, Barbosa IA, Douglas AG, Baptista J, Walker M, Donnelly DE,
Morris AA, Tan HJ, Kurian MA, Gorman K, Mordekar S, Deshpande C, Samanta R,
McFarland R, Hill RB, Taylor RW, Oláhová M. Novel DNM1L variants impair
mitochondrial dynamics through divergent mechanisms. Life Sci Alliance. 2022 Aug
1;5(12):e202101284. doi: 10.26508/lsa.202101284. PMID: 35914810; PMCID:
PMC9354038.
12: Rasulo FA, Hopkins P, Lobo FA, Pandin P, Matta B, Carozzi C, Romagnoli S,
Absalom A, Badenes R, Bleck T, Caricato A, Claassen J, Denault A, Honorato C,
Motta S, Meyfroidt G, Radtke FM, Ricci Z, Robba C, Taccone FS, Vespa P,
Nardiello I, Lamperti M. Processed Electroencephalogram-Based Monitoring to
Guide Sedation in Critically Ill Adult Patients: Recommendations from an
International Expert Panel-Based Consensus. Neurocrit Care. 2022 Jul 27. doi:
10.1007/s12028-022-01565-5. Epub ahead of print. PMID: 35896766.
13: Larivière S, Royer J, Rodríguez-Cruces R, Paquola C, Caligiuri ME,
Gambardella A, Concha L, Keller SS, Cendes F, Yasuda CL, Bonilha L,
Gleichgerrcht E, Focke NK, Domin M, von Podewills F, Langner S, Rummel C, Wiest
R, Martin P, Kotikalapudi R, O'Brien TJ, Sinclair B, Vivash L, Desmond PM, Lui
E, Vaudano AE, Meletti S, Tondelli M, Alhusaini S, Doherty CP, Cavalleri GL,
Delanty N, Kälviäinen R, Jackson GD, Kowalczyk M, Mascalchi M, Semmelroch M,
Thomas RH, Soltanian-Zadeh H, Davoodi-Bojd E, Zhang J, Winston GP, Griffin A,
Singh A, Tiwari VK, Kreilkamp BAK, Lenge M, Guerrini R, Hamandi K, Foley S,
Rüber T, Weber B, Depondt C, Absil J, Carr SJA, Abela E, Richardson MP, Devinsky
O, Severino M, Striano P, Tortora D, Kaestner E, Hatton SN, Vos SB, Caciagli L,
Duncan JS, Whelan CD, Thompson PM, Sisodiya SM, Bernasconi A, Labate A, McDonald
CR, Bernasconi N, Bernhardt BC. Structural network alterations in focal and
generalized epilepsy assessed in a worldwide ENIGMA study follow axes of
epilepsy risk gene expression. Nat Commun. 2022 Jul 27;13(1):4320. doi:
10.1038/s41467-022-31730-5. PMID: 35896547; PMCID: PMC9329287.
14: Markati T, Oskoui M, Farrar MA, Duong T, Goemans N, Servais L. Emerging
therapies for Duchenne muscular dystrophy. Lancet Neurol. 2022
Sep;21(9):814-829. doi: 10.1016/S1474-4422(22)00125-9. Epub 2022 Jul 15. PMID:
35850122.
15: Tsai JW, Cejas P, Wang DK, Patel S, Wu DW, Arounleut P, Wei X, Zhou N,
Syamala S, Dubois FPB, Crane A, Pelton K, Vogelzang J, Sousa C, Baguette A, Chen
X, Condurat AL, Dixon-Clarke SE, Zhou KN, Lu SD, Gonzalez EM, Chacon MS,
Digiacomo JJ, Kumbhani R, Novikov D, Hunter J, Tsoli M, Ziegler DS, Dirksen U,
Jager N, Balasubramanian GP, Kramm CM, Nathrath M, Bielack S, Baker SJ, Zhang J,
McFarland JM, Getz G, Aguet F, Jabado N, Witt O, Pfister SM, Ligon KL, Hovestadt
V, Kleinman CL, Long H, Jones DTW, Bandopadhayay P, Phoenix TN. FOXR2 Is an
Epigenetically Regulated Pan-Cancer Oncogene That Activates ETS Transcriptional
Circuits. Cancer Res. 2022 Sep 2;82(17):2980-3001. doi:
10.1158/0008-5472.CAN-22-0671. PMID: 35802025.
16: Dubois FPB, Shapira O, Greenwald NF, Zack T, Wala J, Tsai JW, Crane A,
Baguette A, Hadjadj D, Harutyunyan AS, Kumar KH, Blattner-Johnson M, Vogelzang
J, Sousa C, Kang KS, Sinai C, Wang DK, Khadka P, Lewis K, Nguyen L, Malkin H, Ho
P, O'Rourke R, Zhang S, Gold R, Deng D, Serrano J, Snuderl M, Jones C, Wright
KD, Chi SN, Grill J, Kleinman CL, Goumnerova LC, Jabado N, Jones DTW, Kieran MW,
Ligon KL, Beroukhim R, Bandopadhayay P. Structural variants shape driver
combinations and outcomes in pediatric high-grade glioma. Nat Cancer. 2022
Aug;3(8):994-1011. doi: 10.1038/s43018-022-00403-z. Epub 2022 Jul 4. PMID:
35788723.
17: Srivastava R, Dunbar M, Shevell M, Oskoui M, Basu A, Rivkin MJ, Shany E, de
Vries LS, Dewey D, Letourneau N, Hill MD, Kirton A. Development and Validation
of a Prediction Model for Perinatal Arterial Ischemic Stroke in Term Neonates.
JAMA Netw Open. 2022 Jun 1;5(6):e2219203. doi:
10.1001/jamanetworkopen.2022.19203. PMID: 35767262; PMCID: PMC9244611.
18: Mirchi A, Richer J, Oskoui M, McMillan HJ. NTRK1-related Hereditary
Sensory and Autonomic Neuropathy Type 4: The Role of the Histamine Challenge
Test. Child Neurol Open. 2022 Jun 20;9:2329048X221108826. doi:
10.1177/2329048X221108826. PMID: 35756968; PMCID: PMC9218906.
19: Bainbridge MN, Mazumder A, Ogasawara D, Abou Jamra R, Bernard G, Bertini E,
Burglen L, Cope H, Crawford A, Derksen A, Dure L, Gantz E, Koch-Hogrebe M, Hurst
ACE, Mahida S, Marshall P, Micalizzi A, Novelli A, Peng H, Rodriguez D, Robbins
SL, Rutledge SL, Scalise R, Schließke S, Shashi V, Srivastava S, Thiffault I,
Topol S; Undiagnosed Disease Network, Qebibo L, Wieczorek D, Cravatt B,
Haricharan S, Torkamani A, Friedman J. Endocannabinoid dysfunction in
neurological disease: neuro-ocular DAGLA-related syndrome (NODRS). Brain. 2022
Jun 23:awac223. doi: 10.1093/brain/awac223. Epub ahead of print. PMID: 35737950.
20: Yaqubi M, Luo JXX, Baig S, Cui QL, Petrecca K, Desu H, Larochelle C,
Afanasiev E, Hall JA, Dudley R, Srour M, Haglund L, Ouellet J, Georgiopoulos M,
Santaguida C, Sonnen JA, Healy LM, Stratton JA, Kennedy TE, Antel JP. Regional
and age-related diversity of human mature oligodendrocytes. Glia. 2022
Oct;70(10):1938-1949. doi: 10.1002/glia.24230. Epub 2022 Jun 23. PMID: 35735919.
21: Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan
HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST,
Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Wigderson M, Tauscher-Wisniewski
S, McGill BE, Macek TA. Onasemnogene abeparvovec for presymptomatic infants with
three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT
trial. Nat Med. 2022 Jul;28(7):1390-1397. doi: 10.1038/s41591-022-01867-3. Epub
2022 Jun 17. PMID: 35715567; PMCID: PMC9205287.
22: Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan
HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST,
Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Tauscher-Wisniewski S, McGill BE,
Macek TA. Onasemnogene abeparvovec for presymptomatic infants with two copies of
SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial. Nat
Med. 2022 Jul;28(7):1381-1389. doi: 10.1038/s41591-022-01866-4. Epub 2022 Jun
17. PMID: 35715566; PMCID: PMC9205281.
23: Severino M, Tortora D, Reid C, Uccella S, Nobili L, Accogli A, Srour M,
Ramaglia A, Sudhakar S, Consales A, Pavanello M, Piatelli G, James G, Ravegnani
M, Rossi A, Mankad K. Imaging characteristics and neurosurgical outcome in
subjects with agenesis of the corpus callosum and interhemispheric cysts.
Neuroradiology. 2022 Jun 7. doi: 10.1007/s00234-022-02990-1. Epub ahead of
print. PMID: 35670822.
24: Hermans D, Houben E, Baeten P, Slaets H, Janssens K, Hoeks C, Hosseinkhani
B, Duran G, Bormans S, Gowing E, Hoornaert C, Beckers L, Fung WK, Schroten H,
Ishikawa H, Fraussen J, Thoelen R, de Vries HE, Kooij G, Zandee S, Prat A,
Hellings N, Broux B. Oncostatin M triggers brain inflammation by compromising
blood-brain barrier integrity. Acta Neuropathol. 2022 Aug;144(2):259-281. doi:
10.1007/s00401-022-02445-0. Epub 2022 Jun 6. PMID: 35666306.
25: Yossofzai O, Fallah A, Maniquis C, Wang S, Ragheb J, Weil AG, Brunette-
Clement T, Andrade A, Ibrahim GM, Mitsakakis N, Widjaja E. Development and
validation of machine learning models for prediction of seizure outcome after
pediatric epilepsy surgery. Epilepsia. 2022 Aug;63(8):1956-1969. doi:
10.1111/epi.17320. Epub 2022 Jun 25. PMID: 35661152.
26: Lopez SM, Aksman LM, Oxtoby NP, Vos SB, Rao J, Kaestner E, Alhusaini S,
Alvim M, Bender B, Bernasconi A, Bernasconi N, Bernhardt B, Bonilha L, Caciagli
L, Caldairou B, Caligiuri ME, Calvet A, Cendes F, Concha L, Conde-Blanco E,
Davoodi-Bojd E, de Bézenac C, Delanty N, Desmond PM, Devinsky O, Domin M, Duncan
JS, Focke NK, Foley S, Fortunato F, Galovic M, Gambardella A, Gleichgerrcht E,
Guerrini R, Hamandi K, Ives-Deliperi V, Jackson GD, Jahanshad N, Keller SS,
Kochunov P, Kotikalapudi R, Kreilkamp BAK, Labate A, Larivière S, Lenge M, Lui
E, Malpas C, Martin P, Mascalchi M, Medland SE, Meletti S, Morita-Sherman ME,
Owen TW, Richardson M, Riva A, Rüber T, Sinclair B, Soltanian-Zadeh H, Stein DJ,
Striano P, Taylor PN, Thomopoulos SI, Thompson PM, Tondelli M, Vaudano AE,
Vivash L, Wang Y, Weber B, Whelan CD, Wiest R, Winston GP, Yasuda CL, McDonald
CR, Alexander DC, Sisodiya SM, Altmann A; ENIGMA-Epilepsy Working Group. Event-
based modeling in temporal lobe epilepsy demonstrates progressive atrophy from
cross-sectional data. Epilepsia. 2022 Aug;63(8):2081-2095. doi:
10.1111/epi.17316. Epub 2022 Jun 25. PMID: 35656586.
27: Paul F, Ng C, Sahari UBM, Nafissi S, Nilipoor Y, Tavasoli AR, Bonnard C,
Wong PM, Nabavizadeh N, Altunoğlu U, Estiar MA, Majoie CB, Lee H, Nelson SF,
Gan-Or Z, Rouleau GA, Van Veldhoven PP, Massie R, Hennekam RC, Kariminejad A,
Reversade B. RABENOSYN separation-of-function mutations uncouple endosomal
recycling from lysosomal degradation, causing a distinct Mendelian Disorder. Hum
Mol Genet. 2022 Jun 2:ddac120. doi: 10.1093/hmg/ddac120. Epub ahead of print.
PMID: 35652444.
28: Marchi M, Elkrief L, Alkema A, van Gastel W, Schubart CD, van Eijk KR, Luykx
JJ, Branje S, Mastrotheodoros S, Galeazzi GM, van Os J, Cecil CA, Conrod PJ,
Boks MP. Childhood maltreatment mediates the effect of the genetic background on
psychosis risk in young adults. Transl Psychiatry. 2022 Jun 1;12(1):219. doi:
10.1038/s41398-022-01975-1. PMID: 35650188; PMCID: PMC9160238.
29: Bong CL, Ho D, Allen JC, Lim GS, Tan HK, Broekman BFP, Fabila T, Reddy S,
Koh WP, Swee-Kim Tan J, Meaney M, Rifkin-Graboi A. Early Neurodevelopmental
Outcomes Following Exposure to General Anesthesia in Infancy: EGAIN, a
Prospective Cohort Study. J Neurosurg Anesthesiol. 2022 May 26. doi:
10.1097/ANA.0000000000000857. Epub ahead of print. PMID: 35613046.
30: Wong C, Barkai O, Wang F, Perez CT, Lev S, Cai W, Tansley S, Yousefpour N,
Hooshmandi M, Lister KC, Latif M, Cuello AC, Prager-Khoutorsky M, Mogil JS,
Séguéla P, De Koninck Y, Ribeiro-da-Silva A, Binshtok AM, Khoutorsky A. mTORC2
mediates structural plasticity in distal nociceptive endings that contributes to
pain hypersensitivity following inflammation. J Clin Invest. 2022 Aug
1;132(15):e152635. doi: 10.1172/JCI152635. PMID: 35579957; PMCID: PMC9337825.
31: Guberman GI, Stojanovski S, Nishat E, Ptito A, Bzdok D, Wheeler AL,
Descoteaux M. Multi-tract multi-symptom relationships in pediatric concussion.
Elife. 2022 May 17;11:e70450. doi: 10.7554/eLife.70450. PMID: 35579325; PMCID:
PMC9132577.
32: Manry J, Bastard P, Gervais A, Le Voyer T, Rosain J, Philippot Q,
Michailidis E, Hoffmann HH, Eto S, Garcia-Prat M, Bizien L, Parra-Martínez A,
Yang R, Haljasmägi L, Migaud M, Särekannu K, Maslovskaja J, de Prost N,
Tandjaoui-Lambiotte Y, Luyt CE, Amador-Borrero B, Gaudet A, Poissy J, Morel P,
Richard P, Cognasse F, Troya J, Trouillet-Assant S, Belot A, Saker K, Garçon P,
Rivière JG, Lagier JC, Gentile S, Rosen LB, Shaw E, Morio T, Tanaka J, Dalmau D,
Tharaux PL, Sene D, Stepanian A, Mégarbane B, Triantafyllia V, Fekkar A, Heath
JR, Franco JL, Anaya JM, Solé-Violán J, Imberti L, Biondi A, Bonfanti P,
Castagnoli R, Delmonte OM, Zhang Y, Snow AL, Holland SM, Biggs CM, Moncada-Vélez
M, Arias AA, Lorenzo L, Boucherit S, Anglicheau D, Planas AM, Haerynck F, Duvlis
S, Ozcelik T, Keles S, Bousfiha AA, El Bakkouri J, Ramirez-Santana C, Paul S,
Pan-Hammarström Q, Hammarström L, Dupont A, Kurolap A, Metz CN, Aiuti A, Casari
G, Lampasona V, Ciceri F, Barreiros LA, Dominguez-Garrido E, Vidigal M, Zatz M,
van de Beek D, Sahanic S, Tancevski I, Stepanovskyy Y, Boyarchuk O, Nukui Y,
Tsumura M, Vidaur L, Tangye SG, Burrel S, Duffy D, Quintana-Murci L, Klocperk A,
Kann NY, Shcherbina A, Lau YL, Leung D, Coulongeat M, Marlet J, Koning R, Reyes
LF, Chauvineau-Grenier A, Venet F, Monneret G, Nussenzweig MC, Arrestier R,
Boudhabhay I, Baris-Feldman H, Hagin D, Wauters J, Meyts I, Dyer AH, Kennelly
SP, Bourke NM, Halwani R, Sharif-Askari FS, Dorgham K, Sallette J, Sedkaoui SM,
AlKhater S, Rigo-Bonnin R, Morandeira F, Roussel L, Vinh DC, Erikstrup C,
Condino-Neto A, Prando C, Bondarenko A, Spaan AN, Gilardin L, Fellay J, Lyonnet
S, Bilguvar K, Lifton RP, Mane S; HGID Lab; COVID Clinicians; COVID-STORM
Clinicians; NIAID Immune Response to COVID Group; NH-COVAIR Study Group; Danish
CHGE; Danish Blood Donor Study; St. James's Hospital, SARS CoV2 Interest Group;
French COVID Cohort Study Group; Imagine COVID-Group; Milieu Intérieur
Consortium; CoV-Contact Cohort; Amsterdam UMC Covid-19 Biobank Investigators;
COVID Human Genetic Effort; CP-COVID-19 Group; CONSTANCES cohort; 3C-Dijon
Study; Cerba Health-Care; Etablissement Français du Sang Study group, Anderson
MS, Boisson B, Béziat V, Zhang SY, Andreakos E, Hermine O, Pujol A, Peterson P,
Mogensen TH, Rowen L, Mond J, Debette S, de Lamballerie X, Burdet C, Bouadma L,
Zins M, Soler-Palacin P, Colobran R, Gorochov G, Solanich X, Susen S, Martinez-
Picado J, Raoult D, Vasse M, Gregersen PK, Piemonti L, Rodríguez-Gallego C,
Notarangelo LD, Su HC, Kisand K, Okada S, Puel A, Jouanguy E, Rice CM,
Tiberghien P, Zhang Q, Casanova JL, Abel L, Cobat A. The risk of COVID-19 death
is much greater and age dependent with type I IFN autoantibodies. Proc Natl Acad
Sci U S A. 2022 May 24;119(21):e2200413119. doi: 10.1073/pnas.2200413119. Epub
2022 May 16. PMID: 35576468; PMCID: PMC9173764.
33: Bartlett A, Lane A, Chaney B, Escorza NY, Black K, Cochrane A, Minturn J,
Bartels U, Warren K, Hansford J, Ziegler D, Diez B, Goldman S, Packer R, Kieran
M, DeWire-Schottmiller M, Erker C, Monje-Deisseroth M, Wagner L, Koschmann C,
Dorris K, Shih CS, Hassall T, Samson Y, Fisher P, Wang SS, Tsui K, Sevlever G,
Zhu X, Dexheimer P, Asher A, Fuller C, Drissi R, Jones B, Leach J, Fouladi M.
Characteristics of Children ≤36 Months of Age with Diffuse Intrinsic Pontine
Glioma (DIPG): A Report from the International DIPG Registry. Neuro Oncol. 2022
May 12:noac123. doi: 10.1093/neuonc/noac123. Epub ahead of print. PMID:
35552452.
34: Cunan ET, Dudley R, Shemie SD. Decompressive craniectomy as a potentially
reversible condition in brain death-brain stunning or skin and pericranium
stretching? Can J Anaesth. 2022 Jul;69(7):811-814. English. doi:
10.1007/s12630-022-02264-7. Epub 2022 May 10. PMID: 35534771.
35: Mirza AI, Zhu F, Knox N, Forbes JD, Bonner C, Van Domselaar G, Bernstein CN,
Graham M, Marrie RA, Hart J, Yeh EA, Arnold DL, Bar-Or A, O'Mahony J, Zhao Y,
Hsiao W, Banwell B, Waubant E, Tremlett H. The metabolic potential of the
paediatric-onset multiple sclerosis gut microbiome. Mult Scler Relat Disord.
2022 Jul;63:103829. doi: 10.1016/j.msard.2022.103829. Epub 2022 Apr 23. PMID:
35500534.
36: Varghaei P, Estiar MA, Ashtiani S, Veyron S, Mufti K, Leveille E, Yu E,
Spiegelman D, Rioux MF, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Suchowersky
O, Trempe JF, Rouleau GA, Gan-Or Z. Genetic, structural and clinical analysis of
spastic paraplegia 4. Parkinsonism Relat Disord. 2022 May;98:62-69. doi:
10.1016/j.parkreldis.2022.03.019. Epub 2022 Apr 16. PMID: 35487127.
37: Birca V, Myers KA. Genetic Generalized Epilepsy and Intrafamilial Phenotypic
Variability with Distal 7q11.23 Deletion. Child Neurol Open. 2022 Apr
21;9:2329048X221093173. doi: 10.1177/2329048X221093173. PMID: 35481155; PMCID:
PMC9036355.
38: Huang J, Saint-Martin C, Tchakarska G, Lavoie J, Myers KA. Cerebral white
matter abnormalities associated with chromosome 18q duplication. Brain Dev. 2022
Sep;44(8):562-566. doi: 10.1016/j.braindev.2022.04.004. Epub 2022 Apr 22. PMID:
35469635.
39: Duncan CJA, Skouboe MK, Howarth S, Hollensen AK, Chen R, Børresen ML,
Thompson BJ, Stremenova Spegarova J, Hatton CF, Stæger FF, Andersen MK,
Whittaker J, Paludan SR, Jørgensen SE, Thomsen MK, Mikkelsen JG, Heilmann C,
Buhas D, Øbro NF, Bay JT, Marquart HV, de la Morena MT, Klejka JA, Hirschfeld M,
Borgwardt L, Forss I, Masmas T, Poulsen A, Noya F, Rouleau G, Hansen T, Zhou S,
Albrechtsen A, Alizadehfar R, Allenspach EJ, Hambleton S, Mogensen TH. Life-
threatening viral disease in a novel form of autosomal recessive IFNAR2
deficiency in the Arctic. J Exp Med. 2022 Jun 6;219(6):e20212427. doi:
10.1084/jem.20212427. Epub 2022 Apr 20. PMID: 35442417; PMCID: PMC9026249.
40: Zhang M, Wong SW, Wright JN, Wagner MW, Toescu S, Han M, Tam LT, Zhou Q,
Ahmadian SS, Shpanskaya K, Lummus S, Lai H, Eghbal A, Radmanesh A, Nemelka J,
Harward S 2nd, Malinzak M, Laughlin S, Perreault S, Braun KRM, Lober RM, Cho YJ,
Ertl-Wagner B, Ho CY, Mankad K, Vogel H, Cheshier SH, Jacques TS, Aquilina K,
Fisher PG, Taylor M, Poussaint T, Vitanza NA, Grant GA, Pfister S, Thompson E,
Jaju A, Ramaswamy V, Yeom KW. MRI Radiogenomics of Pediatric Medulloblastoma: A
Multicenter Study. Radiology. 2022 Aug;304(2):406-416. doi:
10.1148/radiol.212137. Epub 2022 Apr 19. PMID: 35438562; PMCID: PMC9340239.
41: McMillan HJ, Proud CM, Farrar MA, Alexander IE, Muntoni F, Servais L.
Onasemnogene abeparvovec for the treatment of spinal muscular atrophy. Expert
Opin Biol Ther. 2022 May 2:1-16. doi: 10.1080/14712598.2022.2066471. Epub ahead
of print. PMID: 35437095.
42: Siafa L, Argilli E, Sherr EH, Myers KA. De Novo GLI3 Pathogenic Variants May
Cause Hypotonia and a Range of Brain Malformations Without Skeletal
Abnormalities. Pediatr Neurol. 2022 Jun;131:1-3. doi:
10.1016/j.pediatrneurol.2022.03.005. Epub 2022 Mar 31. PMID: 35436645.
43: Enguix V, Easson K, Gilbert G, Saint-Martin C, Rohlicek C, Luck D,
Lodygensky GA, Brossard-Racine M. Altered resting state functional connectivity
in youth with congenital heart disease operated during infancy. PLoS One. 2022
Apr 15;17(4):e0264781. doi: 10.1371/journal.pone.0264781. PMID: 35427374; PMCID:
PMC9012393.
44: Lemaréchal JD, Jedynak M, Trebaul L, Boyer A, Tadel F, Bhattacharjee M,
Deman P, Tuyisenge V, Ayoubian L, Hugues E, Chanteloup-Forêt B, Saubat C,
Zouglech R, Reyes Mejia GC, Tourbier S, Hagmann P, Adam C, Barba C, Bartolomei
F, Blauwblomme T, Curot J, Dubeau F, Francione S, Garcés M, Hirsch E, Landré E,
Liu S, Maillard L, Metsähonkala EL, Mindruta I, Nica A, Pail M, Petrescu AM,
Rheims S, Rocamora R, Schulze-Bonhage A, Szurhaj W, Taussig D, Valentin A, Wang
H, Kahane P, George N, David O; F-TRACT consortium. A brain atlas of axonal and
synaptic delays based on modelling of cortico-cortical evoked potentials. Brain.
2022 Jun 3;145(5):1653-1667. doi: 10.1093/brain/awab362. PMID: 35416942; PMCID:
PMC9166555.
45: D'Onofrio G, Riva A, Di Rosa G, Cali' E, Efthymiou S, Gitto E, Madia F,
Accogli A, Zara F, Houlden H, Salpietro V, Striano P, Soler D. Paroxysmal limb
dystonias associated with GABBR2 pathogenic variant: A case-based literature
review. Brain Dev. 2022 Aug;44(7):469-473. doi: 10.1016/j.braindev.2022.03.010.
Epub 2022 Apr 9. PMID: 35414446.
46: Easson K, Gilbert G, Rohlicek CV, Saint-Martin C, Descoteaux M, Deoni SCL,
Brossard-Racine M. Altered myelination in youth born with congenital heart
disease. Hum Brain Mapp. 2022 Aug 1;43(11):3545-3558. doi: 10.1002/hbm.25866.
Epub 2022 Apr 12. PMID: 35411995; PMCID: PMC9248320.
47: Siegel L, Yan H, Warsi N, Wong S, Suresh H, Weil AG, Ragheb J, Wang S,
Rozzelle C, Albert GW, Raskin J, Abel T, Hauptman J, Schrader DV, Bollo R, Smyth
MD, Lew SM, Lopresti M, Kizek DJ, Weiner HL, Fallah A, Widjaja E, Ibrahim GM.
Connectomic profiling and Vagus nerve stimulation Outcomes Study (CONNECTiVOS):
a prospective observational protocol to identify biomarkers of seizure response
in children and youth. BMJ Open. 2022 Apr 8;12(4):e055886. doi:
10.1136/bmjopen-2021-055886. PMID: 35396292; PMCID: PMC8995963.
48: McAlpine A, Robinson JL, Barton M, Balamohan A, Davies HD, Skar G, Lefebvre
MA, Almadani A, Freire D, Le Saux N, Bowes J, Srigley JA, Passarelli P, Bradley
J, Khan S, Purewal R, Viel-Thériault I, Ranger A, Hawkes MT; Paediatric
Investigators Collaborative Network on Infections in Canada. Cerebrospinal Fluid
Shunt Infections: A Multicenter Pediatric Study. Pediatr Infect Dis J. 2022 Jun
1;41(6):449-454. doi: 10.1097/INF.0000000000003513. Epub 2022 May 6. PMID:
35389956.
49: Bells S, Longoni G, Berenbaum T, de Medeiros CB, Narayanan S, Banwell BL,
Arnold DL, Mabbott DJ, Ann Yeh E. Patterns of white and gray structural
abnormality associated with paediatric demyelinating disorders. Neuroimage Clin.
2022;34:103001. doi: 10.1016/j.nicl.2022.103001. Epub 2022 Mar 31. PMID:
35381508; PMCID: PMC8980471.
50: Longoni G, Brown RA, Oyefiade A, Iruthayanathan R, Wilbur C, Shams S,
Noguera A, Grover SA, O'Mahony J, Chung L, Wan MJ, Mah JK, Costello F, Arnold
DL, Marrie RA, Bar-Or A, Banwell B, Mabbott D, Reginald AY, Yeh EA. Progressive
retinal changes in pediatric multiple sclerosis. Mult Scler Relat Disord. 2022
May;61:103761. doi: 10.1016/j.msard.2022.103761. Epub 2022 Mar 23. PMID:
35349885.
51: Park BY, Larivière S, Rodríguez-Cruces R, Royer J, Tavakol S, Wang Y,
Caciagli L, Caligiuri ME, Gambardella A, Concha L, Keller SS, Cendes F, Alvim
MKM, Yasuda C, Bonilha L, Gleichgerrcht E, Focke NK, Kreilkamp BAK, Domin M, von
Podewils F, Langner S, Rummel C, Rebsamen M, Wiest R, Martin P, Kotikalapudi R,
Bender B, O'Brien TJ, Law M, Sinclair B, Vivash L, Kwan P, Desmond PM, Malpas
CB, Lui E, Alhusaini S, Doherty CP, Cavalleri GL, Delanty N, Kälviäinen R,
Jackson GD, Kowalczyk M, Mascalchi M, Semmelroch M, Thomas RH, Soltanian-Zadeh
H, Davoodi-Bojd E, Zhang J, Lenge M, Guerrini R, Bartolini E, Hamandi K, Foley
S, Weber B, Depondt C, Absil J, Carr SJA, Abela E, Richardson MP, Devinsky O,
Severino M, Striano P, Parodi C, Tortora D, Hatton SN, Vos SB, Duncan JS,
Galovic M, Whelan CD, Bargalló N, Pariente J, Conde-Blanco E, Vaudano AE,
Tondelli M, Meletti S, Kong XZ, Francks C, Fisher SE, Caldairou B, Ryten M,
Labate A, Sisodiya SM, Thompson PM, McDonald CR, Bernasconi A, Bernasconi N,
Bernhardt BC. Topographic divergence of atypical cortical asymmetry and atrophy
patterns in temporal lobe epilepsy. Brain. 2022 May 24;145(4):1285-1298. doi:
10.1093/brain/awab417. PMID: 35333312; PMCID: PMC9128824.
52: Rodden LN, Gilliam KM, Lam C, Rojsajjakul T, Mesaros C, Dionisi C, Pook M,
Pandolfo M, Lynch DR, Blair IA, Bidichandani SI. DNA methylation in Friedreich
ataxia silences expression of frataxin isoform E. Sci Rep. 2022 Mar
23;12(1):5031. doi: 10.1038/s41598-022-09002-5. PMID: 35322126; PMCID:
PMC8943190.
53: Shaw KA, Welborn MC, Matsumoto H, Parent S, Sachwani N, El-Hawary R, Skaggs
D, Newton PO, Blakemore L, Vitale M, Samdani A, Murphy JS; Pediatric Spine Study
Group. To tether or fuse? Significant equipoise remains in treatment
recommendations for idiopathic scoliosis. Spine Deform. 2022 Jul;10(4):763-773.
doi: 10.1007/s43390-022-00497-6. Epub 2022 Mar 22. PMID: 35316524.
54: Wareham LK, Liddelow SA, Temple S, Benowitz LI, Di Polo A, Wellington C,
Goldberg JL, He Z, Duan X, Bu G, Davis AA, Shekhar K, Torre A, Chan DC, Canto-
Soler MV, Flanagan JG, Subramanian P, Rossi S, Brunner T, Bovenkamp DE, Calkins
DJ. Solving neurodegeneration: common mechanisms and strategies for new
treatments. Mol Neurodegener. 2022 Mar 21;17(1):23. doi:
10.1186/s13024-022-00524-0. PMID: 35313950; PMCID: PMC8935795.
55: Myers KA, Barmherzig R, Raj NR, Berrahmoune S, Ingelmo P, Saint-Martin C,
Khan AQ, Kouri M, Morris C, Hershey AD, Kacperski J, Kabbouche MA, Mohamed N,
Rao RR, Lagman-Bartolome AM, Gelfand AA, Szperka CL, Orr SL. The spectrum of
indomethacin-responsive headaches in children and adolescents. Cephalalgia. 2022
Jul;42(8):793-797. doi: 10.1177/03331024221076483. Epub 2022 Mar 18. PMID:
35302385; PMCID: PMC9218410.
56: Bonkhoff AK, Bretzner M, Hong S, Schirmer MD, Cohen A, Regenhardt RW,
Donahue KL, Nardin MJ, Dalca AV, Giese AK, Etherton MR, Hancock BL, Mocking SJT,
McIntosh EC, Attia J, Benavente OR, Bevan S, Cole JW, Donatti A, Griessenauer
CJ, Heitsch L, Holmegaard L, Jood K, Jimenez-Conde J, Kittner SJ, Lemmens R,
Levi CR, McDonough CW, Meschia JF, Phuah CL, Rolfs A, Ropele S, Rosand J, Roquer
J, Rundek T, Sacco RL, Schmidt R, Sharma P, Slowik A, Söderholm M, Sousa A,
Stanne TM, Strbian D, Tatlisumak T, Thijs V, Vagal A, Wasselius J, Woo D, Zand
R, McArdle PF, Worrall BB, Jern C, Lindgren AG, Maguire J, Fox MD, Bzdok D, Wu
O, Rost NS; MRI-GENIE and GISCOME Investigators and the International Stroke
Genetics Consortium. Sex-specific lesion pattern of functional outcomes after
stroke. Brain Commun. 2022 Feb 2;4(2):fcac020. doi: 10.1093/braincomms/fcac020.
PMID: 35282166; PMCID: PMC8914504.
57: Ferreira J, Bowder AN, Faria I, Graner M, Buda AM, Zimmerman K, Truché P,
Pompermaier L, Botelho F, Alonso N, Scheffer MC, Alves Guilloux AG. Evolution of
Gender Disparities Among Brazilian Surgical, Anesthesia, and Obstetric
Providers. J Surg Res. 2022 Jul;275:1-9. doi: 10.1016/j.jss.2021.12.045. Epub
2022 Feb 22. PMID: 35217234.
58: Pernin F, Luo J, Cui QL, Blain M, Fernandes MGF, Yaqubi M, Srour M, Hall J,
Dudley R, Jamann H, Larochelle C, Zandee SEJ, Prat A, Stratton JA, Kennedy TE,
Antel JP. Diverse injury responses of human oligodendrocyte to mediators
implicated in multiple sclerosis. Brain. 2022 Feb 24:awac075. doi:
10.1093/brain/awac075. Epub ahead of print. PMID: 35202462.
59: Michell-Robinson MA, Perrier S, Lucia C, Tran LT, Thiffault I, Köhler W,
Bernard G. Oculodentodigital Dysplasia: A Cause of Hypomyelinating
Leukodystrophy in Adults. Neurology. 2022 Apr 19;98(16):675-677. doi:
10.1212/WNL.0000000000200228. Epub 2022 Feb 21. PMID: 35190466; PMCID:
PMC9052568.
60: Zaghloul MS, Nasr A, Tolba M, Refaat A, Youssef A, Mosaab A, Enayet A, Arafa
O, Maher E, Eldebawy E. Hypofractionated Radiation Therapy For Diffuse Intrinsic
Pontine Glioma: A Noninferiority Randomized Study Including 253 Children. Int J
Radiat Oncol Biol Phys. 2022 Jun 1;113(2):360-368. doi:
10.1016/j.ijrobp.2022.01.054. Epub 2022 Feb 10. PMID: 35150788.
61: Rheault F, Schilling KG, Valcourt-Caron A, Théberge A, Poirier C, Grenier G,
Guberman GI, Begnoche J, Legarreta JH, Y Cai L, Roy M, Edde M, Caceres MP,
Ocampo-Pineda M, Al-Sharif N, Karan P, Bontempi P, Obaid S, Bosticardo S,
Schiavi S, Sairanen V, Daducci A, Cutting LE, Petit L, Descoteaux M, Landman BA.
Tractostorm 2: Optimizing tractography dissection reproducibility with
segmentation protocol dissemination. Hum Brain Mapp. 2022 May;43(7):2134-2147.
doi: 10.1002/hbm.25777. Epub 2022 Feb 10. PMID: 35141980; PMCID: PMC8996349.
62: van der Knaap MS, Bonkowsky JL, Vanderver A, Schiffmann R, Krägeloh-Mann I,
Bertini E, Bernard G, Fatemi SA, Wolf NI, Saunier-Vivar E, Rauner R, Dekker H,
van Bokhoven P, van de Ven P, Leferink PS. Therapy Trial Design in Vanishing
White Matter: An Expert Consortium Opinion. Neurol Genet. 2022 Feb 2;8(2):e657.
doi: 10.1212/NXG.0000000000000657. PMID: 35128050; PMCID: PMC8811717.
63: Cheung A, Argyriou C, Yergeau C, D'Souza Y, Riou É, Lévesque S, Raymond G,
Daba M, Rtskhiladze I, Tkemaladze T, Adang L, La Piana R, Bernard G, Braverman
N. Clinical, neuroradiological, and molecular characterization of patients with
atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series.
Neurogenetics. 2022 Apr;23(2):115-127. doi: 10.1007/s10048-022-00684-7. Epub
2022 Feb 2. PMID: 35106698.
64: Macintosh J, Derksen A, Poulin C, Braverman N, Vanderver A, Thiffault I,
Albrecht S, Bernard G. Novel biallelic variants in NRROS associated with a
lethal microgliopathy, brain calcifications, and neurodegeneration.
Neurogenetics. 2022 Apr;23(2):151-156. doi: 10.1007/s10048-022-00683-8. Epub
2022 Jan 31. PMID: 35099671; PMCID: PMC9289721.
65: Savard M, Pascoal TA, Servaes S, Dhollander T, Iturria-Medina Y, Kang MS,
Vitali P, Therriault J, Mathotaarachchi S, Benedet AL, Gauthier S, Rosa-Neto P;
Frontotemporal Lobar Degeneration Neuroimaging Initiative. Impact of long- and
short-range fibre depletion on the cognitive deficits of fronto-temporal
dementia. Elife. 2022 Jan 24;11:e73510. doi: 10.7554/eLife.73510. PMID:
35073256; PMCID: PMC8824472.
66: Derksen A, Shih HY, Forget D, Darbelli L, Tran LT, Poitras C, Guerrero K,
Tharun S, Alkuraya FS, Kurdi WI, Nguyen CE, Laberge AM, Si Y, Gauthier MS,
Bonkowsky JL, Coulombe B, Bernard G. Variants in LSM7 impair LSM
complexes assembly, neurodevelopment in zebrafish and may be associated with an
ultra-rare neurological disease. HGG Adv. 2021 May 5;2(3):100034. doi:
10.1016/j.xhgg.2021.100034. PMID: 35047835; PMCID: PMC8756503.
67: Katz SL, Parraga G, Luu TM, Santyr G, Abdeen N, Deschenes S, Tse SM, Couch
MJ, Barrowman N, Hayawi L, Momoli F, Blinder H, Thébaud B, Nuyt AM, Ben Fadel N,
Moraes TJ. Pulmonary Magnetic Resonance Imaging of Ex-Preterm Children with and
without Bronchopulmonary Dysplasia. Ann Am Thorac Soc. 2022 Jul;19(7):1149-1157.
doi: 10.1513/AnnalsATS.202106-691OC. PMID: 35030070.
68: Yang JH, Friederich MW, Ellsworth KA, Frederick A, Foreman E, Malicki D,
Dimmock D, Lenberg J, Prasad C, Yu AC, Anthony Rupar C, Hegele RA, Manickam K,
Koboldt DC, Crist E, Choi SS, Farhan SMK, Harvey H, Sattar S, Karp N, Wong T,
Haas R, Van Hove JLK, Wigby K. Expanding the phenotypic and molecular spectrum
of NFS1-related disorders that cause functional deficiencies in mitochondrial
and cytosolic iron-sulfur cluster containing enzymes. Hum Mutat. 2022
Mar;43(3):305-315. doi: 10.1002/humu.24330. Epub 2022 Jan 19. PMID: 35026043;
PMCID: PMC8863643.
69: Nellis ME, Karam O, Valentine SL, Bateman ST, Remy KE, Lacroix J, Cholette
JM, Bembea MM, Russell RT, Steiner ME, Goobie SM, Tucci M, Stricker PA,
Stanworth SJ, Delaney M, Lieberman L, Muszynski JA, Bauer DF, Steffen K,
Nishijima D, Ibla J, Emani S, Vogel AM, Haas T, Goel R, Crighton G, Delgado D,
Demetres M, Parker RI; Pediatric Critical Care Transfusion and Anemia EXpertise
Initiative—Control/Avoidance of Bleeding (TAXI-CAB), in collaboration with the
Pediatric Critical Care Blood Research Network (BloodNet), and the Pediatric
Acute Lung Injury and Sepsis Investigators (PALISI) Network. Executive Summary
of Recommendations and Expert Consensus for Plasma and Platelet Transfusion
Practice in Critically Ill Children: From the Transfusion and Anemia EXpertise
Initiative-Control/Avoidance of Bleeding (TAXI-CAB). Pediatr Crit Care Med. 2022
Jan 1;23(1):34-51. doi: 10.1097/PCC.0000000000002851. PMID: 34989711; PMCID:
PMC8820267.
70: Russell R, Bauer DF, Goobie SM, Haas T, Nellis ME, Nishijima DK, Vogel AM,
Lacroix J; Transfusion and Anemia EXpertise Initiative–Control/Avoidance of
Bleeding (TAXI-CAB), the Pediatric Critical Care Blood Research Network
(BloodNet), and the Pediatric Acute Lung Injury and Sepsis Investigators
(PALISI) Network. Plasma and Platelet Transfusion Strategies in Critically Ill
Children Following Severe Trauma, Traumatic Brain Injury, and/or Intracranial
Hemorrhage: From the Transfusion and Anemia EXpertise Initiative-
Control/Avoidance of Bleeding. Pediatr Crit Care Med. 2022 Jan 1;23(13 Suppl 1
1S):e14-e24. doi: 10.1097/PCC.0000000000002855. PMID: 34989702; PMCID:
PMC8849603.
71: Amir Yazdani P, St-Jean ML, Matovic S, Spahr A, Tran LT, Boucher RM, Poulin
C, Osterman B, Srour M, Rosenblatt B, Chenier S, Soucy JF, Laberge AM, Braverman
N, D'Agostino MD, Nguyen CE, Morsa M, Bernard G. Experience of Parents of
Children with Genetically Determined Leukoencephalopathies Regarding the Adapted
Health Care Services During the COVID-19 Pandemic. J Child Neurol. 2022
Mar;37(4):237-245. doi: 10.1177/08830738211065317. Epub 2022 Jan 5. PMID:
34986037; PMCID: PMC9066235.
72: Liao C, Castonguay CE, Heilbron K, Vuokila V, Medeiros M, Houle G, Akçimen
F, Ross JP, Catoire H, Diez-Fairen M, Kang J, Mueller SH, Girard SL, Hopfner F,
Lorenz D, Clark LN, Soto-Beasley AI, Klebe S, Hallett M, Wszolek ZK, Pendziwiat
M, Lorenzo-Betancor O, Seppi K, Berg D, Vilariño-Güell C, Postuma RB, Bernard G,
Dupré N, Jankovic J, Testa CM, Ross OA, Arzberger T, Chouinard S, Louis ED,
Mandich P, Vitale C, Barone P, García-Martín E, Alonso-Navarro H, Agúndez JAG,
Jiménez-Jiménez FJ, Pastor P, Rajput A, Deuschl G, Kuhlenbaümer G, Meijer IA,
Dion PA, Rouleau GA; 23andMe Research Team. Association of Essential Tremor With
Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. JAMA Neurol.
2022 Feb 1;79(2):185-193. doi: 10.1001/jamaneurol.2021.4781. Erratum in: JAMA
Neurol. 2022 Jan 31;:null. PMID: 34982113; PMCID: PMC8728658.
73: Masnada S, Sarret C, Antonello CE, Fadilah A, Krude H, Mura E, Mordekar S,
Nicita F, Olivotto S, Orcesi S, Porta F, Remerand G, Siri B, Wilpert NM, Amir-
Yazdani P, Bertini E, Schuelke M, Bernard G, Boespflug-Tanguy O, Tonduti D.
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome. Mol Genet
Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec
16. PMID: 34969638.
74: Luo JXX, Cui QL, Yaqubi M, Hall JA, Dudley R, Srour M, Addour N, Jamann H,
Larochelle C, Blain M, Healy LM, Stratton JA, Sonnen JA, Kennedy TE, Antel JP.
Human Oligodendrocyte Myelination Potential; Relation to Age and
Differentiation. Ann Neurol. 2022 Feb;91(2):178-191. doi: 10.1002/ana.26288.
Epub 2022 Jan 10. PMID: 34952986.
75: Mercuri E, Deconinck N, Mazzone ES, Nascimento A, Oskoui M, Saito K,
Vuillerot C, Baranello G, Boespflug-Tanguy O, Goemans N, Kirschner J, Kostera-
Pruszczyk A, Servais L, Gerber M, Gorni K, Khwaja O, Kletzl H, Scalco RS,
Staunton H, Yeung WY, Martin C, Fontoura P, Day JW; SUNFISH Study Group. Safety
and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal
muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-
controlled trial. Lancet Neurol. 2022 Jan;21(1):42-52. doi:
10.1016/S1474-4422(21)00367-7. Erratum in: Lancet Neurol. 2022 Feb;21(2):e2.
Erratum in: Lancet Neurol. 2022 Mar;21(3):e3. Erratum in: Lancet Neurol. 2022
May;21(5):e5. PMID: 34942136.
76: Mirza AI, Zhu F, Knox N, Forbes JD, Van Domselaar G, Bernstein CN, Graham M,
Marrie RA, Hart J, Yeh EA, Arnold DL, Bar-Or A, O'Mahony J, Zhao Y, Hsiao W,
Banwell B, Waubant E, Tremlett H. Metagenomic Analysis of the Pediatric-Onset
Multiple Sclerosis Gut Microbiome. Neurology. 2022 Mar 8;98(10):e1050-e1063.
doi: 10.1212/WNL.0000000000013245. Epub 2021 Dec 22. PMID: 34937787; PMCID:
PMC8967388.
77: Howden K, Chapman S, Serletis D, Kazina C, Rafay MF, Faury D, Hazrati LN,
Jabado N, Vanan MI. Management of Inoperable Supra-Sellar Low-Grade Glioma With
BRAF Mutation in Young Children. Cureus. 2021 Nov 9;13(11):e19400. doi:
10.7759/cureus.19400. PMID: 34926002; PMCID: PMC8656291.
78: Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF,
Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal
M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ripke S, Ware EB,
Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford
S, Crow S, DiBlasi E, Duriez P, Fernández-Aranda F, Fichter MM, Gallinger S,
Glatt SJ, Gorwood P, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Jamain S,
Jiménez-Murcia S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL,
Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR,
Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Ramoz N, Roepke S, Rozanov
V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J,
Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Adolfsson R, Agartz I, Air
TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Soler Artigas
M, Van der Auwera S, Azevedo MH, Bass N, Bau CHD, Baune BT, Bellivier F, Berger
K, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Bosch R, Braff DL,
Bryant R, Budde M, Byrne EM, Cahn W, Casas M, Castelao E, Cervilla JA, Chaumette
B, Cichon S, Corvin A, Craddock N, Craig D, Degenhardt F, Djurovic S, Edenberg
HJ, Fanous AH, Foo JC, Forstner AJ, Frye M, Fullerton JM, Gatt JM, Gejman PV,
Giegling I, Grabe HJ, Green MJ, Grevet EH, Grigoroiu-Serbanescu M, Gutierrez B,
Guzman-Parra J, Hamilton SP, Hamshere ML, Hartmann A, Hauser J, Heilmann-
Heimbach S, Hoffmann P, Ising M, Jones I, Jones LA, Jonsson L, Kahn RS, Kelsoe
JR, Kendler KS, Kloiber S, Koenen KC, Kogevinas M, Konte B, Krebs MO, Landén M,
Lawrence J, Leboyer M, Lee PH, Levinson DF, Liao C, Lissowska J, Lucae S,
Mayoral F, McElroy SL, McGrath P, McGuffin P, McQuillin A, Medland SE, Mehta D,
Melle I, Milaneschi Y, Mitchell PB, Molina E, Morken G, Mortensen PB, Müller-
Myhsok B, Nievergelt C, Nimgaonkar V, Nöthen MM, O'Donovan MC, Ophoff RA, Owen
MJ, Pato C, Pato MT, Penninx BWJH, Pimm J, Pistis G, Potash JB, Power RA,
Preisig M, Quested D, Ramos-Quiroga JA, Reif A, Ribasés M, Richarte V, Rietschel
M, Rivera M, Roberts A, Roberts G, Rouleau GA, Rovaris DL, Rujescu D, Sánchez-
Mora C, Sanders AR, Schofield PR, Schulze TG, Scott LJ, Serretti A, Shi J, Shyn
SI, Sirignano L, Sklar P, Smeland OB, Smoller JW, Sonuga-Barke EJS, Spalletta G,
Strauss JS, Świątkowska B, Trzaskowski M, Turecki G, Vilar-Ribó L, Vincent JB,
Völzke H, Walters JTR, Shannon Weickert C, Weickert TW, Weissman MM, Williams
LM, Wray NR, Zai CC, Ashley-Koch AE, Beckham JC, Hauser ER, Hauser MA, Kimbrel
NA, Lindquist JH, McMahon B, Oslin DW, Qin X; Major Depressive Disorder Working
Group of the Psychiatric Genomics Consortium; Bipolar Disorder Working Group of
the Psychiatric Genomics Consortium; Eating Disorders Working Group of the
Psychiatric Genomics Consortium; German Borderline Genomics Consortium; MVP
Suicide Exemplar Workgroup; VA Million Veteran Program, Agerbo E, Børglum AD,
Breen G, Erlangsen A, Esko T, Gelernter J, Hougaard DM, Kessler RC, Kranzler HR,
Li QS, Martin NG, McIntosh AM, Mors O, Nordentoft M, Olsen CM, Porteous D,
Ursano RJ, Wasserman D, Werge T, Whiteman DC, Bulik CM, Coon H, Demontis D,
Docherty AR, Kuo PH, Lewis CM, Mann JJ, Rentería ME, Smith DJ, Stahl EA, Stein
MB, Streit F, Willour V, Ruderfer DM. Dissecting the Shared Genetic Architecture
of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol
Psychiatry. 2022 Feb 1;91(3):313-327. doi: 10.1016/j.biopsych.2021.05.029. Epub
2021 Sep 9. PMID: 34861974; PMCID: PMC8851871.
79: Moreau JT, Simard-Tremblay E, Albrecht S, Rosenblatt B, Baillet S, Dudley
RWR. Overnight Ictal Magnetoencephalography. Neurol Clin Pract. 2021
Oct;11(5):e732-e735. doi: 10.1212/CPJ.0000000000000937. PMID: 34840892; PMCID:
PMC8610549.
80: Tran TPY, Pouliot P, Assi EB, Rainville P, Myers KA, Robert M, Bouthillier
A, Keezer MR, Nguyen DK. Heart Rate Variability in Insulo-Opercular Epilepsy.
Brain Sci. 2021 Nov 13;11(11):1505. doi: 10.3390/brainsci11111505. PMID:
34827504; PMCID: PMC8615554.
81: Estiar MA, Lail N, Dyment DA, Varghaei P, Hartley T, Gillespie MK, Yoon G,
Boycott KM, Rouleau GA, Gan-Or Z. Heterozygous De Novo KPNA3 Mutations Cause
Complex Hereditary Spastic Paraplegia. Ann Neurol. 2022 May;91(5):730-732. doi:
10.1002/ana.26275. Epub 2021 Dec 14. PMID: 34825409.
82: Suchowersky O, Ashtiani S, Au PB, McLeod S, Estiar MA, Gan-Or Z, Rouleau GA.
Hereditary spastic paraplegia initially diagnosed as cerebral palsy. Clin Park
Relat Disord. 2021 Nov 3;5:100114. doi: 10.1016/j.prdoa.2021.100114. PMID:
34816117; PMCID: PMC8592889.
83: Sahly AN, Shevell M, Sadleir LG, Myers KA. SUDEP risk and autonomic
dysfunction in genetic epilepsies. Auton Neurosci. 2022 Jan;237:102907. doi:
10.1016/j.autneu.2021.102907. Epub 2021 Nov 10. PMID: 34773737.
84: Perrier S, Gauquelin L, Wambach JA, Bernard G. Distinguishing severe
phenotypes associated with pathogenic variants in POLR3A. Am J Med Genet A. 2022
Feb;188(2):708-712. doi: 10.1002/ajmg.a.62553. Epub 2021 Nov 12. PMID: 34773388;
PMCID: PMC8758552.
85: Geva M, Gershoni-Emek N, Naia L, Ly P, Mota S, Rego AC, Hayden MR, Levin LA.
Neuroprotection of retinal ganglion cells by the sigma-1 receptor agonist
pridopidine in models of experimental glaucoma. Sci Rep. 2021 Nov 9;11(1):21975.
doi: 10.1038/s41598-021-01077-w. PMID: 34753986; PMCID: PMC8578336.
86: Vears DF, Minion JT, Roberts SJ, Cummings J, Machirori M, Blell M, Budin-
Ljøsne I, Cowley L, Dyke SOM, Gaff C, Green R, Hall A, Johns AL, Knoppers BM,
Mulrine S, Patch C, Winkler E, Murtagh MJ. Return of individual research results
from genomic research: A systematic review of stakeholder perspectives. PLoS
One. 2021 Nov 8;16(11):e0258646. doi: 10.1371/journal.pone.0258646. PMID:
34748551; PMCID: PMC8575249.
87: Klostranec JM, Vucevic D, Bhatia KD, Kortman HGJ, Krings T, Murphy KP,
terBrugge KG, Mikulis DJ. Current Concepts in Intracranial Interstitial Fluid
Transport and the Glymphatic System: Part II-Imaging Techniques and Clinical
Applications. Radiology. 2021 Dec;301(3):516-532. doi:
10.1148/radiol.2021204088. Epub 2021 Oct 26. PMID: 34698564.
88: Lazow MA, Fuller C, DeWire M, Lane A, Bandopadhayay P, Bartels U, Bouffet E,
Cheng S, Cohen KJ, Cooney TM, Coven SL, Dholaria H, Diez B, Dorris K, El-Ayadi
M, El-Sheikh A, Fisher PG, Fonseca A, Garcia Lombardi M, Greiner RJ, Goldman S,
Gottardo N, Gururangan S, Hansford JR, Hassall T, Hawkins C, Kilburn L,
Koschmann C, Leary SE, Ma J, Minturn JE, Monje-Deisseroth M, Packer R, Samson Y,
Sandler ES, Sevlever G, Tinkle CL, Tsui K, Wagner LM, Zaghloul M, Ziegler DS,
Chaney B, Black K, Asher A, Drissi R, Fouladi M, Jones BV, Leach JL. Accuracy of
central neuro-imaging review of DIPG compared with histopathology in the
International DIPG Registry. Neuro Oncol. 2022 May 4;24(5):821-833. doi:
10.1093/neuonc/noab245. PMID: 34668975; PMCID: PMC9071293.
89: Klostranec JM, Vucevic D, Bhatia KD, Kortman HGJ, Krings T, Murphy KP,
terBrugge KG, Mikulis DJ. Current Concepts in Intracranial Interstitial Fluid
Transport and the Glymphatic System: Part I-Anatomy and Physiology. Radiology.
2021 Dec;301(3):502-514. doi: 10.1148/radiol.2021202043. Epub 2021 Oct 19. PMID:
34665028.
90: Bhatia KD, Lee H, Kortman H, Klostranec J, Guest W, Wälchli T, Radovanovic
I, Krings T, Pereira VM. Endovascular Management of Intracranial Dural AVFs:
Transvenous Approach. AJNR Am J Neuroradiol. 2022 Apr;43(4):510-516. doi:
10.3174/ajnr.A7300. Epub 2021 Oct 14. PMID: 34649915; PMCID: PMC8993200.
91: Munot P, McCrea N, Torelli S, Manzur A, Sewry C, Chambers D, Feng L, Ala P,
Zaharieva I, Ragge N, Roper H, Marton T, Cox P, Milev MP, Liang WC, Maruyama S,
Nishino I, Sacher M, Phadke R, Muntoni F. TRAPPC11-related muscular dystrophy
with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain.
Neuropathol Appl Neurobiol. 2022 Feb;48(2):e12771. doi: 10.1111/nan.12771. Epub
2021 Nov 11. PMID: 34648194.
92: Ashour M, Fortin O, Parent L, Sébire G, Saint-Martin C, Poulin C, Dudley R.
Hirayama Disease in a Patient with a History of Late-Onset Symptomatic Vein of
Galen Aneurysmal Malformation. Pediatr Neurosurg. 2021;56(6):555-562. doi:
10.1159/000519178. Epub 2021 Oct 11. PMID: 34634788.
93: Schur S, Moreau JT, Khoo HM, Koupparis A, Simard Tremblay E, Myers KA,
Osterman B, Rosenblatt B, Farmer JP, Saint-Martin C, Turpin S, Hall J, Olivier
A, Bernasconi A, Bernasconi N, Baillet S, Dubeau F, Gotman J, Dudley RWR. New
interinstitutional, multimodal presurgical evaluation protocol associated with
improved seizure freedom for poorly defined cases of focal epilepsy in children.
J Neurosurg Pediatr. 2021 Oct 8;29(1):74-82. doi: 10.3171/2021.6.PEDS218. PMID:
34624842.
94: Wang S, Sun MZ, Abecassis IJ, Weil AG, Ibrahim GM, Fallah A, Ene C, Leary
SES, Cole BL, Lockwood CM, Olson JM, Geyer JR, Ellenbogen RG, Ojemann JG, Wang
AC. Predictors of mortality and tumor recurrence in desmoplastic infantile
ganglioglioma and astrocytoma-and individual participant data meta-analysis
(IPDMA). J Neurooncol. 2021 Nov;155(2):155-163. doi: 10.1007/s11060-021-03860-1.
Epub 2021 Oct 6. PMID: 34613581; PMCID: PMC9448015.
95: Lemire G, Ito YA, Marshall AE, Chrestian N, Stanley V, Brady L, Tarnopolsky
M, Curry CJ, Hartley T, Mears W, Derksen A, Rioux N, Laflamme N, Hutchison HT,
Pais LS, Zaki MS, Sultan T, Dane AD; Care4Rare Canada Consortium, Gleeson JG,
Vaz FM, Kernohan KD, Bernard G, Boycott KM. ABHD16A deficiency causes a
complicated form of hereditary spastic paraplegia associated with intellectual
disability and cerebral anomalies. Am J Hum Genet. 2021 Oct 7;108(10):2017-2023.
doi: 10.1016/j.ajhg.2021.09.005. Epub 2021 Sep 28. PMID: 34587489; PMCID:
PMC8546048.
96: Abdul Jafar NK, Tham EKH, Pang WW, Fok D, Chua MC, Teoh OH, Goh DYT, Shek
LP, Yap F, Tan KH, Gluckman PD, Chong YS, Meaney MJ, Broekman BFP, Cai S.
Association between breastfeeding and sleep patterns in infants and preschool
children. Am J Clin Nutr. 2021 Dec 1;114(6):1986-1996. doi:
10.1093/ajcn/nqab297. PMID: 34582549.
97: Myers KA, Scheffer IE. Precision Medicine Approaches for Infantile-Onset
Developmental and Epileptic Encephalopathies. Annu Rev Pharmacol Toxicol. 2022
Jan 6;62:641-662. doi: 10.1146/annurev-pharmtox-052120-084449. Epub 2021 Sep 27.
PMID: 34579535.
98: Kalantar-Hormozi A, Moradi E, Hashemi SZ, Kalantar-Hormozi H, Abbaszadeh-
Kasbi A. The Effect of Using In Vitro Fertilization (IVF) on Increasing the
Prevalence of Craniosynostosis. J Craniofac Surg. 2022 Jan-Feb 01;33(1):26-28.
doi: 10.1097/SCS.0000000000008188. PMID: 34545049.
99: Larivière S, Federico P, Chinvarun Y, Jackson G, Morgan V, Rampp S, Vaudano
AE, Wang I, Cendes F, Boelman CG, Bernasconi A, Bernasconi N, Bernhardt BC,
Schrader DV. ILAE Neuroimaging Task Force Highlight: harnessing optimized
imaging protocols for drug-resistant childhood epilepsy. Epileptic Disord. 2021
Oct 1;23(5):675-681. doi: 10.1684/epd.2021.1312. PMID: 34526291.
100: Fallah A, Lewis E, Ibrahim GM, Kola O, Tseng CH, Harris WB, Chen JS, Lin
KM, Cai LX, Liu QZ, Lin JL, Zhou WJ, Mathern GW, Smyth MD, O'Neill BR, Dudley
RWR, Ragheb J, Bhatia S, Delev D, Ramantani G, Zentner J, Wang AC, Dorfer C,
Feucht M, Czech T, Bollo RJ, Issabekov G, Zhu H, Connolly M, Steinbok P, Zhang
JG, Zhang K, Hidalgo ET, Weiner HL, Wong-Kisiel L, Lapalme-Remis S, Tripathi M,
Sarat Chandra P, Hader W, Wang FP, Yao Y, Champagne PO, Brunette-Clément T, Guo
Q, Li SC, Budke M, Pérez-Jiménez MA, Raftopoulos C, Finet P, Michel P, Schaller
K, Stienen MN, Baro V, Cantillano Malone C, Pociecha J, Chamorro N, Muro VL, von
Lehe M, Vieker S, Oluigbo C, Gaillard WD, Al-Khateeb M, Al Otaibi F, Krayenbühl
N, Bolton J, Pearl PL, Weil AG. Comparison of the real-world effectiveness of
vertical versus lateral functional hemispherotomy techniques for pediatric drug-
resistant epilepsy: A post hoc analysis of the HOPS study. Epilepsia. 2021
Nov;62(11):2707-2718. doi: 10.1111/epi.17021. Epub 2021 Sep 12. PMID: 34510448;
PMCID: PMC9290517.
101: Johnson JO, Chia R, Miller DE, Li R, Kumaran R, Abramzon Y, Alahmady N,
Renton AE, Topp SD, Gibbs JR, Cookson MR, Sabir MS, Dalgard CL, Troakes C, Jones
AR, Shatunov A, Iacoangeli A, Al Khleifat A, Ticozzi N, Silani V, Gellera C,
Blair IP, Dobson-Stone C, Kwok JB, Bonkowski ES, Palvadeau R, Tienari PJ,
Morrison KE, Shaw PJ, Al-Chalabi A, Brown RH Jr, Calvo A, Mora G, Al-Saif H,
Gotkine M, Leigh F, Chang IJ, Perlman SJ, Glass I, Scott AI, Shaw CE, Basak AN,
Landers JE, Chiò A, Crawford TO, Smith BN, Traynor BJ; FALS Sequencing
Consortium; American Genome Center; International ALS Genomics Consortium; and
ITALSGEN Consortium, Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp SD, Scotter
EL, Kenna KP, Keagle P, Tiloca C, Vance C, Troakes C, Colombrita C, King A,
Pensato V, Castellotti B, Baas F, Ten Asbroek ALMA, McKenna-Yasek D, McLaughlin
RL, Polak M, Asress S, Esteban-Pérez J, Stevic Z, D'Alfonso S, Mazzini L, Comi
GP, Del Bo R, Ceroni M, Gagliardi S, Querin G, Bertolin C, van Rheenen W,
Rademakers R, van Blitterswijk M, Lauria G, Duga S, Corti S, Cereda C, Corrado
L, Sorarù G, Williams KL, Nicholson GA, Blair IP, Leblond-Manry C, Rouleau GA,
Hardiman O, Morrison KE, Veldink JH, van den Berg LH, Al-Chalabi A, Pall H, Shaw
PJ, Turner MR, Talbot K, Taroni F, García-Redondo A, Wu Z, Glass JD, Gellera C,
Ratti A, Brown RH Jr, Silani V, Shaw CE, Landers JE, Dalgard CL, Adeleye A,
Soltis AR, Alba C, Viollet C, Bacikova D, Hupalo DN, Sukumar G, Pollard HB,
Wilkerson MD, Martinez EM, Abramzon Y, Ahmed S, Arepalli S, Baloh RH, Bowser R,
Brady CB, Brice A, Broach J, Campbell RH, Camu W, Chia R, Cooper-Knock J, Ding
J, Drepper C, Drory VE, Dunckley TL, Eicher JD, England BK, Faghri F, Feldman E,
Floeter MK, Fratta P, Geiger JT, Gerhard G, Gibbs JR, Gibson SB, Glass JD, Hardy
J, Harms MB, Heiman-Patterson TD, Hernandez DG, Jansson L, Kirby J, Kowall NW,
Laaksovirta H, Landeck N, Landi F, Le Ber I, Lumbroso S, MacGowan DJL, Maragakis
NJ, Mora G, Mouzat K, Murphy NA, Myllykangas L, Nalls MA, Orrell RW, Ostrow LW,
Pamphlett R, Pickering-Brown S, Pioro EP, Pletnikova O, Pliner HA, Pulst SM,
Ravits JM, Renton AE, Rivera A, Robberecht W, Rogaeva E, Rollinson S, Rothstein
JD, Scholz SW, Sendtner M, Shaw PJ, Sidle KC, Simmons Z, Singleton AB, Smith N,
Stone DJ, Tienari PJ, Troncoso JC, Valori M, Van Damme P, Van Deerlin VM, Van
Den Bosch L, Zinman L, Landers JE, Chiò A, Traynor BJ, Angelocola SM, Ausiello
FP, Barberis M, Bartolomei I, Battistini S, Bersano E, Bisogni G, Borghero G,
Brunetti M, Cabona C, Calvo A, Canale F, Canosa A, Cantisani TA, Capasso M,
Caponnetto C, Cardinali P, Carrera P, Casale F, Chiò A, Colletti T, Conforti FL,
Conte A, Conti E, Corbo M, Cuccu S, Dalla Bella E, D'Errico E, DeMarco G,
Dubbioso R, Ferrarese C, Ferraro PM, Filippi M, Fini N, Floris G, Fuda G,
Gallone S, Gianferrari G, Giannini F, Grassano M, Greco L, Iazzolino B, Introna
A, La Bella V, Lattante S, Lauria G, Liguori R, Logroscino G, Logullo FO,
Lunetta C, Mandich P, Mandrioli J, Manera U, Manganelli F, Marangi G, Marinou K,
Marrosu MG, Martinelli I, Messina S, Moglia C, Mora G, Mosca L, Murru MR,
Origone P, Passaniti C, Petrelli C, Petrucci A, Pozzi S, Pugliatti M, Quattrini
A, Ricci C, Riolo G, Riva N, Russo M, Sabatelli M, Salamone P, Salivetto M,
Salvi F, Santarelli M, Sbaiz L, Sideri R, Simone I, Simonini C, Spataro R, Tanel
R, Tedeschi G, Ticca A, Torriello A, Tranquilli S, Tremolizzo L, Trojsi F, Vasta
R, Vacchiano V, Vita G, Volanti P, Zollino M, Zucchi E. Association of Variants
in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. JAMA Neurol.
2021 Oct 1;78(10):1236-1248. doi: 10.1001/jamaneurol.2021.2598. PMID: 34459874;
PMCID: PMC8406220.
102: Helman G, Mendes MI, Nicita F, Darbelli L, Sherbini O, Moore T, Derksen A,
Amy Pizzino, Carrozzo R, Torraco A, Catteruccia M, Aiello C, Goffrini P,
Figuccia S, Smith DEC, Hadzsiev K, Hahn A, Biskup S, Brösse I, Kotzaeridou U,
Gauck D, Grebe TA, Elmslie F, Stals K, Gupta R, Bertini E, Thiffault I, Taft RJ,
Schiffmann R, Brandl U, Haack TB, Salomons GS, Simons C, Bernard G, van der
Knaap MS, Vanderver A, Husain RA. Expanded phenotype of AARS1-related white
matter disease. Genet Med. 2021 Dec;23(12):2352-2359. doi:
10.1038/s41436-021-01286-8. Epub 2021 Aug 27. PMID: 34446925.
103: Levitis E, van Praag CDG, Gau R, Heunis S, DuPre E, Kiar G, Bottenhorn KL,
Glatard T, Nikolaidis A, Whitaker KJ, Mancini M, Niso G, Afyouni S, Alonso-Ortiz
E, Appelhoff S, Arnatkeviciute A, Atay SM, Auer T, Baracchini G, Bayer JMM,
Beauvais MJS, Bijsterbosch JD, Bilgin IP, Bollmann S, Bollmann S, Botvinik-Nezer
R, Bright MG, Calhoun VD, Chen X, Chopra S, Chuan-Peng H, Close TG, Cookson SL,
Craddock RC, De La Vega A, De Leener B, Demeter DV, Di Maio P, Dickie EW,
Eickhoff SB, Esteban O, Finc K, Frigo M, Ganesan S, Ganz M, Garner KG, Garza-
Villarreal EA, Gonzalez-Escamilla G, Goswami R, Griffiths JD, Grootswagers T,
Guay S, Guest O, Handwerker DA, Herholz P, Heuer K, Huijser DC, Iacovella V,
Joseph MJE, Karakuzu A, Keator DB, Kobeleva X, Kumar M, Laird AR, Larson-Prior
LJ, Lautarescu A, Lazari A, Legarreta JH, Li XY, Lv J, Mansour L S, Meunier D,
Moraczewski D, Nandi T, Nastase SA, Nau M, Noble S, Norgaard M, Obungoloch J,
Oostenveld R, Orchard ER, Pinho AL, Poldrack RA, Qiu A, Raamana PR, Rokem A,
Rutherford S, Sharan M, Shaw TB, Syeda WT, Testerman MM, Toro R, Valk SL, Van
Den Bossche S, Varoquaux G, Váša F, Veldsman M, Vohryzek J, Wagner AS, Walsh RJ,
White T, Wong FT, Xie X, Yan CG, Yang YF, Yee Y, Zanitti GE, Van Gulick AE, Duff
E, Maumet C. Centering inclusivity in the design of online conferences-An OHBM-
Open Science perspective. Gigascience. 2021 Aug 20;10(8):giab051. doi:
10.1093/gigascience/giab051. PMID: 34414422; PMCID: PMC8377301.
104: Bastard P, Gervais A, Le Voyer T, Rosain J, Philippot Q, Manry J,
Michailidis E, Hoffmann HH, Eto S, Garcia-Prat M, Bizien L, Parra-Martínez A,
Yang R, Haljasmägi L, Migaud M, Särekannu K, Maslovskaja J, de Prost N,
Tandjaoui-Lambiotte Y, Luyt CE, Amador-Borrero B, Gaudet A, Poissy J, Morel P,
Richard P, Cognasse F, Troya J, Trouillet-Assant S, Belot A, Saker K, Garçon P,
Rivière JG, Lagier JC, Gentile S, Rosen LB, Shaw E, Morio T, Tanaka J, Dalmau D,
Tharaux PL, Sene D, Stepanian A, Megarbane B, Triantafyllia V, Fekkar A, Heath
JR, Franco JL, Anaya JM, Solé-Violán J, Imberti L, Biondi A, Bonfanti P,
Castagnoli R, Delmonte OM, Zhang Y, Snow AL, Holland SM, Biggs C, Moncada-Vélez
M, Arias AA, Lorenzo L, Boucherit S, Coulibaly B, Anglicheau D, Planas AM,
Haerynck F, Duvlis S, Nussbaum RL, Ozcelik T, Keles S, Bousfiha AA, El Bakkouri
J, Ramirez-Santana C, Paul S, Pan-Hammarström Q, Hammarström L, Dupont A,
Kurolap A, Metz CN, Aiuti A, Casari G, Lampasona V, Ciceri F, Barreiros LA,
Dominguez-Garrido E, Vidigal M, Zatz M, van de Beek D, Sahanic S, Tancevski I,
Stepanovskyy Y, Boyarchuk O, Nukui Y, Tsumura M, Vidaur L, Tangye SG, Burrel S,
Duffy D, Quintana-Murci L, Klocperk A, Kann NY, Shcherbina A, Lau YL, Leung D,
Coulongeat M, Marlet J, Koning R, Reyes LF, Chauvineau-Grenier A, Venet F,
Monneret G, Nussenzweig MC, Arrestier R, Boudhabhay I, Baris-Feldman H, Hagin D,
Wauters J, Meyts I, Dyer AH, Kennelly SP, Bourke NM, Halwani R, Sharif-Askari
NS, Dorgham K, Sallette J, Sedkaoui SM, AlKhater S, Rigo-Bonnin R, Morandeira F,
Roussel L, Vinh DC, Ostrowski SR, Condino-Neto A, Prando C, Bonradenko A, Spaan
AN, Gilardin L, Fellay J, Lyonnet S, Bilguvar K, Lifton RP, Mane S; HGID Lab;
COVID Clinicians; COVID-STORM Clinicians; NIAID Immune Response to COVID Group;
NH-COVAIR Study Group; Danish CHGE; Danish Blood Donor Study; St. James's
Hospital; SARS CoV2 Interest group; French COVID Cohort Study Group; Imagine
COVID-Group; Milieu Intérieur Consortium; CoV-Contact Cohort; Amsterdam UMC
Covid-19; Biobank Investigators; COVID Human Genetic Effort; CONSTANCES cohort;
3C-Dijon Study; Cerba Health-Care; Etablissement du Sang study group, Anderson
MS, Boisson B, Béziat V, Zhang SY, Vandreakos E, Hermine O, Pujol A, Peterson P,
Mogensen TH, Rowen L, Mond J, Debette S, de Lamballerie X, Duval X, Mentré F,
Zins M, Soler-Palacin P, Colobran R, Gorochov G, Solanich X, Susen S, Martinez-
Picado J, Raoult D, Vasse M, Gregersen PK, Piemonti L, Rodríguez-Gallego C,
Notarangelo LD, Su HC, Kisand K, Okada S, Puel A, Jouanguy E, Rice CM,
Tiberghien P, Zhang Q, Cobat A, Abel L, Casanova JL. Autoantibodies neutralizing
type I IFNs are present in ~4% of uninfected individuals over 70 years
old and account for ~20% of COVID-19 deaths. Sci Immunol. 2021 Aug
19;6(62):eabl4340. doi: 10.1126/sciimmunol.abl4340. PMID: 34413139; PMCID:
PMC8521484.
105: Koupparis A, von Ellenrieder N, Khoo HM, Zazubovits N, Nguyen DK, Hall JA,
Dudley RWR, Dubeau F, Gotman J. Association of EEG-fMRI Responses and Outcome
After Epilepsy Surgery. Neurology. 2021 Aug 16;97(15):e1523–36. doi:
10.1212/WNL.0000000000012660. Epub ahead of print. PMID: 34400584; PMCID:
PMC8575131.
106: Zhang M, Wong SW, Wright JN, Toescu S, Mohammadzadeh M, Han M, Lummus S,
Wagner MW, Yecies D, Lai H, Eghbal A, Radmanesh A, Nemelka J, Harward S,
Malinzak M, Laughlin S, Perreault S, Braun KRM, Vossough A, Poussaint T, Goetti
R, Ertl-Wagner B, Ho CY, Oztekin O, Ramaswamy V, Mankad K, Vitanza NA, Cheshier
SH, Said M, Aquilina K, Thompson E, Jaju A, Grant GA, Lober RM, Yeom KW. Machine
Assist for Pediatric Posterior Fossa Tumor Diagnosis: A Multinational Study.
Neurosurgery. 2021 Oct 13;89(5):892-900. doi: 10.1093/neuros/nyab311. PMID:
34392363; PMCID: PMC8764569.
107: Galosi S, Edani BH, Martinelli S, Hansikova H, Eklund EA, Caputi C,
Masuelli L, Corsten-Janssen N, Srour M, Oegema R, Bosch DGM, Ellis CA, Amlie-
Wolf L, Accogli A, Atallah I, Averdunk L, Barañano KW, Bei R, Bagnasco I, Brusco
A, Demarest S, Alaix AS, Di Bonaventura C, Distelmaier F, Elmslie F, Gan-Or Z,
Good JM, Gripp K, Kamsteeg EJ, Macnamara E, Marcelis C, Mercier N, Peeden J,
Pizzi S, Pannone L, Shinawi M, Toro C, Verbeek NE, Venkateswaran S, Wheeler PG,
Zdrazilova L, Zhang R, Zorzi G, Guerrini R, Sessa WC, Lefeber DJ, Tartaglia M,
Hamdan FF, Grabińska KA, Leuzzi V. De novo DHDDS variants cause a
neurodevelopmental and neurodegenerative disorder with myoclonus. Brain. 2022
Mar 29;145(1):208-223. doi: 10.1093/brain/awab299. PMID: 34382076; PMCID:
PMC8967098.
108: Vitagliano M, Dunbar M, Dyck Holzinger S, Letourneau N, Dewey D, Oskoui M,
Shevell M, Kirton A. Perinatal arterial ischemic stroke and periventricular
venous infarction in infants with unilateral cerebral palsy. Dev Med Child
Neurol. 2022 Jan;64(1):56-62. doi: 10.1111/dmcn.15000. Epub 2021 Aug 10. PMID:
34374437.
109: Sievers P, Henneken SC, Blume C, Sill M, Schrimpf D, Stichel D,
Okonechnikov K, Reuss DE, Benzel J, Maaß KK, Kool M, Sturm D, Zheng T, Ghasemi
DR, Kohlhof-Meinecke P, Cruz O, Suñol M, Lavarino C, Ruf V, Boldt HB, Pagès M,
Pouget C, Schweizer L, Kranendonk MEG, Akhtar N, Bunkowski S, Stadelmann C,
Schüller U, Mueller WC, Dohmen H, Acker T, Harter PN, Mawrin C, Beschorner R,
Brandner S, Snuderl M, Abdullaev Z, Aldape K, Gilbert MR, Armstrong TS, Ellison
DW, Capper D, Ichimura K, Reifenberger G, Grundy RG, Jabado N, Krskova L,
Zapotocky M, Vicha A, Varlet P, Wesseling P, Rutkowski S, Korshunov A, Wick W,
Pfister SM, Jones DTW, von Deimling A, Pajtler KW, Sahm F. Recurrent fusions in
PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial
tumors. Acta Neuropathol. 2021 Nov;142(5):827-839. doi:
10.1007/s00401-021-02356-6. Epub 2021 Aug 5. PMID: 34355256; PMCID: PMC8500895.
110: Myers KA. Response: Sotos Syndrome and the added value of genetic workup in
epilepsy surgery. Epilepsia Open. 2021 Dec;6(4):795-796. doi:
10.1002/epi4.12528. Epub 2021 Aug 5. PMID: 34351709; PMCID: PMC8633461.
111: Gleichgerrcht E, Munsell BC, Alhusaini S, Alvim MKM, Bargalló N, Bender B,
Bernasconi A, Bernasconi N, Bernhardt B, Blackmon K, Caligiuri ME, Cendes F,
Concha L, Desmond PM, Devinsky O, Doherty CP, Domin M, Duncan JS, Focke NK,
Gambardella A, Gong B, Guerrini R, Hatton SN, Kälviäinen R, Keller SS, Kochunov
P, Kotikalapudi R, Kreilkamp BAK, Labate A, Langner S, Larivière S, Lenge M, Lui
E, Martin P, Mascalchi M, Meletti S, O'Brien TJ, Pardoe HR, Pariente JC, Xian
Rao J, Richardson MP, Rodríguez-Cruces R, Rüber T, Sinclair B, Soltanian-Zadeh
H, Stein DJ, Striano P, Taylor PN, Thomas RH, Elisabetta Vaudano A, Vivash L,
von Podewills F, Vos SB, Weber B, Yao Y, Lin Yasuda C, Zhang J, Thompson PM,
Sisodiya SM, McDonald CR, Bonilha L; ENIGMA-Epilepsy Working Group. Artificial
intelligence for classification of temporal lobe epilepsy with ROI-level MRI
data: A worldwide ENIGMA-Epilepsy study. Neuroimage Clin. 2021;31:102765. doi:
10.1016/j.nicl.2021.102765. Epub 2021 Jul 24. PMID: 34339947; PMCID: PMC8346685.
112: Nowicki M, Bourgeois-Tardif S, Diaz PL, Hebert FO, Sanon NT, Champagne PO,
Major P, Sell E, Bitton J, Lewis E, Weil AG. Potential Benefit of Add-on
Δ9-Tetrahydrocannabinol in Pediatric Drug-Resistant Epilepsy: A Case Series. Can
J Neurol Sci. 2022 Jul;49(4):595-597. doi: 10.1017/cjn.2021.151. Epub 2021 Jun
29. PMID: 34183079.
113: Minato E, Myers KA. Age-related evolution of EEG in Dravet syndrome: Meta-
analysis of 155 patients. Seizure. 2021 Oct;91:108-111. doi:
10.1016/j.seizure.2021.06.007. Epub 2021 Jun 11. PMID: 34147886.
114: Erker C, Lane A, Chaney B, Leary S, Minturn JE, Bartels U, Packer RJ,
Dorris K, Gottardo NG, Warren KE, Broniscer A, Kieran MW, Zhu X, White P,
Dexheimer PJ, Black K, Asher A, DeWire M, Hansford JR, Gururangan S, Nazarian J,
Ziegler DS, Sandler E, Bartlett A, Goldman S, Shih CS, Hassall T, Dholaria H,
Bandopadhayay P, Samson Y, Monje M, Fisher PG, Dodgshun A, Parkin S,
Chintagumpala M, Tsui K, Gass D, Larouche V, Broxson E, Garcia Lombardi M, Wang
SS, Ma J, Hawkins C, Hamideh D, Wagner L, Koschmann C, Fuller C, Drissi R, Jones
BV, Leach J, Fouladi M. Characteristics of patients ≥10 years of age with
diffuse intrinsic pontine glioma: a report from the International DIPG/DMG
Registry. Neuro Oncol. 2022 Jan 5;24(1):141-152. doi: 10.1093/neuonc/noab140.
PMID: 34114629; PMCID: PMC8730773.
115: Tremblay-Laganière C, Maroofian R, Nguyen TTM, Karimiani EG, Kirmani S,
Akbar F, Ibrahim S, Afroze B, Doosti M, Ashrafzadeh F, Babaei M, Efthymiou S,
Christoforou M, Sultan T, Ladda RL, McLaughlin HM, Truty R, Mahida S, Cohen JS,
Baranano K, Ismail FY, Patel MS, Lehman A, Edmondson AC, Nagy A, Walker MA,
Mercimek-Andrews S, Maki Y, Sachdev R, Macintosh R, Palmer EE, Mancini GMS,
Barakat TS, Steinfeld R, Rüsch CT, Stettner GM, Wagner M, Wortmann SB, Kini U,
Brady AF, Stals KL, Ismayilova N, Ellard S, Bernardo D, Nugent K, McLean SD,
Antonarakis SE, Houlden H, Kinoshita T, Campeau PM, Murakami Y. PIGG variant
pathogenicity assessment reveals characteristic features within 19 families.
Genet Med. 2021 Oct;23(10):1873-1881. doi: 10.1038/s41436-021-01215-9. Epub 2021
Jun 10. PMID: 34113002.
116: Oskoui M, Gonorazky H, McMillan HJ, Dowling JJ, Amin R, Gagnon C, Selby K.
Guidance on Gene Replacement Therapy in Spinal Muscular Atrophy: A Canadian
Perspective. Can J Neurol Sci. 2022 May;49(3):398-401. doi:
10.1017/cjn.2021.125. Epub 2021 Jun 4. PMID: 34082851.
117: Bouhadoun S, Poulin C, Berrahmoune S, Myers KA. A retrospective analysis of
memantine use in a pediatric neurology clinic. Brain Dev. 2021
Nov;43(10):997-1003. doi: 10.1016/j.braindev.2021.05.012. Epub 2021 May 29.
PMID: 34074563.
118: Donovan LK, Delaidelli A, Joseph SK, Bielamowicz K, Fousek K, Holgado BL,
Manno A, Srikanthan D, Gad AZ, Van Ommeren R, Przelicki D, Richman C, Ramaswamy
V, Daniels C, Pallota JG, Douglas T, Joynt ACM, Haapasalo J, Nor C, Vladoiu MC,
Kuzan-Fischer CM, Garzia L, Mack SC, Varadharajan S, Baker ML, Hendrikse L, Ly
M, Kharas K, Balin P, Wu X, Qin L, Huang N, Stucklin AG, Morrissy AS, Cavalli
FMG, Luu B, Suarez R, De Antonellis P, Michealraj A, Rastan A, Hegde M, Komosa
M, Sirbu O, Kumar SA, Abdullaev Z, Faria CC, Yip S, Hukin J, Tabori U, Hawkins
C, Aldape K, Daugaard M, Maris JM, Sorensen PH, Ahmed N, Taylor MD. Author
Correction: Locoregional delivery of CAR T cells to the cerebrospinal fluid for
treatment of metastatic medulloblastoma and ependymoma. Nat Med. 2021
Jun;27(6):1117-1120. doi: 10.1038/s41591-021-01362-1. Erratum for: Nat Med. 2020
May;26(5):720-731. PMID: 34045740.
119: Spinella PC, El Kassar N, Cap AP, Kindzelski AL, Almond CS, Barkun A,
Gernsheimer TB, Goldstein JN, Holcomb JB, Iorio A, Jensen DM, Key NS, Levy JH,
Mayer SA, Moore EE, Stanworth SJ, Lewis RJ, Steiner ME; Hemostasis Trials
Outcomes Working Group. Recommended primary outcomes for clinical trials
evaluating hemostatic blood products and agents in patients with bleeding:
Proceedings of a National Heart Lung and Blood Institute and US Department of
Defense Consensus Conference. J Trauma Acute Care Surg. 2021 Aug 1;91(2S Suppl
2):S19-S25. doi: 10.1097/TA.0000000000003300. PMID: 34039915; PMCID: PMC9032809.
120: Fortin O, Vincelette C, Khan AQ, Berrahmoune S, Dassi C, Karimi M, Scheffer
IE, Lu J, Davis K, Myers KA. Seizures in Sotos syndrome: Phenotyping in 49
patients. Epilepsia Open. 2021 Jun;6(2):425-430. doi: 10.1002/epi4.12484. Epub
2021 Apr 9. PMID: 34033256; PMCID: PMC8166795.
121: Garbin M, Bertolizio G, Portela DA. Thoracic paravertebral block for an
opioid-free thoracotomy in a dog. Vet Anaesth Analg. 2021 Jul;48(4):622-623.
doi: 10.1016/j.vaa.2021.03.004. Epub 2021 Mar 20. PMID: 34006494.
122: Pathak R, Zin F, Thomas C, Bens S, Gayden T, Karamchandani J, Dudley RW,
Nemes K, Johann PD, Oyen F, Kordes U, Jabado N, Siebert R, Paulus W, Kool M,
Frühwald MC, Albrecht S, Kalpana GV, Hasselblatt M. Inhibition of nuclear export
restores nuclear localization and residual tumor suppressor function of
truncated SMARCB1/INI1 protein in a molecular subset of atypical
teratoid/rhabdoid tumors. Acta Neuropathol. 2021 Aug;142(2):361-374. doi:
10.1007/s00401-021-02328-w. Epub 2021 May 18. PMID: 34003336; PMCID: PMC8270878.
123: Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als
TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars
SP, Ikeda M, Kamitaki N, Kim M, Krebs K, Panagiotaropoulou G, Schilder BM,
Sloofman LG, Steinberg S, Trubetskoy V, Winsvold BS, Won HH, Abramova L, Adorjan
K, Agerbo E, Al Eissa M, Albani D, Alliey-Rodriguez N, Anjorin A, Antilla V,
Antoniou A, Awasthi S, Baek JH, Bækvad-Hansen M, Bass N, Bauer M, Beins EC,
Bergen SE, Birner A, Bøcker Pedersen C, Bøen E, Boks MP, Bosch R, Brum M,
Brumpton BM, Brunkhorst-Kanaan N, Budde M, Bybjerg-Grauholm J, Byerley W, Cairns
M, Casas M, Cervantes P, Clarke TK, Cruceanu C, Cuellar-Barboza A, Cunningham J,
Curtis D, Czerski PM, Dale AM, Dalkner N, David FS, Degenhardt F, Djurovic S,
Dobbyn AL, Douzenis A, Elvsåshagen T, Escott-Price V, Ferrier IN, Fiorentino A,
Foroud TM, Forty L, Frank J, Frei O, Freimer NB, Frisén L, Gade K, Garnham J,
Gelernter J, Giørtz Pedersen M, Gizer IR, Gordon SD, Gordon-Smith K, Greenwood
TA, Grove J, Guzman-Parra J, Ha K, Haraldsson M, Hautzinger M, Heilbronner U,
Hellgren D, Herms S, Hoffmann P, Holmans PA, Huckins L, Jamain S, Johnson JS,
Kalman JL, Kamatani Y, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M,
Koromina M, Kranz TM, Kranzler HR, Kubo M, Kupka R, Kushner SA, Lavebratt C,
Lawrence J, Leber M, Lee HJ, Lee PH, Levy SE, Lewis C, Liao C, Lucae S, Lundberg
M, MacIntyre DJ, Magnusson SH, Maier W, Maihofer A, Malaspina D, Maratou E,
Martinsson L, Mattheisen M, McCarroll SA, McGregor NW, McGuffin P, McKay JD,
Medeiros H, Medland SE, Millischer V, Montgomery GW, Moran JL, Morris DW,
Mühleisen TW, O'Brien N, O'Donovan C, Olde Loohuis LM, Oruc L, Papiol S,
Pardiñas AF, Perry A, Pfennig A, Porichi E, Potash JB, Quested D, Raj T,
Rapaport MH, DePaulo JR, Regeer EJ, Rice JP, Rivas F, Rivera M, Roth J, Roussos
P, Ruderfer DM, Sánchez-Mora C, Schulte EC, Senner F, Sharp S, Shilling PD,
Sigurdsson E, Sirignano L, Slaney C, Smeland OB, Smith DJ, Sobell JL, Søholm
Hansen C, Soler Artigas M, Spijker AT, Stein DJ, Strauss JS, Świątkowska B,
Terao C, Thorgeirsson TE, Toma C, Tooney P, Tsermpini EE, Vawter MP, Vedder H,
Walters JTR, Witt SH, Xi S, Xu W, Yang JMK, Young AH, Young H, Zandi PP, Zhou H,
Zillich L; HUNT All-In Psychiatry, Adolfsson R, Agartz I, Alda M, Alfredsson L,
Babadjanova G, Backlund L, Baune BT, Bellivier F, Bengesser S, Berrettini WH,
Blackwood DHR, Boehnke M, Børglum AD, Breen G, Carr VJ, Catts S, Corvin A,
Craddock N, Dannlowski U, Dikeos D, Esko T, Etain B, Ferentinos P, Frye M,
Fullerton JM, Gawlik M, Gershon ES, Goes FS, Green MJ, Grigoroiu-Serbanescu M,
Hauser J, Henskens F, Hillert J, Hong KS, Hougaard DM, Hultman CM, Hveem K,
Iwata N, Jablensky AV, Jones I, Jones LA, Kahn RS, Kelsoe JR, Kirov G, Landén M,
Leboyer M, Lewis CM, Li QS, Lissowska J, Lochner C, Loughland C, Martin NG,
Mathews CA, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Michie P,
Milani L, Mitchell PB, Morken G, Mors O, Mortensen PB, Mowry B, Müller-Myhsok B,
Myers RM, Neale BM, Nievergelt CM, Nordentoft M, Nöthen MM, O'Donovan MC,
Oedegaard KJ, Olsson T, Owen MJ, Paciga SA, Pantelis C, Pato C, Pato MT,
Patrinos GP, Perlis RH, Posthuma D, Ramos-Quiroga JA, Reif A, Reininghaus EZ,
Ribasés M, Rietschel M, Ripke S, Rouleau GA, Saito T, Schall U, Schalling M,
Schofield PR, Schulze TG, Scott LJ, Scott RJ, Serretti A, Shannon Weickert C,
Smoller JW, Stefansson H, Stefansson K, Stordal E, Streit F, Sullivan PF,
Turecki G, Vaaler AE, Vieta E, Vincent JB, Waldman ID, Weickert TW, Werge T,
Wray NR, Zwart JA, Biernacka JM, Nurnberger JI, Cichon S, Edenberg HJ, Stahl EA,
McQuillin A, Di Florio A, Ophoff RA, Andreassen OA. Genome-wide association
study of more than 40,000 bipolar disorder cases provides new insights into the
underlying biology. Nat Genet. 2021 Jun;53(6):817-829. doi:
10.1038/s41588-021-00857-4. Epub 2021 May 17. PMID: 34002096; PMCID: PMC8192451.
124: Weil AG, Fallah A, Wang S, Ibrahim GM, Elkaim LM, Jayakar P, Miller I,
Bhatia S, Niazi TN, Ragheb J. Functional hemispherectomy: can preoperative
imaging predict outcome? J Neurosurg Pediatr. 2020 Jun 1;25(6). doi:
10.3171/2019.12.PEDS19370. Epub 2020 Feb 21. PMID: 33988937.
125: Durno C, Ercan AB, Bianchi V, Edwards M, Aronson M, Galati M, Atenafu EG,
Abebe-Campino G, Al-Battashi A, Alharbi M, Azad VF, Baris HN, Basel D, Bedgood
R, Bendel A, Ben-Shachar S, Blumenthal DT, Blundell M, Bornhorst M, Bronsema A,
Cairney E, Rhode S, Caspi S, Chamdin A, Chiaravalli S, Constantini S, Crooks B,
Das A, Dvir R, Farah R, Foulkes WD, Frenkel Z, Gallinger B, Gardner S, Gass D,
Ghalibafian M, Gilpin C, Goldberg Y, Goudie C, Hamid SA, Hampel H, Hansford JR,
Harlos C, Hijiya N, Hsu S, Kamihara J, Kebudi R, Knipstein J, Koschmann C, Kratz
C, Larouche V, Lassaletta A, Lindhorst S, Ling SC, Link MP, Loret De Mola R,
Luiten R, Lurye M, Maciaszek JL, MagimairajanIssai V, Maher OM, Massimino M,
McGee RB, Mushtaq N, Mason G, Newmark M, Nicholas G, Nichols KE, Nicolaides T,
Opocher E, Osborn M, Oshrine B, Pearlman R, Pettee D, Rapp J, Rashid M, Reddy A,
Reichman L, Remke M, Robbins G, Roy S, Sabel M, Samuel D, Scheers I, Schneider
KW, Sen S, Stearns D, Sumerauer D, Swallow C, Taylor L, Thomas G, Toledano H,
Tomboc P, Van Damme A, Winer I, Yalon M, Yen LY, Zapotocky M, Zelcer S, Ziegler
DS, Zimmermann S, Hawkins C, Malkin D, Bouffet E, Villani A, Tabori U. Survival
Benefit for Individuals With Constitutional Mismatch Repair Deficiency
Undergoing Surveillance. J Clin Oncol. 2021 Sep 1;39(25):2779-2790. doi:
10.1200/JCO.20.02636. Epub 2021 May 4. PMID: 33945292; PMCID: PMC8407605.
126: Smith JS, Kelly MP, Yanik EL, Baldus CR, Buell TJ, Lurie JD, Edwards C,
Glassman SD, Lenke LG, Boachie-Adjei O, Buchowski JM, Carreon LY, Crawford CH,
Errico TJ, Lewis SJ, Koski T, Parent S, Lafage V, Kim HJ, Ames CP, Bess S,
Schwab FJ, Shaffrey CI, Bridwell KH. Operative versus nonoperative treatment for
adult symptomatic lumbar scoliosis at 5-year follow-up: durability of outcomes
and impact of treatment-related serious adverse events. J Neurosurg Spine. 2021
Apr 30:1-13. doi: 10.3171/2020.9.SPINE201472. Epub ahead of print. PMID:
33930859.
127: Myers KA, Marini C, Carvill GL, McTague A, Panetta J, Stutterd C, Stanley
T, Marin S, Nguyen J, Barba C, Rosati A, Scott RH, Mefford HC, Guerrini R,
Scheffer IE. Phenotypic Spectrum of Seizure Disorders in MBD5-Associated
Neurodevelopmental Disorder. Neurol Genet. 2021 Mar 18;7(2):e579. doi:
10.1212/NXG.0000000000000579. PMID: 33912662; PMCID: PMC8075573.
128: Cai S, Aris IM, Yuan WL, Tan KH, Godfrey KM, Gluckman PD, Shek LP, Chong
YS, Yap F, Fortier MV, Meaney MJ, Lee YS, Qiu A. Neonatal amygdala
microstructure mediates the relationship between gestational glycemia and
offspring adiposity. BMJ Open Diabetes Res Care. 2021 Apr;9(1):e001396. doi:
10.1136/bmjdrc-2020-001396. PMID: 33888539; PMCID: PMC8070871.
129: Slayter J, Hodgkinson V, Lounsberry J, Brais B, Chapman K, Genge A,
Izenberg A, Johnston W, Lochmüller H, O'Ferrall E, Pfeffer G, Plamondon S,
Rodrigue X, Schellenberg K, Shoesmith C, Stables C, Taillon M, Warman-Chardon J,
Korngut L, O'Connell C. A Canadian Adult Spinal Muscular Atrophy Outcome
Measures Toolkit: Results of a National Consensus using a Modified Delphi
Method. J Neuromuscul Dis. 2021;8(4):579-588. doi: 10.3233/JND-200617. PMID:
33867362; PMCID: PMC8385500.
130: Courage C, Oliver KL, Park EJ, Cameron JM, Grabińska KA, Muona M,
Canafoglia L, Gambardella A, Said E, Afawi Z, Baykan B, Brandt C, di Bonaventura
C, Chew HB, Criscuolo C, Dibbens LM, Castellotti B, Riguzzi P, Labate A, Filla
A, Giallonardo AT, Berecki G, Jackson CB, Joensuu T, Damiano JA, Kivity S,
Korczyn A, Palotie A, Striano P, Uccellini D, Giuliano L, Andermann E, Scheffer
IE, Michelucci R, Bahlo M, Franceschetti S, Sessa WC, Berkovic SF, Lehesjoki AE.
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic
heterogeneity including dolichol-dependent protein glycosylation pathway genes.
Am J Hum Genet. 2021 Apr 1;108(4):722-738. doi: 10.1016/j.ajhg.2021.03.013.
PMID: 33798445; PMCID: PMC8059372.
131: Taleghani E, Singh A, Hachem B, Benoit D, Rustagi R, Vithoulkas G, Mac-
Thiong JM, Syed H. Finite element assessment of a disc-replacement implant for
treating scoliotic deformity. Clin Biomech (Bristol, Avon). 2021 Apr;84:105326.
doi: 10.1016/j.clinbiomech.2021.105326. Epub 2021 Mar 17. PMID: 33773168.
132: van Heumen S, Moreau JT, Simard-Tremblay E, Albrecht S, Dudley RW, Baillet
S. Case Report: Aperiodic Fluctuations of Neural Activity in the Ictal MEG of a
Child With Drug-Resistant Fronto-Temporal Epilepsy. Front Hum Neurosci. 2021 Mar
4;15:646426. doi: 10.3389/fnhum.2021.646426. PMID: 33746727; PMCID: PMC7969518.
133: Skowron P, Farooq H, Cavalli FMG, Morrissy AS, Ly M, Hendrikse LD, Wang EY,
Djambazian H, Zhu H, Mungall KL, Trinh QM, Zheng T, Dai S, Stucklin ASG, Vladoiu
MC, Fong V, Holgado BL, Nor C, Wu X, Abd-Rabbo D, Bérubé P, Wang YC, Luu B,
Suarez RA, Rastan A, Gillmor AH, Lee JJY, Zhang XY, Daniels C, Dirks P, Malkin
D, Bouffet E, Tabori U, Loukides J, Doz FP, Bourdeaut F, Delattre OO, Masliah-
Planchon J, Ayrault O, Kim SK, Meyronet D, Grajkowska WA, Carlotti CG, de Torres
C, Mora J, Eberhart CG, Van Meir EG, Kumabe T, French PJ, Kros JM, Jabado N,
Lach B, Pollack IF, Hamilton RL, Rao AAN, Giannini C, Olson JM, Bognár L,
Klekner A, Zitterbart K, Phillips JJ, Thompson RC, Cooper MK, Rubin JB, Liau LM,
Garami M, Hauser P, Li KKW, Ng HK, Poon WS, Yancey Gillespie G, Chan JA, Jung S,
McLendon RE, Thompson EM, Zagzag D, Vibhakar R, Ra YS, Garre ML, Schüller U,
Shofuda T, Faria CC, López-Aguilar E, Zadeh G, Hui CC, Ramaswamy V, Bailey SD,
Jones SJ, Mungall AJ, Moore RA, Calarco JA, Stein LD, Bader GD, Reimand J,
Ragoussis J, Weiss WA, Marra MA, Suzuki H, Taylor MD. The transcriptional
landscape of Shh medulloblastoma. Nat Commun. 2021 Mar 19;12(1):1749. doi:
10.1038/s41467-021-21883-0. PMID: 33741928; PMCID: PMC7979819.
134: Arabzade A, Zhao Y, Varadharajan S, Chen HC, Jessa S, Rivas B, Stuckert AJ,
Solis M, Kardian A, Tlais D, Golbourn BJ, Stanton AJ, Chan YS, Olson C, Karlin
KL, Kong K, Kupp R, Hu B, Injac SG, Ngo M, Wang PR, De León LA, Sahm F, Kawauchi
D, Pfister SM, Lin CY, Hodges HC, Singh I, Westbrook TF, Chintagumpala MM,
Blaney SM, Parsons DW, Pajtler KW, Agnihotri S, Gilbertson RJ, Yi J, Jabado N,
Kleinman CL, Bertrand KC, Deneen B, Mack SC. ZFTA-RELA Dictates Oncogenic
Transcriptional Programs to Drive Aggressive Supratentorial Ependymoma. Cancer
Discov. 2021 Sep;11(9):2200-2215. doi: 10.1158/2159-8290.CD-20-1066. Epub 2021
Mar 19. PMID: 33741710; PMCID: PMC8418998.
135: Murray DS, Richardson L, Tesfaye R, Nadin D, Kelly C, Greenwood P. Black In
Neuro, Beyond One Week. J Neurosci. 2021 Mar 17;41(11):2314-2317. doi:
10.1523/JNEUROSCI.2957-20.2021. PMID: 33731466; PMCID: PMC7984601.
136: Weil AG, Lewis EC, Ibrahim GM, Kola O, Tseng CH, Zhou X, Lin KM, Cai LX,
Liu QZ, Lin JL, Zhou WJ, Mathern GW, Smyth MD, O'Neill BR, Dudley R, Ragheb J,
Bhatia S, Delev D, Ramantani G, Zentner J, Ojemann J, Wang AC, Dorfer C, Feucht
M, Czech T, Bollo RJ, Issabekov G, Zhu H, Connelly M, Steinbok P, Zhang JG,
Zhang K, Hidalgo ET, Weiner HL, Wong-Kisiel L, Lapalme-Remis S, Tripathi M,
Sarat Chandra P, Hader W, Wang FP, Yao Y, Olivier Champagne P, Guo Q, Li SC,
Budke M, Pérez-Jiménez MA, Raftapoulos C, Finet P, Michel P, Schaller K, Stienen
MN, Baro V, Cantillano Malone C, Pociecha J, Chamorro N, Muro VL, von Lehe M,
Vieker S, Oluigbo C, Gaillard WD, Al Khateeb M, Al Otaibi F, Krayenbühl N,
Bolton J, Pearl PL, Fallah A. Hemispherectomy Outcome Prediction Scale:
Development and validation of a seizure freedom prediction tool. Epilepsia. 2021
May;62(5):1064-1073. doi: 10.1111/epi.16861. Epub 2021 Mar 13. PMID: 33713438.
137: Ramezani M, Mouches P, Yoon E, Rajashekar D, Ruskey JA, Leveille E, Martens
K, Kibreab M, Hammer T, Kathol I, Maarouf N, Sarna J, Martino D, Pfeffer G, Gan-
Or Z, Forkert ND, Monchi O. Investigating the relationship between the SNCA gene
and cognitive abilities in idiopathic Parkinson's disease using machine
learning. Sci Rep. 2021 Mar 1;11(1):4917. doi: 10.1038/s41598-021-84316-4. PMID:
33649398; PMCID: PMC7921412.
138: Walter MC, Chiriboga C, Duong T, Goemans N, Mayhew A, Ouillade L, Oskoui M,
Quinlivan R, Vázquez-Costa JF, Vissing J, Servais L. Improving Care and
Empowering Adults Living with SMA: A Call to Action in the New Treatment Era. J
Neuromuscul Dis. 2021;8(4):543-551. doi: 10.3233/JND-200611. PMID: 33646175;
PMCID: PMC8385518.
139: Klionsky DJ, Abdel-Aziz AK, Abdelfatah S, Abdellatif M, Abdoli A, Abel S,
Abeliovich H, Abildgaard MH, Abudu YP, Acevedo-Arozena A, Adamopoulos IE, Adeli
K, Adolph TE, Adornetto A, Aflaki E, Agam G, Agarwal A, Aggarwal BB, Agnello M,
Agostinis P, Agrewala JN, Agrotis A, Aguilar PV, Ahmad ST, Ahmed ZM, Ahumada-
Castro U, Aits S, Aizawa S, Akkoc Y, Akoumianaki T, Akpinar HA, Al-Abd AM, Al-
Akra L, Al-Gharaibeh A, Alaoui-Jamali MA, Alberti S, Alcocer-Gómez E, Alessandri
C, Ali M, Alim Al-Bari MA, Aliwaini S, Alizadeh J, Almacellas E, Almasan A,
Alonso A, Alonso GD, Altan-Bonnet N, Altieri DC, Álvarez ÉMC, Alves S, Alves da
Costa C, Alzaharna MM, Amadio M, Amantini C, Amaral C, Ambrosio S, Amer AO,
Ammanathan V, An Z, Andersen SU, Andrabi SA, Andrade-Silva M, Andres AM,
Angelini S, Ann D, Anozie UC, Ansari MY, Antas P, Antebi A, Antón Z, Anwar T,
Apetoh L, Apostolova N, Araki T, Araki Y, Arasaki K, Araújo WL, Araya J, Arden
C, Arévalo MA, Arguelles S, Arias E, Arikkath J, Arimoto H, Ariosa AR,
Armstrong-James D, Arnauné-Pelloquin L, Aroca A, Arroyo DS, Arsov I, Artero R,
Asaro DML, Aschner M, Ashrafizadeh M, Ashur-Fabian O, Atanasov AG, Au AK,
Auberger P, Auner HW, Aurelian L, Autelli R, Avagliano L, Ávalos Y, Aveic S,
Aveleira CA, Avin-Wittenberg T, Aydin Y, Ayton S, Ayyadevara S, Azzopardi M,
Baba M, Backer JM, Backues SK, Bae DH, Bae ON, Bae SH, Baehrecke EH, Baek A,
Baek SH, Baek SH, Bagetta G, Bagniewska-Zadworna A, Bai H, Bai J, Bai X, Bai Y,
Bairagi N, Baksi S, Balbi T, Baldari CT, Balduini W, Ballabio A, Ballester M,
Balazadeh S, Balzan R, Bandopadhyay R, Banerjee S, Banerjee S, Bánréti Á, Bao Y,
Baptista MS, Baracca A, Barbati C, Bargiela A, Barilà D, Barlow PG, Barmada SJ,
Barreiro E, Barreto GE, Bartek J, Bartel B, Bartolome A, Barve GR,
Basagoudanavar SH, Bassham DC, Bast RC Jr, Basu A, Batoko H, Batten I, Baulieu
EE, Baumgarner BL, Bayry J, Beale R, Beau I, Beaumatin F, Bechara LRG, Beck GR
Jr, Beers MF, Begun J, Behrends C, Behrens GMN, Bei R, Bejarano E, Bel S, Behl
C, Belaid A, Belgareh-Touzé N, Bellarosa C, Belleudi F, Belló Pérez M, Bello-
Morales R, Beltran JSO, Beltran S, Benbrook DM, Bendorius M, Benitez BA, Benito-
Cuesta I, Bensalem J, Berchtold MW, Berezowska S, Bergamaschi D, Bergami M,
Bergmann A, Berliocchi L, Berlioz-Torrent C, Bernard A, Berthoux L, Besirli CG,
Besteiro S, Betin VM, Beyaert R, Bezbradica JS, Bhaskar K, Bhatia-Kissova I,
Bhattacharya R, Bhattacharya S, Bhattacharyya S, Bhuiyan MS, Bhutia SK, Bi L, Bi
X, Biden TJ, Bijian K, Billes VA, Binart N, Bincoletto C, Birgisdottir AB,
Bjorkoy G, Blanco G, Blas-Garcia A, Blasiak J, Blomgran R, Blomgren K, Blum JS,
Boada-Romero E, Boban M, Boesze-Battaglia K, Boeuf P, Boland B, Bomont P,
Bonaldo P, Bonam SR, Bonfili L, Bonifacino JS, Boone BA, Bootman MD, Bordi M,
Borner C, Bornhauser BC, Borthakur G, Bosch J, Bose S, Botana LM, Botas J,
Boulanger CM, Boulton ME, Bourdenx M, Bourgeois B, Bourke NM, Bousquet G, Boya
P, Bozhkov PV, Bozi LHM, Bozkurt TO, Brackney DE, Brandts CH, Braun RJ, Braus
GH, Bravo-Sagua R, Bravo-San Pedro JM, Brest P, Bringer MA, Briones-Herrera A,
Broaddus VC, Brodersen P, Brodsky JL, Brody SL, Bronson PG, Bronstein JM, Brown
CN, Brown RE, Brum PC, Brumell JH, Brunetti-Pierri N, Bruno D, Bryson-Richardson
RJ, Bucci C, Buchrieser C, Bueno M, Buitrago-Molina LE, Buraschi S, Buch S,
Buchan JR, Buckingham EM, Budak H, Budini M, Bultynck G, Burada F, Burgoyne JR,
Burón MI, Bustos V, Büttner S, Butturini E, Byrd A, Cabas I, Cabrera-Benitez S,
Cadwell K, Cai J, Cai L, Cai Q, Cairó M, Calbet JA, Caldwell GA, Caldwell KA,
Call JA, Calvani R, Calvo AC, Calvo-Rubio Barrera M, Camara NO, Camonis JH,
Camougrand N, Campanella M, Campbell EM, Campbell-Valois FX, Campello S, Campesi
I, Campos JC, Camuzard O, Cancino J, Candido de Almeida D, Canesi L, Caniggia I,
Canonico B, Cantí C, Cao B, Caraglia M, Caramés B, Carchman EH, Cardenal-Muñoz
E, Cardenas C, Cardenas L, Cardoso SM, Carew JS, Carle GF, Carleton G, Carloni
S, Carmona-Gutierrez D, Carneiro LA, Carnevali O, Carosi JM, Carra S, Carrier A,
Carrier L, Carroll B, Carter AB, Carvalho AN, Casanova M, Casas C, Casas J,
Cassioli C, Castillo EF, Castillo K, Castillo-Lluva S, Castoldi F, Castori M,
Castro AF, Castro-Caldas M, Castro-Hernandez J, Castro-Obregon S, Catz SD,
Cavadas C, Cavaliere F, Cavallini G, Cavinato M, Cayuela ML, Cebollada Rica P,
Cecarini V, Cecconi F, Cechowska-Pasko M, Cenci S, Ceperuelo-Mallafré V,
Cerqueira JJ, Cerutti JM, Cervia D, Cetintas VB, Cetrullo S, Chae HJ, Chagin AS,
Chai CY, Chakrabarti G, Chakrabarti O, Chakraborty T, Chakraborty T, Chami M,
Chamilos G, Chan DW, Chan EYW, Chan ED, Chan HYE, Chan HH, Chan H, Chan MTV,
Chan YS, Chandra PK, Chang CP, Chang C, Chang HC, Chang K, Chao J, Chapman T,
Charlet-Berguerand N, Chatterjee S, Chaube SK, Chaudhary A, Chauhan S, Chaum E,
Checler F, Cheetham ME, Chen CS, Chen GC, Chen JF, Chen LL, Chen L, Chen L, Chen
M, Chen MK, Chen N, Chen Q, Chen RH, Chen S, Chen W, Chen W, Chen XM, Chen XW,
Chen X, Chen Y, Chen YG, Chen Y, Chen Y, Chen YJ, Chen YQ, Chen ZS, Chen Z, Chen
ZH, Chen ZJ, Chen Z, Cheng H, Cheng J, Cheng SY, Cheng W, Cheng X, Cheng XT,
Cheng Y, Cheng Z, Chen Z, Cheong H, Cheong JK, Chernyak BV, Cherry S, Cheung
CFR, Cheung CHA, Cheung KH, Chevet E, Chi RJ, Chiang AKS, Chiaradonna F,
Chiarelli R, Chiariello M, Chica N, Chiocca S, Chiong M, Chiou SH, Chiramel AI,
Chiurchiù V, Cho DH, Choe SK, Choi AMK, Choi ME, Choudhury KR, Chow NS, Chu CT,
Chua JP, Chua JJE, Chung H, Chung KP, Chung S, Chung SH, Chung YL, Cianfanelli
V, Ciechomska IA, Cifuentes M, Cinque L, Cirak S, Cirone M, Clague MJ, Clarke R,
Clementi E, Coccia EM, Codogno P, Cohen E, Cohen MM, Colasanti T, Colasuonno F,
Colbert RA, Colell A, Čolić M, Coll NS, Collins MO, Colombo MI, Colón-Ramos DA,
Combaret L, Comincini S, Cominetti MR, Consiglio A, Conte A, Conti F, Contu VR,
Cookson MR, Coombs KM, Coppens I, Corasaniti MT, Corkery DP, Cordes N, Cortese
K, Costa MDC, Costantino S, Costelli P, Coto-Montes A, Crack PJ, Crespo JL,
Criollo A, Crippa V, Cristofani R, Csizmadia T, Cuadrado A, Cui B, Cui J, Cui Y,
Cui Y, Culetto E, Cumino AC, Cybulsky AV, Czaja MJ, Czuczwar SJ, D'Adamo S,
D'Amelio M, D'Arcangelo D, D'Lugos AC, D'Orazi G, da Silva JA, Dafsari HS, Dagda
RK, Dagdas Y, Daglia M, Dai X, Dai Y, Dai Y, Dal Col J, Dalhaimer P, Dalla Valle
L, Dallenga T, Dalmasso G, Damme M, Dando I, Dantuma NP, Darling AL, Das H,
Dasarathy S, Dasari SK, Dash S, Daumke O, Dauphinee AN, Davies JS, Dávila VA,
Davis RJ, Davis T, Dayalan Naidu S, De Amicis F, De Bosscher K, De Felice F, De
Franceschi L, De Leonibus C, de Mattos Barbosa MG, De Meyer GRY, De Milito A, De
Nunzio C, De Palma C, De Santi M, De Virgilio C, De Zio D, Debnath J, DeBosch
BJ, Decuypere JP, Deehan MA, Deflorian G, DeGregori J, Dehay B, Del Rio G,
Delaney JR, Delbridge LMD, Delorme-Axford E, Delpino MV, Demarchi F, Dembitz V,
Demers ND, Deng H, Deng Z, Dengjel J, Dent P, Denton D, DePamphilis ML, Der CJ,
Deretic V, Descoteaux A, Devis L, Devkota S, Devuyst O, Dewson G, Dharmasivam M,
Dhiman R, di Bernardo D, Di Cristina M, Di Domenico F, Di Fazio P, Di Fonzo A,
Di Guardo G, Di Guglielmo GM, Di Leo L, Di Malta C, Di Nardo A, Di Rienzo M, Di
Sano F, Diallinas G, Diao J, Diaz-Araya G, Díaz-Laviada I, Dickinson JM,
Diederich M, Dieudé M, Dikic I, Ding S, Ding WX, Dini L, Dinić J, Dinic M,
Dinkova-Kostova AT, Dionne MS, Distler JHW, Diwan A, Dixon IMC, Djavaheri-Mergny
M, Dobrinski I, Dobrovinskaya O, Dobrowolski R, Dobson RCJ, Đokić J, Dokmeci
Emre S, Donadelli M, Dong B, Dong X, Dong Z, Dorn Ii GW, Dotsch V, Dou H, Dou J,
Dowaidar M, Dridi S, Drucker L, Du A, Du C, Du G, Du HN, Du LL, du Toit A, Duan
SB, Duan X, Duarte SP, Dubrovska A, Dunlop EA, Dupont N, Durán RV, Dwarakanath
BS, Dyshlovoy SA, Ebrahimi-Fakhari D, Eckhart L, Edelstein CL, Efferth T,
Eftekharpour E, Eichinger L, Eid N, Eisenberg T, Eissa NT, Eissa S, Ejarque M,
El Andaloussi A, El-Hage N, El-Naggar S, Eleuteri AM, El-Shafey ES, Elgendy M,
Eliopoulos AG, Elizalde MM, Elks PM, Elsasser HP, Elsherbiny ES, Emerling BM,
Emre NCT, Eng CH, Engedal N, Engelbrecht AM, Engelsen AST, Enserink JM,
Escalante R, Esclatine A, Escobar-Henriques M, Eskelinen EL, Espert L, Eusebio
MO, Fabrias G, Fabrizi C, Facchiano A, Facchiano F, Fadeel B, Fader C, Faesen
AC, Fairlie WD, Falcó A, Falkenburger BH, Fan D, Fan J, Fan Y, Fang EF, Fang Y,
Fang Y, Fanto M, Farfel-Becker T, Faure M, Fazeli G, Fedele AO, Feldman AM, Feng
D, Feng J, Feng L, Feng Y, Feng Y, Feng W, Fenz Araujo T, Ferguson TA, Fernández
ÁF, Fernandez-Checa JC, Fernández-Veledo S, Fernie AR, Ferrante AW Jr, Ferraresi
A, Ferrari MF, Ferreira JCB, Ferro-Novick S, Figueras A, Filadi R, Filigheddu N,
Filippi-Chiela E, Filomeni G, Fimia GM, Fineschi V, Finetti F, Finkbeiner S,
Fisher EA, Fisher PB, Flamigni F, Fliesler SJ, Flo TH, Florance I, Florey O,
Florio T, Fodor E, Follo C, Fon EA, Forlino A, Fornai F, Fortini P, Fracassi A,
Fraldi A, Franco B, Franco R, Franconi F, Frankel LB, Friedman SL, Fröhlich LF,
Frühbeck G, Fuentes JM, Fujiki Y, Fujita N, Fujiwara Y, Fukuda M, Fulda S, Furic
L, Furuya N, Fusco C, Gack MU, Gaffke L, Galadari S, Galasso A, Galindo MF,
Gallolu Kankanamalage S, Galluzzi L, Galy V, Gammoh N, Gan B, Ganley IG, Gao F,
Gao H, Gao M, Gao P, Gao SJ, Gao W, Gao X, Garcera A, Garcia MN, Garcia VE,
García-Del Portillo F, Garcia-Escudero V, Garcia-Garcia A, Garcia-Macia M,
García-Moreno D, Garcia-Ruiz C, García-Sanz P, Garg AD, Gargini R, Garofalo T,
Garry RF, Gassen NC, Gatica D, Ge L, Ge W, Geiss-Friedlander R, Gelfi C,
Genschik P, Gentle IE, Gerbino V, Gerhardt C, Germain K, Germain M, Gewirtz DA,
Ghasemipour Afshar E, Ghavami S, Ghigo A, Ghosh M, Giamas G, Giampietri C,
Giatromanolaki A, Gibson GE, Gibson SB, Ginet V, Giniger E, Giorgi C, Girao H,
Girardin SE, Giridharan M, Giuliano S, Giulivi C, Giuriato S, Giustiniani J,
Gluschko A, Goder V, Goginashvili A, Golab J, Goldstone DC, Golebiewska A, Gomes
LR, Gomez R, Gómez-Sánchez R, Gomez-Puerto MC, Gomez-Sintes R, Gong Q, Goni FM,
González-Gallego J, Gonzalez-Hernandez T, Gonzalez-Polo RA, Gonzalez-Reyes JA,
González-Rodríguez P, Goping IS, Gorbatyuk MS, Gorbunov NV, Görgülü K, Gorojod
RM, Gorski SM, Goruppi S, Gotor C, Gottlieb RA, Gozes I, Gozuacik D, Graef M,
Gräler MH, Granatiero V, Grasso D, Gray JP, Green DR, Greenhough A, Gregory SL,
Griffin EF, Grinstaff MW, Gros F, Grose C, Gross AS, Gruber F, Grumati P, Grune
T, Gu X, Guan JL, Guardia CM, Guda K, Guerra F, Guerri C, Guha P, Guillén C,
Gujar S, Gukovskaya A, Gukovsky I, Gunst J, Günther A, Guntur AR, Guo C, Guo C,
Guo H, Guo LW, Guo M, Gupta P, Gupta SK, Gupta S, Gupta VB, Gupta V, Gustafsson
AB, Gutterman DD, H B R, Haapasalo A, Haber JE, Hać A, Hadano S, Hafrén AJ,
Haidar M, Hall BS, Halldén G, Hamacher-Brady A, Hamann A, Hamasaki M, Han W,
Hansen M, Hanson PI, Hao Z, Harada M, Harhaji-Trajkovic L, Hariharan N, Haroon
N, Harris J, Hasegawa T, Hasima Nagoor N, Haspel JA, Haucke V, Hawkins WD, Hay
BA, Haynes CM, Hayrabedyan SB, Hays TS, He C, He Q, He RR, He YW, He YY, Heakal
Y, Heberle AM, Hejtmancik JF, Helgason GV, Henkel V, Herb M, Hergovich A,
Herman-Antosiewicz A, Hernández A, Hernandez C, Hernandez-Diaz S, Hernandez-Gea
V, Herpin A, Herreros J, Hervás JH, Hesselson D, Hetz C, Heussler VT, Higuchi Y,
Hilfiker S, Hill JA, Hlavacek WS, Ho EA, Ho IHT, Ho PW, Ho SL, Ho WY, Hobbs GA,
Hochstrasser M, Hoet PHM, Hofius D, Hofman P, Höhn A, Holmberg CI, Hombrebueno
JR, Yi-Ren Hong CH, Hooper LV, Hoppe T, Horos R, Hoshida Y, Hsin IL, Hsu HY, Hu
B, Hu D, Hu LF, Hu MC, Hu R, Hu W, Hu YC, Hu ZW, Hua F, Hua J, Hua Y, Huan C,
Huang C, Huang C, Huang C, Huang C, Huang H, Huang K, Huang MLH, Huang R, Huang
S, Huang T, Huang X, Huang YJ, Huber TB, Hubert V, Hubner CA, Hughes SM, Hughes
WE, Humbert M, Hummer G, Hurley JH, Hussain S, Hussain S, Hussey PJ, Hutabarat
M, Hwang HY, Hwang S, Ieni A, Ikeda F, Imagawa Y, Imai Y, Imbriano C, Imoto M,
Inman DM, Inoki K, Iovanna J, Iozzo RV, Ippolito G, Irazoqui JE, Iribarren P,
Ishaq M, Ishikawa M, Ishimwe N, Isidoro C, Ismail N, Issazadeh-Navikas S,
Itakura E, Ito D, Ivankovic D, Ivanova S, Iyer AKV, Izquierdo JM, Izumi M,
Jäättelä M, Jabir MS, Jackson WT, Jacobo-Herrera N, Jacomin AC, Jacquin E,
Jadiya P, Jaeschke H, Jagannath C, Jakobi AJ, Jakobsson J, Janji B, Jansen-Dürr
P, Jansson PJ, Jantsch J, Januszewski S, Jassey A, Jean S, Jeltsch-David H,
Jendelova P, Jenny A, Jensen TE, Jessen N, Jewell JL, Ji J, Jia L, Jia R, Jiang
L, Jiang Q, Jiang R, Jiang T, Jiang X, Jiang Y, Jimenez-Sanchez M, Jin EJ, Jin
F, Jin H, Jin L, Jin L, Jin M, Jin S, Jo EK, Joffre C, Johansen T, Johnson GVW,
Johnston SA, Jokitalo E, Jolly MK, Joosten LAB, Jordan J, Joseph B, Ju D, Ju JS,
Ju J, Juárez E, Judith D, Juhász G, Jun Y, Jung CH, Jung SC, Jung YK, Jungbluth
H, Jungverdorben J, Just S, Kaarniranta K, Kaasik A, Kabuta T, Kaganovich D,
Kahana A, Kain R, Kajimura S, Kalamvoki M, Kalia M, Kalinowski DS, Kaludercic N,
Kalvari I, Kaminska J, Kaminskyy VO, Kanamori H, Kanasaki K, Kang C, Kang R,
Kang SS, Kaniyappan S, Kanki T, Kanneganti TD, Kanthasamy AG, Kanthasamy A,
Kantorow M, Kapuy O, Karamouzis MV, Karim MR, Karmakar P, Katare RG, Kato M,
Kaufmann SHE, Kauppinen A, Kaushal GP, Kaushik S, Kawasaki K, Kazan K, Ke PY,
Keating DJ, Keber U, Kehrl JH, Keller KE, Keller CW, Kemper JK, Kenific CM, Kepp
O, Kermorgant S, Kern A, Ketteler R, Keulers TG, Khalfin B, Khalil H, Khambu B,
Khan SY, Khandelwal VKM, Khandia R, Kho W, Khobrekar NV, Khuansuwan S, Khundadze
M, Killackey SA, Kim D, Kim DR, Kim DH, Kim DE, Kim EY, Kim EK, Kim HR, Kim HS,
Hyung-Ryong Kim, Kim JH, Kim JK, Kim JH, Kim J, Kim JH, Kim KI, Kim PK, Kim SJ,
Kimball SR, Kimchi A, Kimmelman AC, Kimura T, King MA, Kinghorn KJ, Kinsey CG,
Kirkin V, Kirshenbaum LA, Kiselev SL, Kishi S, Kitamoto K, Kitaoka Y, Kitazato
K, Kitsis RN, Kittler JT, Kjaerulff O, Klein PS, Klopstock T, Klucken J,
Knævelsrud H, Knorr RL, Ko BCB, Ko F, Ko JL, Kobayashi H, Kobayashi S, Koch I,
Koch JC, Koenig U, Kögel D, Koh YH, Koike M, Kohlwein SD, Kocaturk NM, Komatsu
M, König J, Kono T, Kopp BT, Korcsmaros T, Korkmaz G, Korolchuk VI, Korsnes MS,
Koskela A, Kota J, Kotake Y, Kotler ML, Kou Y, Koukourakis MI, Koustas E, Kovacs
AL, Kovács T, Koya D, Kozako T, Kraft C, Krainc D, Krämer H, Krasnodembskaya AD,
Kretz-Remy C, Kroemer G, Ktistakis NT, Kuchitsu K, Kuenen S, Kuerschner L, Kukar
T, Kumar A, Kumar A, Kumar D, Kumar D, Kumar S, Kume S, Kumsta C, Kundu CN,
Kundu M, Kunnumakkara AB, Kurgan L, Kutateladze TG, Kutlu O, Kwak S, Kwon HJ,
Kwon TK, Kwon YT, Kyrmizi I, La Spada A, Labonté P, Ladoire S, Laface I, Lafont
F, Lagace DC, Lahiri V, Lai Z, Laird AS, Lakkaraju A, Lamark T, Lan SH,
Landajuela A, Lane DJR, Lane JD, Lang CH, Lange C, Langel Ü, Langer R,
Lapaquette P, Laporte J, LaRusso NF, Lastres-Becker I, Lau WCY, Laurie GW,
Lavandero S, Law BYK, Law HK, Layfield R, Le W, Le Stunff H, Leary AY, Lebrun
JJ, Leck LYW, Leduc-Gaudet JP, Lee C, Lee CP, Lee DH, Lee EB, Lee EF, Lee GM,
Lee HJ, Lee HK, Lee JM, Lee JS, Lee JA, Lee JY, Lee JH, Lee M, Lee MG, Lee MJ,
Lee MS, Lee SY, Lee SJ, Lee SY, Lee SB, Lee WH, Lee YR, Lee YH, Lee Y, Lefebvre
C, Legouis R, Lei YL, Lei Y, Leikin S, Leitinger G, Lemus L, Leng S, Lenoir O,
Lenz G, Lenz HJ, Lenzi P, León Y, Leopoldino AM, Leschczyk C, Leskelä S,
Letellier E, Leung CT, Leung PS, Leventhal JS, Levine B, Lewis PA, Ley K, Li B,
Li DQ, Li J, Li J, Li J, Li K, Li L, Li M, Li M, Li M, Li M, Li M, Li PL, Li MQ,
Li Q, Li S, Li T, Li W, Li W, Li X, Li YP, Li Y, Li Z, Li Z, Li Z, Lian J, Liang
C, Liang Q, Liang W, Liang Y, Liang Y, Liao G, Liao L, Liao M, Liao YF, Librizzi
M, Lie PPY, Lilly MA, Lim HJ, Lima TRR, Limana F, Lin C, Lin CW, Lin DS, Lin FC,
Lin JD, Lin KM, Lin KH, Lin LT, Lin PH, Lin Q, Lin S, Lin SJ, Lin W, Lin X, Lin
YX, Lin YS, Linden R, Lindner P, Ling SC, Lingor P, Linnemann AK, Liou YC,
Lipinski MM, Lipovšek S, Lira VA, Lisiak N, Liton PB, Liu C, Liu CH, Liu CF, Liu
CH, Liu F, Liu H, Liu HS, Liu HF, Liu H, Liu J, Liu J, Liu J, Liu L, Liu L, Liu
M, Liu Q, Liu W, Liu W, Liu XH, Liu X, Liu X, Liu X, Liu X, Liu Y, Liu Y, Liu Y,
Liu Y, Liu Y, Livingston JA, Lizard G, Lizcano JM, Ljubojevic-Holzer S, LLeonart
ME, Llobet-Navàs D, Llorente A, Lo CH, Lobato-Márquez D, Long Q, Long YC, Loos
B, Loos JA, López MG, López-Doménech G, López-Guerrero JA, López-Jiménez AT,
López-Pérez Ó, López-Valero I, Lorenowicz MJ, Lorente M, Lorincz P, Lossi L,
Lotersztajn S, Lovat PE, Lovell JF, Lovy A, Lőw P, Lu G, Lu H, Lu JH, Lu JJ, Lu
M, Lu S, Luciani A, Lucocq JM, Ludovico P, Luftig MA, Luhr M, Luis-Ravelo D, Lum
JJ, Luna-Dulcey L, Lund AH, Lund VK, Lünemann JD, Lüningschrör P, Luo H, Luo R,
Luo S, Luo Z, Luparello C, Lüscher B, Luu L, Lyakhovich A, Lyamzaev KG, Lystad
AH, Lytvynchuk L, Ma AC, Ma C, Ma M, Ma NF, Ma QH, Ma X, Ma Y, Ma Z, MacDougald
OA, Macian F, MacIntosh GC, MacKeigan JP, Macleod KF, Maday S, Madeo F, Madesh
M, Madl T, Madrigal-Matute J, Maeda A, Maejima Y, Magarinos M, Mahavadi P,
Maiani E, Maiese K, Maiti P, Maiuri MC, Majello B, Major MB, Makareeva E, Malik
F, Mallilankaraman K, Malorni W, Maloyan A, Mammadova N, Man GCW, Manai F,
Mancias JD, Mandelkow EM, Mandell MA, Manfredi AA, Manjili MH, Manjithaya R,
Manque P, Manshian BB, Manzano R, Manzoni C, Mao K, Marchese C, Marchetti S,
Marconi AM, Marcucci F, Mardente S, Mareninova OA, Margeta M, Mari M, Marinelli
S, Marinelli O, Mariño G, Mariotto S, Marshall RS, Marten MR, Martens S, Martin
APJ, Martin KR, Martin S, Martin S, Martín-Segura A, Martín-Acebes MA, Martin-
Burriel I, Martin-Rincon M, Martin-Sanz P, Martina JA, Martinet W, Martinez A,
Martinez A, Martinez J, Martinez Velazquez M, Martinez-Lopez N, Martinez-Vicente
M, Martins DO, Martins JO, Martins WK, Martins-Marques T, Marzetti E, Masaldan
S, Masclaux-Daubresse C, Mashek DG, Massa V, Massieu L, Masson GR, Masuelli L,
Masyuk AI, Masyuk TV, Matarrese P, Matheu A, Matoba S, Matsuzaki S, Mattar P,
Matte A, Mattoscio D, Mauriz JL, Mauthe M, Mauvezin C, Maverakis E, Maycotte P,
Mayer J, Mazzoccoli G, Mazzoni C, Mazzulli JR, McCarty N, McDonald C, McGill MR,
McKenna SL, McLaughlin B, McLoughlin F, McNiven MA, McWilliams TG, Mechta-
Grigoriou F, Medeiros TC, Medina DL, Megeney LA, Megyeri K, Mehrpour M, Mehta
JL, Meijer AJ, Meijer AH, Mejlvang J, Meléndez A, Melk A, Memisoglu G, Mendes
AF, Meng D, Meng F, Meng T, Menna-Barreto R, Menon MB, Mercer C, Mercier AE,
Mergny JL, Merighi A, Merkley SD, Merla G, Meske V, Mestre AC, Metur SP, Meyer
C, Meyer H, Mi W, Mialet-Perez J, Miao J, Micale L, Miki Y, Milan E, Milczarek
M, Miller DL, Miller SI, Miller S, Millward SW, Milosevic I, Minina EA, Mirzaei
H, Mirzaei HR, Mirzaei M, Mishra A, Mishra N, Mishra PK, Misirkic Marjanovic M,
Misasi R, Misra A, Misso G, Mitchell C, Mitou G, Miura T, Miyamoto S, Miyazaki
M, Miyazaki M, Miyazaki T, Miyazawa K, Mizushima N, Mogensen TH, Mograbi B,
Mohammadinejad R, Mohamud Y, Mohanty A, Mohapatra S, Möhlmann T, Mohmmed A,
Moles A, Moley KH, Molinari M, Mollace V, Møller AB, Mollereau B, Mollinedo F,
Montagna C, Monteiro MJ, Montella A, Montes LR, Montico B, Mony VK, Monzio
Compagnoni G, Moore MN, Moosavi MA, Mora AL, Mora M, Morales-Alamo D, Moratalla
R, Moreira PI, Morelli E, Moreno S, Moreno-Blas D, Moresi V, Morga B, Morgan AH,
Morin F, Morishita H, Moritz OL, Moriyama M, Moriyasu Y, Morleo M, Morselli E,
Moruno-Manchon JF, Moscat J, Mostowy S, Motori E, Moura AF, Moustaid-Moussa N,
Mrakovcic M, Muciño-Hernández G, Mukherjee A, Mukhopadhyay S, Mulcahy Levy JM,
Mulero V, Muller S, Münch C, Munjal A, Munoz-Canoves P, Muñoz-Galdeano T, Münz
C, Murakawa T, Muratori C, Murphy BM, Murphy JP, Murthy A, Myöhänen TT,
Mysorekar IU, Mytych J, Nabavi SM, Nabissi M, Nagy P, Nah J, Nahimana A,
Nakagawa I, Nakamura K, Nakatogawa H, Nandi SS, Nanjundan M, Nanni M, Napolitano
G, Nardacci R, Narita M, Nassif M, Nathan I, Natsumeda M, Naude RJ, Naumann C,
Naveiras O, Navid F, Nawrocki ST, Nazarko TY, Nazio F, Negoita F, Neill T,
Neisch AL, Neri LM, Netea MG, Neubert P, Neufeld TP, Neumann D, Neutzner A,
Newton PT, Ney PA, Nezis IP, Ng CCW, Ng TB, Nguyen HTT, Nguyen LT, Ni HM, Ní
Cheallaigh C, Ni Z, Nicolao MC, Nicoli F, Nieto-Diaz M, Nilsson P, Ning S,
Niranjan R, Nishimune H, Niso-Santano M, Nixon RA, Nobili A, Nobrega C, Noda T,
Nogueira-Recalde U, Nolan TM, Nombela I, Novak I, Novoa B, Nozawa T, Nukina N,
Nussbaum-Krammer C, Nylandsted J, O'Donovan TR, O'Leary SM, O'Rourke EJ,
O'Sullivan MP, O'Sullivan TE, Oddo S, Oehme I, Ogawa M, Ogier-Denis E,
Ogmundsdottir MH, Ogretmen B, Oh GT, Oh SH, Oh YJ, Ohama T, Ohashi Y, Ohmuraya
M, Oikonomou V, Ojha R, Okamoto K, Okazawa H, Oku M, Oliván S, Oliveira JMA,
Ollmann M, Olzmann JA, Omari S, Omary MB, Önal G, Ondrej M, Ong SB, Ong SG,
Onnis A, Orellana JA, Orellana-Muñoz S, Ortega-Villaizan MDM, Ortiz-Gonzalez XR,
Ortona E, Osiewacz HD, Osman AK, Osta R, Otegui MS, Otsu K, Ott C, Ottobrini L,
Ou JJ, Outeiro TF, Oynebraten I, Ozturk M, Pagès G, Pahari S, Pajares M, Pajvani
UB, Pal R, Paladino S, Pallet N, Palmieri M, Palmisano G, Palumbo C, Pampaloni
F, Pan L, Pan Q, Pan W, Pan X, Panasyuk G, Pandey R, Pandey UB, Pandya V, Paneni
F, Pang SY, Panzarini E, Papademetrio DL, Papaleo E, Papinski D, Papp D, Park
EC, Park HT, Park JM, Park JI, Park JT, Park J, Park SC, Park SY, Parola AH,
Parys JB, Pasquier A, Pasquier B, Passos JF, Pastore N, Patel HH, Patschan D,
Pattingre S, Pedraza-Alva G, Pedraza-Chaverri J, Pedrozo Z, Pei G, Pei J, Peled-
Zehavi H, Pellegrini JM, Pelletier J, Peñalva MA, Peng D, Peng Y, Penna F,
Pennuto M, Pentimalli F, Pereira CM, Pereira GJS, Pereira LC, Pereira de Almeida
L, Perera ND, Pérez-Lara Á, Perez-Oliva AB, Pérez-Pérez ME, Periyasamy P, Perl
A, Perrotta C, Perrotta I, Pestell RG, Petersen M, Petrache I, Petrovski G,
Pfirrmann T, Pfister AS, Philips JA, Pi H, Picca A, Pickrell AM, Picot S,
Pierantoni GM, Pierdominici M, Pierre P, Pierrefite-Carle V, Pierzynowska K,
Pietrocola F, Pietruczuk M, Pignata C, Pimentel-Muiños FX, Pinar M, Pinheiro RO,
Pinkas-Kramarski R, Pinton P, Pircs K, Piya S, Pizzo P, Plantinga TS, Platta HW,
Plaza-Zabala A, Plomann M, Plotnikov EY, Plun-Favreau H, Pluta R, Pocock R,
Pöggeler S, Pohl C, Poirot M, Poletti A, Ponpuak M, Popelka H, Popova B, Porta
H, Porte Alcon S, Portilla-Fernandez E, Post M, Potts MB, Poulton J, Powers T,
Prahlad V, Prajsnar TK, Praticò D, Prencipe R, Priault M, Proikas-Cezanne T,
Promponas VJ, Proud CG, Puertollano R, Puglielli L, Pulinilkunnil T, Puri D,
Puri R, Puyal J, Qi X, Qi Y, Qian W, Qiang L, Qiu Y, Quadrilatero J, Quarleri J,
Raben N, Rabinowich H, Ragona D, Ragusa MJ, Rahimi N, Rahmati M, Raia V,
Raimundo N, Rajasekaran NS, Ramachandra Rao S, Rami A, Ramírez-Pardo I, Ramsden
DB, Randow F, Rangarajan PN, Ranieri D, Rao H, Rao L, Rao R, Rathore S,
Ratnayaka JA, Ratovitski EA, Ravanan P, Ravegnini G, Ray SK, Razani B, Rebecca
V, Reggiori F, Régnier-Vigouroux A, Reichert AS, Reigada D, Reiling JH, Rein T,
Reipert S, Rekha RS, Ren H, Ren J, Ren W, Renault T, Renga G, Reue K, Rewitz K,
Ribeiro de Andrade Ramos B, Riazuddin SA, Ribeiro-Rodrigues TM, Ricci JE, Ricci
R, Riccio V, Richardson DR, Rikihisa Y, Risbud MV, Risueño RM, Ritis K, Rizza S,
Rizzuto R, Roberts HC, Roberts LD, Robinson KJ, Roccheri MC, Rocchi S, Rodney
GG, Rodrigues T, Rodrigues Silva VR, Rodriguez A, Rodriguez-Barrueco R,
Rodriguez-Henche N, Rodriguez-Rocha H, Roelofs J, Rogers RS, Rogov VV, Rojo AI,
Rolka K, Romanello V, Romani L, Romano A, Romano PS, Romeo-Guitart D, Romero LC,
Romero M, Roney JC, Rongo C, Roperto S, Rosenfeldt MT, Rosenstiel P, Rosenwald
AG, Roth KA, Roth L, Roth S, Rouschop KMA, Roussel BD, Roux S, Rovere-Querini P,
Roy A, Rozieres A, Ruano D, Rubinsztein DC, Rubtsova MP, Ruckdeschel K,
Ruckenstuhl C, Rudolf E, Rudolf R, Ruggieri A, Ruparelia AA, Rusmini P, Russell
RR, Russo GL, Russo M, Russo R, Ryabaya OO, Ryan KM, Ryu KY, Sabater-Arcis M,
Sachdev U, Sacher M, Sachse C, Sadhu A, Sadoshima J, Safren N, Saftig P, Sagona
AP, Sahay G, Sahebkar A, Sahin M, Sahin O, Sahni S, Saito N, Saito S, Saito T,
Sakai R, Sakai Y, Sakamaki JI, Saksela K, Salazar G, Salazar-Degracia A,
Salekdeh GH, Saluja AK, Sampaio-Marques B, Sanchez MC, Sanchez-Alcazar JA,
Sanchez-Vera V, Sancho-Shimizu V, Sanderson JT, Sandri M, Santaguida S,
Santambrogio L, Santana MM, Santoni G, Sanz A, Sanz P, Saran S, Sardiello M,
Sargeant TJ, Sarin A, Sarkar C, Sarkar S, Sarrias MR, Sarkar S, Sarmah DT,
Sarparanta J, Sathyanarayan A, Sathyanarayanan R, Scaglione KM, Scatozza F,
Schaefer L, Schafer ZT, Schaible UE, Schapira AHV, Scharl M, Schatzl HM, Schein
CH, Scheper W, Scheuring D, Schiaffino MV, Schiappacassi M, Schindl R,
Schlattner U, Schmidt O, Schmitt R, Schmidt SD, Schmitz I, Schmukler E,
Schneider A, Schneider BE, Schober R, Schoijet AC, Schott MB, Schramm M,
Schröder B, Schuh K, Schüller C, Schulze RJ, Schürmanns L, Schwamborn JC,
Schwarten M, Scialo F, Sciarretta S, Scott MJ, Scotto KW, Scovassi AI, Scrima A,
Scrivo A, Sebastian D, Sebti S, Sedej S, Segatori L, Segev N, Seglen PO, Seiliez
I, Seki E, Selleck SB, Sellke FW, Selsby JT, Sendtner M, Senturk S, Seranova E,
Sergi C, Serra-Moreno R, Sesaki H, Settembre C, Setty SRG, Sgarbi G, Sha O,
Shacka JJ, Shah JA, Shang D, Shao C, Shao F, Sharbati S, Sharkey LM, Sharma D,
Sharma G, Sharma K, Sharma P, Sharma S, Shen HM, Shen H, Shen J, Shen M, Shen W,
Shen Z, Sheng R, Sheng Z, Sheng ZH, Shi J, Shi X, Shi YH, Shiba-Fukushima K,
Shieh JJ, Shimada Y, Shimizu S, Shimozawa M, Shintani T, Shoemaker CJ, Shojaei
S, Shoji I, Shravage BV, Shridhar V, Shu CW, Shu HB, Shui K, Shukla AK, Shutt
TE, Sica V, Siddiqui A, Sierra A, Sierra-Torre V, Signorelli S, Sil P, Silva
BJA, Silva JD, Silva-Pavez E, Silvente-Poirot S, Simmonds RE, Simon AK, Simon
HU, Simons M, Singh A, Singh LP, Singh R, Singh SV, Singh SK, Singh SB, Singh S,
Singh SP, Sinha D, Sinha RA, Sinha S, Sirko A, Sirohi K, Sivridis EL, Skendros
P, Skirycz A, Slaninová I, Smaili SS, Smertenko A, Smith MD, Soenen SJ, Sohn EJ,
Sok SPM, Solaini G, Soldati T, Soleimanpour SA, Soler RM, Solovchenko A,
Somarelli JA, Sonawane A, Song F, Song HK, Song JX, Song K, Song Z, Soria LR,
Sorice M, Soukas AA, Soukup SF, Sousa D, Sousa N, Spagnuolo PA, Spector SA,
Srinivas Bharath MM, St Clair D, Stagni V, Staiano L, Stalnecker CA, Stankov MV,
Stathopulos PB, Stefan K, Stefan SM, Stefanis L, Steffan JS, Steinkasserer A,
Stenmark H, Sterneckert J, Stevens C, Stoka V, Storch S, Stork B, Strappazzon F,
Strohecker AM, Stupack DG, Su H, Su LY, Su L, Suarez-Fontes AM, Subauste CS,
Subbian S, Subirada PV, Sudhandiran G, Sue CM, Sui X, Summers C, Sun G, Sun J,
Sun K, Sun MX, Sun Q, Sun Y, Sun Z, Sunahara KKS, Sundberg E, Susztak K,
Sutovsky P, Suzuki H, Sweeney G, Symons JD, Sze SCW, Szewczyk NJ, Tabęcka-
Łonczynska A, Tabolacci C, Tacke F, Taegtmeyer H, Tafani M, Tagaya M, Tai H,
Tait SWG, Takahashi Y, Takats S, Talwar P, Tam C, Tam SY, Tampellini D, Tamura
A, Tan CT, Tan EK, Tan YQ, Tanaka M, Tanaka M, Tang D, Tang J, Tang TS, Tanida
I, Tao Z, Taouis M, Tatenhorst L, Tavernarakis N, Taylor A, Taylor GA, Taylor
JM, Tchetina E, Tee AR, Tegeder I, Teis D, Teixeira N, Teixeira-Clerc F,
Tekirdag KA, Tencomnao T, Tenreiro S, Tepikin AV, Testillano PS, Tettamanti G,
Tharaux PL, Thedieck K, Thekkinghat AA, Thellung S, Thinwa JW, Thirumalaikumar
VP, Thomas SM, Thomes PG, Thorburn A, Thukral L, Thum T, Thumm M, Tian L, Tichy
A, Till A, Timmerman V, Titorenko VI, Todi SV, Todorova K, Toivonen JM,
Tomaipitinca L, Tomar D, Tomas-Zapico C, Tomić S, Tong BC, Tong C, Tong X, Tooze
SA, Torgersen ML, Torii S, Torres-López L, Torriglia A, Towers CG, Towns R,
Toyokuni S, Trajkovic V, Tramontano D, Tran QG, Travassos LH, Trelford CB,
Tremel S, Trougakos IP, Tsao BP, Tschan MP, Tse HF, Tse TF, Tsugawa H, Tsvetkov
AS, Tumbarello DA, Tumtas Y, Tuñón MJ, Turcotte S, Turk B, Turk V, Turner BJ,
Tuxworth RI, Tyler JK, Tyutereva EV, Uchiyama Y, Ugun-Klusek A, Uhlig HH,
Ułamek-Kozioł M, Ulasov IV, Umekawa M, Ungermann C, Unno R, Urbe S, Uribe-
Carretero E, Üstün S, Uversky VN, Vaccari T, Vaccaro MI, Vahsen BF,
Vakifahmetoglu-Norberg H, Valdor R, Valente MJ, Valko A, Vallee RB, Valverde AM,
Van den Berghe G, van der Veen S, Van Kaer L, van Loosdregt J, van Wijk SJL,
Vandenberghe W, Vanhorebeek I, Vannier-Santos MA, Vannini N, Vanrell MC,
Vantaggiato C, Varano G, Varela-Nieto I, Varga M, Vasconcelos MH, Vats S, Vavvas
DG, Vega-Naredo I, Vega-Rubin-de-Celis S, Velasco G, Velázquez AP, Vellai T,
Vellenga E, Velotti F, Verdier M, Verginis P, Vergne I, Verkade P, Verma M,
Verstreken P, Vervliet T, Vervoorts J, Vessoni AT, Victor VM, Vidal M, Vidoni C,
Vieira OV, Vierstra RD, Viganó S, Vihinen H, Vijayan V, Vila M, Vilar M,
Villalba JM, Villalobo A, Villarejo-Zori B, Villarroya F, Villarroya J, Vincent
O, Vindis C, Viret C, Viscomi MT, Visnjic D, Vitale I, Vocadlo DJ,
Voitsekhovskaja OV, Volonté C, Volta M, Vomero M, Von Haefen C, Vooijs MA, Voos
W, Vucicevic L, Wade-Martins R, Waguri S, Waite KA, Wakatsuki S, Walker DW,
Walker MJ, Walker SA, Walter J, Wandosell FG, Wang B, Wang CY, Wang C, Wang C,
Wang C, Wang CY, Wang D, Wang F, Wang F, Wang F, Wang G, Wang H, Wang H, Wang H,
Wang HG, Wang J, Wang J, Wang J, Wang J, Wang K, Wang L, Wang L, Wang MH, Wang
M, Wang N, Wang P, Wang P, Wang P, Wang P, Wang QJ, Wang Q, Wang QK, Wang QA,
Wang WT, Wang W, Wang X, Wang X, Wang Y, Wang Y, Wang Y, Wang YY, Wang Y, Wang
Y, Wang Y, Wang Y, Wang Z, Wang Z, Wang Z, Warnes G, Warnsmann V, Watada H,
Watanabe E, Watchon M, Wawrzyńska A, Weaver TE, Wegrzyn G, Wehman AM, Wei H, Wei
L, Wei T, Wei Y, Weiergräber OH, Weihl CC, Weindl G, Weiskirchen R, Wells A, Wen
RH, Wen X, Werner A, Weykopf B, Wheatley SP, Whitton JL, Whitworth AJ, Wiktorska
K, Wildenberg ME, Wileman T, Wilkinson S, Willbold D, Williams B, Williams RSB,
Williams RL, Williamson PR, Wilson RA, Winner B, Winsor NJ, Witkin SS, Wodrich
H, Woehlbier U, Wollert T, Wong E, Wong JH, Wong RW, Wong VKW, Wong WW, Wu AG,
Wu C, Wu J, Wu J, Wu KK, Wu M, Wu SY, Wu S, Wu SY, Wu S, Wu WKK, Wu X, Wu X, Wu
YW, Wu Y, Xavier RJ, Xia H, Xia L, Xia Z, Xiang G, Xiang J, Xiang M, Xiang W,
Xiao B, Xiao G, Xiao H, Xiao HT, Xiao J, Xiao L, Xiao S, Xiao Y, Xie B, Xie CM,
Xie M, Xie Y, Xie Z, Xie Z, Xilouri M, Xu C, Xu E, Xu H, Xu J, Xu J, Xu L, Xu
WW, Xu X, Xue Y, Yakhine-Diop SMS, Yamaguchi M, Yamaguchi O, Yamamoto A,
Yamashina S, Yan S, Yan SJ, Yan Z, Yanagi Y, Yang C, Yang DS, Yang H, Yang HT,
Yang H, Yang JM, Yang J, Yang J, Yang L, Yang L, Yang M, Yang PM, Yang Q, Yang
S, Yang S, Yang SF, Yang W, Yang WY, Yang X, Yang X, Yang Y, Yang Y, Yao H, Yao
S, Yao X, Yao YG, Yao YM, Yasui T, Yazdankhah M, Yen PM, Yi C, Yin XM, Yin Y,
Yin Z, Yin Z, Ying M, Ying Z, Yip CK, Yiu SPT, Yoo YH, Yoshida K, Yoshii SR,
Yoshimori T, Yousefi B, Yu B, Yu H, Yu J, Yu J, Yu L, Yu ML, Yu SW, Yu VC, Yu
WH, Yu Z, Yu Z, Yuan J, Yuan LQ, Yuan S, Yuan SF, Yuan Y, Yuan Z, Yue J, Yue Z,
Yun J, Yung RL, Zacks DN, Zaffagnini G, Zambelli VO, Zanella I, Zang QS, Zanivan
S, Zappavigna S, Zaragoza P, Zarbalis KS, Zarebkohan A, Zarrouk A, Zeitlin SO,
Zeng J, Zeng JD, Žerovnik E, Zhan L, Zhang B, Zhang DD, Zhang H, Zhang H, Zhang
H, Zhang H, Zhang H, Zhang H, Zhang H, Zhang HL, Zhang J, Zhang J, Zhang JP,
Zhang KYB, Zhang LW, Zhang L, Zhang L, Zhang L, Zhang L, Zhang M, Zhang P, Zhang
S, Zhang W, Zhang X, Zhang XW, Zhang X, Zhang X, Zhang X, Zhang X, Zhang XD,
Zhang Y, Zhang Y, Zhang Y, Zhang YD, Zhang Y, Zhang YY, Zhang Y, Zhang Z, Zhang
Z, Zhang Z, Zhang Z, Zhang Z, Zhang Z, Zhao H, Zhao L, Zhao S, Zhao T, Zhao XF,
Zhao Y, Zhao Y, Zhao Y, Zhao Y, Zheng G, Zheng K, Zheng L, Zheng S, Zheng XL,
Zheng Y, Zheng ZG, Zhivotovsky B, Zhong Q, Zhou A, Zhou B, Zhou C, Zhou G, Zhou
H, Zhou H, Zhou H, Zhou J, Zhou J, Zhou J, Zhou J, Zhou K, Zhou R, Zhou XJ, Zhou
Y, Zhou Y, Zhou Y, Zhou ZY, Zhou Z, Zhu B, Zhu C, Zhu GQ, Zhu H, Zhu H, Zhu H,
Zhu WG, Zhu Y, Zhu Y, Zhuang H, Zhuang X, Zientara-Rytter K, Zimmermann CM,
Ziviani E, Zoladek T, Zong WX, Zorov DB, Zorzano A, Zou W, Zou Z, Zou Z, Zuryn
S, Zwerschke W, Brand-Saberi B, Dong XC, Kenchappa CS, Li Z, Lin Y, Oshima S,
Rong Y, Sluimer JC, Stallings CL, Tong CK. Guidelines for the use and
interpretation of assays for monitoring autophagy (4th edition)1.
Autophagy. 2021 Jan;17(1):1-382. doi: 10.1080/15548627.2020.1797280. Epub 2021
Feb 8. PMID: 33634751; PMCID: PMC7996087.
140: Perrier S, Michell-Robinson MA, Bernard G. POLR3-Related Leukodystrophy:
Exploring Potential Therapeutic Approaches. Front Cell Neurosci. 2021 Jan
28;14:631802. doi: 10.3389/fncel.2020.631802. PMID: 33633543; PMCID: PMC7902007.
141: Jin JW, Fan X, Del Cid-Pellitero E, Liu XX, Zhou L, Dai C, Gibbs E, He W,
Li H, Wu X, Hill A, Leavitt BR, Cashman N, Liu L, Lu J, Durcan TM, Dong Z, Fon
EA, Wang YT. Development of an α-synuclein knockdown peptide and evaluation of
its efficacy in Parkinson's disease models. Commun Biol. 2021 Feb 19;4(1):232.
doi: 10.1038/s42003-021-01746-6. PMID: 33608634; PMCID: PMC7895943.
142: Moreau JT, Saint-Martin C, Baillet S, Dudley RWR. MNI SISCOM: an Open-
Source Tool for Computing Subtraction Ictal Single-Photon Emission CT
Coregistered to MRI. J Digit Imaging. 2021 Apr;34(2):357-361. doi:
10.1007/s10278-021-00422-9. Epub 2021 Feb 18. PMID: 33604806; PMCID: PMC8289986.
143: Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E,
Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM,
Dupre N, Dion PA, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. Evidence for
Non-Mendelian Inheritance in Spastic Paraplegia 7. Mov Disord. 2021
Jul;36(7):1664-1675. doi: 10.1002/mds.28528. Epub 2021 Feb 17. PMID: 33598982.
144: Escartin C, Galea E, Lakatos A, O'Callaghan JP, Petzold GC, Serrano-Pozo A,
Steinhäuser C, Volterra A, Carmignoto G, Agarwal A, Allen NJ, Araque A, Barbeito
L, Barzilai A, Bergles DE, Bonvento G, Butt AM, Chen WT, Cohen-Salmon M,
Cunningham C, Deneen B, De Strooper B, Díaz-Castro B, Farina C, Freeman M, Gallo
V, Goldman JE, Goldman SA, Götz M, Gutiérrez A, Haydon PG, Heiland DH, Hol EM,
Holt MG, Iino M, Kastanenka KV, Kettenmann H, Khakh BS, Koizumi S, Lee CJ,
Liddelow SA, MacVicar BA, Magistretti P, Messing A, Mishra A, Molofsky AV, Murai
KK, Norris CM, Okada S, Oliet SHR, Oliveira JF, Panatier A, Parpura V, Pekna M,
Pekny M, Pellerin L, Perea G, Pérez-Nievas BG, Pfrieger FW, Poskanzer KE,
Quintana FJ, Ransohoff RM, Riquelme-Perez M, Robel S, Rose CR, Rothstein JD,
Rouach N, Rowitch DH, Semyanov A, Sirko S, Sontheimer H, Swanson RA, Vitorica J,
Wanner IB, Wood LB, Wu J, Zheng B, Zimmer ER, Zorec R, Sofroniew MV, Verkhratsky
A. Reactive astrocyte nomenclature, definitions, and future directions. Nat
Neurosci. 2021 Mar;24(3):312-325. doi: 10.1038/s41593-020-00783-4. Epub 2021 Feb
15. PMID: 33589835; PMCID: PMC8007081.
145: Shemie SD, Torrance S, Wilson L, Hornby L, MacLean J, Mohr J, Gillrie C,
Badiwala MV, Baker A, Freed DH, Simpson C, Teitelbaum J, Brodrecht D, Healey A.
Heart donation and transplantation after circulatory determination of death:
expert guidance from a Canadian consensus building process. Can J Anaesth. 2021
May;68(5):661-671. doi: 10.1007/s12630-021-01926-2. Epub 2021 Feb 5. PMID:
33543427; PMCID: PMC8035095.
146: Nyirenda MH, Fadda G, Healy LM, Mexhitaj I, Poliquin-Lasnier L, Hanwell H,
Saveriano AW, Rozenberg A, Li R, Moore CS, Belabani C, Johnson T, O'Mahony J,
Arnold DL, Yeh EA, Marrie RA, Dunn S, Banwell B, Bar-Or A. Pro-inflammatory
adiponectin in pediatric-onset multiple sclerosis. Mult Scler. 2021
Oct;27(12):1948-1959. doi: 10.1177/1352458521989090. Epub 2021 Feb 1. PMID:
33522403.
147: Dhanani S, Hornby L, van Beinum A, Scales NB, Hogue M, Baker A, Beed S,
Boyd JG, Chandler JA, Chassé M, D'Aragon F, Dezfulian C, Doig CJ, Duska F,
Friedrich JO, Gardiner D, Gofton T, Harvey D, Herry C, Isac G, Kramer AH,
Kutsogiannis DJ, Maslove DM, Meade M, Mehta S, Munshi L, Norton L, Pagliarello
G, Ramsay T, Rusinova K, Scales D, Schmidt M, Seely A, Shahin J, Slessarev M, So
D, Talbot H, van Mook WNKA, Waldauf P, Weiss M, Wind JT, Shemie SD; Canadian
Critical Care Trials Group; Canadian Donation and Transplantation Research
Program. Resumption of Cardiac Activity after Withdrawal of Life-Sustaining
Measures. N Engl J Med. 2021 Jan 28;384(4):345-352. doi: 10.1056/NEJMoa2022713.
PMID: 33503343.
148: Kumar R, Smith KS, Deng M, Terhune C, Robinson GW, Orr BA, Liu APY, Lin T,
Billups CA, Chintagumpala M, Bowers DC, Hassall TE, Hansford JR, Khuong-Quang
DA, Crawford JR, Bendel AE, Gururangan S, Schroeder K, Bouffet E, Bartels U,
Fisher MJ, Cohn R, Partap S, Kellie SJ, McCowage G, Paulino AC, Rutkowski S,
Fleischhack G, Dhall G, Klesse LJ, Leary S, Nazarian J, Kool M, Wesseling P,
Ryzhova M, Zheludkova O, Golanov AV, McLendon RE, Packer RJ, Dunham C, Hukin J,
Fouladi M, Faria CC, Pimentel J, Walter AW, Jabado N, Cho YJ, Perreault S, Croul
SE, Zapotocky M, Hawkins C, Tabori U, Taylor MD, Pfister SM, Klimo P Jr, Boop
FA, Ellison DW, Merchant TE, Onar-Thomas A, Korshunov A, Jones DTW, Gajjar A,
Ramaswamy V, Northcott PA. Clinical Outcomes and Patient-Matched Molecular
Composition of Relapsed Medulloblastoma. J Clin Oncol. 2021 Mar 1;39(7):807-821.
doi: 10.1200/JCO.20.01359. Epub 2021 Jan 27. PMID: 33502920; PMCID: PMC8078396.
149: Perrier S, Matovic S, Bernard G. Classifying Hypomyelination: A Critical
(White) Matter. Child Neurol Open. 2020 Dec 24;7:2329048X20983761. doi:
10.1177/2329048X20983761. PMID: 33490304; PMCID: PMC7768829.
150: Zhan D, Li H, Shi W, Zhao R. Social-emotional, sleep and feeding problems
in young patients with agenesis of the corpus callosum and the life quality of
their parents. Soc Neurosci. 2021 Apr;16(2):166-173. doi:
10.1080/17470919.2021.1879931. Epub 2021 Feb 8. PMID: 33471630.
151: Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM,
Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA,
Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados MA, Singer
HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C, Tarnok Z,
Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ, McMahon
WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee PC,
Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A, Hoekstra
PJ, Kuperman S, Zinner SH, Wagner M, Knowles JA, Jeremy Willsey A, Tischfield
JA, Heiman GA, Cox NJ, Freimer NB, Neale BM, Davis LK, Coppola G, Mathews CA,
Scharf JM, Paschou P; Tourette Association of America International Consortium
for Genetics, Barr CL, Batterson JR, Berlin C, Budman CL, Cath DC, Coppola G,
Cox NJ, Darrow S, Davis LK, Dion Y, Freimer NB, Grados MA, Greenberg E,
Hirschtritt ME, Huang AY, Illmann C, King RA, Kurlan R, Leckman JF, Lyon GJ,
Malaty IA, Mathews CA, McMahon WM, Neale BM, Okun MS, Osiecki L, Robertson MM,
Rouleau GA, Sandor P, Scharf JM, Singer HS, Smit JH, Sul JH, Yu D; Gilles de la
Tourette GWAS Replication Initiative, Aschauer HAH, Barta C, Budman CL, Cath DC,
Depienne C, Hartmann A, Hebebrand J, Konstantinidis A, Mathews CA, Müller-Vahl
K, Nagy P, Nöthen MM, Paschou P, Rizzo R, Rouleau GA, Sandor P, Scharf JM,
Schlögelhofer M, Stamenkovic M, Stuhrmann M, Tsetsos F, Tarnok Z, Wolanczyk T,
Worbe Y; Tourette International Collaborative Genetics Study, Brown L, Cheon KA,
Coffey BJ, Dietrich A, Fernandez TV, Garcia-Delgar B, Gilbert D, Grice DE,
Hagstrøm J, Hedderly T, Heiman GA, Heyman I, Hoekstra PJ, Huyser C, Kim YK, Kim
YS, King RA, Koh YJ, Kook S, Kuperman S, Leventhal BL, Madruga-Garrido M, Mir P,
Morer A, Münchau A, Plessen KJ, Roessner V, Shin EY, Song DH, Song J, Tischfield
JA, Willsey AJ, Zinner S; Psychiatric Genomics Consortium Tourette Syndrome
Working Group, Aschauer H, Barr CL, Barta C, Batterson JR, Berlin C, Brown L,
Budman CL, Cath DC, Coffey BJ, Coppola G, Cox NJ, Darrow S, Davis LK, Depienne
C, Dietrich A, Dion Y, Fernandez T, Freimer NB, Gilbert D, Grados MA, Greenberg
E, Hartmann A, Hebebrand J, Heiman G, Hirschtritt ME, Hoekstra P, Huang AY,
Illmann C, Jankovic J, King RA, Kuperman S, Lee PC, Lyon GJ, Malaty IA, Mathews
CA, McMahon WM, Müller-Vahl K, Nagy P, Neale BM, Nöthen MM, Okun MS, Osiecki L,
Paschou P, Rizzo R, Robertson MM, Rouleau GA, Sandor P, Scharf JM, Schlögelhofer
M, Singer HS, Stamenkovic M, Stuhrmann M, Sul JH, Tarnok Z, Tischfield J,
Tsetsos F, Willsey AJ, Woods D, Worbe Y, Yu D, Zinner S. Synaptic processes and
immune-related pathways implicated in Tourette syndrome. Transl Psychiatry. 2021
Jan 18;11(1):56. doi: 10.1038/s41398-020-01082-z. PMID: 33462189; PMCID:
PMC7814139.
152: Myers KA, Bennett MF, Grinton BE, Dabscheck G, Chan EK, Bello-Espinosa LE,
Sadleir LG, D'Alfonso S, Schneider AL, Damiano JA, Hildebrand MS, Bahlo M,
Berkovic SF, Buchhalter J, Scheffer IE. Contribution of rare genetic variants to
drug response in absence epilepsy. Epilepsy Res. 2021 Feb;170:106537. doi:
10.1016/j.eplepsyres.2020.106537. Epub 2021 Jan 4. PMID: 33421703.
153: Djordjevic D, Pinard M, Gauthier MS, Smith-Hicks C, Hoffman TL, Wolf NI,
Oegema R, van Binsbergen E, Baskin B, Bernard G, Fribourg S, Coulombe B, Yoon G.
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating
neuropathy. Am J Hum Genet. 2021 Jan 7;108(1):186-193. doi:
10.1016/j.ajhg.2020.12.002. Erratum in: Am J Hum Genet. 2022 Apr
7;109(4):759-763. PMID: 33417887; PMCID: PMC7820722.
154: Fernandes MGF, Luo JXX, Cui QL, Perlman K, Pernin F, Yaqubi M, Hall JA,
Dudley R, Srour M, Couturier CP, Petrecca K, Larochelle C, Healy LM, Stratton
JA, Kennedy TE, Antel JP. Age-related injury responses of human oligodendrocytes
to metabolic insults: link to BCL-2 and autophagy pathways. Commun Biol. 2021
Jan 4;4(1):20. doi: 10.1038/s42003-020-01557-1. PMID: 33398046; PMCID:
PMC7782481.
155: Alawadhi A, Morgan AT, Mucha BE, Scheffer IE, Myers KA. Self-limited focal
epilepsy and childhood apraxia of speech with WAC pathogenic variants. Eur J
Paediatr Neurol. 2021 Jan;30:25-28. doi: 10.1016/j.ejpn.2020.12.010. Epub 2020
Dec 24. PMID: 33387902.
156: Lam J, Moreau JT, Chen JK, Albrecht S, Saint-Martin C, Simard-Tremblay E,
Baillet S, Klein D, Dudley RW. Prosopagnosia seizure semiology in a 10-year-old
boy: a functional neuroimaging study. BMJ Case Rep. 2020 Dec 22;13(12):e237228.
doi: 10.1136/bcr-2020-237228. PMID: 33370980; PMCID: PMC7757463.
157: Opheim G, van der Kolk A, Markenroth Bloch K, Colon AJ, Davis KA, Henry TR,
Jansen JFA, Jones SE, Pan JW, Rössler K, Stein JM, Strandberg MC, Trattnig S,
Van de Moortele PF, Vargas MI, Wang I, Bartolomei F, Bernasconi N, Bernasconi A,
Bernhardt B, Björkman-Burtscher I, Cosottini M, Das SR, Hertz-Pannier L, Inati
S, Jurkiewicz MT, Khan AR, Liang S, Ma RE, Mukundan S, Pardoe H, Pinborg LH,
Polimeni JR, Ranjeva JP, Steijvers E, Stufflebeam S, Veersema TJ, Vignaud A,
Voets N, Vulliemoz S, Wiggins CJ, Xue R, Guerrini R, Guye M. 7T Epilepsy Task
Force Consensus Recommendations on the Use of 7T MRI in Clinical Practice.
Neurology. 2021 Feb 16;96(7):327-341. doi: 10.1212/WNL.0000000000011413. Epub
2020 Dec 22. PMID: 33361257; PMCID: PMC8055334.
158: Chung J, Maruvka YE, Sudhaman S, Kelly J, Haradhvala NJ, Bianchi V, Edwards
M, Forster VJ, Nunes NM, Galati MA, Komosa M, Deshmukh S, Cabric V, Davidson S,
Zatzman M, Light N, Hayes R, Brunga L, Anderson ND, Ho B, Hodel KP, Siddaway R,
Morrissy AS, Bowers DC, Larouche V, Bronsema A, Osborn M, Cole KA, Opocher E,
Mason G, Thomas GA, George B, Ziegler DS, Lindhorst S, Vanan M, Yalon-Oren M,
Reddy AT, Massimino M, Tomboc P, Van Damme A, Lossos A, Durno C, Aronson M,
Morgenstern DA, Bouffet E, Huang A, Taylor MD, Villani A, Malkin D, Hawkins CE,
Pursell ZF, Shlien A, Kunkel TA, Getz G, Tabori U. DNA Polymerase and Mismatch
Repair Exert Distinct Microsatellite Instability Signatures in Normal and
Malignant Human Cells. Cancer Discov. 2021 May;11(5):1176-1191. doi:
10.1158/2159-8290.CD-20-0790. Epub 2020 Dec 18. PMID: 33355208; PMCID:
PMC8223607.
159: Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler
IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin
K, Li L, Millwood IY, Chen Z, Rouleau GA, Zhou S, Rannikmäe K, Sudlow CLM,
Houlden H, van den Berg LH, Dina C, Naggara O, Gentric JC, Shotar E, Eugène F,
Desal H, Winsvold BS, Børte S, Johnsen MB, Brumpton BM, Sandvei MS, Willer CJ,
Hveem K, Zwart JA, Verschuren WMM, Friedrich CM, Hirsch S, Schilling S,
Dauvillier J, Martin O; HUNT All-In Stroke; China Kadoorie Biobank Collaborative
Group; BioBank Japan Project Consortium; ICAN Study Group; CADISP Group;
Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigators;
International Stroke Genetics Consortium (ISGC), Jones GT, Bown MJ, Ko NU, Kim
H, Coleman JRI, Breen G, Zaroff JG, Klijn CJM, Malik R, Dichgans M,
Sargurupremraj M, Tatlisumak T, Amouyel P, Debette S, Rinkel GJE, Worrall BB,
Pera J, Slowik A, Gaál-Paavola EI, Niemelä M, Jääskeläinen JE, von Und Zu
Fraunberg M, Lindgren A, Broderick JP, Werring DJ, Woo D, Redon R, Bijlenga P,
Kamatani Y, Veldink JH, Ruigrok YM. Author Correction: Genome-wide association
study of intracranial aneurysms identifies 17 risk loci and genetic overlap with
clinical risk factors. Nat Genet. 2021 Feb;53(2):254. doi:
10.1038/s41588-020-00760-4. Erratum for: Nat Genet. 2020 Dec;52(12):1303-1313.
PMID: 33353957.
160: Hutcheon JA, Harper S, Liauw J, Skoll MA, Srour M, Strumpf EC. Antenatal
corticosteroid administration and early school age child development: A
regression discontinuity study in British Columbia, Canada. PLoS Med. 2020 Dec
7;17(12):e1003435. doi: 10.1371/journal.pmed.1003435. PMID: 33284805; PMCID:
PMC7721186.
161: Diez-Fairen M, Houle G, Ortega-Cubero S, Bandres-Ciga S, Alvarez I, Carcel
M, Ibañez L, Fernandez MV, Budde JP, Trotta JR, Tonda R, Chong JX, Bamshad MJ,
Nickerson DA; University of Washington Center for Mendelian Genomics (UWCMG),
Aguilar M, Tartari JP, Gironell A, García-Martín E, Agundez JA, Alonso-Navarro
H, Jimenez-Jimenez FJ, Fernandez M, Valldeoriola F, Marti MJ, Tolosa E, Coria F,
Pastor MA, Vilariño-Güell C, Rajput A, Dion PA, Cruchaga C, Rouleau GA, Pastor
P. Exome-wide rare variant analysis in familial essential tremor. Parkinsonism
Relat Disord. 2021 Jan;82:109-116. doi: 10.1016/j.parkreldis.2020.11.021. Epub
2020 Nov 24. PMID: 33279834; PMCID: PMC7856267.
162: Fallah A, Subramaniam T, Phillips HW, Michalet X, Vinters HV, Yong WH, Wu
JY, Salamon N, Ellingson BM, Wang AC, Reyes SD, Ibrahim GM, Weil AG, Chang JW,
Babayan D, Nguyen JC, Behnke E, Tseng CH, Mathern GW. Novel tonometer device
distinguishes brain stiffness in epilepsy surgery. Sci Rep. 2020 Dec
1;10(1):20978. doi: 10.1038/s41598-020-77888-0. PMID: 33262385; PMCID:
PMC7708453.
163: Chen CCL, Deshmukh S, Jessa S, Hadjadj D, Lisi V, Andrade AF, Faury D,
Jawhar W, Dali R, Suzuki H, Pathania M, A D, Dubois F, Woodward E, Hébert S,
Coutelier M, Karamchandani J, Albrecht S, Brandner S, De Jay N, Gayden T, Bajic
A, Harutyunyan AS, Marchione DM, Mikael LG, Juretic N, Zeinieh M, Russo C,
Maestro N, Bassenden AV, Hauser P, Virga J, Bognar L, Klekner A, Zapotocky M,
Vicha A, Krskova L, Vanova K, Zamecnik J, Sumerauer D, Ekert PG, Ziegler DS,
Ellezam B, Filbin MG, Blanchette M, Hansford JR, Khuong-Quang DA, Berghuis AM,
Weil AG, Garcia BA, Garzia L, Mack SC, Beroukhim R, Ligon KL, Taylor MD,
Bandopadhayay P, Kramm C, Pfister SM, Korshunov A, Sturm D, Jones DTW, Salomoni
P, Kleinman CL, Jabado N. Histone H3.3G34-Mutant Interneuron Progenitors Co-opt
PDGFRA for Gliomagenesis. Cell. 2020 Dec 10;183(6):1617-1633.e22. doi:
10.1016/j.cell.2020.11.012. Epub 2020 Nov 30. PMID: 33259802; PMCID: PMC7791404.
164: Crevier-Sorbo G, Brunette-Clément T, Medawar E, Mathieu F, Morgan BR,
Hachem LD, Dewan MC, Fallah A, Weil AG, Ibrahim GM. A needs assessment of
pediatric epilepsy surgery in Haiti. J Neurosurg Pediatr. 2020 Nov
27;27(2):189-195. doi: 10.3171/2020.7.PEDS20256. PMID: 33254133.
165: Thomas C, Soschinski P, Zwaig M, Oikonomopoulos S, Okonechnikov K, Pajtler
KW, Sill M, Schweizer L, Koch A, Neumann J, Schüller U, Sahm F, Rauschenbach L,
Keyvani K, Proescholdt M, Riemenschneider MJ, Segewiß J, Ruckert C, Grauer O,
Monoranu CM, Lamszus K, Patrizi A, Kordes U, Siebert R, Kool M, Ragoussis J,
Foulkes WD, Paulus W, Rivera B, Hasselblatt M. The genetic landscape of choroid
plexus tumors in children and adults. Neuro Oncol. 2021 Apr 12;23(4):650-660.
doi: 10.1093/neuonc/noaa267. PMID: 33249490; PMCID: PMC8041331.
166: van Beinum A, Healey A, Chandler J, Dhanani S, Hartwick M, Lewis A,
Marshall C, Marshall J, Shemie S, Singh JM. Correction to: Requests for somatic
support after neurologic death determination: Canadian physician experiences;
Demandes de soutien des fonctions vitales après un diagnostic de décès
neurologique : les expériences des médecins canadiens. Can J Anaesth. 2021
Aug;68(8):1304. doi: 10.1007/s12630-020-01871-6. Erratum for: Can J Anaesth.
2021 Mar;68(3):293-314. PMID: 33236279; PMCID: PMC9119271.
167: Mireault D, Cawthorn TR, Todd AR, Spencer AO. Suprazygomatic maxillary
nerve block: an ultrasound and cadaveric study to identify correct
sonoanatomical landmarks. J Anesth. 2021 Feb;35(1):150-153. doi:
10.1007/s00540-020-02877-6. Epub 2020 Nov 23. PMID: 33230676.
168: Bolduc ME, Dionne E, Gagnon I, Rennick JE, Majnemer A, Brossard-Racine M.
Motor Impairment in Children With Congenital Heart Defects: A Systematic Review.
Pediatrics. 2020 Dec;146(6):e20200083. doi: 10.1542/peds.2020-0083. PMID:
33208496.
169: Larivière S, Rodríguez-Cruces R, Royer J, Caligiuri ME, Gambardella A,
Concha L, Keller SS, Cendes F, Yasuda C, Bonilha L, Gleichgerrcht E, Focke NK,
Domin M, von Podewills F, Langner S, Rummel C, Wiest R, Martin P, Kotikalapudi
R, O'Brien TJ, Sinclair B, Vivash L, Desmond PM, Alhusaini S, Doherty CP,
Cavalleri GL, Delanty N, Kälviäinen R, Jackson GD, Kowalczyk M, Mascalchi M,
Semmelroch M, Thomas RH, Soltanian-Zadeh H, Davoodi-Bojd E, Zhang J, Lenge M,
Guerrini R, Bartolini E, Hamandi K, Foley S, Weber B, Depondt C, Absil J, Carr
SJA, Abela E, Richardson MP, Devinsky O, Severino M, Striano P, Tortora D,
Hatton SN, Vos SB, Duncan JS, Whelan CD, Thompson PM, Sisodiya SM, Bernasconi A,
Labate A, McDonald CR, Bernasconi N, Bernhardt BC. Network-based atrophy
modeling in the common epilepsies: A worldwide ENIGMA study. Sci Adv. 2020 Nov
18;6(47):eabc6457. doi: 10.1126/sciadv.abc6457. PMID: 33208365; PMCID:
PMC7673818.
170: Teel E, Brossard-Racine M, Corbin-Berrigan LA, Gagnon I. Perceptual
Cognitive Training Does Not Improve Clinical Outcomes at 4 and 12 Weeks
Following Concussion in Children and Adolescents: A Randomized Controlled Trial.
J Head Trauma Rehabil. 2021 Mar-Apr 01;36(2):E97-E107. doi:
10.1097/HTR.0000000000000633. PMID: 33201041.
171: Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler
IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin
K, Li L, Millwood IY, Chen Z, Rouleau GA, Zhou S, Rannikmäe K, Sudlow CLM,
Houlden H, van den Berg LH, Dina C, Naggara O, Gentric JC, Shotar E, Eugène F,
Desal H, Winsvold BS, Børte S, Johnsen MB, Brumpton BM, Sandvei MS, Willer CJ,
Hveem K, Zwart JA, Verschuren WMM, Friedrich CM, Hirsch S, Schilling S,
Dauvillier J, Martin O; HUNT All-In Stroke; China Kadoorie Biobank Collaborative
Group; BioBank Japan Project Consortium; ICAN Study Group; CADISP Group;
Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigators;
International Stroke Genetics Consortium (ISGC), Jones GT, Bown MJ, Ko NU, Kim
H, Coleman JRI, Breen G, Zaroff JG, Klijn CJM, Malik R, Dichgans M,
Sargurupremraj M, Tatlisumak T, Amouyel P, Debette S, Rinkel GJE, Worrall BB,
Pera J, Slowik A, Gaál-Paavola EI, Niemelä M, Jääskeläinen JE, von Und Zu
Fraunberg M, Lindgren A, Broderick JP, Werring DJ, Woo D, Redon R, Bijlenga P,
Kamatani Y, Veldink JH, Ruigrok YM. Genome-wide association study of
intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical
risk factors. Nat Genet. 2020 Dec;52(12):1303-1313. doi:
10.1038/s41588-020-00725-7. Epub 2020 Nov 16. Erratum in: Nat Genet. 2020 Dec
22;: PMID: 33199917; PMCID: PMC7116530.
172: van Beinum A, Healey A, Chandler J, Dhanani S, Hartwick M, Lewis A,
Marshall C, Marshall J, Shemie S, Singh JM. Requests for somatic support after
neurologic death determination: Canadian physician experiences. Can J Anaesth.
2021 Mar;68(3):293-314. doi: 10.1007/s12630-020-01852-9. Epub 2020 Nov 10.
Erratum in: Can J Anaesth. 2020 Nov 24;: PMID: 33174163; PMCID: PMC7654566.
173: Gauquelin L, Hartley T, Tarnopolsky M, Dyment DA, Brais B, Geraghty MT,
Tétreault M, Ahmed S, Rojas S, Choquet K, Majewski J, Bernier F, Innes AM,
Rouleau G, Suchowersky O, Boycott KM, Yoon G. Channelopathies Are a Frequent
Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Mov Disord Clin
Pract. 2020 Sep 29;7(8):940-949. doi: 10.1002/mdc3.13086. PMID: 33163565; PMCID:
PMC7604675.
174: Tremblay-Laganière C, Kaiyrzhanov R, Maroofian R, Nguyen TTM, Salayev K,
Chilton IT, Chung WK, Madden JA, Phornphutkul C, Agrawal PB, Houlden H, Campeau
PM. PIGH deficiency can be associated with severe neurodevelopmental and
skeletal manifestations. Clin Genet. 2021 Feb;99(2):313-317. doi:
10.1111/cge.13877. Epub 2020 Nov 27. PMID: 33156547; PMCID: PMC7839508.
175: Weil AG, Mathews N, Farmer JP, St Martin C, Albrecht S, Jabado N, Dudley
RWR. Successful treatment of non-midline primary malignant germ cell tumors with
yolk sac components in neonates: report of 2 cases. J Neurosurg Pediatr. 2020
Oct 30;27(1):47-51. doi: 10.3171/2020.6.PEDS19719. PMID: 33126205.
176: Balakrishnan I, Danis E, Pierce A, Madhavan K, Wang D, Dahl N, Sanford B,
Birks DK, Davidson N, Metselaar DS, Meel MH, Lemma R, Donson A, Vijmasi T,
Katagi H, Sola I, Fosmire S, Alimova I, Steiner J, Gilani A, Hulleman E, Serkova
NJ, Hashizume R, Hawkins C, Carcaboso AM, Gupta N, Monje M, Jabado N, Jones K,
Foreman N, Green A, Vibhakar R, Venkataraman S. Senescence Induced by BMI1
Inhibition Is a Therapeutic Vulnerability in H3K27M-Mutant DIPG. Cell Rep. 2020
Oct 20;33(3):108286. doi: 10.1016/j.celrep.2020.108286. PMID: 33086074; PMCID:
PMC7574900.
177: Appendino JP, Baker S, Chapman KM, Dykstra T, Hussein T, Jones ML, Mezei
MM, Mirsattari SM, Ng M, Nikkel J, Obradovic V, Phan C, Robinson L, Scott A,
Téllez-Zenteno J, Van Niekerk M, Venance S, Moore F. Response from Authors to
the Letter to the Editor. Can J Neurol Sci. 2021 Jan;48(1):135-137. doi:
10.1017/cjn.2020.225. Epub 2020 Oct 15. PMID: 33054869; PMCID: PMC7853747.
178: Aravamuthan BR, Shevell M, Kim YM, Wilson JL, O'Malley JA, Pearson TS,
Kruer MC, Fahey M, Waugh JL, Russman B, Shapiro B, Tilton A. Role of child
neurologists and neurodevelopmentalists in the diagnosis of cerebral palsy: A
survey study. Neurology. 2020 Nov 24;95(21):962-972. doi:
10.1212/WNL.0000000000011036. Epub 2020 Oct 12. PMID: 33046609; PMCID:
PMC7734737.
179: van Lee L, Chia A, Phua D, Colega M, Padmapriya N, Bernard JY, Cai S, Tham
EKH, Teoh OH, Goh D, Gooley JJ, Gluckman PD, Yap F, Shek LPC, Godfrey KM, Tan
KH, Chong YS, Müller-Riemenschneider F, Broekman B, Meaney M, Chen H, Chong MFF.
Multiple modifiable lifestyle factors and the risk of perinatal depression
during pregnancy: Findings from the GUSTO cohort. Compr Psychiatry. 2020
Nov;103:152210. doi: 10.1016/j.comppsych.2020.152210. Epub 2020 Sep 30. PMID:
33045668.
180: Prince EW, Whelan R, Mirsky DM, Stence N, Staulcup S, Klimo P, Anderson
RCE, Niazi TN, Grant G, Souweidane M, Johnston JM, Jackson EM, Limbrick DD Jr,
Smith A, Drapeau A, Chern JJ, Kilburn L, Ginn K, Naftel R, Dudley R, Tyler-
Kabara E, Jallo G, Handler MH, Jones K, Donson AM, Foreman NK, Hankinson TC.
Robust deep learning classification of adamantinomatous craniopharyngioma from
limited preoperative radiographic images. Sci Rep. 2020 Oct 9;10(1):16885. doi:
10.1038/s41598-020-73278-8. PMID: 33037266; PMCID: PMC7547020.
181: Myers KA. Response to Canadian Neurophysiology Laboratory COVID-19 Practice
Guidelines. Can J Neurol Sci. 2021 Jan;48(1):133-134. doi: 10.1017/cjn.2020.220.
Epub 2020 Oct 6. PMID: 33019956; PMCID: PMC7853735.
182: Pelletier F, Perrier S, Cayami FK, Mirchi A, Saikali S, Tran LT, Ulrick N,
Guerrero K, Rampakakis E, van Spaendonk RML, Naidu S, Pohl D, Gibson WT, Demos
M, Goizet C, Tejera-Martin I, Potic A, Fogel BL, Brais B, Sylvain M, Sébire G,
Lourenço CM, Bonkowsky JL, Catsman-Berrevoets C, Pinto PS, Tirupathi S, Strømme
P, de Grauw T, Gieruszczak-Bialek D, Krägeloh-Mann I, Mierzewska H, Philippi H,
Rankin J, Atik T, Banwell B, Benko WS, Blaschek A, Bley A, Boltshauser E,
Bratkovic D, Brozova K, Cimas I, Clough C, Corenblum B, Dinopoulos A, Dolan G,
Faletra F, Fernandez R, Fletcher J, Garcia Garcia ME, Gasparini P, Gburek-
Augustat J, Gonzalez Moron D, Hamati A, Harting I, Hertzberg C, Hill A, Hobson
GM, Innes AM, Kauffman M, Kirwin SM, Kluger G, Kolditz P, Kotzaeridou U, La
Piana R, Liston E, McClintock W, McEntagart M, McKenzie F, Melançon S,
Misbahuddin A, Suri M, Monton FI, Moutton S, Murphy RPJ, Nickel M, Onay H,
Orcesi S, Özkınay F, Patzer S, Pedro H, Pekic S, Pineda Marfa M, Pizzino A,
Plecko B, Poll-The BT, Popovic V, Rating D, Rioux MF, Rodriguez Espinosa N,
Ronan A, Ostergaard JR, Rossignol E, Sanchez-Carpintero R, Schossig A, Senbil N,
Sønderberg Roos LK, Stevens CA, Synofzik M, Sztriha L, Tibussek D, Timmann D,
Tonduti D, van de Warrenburg BP, Vázquez-López M, Venkateswaran S, Wasling P,
Wassmer E, Webster RI, Wiegand G, Yoon G, Rotteveel J, Schiffmann R, van der
Knaap MS, Vanderver A, Martos-Moreno GÁ, Polychronakos C, Wolf NI, Bernard G.
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in
POLR3A, POLR3B, and POLR1C. J Clin Endocrinol Metab. 2021 Jan
23;106(2):e660-e674. doi: 10.1210/clinem/dgaa700. PMID: 33005949; PMCID:
PMC7823228.
183: Cristini J, Weiss M, De Las Heras B, Medina-Rincón A, Dagher A, Postuma RB,
Huber R, Doyon J, Rosa-Neto P, Carrier J, Amara AW, Roig M. The effects of
exercise on sleep quality in persons with Parkinson's disease: A systematic
review with meta-analysis. Sleep Med Rev. 2021 Feb;55:101384. doi:
10.1016/j.smrv.2020.101384. Epub 2020 Sep 8. PMID: 32987321.
184: Al-Roubaie Z, Guadagno E, Ramanakumar AV, Khan AQ, Myers KA. Clinical
utility of therapeutic drug monitoring of antiepileptic drugs: Systematic
review. Neurol Clin Pract. 2020 Aug;10(4):344-355. doi:
10.1212/CPJ.0000000000000722. PMID: 32983615; PMCID: PMC7508342.
185: Garbin M, Portela DA, Bertolizio G, Gallastegui A, Otero PE. A novel
ultrasound-guided lateral quadratus lumborum block in dogs: a comparative
cadaveric study of two approaches. Vet Anaesth Analg. 2020 Nov;47(6):810-818.
doi: 10.1016/j.vaa.2020.08.003. Epub 2020 Aug 13. PMID: 32981838.
186: Yan H, Siegel L, Breitbart S, Gorodetsky C, Gonorazky HD, Yau I, Go C,
Donner E, Kalia SK, Fasano A, Weil AG, Fallah A, Ibrahim GM. The Child & Youth
CompreHensIve Longitudinal Database for Deep Brain Stimulation (CHILD-DBS).
Childs Nerv Syst. 2021 Feb;37(2):607-615. doi: 10.1007/s00381-020-04880-4. Epub
2020 Sep 15. PMID: 32935233.
187: Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich
K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L,
Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor
J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. Correction: DOORS
syndrome and a recurrent truncating ATP6V1B2 variant. Genet Med. 2021
Jan;23(1):237. doi: 10.1038/s41436-020-00969-y. Erratum for: Genet Med. 2021
Jan;23(1):149-154. PMID: 32934366.
188: Douard E, Zeribi A, Schramm C, Tamer P, Loum MA, Nowak S, Saci Z, Lord MP,
Rodríguez-Herreros B, Jean-Louis M, Moreau C, Loth E, Schumann G, Pausova Z,
Elsabbagh M, Almasy L, Glahn DC, Bourgeron T, Labbe A, Paus T, Mottron L,
Greenwood CMT, Huguet G, Jacquemont S. Effect Sizes of Deletions and
Duplications on Autism Risk Across the Genome. Am J Psychiatry. 2021 Jan
1;178(1):87-98. doi: 10.1176/appi.ajp.2020.19080834. Epub 2020 Sep 11. PMID:
32911998; PMCID: PMC8931740.
189: Sahly AN, Krochmalnek E, St-Onge J, Srour M, Myers KA. Severe DNM1
encephalopathy with dysmyelination due to recurrent splice site pathogenic
variant. Hum Genet. 2020 Dec;139(12):1575-1578. doi: 10.1007/s00439-020-02224-5.
Epub 2020 Sep 9. PMID: 32909139.
190: Rezk A, Li R, Bar-Or A. Multiplexed detection and isolation of viable low-
frequency cytokine-secreting human B cells using cytokine secretion assay and
flow cytometry (CSA-Flow). Sci Rep. 2020 Sep 9;10(1):14823. doi:
10.1038/s41598-020-71750-z. PMID: 32908164; PMCID: PMC7481209.
191: Smith EE, Couillard P, Fisk JD, Ismail Z, Montero-Odasso M, Robillard JM,
Vedel I, Sivananthan S, Gauthier S. Pandemic Dementia Scarce Resource
Allocation. Can Geriatr J. 2020 Sep 1;23(3):216-218. doi: 10.5770/cgj.23.457.
PMID: 32904792; PMCID: PMC7458602.
192: Zha C, Farah CA, Holt RJ, Ceroni F, Al-Abdi L, Thuriot F, Khan AO, Helaby
R, Lévesque S, Alkuraya FS, Kraus A, Ragge NK, Sossin WS. Biallelic variants in
the small optic lobe calpain CAPN15 are associated with congenital eye
anomalies, deafness and other neurodevelopmental deficits. Hum Mol Genet. 2020
Nov 4;29(18):3054-3063. doi: 10.1093/hmg/ddaa198. PMID: 32885237; PMCID:
PMC7645705.
193: Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich
K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L,
Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor
J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. DOORS syndrome and a
recurrent truncating ATP6V1B2 variant. Genet Med. 2021 Jan;23(1):149-154. doi:
10.1038/s41436-020-00950-9. Epub 2020 Sep 2. Erratum in: Genet Med. 2020 Sep
15;: PMID: 32873933.
194: Chivukula S, Modiri O, Kashanian A, Babayan D, Ibrahim GM, Weil AG, Tu A,
Wu JY, Mathern GW, Fallah A. Effect of Gene Mutation on Seizures in Surgery for
Tuberous Sclerosis Complex. Can J Neurol Sci. 2021 May;48(3):327-334. doi:
10.1017/cjn.2020.185. Epub 2020 Aug 28. PMID: 32854808.
195: Oskoui M, Ng P, Zaman M, Buckley D, Kirton A, van Rensburg E, Wood E,
Shevell M, Majnemer A. Complementary and Alternative Therapy Use in Children
with Cerebral Palsy. Can J Neurol Sci. 2021 May;48(3):408-414. doi:
10.1017/cjn.2020.188. Epub 2020 Aug 28. PMID: 32854793.
196: Moreau JT, Baillet S, Dudley RW. Biased intelligence: on the subjectivity
of digital objectivity. BMJ Health Care Inform. 2020 Aug;27(3):e100146. doi:
10.1136/bmjhci-2020-100146. PMID: 32830107; PMCID: PMC7445351.
197: Hatton SN, Huynh KH, Bonilha L, Abela E, Alhusaini S, Altmann A, Alvim MKM,
Balachandra AR, Bartolini E, Bender B, Bernasconi N, Bernasconi A, Bernhardt B,
Bargallo N, Caldairou B, Caligiuri ME, Carr SJA, Cavalleri GL, Cendes F, Concha
L, Davoodi-Bojd E, Desmond PM, Devinsky O, Doherty CP, Domin M, Duncan JS, Focke
NK, Foley SF, Gambardella A, Gleichgerrcht E, Guerrini R, Hamandi K, Ishikawa A,
Keller SS, Kochunov PV, Kotikalapudi R, Kreilkamp BAK, Kwan P, Labate A, Langner
S, Lenge M, Liu M, Lui E, Martin P, Mascalchi M, Moreira JCV, Morita-Sherman ME,
O'Brien TJ, Pardoe HR, Pariente JC, Ribeiro LF, Richardson MP, Rocha CS,
Rodríguez-Cruces R, Rosenow F, Severino M, Sinclair B, Soltanian-Zadeh H,
Striano P, Taylor PN, Thomas RH, Tortora D, Velakoulis D, Vezzani A, Vivash L,
von Podewils F, Vos SB, Weber B, Winston GP, Yasuda CL, Zhu AH, Thompson PM,
Whelan CD, Jahanshad N, Sisodiya SM, McDonald CR. White matter abnormalities
across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain.
2020 Aug 1;143(8):2454-2473. doi: 10.1093/brain/awaa200. PMID: 32814957; PMCID:
PMC7567169.
198: Canadian Society of Clinical Neurophysiologists (CSCN); Canadian
Association of Electroneurophysiology Technologists (CAET); Association of
Electromyography Technologists of Canada (AETC); Board of Registration of
Electromyography Technologists of Canada (BRETC), Canadian Board of Registration
of Electroencephalograph Technologists (CBRET), Appendino JP, Baker SK, Chapman
KM, Dykstra T, Hussein T, Jones ML, Mezei MM, Mirsattari SM, Ng M, Nikkel J,
Obradovic V, Phan C, Robinson L, Scott A, Tellez-Zenteno J, Van Niekerk M,
Venance S, Moore F. Practice Guidelines for Canadian Neurophysiology
Laboratories During the COVID-19 Pandemic. Can J Neurol Sci. 2021
Jan;48(1):25-30. doi: 10.1017/cjn.2020.184. Epub 2020 Aug 19. PMID: 32811585;
PMCID: PMC7578631.
199: Boychuck Z, Andersen J, Bussières A, Fehlings D, Kirton A, Li P, Oskoui M,
Rodriguez C, Shevell M, Snider L, Majnemer A; PROMPT Group. Use of consensus
methods to determine the early clinical signs of cerebral palsy. Paediatr Child
Health. 2020 Aug;25(5):300-307. doi: 10.1093/pch/pxz061. Epub 2019 May 8. PMID:
32765166; PMCID: PMC7395325.
200: Hwang P, Hechtman L, Carboni-Jiménez A, Demchenko I, Maduro A, Mady N,
Tounkara F, Sapkota RP, Brunet A. In Response to "Clinical Characteristics
Associated with Early Phase Psychosis and Comorbid Substance Use":
Methodological Concerns. Can J Psychiatry. 2021 Feb;66(2):183-184. doi:
10.1177/0706743720947636. Epub 2020 Aug 7. PMID: 32762339; PMCID: PMC7918869.
201: Greer DM, Shemie SD, Lewis A, Torrance S, Varelas P, Goldenberg FD, Bernat
JL, Souter M, Topcuoglu MA, Alexandrov AW, Baldisseri M, Bleck T, Citerio G,
Dawson R, Hoppe A, Jacobe S, Manara A, Nakagawa TA, Pope TM, Silvester W,
Thomson D, Al Rahma H, Badenes R, Baker AJ, Cerny V, Chang C, Chang TR,
Gnedovskaya E, Han MK, Honeybul S, Jimenez E, Kuroda Y, Liu G, Mallick UK,
Marquevich V, Mejia-Mantilla J, Piradov M, Quayyum S, Shrestha GS, Su YY,
Timmons SD, Teitelbaum J, Videtta W, Zirpe K, Sung G. Determination of Brain
Death/Death by Neurologic Criteria: The World Brain Death Project. JAMA. 2020
Sep 15;324(11):1078-1097. doi: 10.1001/jama.2020.11586. PMID: 32761206.
202: Schneeberger PE, Kortüm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D,
Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M,
Biskup S, Heller C, Maier EM, Javaher-Haghighi P, Bedeschi MF, Ajmone PF,
Iascone M, Peeters H, Ballon K, Jaeken J, Rodríguez Alonso A, Palomares-Bralo M,
Santos-Simarro F, Meuwissen MEC, Beysen D, Kooy RF, Houlden H, Murphy D, Doosti
M, Karimiani EG, Mojarrad M, Maroofian R, Noskova L, Kmoch S, Honzik T, Cope H,
Sanchez-Valle A; Undiagnosed Diseases Network, Gelb BD, Kurth I, Hempel M,
Kutsche K. Biallelic MADD variants cause a phenotypic spectrum ranging from
developmental delay to a multisystem disorder. Brain. 2020 Aug
1;143(8):2437-2453. doi: 10.1093/brain/awaa204. PMID: 32761064; PMCID:
PMC7447524.
203: Bis-Brewer DM, Gan-Or Z, Sleiman P; Inherited Neuropathy Consortium,
Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M,
Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle
R, Züchner S. Assessing non-Mendelian inheritance in inherited axonopathies.
Genet Med. 2020 Dec;22(12):2114-2119. doi: 10.1038/s41436-020-0924-0. Epub 2020
Aug 3. PMID: 32741968; PMCID: PMC7710562.
204: Dermer E, Spahr A, Tran LT, Mirchi A, Pelletier F, Guerrero K, Ahmed S,
Brais B, Braverman N, Buhas D, Chandratre S, Chenier S, Chrestian N, Desmeules
M, Dilenge ME, Laflamme J, Larbrisseau A, Legault G, Lim KY, Maftei C, Major P,
Malvey-Dorn E, Marois P, Mitchell J, Nadeau A, Osterman B, Paradis I, Pohl D,
Reggin J, Riou E, Roedde G, Rossignol E, Sébire G, Shevell M, Srour M, Sylvain
M, Tarnopolsky M, Venkateswaran S, Sullivan M, Bernard G. Stress in Parents of
Children With Genetically Determined Leukoencephalopathies: A Pilot Study. J
Child Neurol. 2020 Nov;35(13):901-907. doi: 10.1177/0883073820938645. Epub 2020
Jul 28. PMID: 32720856.
205: Al Amrani F, Racine E, Shevell M, Wintermark P. Death after Birth Asphyxia
in the Cooling Era. J Pediatr. 2020 Nov;226:289-293. doi:
10.1016/j.jpeds.2020.07.041. Epub 2020 Jul 16. PMID: 32682749.
206: Lewis A, Liebman J, Kreiger-Benson E, Kumpfbeck A, Bakkar A, Shemie SD,
Sung G, Torrance S, Greer D. Ancillary Testing for Determination of Death by
Neurologic Criteria Around the World. Neurocrit Care. 2021 Apr;34(2):473-484.
doi: 10.1007/s12028-020-01039-6. PMID: 32648194.
207: Fortin O, Ashour M, Lacroix C, Sabapathy CA, Myers KA. Megalencephaly-
Capillary Malformation-Polymicrogyria with Cerebral Venous Thrombosis. Can J
Neurol Sci. 2020 Nov;47(6):828-829. doi: 10.1017/cjn.2020.127. Epub 2020 Jun 23.
PMID: 32631464.
208: Healey A, Leeies M, Hrymak C, Chochinov A, Grunau B, Paunovic B, Teitelbaum
J, Wilson LC, Shemie SD. CAEP Position Statement - Management of devastating
brain injuries in the emergency department: Enhancing neuroprognostication and
maintaining the opportunity for organ and tissue donation. CJEM. 2020
Sep;22(5):658-660. doi: 10.1017/cem.2020.357. Erratum in: CJEM. 2020
Sep;22(5):E9. PMID: 32618532; PMCID: PMC7509745.
209: Mirchi A, Saint-Martin C, Myers KA. Spontaneous Multilevel Cerebrospinal
Fluid Leak in Marfan Syndrome. Ann Neurol. 2020 Oct;88(4):855-856. doi:
10.1002/ana.25837. Epub 2020 Jul 14. PMID: 32613612.
210: Fortin O, Vincelette C, Chénier S, Ghais A, Shevell MI, Simard-Tremblay E,
Myers KA. Copy number variation in genetic epilepsy with febrile seizures plus.
Eur J Paediatr Neurol. 2020 Jul;27:111-115. doi: 10.1016/j.ejpn.2020.05.005.
Epub 2020 Jun 20. PMID: 32595013.
211: Jenkins DJA, Jayalath VH, Choo VL, Viguiliouk E, Kendall CWC, Srichaikul K,
Mirrahimi A, Bernstein CN, Chang TM, Gold P, Haynes RB, Hollenberg MD, Lozano
AM, Posner BI, Ronald AR, Vranic M, Wang YT, Chiavaroli L, de Souza RJ, Nishi S,
Pichika SC, Gillett C, Tsirakis T, Sievenpiper JL. Does conventional early life
academic excellence predict later life scientific discovery? An assessment of
the lives of great medical innovators. QJM. 2021 Oct 7;114(6):381-389. doi:
10.1093/qjmed/hcaa210. PMID: 32589722; PMCID: PMC8497073.
212: Perrier S, Gauquelin L, Fallet-Bianco C, Dishop MK, Michell-Robinson MA,
Tran LT, Guerrero K, Darbelli L, Srour M, Petrecca K, Renaud DL, Saito M, Cohen
S, Leiz S, Alhaddad B, Haack TB, Tejera-Martin I, Monton FI, Rodriguez-Espinosa
N, Pohl D, Nageswaran S, Grefe A, Glamuzina E, Bernard G. Expanding the
phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophy.
Neurol Genet. 2020 May 11;6(3):e425. doi: 10.1212/NXG.0000000000000425. PMID:
32582862; PMCID: PMC7238899.
213: Syn NL, Chan SY, Chia EWY, Ong WX, Phua D, Cai S, Shek LPC, Chong YS,
Daniel LM, Broekman BFP, Godfrey KM, Meaney MJ, Law EC. Severity of nausea and
vomiting in pregnancy and early childhood neurobehavioural outcomes: The Growing
Up in Singapore Towards Healthy Outcomes study. Paediatr Perinat Epidemiol. 2021
Jan;35(1):98-108. doi: 10.1111/ppe.12703. Epub 2020 Jun 23. PMID: 32578237;
PMCID: PMC7116637.
214: Gardiner E, Miller AR, Lach LM. Service adequacy and the relation between
child behavior problems and negative family impact reported by primary
caregivers of children with neurodevelopmental conditions. Res Dev Disabil. 2020
Sep;104:103712. doi: 10.1016/j.ridd.2020.103712. Epub 2020 Jun 15. PMID:
32554267.
215: Cadieux-Dion M, Meneghini S, Villa C, Toffa DH, Wickstrom R, Bouthillier A,
Sandvik U, Gustavsson B, Mohamed I, Cossette P, Combi R, Becchetti A, Nguyen DK.
Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular
Epilepsy. Can J Neurol Sci. 2020 Nov;47(6):800-809. doi: 10.1017/cjn.2020.126.
Epub 2020 Jun 15. PMID: 32536355.
216: Crevier-Sorbo G, Brunette-Clément T, Medawar E, Mathieu F, Morgan BR,
Hachem L, Fallah A, Weil AG, Ibrahim GM. Assessment and treatment of childhood
epilepsy in Haiti. Epilepsia Open. 2020 Mar 2;5(2):190-197. doi:
10.1002/epi4.12384. PMID: 32524044; PMCID: PMC7278551.
217: Hodgkinson VL, Oskoui M, Lounsberry J, M'Dahoma S, Butler E, Campbell C,
MacKenzie A, McMillan HJ, Simard L, Vajsar J, Brais B, Chapman KM, Chrestian N,
Crone M, Dobrowolski P, Dojeiji S, Dowling JJ, Dupré N, Genge A, Gonorazky H,
Hasal S, Izenberg A, Johnston W, Leung E, Lochmüller H, Mah JK, Marerro A,
Massie R, McAdam L, McCormick A, Melanson M, Mezei MM, Nguyen CE, O'Connell C,
O'Ferrall EK, Pfeffer G, Phan C, Plamondon S, Poulin C, Rodrigue X, Schellenberg
KL, Selby K, Sheriko J, Shoesmith C, Smith G, Taillon M, Taylor S, Warman
Chardon J, Worley S, Korngut L. A National Spinal Muscular Atrophy Registry for
Real-World Evidence. Can J Neurol Sci. 2020 Nov;47(6):810-815. doi:
10.1017/cjn.2020.111. Epub 2020 Jun 4. PMID: 32493524; PMCID: PMC7656664.
218: Sisodiya SM, Whelan CD, Hatton SN, Huynh K, Altmann A, Ryten M, Vezzani A,
Caligiuri ME, Labate A, Gambardella A, Ives-Deliperi V, Meletti S, Munsell BC,
Bonilha L, Tondelli M, Rebsamen M, Rummel C, Vaudano AE, Wiest R, Balachandra
AR, Bargalló N, Bartolini E, Bernasconi A, Bernasconi N, Bernhardt B, Caldairou
B, Carr SJA, Cavalleri GL, Cendes F, Concha L, Desmond PM, Domin M, Duncan JS,
Focke NK, Guerrini R, Hamandi K, Jackson GD, Jahanshad N, Kälviäinen R, Keller
SS, Kochunov P, Kowalczyk MA, Kreilkamp BAK, Kwan P, Lariviere S, Lenge M, Lopez
SM, Martin P, Mascalchi M, Moreira JCV, Morita-Sherman ME, Pardoe HR, Pariente
JC, Raviteja K, Rocha CS, Rodríguez-Cruces R, Seeck M, Semmelroch MKHG, Sinclair
B, Soltanian-Zadeh H, Stein DJ, Striano P, Taylor PN, Thomas RH, Thomopoulos SI,
Velakoulis D, Vivash L, Weber B, Yasuda CL, Zhang J, Thompson PM, McDonald CR;
ENIGMA Consortium Epilepsy Working Group. The ENIGMA-Epilepsy working group:
Mapping disease from large data sets. Hum Brain Mapp. 2020 May 29;43(1):113–28.
doi: 10.1002/hbm.25037. Epub ahead of print. PMID: 32468614; PMCID: PMC8675408.
219: Alhajaj G, Atkinson J, Keezer MR, Nikolic A, Myers KA. A proposed guideline
for vagus nerve stimulator handling in palliative care and after death.
Epilepsia. 2020 Jul;61(7):1336-1340. doi: 10.1111/epi.16553. Epub 2020 May 28.
PMID: 32463125.
220: Michealraj KA, Kumar SA, Kim LJY, Cavalli FMG, Przelicki D, Wojcik JB,
Delaidelli A, Bajic A, Saulnier O, MacLeod G, Vellanki RN, Vladoiu MC, Guilhamon
P, Ong W, Lee JJY, Jiang Y, Holgado BL, Rasnitsyn A, Malik AA, Tsai R, Richman
CM, Juraschka K, Haapasalo J, Wang EY, De Antonellis P, Suzuki H, Farooq H,
Balin P, Kharas K, Van Ommeren R, Sirbu O, Rastan A, Krumholtz SL, Ly M, Ahmadi
M, Deblois G, Srikanthan D, Luu B, Loukides J, Wu X, Garzia L, Ramaswamy V,
Kanshin E, Sánchez-Osuna M, El-Hamamy I, Coutinho FJ, Prinos P, Singh S, Donovan
LK, Daniels C, Schramek D, Tyers M, Weiss S, Stein LD, Lupien M, Wouters BG,
Garcia BA, Arrowsmith CH, Sorensen PH, Angers S, Jabado N, Dirks PB, Mack SC,
Agnihotri S, Rich JN, Taylor MD. Metabolic Regulation of the Epigenome Drives
Lethal Infantile Ependymoma. Cell. 2020 Jun 11;181(6):1329-1345.e24. doi:
10.1016/j.cell.2020.04.047. Epub 2020 May 22. PMID: 32445698.
221: Lai JS, Cai S, Lee BL, Godfrey KM, Gluckman PD, Shek LP, Yap F, Tan KH,
Chong YS, Ong CN, Meaney MJ, Rifkin-Graboi A, Broekman BFP, Chong MFF. Higher
maternal plasma β-cryptoxanthin concentration is associated with better
cognitive and motor development in offspring at 2 years of age. Eur J Nutr. 2021
Mar;60(2):703-714. doi: 10.1007/s00394-020-02277-2. Epub 2020 May 20. PMID:
32435993; PMCID: PMC7116811.
222: Prince E, Whelan R, Donson A, Staulcup S, Hengartner A, Vijmasi T, Agwu C,
Lillehei KO, Foreman NK, Johnston JM, Massimi L, Anderson RCE, Souweidane MM,
Naftel RP, Limbrick DD, Grant G, Niazi TN, Dudley R, Kilburn L, Jackson EM,
Jallo GI, Ginn K, Smith A, Chern JJ, Lee A, Drapeau A, Krieger MD, Handler MH,
Hankinson TC; Advancing Treatment for Pediatric Craniopharyngioma Consortium.
Transcriptional analyses of adult and pediatric adamantinomatous
craniopharyngioma reveals similar expression signatures regarding potential
therapeutic targets. Acta Neuropathol Commun. 2020 May 13;8(1):68. doi:
10.1186/s40478-020-00939-0. PMID: 32404202; PMCID: PMC7222517.
223: Sévère M, Ng P, Messerlian C, Andersen J, Buckley D, Fehlings D, Kirton A,
Koclas L, Pigeon N, Van Rensburg E, Wood E, Shevell M, Oskoui M. Congenital
Malformations in Children With Cerebral Palsy: Is Prematurity Protective?
Pediatr Neurol. 2020 Jul;108:70-76. doi: 10.1016/j.pediatrneurol.2020.02.002.
Epub 2020 Feb 12. PMID: 32386793.
224: Birca V, Saint-Martin C, Myers KA. Teaching Video NeuroImages: Pathologic
yawning: A sign of brainstem involvement in acute disseminated
encephalomyelitis? Neurology. 2020 Jun 9;94(23):e2497-e2498. doi:
10.1212/WNL.0000000000009595. Epub 2020 May 4. PMID: 32366540.
225: Vanderver A, Bernard G, Helman G, Sherbini O, Boeck R, Cohn J, Collins A,
Demarest S, Dobbins K, Emrick L, Fraser JL, Masser-Frye D, Hayward J, Karmarkar
S, Keller S, Mirrop S, Mitchell W, Pathak S, Sherr E, van Haren K, Waters E,
Wilson JL, Zhorne L, Schiffmann R, van der Knaap MS, Pizzino A, Dubbs H, Shults
J, Simons C, Taft RJ; LeukoSEQ Workgroup. Randomized Clinical Trial of First-
Line Genome Sequencing in Pediatric White Matter Disorders. Ann Neurol. 2020
Aug;88(2):264-273. doi: 10.1002/ana.25757. Epub 2020 Jun 9. PMID: 32342562;
PMCID: PMC8061316.
226: Donovan LK, Delaidelli A, Joseph SK, Bielamowicz K, Fousek K, Holgado BL,
Manno A, Srikanthan D, Gad AZ, Van Ommeren R, Przelicki D, Richman C, Ramaswamy
V, Daniels C, Pallota JG, Douglas T, Joynt ACM, Haapasalo J, Nor C, Vladoiu MC,
Kuzan-Fischer CM, Garzia L, Mack SC, Varadharajan S, Baker ML, Hendrikse L, Ly
M, Kharas K, Balin P, Wu X, Qin L, Huang N, Stucklin AG, Morrissy AS, Cavalli
FMG, Luu B, Suarez R, De Antonellis P, Michealraj A, Rastan A, Hegde M, Komosa
M, Sirbu O, Kumar SA, Abdullaev Z, Faria CC, Yip S, Hukin J, Tabori U, Hawkins
C, Aldape K, Daugaard M, Maris JM, Sorensen PH, Ahmed N, Taylor MD. Locoregional
delivery of CAR T cells to the cerebrospinal fluid for treatment of metastatic
medulloblastoma and ependymoma. Nat Med. 2020 May;26(5):720-731. doi:
10.1038/s41591-020-0827-2. Epub 2020 Apr 27. Erratum in: Nat Med. 2021
Jun;27(6):1117-1120. PMID: 32341580; PMCID: PMC8815773.
227: Myers KA, Tamon U, Agnihotram RV, Berrahmoune S. Serum Levels of Valproic
Acid and Carbamazepine Do Not Correlate Well with End-Organ Dysfunction.
Epilepsy Res. 2020 Jul;163:106343. doi: 10.1016/j.eplepsyres.2020.106343. Epub
2020 Apr 19. PMID: 32339984.
228: Bogossian A, Majnemer A, Racine E. Contextualized Autonomy in Transitional
Care for Youth With Neurologic Conditions: The Role of the Pediatric
Neurologist. J Child Neurol. 2020 Jul;35(8):536-542. doi:
10.1177/0883073820918454. Epub 2020 Apr 26. PMID: 32338583.
229: DeGasperis SM, Bernard G, Wolf NI, Miller E, Pohl D. 4H leukodystrophy:
Mild clinical phenotype and comorbidity with multiple sclerosis. Neurol Genet.
2020 Mar 11;6(2):e409. doi: 10.1212/NXG.0000000000000409. PMID: 32337336; PMCID:
PMC7164972.
230: Iorio-Morin C, Hodaie M, Sarica C, Dea N, Westwick HJ, Christie SD,
McDonald PJ, Labidi M, Farmer JP, Brisebois S, D'Aragon F, Carignan A, Fortin D.
Letter: The Risk of COVID-19 Infection During Neurosurgical Procedures: A Review
of Severe Acute Respiratory Distress Syndrome Coronavirus 2 (SARS-CoV-2) Modes
of Transmission and Proposed Neurosurgery-Specific Measures for Mitigation.
Neurosurgery. 2020 Aug 1;87(2):E178-E185. doi: 10.1093/neuros/nyaa157. PMID:
32335684; PMCID: PMC7188127.
231: Levy JP, Oskoui M, Ng P, Andersen J, Buckley D, Fehlings D, Kirton A,
Koclas L, Pigeon N, van Rensburg E, Wood E, Shevell M. Ataxic-hypotonic cerebral
palsy in a cerebral palsy registry: Insights into a distinct subtype. Neurol
Clin Pract. 2020 Apr;10(2):131-139. doi: 10.1212/CPJ.0000000000000713. PMID:
32309031; PMCID: PMC7156190.
232: Thebault S, Lee H, Bose G, Tessier D, Abdoli M, Bowman M, Berard J, Walker
L, Rush CA, MacLean H, Booth RA, Narayanan S, Arnold DL, Tabard-Cossa V, Atkins
HL, Bar-Or A, Freedman MS. Neurotoxicity after hematopoietic stem cell
transplant in multiple sclerosis. Ann Clin Transl Neurol. 2020 May;7(5):767-775.
doi: 10.1002/acn3.51045. Epub 2020 Apr 18. PMID: 32304358; PMCID: PMC7261754.
233: Myers KA, Simard-Tremblay E, Saint-Martin C. X-Linked Familial Focal
Epilepsy Associated With Xp22.31 Deletion. Pediatr Neurol. 2020 Jul;108:113-116.
doi: 10.1016/j.pediatrneurol.2020.02.008. Epub 2020 Apr 13. PMID: 32299744.
234: Eid H, Crevier-Sorbo G, Moreau JT, Saint-Martin C, Elzawawi MS, Mousa WA,
Dudley RWR, Wilson N. Eight-Year Experience With 3-T Intraoperative MRI
Integration in Focal Pediatric Epilepsy Surgery: Impact on Extent of Resection,
Residual Volumes, and Seizure Outcomes. AJR Am J Roentgenol. 2020
Jun;214(6):1343-1351. doi: 10.2214/AJR.19.22336. Epub 2020 Mar 24. PMID:
32208007.
235: Solstrand Dahlberg L, Viessmann O, Linnman C. Heritability of cervical
spinal cord structure. Neurol Genet. 2020 Feb 26;6(2):e401. doi:
10.1212/NXG.0000000000000401. Erratum in: Neurol Genet. 2020 Mar 18;6(2):e419.
PMID: 32185240; PMCID: PMC7061306.
236: Borlot F, Abushama A, Morrison-Levy N, Jain P, Puthenveettil Vinayan K,
Abukhalid M, Aldhalaan HM, Almuzaini HS, Gulati S, Hershkovitz T, Konanki R,
Lingappa L, Luat AF, Shafi S, Tabarki B, Thomas M, Yoganathan S, Alfadhel M,
Arya R, Donner EJ, Ehaideb SN, Gowda VK, Jain V, Madaan P, Myers KA, Otsubo H,
Panda P, Sahu JK, Sampaio LPB, Sharma S, Simard-Tremblay E, Zak M, Whitney R.
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric
cases. Epilepsia. 2020 Apr;61(4):679-692. doi: 10.1111/epi.16480. Epub 2020 Mar
13. PMID: 32167590.
237: Chevin M, Chabrier S, Dinomais M, Bedell BJ, Sébire G. Benefits of
hypothermia in neonatal arterial ischemic strokes: A preclinical study. Int J
Dev Neurosci. 2020 Jun;80(4):257-266. doi: 10.1002/jdn.10022. Epub 2020 Mar 24.
PMID: 32115740.
238: Westwick HJ, Elkaim LM, Obaid S, Fallah A, Tu A, Ibrahim GM, Weil AG.
Interest and participation in global neurosurgery: a survey of Canadian
neurosurgery residents. Neurosurg Focus. 2020 Mar 1;48(3):E21. doi:
10.3171/2019.12.FOCUS19767. PMID: 32114558.
239: Sardaar S, Qi B, Dionne-Laporte A, Rouleau GA, Rabbany R, Trakadis YJ.
Machine learning analysis of exome trios to contrast the genomic architecture of
autism and schizophrenia. BMC Psychiatry. 2020 Feb 28;20(1):92. doi:
10.1186/s12888-020-02503-5. PMID: 32111185; PMCID: PMC7049199.
240: Chocron Y, Azzi AJ, Galli R, Alnaif N, Atkinson J, Dudley R, Farmer JP,
Gilardino MS. Operative Time as the Predominant Risk Factor for Transfusion
Requirements in Nonsyndromic Craniosynostosis Repair. Plast Reconstr Surg Glob
Open. 2020 Jan 17;8(1):e2592. doi: 10.1097/GOX.0000000000002592. PMID: 32095402;
PMCID: PMC7015599.
241: Fokkens WJ, Lund VJ, Hopkins C, Hellings PW, Kern R, Reitsma S, Toppila-
Salmi S, Bernal-Sprekelsen M, Mullol J, Alobid I, Terezinha Anselmo-Lima W,
Bachert C, Baroody F, von Buchwald C, Cervin A, Cohen N, Constantinidis J, De
Gabory L, Desrosiers M, Diamant Z, Douglas RG, Gevaert PH, Hafner A, Harvey RJ,
Joos GF, Kalogjera L, Knill A, Kocks JH, Landis BN, Limpens J, Lebeer S,
Lourenco O, Meco C, Matricardi PM, O'Mahony L, Philpott CM, Ryan D, Schlosser R,
Senior B, Smith TL, Teeling T, Tomazic PV, Wang DY, Wang D, Zhang L, Agius AM,
Ahlstrom-Emanuelsson C, Alabri R, Albu S, Alhabash S, Aleksic A, Aloulah M, Al-
Qudah M, Alsaleh S, Baban MA, Baudoin T, Balvers T, Battaglia P, Bedoya JD,
Beule A, Bofares KM, Braverman I, Brozek-Madry E, Richard B, Callejas C, Carrie
S, Caulley L, Chussi D, de Corso E, Coste A, El Hadi U, Elfarouk A, Eloy PH,
Farrokhi S, Felisati G, Ferrari MD, Fishchuk R, Grayson W, Goncalves PM, Grdinic
B, Grgic V, Hamizan AW, Heinichen JV, Husain S, Ping TI, Ivaska J, Jakimovska F,
Jovancevic L, Kakande E, Kamel R, Karpischenko S, Kariyawasam HH, Kawauchi H,
Kjeldsen A, Klimek L, Krzeski A, Kopacheva Barsova G, Kim SW, Lal D, Letort JJ,
Lopatin A, Mahdjoubi A, Mesbahi A, Netkovski J, Nyenbue Tshipukane D, Obando-
Valverde A, Okano M, Onerci M, Ong YK, Orlandi R, Otori N, Ouennoughy K, Ozkan
M, Peric A, Plzak J, Prokopakis E, Prepageran N, Psaltis A, Pugin B, Raftopulos
M, Rombaux P, Riechelmann H, Sahtout S, Sarafoleanu CC, Searyoh K, Rhee CS, Shi
J, Shkoukani M, Shukuryan AK, Sicak M, Smyth D, Sindvongs K, Soklic Kosak T,
Stjarne P, Sutikno B, Steinsvag S, Tantilipikorn P, Thanaviratananich S, Tran T,
Urbancic J, Valiulius A, Vasquez de Aparicio C, Vicheva D, Virkkula PM, Vicente
G, Voegels R, Wagenmann MM, Wardani RS, Welge-Lussen A, Witterick I, Wright E,
Zabolotniy D, Zsolt B, Zwetsloot CP. European Position Paper on Rhinosinusitis
and Nasal Polyps 2020. Rhinology. 2020 Feb 20;58(Suppl S29):1-464. doi:
10.4193/Rhin20.600. PMID: 32077450.
242: Wheeler MA, Clark IC, Tjon EC, Li Z, Zandee SEJ, Couturier CP, Watson BR,
Scalisi G, Alkwai S, Rothhammer V, Rotem A, Heyman JA, Thaploo S, Sanmarco LM,
Ragoussis J, Weitz DA, Petrecca K, Moffitt JR, Becher B, Antel JP, Prat A,
Quintana FJ. MAFG-driven astrocytes promote CNS inflammation. Nature. 2020
Feb;578(7796):593-599. doi: 10.1038/s41586-020-1999-0. Epub 2020 Feb 12. PMID:
32051591; PMCID: PMC8049843.
243: Amankwah N, Oskoui M, Garner R, Bancej C, Manuel DG, Wall R, Finès P,
Bernier J, Tu K, Reimer K. Cerebral palsy in Canada, 2011-2031: results of a
microsimulation modelling study of epidemiological and cost impacts. Health
Promot Chronic Dis Prev Can. 2020 Feb;40(2):25-37. doi: 10.24095/hpcdp.40.2.01.
PMID: 32049464; PMCID: PMC7053851.
244: Wang S, Weil AG, Ibrahim GM, Fallah A, Korman B, Ragheb J, Bhatia S,
Duchowny M. Surgical management of pediatric patients with encephalopathy due to
electrical status epilepticus during sleep (ESES). Epileptic Disord. 2020 Feb
1;22(1):39-54. doi: 10.1684/epd.2020.1129. PMID: 32043470.
245: Gauquelin L, Cayami FK, Sztriha L, Yoon G, Tran LT, Guerrero K, Hocke F,
van Spaendonk RML, Fung EL, D'Arrigo S, Vasco G, Thiffault I, Niyazov DM, Person
R, Lewis KS, Wassmer E, Prescott T, Fallon P, McEntagart M, Rankin J, Webster R,
Philippi H, van de Warrenburg B, Timmann D, Dixit A, Searle C; DDD Study,,
Thakur N, Kruer MC, Sharma S, Vanderver A, Tonduti D, van der Knaap MS, Bertini
E, Goizet C, Fribourg S, Wolf NI, Bernard G. Clinical spectrum of POLR3-related
leukodystrophy caused by biallelic POLR1C pathogenic variants. Neurol
Genet. 2019 Oct 30;5(6):e369. doi: 10.1212/NXG.0000000000000369. PMID: 32042905;
PMCID: PMC6927361.
246: Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y,
Kuentz P, Courcet JB, Carmignac V, Garret P, Bessis D, Boute O, Bron A, Captier
G, Carmi E, Devauchelle B, Geneviève D, Gondry-Jouet C, Guibaud L, Lafon A,
Mathieu-Dramard M, Thevenon J, Dobyns WB, Bernard G, Polubothu S, Faravelli F,
Kinsler VA, Thauvin C, Faivre L, Ross ME, Rivière JB. Author Correction:
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal
syndrome. Nat Genet. 2020 Mar;52(3):353. doi: 10.1038/s41588-019-0565-x. Erratum
for: Nat Genet. 2019 Oct;51(10):1438-1441. PMID: 32034319.
247: Luo L, Ambrozkiewicz MC, Benseler F, Chen C, Dumontier E, Falkner S,
Furlanis E, Gomez AM, Hoshina N, Huang WH, Hutchison MA, Itoh-Maruoka Y, Lavery
LA, Li W, Maruo T, Motohashi J, Pai EL, Pelkey KA, Pereira A, Philips T,
Sinclair JL, Stogsdill JA, Traunmüller L, Wang J, Wortel J, You W, Abumaria N,
Beier KT, Brose N, Burgess HA, Cepko CL, Cloutier JF, Eroglu C, Goebbels S,
Kaeser PS, Kay JN, Lu W, Luo L, Mandai K, McBain CJ, Nave KA, Prado MAM, Prado
VF, Rothstein J, Rubenstein JLR, Saher G, Sakimura K, Sanes JR, Scheiffele P,
Takai Y, Umemori H, Verhage M, Yuzaki M, Zoghbi HY, Kawabe H, Craig AM.
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines:
Prevalence of Germline Recombination and Influencing Factors. Neuron. 2020 Apr
8;106(1):37-65.e5. doi: 10.1016/j.neuron.2020.01.008. Epub 2020 Feb 5. PMID:
32027825; PMCID: PMC7377387.
248: Moreau JT, Hankinson TC, Baillet S, Dudley RWR. Individual-patient
prediction of meningioma malignancy and survival using the Surveillance,
Epidemiology, and End Results database. NPJ Digit Med. 2020 Jan 30;3:12. doi:
10.1038/s41746-020-0219-5. PMID: 32025573; PMCID: PMC6992687.
249: Garbin M, Portela DA, Bertolizio G, Garcia-Pereira F, Gallastegui A, Otero
PE. Description of ultrasound-guided quadratus lumborum block technique and
evaluation of injectate spread in canine cadavers. Vet Anaesth Analg. 2020
Mar;47(2):249-258. doi: 10.1016/j.vaa.2019.12.005. Epub 2019 Dec 31. PMID:
32014397.
250: Pellerin D, Aykanat A, Ellezam B, Troiano EC, Karamchandani J, Dicaire MJ,
Petitclerc M, Robertson R, Allard-Chamard X, Brunet D, Konersman CG, Mathieu J,
Warman Chardon J, Gupta VA, Beggs AH, Brais B, Chrestian N. Novel Recessive
TNNT1 Congenital Core-Rod Myopathy in French Canadians. Ann Neurol. 2020
Apr;87(4):568-583. doi: 10.1002/ana.25685. Epub 2020 Feb 8. PMID: 31970803;
PMCID: PMC7078025.
251: Perlman K, Couturier CP, Yaqubi M, Tanti A, Cui QL, Pernin F, Stratton JA,
Ragoussis J, Healy L, Petrecca K, Dudley R, Srour M, Hall JA, Kennedy TE,
Mechawar N, Antel JP. Developmental trajectory of oligodendrocyte progenitor
cells in the human brain revealed by single cell RNA sequencing. Glia. 2020
Jun;68(6):1291-1303. doi: 10.1002/glia.23777. Epub 2020 Jan 20. PMID: 31958186.
252: Harting I, Al-Saady M, Krägeloh-Mann I, Bley A, Hempel M, Bierhals T, Karch
S, Moog U, Bernard G, Huntsman R, van Spaendonk RML, Vreeburg M, Rodríguez-
Palmero A, Pujol A, van der Knaap MS, Pouwels PJW, Wolf NI. POLR3A variants with
striatal involvement and extrapyramidal movement disorder. Neurogenetics. 2020
Apr;21(2):121-133. doi: 10.1007/s10048-019-00602-4. Epub 2020 Jan 15. PMID:
31940116; PMCID: PMC7064625.
253: Myers KA, Oskoui M. Seizures in Epilepsy With Eyelid Myoclonia May Be
Provoked by Eye Closure, Not Fixation Removal. Pediatr Neurol. 2020
Apr;105:62-64. doi: 10.1016/j.pediatrneurol.2019.10.001. Epub 2019 Oct 19. PMID:
31932118.
254: Manara A, Shemie SD, Large S, Healey A, Baker A, Badiwala M, Berman M,
Butler AJ, Chaudhury P, Dark J, Forsythe J, Freed DH, Gardiner D, Harvey D,
Hornby L, MacLean J, Messer S, Oniscu GC, Simpson C, Teitelbaum J, Torrance S,
Wilson LC, Watson CJE. Maintaining the permanence principle for death during in
situ normothermic regional perfusion for donation after circulatory death organ
recovery: A United Kingdom and Canadian proposal. Am J Transplant. 2020
Aug;20(8):2017-2025. doi: 10.1111/ajt.15775. Epub 2020 Jan 27. PMID: 31922653;
PMCID: PMC7540256.
255: Helman G, Lajoie BR, Crawford J, Takanohashi A, Walkiewicz M, Dolzhenko E,
Gross AM, Gainullin VG, Bent SJ, Jenkinson EM, Ferdinandusse S, Waterham HR,
Dorboz I, Bertini E, Miyake N, Wolf NI, Abbink TEM, Kirwin SM, Tan CM, Hobson
GM, Guo L, Ikegawa S, Pizzino A, Schmidt JL, Bernard G, Schiffmann R, van der
Knaap MS, Simons C, Taft RJ, Vanderver A. Genome sequencing in persistently
unsolved white matter disorders. Ann Clin Transl Neurol. 2020 Jan;7(1):144-152.
doi: 10.1002/acn3.50957. Epub 2020 Jan 7. PMID: 31912665; PMCID: PMC6952322.
256: Guberman GI, Houde JC, Ptito A, Gagnon I, Descoteaux M. Structural
abnormalities in thalamo-prefrontal tracks revealed by high angular resolution
diffusion imaging predict working memory scores in concussed children. Brain
Struct Funct. 2020 Jan;225(1):441-459. doi: 10.1007/s00429-019-02002-8. Epub
2020 Jan 1. PMID: 31894406.
257: Sarubbo S, Tate M, De Benedictis A, Merler S, Moritz-Gasser S, Herbet G,
Duffau H. A normalized dataset of 1821 cortical and subcortical functional
responses collected during direct electrical stimulation in patients undergoing
awake brain surgery. Data Brief. 2019 Dec 5;28:104892. doi:
10.1016/j.dib.2019.104892. PMID: 31886348; PMCID: PMC6921148.
258: Deng MY, Sill M, Sturm D, Stichel D, Witt H, Ecker J, Wittmann A,
Schittenhelm J, Ebinger M, Schuhmann MU, Figarella-Branger D, Aronica E,
Staszewski O, Preusser M, Haberler C, Lauten M, Schüller U, Hartmann C, Snuderl
M, Dunham C, Jabado N, Wesseling P, Deckert M, Keyvani K, Gottardo N,
Giangaspero F, von Hoff K, Ellison DW, Pietsch T, Herold-Mende C, Milde T, Witt
O, Kool M, Korshunov A, Wick W, von Deimling A, Pfister SM, Jones DTW, Sahm F.
Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear
clusters (DGONC) - a molecularly defined glioneuronal CNS tumour class
displaying recurrent monosomy 14. Neuropathol Appl Neurobiol. 2020
Aug;46(5):422-430. doi: 10.1111/nan.12590. Epub 2020 Feb 5. PMID: 31867747.
259: Myers KA. Can academic satire exist in the age of "fake news?" Tracking the
citation record of a "holiday review" paper. BMJ. 2019 Dec 16;367:l6763. doi:
10.1136/bmj.l6763. PMID: 31843746.
260: Li BK, Vasiljevic A, Dufour C, Yao F, Ho BLB, Lu M, Hwang EI, Gururangan S,
Hansford JR, Fouladi M, Nobusawa S, Laquerriere A, Delisle MB, Fangusaro J,
Forest F, Toledano H, Solano-Paez P, Leary S, Birks D, Hoffman LM, Szathmari A,
Faure-Conter C, Fan X, Catchpoole D, Zhou L, Schultz KAP, Ichimura K, Gauchotte
G, Jabado N, Jones C, Loussouarn D, Mokhtari K, Rousseau A, Ziegler DS, Tanaka
S, Pomeroy SL, Gajjar A, Ramaswamy V, Hawkins C, Grundy RG, Hill DA, Bouffet E,
Huang A, Jouvet A. Pineoblastoma segregates into molecular sub-groups with
distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry
study. Acta Neuropathol. 2020 Feb;139(2):223-241. doi:
10.1007/s00401-019-02111-y. Epub 2019 Dec 9. PMID: 31820118; PMCID: PMC7673644.
261: Mithani K, Boutet A, Germann J, Elias GJB, Weil AG, Shah A, Guillen M,
Bernal B, Achua JK, Ragheb J, Donner E, Lozano AM, Widjaja E, Ibrahim GM. Lesion
Network Localization of Seizure Freedom following MR-guided Laser Interstitial
Thermal Ablation. Sci Rep. 2019 Dec 9;9(1):18598. doi:
10.1038/s41598-019-55015-y. PMID: 31819108; PMCID: PMC6901556.
262: Mendes MI, Green LMC, Bertini E, Tonduti D, Aiello C, Smith D, Salsano E,
Beerepoot S, Hertecant J, von Spiczak S, Livingston JH, Emrick L, Fraser J,
Russell L, Bernard G, Magri S, Di Bella D, Taroni F, Koenig MK, Moroni I,
Cappuccio G, Brunetti-Pierri N, Rhee J, Mendelsohn BA, Helbig I, Helbig K, Muhle
H, Ismayl O, Vanderver AL, Salomons GS, van der Knaap MS, Wolf NI. RARS1-related
hypomyelinating leukodystrophy: Expanding the spectrum. Ann Clin Transl Neurol.
2020 Jan;7(1):83-93. doi: 10.1002/acn3.50960. Epub 2019 Dec 8. PMID: 31814314;
PMCID: PMC6952319.
263: Le A, Yeganeh M, Buhas D, Trempe MJ, Myers KA. Monocarboxylate
transporter-1 deficiency results in severe metabolic acidosis with ketogenic
diet in early onset absence epilepsy: Case report. Seizure. 2020 Jan;74:31-32.
doi: 10.1016/j.seizure.2019.11.008. Epub 2019 Nov 28. PMID: 31812089.
264: Rivera B, Nadaf J, Fahiminiya S, Apellaniz-Ruiz M, Saskin A, Chong AS,
Sharma S, Wagener R, Revil T, Condello V, Harra Z, Hamel N, Sabbaghian N,
Muchantef K, Thomas C, de Kock L, Hébert-Blouin MN, Bassenden AV, Rabenstein H,
Mete O, Paschke R, Pusztaszeri MP, Paulus W, Berghuis A, Ragoussis J, Nikiforov
YE, Siebert R, Albrecht S, Turcotte R, Hasselblatt M, Fabian MR, Foulkes WD.
DGCR8 microprocessor defect characterizes familial multinodular goiter with
schwannomatosis. J Clin Invest. 2020 Mar 2;130(3):1479-1490. doi:
10.1172/JCI130206. PMID: 31805011; PMCID: PMC7269565.
265: Lambo S, Gröbner SN, Rausch T, Waszak SM, Schmidt C, Gorthi A, Romero JC,
Mauermann M, Brabetz S, Krausert S, Buchhalter I, Koster J, Zwijnenburg DA, Sill
M, Hübner JM, Mack N, Schwalm B, Ryzhova M, Hovestadt V, Papillon-Cavanagh S,
Chan JA, Landgraf P, Ho B, Milde T, Witt O, Ecker J, Sahm F, Sumerauer D,
Ellison DW, Orr BA, Darabi A, Haberler C, Figarella-Branger D, Wesseling P,
Schittenhelm J, Remke M, Taylor MD, Gil-da-Costa MJ, Łastowska M, Grajkowska W,
Hasselblatt M, Hauser P, Pietsch T, Uro-Coste E, Bourdeaut F, Masliah-Planchon
J, Rigau V, Alexandrescu S, Wolf S, Li XN, Schüller U, Snuderl M, Karajannis MA,
Giangaspero F, Jabado N, von Deimling A, Jones DTW, Korbel JO, von Hoff K,
Lichter P, Huang A, Bishop AJR, Pfister SM, Korshunov A, Kool M. The molecular
landscape of ETMR at diagnosis and relapse. Nature. 2019 Dec;576(7786):274-280.
doi: 10.1038/s41586-019-1815-x. Epub 2019 Dec 4. PMID: 31802000; PMCID:
PMC6908757.
266: Van Bergen NJ, Guo Y, Al-Deri N, Lipatova Z, Stanga D, Zhao S, Murtazina R,
Gyurkovska V, Pehlivan D, Mitani T, Gezdirici A, Antony J, Collins F, Willis
MJH, Coban Akdemir ZH, Liu P, Punetha J, Hunter JV, Jhangiani SN, Fatih JM,
Rosenfeld JA, Posey JE, Gibbs RA, Karaca E, Massey S, Ranasinghe TG, Sleiman P,
Troedson C, Lupski JR, Sacher M, Segev N, Hakonarson H, Christodoulou J.
Deficiencies in vesicular transport mediated by TRAPPC4 are associated with
severe syndromic intellectual disability. Brain. 2020 Jan 1;143(1):112-130. doi:
10.1093/brain/awz374. Erratum in: Brain. 2020 Mar 1;143(3):e24. PMID: 31794024;
PMCID: PMC6935753.
267: Laflamme P, Kondyli M, Aljared T, Miconiatis S, Saint-Martin C, Farmer JP,
Dudley RW, Perreault S, Jabado N, Larouche V. Correction to: Efficacy of
Dabrafenib for three children with brainstem BRAFV600E positive
ganglioglioma. J Neurooncol. 2019 Dec;145(3):595. doi:
10.1007/s11060-019-03350-5. Erratum for: J Neurooncol. 2019 Oct;145(1):135-141.
PMID: 31768714.
268: Jessa S, Blanchet-Cohen A, Krug B, Vladoiu M, Coutelier M, Faury D, Poreau
B, De Jay N, Hébert S, Monlong J, Farmer WT, Donovan LK, Hu Y, McConechy MK,
Cavalli FMG, Mikael LG, Ellezam B, Richer M, Allaire A, Weil AG, Atkinson J,
Farmer JP, Dudley RWR, Larouche V, Crevier L, Albrecht S, Filbin MG, Sartelet H,
Lutz PE, Nagy C, Turecki G, Costantino S, Dirks PB, Murai KK, Bourque G,
Ragoussis J, Garzia L, Taylor MD, Jabado N, Kleinman CL. Stalled developmental
programs at the root of pediatric brain tumors. Nat Genet. 2019
Dec;51(12):1702-1713. doi: 10.1038/s41588-019-0531-7. Epub 2019 Nov 25. PMID:
31768071; PMCID: PMC6885128.
269: Alawadhi A, Saint-Martin C, Sabapathy C, Sebire G, Shevell M. Lateral
Medullary Syndrome Due to Left Vertebral Artery Occlusion in a Boy Postflexion
Neck Injury. Child Neurol Open. 2019 Aug 6;6:2329048X19867800. doi:
10.1177/2329048X19867800. PMID: 31763345; PMCID: PMC6852355.
270: Blauwendraat C, Reed X, Krohn L, Heilbron K, Bandres-Ciga S, Tan M, Gibbs
JR, Hernandez DG, Kumaran R, Langston R, Bonet-Ponce L, Alcalay RN, Hassin-Baer
S, Greenbaum L, Iwaki H, Leonard HL, Grenn FP, Ruskey JA, Sabir M, Ahmed S,
Makarious MB, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J, Schulte C,
Brockmann K, Sharma M, Siitonen A, Majamaa K, Eerola-Rautio J, Tienari PJ;
23andMe Research Team, Pantelyat A, Hillis AE, Dawson TM, Rosenthal LS, Albert
MS, Resnick SM, Ferrucci L, Morris CM, Pletnikova O, Troncoso J, Grosset D,
Lesage S, Corvol JC, Brice A, Noyce AJ, Masliah E, Wood N, Hardy J, Shulman LM,
Jankovic J, Shulman JM, Heutink P, Gasser T, Cannon P, Scholz SW, Morris H,
Cookson MR, Nalls MA, Gan-Or Z, Singleton AB. Genetic modifiers of risk and age
at onset in GBA associated Parkinson's disease and Lewy body dementia. Brain.
2020 Jan 1;143(1):234-248. doi: 10.1093/brain/awz350. Erratum in: Brain. 2020
Apr 1;143(4):e33. Erratum in: Brain. 2020 Mar 1;143(3):e24. PMID: 31755958;
PMCID: PMC6935749.
271: Sievers P, Chiang J, Schrimpf D, Stichel D, Paramasivam N, Sill M, Gayden
T, Casalini B, Reuss DE, Dalton J, Pajtler KW, Hänggi D, Herold-Mende C, Rushing
E, Korshunov A, Mawrin C, Weller M, Schlesner M, Wick W, Jabado N, Jones DTW,
Pfister SM, von Deimling A, Ellison DW, Sahm F. YAP1-fusions in pediatric
NF2-wildtype meningioma. Acta Neuropathol. 2020 Jan;139(1):215-218. doi:
10.1007/s00401-019-02095-9. Epub 2019 Nov 16. PMID: 31734728.
272: Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D,
Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J,
Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H,
Faghri F, Gibbs JR, Hernandez DG, Scholz SW, Botia JA, Martinez M, Corvol JC,
Lesage S, Jankovic J, Shulman LM, Sutherland M, Tienari P, Majamaa K, Toft M,
Andreassen OA, Bangale T, Brice A, Yang J, Gan-Or Z, Gasser T, Heutink P,
Shulman JM, Wood NW, Hinds DA, Hardy JA, Morris HR, Gratten J, Visscher PM,
Graham RR, Singleton AB; 23andMe Research Team; System Genomics of Parkinson's
Disease Consortium; International Parkinson's Disease Genomics Consortium.
Identification of novel risk loci, causal insights, and heritable risk for
Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet
Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5. PMID:
31701892; PMCID: PMC8422160.
273: Rtshiladze MA, Roy AA, Goltsman D, Hunt J, Reddy R, Gianoutsos MP. The
removal of cranial springs used in the treatment of scaphocephaly: A minimal
access approach. J Craniomaxillofac Surg. 2019 Nov;47(11):1706-1711. doi:
10.1016/j.jcms.2019.04.001. Epub 2019 Apr 16. PMID: 31677988.
274: Suzuki H, Kumar SA, Shuai S, Diaz-Navarro A, Gutierrez-Fernandez A, De
Antonellis P, Cavalli FMG, Juraschka K, Farooq H, Shibahara I, Vladoiu MC, Zhang
J, Abeysundara N, Przelicki D, Skowron P, Gauer N, Luu B, Daniels C, Wu X,
Forget A, Momin A, Wang J, Dong W, Kim SK, Grajkowska WA, Jouvet A, Fèvre-
Montange M, Garrè ML, Nageswara Rao AA, Giannini C, Kros JM, French PJ, Jabado
N, Ng HK, Poon WS, Eberhart CG, Pollack IF, Olson JM, Weiss WA, Kumabe T, López-
Aguilar E, Lach B, Massimino M, Van Meir EG, Rubin JB, Vibhakar R, Chambless LB,
Kijima N, Klekner A, Bognár L, Chan JA, Faria CC, Ragoussis J, Pfister SM,
Goldenberg A, Wechsler-Reya RJ, Bailey SD, Garzia L, Morrissy AS, Marra MA,
Huang X, Malkin D, Ayrault O, Ramaswamy V, Puente XS, Calarco JA, Stein L,
Taylor MD. Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH
medulloblastoma. Nature. 2019 Oct;574(7780):707-711. doi:
10.1038/s41586-019-1650-0. Epub 2019 Oct 9. PMID: 31664194; PMCID: PMC7141958.
275: Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J,
Andermann F, Andermann E, Walsh CA, Dobyns WB. Duplication 2p16 is associated
with perisylvian polymicrogyria. Am J Med Genet A. 2019 Dec;179(12):2343-2356.
doi: 10.1002/ajmg.a.61342. Epub 2019 Oct 29. PMID: 31660690.
276: Smith ER, Concepcion TL, Shrime M, Niemeier K, Mohamed M, Dahir S, Ismail
EA, Poenaru D, Rice HE; Global Initiative for Children’s Surgery. Waiting Too
Long: The Contribution of Delayed Surgical Access to Pediatric Disease Burden in
Somaliland. World J Surg. 2020 Mar;44(3):656-664. doi:
10.1007/s00268-019-05239-w. PMID: 31654200.
277: Stevelink R, Pangilinan F, Jansen FE, Braun KPJ; International League
Against Epilepsy Consortium on Complex Epilepsies, Molloy AM, Brody LC, Koeleman
BPC. Assessing the genetic association between vitamin B6 metabolism and genetic
generalized epilepsy. Mol Genet Metab Rep. 2019 Oct 11;21:100518. doi:
10.1016/j.ymgmr.2019.100518. PMID: 31641590; PMCID: PMC6796782.
278: Horwood L, Li P, Mok E, Oskoui M, Shevell M, Constantin E. Behavioral
difficulties, sleep problems, and nighttime pain in children with cerebral
palsy. Res Dev Disabil. 2019 Dec;95:103500. doi: 10.1016/j.ridd.2019.103500.
Epub 2019 Oct 17. PMID: 31630025.
279: Iorio-Morin C, Yap R, Dudley RWR, Poulin C, Cantin MA, Benaroch TE, Farmer
JP. Selective Dorsal Root Rhizotomy for Spastic Cerebral Palsy: A Longitudinal
Case-Control Analysis of Functional Outcome. Neurosurgery. 2020 Aug
1;87(2):186-192. doi: 10.1093/neuros/nyz422. PMID: 31620799.
280: Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus
A, Trivisano M, Gill D; EIMFS Consortium, Sadleir LG, Specchio N, Guerrini R,
Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE. The Genetic
Landscape of Epilepsy of Infancy with Migrating Focal Seizures. Ann Neurol. 2019
Dec;86(6):821-831. doi: 10.1002/ana.25619. Erratum in: Ann Neurol. 2020
Apr;87(4):658. PMID: 31618474; PMCID: PMC7423163.
281: Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y,
Kuentz P, Courcet JB, Carmignac V, Garret P, Bessis D, Boute O, Bron A, Captier
G, Carmi E, Devauchelle B, Geneviève D, Gondry-Jouet C, Guibaud L, Lafon A,
Mathieu-Dramard M, Thevenon J, Dobyns WB, Bernard G, Polubothu S, Faravelli F,
Kinsler VA, Thauvin C, Faivre L, Ross ME, Rivière JB. Author Correction:
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal
syndrome. Nat Genet. 2019 Nov;51(11):1660. doi: 10.1038/s41588-019-0527-3.
Erratum for: Nat Genet. 2019 Sep 30;: PMID: 31611689.
282: Easson K, Rohlicek CV, Houde JC, Gilbert G, Saint-Martin C, Fontes K,
Majnemer A, Marelli A, Wintermark P, Descoteaux M, Brossard-Racine M.
Quantification of apparent axon density and orientation dispersion in the white
matter of youth born with congenital heart disease. Neuroimage. 2020 Jan
15;205:116255. doi: 10.1016/j.neuroimage.2019.116255. Epub 2019 Oct 9. PMID:
31605826.
283: Ademuyiwa AO, Odugbemi TO, Bode CO, Elebute OA, Alakaloko FM, Alabi EO,
Bankole O, Ladipo-Ajayi O, Seyi-Olajide JO, Okusanya B, Abazie O, Ademuyiwa IY,
Onwuka A, Tran T, Makanjuola A, Gupta S, Ots R, Harrison EM, Poenaru D, Nwomeh
BC. Prevalence of surgically correctable conditions among children in a mixed
urban-rural community in Nigeria using the SOSAS survey tool: Implications for
paediatric surgical capacity-building. PLoS One. 2019 Oct 10;14(10):e0223423.
doi: 10.1371/journal.pone.0223423. PMID: 31600252; PMCID: PMC6786634.
284: Wheelwright M, Selvey PJ, Steinbok P, Singhal A, Ibrahim G, Fallah A, Weil
AG, Halvorson K, Tu A. Systematic review of spinal deformities following multi-
level selective dorsal rhizotomy. Childs Nerv Syst. 2020 May;36(5):1025-1035.
doi: 10.1007/s00381-019-04375-x. Epub 2019 Oct 8. PMID: 31595313.
285: Accogli A, Calabretta S, St-Onge J, Boudrahem-Addour N, Dionne-Laporte A,
Joset P, Azzarello-Burri S, Rauch A, Krier J, Fieg E, Pallais JC; Undiagnosed
Diseases Network, McConkie-Rosell A, McDonald M, Freedman SF, Rivière JB,
Lafond-Lapalme J, Simpson BN, Hopkin RJ, Trimouille A, Van-Gils J, Begtrup A,
McWalter K, Delphine H, Keren B, Genevieve D, Argilli E, Sherr EH, Severino M,
Rouleau GA, Yam PT, Charron F, Srour M. De Novo Pathogenic Variants in
N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum,
Axon, Cardiac, Ocular, and Genital Defects. Am J Hum Genet. 2019 Oct
3;105(4):854-868. doi: 10.1016/j.ajhg.2019.09.005. PMID: 31585109; PMCID:
PMC6817525.
286: Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y,
Kuentz P, Courcet JB, Carmignac V, Garret P, Bessis D, Boute O, Bron A, Captier
G, Carmi E, Devauchelle B, Geneviève D, Gondry-Jouet C, Guibaud L, Lafon A,
Mathieu-Dramard M, Thevenon J, Dobyns WB, Bernard G, Polubothu S, Faravelli F,
Kinsler VA, Thauvin C, Faivre L, Ross ME, Rivière JB. Postzygotic inactivating
mutations of RHOA cause a mosaic neuroectodermal syndrome. Nat Genet. 2019
Oct;51(10):1438-1441. doi: 10.1038/s41588-019-0498-4. Epub 2019 Sep 30. Erratum
in: Nat Genet. 2019 Nov;51(11):1660. Erratum in: Nat Genet. 2020 Mar;52(3):353.
PMID: 31570889; PMCID: PMC6858542.
287: Guerreiro Stucklin AS, Ryall S, Fukuoka K, Zapotocky M, Lassaletta A, Li C,
Bridge T, Kim B, Arnoldo A, Kowalski PE, Zhong Y, Johnson M, Li C, Ramani AK,
Siddaway R, Nobre LF, de Antonellis P, Dunham C, Cheng S, Boué DR, Finlay JL,
Coven SL, de Prada I, Perez-Somarriba M, Faria CC, Grotzer MA, Rushing E,
Sumerauer D, Zamecnik J, Krskova L, Garcia Ariza M, Cruz O, Morales La Madrid A,
Solano P, Terashima K, Nakano Y, Ichimura K, Nagane M, Sakamoto H, Gil-da-Costa
MJ, Silva R, Johnston DL, Michaud J, Wilson B, van Landeghem FKH, Oviedo A,
McNeely PD, Crooks B, Fried I, Zhukova N, Hansford JR, Nageswararao A, Garzia L,
Shago M, Brudno M, Irwin MS, Bartels U, Ramaswamy V, Bouffet E, Taylor MD,
Tabori U, Hawkins C. Alterations in ALK/ROS1/NTRK/MET drive a group of infantile
hemispheric gliomas. Nat Commun. 2019 Sep 25;10(1):4343. doi:
10.1038/s41467-019-12187-5. PMID: 31554817; PMCID: PMC6761184.
288: Faltermeier C, Chai T, Syed S, Lau N, Elkaim L, Ibrahim G, Wang A, Weil A,
Bendel A, Fallah A, Tu A. Survival of infants ≤24 months of age with brain
tumors: A population-based study using the SEER database. PLoS One. 2019 Sep
25;14(9):e0223051. doi: 10.1371/journal.pone.0223051. Erratum in: PLoS One. 2019
Oct 24;14(10):e0224570. PMID: 31553771; PMCID: PMC6760899.
289: Oskoui M, Pringsheim T, Holler-Managan Y, Potrebic S, Billinghurst L, Gloss
D, Hershey AD, Licking N, Sowell M, Victorio MC, Gersz EM, Leininger E, Zanitsch
H, Yonker M, Mack K. Practice guideline update summary: Acute treatment of
migraine in children and adolescents: Report of the Guideline Development,
Dissemination, and Implementation Subcommittee of the American Academy of
Neurology and the American Headache Society. Headache. 2019 Sep;59(8):1158-1173.
doi: 10.1111/head.13628. PMID: 31529481.
290: Hershey AD, Oskoui M, Pringsheim T, Holler-Managan Y, Potrebic S,
Billinghurst L, Gloss D, Licking N, Sowell M, Victorio MC, Gersz E, Vrijsen E,
Zanitsch H, Yonker M, Mack K, Gelfand AA, Szperka CL, Powers SW. New Guidelines:
Interpretation, Application and the Future. Headache. 2019 Sep;59(8):1133-1143.
doi: 10.1111/head.13629. PMID: 31529478.
291: Oskoui M, Pringsheim T, Billinghurst L, Potrebic S, Gersz EM, Gloss D,
Holler-Managan Y, Leininger E, Licking N, Mack K, Powers SW, Sowell M, Cristina
Victorio M, Yonker M, Zanitsch H, Hershey AD. Practice guideline update summary:
Pharmacologic treatment for pediatric migraine prevention: Report of the
Guideline Development, Dissemination, and Implementation Subcommittee of the
American Academy of Neurology and the American Headache Society. Headache. 2019
Sep;59(8):1144-1157. doi: 10.1111/head.13625. PMID: 31529477.
292: Philippe L, Maria K, Tariq A, Sofia M, Christine SM, Jean-Pierre F, Dudley
RW, Sébastien P, Nada J, Valérie L. Efficacy of Dabrafenib for three children
with brainstem BRAFV600E positive ganglioglioma. J Neurooncol. 2019
Oct;145(1):135-141. doi: 10.1007/s11060-019-03280-2. Epub 2019 Sep 9. Erratum
in: J Neurooncol. 2019 Dec;145(3):595. PMID: 31502039.
293: Shevell M. Health Professional Burnout: An (Un)Ethical Consequence of
Modern Health Care? Can J Neurol Sci. 2019 Nov;46(6):682-683. doi:
10.1017/cjn.2019.280. PMID: 31500677.
294: Juhász C, Shevell M. When white matter lesions cross the (midventricle)
line: Predicting outcome in preterm infants. Neurology. 2019 Sep
24;93(13):569-570. doi: 10.1212/WNL.0000000000008165. Epub 2019 Aug 29. PMID:
31467254.
295: Appendino JP, Boelman C, Brna PM, Burneo JG, Claassen CS, Connolly MB, De
Guzman MVT, Federico P, Floyd D, Huntsman RJ, Javidan M, Jette N, Jurasek LL,
Keezer MR, Lau JC, McCoy B, McLachlan RS, Ng MC, Nguyen DK, Reid AY, Rho JM,
Snead OC, Téllez-Zenteno JF, Wang L, Zak MM. Position Statement on the Use of
Medical Cannabis for the Treatment of Epilepsy in Canada. Can J Neurol Sci. 2019
Nov;46(6):645-652. doi: 10.1017/cjn.2019.282. PMID: 31466531.
296: Machado I, Toews M, George E, Unadkat P, Essayed W, Luo J, Teodoro P,
Carvalho H, Martins J, Golland P, Pieper S, Frisken S, Golby A, Wells Iii W, Ou
Y. Deformable MRI-Ultrasound registration using correlation-based attribute
matching for brain shift correction: Accuracy and generality in multi-site data.
Neuroimage. 2019 Nov 15;202:116094. doi: 10.1016/j.neuroimage.2019.116094. Epub
2019 Aug 22. PMID: 31446127; PMCID: PMC6819249.
297: Myers KA, van 't Hof FNG, Sadleir LG, Legault G, Simard-Tremblay E, Amor
DJ, Scheffer IE. Fragile Females: Case Series of Epilepsy in Girls With
FMR1 Disruption. Pediatrics. 2019 Sep;144(3):e20190599. doi:
10.1542/peds.2019-0599. Epub 2019 Aug 22. PMID: 31439621.
298: Vissoci JRN, Ong CT, Andrade L, Rocha TAH, Silva NCD, Poenaru D, Smith ER,
Rice HE; Global Initiative for Children’s Surgery. Disparities in surgical care
for children across Brazil: Use of geospatial analysis. PLoS One. 2019 Aug
20;14(8):e0220959. doi: 10.1371/journal.pone.0220959. PMID: 31430312; PMCID:
PMC6701804.
299: Aishworiya R, Cai S, Chen HY, Phua DY, Broekman BFP, Daniel LM, Chong YS,
Shek LP, Yap F, Chan SY, Meaney MJ, Law EC. Television viewing and child
cognition in a longitudinal birth cohort in Singapore: the role of maternal
factors. BMC Pediatr. 2019 Aug 16;19(1):286. doi: 10.1186/s12887-019-1651-z.
PMID: 31419962; PMCID: PMC6696668.
300: Oskoui M, Pringsheim T, Holler-Managan Y, Potrebic S, Billinghurst L, Gloss
D, Hershey AD, Licking N, Sowell M, Victorio MC, Gersz EM, Leininger E, Zanitsch
H, Yonker M, Mack K. Practice guideline update summary: Acute treatment of
migraine in children and adolescents: Report of the Guideline Development,
Dissemination, and Implementation Subcommittee of the American Academy of
Neurology and the American Headache Society. Neurology. 2019 Sep
10;93(11):487-499. doi: 10.1212/WNL.0000000000008095. Epub 2019 Aug 14. Erratum
in: Neurology. 2020 Jan 7;94(1):50. PMID: 31413171.
301: Oskoui M, Pringsheim T, Billinghurst L, Potrebic S, Gersz EM, Gloss D,
Holler-Managan Y, Leininger E, Licking N, Mack K, Powers SW, Sowell M, Victorio
MC, Yonker M, Zanitsch H, Hershey AD. Practice guideline update summary:
Pharmacologic treatment for pediatric migraine prevention: Report of the
Guideline Development, Dissemination, and Implementation Subcommittee of the
American Academy of Neurology and the American Headache Society. Neurology. 2019
Sep 10;93(11):500-509. doi: 10.1212/WNL.0000000000008105. Epub 2019 Aug 14.
Erratum in: Neurology. 2020 Jan 7;94(1):50. PMID: 31413170; PMCID: PMC6746206.
302: Mithani K, Mikhail M, Morgan BR, Wong S, Weil AG, Deschenes S, Wang S,
Bernal B, Guillen MR, Ochi A, Otsubo H, Yau I, Lo W, Pang E, Holowka S, Snead
OC, Donner E, Rutka JT, Go C, Widjaja E, Ibrahim GM. Connectomic Profiling
Identifies Responders to Vagus Nerve Stimulation. Ann Neurol. 2019
Nov;86(5):743-753. doi: 10.1002/ana.25574. Epub 2019 Aug 27. PMID: 31393626.
303: Cronin SJF, Seehus C, Weidinger A, Talbot S, Reissig S, Seifert M, Pierson
Y, McNeill E, Longhi MS, Turnes BL, Kreslavsky T, Kogler M, Hoffmann D, Ticevic
M, da Luz Scheffer D, Tortola L, Cikes D, Jais A, Rangachari M, Rao S, Paolino
M, Novatchkova M, Aichinger M, Barrett L, Latremoliere A, Wirnsberger G,
Lametschwandtner G, Busslinger M, Zicha S, Latini A, Robson SC, Waisman A,
Andrews N, Costigan M, Channon KM, Weiss G, Kozlov AV, Tebbe M, Johnsson K,
Woolf CJ, Penninger JM. Publisher Correction: The metabolite BH4 controls T cell
proliferation in autoimmunity and cancer. Nature. 2019 Aug;572(7769):E18. doi:
10.1038/s41586-019-1459-x. Erratum for: Nature. 2018 Nov;563(7732):564-568.
PMID: 31363232.
304: Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM,
Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ,
Borowitz MJ, Wood BL, Carroll WL, Raetz EA, Feingold E, Devidas M, Barcellos LF,
Hansen HM, Morimoto L, Kang AY, Smirnov I, Healy J, Laverdière C, Sinnett D,
Taub JW, Birch JM, Thompson P, Spector LG, Pombo-de-Oliveira MS, DeWan AT,
Mullighan CG, Hunger SP, Pui CH, Loh ML, Zwick ME, Metayer C, Ma X, Mueller BA,
Sherman SL, Wiemels JL, Relling MV, Yang JJ, Lupo PJ, Rabin KR. Inherited
genetic susceptibility to acute lymphoblastic leukemia in Down syndrome. Blood.
2019 Oct 10;134(15):1227-1237. doi: 10.1182/blood.2018890764. PMID: 31350265;
PMCID: PMC6788009.
305: Lai JS, Cai S, Feng L, Shek LP, Yap F, Tan KH, Chong YS, Godfrey KM, Meaney
MJ, Rifkin-Graboi A, Broekman BFP, Chong MFF. Associations of maternal zinc and
magnesium with offspring learning abilities and cognitive development at 4 years
in GUSTO. Nutr Neurosci. 2021 Jun;24(6):467-476. doi:
10.1080/1028415X.2019.1643624. Epub 2019 Jul 22. PMID: 31331255.
306: de Smith AJ, Walsh KM, Morimoto LM, Francis SS, Hansen HM, Jeon S, Gonseth
S, Chen M, Sun H, Luna-Fineman S, Antillón F, Girón V, Kang AY, Smirnov I, Shao
X, Whitehead TP, Barcellos LF, Jolly KW, Healy J, Laverdière C, Sinnett D, Taub
JW, Birch JM, Thompson PD, Pombo-de-Oliveira MS, Spector LG, DeWan AT, Mueller
BA, Chiang C, Metayer C, Ma X, Wiemels JL. Heritable variation at the chromosome
21 gene ERG is associated with acute lymphoblastic leukemia risk in children
with and without Down syndrome. Leukemia. 2019 Nov;33(11):2746-2751. doi:
10.1038/s41375-019-0514-9. Epub 2019 Jul 11. PMID: 31296947; PMCID: PMC6858994.
307: Sin-Chan P, Mumal I, Suwal T, Ho B, Fan X, Singh I, Du Y, Lu M, Patel N,
Torchia J, Popovski D, Fouladi M, Guilhamon P, Hansford JR, Leary S, Hoffman LM,
Mulcahy Levy JM, Lassaletta A, Solano-Paez P, Rivas E, Reddy A, Gillespie GY,
Gupta N, Van Meter TE, Nakamura H, Wong TT, Ra YS, Kim SK, Massimi L, Grundy RG,
Fangusaro J, Johnston D, Chan J, Lafay-Cousin L, Hwang EI, Wang Y, Catchpoole D,
Michaud J, Ellezam B, Ramanujachar R, Lindsay H, Taylor MD, Hawkins CE, Bouffet
E, Jabado N, Singh SK, Kleinman CL, Barsyte-Lovejoy D, Li XN, Dirks PB, Lin CY,
Mack SC, Rich JN, Huang A. A C19MC-LIN28A-MYCN Oncogenic Circuit Driven by
Hijacked Super-enhancers Is a Distinct Therapeutic Vulnerability in ETMRs: A
Lethal Brain Tumor. Cancer Cell. 2019 Jul 8;36(1):51-67.e7. doi:
10.1016/j.ccell.2019.06.002. PMID: 31287992.
308: Qi Y, Zheng Y, Li Z, Liu Z, Xiong L. Genetic Studies of Tic Disorders and
Tourette Syndrome. Methods Mol Biol. 2019;2011:547-571. doi:
10.1007/978-1-4939-9554-7_32. PMID: 31273721.
309: Bedognetti D, Ceccarelli M, Galluzzi L, Lu R, Palucka K, Samayoa J,
Spranger S, Warren S, Wong KK, Ziv E, Chowell D, Coussens LM, De Carvalho DD,
DeNardo DG, Galon J, Kaufman HL, Kirchhoff T, Lotze MT, Luke JJ, Minn AJ, Politi
K, Shultz LD, Simon R, Thórsson V, Weidhaas JB, Ascierto ML, Ascierto PA, Barnes
JM, Barsan V, Bommareddy PK, Bot A, Church SE, Ciliberto G, De Maria A, Draganov
D, Ho WS, McGee HM, Monette A, Murphy JF, Nisticò P, Park W, Patel M, Quigley M,
Radvanyi L, Raftopoulos H, Rudqvist NP, Snyder A, Sweis RF, Valpione S,
Zappasodi R, Butterfield LH, Disis ML, Fox BA, Cesano A, Marincola FM; Society
for Immunotherapy of Cancer (SITC) Cancer Immune Responsiveness Task Force and
Working Groups. Correction to: Toward a comprehensive view of cancer immune
responsiveness: a synopsis from the SITC workshop. J Immunother Cancer. 2019 Jul
4;7(1):167. doi: 10.1186/s40425-019-0640-y. Erratum for: J Immunother Cancer.
2019 May 22;7(1):131. PMID: 31272507; PMCID: PMC6610889.
310: Akyol MU, Alden TD, Amartino H, Ashworth J, Belani K, Berger KI, Borgo A,
Braunlin E, Eto Y, Gold JI, Jester A, Jones SA, Karsli C, Mackenzie W, Marinho
DR, McFadyen A, McGill J, Mitchell JJ, Muenzer J, Okuyama T, Orchard PJ, Stevens
B, Thomas S, Walker R, Wynn R, Giugliani R, Harmatz P, Hendriksz C, Scarpa M;
MPS Consensus Programme Steering Committee; MPS Consensus Programme Co-Chairs.
Recommendations for the management of MPS IVA: systematic evidence- and
consensus-based guidance. Orphanet J Rare Dis. 2019 Jun 13;14(1):137. doi:
10.1186/s13023-019-1074-9. PMID: 31196221; PMCID: PMC6567385.
311: Saint-Martin C, Apuzzo S, Salman A, Farmer JP. Hyperacute Infarct on
Intraoperative Diffusion Imaging of Pediatric Brain Tumor Surgery. Can J Neurol
Sci. 2019 Sep;46(5):550-558. doi: 10.1017/cjn.2019.226. Epub 2019 Jul 29. PMID:
31179961.
312: Polosa A, Lv S, Ait Igrine W, Chevrolat LA, Bessaklia H, Lachapelle P.
Evidences Suggesting that Distinct Immunological and Cellular Responses to Light
Damage Distinguishes Juvenile and Adult Rat Retinas. Int J Mol Sci. 2019 Jun
4;20(11):2744. doi: 10.3390/ijms20112744. PMID: 31167447; PMCID: PMC6600267.
313: Alhajaj G, Myers KA. Incorporation of fixation-removal with Fresnel glasses
in a routine EEG protocol. Clin Neurophysiol. 2019 Aug;130(8):1185-1187. doi:
10.1016/j.clinph.2019.04.716. Epub 2019 May 24. PMID: 31163362.
314: Akyol MU, Alden TD, Amartino H, Ashworth J, Belani K, Berger KI, Borgo A,
Braunlin E, Eto Y, Gold JI, Jester A, Jones SA, Karsli C, Mackenzie W, Marinho
DR, McFadyen A, McGill J, Mitchell JJ, Muenzer J, Okuyama T, Orchard PJ, Stevens
B, Thomas S, Walker R, Wynn R, Giugliani R, Harmatz P, Hendriksz C, Scarpa M;
MPS Consensus Programme Steering Committee; MPS Consensus Programme Co-Chairs.
Recommendations for the management of MPS VI: systematic evidence- and
consensus-based guidance. Orphanet J Rare Dis. 2019 May 29;14(1):118. doi:
10.1186/s13023-019-1080-y. PMID: 31142378; PMCID: PMC6541999.
315: Darras BT, Crawford TO, Finkel RS, Mercuri E, De Vivo DC, Oskoui M, Tizzano
EF, Ryan MM, Muntoni F, Zhao G, Staropoli J, McCampbell A, Petrillo M, Stebbins
C, Fradette S, Farwell W, Sumner CJ. Neurofilament as a potential biomarker for
spinal muscular atrophy. Ann Clin Transl Neurol. 2019 Apr 17;6(5):932-944. doi:
10.1002/acn3.779. PMID: 31139691; PMCID: PMC6530526.
316: Springer A, Dyck Holzinger S, Andersen J, Buckley D, Fehlings D, Kirton A,
Koclas L, Pigeon N, Van Rensburg E, Wood E, Oskoui M, Shevell M. Profile of
children with cerebral palsy spectrum disorder and a normal MRI study.
Neurology. 2019 Jul 2;93(1):e88-e96. doi: 10.1212/WNL.0000000000007726. Epub
2019 May 24. PMID: 31127072.
317: Williams MA, Nagel SJ, Luciano MG, Relkin N, Zwimpfer TJ, Katzen H,
Holubkov R, Moghekar A, Wisoff JH, McKhann GM, Golomb J, Edwards RJ, Hamilton
MG. The clinical spectrum of hydrocephalus in adults: report of the first 517
patients of the Adult Hydrocephalus Clinical Research Network registry. J
Neurosurg. 2019 May 24;132(6):1773-1784. doi: 10.3171/2019.2.JNS183538. PMID:
31125971.
318: Bedognetti D, Ceccarelli M, Galluzzi L, Lu R, Palucka K, Samayoa J,
Spranger S, Warren S, Wong KK, Ziv E, Chowell D, Coussens LM, De Carvalho DD,
DeNardo DG, Galon J, Kaufman HL, Kirchhoff T, Lotze MT, Luke JJ, Minn AJ, Politi
K, Shultz LD, Simon R, Thórsson V, Weidhaas JB, Ascierto ML, Ascierto PA, Barnes
JM, Barsan V, Bommareddy PK, Bot A, Church SE, Ciliberto G, De Maria A, Draganov
D, Ho WS, McGee HM, Monette A, Murphy JF, Nisticò P, Park W, Patel M, Quigley M,
Radvanyi L, Raftopoulos H, Rudqvist NP, Snyder A, Sweis RF, Valpione S,
Zappasodi R, Butterfield LH, Disis ML, Fox BA, Cesano A, Marincola FM; Society
for Immunotherapy of Cancer (SITC) Cancer Immune Responsiveness Task Force and
Working Groups. Toward a comprehensive view of cancer immune responsiveness: a
synopsis from the SITC workshop. J Immunother Cancer. 2019 May 22;7(1):131. doi:
10.1186/s40425-019-0602-4. Erratum in: J Immunother Cancer. 2019 Jul 4;7(1):167.
PMID: 31113486; PMCID: PMC6529999.
319: de Smith AJ, Lavoie G, Walsh KM, Aujla S, Evans E, Hansen HM, Smirnov I,
Kang AY, Zenker M, Ceremsak JJ, Stieglitz E, Muskens IS, Roberts W, McKean-
Cowdin R, Metayer C, Roux PP, Wiemels JL. Predisposing germline mutations in
high hyperdiploid acute lymphoblastic leukemia in children. Genes Chromosomes
Cancer. 2019 Oct;58(10):723-730. doi: 10.1002/gcc.22765. Epub 2019 May 27. PMID:
31102422; PMCID: PMC6684857.
320: Krug B, De Jay N, Harutyunyan AS, Deshmukh S, Marchione DM, Guilhamon P,
Bertrand KC, Mikael LG, McConechy MK, Chen CCL, Khazaei S, Koncar RF, Agnihotri
S, Faury D, Ellezam B, Weil AG, Ursini-Siegel J, De Carvalho DD, Dirks PB, Lewis
PW, Salomoni P, Lupien M, Arrowsmith C, Lasko PF, Garcia BA, Kleinman CL, Jabado
N, Mack SC. Pervasive H3K27 Acetylation Leads to ERV Expression and a
Therapeutic Vulnerability in H3K27M Gliomas. Cancer Cell. 2019 May
13;35(5):782-797.e8. doi: 10.1016/j.ccell.2019.04.004. Erratum in: Cancer Cell.
2019 Sep 16;36(3):338-339. PMID: 31085178; PMCID: PMC6521975.
321: O'Donnell-Luria AH, Pais LS, Faundes V, Wood JC, Sveden A, Luria V, Abou
Jamra R, Accogli A, Amburgey K, Anderlid BM, Azzarello-Burri S, Basinger AA,
Bianchini C, Bird LM, Buchert R, Carre W, Ceulemans S, Charles P, Cox H,
Culliton L, Currò A; Deciphering Developmental Disorders (DDD) Study, Demurger
F, Dowling JJ, Duban-Bedu B, Dubourg C, Eiset SE, Escobar LF, Ferrarini A, Haack
TB, Hashim M, Heide S, Helbig KL, Helbig I, Heredia R, Héron D, Isidor B,
Jonasson AR, Joset P, Keren B, Kok F, Kroes HY, Lavillaureix A, Lu X, Maas SM,
Maegawa GHB, Marcelis CLM, Mark PR, Masruha MR, McLaughlin HM, McWalter K,
Melchinger EU, Mercimek-Andrews S, Nava C, Pendziwiat M, Person R, Ramelli GP,
Ramos LLP, Rauch A, Reavey C, Renieri A, Rieß A, Sanchez-Valle A, Sattar S,
Saunders C, Schwarz N, Smol T, Srour M, Steindl K, Syrbe S, Taylor JC, Telegrafi
A, Thiffault I, Trauner DA, van der Linden H Jr, van Koningsbruggen S, Villard
L, Vogel I, Vogt J, Weber YG, Wentzensen IM, Widjaja E, Zak J, Baxter S, Banka
S, Rodan LH. Heterozygous Variants in KMT2E Cause a Spectrum of
Neurodevelopmental Disorders and Epilepsy. Am J Hum Genet. 2019 Jun
6;104(6):1210-1222. doi: 10.1016/j.ajhg.2019.03.021. Epub 2019 May 9. PMID:
31079897; PMCID: PMC6556837.
322: Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V,
Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides
JMW, Trzaskowski M, Byrne EM, Pers TH, Holmans PA, Richards AL, Abbott L, Agerbo
E, Akil H, Albani D, Alliey-Rodriguez N, Als TD, Anjorin A, Antilla V, Awasthi
S, Badner JA, Bækvad-Hansen M, Barchas JD, Bass N, Bauer M, Belliveau R, Bergen
SE, Pedersen CB, Bøen E, Boks MP, Boocock J, Budde M, Bunney W, Burmeister M,
Bybjerg-Grauholm J, Byerley W, Casas M, Cerrato F, Cervantes P, Chambert K,
Charney AW, Chen D, Churchhouse C, Clarke TK, Coryell W, Craig DW, Cruceanu C,
Curtis D, Czerski PM, Dale AM, de Jong S, Degenhardt F, Del-Favero J, DePaulo
JR, Djurovic S, Dobbyn AL, Dumont A, Elvsåshagen T, Escott-Price V, Fan CC,
Fischer SB, Flickinger M, Foroud TM, Forty L, Frank J, Fraser C, Freimer NB,
Frisén L, Gade K, Gage D, Garnham J, Giambartolomei C, Pedersen MG, Goldstein J,
Gordon SD, Gordon-Smith K, Green EK, Green MJ, Greenwood TA, Grove J, Guan W,
Guzman-Parra J, Hamshere ML, Hautzinger M, Heilbronner U, Herms S, Hipolito M,
Hoffmann P, Holland D, Huckins L, Jamain S, Johnson JS, Juréus A, Kandaswamy R,
Karlsson R, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koller AC,
Kupka R, Lavebratt C, Lawrence J, Lawson WB, Leber M, Lee PH, Levy SE, Li JZ,
Liu C, Lucae S, Maaser A, MacIntyre DJ, Mahon PB, Maier W, Martinsson L,
McCarroll S, McGuffin P, McInnis MG, McKay JD, Medeiros H, Medland SE, Meng F,
Milani L, Montgomery GW, Morris DW, Mühleisen TW, Mullins N, Nguyen H,
Nievergelt CM, Adolfsson AN, Nwulia EA, O'Donovan C, Loohuis LMO, Ori APS, Oruc
L, Ösby U, Perlis RH, Perry A, Pfennig A, Potash JB, Purcell SM, Regeer EJ, Reif
A, Reinbold CS, Rice JP, Rivas F, Rivera M, Roussos P, Ruderfer DM, Ryu E,
Sánchez-Mora C, Schatzberg AF, Scheftner WA, Schork NJ, Shannon Weickert C,
Shehktman T, Shilling PD, Sigurdsson E, Slaney C, Smeland OB, Sobell JL, Søholm
Hansen C, Spijker AT, St Clair D, Steffens M, Strauss JS, Streit F, Strohmaier
J, Szelinger S, Thompson RC, Thorgeirsson TE, Treutlein J, Vedder H, Wang W,
Watson SJ, Weickert TW, Witt SH, Xi S, Xu W, Young AH, Zandi P, Zhang P, Zöllner
S; eQTLGen Consortium; BIOS Consortium, Adolfsson R, Agartz I, Alda M, Backlund
L, Baune BT, Bellivier F, Berrettini WH, Biernacka JM, Blackwood DHR, Boehnke M,
Børglum AD, Corvin A, Craddock N, Daly MJ, Dannlowski U, Esko T, Etain B, Frye
M, Fullerton JM, Gershon ES, Gill M, Goes F, Grigoroiu-Serbanescu M, Hauser J,
Hougaard DM, Hultman CM, Jones I, Jones LA, Kahn RS, Kirov G, Landén M, Leboyer
M, Lewis CM, Li QS, Lissowska J, Martin NG, Mayoral F, McElroy SL, McIntosh AM,
McMahon FJ, Melle I, Metspalu A, Mitchell PB, Morken G, Mors O, Mortensen PB,
Müller-Myhsok B, Myers RM, Neale BM, Nimgaonkar V, Nordentoft M, Nöthen MM,
O'Donovan MC, Oedegaard KJ, Owen MJ, Paciga SA, Pato C, Pato MT, Posthuma D,
Ramos-Quiroga JA, Ribasés M, Rietschel M, Rouleau GA, Schalling M, Schofield PR,
Schulze TG, Serretti A, Smoller JW, Stefansson H, Stefansson K, Stordal E,
Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Werge T, Nurnberger JI,
Wray NR, Di Florio A, Edenberg HJ, Cichon S, Ophoff RA, Scott LJ, Andreassen OA,
Kelsoe J, Sklar P; Bipolar Disorder Working Group of the Psychiatric Genomics
Consortium. Genome-wide association study identifies 30 loci associated with
bipolar disorder. Nat Genet. 2019 May;51(5):793-803. doi:
10.1038/s41588-019-0397-8. Epub 2019 May 1. PMID: 31043756; PMCID: PMC6956732.
323: Vladoiu MC, El-Hamamy I, Donovan LK, Farooq H, Holgado BL, Sundaravadanam
Y, Ramaswamy V, Hendrikse LD, Kumar S, Mack SC, Lee JJY, Fong V, Juraschka K,
Przelicki D, Michealraj A, Skowron P, Luu B, Suzuki H, Morrissy AS, Cavalli FMG,
Garzia L, Daniels C, Wu X, Qazi MA, Singh SK, Chan JA, Marra MA, Malkin D, Dirks
P, Heisler L, Pugh T, Ng K, Notta F, Thompson EM, Kleinman CL, Joyner AL, Jabado
N, Stein L, Taylor MD. Childhood cerebellar tumours mirror conserved fetal
transcriptional programs. Nature. 2019 Aug;572(7767):67-73. doi:
10.1038/s41586-019-1158-7. Epub 2019 May 1. PMID: 31043743; PMCID: PMC6675628.
324: Callaghan DB, Rogic S, Tan PPC, Calli K, Qiao Y, Baldwin R, Jacobson M,
Belmadani M, Holmes N, Yu C, Li Y, Li Y, Kurtzke FE, Kuzeljevic B, Yu AY, Hudson
M, Mcaughton AJM, Xu Y, Dionne-Laporte A, Girard S, Liang P, Separovic ER, Liu
X, Rouleau G, Pavlidis P, Lewis MES. Whole genome sequencing and variant
discovery in the ASPIRE autism spectrum disorder cohort. Clin Genet. 2019
Sep;96(3):199-206. doi: 10.1111/cge.13556. Epub 2019 May 30. PMID: 31038196.
325: Mannix R, Zemek R, Yeates KO, Arbogast K, Atabaki S, Badawy M, Beauchamp
MH, Beer D, Bin S, Burstein B, Craig W, Corwin D, Doan Q, Ellis M, Freedman SB,
Gagnon I, Gravel J, Leddy J, Lumba-Brown A, Master C, Mayer AR, Park G, Penque
M, Rhine T, Russell K, Schneider K, Bell M, Wisniewski S. Practice Patterns in
Pharmacological and Non-Pharmacological Therapies for Children with Mild
Traumatic Brain Injury: A Survey of 15 Canadian and United States Centers. J
Neurotrauma. 2019 Oct 15;36(20):2886-2894. doi: 10.1089/neu.2018.6290. Epub 2019
Jun 17. PMID: 31025612.
326: Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R,
Pihlstrøm L, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Siitonen A, Iwaki H,
Leonard H, Noyce AJ, Tan M, Gibbs JR, Hernandez DG, Scholz SW, Jankovic J,
Shulman LM, Lesage S, Corvol JC, Brice A, van Hilten JJ, Marinus J; 23andMe
Research Team, Eerola-Rautio J, Tienari P, Majamaa K, Toft M, Grosset DG, Gasser
T, Heutink P, Shulman JM, Wood N, Hardy J, Morris HR, Hinds DA, Gratten J,
Visscher PM, Gan-Or Z, Nalls MA, Singleton AB; International Parkinson's Disease
Genomics Consortium (IPDGC). Parkinson's disease age at onset genome-wide
association study: Defining heritability, genetic loci, and α-synuclein
mechanisms. Mov Disord. 2019 Jun;34(6):866-875. doi: 10.1002/mds.27659. Epub
2019 Apr 7. PMID: 30957308; PMCID: PMC6579628.
327: Accogli A, Russell L, Sébire G, Rivière JB, St-Onge J, Addour-Boudrahem N,
Laporte AD, Rouleau GA, Saint-Martin C, Srour M. Pathogenic variants in AIMP1
cause pontocerebellar hypoplasia. Neurogenetics. 2019 May;20(2):103-108. doi:
10.1007/s10048-019-00572-7. Epub 2019 Mar 28. PMID: 30924036.
328: Bong CL, Tan J, Lim S, Low Y, Sim SW, Rajadurai VS, Khoo PC, Allen J,
Meaney M, Koh WP. Randomised controlled trial of dexmedetomidine sedation vs
general anaesthesia for inguinal hernia surgery on perioperative outcomes in
infants. Br J Anaesth. 2019 May;122(5):662-670. doi: 10.1016/j.bja.2018.12.027.
Epub 2019 Mar 7. PMID: 30916007.
329: Choquet K, Forget D, Meloche E, Dicaire MJ, Bernard G, Vanderver A,
Schiffmann R, Fabian MR, Teichmann M, Coulombe B, Brais B, Kleinman CL.
Leukodystrophy-associated POLR3A mutations down-regulate the RNA
polymerase III transcript and important regulatory RNA BC200. J Biol
Chem. 2019 May 3;294(18):7445-7459. doi: 10.1074/jbc.RA118.006271. Epub 2019 Mar
21. PMID: 30898877; PMCID: PMC6509492.
330: Harutyunyan AS, Krug B, Chen H, Papillon-Cavanagh S, Zeinieh M, De Jay N,
Deshmukh S, Chen CCL, Belle J, Mikael LG, Marchione DM, Li R, Nikbakht H, Hu B,
Cagnone G, Cheung WA, Mohammadnia A, Bechet D, Faury D, McConechy MK, Pathania
M, Jain SU, Ellezam B, Weil AG, Montpetit A, Salomoni P, Pastinen T, Lu C, Lewis
PW, Garcia BA, Kleinman CL, Jabado N, Majewski J. H3K27M induces defective
chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for
glioma tumorigenesis. Nat Commun. 2019 Mar 19;10(1):1262. doi:
10.1038/s41467-019-09140-x. PMID: 30890717; PMCID: PMC6425035.
331: Sonjak V, Jacob KJ, Spendiff S, Vuda M, Perez A, Miguez K, Minozzo FC,
Spake C, Morais JA, Hepple RT. Reduced Mitochondrial Content, Elevated Reactive
Oxygen Species, and Modulation by Denervation in Skeletal Muscle of Prefrail or
Frail Elderly Women. J Gerontol A Biol Sci Med Sci. 2019 Nov
13;74(12):1887-1895. doi: 10.1093/gerona/glz066. PMID: 30855073.
332: Sarubbo S, Petit L, De Benedictis A, Chioffi F, Ptito M, Dyrby TB.
Uncovering the inferior fronto-occipital fascicle and its topological
organization in non-human primates: the missing connection for language
evolution. Brain Struct Funct. 2019 May;224(4):1553-1567. doi:
10.1007/s00429-019-01856-2. Epub 2019 Mar 7. PMID: 30847641.
333: Gauthier M, Gauvin M, Lina JM, Lachapelle P. The effects of bandpass
filtering on the oscillatory potentials of the electroretinogram. Doc
Ophthalmol. 2019 Jun;138(3):247-254. doi: 10.1007/s10633-019-09683-w. Epub 2019
Mar 7. PMID: 30847633.
334: Al Yazidi G, Tran LT, Guerrero K, Vanderver A, Schiffmann R, Wolf NI,
Chouinard S, Bernard G. Dystonia in RNA Polymerase III-Related Leukodystrophy.
Mov Disord Clin Pract. 2019 Jan 9;6(2):155-159. doi: 10.1002/mdc3.12715. PMID:
30838315; PMCID: PMC6384176.
335: Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki
L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y,
Rouleau G, Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados
M, Singer HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C,
Tarnok Z, Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ,
McMahon WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee
PC, Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A,
Hoekstra PJ, Kuperman S, Zinner SH, Luðvigsson P, Sæmundsen E, Thorarensen Ó,
Atzmon G, Barzilai N, Wagner M, Moessner R, Ophoff R, Pato CN, Pato MT, Knowles
JA, Roffman JL, Smoller JW, Buckner RL, Willsey AJ, Tischfield JA, Heiman GA,
Stefansson H, Stefansson K, Posthuma D, Cox NJ, Pauls DL, Freimer NB, Neale BM,
Davis LK, Paschou P, Coppola G, Mathews CA, Scharf JM; Tourette Association of
America International Consortium for Genetics, the Gilles de la Tourette GWAS
Replication Initiative, the Tourette International Collaborative Genetics Study,
and the Psychiatric Genomics Consortium Tourette Syndrome Working Group.
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic
Disorders Through Genome-Wide Association Studies. Am J Psychiatry. 2019 Mar
1;176(3):217-227. doi: 10.1176/appi.ajp.2018.18070857. PMID: 30818990; PMCID:
PMC6677250.
336: Fokkens W, Desrosiers M, Harvey R, Hopkins C, Mullol J, Philpott C, Alobid
I, Anselmo-Lima WT, Bachert C, Baroody F, Bernal-Sprekelsen M, von Buchwald C,
Cervin A, Cohen N, Constantinidis J, De Gabory L, Douglas R, Gevaert P, Hafner
A, Hellings P, Joos G, Kalogjera L, Kern R, Knill A, Kocks J, Landis BN, Limpens
J, Lebeer S, Lourenco O, Matricardi PM, Meco C, O Mahony L, Reitsma S, Ryan D,
Schlosser R, Senior B, Smith T, Teeling T, Tomazic PV, Toppila-Salmi S, Wang DY,
Wang D, Zhang L, Lund V. EPOS2020: development strategy and goals for the latest
European Position Paper on Rhinosinusitis. Rhinology. 2019 Jun 1;57(3):162-168.
doi: 10.4193/Rhin19.080. PMID: 30810118.
337: Mexhitaj I, Nyirenda MH, Li R, O'Mahony J, Rezk A, Rozenberg A, Moore CS,
Johnson T, Sadovnick D, Collins DL, Arnold DL, Gran B, Yeh EA, Marrie RA,
Banwell B, Bar-Or A. Abnormal effector and regulatory T cell subsets in
paediatric-onset multiple sclerosis. Brain. 2019 Mar 1;142(3):617-632. doi:
10.1093/brain/awz017. PMID: 30759186; PMCID: PMC6391601.
338: Friedman J, Smith DE, Issa MY, Stanley V, Wang R, Mendes MI, Wright MS,
Wigby K, Hildreth A, Crawford JR, Koehler AE, Chowdhury S, Nahas S, Zhai L, Xu
Z, Lo WS, James KN, Musaev D, Accogli A, Guerrero K, Tran LT, Omar TEI, Ben-
Omran T, Dimmock D, Kingsmore SF, Salomons GS, Zaki MS, Bernard G, Gleeson JG.
Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a
progressive neurodevelopmental epileptic encephalopathy. Nat Commun. 2019 Feb
12;10(1):707. doi: 10.1038/s41467-018-07067-3. PMID: 30755602; PMCID:
PMC6372641.
339: Illes J, Weiss S, Bains J, Chandler JA, Conrod P, De Koninck Y, Fellows LK,
Groetzinger D, Racine E, Robillard JM, Sokolowski MB. A Neuroethics Backbone for
the Evolving Canadian Brain Research Strategy. Neuron. 2019 Feb
6;101(3):370-374. doi: 10.1016/j.neuron.2018.12.021. PMID: 30731060.
340: Théry C, Witwer KW, Aikawa E, Alcaraz MJ, Anderson JD, Andriantsitohaina R,
Antoniou A, Arab T, Archer F, Atkin-Smith GK, Ayre DC, Bach JM, Bachurski D,
Baharvand H, Balaj L, Baldacchino S, Bauer NN, Baxter AA, Bebawy M, Beckham C,
Bedina Zavec A, Benmoussa A, Berardi AC, Bergese P, Bielska E, Blenkiron C,
Bobis-Wozowicz S, Boilard E, Boireau W, Bongiovanni A, Borràs FE, Bosch S,
Boulanger CM, Breakefield X, Breglio AM, Brennan MÁ, Brigstock DR, Brisson A,
Broekman ML, Bromberg JF, Bryl-Górecka P, Buch S, Buck AH, Burger D, Busatto S,
Buschmann D, Bussolati B, Buzás EI, Byrd JB, Camussi G, Carter DR, Caruso S,
Chamley LW, Chang YT, Chen C, Chen S, Cheng L, Chin AR, Clayton A, Clerici SP,
Cocks A, Cocucci E, Coffey RJ, Cordeiro-da-Silva A, Couch Y, Coumans FA, Coyle
B, Crescitelli R, Criado MF, D'Souza-Schorey C, Das S, Datta Chaudhuri A, de
Candia P, De Santana EF, De Wever O, Del Portillo HA, Demaret T, Deville S,
Devitt A, Dhondt B, Di Vizio D, Dieterich LC, Dolo V, Dominguez Rubio AP,
Dominici M, Dourado MR, Driedonks TA, Duarte FV, Duncan HM, Eichenberger RM,
Ekström K, El Andaloussi S, Elie-Caille C, Erdbrügger U, Falcón-Pérez JM, Fatima
F, Fish JE, Flores-Bellver M, Försönits A, Frelet-Barrand A, Fricke F, Fuhrmann
G, Gabrielsson S, Gámez-Valero A, Gardiner C, Gärtner K, Gaudin R, Gho YS,
Giebel B, Gilbert C, Gimona M, Giusti I, Goberdhan DC, Görgens A, Gorski SM,
Greening DW, Gross JC, Gualerzi A, Gupta GN, Gustafson D, Handberg A, Haraszti
RA, Harrison P, Hegyesi H, Hendrix A, Hill AF, Hochberg FH, Hoffmann KF, Holder
B, Holthofer H, Hosseinkhani B, Hu G, Huang Y, Huber V, Hunt S, Ibrahim AG,
Ikezu T, Inal JM, Isin M, Ivanova A, Jackson HK, Jacobsen S, Jay SM,
Jayachandran M, Jenster G, Jiang L, Johnson SM, Jones JC, Jong A, Jovanovic-
Talisman T, Jung S, Kalluri R, Kano SI, Kaur S, Kawamura Y, Keller ET, Khamari
D, Khomyakova E, Khvorova A, Kierulf P, Kim KP, Kislinger T, Klingeborn M,
Klinke DJ 2nd, Kornek M, Kosanović MM, Kovács ÁF, Krämer-Albers EM, Krasemann S,
Krause M, Kurochkin IV, Kusuma GD, Kuypers S, Laitinen S, Langevin SM, Languino
LR, Lannigan J, Lässer C, Laurent LC, Lavieu G, Lázaro-Ibáñez E, Le Lay S, Lee
MS, Lee YXF, Lemos DS, Lenassi M, Leszczynska A, Li IT, Liao K, Libregts SF,
Ligeti E, Lim R, Lim SK, Linē A, Linnemannstöns K, Llorente A, Lombard CA,
Lorenowicz MJ, Lörincz ÁM, Lötvall J, Lovett J, Lowry MC, Loyer X, Lu Q,
Lukomska B, Lunavat TR, Maas SL, Malhi H, Marcilla A, Mariani J, Mariscal J,
Martens-Uzunova ES, Martin-Jaular L, Martinez MC, Martins VR, Mathieu M,
Mathivanan S, Maugeri M, McGinnis LK, McVey MJ, Meckes DG Jr, Meehan KL, Mertens
I, Minciacchi VR, Möller A, Møller Jørgensen M, Morales-Kastresana A, Morhayim
J, Mullier F, Muraca M, Musante L, Mussack V, Muth DC, Myburgh KH, Najrana T,
Nawaz M, Nazarenko I, Nejsum P, Neri C, Neri T, Nieuwland R, Nimrichter L, Nolan
JP, Nolte-'t Hoen EN, Noren Hooten N, O'Driscoll L, O'Grady T, O'Loghlen A,
Ochiya T, Olivier M, Ortiz A, Ortiz LA, Osteikoetxea X, Østergaard O, Ostrowski
M, Park J, Pegtel DM, Peinado H, Perut F, Pfaffl MW, Phinney DG, Pieters BC,
Pink RC, Pisetsky DS, Pogge von Strandmann E, Polakovicova I, Poon IK, Powell
BH, Prada I, Pulliam L, Quesenberry P, Radeghieri A, Raffai RL, Raimondo S, Rak
J, Ramirez MI, Raposo G, Rayyan MS, Regev-Rudzki N, Ricklefs FL, Robbins PD,
Roberts DD, Rodrigues SC, Rohde E, Rome S, Rouschop KM, Rughetti A, Russell AE,
Saá P, Sahoo S, Salas-Huenuleo E, Sánchez C, Saugstad JA, Saul MJ, Schiffelers
RM, Schneider R, Schøyen TH, Scott A, Shahaj E, Sharma S, Shatnyeva O, Shekari
F, Shelke GV, Shetty AK, Shiba K, Siljander PR, Silva AM, Skowronek A, Snyder OL
2nd, Soares RP, Sódar BW, Soekmadji C, Sotillo J, Stahl PD, Stoorvogel W, Stott
SL, Strasser EF, Swift S, Tahara H, Tewari M, Timms K, Tiwari S, Tixeira R,
Tkach M, Toh WS, Tomasini R, Torrecilhas AC, Tosar JP, Toxavidis V, Urbanelli L,
Vader P, van Balkom BW, van der Grein SG, Van Deun J, van Herwijnen MJ, Van
Keuren-Jensen K, van Niel G, van Royen ME, van Wijnen AJ, Vasconcelos MH,
Vechetti IJ Jr, Veit TD, Vella LJ, Velot É, Verweij FJ, Vestad B, Viñas JL,
Visnovitz T, Vukman KV, Wahlgren J, Watson DC, Wauben MH, Weaver A, Webber JP,
Weber V, Wehman AM, Weiss DJ, Welsh JA, Wendt S, Wheelock AM, Wiener Z, Witte L,
Wolfram J, Xagorari A, Xander P, Xu J, Yan X, Yáñez-Mó M, Yin H, Yuana Y,
Zappulli V, Zarubova J, Žėkas V, Zhang JY, Zhao Z, Zheng L, Zheutlin AR, Zickler
AM, Zimmermann P, Zivkovic AM, Zocco D, Zuba-Surma EK. Minimal information for
studies of extracellular vesicles 2018 (MISEV2018): a position statement of the
International Society for Extracellular Vesicles and update of the MISEV2014
guidelines. J Extracell Vesicles. 2018 Nov 23;7(1):1535750. doi:
10.1080/20013078.2018.1535750. PMID: 30637094; PMCID: PMC6322352.
341: Yeates KO, Tang K, Barrowman N, Freedman SB, Gravel J, Gagnon I, Sangha G,
Boutis K, Beer D, Craig W, Burns E, Farion KJ, Mikrogianakis A, Barlow K,
Dubrovsky AS, Meeuwisse W, Gioia G, Meehan WP 3rd, Beauchamp MH, Kamil Y, Grool
AM, Hoshizaki B, Anderson P, Brooks BL, Vassilyadi M, Klassen T, Keightley M,
Richer L, DeMatteo C, Osmond MH, Zemek R; Pediatric Emergency Research Canada
(PERC) Predicting Persistent Postconcussive Problems in Pediatrics (5P)
Concussion Team. Derivation and Initial Validation of Clinical Phenotypes of
Children Presenting with Concussion Acutely in the Emergency Department: Latent
Class Analysis of a Multi-Center, Prospective Cohort, Observational Study. J
Neurotrauma. 2019 Jun;36(11):1758-1767. doi: 10.1089/neu.2018.6009. Epub 2019
Mar 6. PMID: 30618356.
342: Horwood L, Li P, Mok E, Oskoui M, Shevell M, Constantin E. Health-related
quality of life in Canadian children with cerebral palsy: what role does sleep
play? Sleep Med. 2019 Feb;54:213-222. doi: 10.1016/j.sleep.2018.10.022. Epub
2018 Nov 5. PMID: 30583275.
343: Shevell M. Cerebral palsy to cerebral palsy spectrum disorder: Time for a
name change? Neurology. 2018 Dec 19:10.1212/WNL.0000000000006747. doi:
10.1212/WNL.0000000000006747. Epub ahead of print. PMID: 30568002.
344: Luo RT, Wang PJ, Deng XF, Zhou SJ, Zhao M, Qian J, Zhang D, Wang R, Zhang
Y. An Integrated Analysis of Risk Factors of Cognitive Impairment in Patients
with Severe Carotid Artery Stenosis. Biomed Environ Sci. 2018
Nov;31(11):797-804. doi: 10.3967/bes2018.107. PMID: 30558700.
345: Klieverik VM, Miller KJ, Han KS, Singhal A, Vassilyadi M, Touchette CJ,
Weil AG, Woerdeman PA. Cranioplasties following craniectomies in children-a
multicenter, retrospective cohort study. Childs Nerv Syst. 2019
Sep;35(9):1473-1480. doi: 10.1007/s00381-018-4024-2. Epub 2018 Dec 15. PMID:
30554262.
346: Iv M, Zhou M, Shpanskaya K, Perreault S, Wang Z, Tranvinh E, Lanzman B,
Vajapeyam S, Vitanza NA, Fisher PG, Cho YJ, Laughlin S, Ramaswamy V, Taylor MD,
Cheshier SH, Grant GA, Young Poussaint T, Gevaert O, Yeom KW. MR Imaging-Based
Radiomic Signatures of Distinct Molecular Subgroups of Medulloblastoma. AJNR Am
J Neuroradiol. 2019 Jan;40(1):154-161. doi: 10.3174/ajnr.A5899. Epub 2018 Dec 6.
PMID: 30523141; PMCID: PMC6330121.
347: Myers KA, Dudley RW, Srour M. Hemiconvulsion-Hemiplegia-Epilepsy in a girl
with cobalamin C deficiency. Epileptic Disord. 2018 Dec 1;20(6):545-550. doi:
10.1684/epd.2018.1017. PMID: 30530444; PMCID: PMC7163536.
348: Easson K, Dahan-Oliel N, Rohlicek C, Sahakian S, Brossard-Racine M, Mazer
B, Riley P, Maltais DB, Nadeau L, Hatzigeorgiou S, Schmitz N, Majnemer A. A
Comparison of Developmental Outcomes of Adolescent Neonatal Intensive Care Unit
Survivors Born with a Congenital Heart Defect or Born Preterm. J Pediatr. 2019
Apr;207:34-41.e2. doi: 10.1016/j.jpeds.2018.11.002. Epub 2018 Dec 6. PMID:
30528759.
349: Holmes SA, Singh-Saluja R, Chen JK, Gagnon I, Ptito A. Evaluating task-
based brain network activity in pediatric subjects with an mTBI: mechanisms of
functional compensation are symptom-level dependent. Brain Inj.
2019;33(3):383-393. doi: 10.1080/02699052.2018.1552023. Epub 2018 Dec 3. PMID:
30507312.
350: Coulombe MA, Elkaim LM, Alotaibi NM, Gorman DA, Weil AG, Fallah A, Kalia
SK, Lipsman N, Lozano AM, Ibrahim GM. Deep brain stimulation for Gilles de la
Tourette syndrome in children and youth: a meta-analysis with individual
participant data. J Neurosurg Pediatr. 2018 Oct 26;23(2):236-246. doi:
10.3171/2018.7.PEDS18300. PMID: 30497215.
351: Mansouri A, Taslimi S, Abbasian A, Badhiwala JH, Akbar MA, Alotaibi NM,
Almenawer SA, Weil AG, Fallah A, Carmant L, Ibrahim GM. Surgical outcomes for
medically intractable epilepsy in low- and middle-income countries: a systematic
review and meta-analysis. J Neurosurg. 2018 Nov 1:1-11. doi:
10.3171/2018.5.JNS18599. Epub ahead of print. PMID: 30497170.
352: Accogli A, Guerrero K, D'Agostino MD, Tran L, Cieuta-Walti C, Thiffault I,
Chénier S, Schwartzentruber J, Majewski J; Care4Rare Canada Consortium, Bernard
G. Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative
Disease. J Child Neurol. 2019 Feb;34(2):74-80. doi: 10.1177/0883073818811223.
Epub 2018 Nov 28. PMID: 30486714.
353: Shevell M. What We Need to Know? Pediatr Neurol. 2019 Jan;90:3-7. doi:
10.1016/j.pediatrneurol.2018.07.017. Epub 2018 Aug 6. PMID: 30477742.
354: Wells E, Hacohen Y, Waldman A, Tillema JM, Soldatos A, Ances B, Benseler S,
Bielekova B, Dale RC, Dalmau J, Gaillard W, Gorman M, Greenberg B, Hyslop A,
Pardo CA, Tasker RC, Yeh EA, Bar-Or A, Pittock S, Vanderver A, Banwell B;
attendees of the International Neuroimmune Meeting. Author Correction:
Neuroimmune disorders of the central nervous system in children in the molecular
era. Nat Rev Neurol. 2018 Dec;14(12):749. doi: 10.1038/s41582-018-0077-9.
Erratum for: Nat Rev Neurol. 2018 Jul;14(7):433-445. PMID: 30442924.
355: Lambrinakos-Raymond K, Dubrovsky AS. Nerve blocks in paediatric and
adolescent headache disorders. Curr Opin Pediatr. 2018 Dec;30(6):780-785. doi:
10.1097/MOP.0000000000000687. PMID: 30407973.
356: Cronin SJF, Seehus C, Weidinger A, Talbot S, Reissig S, Seifert M, Pierson
Y, McNeill E, Longhi MS, Turnes BL, Kreslavsky T, Kogler M, Hoffmann D, Ticevic
M, da Luz Scheffer D, Tortola L, Cikes D, Jais A, Rangachari M, Rao S, Paolino
M, Novatchkova M, Aichinger M, Barrett L, Latremoliere A, Wirnsberger G,
Lametschwandtner G, Busslinger M, Zicha S, Latini A, Robson SC, Waisman A,
Andrews N, Costigan M, Channon KM, Weiss G, Kozlov AV, Tebbe M, Johnsson K,
Woolf CJ, Penninger JM. The metabolite BH4 controls T cell proliferation in
autoimmunity and cancer. Nature. 2018 Nov;563(7732):564-568. doi:
10.1038/s41586-018-0701-2. Epub 2018 Nov 7. Erratum in: Nature. 2019
Aug;572(7769):E18. PMID: 30405245; PMCID: PMC6438708.
357: Garcia ADR, Han YG, Triplett JW, Farmer WT, Harwell CC, Ihrie RA. The
Elegance of Sonic Hedgehog: Emerging Novel Functions for a Classic Morphogen. J
Neurosci. 2018 Oct 31;38(44):9338-9345. doi: 10.1523/JNEUROSCI.1662-18.2018.
PMID: 30381425; PMCID: PMC6209836.
358: Myers KA, Davey MJ, Ching M, Ellis C, Grinton BE, Roten A, Lightfoot PA,
Scheffer IE. Randomized Controlled Trial of Melatonin for Sleep Disturbance in
Dravet Syndrome: The DREAMS Study. J Clin Sleep Med. 2018 Oct
15;14(10):1697-1704. doi: 10.5664/jcsm.7376. PMID: 30353809; PMCID: PMC6175806.
359: Pinchefsky EF, Accogli A, Shevell MI, Saint-Martin C, Srour M.
Developmental outcomes in children with congenital cerebellar malformations. Dev
Med Child Neurol. 2019 Mar;61(3):350-358. doi: 10.1111/dmcn.14059. Epub 2018 Oct
15. PMID: 30320441.
360: Shevell M. The Role of the Pediatric Neurologist in the Care of Children
With Neurodevelopmental Disabilities. Pediatr Neurol. 2018 Nov;88:3-9. doi:
10.1016/j.pediatrneurol.2018.08.004. Epub 2018 Aug 10. PMID: 30318285.
361: Gardiner E, Miller AR, Lach LM. Family impact of childhood
neurodevelopmental disability: considering adaptive and maladaptive behaviour. J
Intellect Disabil Res. 2018 Oct;62(10):888-899. doi: 10.1111/jir.12547. PMID:
30230656.
362: Auvin S, Wirrell E, Donald KA, Berl M, Hartmann H, Valente KD, Van Bogaert
P, Cross JH, Osawa M, Kanemura H, Aihara M, Guerreiro MM, Samia P, Vinayan KP,
Smith ML, Carmant L, Kerr M, Hermann B, Dunn D, Wilmshurst JM. Systematic review
of the screening, diagnosis, and management of ADHD in children with epilepsy.
Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric
Commission. Epilepsia. 2018 Oct;59(10):1867-1880. doi: 10.1111/epi.14549. Epub
2018 Sep 3. PMID: 30178479.
363: Larouche V, Atkinson J, Albrecht S, Laframboise R, Jabado N, Tabori U,
Bouffet E; international bMMRD consortium. Sustained complete response of
recurrent glioblastoma to combined checkpoint inhibition in a young patient with
constitutional mismatch repair deficiency. Pediatr Blood Cancer. 2018
Dec;65(12):e27389. doi: 10.1002/pbc.27389. Epub 2018 Aug 29. PMID: 30160041.
364: Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS,
Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht
JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha
L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK.
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical
Folding and Oral Motor Development. Neuron. 2018 Sep 5;99(5):905-913.e7. doi:
10.1016/j.neuron.2018.07.052. Epub 2018 Aug 23. PMID: 30146301; PMCID:
PMC6226006.
365: Valera ET, McConechy MK, Gayden T, Rivera B, Jones DTW, Wittmann A, Han H,
Bareke E, Nikbakht H, Mikael L, Queiroz RG, Suazo VK, Phi JH, Kim SK, Park SH,
Fukaya R, Yum MS, Ko TS, de Oliveira RS, Machado HR, Brassesco MS, do Santos AC,
Simão GN, Ramalho LNZ, Neder L, Scrideli CA, Tone LG, Majewski J, Jabado N.
Methylome analysis and whole-exome sequencing reveal that brain tumors
associated with encephalocraniocutaneous lipomatosis are midline pilocytic
astrocytomas. Acta Neuropathol. 2018 Oct;136(4):657-660. doi:
10.1007/s00401-018-1898-8. Epub 2018 Aug 24. PMID: 30143858; PMCID: PMC6132939.
366: Jacobs J, Wu JY, Perucca P, Zelmann R, Mader M, Dubeau F, Mathern GW,
Schulze-Bonhage A, Gotman J. Removing high-frequency oscillations: A prospective
multicenter study on seizure outcome. Neurology. 2018 Sep 11;91(11):e1040-e1052.
doi: 10.1212/WNL.0000000000006158. Epub 2018 Aug 17. PMID: 30120133; PMCID:
PMC6140372.
367: Ibrahim GM, Weil AG, Sedighim S, Schoen NB, Mikhail M, Sharma P, Guillen
MR, Morgan BR, Wong S, Cajigas I, Jermakowicz WJ, Sandoval-Garcia C, Lewis EC,
Fallah A, Altman N, Medina S, Pacheco-Jacome E, Jayakar P, Hyslop A, Miller I,
Ragheb J, Bhatia S, Bernal B. Presurgical hyperconnectivity of the ablation
volume is associated with seizure-freedom after magnetic resonance-guided laser
interstitial thermal therapy. Seizure. 2018 Oct;61:89-93. doi:
10.1016/j.seizure.2018.08.006. Epub 2018 Aug 9. PMID: 30118930.
368: Tejada Neyra MA, Neuberger U, Reinhardt A, Brugnara G, Bonekamp D, Sill M,
Wick A, Jones DTW, Radbruch A, Unterberg A, Debus J, Heiland S, Schlemmer HP,
Herold-Mende C, Pfister S, von Deimling A, Wick W, Capper D, Bendszus M,
Kickingereder P. Voxel-wise radiogenomic mapping of tumor location with key
molecular alterations in patients with glioma. Neuro Oncol. 2018 Oct
9;20(11):1517-1524. doi: 10.1093/neuonc/noy134. PMID: 30107597; PMCID:
PMC6176804.
369: Kondyli M, Larouche V, Saint-Martin C, Ellezam B, Pouliot L, Sinnett D,
Legault G, Crevier L, Weil A, Farmer JP, Jabado N, Perreault S. Trametinib for
progressive pediatric low-grade gliomas. J Neurooncol. 2018 Nov;140(2):435-444.
doi: 10.1007/s11060-018-2971-9. Epub 2018 Aug 10. PMID: 30097824.
370: Lord C, Elsabbagh M, Baird G, Veenstra-Vanderweele J. Autism spectrum
disorder. Lancet. 2018 Aug 11;392(10146):508-520. doi:
10.1016/S0140-6736(18)31129-2. Epub 2018 Aug 2. PMID: 30078460; PMCID:
PMC7398158.
371: Gagnon I, Friedman D, Beauchamp MH, Christie B, DeMatteo C, Macartney G,
McFadyen BJ, Sirois K, Taneja C, Zabjek K, Zemek R, Mrazik M. The Canadian
Pediatric Mild Traumatic Brain Injury Common Data Elements Project: Harmonizing
Outcomes to Increase Understanding of Pediatric Concussion. J Neurotrauma. 2018
Aug 15;35(16):1849-1857. doi: 10.1089/neu.2018.5887. PMID: 30074870.
372: Campbell C, Selby K, McMillan H, Vajsar J, Korngut L, Brais B, MacKenzie A,
Oskoui M. Response to the Canadian Agency for Drugs and Technologies in Health
and Institut national d'excellence en santé et en services sociaux decision
regarding nusinersen for Spinal Muscular Atrophy. Can J Neurol Sci. 2018
Sep;45(5):516-517. doi: 10.1017/cjn.2018.59. Epub 2018 Jul 24. PMID: 30039778.
373: Dewan MC, Baticulon RE, Ravindran K, Bonfield CM, Poenaru D, Harkness W.
Pediatric neurosurgical bellwether procedures for infrastructure capacity
building in hospitals and healthcare systems worldwide. Childs Nerv Syst. 2018
Oct;34(10):1837-1846. doi: 10.1007/s00381-018-3902-y. Epub 2018 Jul 21. PMID:
30030605.
374: Trebaul L, Deman P, Tuyisenge V, Jedynak M, Hugues E, Rudrauf D,
Bhattacharjee M, Tadel F, Chanteloup-Foret B, Saubat C, Reyes Mejia GC, Adam C,
Nica A, Pail M, Dubeau F, Rheims S, Trébuchon A, Wang H, Liu S, Blauwblomme T,
Garcés M, De Palma L, Valentin A, Metsähonkala EL, Petrescu AM, Landré E,
Szurhaj W, Hirsch E, Valton L, Rocamora R, Schulze-Bonhage A, Mindruta I,
Francione S, Maillard L, Taussig D, Kahane P, David O. Probabilistic functional
tractography of the human cortex revisited. Neuroimage. 2018 Nov 1;181:414-429.
doi: 10.1016/j.neuroimage.2018.07.039. Epub 2018 Jul 17. PMID: 30025851; PMCID:
PMC6150949.
375: Osmond MH, Klassen TP, Wells GA, Davidson J, Correll R, Boutis K, Joubert
G, Gouin S, Khangura S, Turner T, Belanger F, Silver N, Taylor B, Curran J,
Stiell IG; Pediatric Emergency Research Canada (PERC) Head Injury Study Group.
Validation and refinement of a clinical decision rule for the use of computed
tomography in children with minor head injury in the emergency department. CMAJ.
2018 Jul 9;190(27):E816-E822. doi: 10.1503/cmaj.170406. PMID: 29986857; PMCID:
PMC6041249.
376: Yan H, Abel TJ, Alotaibi NM, Anderson M, Niazi TN, Weil AG, Fallah A,
Phillips JH, Forrest CR, Kulkarni AV, Drake JM, Ibrahim GM. A systematic review
and meta-analysis of endoscopic versus open treatment of craniosynostosis. Part
1: the sagittal suture. J Neurosurg Pediatr. 2018 Oct;22(4):352-360. doi:
10.3171/2018.4.PEDS17729. Epub 2018 Jul 6. PMID: 29979135.
377: Yan H, Abel TJ, Alotaibi NM, Anderson M, Niazi TN, Weil AG, Fallah A,
Phillips JH, Forrest CR, Kulkarni AV, Drake JM, Ibrahim GM. A systematic review
of endoscopic versus open treatment of craniosynostosis. Part 2: the nonsagittal
single sutures. J Neurosurg Pediatr. 2018 Oct;22(4):361-368. doi:
10.3171/2018.4.PEDS17730. Epub 2018 Jul 6. PMID: 29979132.
378: Horwood L, Mok E, Li P, Oskoui M, Shevell M, Constantin E. Prevalence of
sleep problems and sleep-related characteristics in preschool- and school-aged
children with cerebral palsy. Sleep Med. 2018 Oct;50:1-6. doi:
10.1016/j.sleep.2018.05.008. Epub 2018 May 24. PMID: 29966807.
379: Bell S, Maussion G, Jefri M, Peng H, Theroux JF, Silveira H, Soubannier V,
Wu H, Hu P, Galat E, Torres-Platas SG, Boudreau-Pinsonneault C, O'Leary LA,
Galat V, Turecki G, Durcan TM, Fon EA, Mechawar N, Ernst C. Disruption of GRIN2B
Impairs Differentiation in Human Neurons. Stem Cell Reports. 2018 Jul
10;11(1):183-196. doi: 10.1016/j.stemcr.2018.05.018. Epub 2018 Jun 21. PMID:
29937144; PMCID: PMC6067152.
380: Grassia F, Poliakov AV, Poliachik SL, Casimo K, Friedman SD, Shurtleff H,
Giussani C, Novotny EJ, Ojemann JG, Hauptman JS. Changes in resting-state
connectivity in pediatric temporal lobe epilepsy. J Neurosurg Pediatr. 2018
Sep;22(3):270-275. doi: 10.3171/2018.3.PEDS17701. Epub 2018 Jun 22. PMID:
29932365.
381: Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters
RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R,
Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B,
Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A,
Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI,
Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA,
Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye
JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin
AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ,
Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel
H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK,
Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A,
Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind
DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT,
Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N,
Kurth T, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams
HHH, Lehtimäki T, Wedenoja J, Buring JE, Schürks M, Hrafnsdottir M, Hottenga JJ,
Penninx B, Artto V, Kaunisto M, Vepsäläinen S, Martin NG, Montgomery GW, Kurki
MI, Hämäläinen E, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B,
Schreiber S, Salomaa V, Loehrer E, Göbel H, Macaya A, Pozo-Rosich P, Hansen T,
Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den
Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt
DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono RJ, Catarino CB, Cossette
P, De Jonghe P, Depondt C, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-
Khoda J, Kälviäinen R, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D,
McCormack M, Møller RS, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R,
Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya
SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD,
Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gasser T, Gibbs
R, Heutink P, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan
S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B,
Rothwell P, Sharma P, Sudlow C, Vicente A, Markus H, Kourkoulis C, Pera J,
Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner
N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI,
Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK,
Trace SE, Davis OSP, Helder SG, Ehrlich S, Herpertz-Dahlmann B, Danner UN, van
Elburg AA, Clementi M, Forzan M, Docampo E, Lissowska J, Hauser J, Tortorella A,
Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S,
Herms S, Julià A, Rabionet R, Dick DM, Ripatti S, Andreassen OA, Espeseth T,
Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson
L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz
JP, Cormand B, Ramos-Quiroga JA, Sánchez-Mora C, Ribasés M, Casas M, Hervas A,
Arranz MJ, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger
A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A,
Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley
K, Rietschel M, Witt SH, Dalsgaard S, Børglum AD, Waldman I, Wilmot B, Molly N,
Bau CHD, Crosbie J, Schachar R, Loo SK, McGough JJ, Grevet EH, Medland SE,
Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Betancur C,
Bolton P, Cantor R, Celestino-Soper P, Dawson G, De Rubeis S, Duque F, Green A,
Klauck SM, Leboyer M, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan
R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo
S, Delorme R, Rogé B, Magalhaes T, Arking D, Schulze TG, Thompson RC, Strohmaier
J, Matthews K, Melle I, Morris D, Blackwood D, McIntosh A, Bergen SE, Schalling
M, Jamain S, Maaser A, Fischer SB, Reinbold CS, Fullerton JM, Guzman-Parra J,
Mayoral F, Schofield PR, Cichon S, Mühleisen TW, Degenhardt F, Schumacher J,
Bauer M, Mitchell PB, Gershon ES, Rice J, Potash JB, Zandi PP, Craddock N,
Ferrier IN, Alda M, Rouleau GA, Turecki G, Ophoff R, Pato C, Anjorin A, Stahl E,
Leber M, Czerski PM, Cruceanu C, Jones IR, Posthuma D, Andlauer TFM, Forstner
AJ, Streit F, Baune BT, Air T, Sinnamon G, Wray NR, MacIntyre DJ, Porteous D,
Homuth G, Rivera M, Grove J, Middeldorp CM, Hickie I, Pergadia M, Mehta D, Smit
JH, Jansen R, de Geus E, Dunn E, Li QS, Nauck M, Schoevers RA, Beekman AT,
Knowles JA, Viktorin A, Arnold P, Barr CL, Bedoya-Berrio G, Bienvenu OJ,
Brentani H, Burton C, Camarena B, Cappi C, Cath D, Cavallini M, Cusi D, Darrow
S, Denys D, Derks EM, Dietrich A, Fernandez T, Figee M, Freimer N, Gerber G,
Grados M, Greenberg E, Hanna GL, Hartmann A, Hirschtritt ME, Hoekstra PJ, Huang
A, Huyser C, Illmann C, Jenike M, Kuperman S, Leventhal B, Lochner C, Lyon GJ,
Macciardi F, Madruga-Garrido M, Malaty IA, Maras A, McGrath L, Miguel EC, Mir P,
Nestadt G, Nicolini H, Okun MS, Pakstis A, Paschou P, Piacentini J, Pittenger C,
Plessen K, Ramensky V, Ramos EM, Reus V, Richter MA, Riddle MA, Robertson MM,
Roessner V, Rosário M, Samuels JF, Sandor P, Stein DJ, Tsetsos F, Van
Nieuwerburgh F, Weatherall S, Wendland JR, Wolanczyk T, Worbe Y, Zai G, Goes FS,
McLaughlin N, Nestadt PS, Grabe HJ, Depienne C, Konkashbaev A, Lanzagorta N,
Valencia-Duarte A, Bramon E, Buccola N, Cahn W, Cairns M, Chong SA, Cohen D,
Crespo-Facorro B, Crowley J, Davidson M, DeLisi L, Dinan T, Donohoe G, Drapeau
E, Duan J, Haan L, Hougaard D, Karachanak-Yankova S, Khrunin A, Klovins J,
Kučinskas V, Lee Chee Keong J, Limborska S, Loughland C, Lönnqvist J, Maher B,
Mattheisen M, McDonald C, Murphy KC, Nenadic I, van Os J, Pantelis C, Pato M,
Petryshen T, Quested D, Roussos P, Sanders AR, Schall U, Schwab SG, Sim K, So
HC, Stögmann E, Subramaniam M, Toncheva D, Waddington J, Walters J, Weiser M,
Cheng W, Cloninger R, Curtis D, Gejman PV, Henskens F, Mattingsdal M, Oh SY,
Scott R, Webb B, Breen G, Churchhouse C, Bulik CM, Daly M, Dichgans M, Faraone
SV, Guerreiro R, Holmans P, Kendler KS, Koeleman B, Mathews CA, Price A, Scharf
J, Sklar P, Williams J, Wood NW, Cotsapas C, Palotie A, Smoller JW, Sullivan P,
Rosand J, Corvin A, Neale BM, Schott JM, Anney R, Elia J, Grigoroiu-Serbanescu
M, Edenberg HJ, Murray R. Analysis of shared heritability in common disorders of
the brain. Science. 2018 Jun 22;360(6395):eaap8757. doi:
10.1126/science.aap8757. PMID: 29930110; PMCID: PMC6097237.
382: Wells E, Hacohen Y, Waldman A, Tillema JM, Soldatos A, Ances B, Benseler S,
Bielekova B, Dale RC, Dalmau J, Gaillard W, Gorman M, Greenberg B, Hyslop A,
Pardo CA, Tasker RC, Yeh EA, Bar-Or A, Pittock S, Vanderver A, Banwell B;
attendees of the International Neuroimmune Meeting. Neuroimmune disorders of the
central nervous system in children in the molecular era. Nat Rev Neurol. 2018
Jul;14(7):433-445. doi: 10.1038/s41582-018-0024-9. Erratum in: Nat Rev Neurol.
2018 Dec;14(12):749. PMID: 29925924.
383: Weil AG, Muir K, Hukin J, Desautels A, Martel V, Perreault S. Narcolepsy
and Hypothalamic Region Tumors: Presentation and Evolution. Pediatr Neurol. 2018
Jul;84:27-31. doi: 10.1016/j.pediatrneurol.2017.12.016. Epub 2018 Feb 14. PMID:
29909138.
384: Reinbold CS, Forstner AJ, Hecker J, Fullerton JM, Hoffmann P, Hou L,
Heilbronner U, Degenhardt F, Adli M, Akiyama K, Akula N, Ardau R, Arias B,
Backlund L, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A,
Marie-Claire C, Cervantes P, Chen GB, Chen HC, Chillotti C, Clark SR, Colom F,
Cousins DA, Cruceanu C, Czerski PM, Dayer A, Étain B, Falkai P, Frisén L, Gard
S, Garnham JS, Goes FS, Grof P, Gruber O, Hashimoto R, Hauser J, Herms S, Jamain
S, Jiménez E, Kahn JP, Kassem L, Kittel-Schneider S, Kliwicki S, König B, Kusumi
I, Lackner N, Laje G, Landén M, Lavebratt C, Leboyer M, Leckband SG, López
Jaramillo CA, MacQueen G, Manchia M, Martinsson L, Mattheisen M, McCarthy MJ,
McElroy SL, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, Ösby U, Ozaki
N, Perlis RH, Pfennig A, Reich-Erkelenz D, Rouleau GA, Schofield PR, Schubert
KO, Schweizer BW, Seemüller F, Severino G, Shekhtman T, Shilling PD, Shimoda K,
Simhandl C, Slaney CM, Smoller JW, Squassina A, Stamm TJ, Stopkova P, Tighe SK,
Tortorella A, Turecki G, Volkert J, Witt SH, Wright AJ, Young LT, Zandi PP,
Potash JB, DePaulo JR, Bauer M, Reininghaus E, Novák T, Aubry JM, Maj M, Baune
BT, Mitchell PB, Vieta E, Frye MA, Rybakowski JK, Kuo PH, Kato T, Grigoroiu-
Serbanescu M, Reif A, Del Zompo M, Bellivier F, Schalling M, Wray NR, Kelsoe JR,
Alda M, McMahon FJ, Schulze TG, Rietschel M, Nöthen MM, Cichon S. Analysis of
the Influence of microRNAs in Lithium Response in Bipolar Disorder. Front
Psychiatry. 2018 May 31;9:207. doi: 10.3389/fpsyt.2018.00207. PMID: 29904359;
PMCID: PMC5991073.
385: Mirchi A, Pelletier F, Tran LT, Keller S, Braverman N, Tonduti D, Vanderver
A, Pizzino A, Dilenge ME, Poulin C, Shevell M, Majnemer A, Sébire G, Srour M,
Osterman B, Boucher RM, Vanasse M, Rossignol E, Mitchell J, Venkateswaran S,
Pohl D, Kauffman M, Schiffmann R, Goizet C, Moutton S, Roncarolo F, Bernard G.
Health-Related Quality of Life for Patients With Genetically Determined
Leukoencephalopathy. Pediatr Neurol. 2018 Jul;84:21-26. doi:
10.1016/j.pediatrneurol.2018.03.015. Epub 2018 Apr 9. PMID: 29859719.
386: Maranzano J, Till C, Assemlal HE, Fonov V, Brown R, Araujo D, O'Mahony J,
Yeh EA, Bar-Or A, Marrie RA, Collins L, Banwell B, Arnold DL, Narayanan S.
Detection and clinical correlation of leukocortical lesions in pediatric-onset
multiple sclerosis on multi-contrast MRI. Mult Scler. 2019 Jun;25(7):980-986.
doi: 10.1177/1352458518779952. Epub 2018 Jun 1. PMID: 29852831.
387: Waszak SM, Northcott PA, Buchhalter I, Robinson GW, Sutter C, Groebner S,
Grund KB, Brugières L, Jones DTW, Pajtler KW, Morrissy AS, Kool M, Sturm D,
Chavez L, Ernst A, Brabetz S, Hain M, Zichner T, Segura-Wang M, Weischenfeldt J,
Rausch T, Mardin BR, Zhou X, Baciu C, Lawerenz C, Chan JA, Varlet P, Guerrini-
Rousseau L, Fults DW, Grajkowska W, Hauser P, Jabado N, Ra YS, Zitterbart K,
Shringarpure SS, De La Vega FM, Bustamante CD, Ng HK, Perry A, MacDonald TJ,
Hernáiz Driever P, Bendel AE, Bowers DC, McCowage G, Chintagumpala MM, Cohn R,
Hassall T, Fleischhack G, Eggen T, Wesenberg F, Feychting M, Lannering B, Schüz
J, Johansen C, Andersen TV, Röösli M, Kuehni CE, Grotzer M, Kjaerheim K,
Monoranu CM, Archer TC, Duke E, Pomeroy SL, Shelagh R, Frank S, Sumerauer D,
Scheurlen W, Ryzhova MV, Milde T, Kratz CP, Samuel D, Zhang J, Solomon DA, Marra
M, Eils R, Bartram CR, von Hoff K, Rutkowski S, Ramaswamy V, Gilbertson RJ,
Korshunov A, Taylor MD, Lichter P, Malkin D, Gajjar A, Korbel JO, Pfister SM.
Spectrum and prevalence of genetic predisposition in medulloblastoma: a
retrospective genetic study and prospective validation in a clinical trial
cohort. Lancet Oncol. 2018 Jun;19(6):785-798. doi:
10.1016/S1470-2045(18)30242-0. Epub 2018 May 9. PMID: 29753700; PMCID:
PMC5984248.
388: Schur S, Allen V, White A, Mirsky D, Stence N, O'Neill B, Handler M, Dudley
R, Laoprasert P. Significance of FDG-PET Hypermetabolism in Children with
Intractable Focal Epilepsy. Pediatr Neurosurg. 2018;53(3):153-162. doi:
10.1159/000487088. Epub 2018 Apr 19. PMID: 29672310.
389: Schneider RE, Ng P, Zhang X, Andersen J, Buckley D, Fehlings D, Kirton A,
Wood E, van Rensburg E, Shevell MI, Oskoui M. The Association Between Maternal
Age and Cerebral Palsy Risk Factors. Pediatr Neurol. 2018 May;82:25-28. doi:
10.1016/j.pediatrneurol.2018.01.005. Epub 2018 Feb 12. PMID: 29622489.
390: Alawadhi A, Saint-Martin C, Bhanji F, Srour M, Atkinson J, Sébire G. Acute
Hemorrhagic Encephalitis Responding to Combined Decompressive Craniectomy,
Intravenous Immunoglobulin, and Corticosteroid Therapies: Association with Novel
RANBP2 Variant. Front Neurol. 2018 Mar 12;9:130. doi:
10.3389/fneur.2018.00130. PMID: 29593631; PMCID: PMC5857578.
391: Cooper YA, Pianka ST, Alotaibi NM, Babayan D, Salavati B, Weil AG, Ibrahim
GM, Wang AC, Fallah A. Repetitive transcranial magnetic stimulation for the
treatment of drug-resistant epilepsy: A systematic review and individual
participant data meta-analysis of real-world evidence. Epilepsia Open. 2017 Dec
27;3(1):55-65. doi: 10.1002/epi4.12092. PMID: 29588988; PMCID: PMC5839309.
392: Mendes MI, Gutierrez Salazar M, Guerrero K, Thiffault I, Salomons GS,
Gauquelin L, Tran LT, Forget D, Gauthier MS, Waisfisz Q, Smith DEC, Simons C,
van der Knaap MS, Marquardt I, Lemes A, Mierzewska H, Weschke B, Koehler W,
Coulombe B, Wolf NI, Bernard G. Bi-allelic Mutations in EPRS, Encoding the
Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating
Leukodystrophy. Am J Hum Genet. 2018 Apr 5;102(4):676-684. doi:
10.1016/j.ajhg.2018.02.011. Epub 2018 Mar 22. PMID: 29576217; PMCID: PMC5985283.
393: Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA,
Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt
JJFA, Geiger JT, Van der Spek RA, Pliner HA, Shankaracharya, Smith BN, Marangi
G, Topp SD, Abramzon Y, Gkazi AS, Eicher JD, Kenna A; ITALSGEN Consortium, Mora
G, Calvo A, Mazzini L, Riva N, Mandrioli J, Caponnetto C, Battistini S, Volanti
P, La Bella V, Conforti FL, Borghero G, Messina S, Simone IL, Trojsi F, Salvi F,
Logullo FO, D'Alfonso S, Corrado L, Capasso M, Ferrucci L; Genomic Translation
for ALS Care (GTAC) Consortium, Moreno CAM, Kamalakaran S, Goldstein DB; ALS
Sequencing Consortium, Gitler AD, Harris T, Myers RM; NYGC ALS Consortium,
Phatnani H, Musunuri RL, Evani US, Abhyankar A, Zody MC; Answer ALS Foundation,
Kaye J, Finkbeiner S, Wyman SK, LeNail A, Lima L, Fraenkel E, Svendsen CN,
Thompson LM, Van Eyk JE, Berry JD, Miller TM, Kolb SJ, Cudkowicz M, Baxi E;
Clinical Research in ALS and Related Disorders for Therapeutic Development
(CReATe) Consortium, Benatar M, Taylor JP, Rampersaud E, Wu G, Wuu J; SLAGEN
Consortium, Lauria G, Verde F, Fogh I, Tiloca C, Comi GP, Sorarù G, Cereda C;
French ALS Consortium, Corcia P, Laaksovirta H, Myllykangas L, Jansson L, Valori
M, Ealing J, Hamdalla H, Rollinson S, Pickering-Brown S, Orrell RW, Sidle KC,
Malaspina A, Hardy J, Singleton AB, Johnson JO, Arepalli S, Sapp PC, McKenna-
Yasek D, Polak M, Asress S, Al-Sarraj S, King A, Troakes C, Vance C, de
Belleroche J, Baas F, Ten Asbroek ALMA, Muñoz-Blanco JL, Hernandez DG, Ding J,
Gibbs JR, Scholz SW, Floeter MK, Campbell RH, Landi F, Bowser R, Pulst SM,
Ravits JM, MacGowan DJL, Kirby J, Pioro EP, Pamphlett R, Broach J, Gerhard G,
Dunckley TL, Brady CB, Kowall NW, Troncoso JC, Le Ber I, Mouzat K, Lumbroso S,
Heiman-Patterson TD, Kamel F, Van Den Bosch L, Baloh RH, Strom TM, Meitinger T,
Shatunov A, Van Eijk KR, de Carvalho M, Kooyman M, Middelkoop B, Moisse M,
McLaughlin RL, Van Es MA, Weber M, Boylan KB, Van Blitterswijk M, Rademakers R,
Morrison KE, Basak AN, Mora JS, Drory VE, Shaw PJ, Turner MR, Talbot K, Hardiman
O, Williams KL, Fifita JA, Nicholson GA, Blair IP, Rouleau GA, Esteban-Pérez J,
García-Redondo A, Al-Chalabi A; Project MinE ALS Sequencing Consortium, Rogaeva
E, Zinman L, Ostrow LW, Maragakis NJ, Rothstein JD, Simmons Z, Cooper-Knock J,
Brice A, Goutman SA, Feldman EL, Gibson SB, Taroni F, Ratti A, Gellera C, Van
Damme P, Robberecht W, Fratta P, Sabatelli M, Lunetta C, Ludolph AC, Andersen
PM, Weishaupt JH, Camu W, Trojanowski JQ, Van Deerlin VM, Brown RH Jr, van den
Berg LH, Veldink JH, Harms MB, Glass JD, Stone DJ, Tienari P, Silani V, Chiò A,
Shaw CE, Traynor BJ, Landers JE. Genome-wide Analyses Identify KIF5A as a Novel
ALS Gene. Neuron. 2018 Mar 21;97(6):1268-1283.e6. doi:
10.1016/j.neuron.2018.02.027. PMID: 29566793; PMCID: PMC5867896.
394: Zomerman WW, Plasschaert SLA, Conroy S, Scherpen FJ, Meeuwsen-de Boer TGJ,
Lourens HJ, Guerrero Llobet S, Smit MJ, Slagter-Menkema L, Seitz A, Gidding CEM,
Hulleman E, Wesseling P, Meijer L, van Kempen LC, van den Berg A, Warmerdam DO,
Kruyt FAE, Foijer F, van Vugt MATM, den Dunnen WFA, Hoving EW, Guryev V, de Bont
ESJM, Bruggeman SWM. Identification of Two Protein-Signaling States Delineating
Transcriptionally Heterogeneous Human Medulloblastoma. Cell Rep. 2018 Mar
20;22(12):3206-3216. doi: 10.1016/j.celrep.2018.02.089. PMID: 29562177.
395: Capper D, Jones DTW, Sill M, Hovestadt V, Schrimpf D, Sturm D, Koelsche C,
Sahm F, Chavez L, Reuss DE, Kratz A, Wefers AK, Huang K, Pajtler KW, Schweizer
L, Stichel D, Olar A, Engel NW, Lindenberg K, Harter PN, Braczynski AK, Plate
KH, Dohmen H, Garvalov BK, Coras R, Hölsken A, Hewer E, Bewerunge-Hudler M,
Schick M, Fischer R, Beschorner R, Schittenhelm J, Staszewski O, Wani K, Varlet
P, Pages M, Temming P, Lohmann D, Selt F, Witt H, Milde T, Witt O, Aronica E,
Giangaspero F, Rushing E, Scheurlen W, Geisenberger C, Rodriguez FJ, Becker A,
Preusser M, Haberler C, Bjerkvig R, Cryan J, Farrell M, Deckert M, Hench J,
Frank S, Serrano J, Kannan K, Tsirigos A, Brück W, Hofer S, Brehmer S, Seiz-
Rosenhagen M, Hänggi D, Hans V, Rozsnoki S, Hansford JR, Kohlhof P, Kristensen
BW, Lechner M, Lopes B, Mawrin C, Ketter R, Kulozik A, Khatib Z, Heppner F, Koch
A, Jouvet A, Keohane C, Mühleisen H, Mueller W, Pohl U, Prinz M, Benner A,
Zapatka M, Gottardo NG, Driever PH, Kramm CM, Müller HL, Rutkowski S, von Hoff
K, Frühwald MC, Gnekow A, Fleischhack G, Tippelt S, Calaminus G, Monoranu CM,
Perry A, Jones C, Jacques TS, Radlwimmer B, Gessi M, Pietsch T, Schramm J,
Schackert G, Westphal M, Reifenberger G, Wesseling P, Weller M, Collins VP,
Blümcke I, Bendszus M, Debus J, Huang A, Jabado N, Northcott PA, Paulus W,
Gajjar A, Robinson GW, Taylor MD, Jaunmuktane Z, Ryzhova M, Platten M, Unterberg
A, Wick W, Karajannis MA, Mittelbronn M, Acker T, Hartmann C, Aldape K, Schüller
U, Buslei R, Lichter P, Kool M, Herold-Mende C, Ellison DW, Hasselblatt M,
Snuderl M, Brandner S, Korshunov A, von Deimling A, Pfister SM. DNA methylation-
based classification of central nervous system tumours. Nature. 2018 Mar
22;555(7697):469-474. doi: 10.1038/nature26000. Epub 2018 Mar 14. PMID:
29539639; PMCID: PMC6093218.
396: Dudley RWR, Torok MR, Randall S, Béland B, Handler MH, Mulcahy-Levy JM, Liu
AK, Hankinson TC. Pediatric versus adult meningioma: comparison of epidemiology,
treatments, and outcomes using the Surveillance, Epidemiology, and End Results
database. J Neurooncol. 2018 May;137(3):621-629. doi: 10.1007/s11060-018-2756-1.
Epub 2018 Mar 9. PMID: 29520612.
397: Gauthier J, Meijer IA, Lessel D, Mencacci NE, Krainc D, Hempel M, Tsiakas
K, Prokisch H, Rossignol E, Helm MH, Rodan LH, Karamchandani J, Carecchio M,
Lubbe SJ, Telegrafi A, Henderson LB, Lorenzo K, Wallace SE, Glass IA, Hamdan FF,
Michaud JL, Rouleau GA, Campeau PM. Recessive mutations in VPS13D cause
childhood onset movement disorders. Ann Neurol. 2018 Jun;83(6):1089-1095. doi:
10.1002/ana.25204. Epub 2018 Apr 10. PMID: 29518281.
398: Wei Y, McCormick A, MacKenzie A, O'Ferrall E, Venance S, Mah JK, Selby K,
McMillan HJ, Smith G, Oskoui M, Hogan G, McAdam L, Mabaya G, Hodgkinson V,
Lounsberry J, Korngut L, Campbell C. The Canadian Neuromuscular Disease
Registry: Connecting patients to national and international research
opportunities. Paediatr Child Health. 2018 Feb;23(1):20-26. doi:
10.1093/pch/pxx125. Epub 2017 Dec 8. PMID: 29479275; PMCID: PMC5814813.
399: Al-Olabi L, Polubothu S, Dowsett K, Andrews KA, Stadnik P, Joseph AP, Knox
R, Pittman A, Clark G, Baird W, Bulstrode N, Glover M, Gordon K, Hargrave D,
Huson SM, Jacques TS, James G, Kondolf H, Kangesu L, Keppler-Noreuil KM, Khan A,
Lindhurst MJ, Lipson M, Mansour S, O'Hara J, Mahon C, Mosica A, Moss C, Murthy
A, Ong J, Parker VE, Rivière JB, Sapp JC, Sebire NJ, Shah R, Sivakumar B, Thomas
A, Virasami A, Waelchli R, Zeng Z, Biesecker LG, Barnacle A, Topf M, Semple RK,
Patton EE, Kinsler VA. Mosaic RAS/MAPK variants cause sporadic vascular
malformations which respond to targeted therapy. J Clin Invest. 2018 Apr
2;128(4):1496-1508. doi: 10.1172/JCI98589. Epub 2018 Mar 12. Erratum in: J Clin
Invest. 2018 Nov 1;128(11):5185. PMID: 29461977; PMCID: PMC5873857.
400: Smilga AS, Garfinkle J, Ng P, Andersen J, Buckley D, Fehlings D, Kirton A,
Wood E, van Rensburg E, Shevell M, Oskoui M. Neonatal Infection in Children With
Cerebral Palsy: A Registry-Based Cohort Study. Pediatr Neurol. 2018
Mar;80:77-83. doi: 10.1016/j.pediatrneurol.2017.11.006. Epub 2017 Dec 13. PMID:
29428154.
401: da Silva RV, Johannssen HC, Wyss MT, Roome RB, Bourojeni FB, Stifani N,
Marsh APL, Ryan MM, Lockhart PJ, Leventer RJ, Richards LJ, Rosenblatt B, Srour
M, Weber B, Zeilhofer HU, Kania A. DCC Is Required for the Development of
Nociceptive Topognosis in Mice and Humans. Cell Rep. 2018 Jan
30;22(5):1105-1114. doi: 10.1016/j.celrep.2018.01.004. PMID: 29386099.
402: Alcalay RN, Wolf P, Levy OA, Kang UJ, Waters C, Fahn S, Ford B, Kuo SH,
Vanegas N, Shah H, Liong C, Narayan S, Pauciulo MW, Nichols WC, Gan-Or Z,
Rouleau GA, Chung WK, Oliva P, Keutzer J, Marder K, Zhang XK. Alpha
galactosidase A activity in Parkinson's disease. Neurobiol Dis. 2018
Apr;112:85-90. doi: 10.1016/j.nbd.2018.01.012. Epub 2018 Feb 2. PMID: 29369793;
PMCID: PMC5811339.
403: Whelan CD, Altmann A, Botía JA, Jahanshad N, Hibar DP, Absil J, Alhusaini
S, Alvim MKM, Auvinen P, Bartolini E, Bergo FPG, Bernardes T, Blackmon K, Braga
B, Caligiuri ME, Calvo A, Carr SJ, Chen J, Chen S, Cherubini A, David P, Domin
M, Foley S, França W, Haaker G, Isaev D, Keller SS, Kotikalapudi R, Kowalczyk
MA, Kuzniecky R, Langner S, Lenge M, Leyden KM, Liu M, Loi RQ, Martin P,
Mascalchi M, Morita ME, Pariente JC, Rodríguez-Cruces R, Rummel C, Saavalainen
T, Semmelroch MK, Severino M, Thomas RH, Tondelli M, Tortora D, Vaudano AE,
Vivash L, von Podewils F, Wagner J, Weber B, Yao Y, Yasuda CL, Zhang G, Bargalló
N, Bender B, Bernasconi N, Bernasconi A, Bernhardt BC, Blümcke I, Carlson C,
Cavalleri GL, Cendes F, Concha L, Delanty N, Depondt C, Devinsky O, Doherty CP,
Focke NK, Gambardella A, Guerrini R, Hamandi K, Jackson GD, Kälviäinen R,
Kochunov P, Kwan P, Labate A, McDonald CR, Meletti S, O'Brien TJ, Ourselin S,
Richardson MP, Striano P, Thesen T, Wiest R, Zhang J, Vezzani A, Ryten M,
Thompson PM, Sisodiya SM. Structural brain abnormalities in the common
epilepsies assessed in a worldwide ENIGMA study. Brain. 2018 Feb
1;141(2):391-408. doi: 10.1093/brain/awx341. PMID: 29365066; PMCID: PMC5837616.
404: Ibrahim GM, Wong S, Morgan BR, Lipsman N, Fallah A, Weil AG, Krishna V,
Wennberg RA, Lozano AA. Phase-amplitude coupling within the anterior thalamic
nuclei during seizures. J Neurophysiol. 2018 Apr 1;119(4):1497-1505. doi:
10.1152/jn.00832.2017. Epub 2017 Dec 27. PMID: 29357461.
405: Lam Van Ba O, Barbe MF, Caremel R, Aharony S, Loutochin O, Jacques L, Wood
MW, Tiwari E, Tuite GF, Campeau L, Corcos J, Ruggieri MR Sr. Lumbar to sacral
root rerouting to restore bladder function in a feline spinal cord injury model:
Urodynamic and retrograde nerve tracing results from a pilot study. Neurourol
Urodyn. 2018 Jan;37(1):153-162. doi: 10.1002/nau.23394. Epub 2018 Jan 4. PMID:
29314212; PMCID: PMC5785433.
406: Mack SC, Pajtler KW, Chavez L, Okonechnikov K, Bertrand KC, Wang X, Erkek
S, Federation A, Song A, Lee C, Wang X, McDonald L, Morrow JJ, Saiakhova A, Sin-
Chan P, Wu Q, Michaelraj KA, Miller TE, Hubert CG, Ryzhova M, Garzia L, Donovan
L, Dombrowski S, Factor DC, Luu B, Valentim CLL, Gimple RC, Morton A, Kim L,
Prager BC, Lee JJY, Wu X, Zuccaro J, Thompson Y, Holgado BL, Reimand J, Ke SQ,
Tropper A, Lai S, Vijayarajah S, Doan S, Mahadev V, Miñan AF, Gröbner SN,
Lienhard M, Zapatka M, Huang Z, Aldape KD, Carcaboso AM, Houghton PJ, Keir ST,
Milde T, Witt H, Li Y, Li CJ, Bian XW, Jones DTW, Scott I, Singh SK, Huang A,
Dirks PB, Bouffet E, Bradner JE, Ramaswamy V, Jabado N, Rutka JT, Northcott PA,
Lupien M, Lichter P, Korshunov A, Scacheri PC, Pfister SM, Kool M, Taylor MD,
Rich JN. Therapeutic targeting of ependymoma as informed by oncogenic enhancer
profiling. Nature. 2018 Jan 4;553(7686):101-105. doi: 10.1038/nature25169. Epub
2017 Dec 20. PMID: 29258295; PMCID: PMC5993422.
407: Ritzema AM, Lach LM, Nicholas D, Sladeczek IE. A model of well-being for
children with neurodevelopmental disorders: Parental perceptions of functioning,
services, and support. Child Care Health Dev. 2018 Mar;44(2):240-248. doi:
10.1111/cch.12541. Epub 2017 Dec 18. PMID: 29250821.
408: Gnekow AK, Walker DA, Kandels D, Picton S, Giorgio Perilongo, Grill J,
Stokland T, Sandstrom PE, Warmuth-Metz M, Pietsch T, Giangaspero F, Schmidt R,
Faldum A, Kilmartin D, De Paoli A, De Salvo GL; low-grade glioma Consortium and
the participating centers. Corrigendum to "A European randomised controlled
trial of the addition of etoposide to standard vincristine and carboplatin
induction as part of an 18-month treatment programme for childhood (≤16 years)
low-grade glioma - A final report" [Eur J of Canc (2017) 206-225]. Eur J Cancer.
2018 Feb;90:156-157. doi: 10.1016/j.ejca.2017.11.017. Epub 2017 Dec 14. Erratum
for: Eur J Cancer. 2017 Aug;81:206-225. PMID: 29248309; PMCID: PMC6854447.
409: Gauquelin L, Tétreault M, Thiffault I, Farrow E, Miller N, Yoo B, Bareke E,
Yoon G, Suchowersky O, Dupré N, Tarnopolsky M, Brais B, Wolf NI, Majewski J,
Rouleau GA, Gan-Or Z, Bernard G. POLR3A variants in hereditary spastic
paraplegia and ataxia. Brain. 2018 Jan 1;141(1):e1. doi: 10.1093/brain/awx290.
PMID: 29228109; PMCID: PMC5837469.
410: Gauvin M, Dorfman AL, Lachapelle P. Recording and Analysis of the Human
Clinical Electroretinogram. Methods Mol Biol. 2018;1715:313-325. doi:
10.1007/978-1-4939-7522-8_23. PMID: 29188524.
411: Cayami FK, Bugiani M, Pouwels PJW, Bernard G, van der Knaap MS, Wolf NI. 4H
Leukodystrophy: Lessons from 3T Imaging. Neuropediatrics. 2018
Apr;49(2):112-117. doi: 10.1055/s-0037-1608780. Epub 2017 Nov 27. PMID:
29179231.
412: Dubrovsky AS. Nerve Blocks in Pediatric and Adolescent Headache Disorders.
Curr Pain Headache Rep. 2017 Nov 9;21(12):50. doi: 10.1007/s11916-017-0650-8.
PMID: 29124490.
413: Gauquelin L, Tran LT, Chouinard S, Bernard G. The Movement Disorder of
Brain-Lung-Thyroid Syndrome Can be Responsive to Methylphenidate. Tremor Other
Hyperkinet Mov (N Y). 2017 Oct 26;7:508. doi: 10.7916/D84X5M9Z. PMID: 29109906;
PMCID: PMC5666014.
414: Wolf P, Alcalay RN, Liong C, Cullen E, Pauciulo MW, Nichols WC, Gan-Or Z,
Chung WK, Faulkner T, Bentis C, Pomponio RJ, Ma X, Kate Zhang X, Keutzer JM,
Oliva P. Tandem mass spectrometry assay of β-glucocerebrosidase activity in
dried blood spots eliminates false positives detected in fluorescence assay. Mol
Genet Metab. 2018 Feb;123(2):135-139. doi: 10.1016/j.ymgme.2017.10.011. Epub
2017 Oct 23. PMID: 29100779; PMCID: PMC5808899.
415: Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif
C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K,
Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K,
Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study,
FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH,
Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L,
Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg
EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF,
Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA,
Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ,
Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C,
Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE,
Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major
P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau
PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau
GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL.
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic
Encephalopathies. Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi:
10.1016/j.ajhg.2017.09.008. PMID: 29100083; PMCID: PMC5673604.
416: Wang AC, Ibrahim GM, Poliakov AV, Wang PI, Fallah A, Mathern GW, Buckley
RT, Collins K, Weil AG, Shurtleff HA, Warner MH, Perez FA, Shaw DW, Wright JN,
Saneto RP, Novotny EJ, Lee A, Browd SR, Ojemann JG. Corticospinal tract atrophy
and motor fMRI predict motor preservation after functional cerebral
hemispherectomy. J Neurosurg Pediatr. 2018 Jan;21(1):81-89. doi:
10.3171/2017.7.PEDS17137. Epub 2017 Nov 3. PMID: 29099351.
417: Karamanou M, Tsoucalas G, Themistocleous M, Giakoumettis D, Stranjalis G,
Androutsos G. Epilepsy and Neurosurgery: Historical Highlights. Curr Pharm Des.
2017;23(42):6373-6375. doi: 10.2174/1381612823666171024150121. PMID: 29076417.
418: Marsh APL, Edwards TJ, Galea C, Cooper HM, Engle EC, Jamuar SS, Méneret A,
Moutard ML, Nava C, Rastetter A, Robinson G, Rouleau G, Roze E, Spencer-Smith M,
Trouillard O, Billette de Villemeur T, Walsh CA, Yu TW; IRC5 Consortium, Heron
D, Sherr EH, Richards LJ, Depienne C, Leventer RJ, Lockhart PJ. DCC mutation
update: Congenital mirror movements, isolated agenesis of the corpus callosum,
and developmental split brain syndrome. Hum Mutat. 2018 Jan;39(1):23-39. doi:
10.1002/humu.23361. Epub 2017 Nov 11. PMID: 29068161; PMCID: PMC5722687.
419: Maillard LG, Tassi L, Bartolomei F, Catenoix H, Dubeau F, Szurhaj W, Kahane
P, Nica A, Marusic P, Mindruta I, Chassoux F, Ramantani G.
Stereoelectroencephalography and surgical outcome in polymicrogyria-related
epilepsy: A multicentric study. Ann Neurol. 2017 Nov;82(5):781-794. doi:
10.1002/ana.25081. Epub 2017 Nov 11. PMID: 29059488.
420: Jones DTW, Kieran MW, Bouffet E, Alexandrescu S, Bandopadhayay P, Bornhorst
M, Ellison D, Fangusaro J, Fisher MJ, Foreman N, Fouladi M, Hargrave D, Hawkins
C, Jabado N, Massimino M, Mueller S, Perilongo G, Schouten van Meeteren AYN,
Tabori U, Warren K, Waanders AJ, Walker D, Weiss W, Witt O, Wright K, Zhu Y,
Bowers DC, Pfister SM, Packer RJ. Pediatric low-grade gliomas: next biologically
driven steps. Neuro Oncol. 2018 Jan 22;20(2):160-173. doi:
10.1093/neuonc/nox141. Erratum in: Neuro Oncol. 2018 Jan 22;20(2):293. PMID:
29016845; PMCID: PMC5786244.
421: Fallah A, Weil AG, Juraschka K, Ibrahim GM, Wang AC, Crevier L, Tseng CH,
Kulkarni AV, Ragheb J, Bhatia S. The importance of extent of choroid plexus
cauterization in addition to endoscopic third ventriculostomy for infantile
hydrocephalus: a retrospective North American observational study using
propensity score-adjusted analysis. J Neurosurg Pediatr. 2017 Dec;20(6):503-510.
doi: 10.3171/2017.7.PEDS16379. Epub 2017 Oct 6. PMID: 28984539.
422: Ibrahim GM, Sharma P, Hyslop A, Guillen MR, Morgan BR, Wong S, Abel TJ,
Elkaim L, Cajigas I, Shah AH, Fallah A, Weil AG, Altman N, Bernal B, Medina S,
Widjaja E, Jayakar P, Ragheb J, Bhatia S. Presurgical thalamocortical
connectivity is associated with response to vagus nerve stimulation in children
with intractable epilepsy. Neuroimage Clin. 2017 Sep 22;16:634-642. doi:
10.1016/j.nicl.2017.09.015. PMID: 28971013; PMCID: PMC5619991.
423: Al Amrani F, Dudley R, Bello-Espinosa LE, Rosenblatt B, Srour M, Sébire G.
Intravenous Immunoglobulin as a Treatment for Intractable Epilepsy Secondary to
Focal Cortical Dysplasia: A Meta-analysis. Pediatr Neurol. 2017 Nov;76:79-81.
doi: 10.1016/j.pediatrneurol.2017.07.009. Epub 2017 Jul 19. PMID: 28969879.
424: Mackay A, Burford A, Carvalho D, Izquierdo E, Fazal-Salom J, Taylor KR,
Bjerke L, Clarke M, Vinci M, Nandhabalan M, Temelso S, Popov S, Molinari V,
Raman P, Waanders AJ, Han HJ, Gupta S, Marshall L, Zacharoulis S, Vaidya S,
Mandeville HC, Bridges LR, Martin AJ, Al-Sarraj S, Chandler C, Ng HK, Li X, Mu
K, Trabelsi S, Brahim DH, Kisljakov AN, Konovalov DM, Moore AS, Carcaboso AM,
Sunol M, de Torres C, Cruz O, Mora J, Shats LI, Stavale JN, Bidinotto LT, Reis
RM, Entz-Werle N, Farrell M, Cryan J, Crimmins D, Caird J, Pears J, Monje M,
Debily MA, Castel D, Grill J, Hawkins C, Nikbakht H, Jabado N, Baker SJ, Pfister
SM, Jones DTW, Fouladi M, von Bueren AO, Baudis M, Resnick A, Jones C.
Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse
Intrinsic Pontine Glioma. Cancer Cell. 2017 Oct 9;32(4):520-537.e5. doi:
10.1016/j.ccell.2017.08.017. Epub 2017 Sep 28. PMID: 28966033; PMCID:
PMC5637314.
425: Kay-Rivest E, Khendek L, Bernard G, Daniel SJ. Pediatric leukodystrophies:
The role of the otolaryngologist. Int J Pediatr Otorhinolaryngol. 2017
Oct;101:141-144. doi: 10.1016/j.ijporl.2017.07.039. Epub 2017 Jul 27. PMID:
28964285.
426: Adang LA, Sherbini O, Ball L, Bloom M, Darbari A, Amartino H, DiVito D,
Eichler F, Escolar M, Evans SH, Fatemi A, Fraser J, Hollowell L, Jaffe N, Joseph
C, Karpinski M, Keller S, Maddock R, Mancilla E, McClary B, Mertz J, Morgart K,
Langan T, Leventer R, Parikh S, Pizzino A, Prange E, Renaud DL, Rizzo W, Shapiro
J, Suhr D, Suhr T, Tonduti D, Waggoner J, Waldman A, Wolf NI, Zerem A, Bonkowsky
JL, Bernard G, van Haren K, Vanderver A; Global Leukodystrophy Initiative (GLIA)
Consortium. Revised consensus statement on the preventive and symptomatic care
of patients with leukodystrophies. Mol Genet Metab. 2017 Sep;122(1-2):18-32.
doi: 10.1016/j.ymgme.2017.08.006. Epub 2017 Aug 20. PMID: 28863857; PMCID:
PMC8018711.
427: Perrier S, Gauquelin L, Tétreault M, Tran LT, Webb N, Srour M, Mitchell JJ,
Brunel-Guitton C, Majewski J, Long V, Keller S, Gambello MJ, Simons C; Care4Rare
Canada Consortium, Vanderver A, Bernard G. Recessive mutations in NDUFA2 cause
mitochondrial leukoencephalopathy. Clin Genet. 2018 Feb;93(2):396-400. doi:
10.1111/cge.13126. Epub 2017 Dec 21. PMID: 28857146.
428: Karlberg A, Berntsen EM, Johansen H, Myrthue M, Skjulsvik AJ, Reinertsen I,
Esmaeili M, Dai HY, Xiao Y, Rivaz H, Borghammer P, Solheim O, Eikenes L.
Multimodal 18F-Fluciclovine PET/MRI and Ultrasound-Guided
Neurosurgery of an Anaplastic Oligodendroglioma. World Neurosurg. 2017
Dec;108:989.e1-989.e8. doi: 10.1016/j.wneu.2017.08.085. Epub 2017 Aug 24. PMID:
28844925.
429: Graber TE, Freemantle E, Anadolu MN, Hébert-Seropian S, MacAdam RL, Shin U,
Hoang HD, Alain T, Lacaille JC, Sossin WS. UPF1 Governs Synaptic Plasticity
through Association with a STAU2 RNA Granule. J Neurosci. 2017 Sep
20;37(38):9116-9131. doi: 10.1523/JNEUROSCI.0088-17.2017. Epub 2017 Aug 18.
Erratum in: J Neurosci. 2017 Oct 18;37(42):10253. PMID: 28821679; PMCID:
PMC6596739.
430: Woo J, Jung S, Gauvin M, Lachapelle P. The DTL ERG electrode comes in
different shapes and sizes: Are they all good? Doc Ophthalmol. 2017
Oct;135(2):155-164. doi: 10.1007/s10633-017-9600-3. Epub 2017 Jul 24. PMID:
28741115.
431: Panwalkar P, Clark J, Ramaswamy V, Hawes D, Yang F, Dunham C, Yip S, Hukin
J, Sun Y, Schipper MJ, Chavez L, Margol A, Pekmezci M, Chung C, Banda A, Bayliss
JM, Curry SJ, Santi M, Rodriguez FJ, Snuderl M, Karajannis MA, Saratsis AM,
Horbinski CM, Carret AS, Wilson B, Johnston D, Lafay-Cousin L, Zelcer S,
Eisenstat D, Silva M, Scheinemann K, Jabado N, McNeely PD, Kool M, Pfister SM,
Taylor MD, Hawkins C, Korshunov A, Judkins AR, Venneti S. Immunohistochemical
analysis of H3K27me3 demonstrates global reduction in group-A childhood
posterior fossa ependymoma and is a powerful predictor of outcome. Acta
Neuropathol. 2017 Nov;134(5):705-714. doi: 10.1007/s00401-017-1752-4. Epub 2017
Jul 21. PMID: 28733933; PMCID: PMC5647236.
432: Northcott PA, Buchhalter I, Morrissy AS, Hovestadt V, Weischenfeldt J,
Ehrenberger T, Gröbner S, Segura-Wang M, Zichner T, Rudneva VA, Warnatz HJ,
Sidiropoulos N, Phillips AH, Schumacher S, Kleinheinz K, Waszak SM, Erkek S,
Jones DTW, Worst BC, Kool M, Zapatka M, Jäger N, Chavez L, Hutter B, Bieg M,
Paramasivam N, Heinold M, Gu Z, Ishaque N, Jäger-Schmidt C, Imbusch CD, Jugold
A, Hübschmann D, Risch T, Amstislavskiy V, Gonzalez FGR, Weber UD, Wolf S,
Robinson GW, Zhou X, Wu G, Finkelstein D, Liu Y, Cavalli FMG, Luu B, Ramaswamy
V, Wu X, Koster J, Ryzhova M, Cho YJ, Pomeroy SL, Herold-Mende C, Schuhmann M,
Ebinger M, Liau LM, Mora J, McLendon RE, Jabado N, Kumabe T, Chuah E, Ma Y,
Moore RA, Mungall AJ, Mungall KL, Thiessen N, Tse K, Wong T, Jones SJM, Witt O,
Milde T, Von Deimling A, Capper D, Korshunov A, Yaspo ML, Kriwacki R, Gajjar A,
Zhang J, Beroukhim R, Fraenkel E, Korbel JO, Brors B, Schlesner M, Eils R, Marra
MA, Pfister SM, Taylor MD, Lichter P. The whole-genome landscape of
medulloblastoma subtypes. Nature. 2017 Jul 19;547(7663):311-317. doi:
10.1038/nature22973. PMID: 28726821; PMCID: PMC5905700.
433: Frauscher B, Bartolomei F, Kobayashi K, Cimbalnik J, van 't Klooster MA,
Rampp S, Otsubo H, Höller Y, Wu JY, Asano E, Engel J Jr, Kahane P, Jacobs J,
Gotman J. High-frequency oscillations: The state of clinical research.
Epilepsia. 2017 Aug;58(8):1316-1329. doi: 10.1111/epi.13829. Epub 2017 Jun 30.
PMID: 28666056; PMCID: PMC5806699.
434: Gnekow AK, Walker DA, Kandels D, Picton S, Giorgio Perilongo, Grill J,
Stokland T, Sandstrom PE, Warmuth-Metz M, Pietsch T, Giangaspero F, Schmidt R,
Faldum A, Kilmartin D, De Paoli A, De Salvo GL; of the low-grade glioma
Consortium and the participating centers. A European randomised controlled trial
of the addition of etoposide to standard vincristine and carboplatin induction
as part of an 18-month treatment programme for childhood (≤16 years) low grade
glioma - A final report. Eur J Cancer. 2017 Aug;81:206-225. doi:
10.1016/j.ejca.2017.04.019. Epub 2017 Jun 22. Erratum in: Eur J Cancer. 2017 Dec
13;: PMID: 28649001; PMCID: PMC5517338.
435: Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos
EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M,
Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL,
Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H,
Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C,
Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty
IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls
DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G;
Tourette Syndrome Association International Consortium for Genetics (TSAICG);
Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI). Rare Copy
Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron.
2017 Jun 21;94(6):1101-1111.e7. doi: 10.1016/j.neuron.2017.06.010. PMID:
28641109; PMCID: PMC5568251.
436: Leyton M, Kennedy SH. Neuroimaging tests for clinical psychiatry: Are we
there yet? J Psychiatry Neurosci. 2017 Jun;42(4):219-221. doi:
10.1503/jpn.170109. PMID: 28639935; PMCID: PMC5487268.
437: Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh
M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A,
Atkinson D, Hartley T, Tetreault M, Cuppen I, van der Pol WL, Candayan A,
Battaloglu E, Parman Y, van Gassen KLI, van den Boogaard MH, Boycott KM, Kauppi
L, Jordanova A, Lönnqvist T, Tyynismaa H. MCM3AP in recessive Charcot-Marie-
Tooth neuropathy and mild intellectual disability. Brain. 2017 Aug
1;140(8):2093-2103. doi: 10.1093/brain/awx138. PMID: 28633435.
438: Cavalli FMG, Remke M, Rampasek L, Peacock J, Shih DJH, Luu B, Garzia L,
Torchia J, Nor C, Morrissy AS, Agnihotri S, Thompson YY, Kuzan-Fischer CM,
Farooq H, Isaev K, Daniels C, Cho BK, Kim SK, Wang KC, Lee JY, Grajkowska WA,
Perek-Polnik M, Vasiljevic A, Faure-Conter C, Jouvet A, Giannini C, Nageswara
Rao AA, Li KKW, Ng HK, Eberhart CG, Pollack IF, Hamilton RL, Gillespie GY, Olson
JM, Leary S, Weiss WA, Lach B, Chambless LB, Thompson RC, Cooper MK, Vibhakar R,
Hauser P, van Veelen MC, Kros JM, French PJ, Ra YS, Kumabe T, López-Aguilar E,
Zitterbart K, Sterba J, Finocchiaro G, Massimino M, Van Meir EG, Osuka S,
Shofuda T, Klekner A, Zollo M, Leonard JR, Rubin JB, Jabado N, Albrecht S, Mora
J, Van Meter TE, Jung S, Moore AS, Hallahan AR, Chan JA, Tirapelli DPC, Carlotti
CG, Fouladi M, Pimentel J, Faria CC, Saad AG, Massimi L, Liau LM, Wheeler H,
Nakamura H, Elbabaa SK, Perezpeña-Diazconti M, Chico Ponce de León F, Robinson
S, Zapotocky M, Lassaletta A, Huang A, Hawkins CE, Tabori U, Bouffet E, Bartels
U, Dirks PB, Rutka JT, Bader GD, Reimand J, Goldenberg A, Ramaswamy V, Taylor
MD. Intertumoral Heterogeneity within Medulloblastoma Subgroups. Cancer Cell.
2017 Jun 12;31(6):737-754.e6. doi: 10.1016/j.ccell.2017.05.005. PMID: 28609654;
PMCID: PMC6163053.
439: Vrij-van den Bos S, Hol JA, La Piana R, Harting I, Vanderver A, Barkhof F,
Cayami F, van Wieringen WN, Pouwels PJW, van der Knaap MS, Bernard G, Wolf NI.
4H Leukodystrophy: A Brain Magnetic Resonance Imaging Scoring System.
Neuropediatrics. 2017 Jun;48(3):152-160. doi: 10.1055/s-0037-1599141. Epub 2017
Mar 1. PMID: 28561206.
440: van den Bruck R, Weil PP, Ziegenhals T, Schreiner P, Juranek S, Gödde D,
Vogel S, Schuster F, Orth V, Dörner J, Pembaur D, Röper M, Störkel S, Zirngibl
H, Wirth S, Jenke ACW, Postberg J, Boy N, Heringer J, Haege G, Glahn EM,
Hoffmann GF, Garbade SF, Burgard P, Kölker S, Chao CM, Yahya F, Moiseenko A,
Shrestha A, Ahmadvand N, Quantius J, Wilhelm J, El-Agha E, Zimmer KP, Bellusci
S, Staufner C, Kölker S, Prokisch H, Hoffmann GF, Seeliger S, Müller M, Hippe A,
Steinkraus H, Wauer R, Lachmann B, Hofmann SR, Hedrich CM, Zierk J, Arzideh F,
Haeckel R, Rascher W, Rauh M, Metzler M, Thieme S, Bandoła J, Richter C, Ryser
M, Jamal A, Ashton MP, von Bonin M, Kuhn M, Hedrich CM, Bonifacio E, Berner R,
Brenner S, Hammersen J, Has C, Naumann-Bartsch N, Stachel D, Kiritsi D, Söder S,
Tardieu M, Metzler M, Bruckner-Tuderman L, Schneider H, Bohne F, Langer D,
Cencic R, Eggermann T, Zechner U, Pelletier J, Zepp F, Enklaar T, Prawitt D,
Pech M, Weckmann M, Heinsen FA, Franke A, Happle C, Dittrich AM, Hansen G, Fuchs
O, von Mutius E, Oliver BG, Kopp MV, Paret C, Russo A, Theruvath J, Keller B, El
Malki K, Lehmann N, Wingerter A, Neu MA, Aslihan GA, Wagner W, Sommer C, Pietsch
T, Seidmann L, Faber J, Schreiner F, Ackermann M, Michalik M, Rother E, Bilkei-
Gorzo A, Racz I, Bindila L, Lutz B, Dötsch J, Zimmer A, Woelfle J, Fischer HS,
Ullrich TL, Bührer C, Czernik C, Schmalisch G, Stein R, Hofmann SR, Hagenbuchner
J, Kiechl-Kohlendorfer U, Obexer P, Ausserlechner MJ, Loges NT, Frommer AT,
Wallmeier J, Omran H, Öner-Sieben S, Gimpfl M, Rozman J, Irmler M, Beckers J, De
Angelis MH, Roscher A, Wolf E, Ensenauer R, Nemes K, Frühwald M, Hasselblatt M,
Siebert R, Kordes U, Kool M, Wang H, Hardy H, Refai O, Barwick KES, Zimmerman
HH, Weis J, Baple EL, Crosby AH, Cirak S, Hellmuth C, Uhl O, Standl M, Heinrich
J, Thiering E, Koletzko B, Blümel L, Kerl K, Picard D, Frühwald MC, Liebau MC,
Reifenberger G, Borkhardt A, Hasselblatt M, Remke M, Tews D, Wabitsch M,
Fischer-Posovszky P, Westhoff MA, Nonnenmacher L, Langhans J, Schneele L,
Trenkler N, Debatin KM. Abstracts of the 52nd Workshop for Pediatric Research :
Frankfurt, Germany. 27-28 October 2016. Mol Cell Pediatr. 2017 May;4(Suppl 1):5.
doi: 10.1186/s40348-017-0071-0. PMID: 28516419; PMCID: PMC5435609.
441: Al Yazidi G, Shevell MI, Srour M. Two Novel KCNQ2 Mutations in 2
Families With Benign Familial Neonatal Convulsions. Child Neurol Open. 2017 Feb
23;4:2329048X17691396. doi: 10.1177/2329048X17691396. PMID: 28503627; PMCID:
PMC5417349.
442: Sabouny R, Fraunberger E, Geoffrion M, Ng AC, Baird SD, Screaton RA, Milne
R, McBride HM, Shutt TE. The Keap1-Nrf2 Stress Response Pathway Promotes
Mitochondrial Hyperfusion Through Degradation of the Mitochondrial Fission
Protein Drp1. Antioxid Redox Signal. 2017 Dec 20;27(18):1447-1459. doi:
10.1089/ars.2016.6855. Epub 2017 Jul 7. PMID: 28494652.
443: Bernard G, Vanderver A. POLR3-Related Leukodystrophy. 2012 Aug 2 [updated
2017 May 11]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean
LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle
(WA): University of Washington, Seattle; 1993–2022. PMID: 22855961.
444: Alt C, Shevell MI, Poulin C, Rosenblatt B, Saint-Martin C, Srour M.
Clinical and Radiologic Spectrum of Septo-optic Dysplasia: Review of 17 Cases. J
Child Neurol. 2017 Aug;32(9):797-803. doi: 10.1177/0883073817707300. Epub 2017
May 8. PMID: 28482731.
445: van Lee L, Quah PL, Saw SM, Yap FKP, Godfrey KM, Chong YS, Meaney MJ, Chen
H, Chong MF. Maternal choline status during pregnancy, but not that of betaine,
is related to antenatal mental well-being: The growing up in Singapore toward
healthy outcomes cohort. Depress Anxiety. 2017 Oct;34(10):877-887. doi:
10.1002/da.22637. Epub 2017 May 4. PMID: 28471488; PMCID: PMC5553109.
446: Shemie SD, Simpson C, Blackmer J, MacDonald S, Dhanani S, Torrance S, Byrne
P; Donation Physician Ethics Guide Meeting Participants. Ethics Guide
Recommendations for Organ-Donation-Focused Physicians: Endorsed by the Canadian
Medical Association. Transplantation. 2017 May;101(5S Suppl 1):S41-S47. doi:
10.1097/TP.0000000000001694. PMID: 28437370.
447: Lacaria M, Srour M, Michaud JL, Doja A, Miller E, Schwartzentruber J,
Goldsmith C, Majewski J; FORGE Canada Consortium, Boycott KM. Expansion of the
clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and
hyperemia of the hands and feet. Am J Med Genet A. 2017 Jun;173(6):1611-1619.
doi: 10.1002/ajmg.a.38231. Epub 2017 Apr 21. PMID: 28432728.
448: Choquet K, Yang S, Moir RD, Forget D, Larivière R, Bouchard A, Poitras C,
Sgarioto N, Dicaire MJ, Noohi F, Kennedy TE, Rochford J, Bernard G, Teichmann M,
Coulombe B, Willis IM, Kleinman CL, Brais B. Absence of neurological
abnormalities in mice homozygous for the Polr3a G672E hypomyelinating
leukodystrophy mutation. Mol Brain. 2017 Apr 13;10(1):13. doi:
10.1186/s13041-017-0294-y. PMID: 28407788; PMCID: PMC5391615.
449: Morrissy AS, Cavalli FMG, Remke M, Ramaswamy V, Shih DJH, Holgado BL,
Farooq H, Donovan LK, Garzia L, Agnihotri S, Kiehna EN, Mercier E, Mayoh C,
Papillon-Cavanagh S, Nikbakht H, Gayden T, Torchia J, Picard D, Merino DM,
Vladoiu M, Luu B, Wu X, Daniels C, Horswell S, Thompson YY, Hovestadt V,
Northcott PA, Jones DTW, Peacock J, Wang X, Mack SC, Reimand J, Albrecht S,
Fontebasso AM, Thiessen N, Li Y, Schein JE, Lee D, Carlsen R, Mayo M, Tse K, Tam
A, Dhalla N, Ally A, Chuah E, Cheng Y, Plettner P, Li HI, Corbett RD, Wong T,
Long W, Loukides J, Buczkowicz P, Hawkins CE, Tabori U, Rood BR, Myseros JS,
Packer RJ, Korshunov A, Lichter P, Kool M, Pfister SM, Schüller U, Dirks P,
Huang A, Bouffet E, Rutka JT, Bader GD, Swanton C, Ma Y, Moore RA, Mungall AJ,
Majewski J, Jones SJM, Das S, Malkin D, Jabado N, Marra MA, Taylor MD. Spatial
heterogeneity in medulloblastoma. Nat Genet. 2017 May;49(5):780-788. doi:
10.1038/ng.3838. Epub 2017 Apr 10. PMID: 28394352; PMCID: PMC5553617.
450: Aubert-Broche B, Weier K, Longoni G, Fonov VS, Bar-Or A, Marrie RA, Yeh EA,
Narayanan S, Arnold DL, Verhey LH, Banwell B, Collins DL; Canadian Pediatric
Demyelinating Disease Network. Monophasic demyelination reduces brain growth in
children. Neurology. 2017 May 2;88(18):1744-1750. doi:
10.1212/WNL.0000000000003884. Epub 2017 Apr 5. PMID: 28381515; PMCID:
PMC5409842.
451: Oliver KL, Franceschetti S, Milligan CJ, Muona M, Mandelstam SA, Canafoglia
L, Boguszewska-Chachulska AM, Korczyn AD, Bisulli F, Di Bonaventura C, Ragona F,
Michelucci R, Ben-Zeev B, Straussberg R, Panzica F, Massano J, Friedman D,
Crespel A, Engelsen BA, Andermann F, Andermann E, Spodar K, Lasek-Bal A, Riguzzi
P, Pasini E, Tinuper P, Licchetta L, Gardella E, Lindenau M, Wulf A, Møller RS,
Benninger F, Afawi Z, Rubboli G, Reid CA, Maljevic S, Lerche H, Lehesjoki AE,
Petrou S, Berkovic SF. Myoclonus epilepsy and ataxia due to KCNC1 mutation:
Analysis of 20 cases and K+ channel properties. Ann Neurol. 2017
May;81(5):677-689. doi: 10.1002/ana.24929. PMID: 28380698.
452: Longoni G, Brown RA, MomayyezSiahkal P, Elliott C, Narayanan S, Bar-Or A,
Marrie RA, Yeh EA, Filippi M, Banwell B, Arnold DL; Canadian Pediatric
Demyelinating Disease Network. White matter changes in paediatric multiple
sclerosis and monophasic demyelinating disorders. Brain. 2017 May
1;140(5):1300-1315. doi: 10.1093/brain/awx041. PMID: 28334875.
453: Wang S, Stone S, Weil AG, Fallah A, Warf BC, Ragheb J, Bhatia S, Kulkarni
AV. Comparative effectiveness of flexible versus rigid neuroendoscopy for
endoscopic third ventriculostomy and choroid plexus cauterization: a propensity
score-matched cohort and survival analysis. J Neurosurg Pediatr. 2017
May;19(5):585-591. doi: 10.3171/2016.12.PEDS16443. Epub 2017 Mar 17. PMID:
28304218.
454: Rosewich H, Sweney MT, DeBrosse S, Ess K, Ozelius L, Andermann E, Andermann
F, Andrasco G, Belgrade A, Brashear A, Ciccodicola S, Egan L, George AL Jr,
Lewelt A, Magelby J, Merida M, Newcomb T, Platt V, Poncelin D, Reyna S, Sasaki
M, Sotero de Menezes M, Sweadner K, Viollet L, Zupanc M, Silver K, Swoboda K.
Research conference summary from the 2014 International Task Force on
ATP1A3-Related Disorders. Neurol Genet. 2017 Mar 2;3(2):e139. doi:
10.1212/NXG.0000000000000139. PMID: 28293679; PMCID: PMC5335249.
455: Yang GZ, Cambias J, Cleary K, Daimler E, Drake J, Dupont PE, Hata N,
Kazanzides P, Martel S, Patel RV, Santos VJ, Taylor RH. Medical robotics-
Regulatory, ethical, and legal considerations for increasing levels of autonomy.
Sci Robot. 2017 Mar 15;2(4):eaam8638. doi: 10.1126/scirobotics.aam8638. Epub
2017 Mar 15. PMID: 33157870.
456: Lee BS, Hwang LS, Doumit GD, Wooley J, Papay FA, Luciano MG, Recinos VM.
Management options of non-syndromic sagittal craniosynostosis. J Clin Neurosci.
2017 May;39:28-34. doi: 10.1016/j.jocn.2017.02.042. Epub 2017 Mar 6. PMID:
28279556.
457: Marsh AP, Heron D, Edwards TJ, Quartier A, Galea C, Nava C, Rastetter A,
Moutard ML, Anderson V, Bitoun P, Bunt J, Faudet A, Garel C, Gillies G, Gobius
I, Guegan J, Heide S, Keren B, Lesne F, Lukic V, Mandelstam SA, McGillivray G,
McIlroy A, Méneret A, Mignot C, Morcom LR, Odent S, Paolino A, Pope K, Riant F,
Robinson GA, Spencer-Smith M, Srour M, Stephenson SE, Tankard R, Trouillard O,
Welniarz Q, Wood A, Brice A, Rouleau G, Attié-Bitach T, Delatycki MB, Mandel JL,
Amor DJ, Roze E, Piton A, Bahlo M, Billette de Villemeur T, Sherr EH, Leventer
RJ, Richards LJ, Lockhart PJ, Depienne C. Mutations in DCC cause isolated
agenesis of the corpus callosum with incomplete penetrance. Nat Genet. 2017
Apr;49(4):511-514. doi: 10.1038/ng.3794. Epub 2017 Feb 27. PMID: 28250454;
PMCID: PMC5894478.
458: Yea C, Bitnun A, Robinson J, Mineyko A, Barton M, Mah JK, Vajsar J,
Richardson S, Licht C, Brophy J, Crone M, Desai S, Hukin J, Jones K, Muir K,
Pernica JM, Pless R, Pohl D, Rafay MF, Selby K, Venkateswaran S, Bernard G, Yeh
EA. Longitudinal Outcomes in the 2014 Acute Flaccid Paralysis Cluster in Canada.
J Child Neurol. 2017 Mar;32(3):301-307. doi: 10.1177/0883073816680770. Epub 2016
Dec 20. PMID: 28193112.
459: Sola C, Vega E, Ingelmo P. TAP block in neonates: need to think beyond
effectiveness. Minerva Anestesiol. 2017 Mar;83(3):242-243. doi:
10.23736/S0375-9393.17.11848-1. Epub 2017 Jan 25. PMID: 28124865.
460: Gauvin M, Dorfman AL, Trang N, Gauthier M, Little JM, Lina JM, Lachapelle
P. Assessing the Contribution of the Oscillatory Potentials to the Genesis of
the Photopic ERG with the Discrete Wavelet Transform. Biomed Res Int.
2016;2016:2790194. doi: 10.1155/2016/2790194. Epub 2016 Dec 22. PMID: 28101507;
PMCID: PMC5217158.
461: Hibar DP, Adams HHH, Jahanshad N, Chauhan G, Stein JL, Hofer E, Renteria
ME, Bis JC, Arias-Vasquez A, Ikram MK, Desrivières S, Vernooij MW, Abramovic L,
Alhusaini S, Amin N, Andersson M, Arfanakis K, Aribisala BS, Armstrong NJ,
Athanasiu L, Axelsson T, Beecham AH, Beiser A, Bernard M, Blanton SH, Bohlken
MM, Boks MP, Bralten J, Brickman AM, Carmichael O, Chakravarty MM, Chen Q, Ching
CRK, Chouraki V, Cuellar-Partida G, Crivello F, Den Braber A, Doan NT, Ehrlich
S, Giddaluru S, Goldman AL, Gottesman RF, Grimm O, Griswold ME, Guadalupe T,
Gutman BA, Hass J, Haukvik UK, Hoehn D, Holmes AJ, Hoogman M, Janowitz D, Jia T,
Jørgensen KN, Karbalai N, Kasperaviciute D, Kim S, Klein M, Kraemer B, Lee PH,
Liewald DCM, Lopez LM, Luciano M, Macare C, Marquand AF, Matarin M, Mather KA,
Mattheisen M, McKay DR, Milaneschi Y, Muñoz Maniega S, Nho K, Nugent AC, Nyquist
P, Loohuis LMO, Oosterlaan J, Papmeyer M, Pirpamer L, Pütz B, Ramasamy A,
Richards JS, Risacher SL, Roiz-Santiañez R, Rommelse N, Ropele S, Rose EJ, Royle
NA, Rundek T, Sämann PG, Saremi A, Satizabal CL, Schmaal L, Schork AJ, Shen L,
Shin J, Shumskaya E, Smith AV, Sprooten E, Strike LT, Teumer A, Tordesillas-
Gutierrez D, Toro R, Trabzuni D, Trompet S, Vaidya D, Van der Grond J, Van der
Lee SJ, Van der Meer D, Van Donkelaar MMJ, Van Eijk KR, Van Erp TGM, Van Rooij
D, Walton E, Westlye LT, Whelan CD, Windham BG, Winkler AM, Wittfeld K,
Woldehawariat G, Wolf C, Wolfers T, Yanek LR, Yang J, Zijdenbos A, Zwiers MP,
Agartz I, Almasy L, Ames D, Amouyel P, Andreassen OA, Arepalli S, Assareh AA,
Barral S, Bastin ME, Becker DM, Becker JT, Bennett DA, Blangero J, van Bokhoven
H, Boomsma DI, Brodaty H, Brouwer RM, Brunner HG, Buckner RL, Buitelaar JK,
Bulayeva KB, Cahn W, Calhoun VD, Cannon DM, Cavalleri GL, Cheng CY, Cichon S,
Cookson MR, Corvin A, Crespo-Facorro B, Curran JE, Czisch M, Dale AM, Davies GE,
De Craen AJM, De Geus EJC, De Jager PL, De Zubicaray GI, Deary IJ, Debette S,
DeCarli C, Delanty N, Depondt C, DeStefano A, Dillman A, Djurovic S, Donohoe G,
Drevets WC, Duggirala R, Dyer TD, Enzinger C, Erk S, Espeseth T, Fedko IO,
Fernández G, Ferrucci L, Fisher SE, Fleischman DA, Ford I, Fornage M, Foroud TM,
Fox PT, Francks C, Fukunaga M, Gibbs JR, Glahn DC, Gollub RL, Göring HHH, Green
RC, Gruber O, Gudnason V, Guelfi S, Håberg AK, Hansell NK, Hardy J, Hartman CA,
Hashimoto R, Hegenscheid K, Heinz A, Le Hellard S, Hernandez DG, Heslenfeld DJ,
Ho BC, Hoekstra PJ, Hoffmann W, Hofman A, Holsboer F, Homuth G, Hosten N,
Hottenga JJ, Huentelman M, Hulshoff Pol HE, Ikeda M, Jack CR Jr, Jenkinson M,
Johnson R, Jönsson EG, Jukema JW, Kahn RS, Kanai R, Kloszewska I, Knopman DS,
Kochunov P, Kwok JB, Lawrie SM, Lemaître H, Liu X, Longo DL, Lopez OL, Lovestone
S, Martinez O, Martinot JL, Mattay VS, McDonald C, McIntosh AM, McMahon FJ,
McMahon KL, Mecocci P, Melle I, Meyer-Lindenberg A, Mohnke S, Montgomery GW,
Morris DW, Mosley TH, Mühleisen TW, Müller-Myhsok B, Nalls MA, Nauck M, Nichols
TE, Niessen WJ, Nöthen MM, Nyberg L, Ohi K, Olvera RL, Ophoff RA, Pandolfo M,
Paus T, Pausova Z, Penninx BWJH, Pike GB, Potkin SG, Psaty BM, Reppermund S,
Rietschel M, Roffman JL, Romanczuk-Seiferth N, Rotter JI, Ryten M, Sacco RL,
Sachdev PS, Saykin AJ, Schmidt R, Schmidt H, Schofield PR, Sigursson S, Simmons
A, Singleton A, Sisodiya SM, Smith C, Smoller JW, Soininen H, Steen VM, Stott
DJ, Sussmann JE, Thalamuthu A, Toga AW, Traynor BJ, Troncoso J, Tsolaki M,
Tzourio C, Uitterlinden AG, Hernández MCV, Van der Brug M, van der Lugt A, van
der Wee NJA, Van Haren NEM, van 't Ent D, Van Tol MJ, Vardarajan BN, Vellas B,
Veltman DJ, Völzke H, Walter H, Wardlaw JM, Wassink TH, Weale ME, Weinberger DR,
Weiner MW, Wen W, Westman E, White T, Wong TY, Wright CB, Zielke RH, Zonderman
AB, Martin NG, Van Duijn CM, Wright MJ, Longstreth WT, Schumann G, Grabe HJ,
Franke B, Launer LJ, Medland SE, Seshadri S, Thompson PM, Ikram MA. Novel
genetic loci associated with hippocampal volume. Nat Commun. 2017 Jan
18;8:13624. doi: 10.1038/ncomms13624. PMID: 28098162; PMCID: PMC5253632.
462: Gauvin M, Sustar M, Little JM, Brecelj J, Lina JM, Lachapelle P.
Quantifying the ON and OFF Contributions to the Flash ERG with the Discrete
Wavelet Transform. Transl Vis Sci Technol. 2017 Jan 10;6(1):3. doi:
10.1167/tvst.6.1.3. PMID: 28097047; PMCID: PMC5235331.
463: Vezina N, Al-Halabi B, Shash H, Dudley RR, Gilardino MS. A Review of
Techniques Used in the Management of Growing Skull Fractures. J Craniofac Surg.
2017 May;28(3):604-609. doi: 10.1097/SCS.0000000000003379. PMID: 28060103.
464: Nguyen TV, Lew J, Albaugh MD, Botteron KN, Hudziak JJ, Fonov VS, Collins
DL, Ducharme S, McCracken JT. Sex-specific associations of testosterone with
prefrontal-hippocampal development and executive function.
Psychoneuroendocrinology. 2017 Feb;76:206-217. doi:
10.1016/j.psyneuen.2016.12.005. Epub 2016 Dec 8. PMID: 27984812; PMCID:
PMC5272813.
465: Weil AG, Wang AC, Westwick HJ, Ibrahim GM, Ariani RT, Crevier L, Perreault
S, Davidson T, Tseng CH, Fallah A. Survival in pediatric medulloblastoma: a
population-based observational study to improve prognostication. J Neurooncol.
2017 Mar;132(1):99-107. doi: 10.1007/s11060-016-2341-4. Epub 2016 Dec 15. PMID:
27981412.
466: Torchia J, Golbourn B, Feng S, Ho KC, Sin-Chan P, Vasiljevic A, Norman JD,
Guilhamon P, Garzia L, Agamez NR, Lu M, Chan TS, Picard D, de Antonellis P,
Khuong-Quang DA, Planello AC, Zeller C, Barsyte-Lovejoy D, Lafay-Cousin L,
Letourneau L, Bourgey M, Yu M, Gendoo DMA, Dzamba M, Barszczyk M, Medina T,
Riemenschneider AN, Morrissy AS, Ra YS, Ramaswamy V, Remke M, Dunham CP, Yip S,
Ng HK, Lu JQ, Mehta V, Albrecht S, Pimentel J, Chan JA, Somers GR, Faria CC,
Roque L, Fouladi M, Hoffman LM, Moore AS, Wang Y, Choi SA, Hansford JR,
Catchpoole D, Birks DK, Foreman NK, Strother D, Klekner A, Bognár L, Garami M,
Hauser P, Hortobágyi T, Wilson B, Hukin J, Carret AS, Van Meter TE, Hwang EI,
Gajjar A, Chiou SH, Nakamura H, Toledano H, Fried I, Fults D, Wataya T, Fryer C,
Eisenstat DD, Scheinemann K, Fleming AJ, Johnston DL, Michaud J, Zelcer S,
Hammond R, Afzal S, Ramsay DA, Sirachainan N, Hongeng S, Larbcharoensub N,
Grundy RG, Lulla RR, Fangusaro JR, Druker H, Bartels U, Grant R, Malkin D,
McGlade CJ, Nicolaides T, Tihan T, Phillips J, Majewski J, Montpetit A, Bourque
G, Bader GD, Reddy AT, Gillespie GY, Warmuth-Metz M, Rutkowski S, Tabori U,
Lupien M, Brudno M, Schüller U, Pietsch T, Judkins AR, Hawkins CE, Bouffet E,
Kim SK, Dirks PB, Taylor MD, Erdreich-Epstein A, Arrowsmith CH, De Carvalho DD,
Rutka JT, Jabado N, Huang A. Integrated (epi)-Genomic Analyses Identify
Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors. Cancer Cell. 2016
Dec 12;30(6):891-908. doi: 10.1016/j.ccell.2016.11.003. PMID: 27960086; PMCID:
PMC5500911.
467: Chrestian N, Dupré N, Gan-Or Z, Szuto A, Chen S, Venkitachalam A, Brisson
JD, Warman-Chardon J, Ahmed S, Ashtiani S, MacDonald H, Mohsin N, Mourabit-Amari
K, Provencher P, Boycott KM, Stavropoulos DJ, Dion PA, Ray PN, Suchowersky O,
Rouleau GA, Yoon G. Clinical and genetic study of hereditary spastic paraplegia
in Canada. Neurol Genet. 2016 Dec 5;3(1):e122. doi:
10.1212/NXG.0000000000000122. PMID: 27957547; PMCID: PMC5141523.
468: Foveau B, Albrecht S, Bennett DA, Correa JA, LeBlanc AC. Increased
Caspase-6 activity in the human anterior olfactory nuclei of the olfactory bulb
is associated with cognitive impairment. Acta Neuropathol Commun. 2016 Dec
8;4(1):127. doi: 10.1186/s40478-016-0400-x. PMID: 27931265; PMCID: PMC5146837.
469: Trickey K, Hornby L, Shemie SD, Teitelbaum J. Mechanism of Death after
Decompressive Craniectomy in Non-Traumatic Brain Injury. Can J Neurol Sci. 2017
Jan;44(1):112-115. doi: 10.1017/cjn.2016.320. Epub 2016 Dec 5. PMID: 27917726.
470: Xue D, Kaufman GN, Dembele M, Beland M, Massoud AH, Mindt BC, Fiter R,
Fixman ED, Martin JG, Friedel RH, Divangahi M, Fritz JH, Mazer BD. Semaphorin 4C
Protects against Allergic Inflammation: Requirement of Regulatory CD138+ Plasma
Cells. J Immunol. 2017 Jan 1;198(1):71-81. doi: 10.4049/jimmunol.1600831. Epub
2016 Nov 23. PMID: 27881703.
471: Burstein B, Fauteux-Lamarre E, Cheng A, Chalut D, Bretholz A. Simulation
and Web-based learning increases utilization of Bier block for forearm fracture
reduction in the pediatric emergency department. CJEM. 2017 Nov;19(6):434-440.
doi: 10.1017/cem.2016.392. Epub 2016 Nov 21. PMID: 27866507.
472: Ulrick N, Goldstein A, Simons C, Taft RJ, Helman G, Pizzino A, Bloom M,
Vogt J, Pysden K, Diodato D, Martinelli D, Monavari A, Buhas D, van Karnebeek
CD, Dorboz I, Boespflug-Tanguy O, Rodriguez D, Tétreault M, Majewski J, Bernard
G, Ng YS; Care4Rare Canada Consortium, McFarland R, Vanderver A. RMND1-Related
Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss-Another Mendelian
Mimicker of Congenital Cytomegalovirus Infection. Pediatr Neurol. 2017
Jan;66:59-62. doi: 10.1016/j.pediatrneurol.2016.09.003. Epub 2016 Sep 13. PMID:
27843092.
473: Hughes DA, Nicholls K, Shankar SP, Sunder-Plassmann G, Koeller D, Nedd K,
Vockley G, Hamazaki T, Lachmann R, Ohashi T, Olivotto I, Sakai N, Deegan P,
Dimmock D, Eyskens F, Germain DP, Goker-Alpan O, Hachulla E, Jovanovic A,
Lourenco CM, Narita I, Thomas M, Wilcox WR, Bichet DG, Schiffmann R, Ludington
E, Viereck C, Kirk J, Yu J, Johnson F, Boudes P, Benjamin ER, Lockhart DJ,
Barlow C, Skuban N, Castelli JP, Barth J, Feldt-Rasmussen U. Oral
pharmacological chaperone migalastat compared with enzyme replacement therapy in
Fabry disease: 18-month results from the randomised phase III ATTRACT study. J
Med Genet. 2017 Apr;54(4):288-296. doi: 10.1136/jmedgenet-2016-104178. Epub 2016
Nov 10. Erratum in: J Med Genet. 2018 Apr 16;: PMID: 27834756; PMCID:
PMC5502308.
474: Müller SH, Girard SL, Hopfner F, Merner ND, Bourassa CV, Lorenz D, Clark
LN, Tittmann L, Soto-Ortolaza AI, Klebe S, Hallett M, Schneider SA, Hodgkinson
CA, Lieb W, Wszolek ZK, Pendziwiat M, Lorenzo-Betancor O, Poewe W, Ortega-Cubero
S, Seppi K, Rajput A, Hussl A, Rajput AH, Berg D, Dion PA, Wurster I, Shulman
JM, Srulijes K, Haubenberger D, Pastor P, Vilariño-Güell C, Postuma RB, Bernard
G, Ladwig KH, Dupré N, Jankovic J, Strauch K, Panisset M, Winkelmann J, Testa
CM, Reischl E, Zeuner KE, Ross OA, Arzberger T, Chouinard S, Deuschl G, Louis
ED, Kuhlenbäumer G, Rouleau GA. Genome-wide association study in essential
tremor identifies three new loci. Brain. 2016 Dec;139(Pt 12):3163-3169. doi:
10.1093/brain/aww242. Epub 2016 Oct 20. PMID: 27797806; PMCID: PMC5382938.
475: Adams HH, Hibar DP, Chouraki V, Stein JL, Nyquist PA, Rentería ME, Trompet
S, Arias-Vasquez A, Seshadri S, Desrivières S, Beecham AH, Jahanshad N, Wittfeld
K, Van der Lee SJ, Abramovic L, Alhusaini S, Amin N, Andersson M, Arfanakis K,
Aribisala BS, Armstrong NJ, Athanasiu L, Axelsson T, Beiser A, Bernard M, Bis
JC, Blanken LM, Blanton SH, Bohlken MM, Boks MP, Bralten J, Brickman AM,
Carmichael O, Chakravarty MM, Chauhan G, Chen Q, Ching CR, Cuellar-Partida G,
Braber AD, Doan NT, Ehrlich S, Filippi I, Ge T, Giddaluru S, Goldman AL,
Gottesman RF, Greven CU, Grimm O, Griswold ME, Guadalupe T, Hass J, Haukvik UK,
Hilal S, Hofer E, Hoehn D, Holmes AJ, Hoogman M, Janowitz D, Jia T,
Kasperaviciute D, Kim S, Klein M, Kraemer B, Lee PH, Liao J, Liewald DC, Lopez
LM, Luciano M, Macare C, Marquand A, Matarin M, Mather KA, Mattheisen M, Mazoyer
B, McKay DR, McWhirter R, Milaneschi Y, Mirza-Schreiber N, Muetzel RL, Maniega
SM, Nho K, Nugent AC, Loohuis LM, Oosterlaan J, Papmeyer M, Pappa I, Pirpamer L,
Pudas S, Pütz B, Rajan KB, Ramasamy A, Richards JS, Risacher SL, Roiz-Santiañez
R, Rommelse N, Rose EJ, Royle NA, Rundek T, Sämann PG, Satizabal CL, Schmaal L,
Schork AJ, Shen L, Shin J, Shumskaya E, Smith AV, Sprooten E, Strike LT, Teumer
A, Thomson R, Tordesillas-Gutierrez D, Toro R, Trabzuni D, Vaidya D, Van der
Grond J, Van der Meer D, Van Donkelaar MM, Van Eijk KR, Van Erp TG, Van Rooij D,
Walton E, Westlye LT, Whelan CD, Windham BG, Winkler AM, Woldehawariat G, Wolf
C, Wolfers T, Xu B, Yanek LR, Yang J, Zijdenbos A, Zwiers MP, Agartz I, Aggarwal
NT, Almasy L, Ames D, Amouyel P, Andreassen OA, Arepalli S, Assareh AA, Barral
S, Bastin ME, Becker DM, Becker JT, Bennett DA, Blangero J, van Bokhoven H,
Boomsma DI, Brodaty H, Brouwer RM, Brunner HG, Buckner RL, Buitelaar JK,
Bulayeva KB, Cahn W, Calhoun VD, Cannon DM, Cavalleri GL, Chen C, Cheng CY,
Cichon S, Cookson MR, Corvin A, Crespo-Facorro B, Curran JE, Czisch M, Dale AM,
Davies GE, De Geus EJ, De Jager PL, de Zubicaray GI, Delanty N, Depondt C,
DeStefano AL, Dillman A, Djurovic S, Donohoe G, Drevets WC, Duggirala R, Dyer
TD, Erk S, Espeseth T, Evans DA, Fedko IO, Fernández G, Ferrucci L, Fisher SE,
Fleischman DA, Ford I, Foroud TM, Fox PT, Francks C, Fukunaga M, Gibbs JR, Glahn
DC, Gollub RL, Göring HH, Grabe HJ, Green RC, Gruber O, Gudnason V, Guelfi S,
Hansell NK, Hardy J, Hartman CA, Hashimoto R, Hegenscheid K, Heinz A, Le Hellard
S, Hernandez DG, Heslenfeld DJ, Ho BC, Hoekstra PJ, Hoffmann W, Hofman A,
Holsboer F, Homuth G, Hosten N, Hottenga JJ, Hulshoff Pol HE, Ikeda M, Ikram MK,
Jack CR Jr, Jenkinson M, Johnson R, Jönsson EG, Jukema JW, Kahn RS, Kanai R,
Kloszewska I, Knopman DS, Kochunov P, Kwok JB, Lawrie SM, Lemaître H, Liu X,
Longo DL, Longstreth WT Jr, Lopez OL, Lovestone S, Martinez O, Martinot JL,
Mattay VS, McDonald C, McIntosh AM, McMahon KL, McMahon FJ, Mecocci P, Melle I,
Meyer-Lindenberg A, Mohnke S, Montgomery GW, Morris DW, Mosley TH, Mühleisen TW,
Müller-Myhsok B, Nalls MA, Nauck M, Nichols TE, Niessen WJ, Nöthen MM, Nyberg L,
Ohi K, Olvera RL, Ophoff RA, Pandolfo M, Paus T, Pausova Z, Penninx BW, Pike GB,
Potkin SG, Psaty BM, Reppermund S, Rietschel M, Roffman JL, Romanczuk-Seiferth
N, Rotter JI, Ryten M, Sacco RL, Sachdev PS, Saykin AJ, Schmidt R, Schofield PR,
Sigurdsson S, Simmons A, Singleton A, Sisodiya SM, Smith C, Smoller JW, Soininen
H, Srikanth V, Steen VM, Stott DJ, Sussmann JE, Thalamuthu A, Tiemeier H, Toga
AW, Traynor BJ, Troncoso J, Turner JA, Tzourio C, Uitterlinden AG, Hernández MC,
Van der Brug M, Van der Lugt A, Van der Wee NJ, Van Duijn CM, Van Haren NE, Van
T Ent D, Van Tol MJ, Vardarajan BN, Veltman DJ, Vernooij MW, Völzke H, Walter H,
Wardlaw JM, Wassink TH, Weale ME, Weinberger DR, Weiner MW, Wen W, Westman E,
White T, Wong TY, Wright CB, Zielke HR, Zonderman AB, Deary IJ, DeCarli C,
Schmidt H, Martin NG, De Craen AJ, Wright MJ, Launer LJ, Schumann G, Fornage M,
Franke B, Debette S, Medland SE, Ikram MA, Thompson PM. Novel genetic loci
underlying human intracranial volume identified through genome-wide association.
Nat Neurosci. 2016 Dec;19(12):1569-1582. doi: 10.1038/nn.4398. Epub 2016 Oct 3.
PMID: 27694991; PMCID: PMC5227112.
476: Weil AG, Westwick H, Wang S, Alotaibi NM, Elkaim L, Ibrahim GM, Wang AC,
Ariani RT, Crevier L, Myers B, Fallah A. Efficacy and safety of endoscopic third
ventriculostomy and choroid plexus cauterization for infantile hydrocephalus: a
systematic review and meta-analysis. Childs Nerv Syst. 2016
Nov;32(11):2119-2131. doi: 10.1007/s00381-016-3236-6. Epub 2016 Sep 9. PMID:
27613635.
477: Garzon MC, Epstein LG, Heyer GL, Frommelt PC, Orbach DB, Baylis AL, Blei F,
Burrows PE, Chamlin SL, Chun RH, Hess CP, Joachim S, Johnson K, Kim W, Liang MG,
Maheshwari M, McCoy GN, Metry DW, Monrad PA, Pope E, Powell J, Shwayder TA,
Siegel DH, Tollefson MM, Vadivelu S, Lew SM, Frieden IJ, Drolet BA. PHACE
Syndrome: Consensus-Derived Diagnosis and Care Recommendations. J Pediatr. 2016
Nov;178:24-33.e2. doi: 10.1016/j.jpeds.2016.07.054. Epub 2016 Sep 19. PMID:
27659028; PMCID: PMC6599593.
478: Warsi NM, Lasry O, Farah A, Saint-Martin C, Montes JL, Atkinson J, Farmer
JP, Dudley RW. 3-T intraoperative MRI (iMRI) for pediatric epilepsy surgery.
Childs Nerv Syst. 2016 Dec;32(12):2415-2422. doi: 10.1007/s00381-016-3263-3.
Epub 2016 Oct 18. PMID: 27757571.
479: Pal GD, Hall D, Ouyang B, Phelps J, Alcalay R, Pauciulo MW, Nichols WC,
Clark L, Mejia-Santana H, Blasucci L, Goetz CG, Comella C, Colcher A, Gan-Or Z,
Rouleau GA, Marder K; Consortium on Risk for Early Onset Parkinson's Disease
(CORE-PD) Investigators. Genetic and Clinical Predictors of Deep Brain
Stimulation in Young-Onset Parkinson's Disease. Mov Disord Clin Pract. 2016 Sep-
Oct;3(5):465-471. doi: 10.1002/mdc3.12309. Epub 2016 Jan 18. PMID: 27709117;
PMCID: PMC5047521.
480: Jayakar P, Gotman J, Harvey AS, Palmini A, Tassi L, Schomer D, Dubeau F,
Bartolomei F, Yu A, Kršek P, Velis D, Kahane P. Diagnostic utility of invasive
EEG for epilepsy surgery: Indications, modalities, and techniques. Epilepsia.
2016 Nov;57(11):1735-1747. doi: 10.1111/epi.13515. Epub 2016 Sep 28. PMID:
27677490.
481: Albaladejo P, Bonhomme F, Blais N, Collet JP, Faraoni D, Fontana P, Godier
A, Llau J, Longrois D, Marret E, Mismetti P, Rosencher N, Roullet S, Samama CM,
Schved JF, Sié P, Steib A, Susen S; French Working Group on Perioperative
Hemostasis (GIHP). Management of direct oral anticoagulants in patients
undergoing elective surgeries and invasive procedures: Updated guidelines from
the French Working Group on Perioperative Hemostasis (GIHP) - September 2015.
Anaesth Crit Care Pain Med. 2017 Feb;36(1):73-76. doi:
10.1016/j.accpm.2016.09.002. Epub 2016 Sep 20. PMID: 27659969.
482: Harel T, Yoon WH, Garone C, Gu S, Coban-Akdemir Z, Eldomery MK, Posey JE,
Jhangiani SN, Rosenfeld JA, Cho MT, Fox S, Withers M, Brooks SM, Chiang T,
Duraine L, Erdin S, Yuan B, Shao Y, Moussallem E, Lamperti C, Donati MA, Smith
JD, McLaughlin HM, Eng CM, Walkiewicz M, Xia F, Pippucci T, Magini P, Seri M,
Zeviani M, Hirano M, Hunter JV, Srour M, Zanigni S, Lewis RA, Muzny DM, Lotze
TE, Boerwinkle E; Baylor-Hopkins Center for Mendelian Genomics; University of
Washington Center for Mendelian Genomics, Gibbs RA, Hickey SE, Graham BH, Yang
Y, Buhas D, Martin DM, Potocki L, Graziano C, Bellen HJ, Lupski JR. Recurrent De
Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane
Protein, Results in Distinct Neurological Syndromes. Am J Hum Genet. 2016 Oct
6;99(4):831-845. doi: 10.1016/j.ajhg.2016.08.007. Epub 2016 Sep 15. PMID:
27640307; PMCID: PMC5065660.
483: Aljared T, Farmer JP, Tampieri D. Feasibility and value of preoperative
embolization of a congenital choroid plexus tumour in the premature infant: An
illustrative case report with technical details. Interv Neuroradiol. 2016
Dec;22(6):732-735. doi: 10.1177/1591019916665346. Epub 2016 Sep 7. PMID:
27605545; PMCID: PMC5564368.
484: Jung S, Johnstone A, Khoja Z, Rampakakis E, Lachapelle P, Wintermark P.
Sildenafil Improves Functional and Structural Outcome of Retinal Injury
Following Term Neonatal Hypoxia-Ischemia. Invest Ophthalmol Vis Sci. 2016 Aug
1;57(10):4306-14. doi: 10.1167/iovs.16-19385. PMID: 27552408.
485: Thiffault I, Bernard G. Expert opinion and caution are imperative for
interpretation of next generation sequencing data. Eur J Med Genet. 2016
Oct;59(10):519-21. doi: 10.1016/j.ejmg.2016.08.002. Epub 2016 Aug 12. PMID:
27535217.
486: Sharpee TO, Destexhe A, Kawato M, Sekulić V, Skinner FK, Wójcik DK,
Chintaluri C, Cserpán D, Somogyvári Z, Kim JK, Kilpatrick ZP, Bennett MR, Josić
K, Elices I, Arroyo D, Levi R, Rodriguez FB, Varona P, Hwang E, Kim B, Han HB,
Kim T, McKenna JT, Brown RE, McCarley RW, Choi JH, Rankin J, Popp PO, Rinzel J,
Tabas A, Rupp A, Balaguer-Ballester E, Maturana MI, Grayden DB, Cloherty SL,
Kameneva T, Ibbotson MR, Meffin H, Koren V, Lochmann T, Dragoi V, Obermayer K,
Psarrou M, Schilstra M, Davey N, Torben-Nielsen B, Steuber V, Ju H, Yu J, Hines
ML, Chen L, Yu Y, Kim J, Leahy W, Shlizerman E, Birgiolas J, Gerkin RC, Crook
SM, Viriyopase A, Memmesheimer RM, Gielen S, Dabaghian Y, DeVito J, Perotti L,
Kim AJ, Fenk LM, Cheng C, Maimon G, Zhao C, Widmer Y, Sprecher S, Senn W, Halnes
G, Mäki-Marttunen T, Keller D, Pettersen KH, Andreassen OA, Einevoll GT, Yamada
Y, Steyn-Ross ML, Alistair Steyn-Ross D, Mejias JF, Murray JD, Kennedy H, Wang
XJ, Kruscha A, Grewe J, Benda J, Lindner B, Badel L, Ohta K, Tsuchimoto Y,
Kazama H, Kahng B, Tam ND, Pollonini L, Zouridakis G, Soh J, Kim D, Yoo M,
Palmer SE, Culmone V, Bojak I, Ferrario A, Merrison-Hort R, Borisyuk R, Kim CS,
Tezuka T, Joo P, Rho YA, Burton SD, Bard Ermentrout G, Jeong J, Urban NN,
Marsalek P, Kim HH, Moon SH, Lee DW, Lee SB, Lee JY, Molkov YI, Hamade K, Teka
W, Barnett WH, Kim T, Markin S, Rybak IA, Forro C, Dermutz H, Demkó L, Vörös J,
Babichev A, Huang H, Verduzco-Flores S, Dos Santos F, Andras P, Metzner C,
Schweikard A, Zurowski B, Roach JP, Sander LM, Zochowski MR, Skilling QM,
Ognjanovski N, Aton SJ, Zochowski M, Wang SJ, Ouyang G, Guang J, Zhang M,
Michael Wong KY, Zhou C, Robinson PA, Sanz-Leon P, Drysdale PM, Fung F,
Abeysuriya RG, Rennie CJ, Zhao X, Choe Y, Yang HF, Mi Y, Lin X, Wu S, Liedtke J,
Schottdorf M, Wolf F, Yamamura Y, Wickens JR, Rumbell T, Ramsey J, Reyes A,
Draguljić D, Hof PR, Luebke J, Weaver CM, He H, Yang X, Ma H, Xu Z, Wang Y, Baek
K, Morris LS, Kundu P, Voon V, Agnes EJ, Vogels TP, Podlaski WF, Giese M, Kuravi
P, Vogels R, Seeholzer A, Podlaski W, Ranjan R, Vogels T, Torres JJ, Baroni F,
Latorre R, Gips B, Lowet E, Roberts MJ, de Weerd P, Jensen O, van der Eerden J,
Goodarzinick A, Niry MD, Valizadeh A, Pariz A, Parsi SS, Warburton JM, Marucci
L, Tamagnini F, Brown J, Tsaneva-Atanasova K, Kleberg FI, Triesch J, Moezzi B,
Iannella N, Schaworonkow N, Plogmacher L, Goldsworthy MR, Hordacre B, McDonnell
MD, Ridding MC, Zapotocky M, Smit D, Fouquet C, Trembleau A, Dasgupta S,
Nishikawa I, Aihara K, Toyoizumi T, Robb DT, Mellen N, Toporikova N, Tang R,
Tang YY, Liang G, Kiser SA, Howard JH Jr, Goncharenko J, Voronenko SO, Ahamed T,
Stephens G, Yger P, Lefebvre B, Spampinato GLB, Esposito E, et Olivier Marre MS,
Choi H, Song MH, Chung S, Lee DD, Sompolinsky H, Phillips RS, Smith J,
Chatzikalymniou AP, Ferguson K, Alex Cayco Gajic N, Clopath C, Angus Silver R,
Gleeson P, Marin B, Sadeh S, Quintana A, Cantarelli M, Dura-Bernal S, Lytton WW,
Davison A, Li L, Zhang W, Wang D, Song Y, Park S, Choi I, Shin HS, Choi H,
Pasupathy A, Shea-Brown E, Huh D, Sejnowski TJ, Vogt SM, Kumar A, Schmidt R, Van
Wert S, Schiff SJ, Veale R, Scheutz M, Lee SW, Gallinaro J, Rotter S, Rubchinsky
LL, Cheung CC, Ratnadurai-Giridharan S, Shomali SR, Ahmadabadi MN, Shimazaki H,
Nader Rasuli S, Zhao X, Rasch MJ, Wilting J, Priesemann V, Levina A, Rudelt L,
Lizier JT, Spinney RE, Rubinov M, Wibral M, Bak JH, Pillow J, Zaho Y, Park IM,
Kang J, Park HJ, Jang J, Paik SB, Choi W, Lee C, Song M, Lee H, Park Y, Yilmaz
E, Baysal V, Ozer M, Saska D, Nowotny T, Chan HK, Diamond A, Herrmann CS, Murray
MM, Ionta S, Hutt A, Lefebvre J, Weidel P, Duarte R, Morrison A, Lee JH, Iyer R,
Mihalas S, Koch C, Petrovici MA, Leng L, Breitwieser O, Stöckel D, Bytschok I,
Martel R, Bill J, Schemmel J, Meier K, Esler TB, Burkitt AN, Kerr RR, Tahayori
B, Nolte M, Reimann MW, Muller E, Markram H, Parziale A, Senatore R, Marcelli A,
Skiker K, Maouene M, Neymotin SA, Seidenstein A, Lakatos P, Sanger TD, Menzies
RJ, McLauchlan C, van Albada SJ, Kedziora DJ, Neymotin S, Kerr CC, Suter BA,
Shepherd GMG, Ryu J, Lee SH, Lee J, Lee HJ, Lim D, Wang J, Lee H, Jung N, Anh
Quang L, Maeng SE, Lee TH, Lee JW, Park CH, Ahn S, Moon J, Choi YS, Kim J, Jun
SB, Lee S, Lee HW, Jo S, Jun E, Yu S, Goetze F, Lai PY, Kim S, Kwag J, Jang HJ,
Filipović M, Reig R, Aertsen A, Silberberg G, Bachmann C, Buttler S, Jacobs H,
Dillen K, Fink GR, Kukolja J, Kepple D, Giaffar H, Rinberg D, Shea S, Koulakov
A, Bahuguna J, Tetzlaff T, Kotaleski JH, Kunze T, Peterson A, Knösche T, Kim M,
Kim H, Park JS, Yeon JW, Kim SP, Kang JH, Lee C, Spiegler A, Petkoski S, Palva
MJ, Jirsa VK, Saggio ML, Siep SF, Stacey WC, Bernar C, Choung OH, Jeong Y, Lee
YI, Kim SH, Jeong M, Lee J, Kwon J, Kralik JD, Jahng J, Hwang DU, Kwon JH, Park
SM, Kim S, Kim H, Kim PS, Yoon S, Lim S, Park C, Miller T, Clements K, Ahn S, Ji
EH, Issa FA, Baek J, Oba S, Yoshimoto J, Doya K, Ishii S, Mosqueiro TS, Strube-
Bloss MF, Smith B, Huerta R, Hadrava M, Hlinka J, Bos H, Helias M, Welzig CM,
Harper ZJ, Kim WS, Shin IS, Baek HM, Han SK, Richter R, Vitay J, Beuth F, Hamker
FH, Toppin K, Guo Y, Graham BP, Kale PJ, Gollo LL, Stern M, Abbott LF, Fedorov
LA, Giese MA, Ardestani MH, Faraji MJ, Preuschoff K, Gerstner W, van Gendt MJ,
Briaire JJ, Kalkman RK, Frijns JHM, Lee WH, Frangou S, Fulcher BD, Tran PHP,
Fornito A, Gliske SV, Lim E, Holman KA, Fink CG, Kim JS, Mu S, Briggman KL,
Sebastian Seung H; the EyeWirers, Wegener D, Bohnenkamp L, Ernst UA, Devor A,
Dale AM, Lines GT, Edwards A, Tveito A, Hagen E, Senk J, Diesmann M, Schmidt M,
Bakker R, Shen K, Bezgin G, Hilgetag CC, van Albada SJ, Sun H, Sourina O, Huang
GB, Klanner F, Denk C, Glomb K, Ponce-Alvarez A, Gilson M, Ritter P, Deco G,
Witek MAG, Clarke EF, Hansen M, Wallentin M, Kringelbach ML, Vuust P, Klingbeil
G, De Schutter E, Chen W, Zang Y, Hong S, Takashima A, Zamora C, Gallimore AR,
Goldschmidt D, Manoonpong P, Karoly PJ, Freestone DR, Soundry D, Kuhlmann L,
Paninski L, Cook M, Lee J, Fishman YI, Cohen YE, Roberts JA, Cocchi L, Sweeney
Y, Lee S, Jung WS, Kim Y, Jung Y, Song YK, Chavane F, Soman K, Muralidharan V,
Srinivasa Chakravarthy V, Shivkumar S, Mandali A, Pragathi Priyadharsini B,
Mehta H, Davey CE, Brinkman BAW, Kekona T, Rieke F, Buice M, De Pittà M, Berry
H, Brunel N, Breakspear M, Marsat G, Drew J, Chapman PD, Daly KC, Bradle SP, Seo
SB, Su J, Kavalali ET, Blackwell J, Shiau L, Buhry L, Basnayake K, Lee SH, Levy
BA, Baker CI, Leleu T, Philips RT, Chhabria K. 25th Annual Computational
Neuroscience Meeting: CNS-2016. BMC Neurosci. 2016 Aug 18;17 Suppl 1(Suppl
1):54. doi: 10.1186/s12868-016-0283-6. PMID: 27534393; PMCID: PMC5001212.
487: Lechpammer M, Tran YP, Wintermark P, Martínez-Cerdeño V, Krishnan VV, Ahmed
W, Berman RF, Jensen FE, Nudler E, Zagzag D. Upregulation of cystathionine
β-synthase and p70S6K/S6 in neonatal hypoxic ischemic brain injury. Brain
Pathol. 2017 Jul;27(4):449-458. doi: 10.1111/bpa.12421. Epub 2016 Aug 28.
Erratum in: Brain Pathol. 2017 Nov;27(6):856. PMID: 27465493; PMCID: PMC8028969.
488: Dudley RW, Torok MR, Hoffman L, Levy JM, Handler MH, Liu AK, Hankinson TC.
Response to Journal Club: Pediatric Low-Grade Ganglioglioma: Epidemiology,
Treatments, and Outcome Analysis of 348 Children From the Surveillance,
Epidemiology, and End Results Database. Neurosurgery. 2016 Aug;79(2):309. doi:
10.1227/NEU.0000000000001275. PMID: 27428632.
489: Lasry O, Dudley RW, Fuhrer R, Torrie J, Carlin R, Marcoux J. Traumatic
brain injury in a rural indigenous population in Canada: a community-based
approach to surveillance. CMAJ Open. 2016 May 25;4(2):E249-59. doi:
10.9778/cmajo.20150105. PMID: 27398371; PMCID: PMC4933602.
490: Baird R, Poenaru D, Ganey M, Hansen E, Emil S. Partnership in fellowship:
Comparative analysis of pediatric surgical training and evaluation of a fellow
exchange between Canada and Kenya. J Pediatr Surg. 2016 Oct;51(10):1704-10. doi:
10.1016/j.jpedsurg.2016.06.002. Epub 2016 Jun 13. PMID: 27389051.
491: Mitchell J, Berger KI, Borgo A, Braunlin EA, Burton BK, Ghotme KA, Kircher
SG, Molter D, Orchard PJ, Palmer J, Pastores GM, Rapoport DM, Wang RY, White K.
Unique medical issues in adult patients with mucopolysaccharidoses. Eur J Intern
Med. 2016 Oct;34:2-10. doi: 10.1016/j.ejim.2016.05.017. Epub 2016 Jun 11. PMID:
27296591.
492: Pana R, Hornby L, Shemie SD, Dhanani S, Teitelbaum J. Time to loss of brain
function and activity during circulatory arrest. J Crit Care. 2016 Aug;34:77-83.
doi: 10.1016/j.jcrc.2016.04.001. Epub 2016 Apr 11. PMID: 27288615.
493: Vanderver A, Simons C, Helman G, Crawford J, Wolf NI, Bernard G, Pizzino A,
Schmidt JL, Takanohashi A, Miller D, Khouzam A, Rajan V, Ramos E, Chowdhury S,
Hambuch T, Ru K, Baillie GJ, Grimmond SM, Caldovic L, Devaney J, Bloom M, Evans
SH, Murphy JLP, McNeill N, Fogel BL; Leukodystrophy Study Group, Schiffmann R,
van der Knaap MS, Taft RJ. Whole exome sequencing in patients with white matter
abnormalities. Ann Neurol. 2016 Jun;79(6):1031-1037. doi: 10.1002/ana.24650.
Epub 2016 May 9. PMID: 27159321; PMCID: PMC5354169.
494: Gauvin M, Chakor H, Koenekoop RK, Little JM, Lina JM, Lachapelle P. Erratum
to: Witnessing the first sign of retinitis pigmentosa onset in the allegedly
normal eye of a case of unilateral RP: a 30-year follow-up. Doc Ophthalmol. 2016
Jun;132(3):231. doi: 10.1007/s10633-016-9542-1. Erratum for: Doc Ophthalmol.
2016 Jun;132(3):213-229. Epub 2016 Apr 4. PMID: 27126338.
495: Srour M, Caron V, Pearson T, Nielsen SB, Lévesque S, Delrue MA, Becker TA,
Hamdan FF, Kibar Z, Sattler SG, Schneider MC, Bitoun P, Chassaing N, Rosenfeld
JA, Xia F, Desai S, Roeder E, Kimonis V, Schneider A, Littlejohn RO, Douzgou S,
Tremblay A, Michaud JL. Gain-of-Function Mutations in RARB Cause Intellectual
Disability with Progressive Motor Impairment. Hum Mutat. 2016 Aug;37(8):786-93.
doi: 10.1002/humu.23004. Epub 2016 May 9. PMID: 27120018.
496: Alsowayan O, Alzahrani A, Farmer JP, Capolicchio JP, Jednak R, El-Sherbiny
M. Comprehensive analysis of the clinical and urodynamic outcomes of primary
tethered spinal cord before and after spinal cord untethering. J Pediatr Urol.
2016 Oct;12(5):285.e1-285.e5. doi: 10.1016/j.jpurol.2016.02.012. Epub 2016 Mar
15. PMID: 27049673.
497: Nikbakht H, Panditharatna E, Mikael LG, Li R, Gayden T, Osmond M, Ho CY,
Kambhampati M, Hwang EI, Faury D, Siu A, Papillon-Cavanagh S, Bechet D, Ligon
KL, Ellezam B, Ingram WJ, Stinson C, Moore AS, Warren KE, Karamchandani J,
Packer RJ, Jabado N, Majewski J, Nazarian J. Spatial and temporal homogeneity of
driver mutations in diffuse intrinsic pontine glioma. Nat Commun. 2016 Apr
6;7:11185. doi: 10.1038/ncomms11185. PMID: 27048880; PMCID: PMC4823825.
498: Gauvin M, Chakor H, Koenekoop RK, Little JM, Lina JM, Lachapelle P.
Witnessing the first sign of retinitis pigmentosa onset in the allegedly normal
eye of a case of unilateral RP: a 30-year follow-up. Doc Ophthalmol. 2016
Jun;132(3):213-29. doi: 10.1007/s10633-016-9537-y. Epub 2016 Apr 4. Erratum in:
Doc Ophthalmol. 2016 Jun;132(3):231. PMID: 27041556.
499: La Piana R, Cayami FK, Tran LT, Guerrero K, van Spaendonk R, Õunap K,
Pajusalu S, Haack T, Wassmer E, Timmann D, Mierzewska H, Poll-Thé BT, Patel C,
Cox H, Atik T, Onay H, Ozkınay F, Vanderver A, van der Knaap MS, Wolf NI,
Bernard G. Diffuse hypomyelination is not obligate for POLR3-related disorders.
Neurology. 2016 Apr 26;86(17):1622-6. doi: 10.1212/WNL.0000000000002612. Epub
2016 Mar 30. PMID: 27029625; PMCID: PMC4844237.
500: Kahle KT, Schmouth JF, Lavastre V, Latremoliere A, Zhang J, Andrews N,
Omura T, Laganière J, Rochefort D, Hince P, Castonguay G, Gaudet R, Mapplebeck
JC, Sotocinal SG, Duan J, Ward C, Khanna AR, Mogil JS, Dion PA, Woolf CJ,
Inquimbert P, Rouleau GA. Inhibition of the kinase WNK1/HSN2 ameliorates
neuropathic pain by restoring GABA inhibition. Sci Signal. 2016 Mar
29;9(421):ra32. doi: 10.1126/scisignal.aad0163. PMID: 27025876; PMCID:
PMC5723157.
501: Thompson EM, Hielscher T, Bouffet E, Remke M, Luu B, Gururangan S, McLendon
RE, Bigner DD, Lipp ES, Perreault S, Cho YJ, Grant G, Kim SK, Lee JY, Rao AAN,
Giannini C, Li KKW, Ng HK, Yao Y, Kumabe T, Tominaga T, Grajkowska WA, Perek-
Polnik M, Low DCY, Seow WT, Chang KTE, Mora J, Pollack IF, Hamilton RL, Leary S,
Moore AS, Ingram WJ, Hallahan AR, Jouvet A, Fèvre-Montange M, Vasiljevic A,
Faure-Conter C, Shofuda T, Kagawa N, Hashimoto N, Jabado N, Weil AG, Gayden T,
Wataya T, Shalaby T, Grotzer M, Zitterbart K, Sterba J, Kren L, Hortobágyi T,
Klekner A, László B, Pócza T, Hauser P, Schüller U, Jung S, Jang WY, French PJ,
Kros JM, van Veelen MC, Massimi L, Leonard JR, Rubin JB, Vibhakar R, Chambless
LB, Cooper MK, Thompson RC, Faria CC, Carvalho A, Nunes S, Pimentel J, Fan X,
Muraszko KM, López-Aguilar E, Lyden D, Garzia L, Shih DJH, Kijima N, Schneider
C, Adamski J, Northcott PA, Kool M, Jones DTW, Chan JA, Nikolic A, Garre ML, Van
Meir EG, Osuka S, Olson JJ, Jahangiri A, Castro BA, Gupta N, Weiss WA, Moxon-
Emre I, Mabbott DJ, Lassaletta A, Hawkins CE, Tabori U, Drake J, Kulkarni A,
Dirks P, Rutka JT, Korshunov A, Pfister SM, Packer RJ, Ramaswamy V, Taylor MD.
Prognostic value of medulloblastoma extent of resection after accounting for
molecular subgroup: a retrospective integrated clinical and molecular analysis.
Lancet Oncol. 2016 Apr;17(4):484-495. doi: 10.1016/S1470-2045(15)00581-1. Epub
2016 Mar 12. Erratum in: Lancet Oncol. 2022 Feb;23(2):e59. PMID: 26976201;
PMCID: PMC4907853.
502: Zemek R, Barrowman N, Freedman SB, Gravel J, Gagnon I, McGahern C, Aglipay
M, Sangha G, Boutis K, Beer D, Craig W, Burns E, Farion KJ, Mikrogianakis A,
Barlow K, Dubrovsky AS, Meeuwisse W, Gioia G, Meehan WP 3rd, Beauchamp MH, Kamil
Y, Grool AM, Hoshizaki B, Anderson P, Brooks BL, Yeates KO, Vassilyadi M,
Klassen T, Keightley M, Richer L, DeMatteo C, Osmond MH; Pediatric Emergency
Research Canada (PERC) Concussion Team. Clinical Risk Score for Persistent
Postconcussion Symptoms Among Children With Acute Concussion in the ED. JAMA.
2016 Mar 8;315(10):1014-25. doi: 10.1001/jama.2016.1203. Erratum in: JAMA. 2016
Jun 21;315(23):2624. PMID: 26954410.
503: Rivera B, Gayden T, Carrot-Zhang J, Nadaf J, Boshari T, Faury D, Zeinieh M,
Blanc R, Burk DL, Fahiminiya S, Bareke E, Schüller U, Monoranu CM, Sträter R,
Kerl K, Niederstadt T, Kurlemann G, Ellezam B, Michalak Z, Thom M, Lockhart PJ,
Leventer RJ, Ohm M, MacGregor D, Jones D, Karamchandani J, Greenwood CM,
Berghuis AM, Bens S, Siebert R, Zakrzewska M, Liberski PP, Zakrzewski K,
Sisodiya SM, Paulus W, Albrecht S, Hasselblatt M, Jabado N, Foulkes WD, Majewski
J. Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial
tumors. Acta Neuropathol. 2016 Jun;131(6):847-63. doi:
10.1007/s00401-016-1549-x. Epub 2016 Feb 26. PMID: 26920151; PMCID: PMC5039033.
504: Sturm D, Orr BA, Toprak UH, Hovestadt V, Jones DTW, Capper D, Sill M,
Buchhalter I, Northcott PA, Leis I, Ryzhova M, Koelsche C, Pfaff E, Allen SJ,
Balasubramanian G, Worst BC, Pajtler KW, Brabetz S, Johann PD, Sahm F, Reimand
J, Mackay A, Carvalho DM, Remke M, Phillips JJ, Perry A, Cowdrey C, Drissi R,
Fouladi M, Giangaspero F, Łastowska M, Grajkowska W, Scheurlen W, Pietsch T,
Hagel C, Gojo J, Lötsch D, Berger W, Slavc I, Haberler C, Jouvet A, Holm S,
Hofer S, Prinz M, Keohane C, Fried I, Mawrin C, Scheie D, Mobley BC,
Schniederjan MJ, Santi M, Buccoliero AM, Dahiya S, Kramm CM, von Bueren AO, von
Hoff K, Rutkowski S, Herold-Mende C, Frühwald MC, Milde T, Hasselblatt M,
Wesseling P, Rößler J, Schüller U, Ebinger M, Schittenhelm J, Frank S, Grobholz
R, Vajtai I, Hans V, Schneppenheim R, Zitterbart K, Collins VP, Aronica E,
Varlet P, Puget S, Dufour C, Grill J, Figarella-Branger D, Wolter M, Schuhmann
MU, Shalaby T, Grotzer M, van Meter T, Monoranu CM, Felsberg J, Reifenberger G,
Snuderl M, Forrester LA, Koster J, Versteeg R, Volckmann R, van Sluis P, Wolf S,
Mikkelsen T, Gajjar A, Aldape K, Moore AS, Taylor MD, Jones C, Jabado N,
Karajannis MA, Eils R, Schlesner M, Lichter P, von Deimling A, Pfister SM,
Ellison DW, Korshunov A, Kool M. New Brain Tumor Entities Emerge from Molecular
Classification of CNS-PNETs. Cell. 2016 Feb 25;164(5):1060-1072. doi:
10.1016/j.cell.2016.01.015. PMID: 26919435; PMCID: PMC5139621.
505: Shao YH, Choquet K, La Piana R, Tétreault M, Dicaire MJ; Care4Rare Canada
Consortium, Boycott KM, Majewski J, Brais B. Mutations in GALC cause late-onset
Krabbe disease with predominant cerebellar ataxia. Neurogenetics. 2016
Apr;17(2):137-41. doi: 10.1007/s10048-016-0476-2. Epub 2016 Feb 26. PMID:
26915362.
506: Bandopadhayay P, Ramkissoon LA, Jain P, Bergthold G, Wala J, Zeid R,
Schumacher SE, Urbanski L, O'Rourke R, Gibson WJ, Pelton K, Ramkissoon SH, Han
HJ, Zhu Y, Choudhari N, Silva A, Boucher K, Henn RE, Kang YJ, Knoff D, Paolella
BR, Gladden-Young A, Varlet P, Pages M, Horowitz PM, Federation A, Malkin H,
Tracy AA, Seepo S, Ducar M, Van Hummelen P, Santi M, Buccoliero AM, Scagnet M,
Bowers DC, Giannini C, Puget S, Hawkins C, Tabori U, Klekner A, Bognar L, Burger
PC, Eberhart C, Rodriguez FJ, Hill DA, Mueller S, Haas-Kogan DA, Phillips JJ,
Santagata S, Stiles CD, Bradner JE, Jabado N, Goren A, Grill J, Ligon AH,
Goumnerova L, Waanders AJ, Storm PB, Kieran MW, Ligon KL, Beroukhim R, Resnick
AC. MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a
tripartite mechanism. Nat Genet. 2016 Mar;48(3):273-82. doi: 10.1038/ng.3500.
Epub 2016 Feb 1. PMID: 26829751; PMCID: PMC4767685.
507: Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena
A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G,
Agarwal R, Aghi MK, Agnello M, Agostinis P, Aguilar PV, Aguirre-Ghiso J, Airoldi
EM, Ait-Si-Ali S, Akematsu T, Akporiaye ET, Al-Rubeai M, Albaiceta GM, Albanese
C, Albani D, Albert ML, Aldudo J, Algül H, Alirezaei M, Alloza I, Almasan A,
Almonte-Beceril M, Alnemri ES, Alonso C, Altan-Bonnet N, Altieri DC, Alvarez S,
Alvarez-Erviti L, Alves S, Amadoro G, Amano A, Amantini C, Ambrosio S, Amelio I,
Amer AO, Amessou M, Amon A, An Z, Anania FA, Andersen SU, Andley UP, Andreadi
CK, Andrieu-Abadie N, Anel A, Ann DK, Anoopkumar-Dukie S, Antonioli M, Aoki H,
Apostolova N, Aquila S, Aquilano K, Araki K, Arama E, Aranda A, Araya J, Arcaro
A, Arias E, Arimoto H, Ariosa AR, Armstrong JL, Arnould T, Arsov I, Asanuma K,
Askanas V, Asselin E, Atarashi R, Atherton SS, Atkin JD, Attardi LD, Auberger P,
Auburger G, Aurelian L, Autelli R, Avagliano L, Avantaggiati ML, Avrahami L,
Awale S, Azad N, Bachetti T, Backer JM, Bae DH, Bae JS, Bae ON, Bae SH,
Baehrecke EH, Baek SH, Baghdiguian S, Bagniewska-Zadworna A, Bai H, Bai J, Bai
XY, Bailly Y, Balaji KN, Balduini W, Ballabio A, Balzan R, Banerjee R, Bánhegyi
G, Bao H, Barbeau B, Barrachina MD, Barreiro E, Bartel B, Bartolomé A, Bassham
DC, Bassi MT, Bast RC Jr, Basu A, Batista MT, Batoko H, Battino M, Bauckman K,
Baumgarner BL, Bayer KU, Beale R, Beaulieu JF, Beck GR Jr, Becker C, Beckham JD,
Bédard PA, Bednarski PJ, Begley TJ, Behl C, Behrends C, Behrens GM, Behrns KE,
Bejarano E, Belaid A, Belleudi F, Bénard G, Berchem G, Bergamaschi D, Bergami M,
Berkhout B, Berliocchi L, Bernard A, Bernard M, Bernassola F, Bertolotti A, Bess
AS, Besteiro S, Bettuzzi S, Bhalla S, Bhattacharyya S, Bhutia SK, Biagosch C,
Bianchi MW, Biard-Piechaczyk M, Billes V, Bincoletto C, Bingol B, Bird SW,
Bitoun M, Bjedov I, Blackstone C, Blanc L, Blanco GA, Blomhoff HK, Boada-Romero
E, Böckler S, Boes M, Boesze-Battaglia K, Boise LH, Bolino A, Boman A, Bonaldo
P, Bordi M, Bosch J, Botana LM, Botti J, Bou G, Bouché M, Bouchecareilh M,
Boucher MJ, Boulton ME, Bouret SG, Boya P, Boyer-Guittaut M, Bozhkov PV, Brady
N, Braga VM, Brancolini C, Braus GH, Bravo-San Pedro JM, Brennan LA, Bresnick
EH, Brest P, Bridges D, Bringer MA, Brini M, Brito GC, Brodin B, Brookes PS,
Brown EJ, Brown K, Broxmeyer HE, Bruhat A, Brum PC, Brumell JH, Brunetti-Pierri
N, Bryson-Richardson RJ, Buch S, Buchan AM, Budak H, Bulavin DV, Bultman SJ,
Bultynck G, Bumbasirevic V, Burelle Y, Burke RE, Burmeister M, Bütikofer P,
Caberlotto L, Cadwell K, Cahova M, Cai D, Cai J, Cai Q, Calatayud S, Camougrand
N, Campanella M, Campbell GR, Campbell M, Campello S, Candau R, Caniggia I,
Cantoni L, Cao L, Caplan AB, Caraglia M, Cardinali C, Cardoso SM, Carew JS,
Carleton LA, Carlin CR, Carloni S, Carlsson SR, Carmona-Gutierrez D, Carneiro
LA, Carnevali O, Carra S, Carrier A, Carroll B, Casas C, Casas J, Cassinelli G,
Castets P, Castro-Obregon S, Cavallini G, Ceccherini I, Cecconi F, Cederbaum AI,
Ceña V, Cenci S, Cerella C, Cervia D, Cetrullo S, Chaachouay H, Chae HJ, Chagin
AS, Chai CY, Chakrabarti G, Chamilos G, Chan EY, Chan MT, Chandra D, Chandra P,
Chang CP, Chang RC, Chang TY, Chatham JC, Chatterjee S, Chauhan S, Che Y,
Cheetham ME, Cheluvappa R, Chen CJ, Chen G, Chen GC, Chen G, Chen H, Chen JW,
Chen JK, Chen M, Chen M, Chen P, Chen Q, Chen Q, Chen SD, Chen S, Chen SS, Chen
W, Chen WJ, Chen WQ, Chen W, Chen X, Chen YH, Chen YG, Chen Y, Chen Y, Chen Y,
Chen YJ, Chen YQ, Chen Y, Chen Z, Chen Z, Cheng A, Cheng CH, Cheng H, Cheong H,
Cherry S, Chesney J, Cheung CH, Chevet E, Chi HC, Chi SG, Chiacchiera F, Chiang
HL, Chiarelli R, Chiariello M, Chieppa M, Chin LS, Chiong M, Chiu GN, Cho DH,
Cho SG, Cho WC, Cho YY, Cho YS, Choi AM, Choi EJ, Choi EK, Choi J, Choi ME, Choi
SI, Chou TF, Chouaib S, Choubey D, Choubey V, Chow KC, Chowdhury K, Chu CT,
Chuang TH, Chun T, Chung H, Chung T, Chung YL, Chwae YJ, Cianfanelli V, Ciarcia
R, Ciechomska IA, Ciriolo MR, Cirone M, Claerhout S, Clague MJ, Clària J, Clarke
PG, Clarke R, Clementi E, Cleyrat C, Cnop M, Coccia EM, Cocco T, Codogno P,
Coers J, Cohen EE, Colecchia D, Coletto L, Coll NS, Colucci-Guyon E, Comincini
S, Condello M, Cook KL, Coombs GH, Cooper CD, Cooper JM, Coppens I, Corasaniti
MT, Corazzari M, Corbalan R, Corcelle-Termeau E, Cordero MD, Corral-Ramos C,
Corti O, Cossarizza A, Costelli P, Costes S, Cotman SL, Coto-Montes A, Cottet S,
Couve E, Covey LR, Cowart LA, Cox JS, Coxon FP, Coyne CB, Cragg MS, Craven RJ,
Crepaldi T, Crespo JL, Criollo A, Crippa V, Cruz MT, Cuervo AM, Cuezva JM, Cui
T, Cutillas PR, Czaja MJ, Czyzyk-Krzeska MF, Dagda RK, Dahmen U, Dai C, Dai W,
Dai Y, Dalby KN, Dalla Valle L, Dalmasso G, D'Amelio M, Damme M, Darfeuille-
Michaud A, Dargemont C, Darley-Usmar VM, Dasarathy S, Dasgupta B, Dash S, Dass
CR, Davey HM, Davids LM, Dávila D, Davis RJ, Dawson TM, Dawson VL, Daza P, de
Belleroche J, de Figueiredo P, de Figueiredo RC, de la Fuente J, De Martino L,
De Matteis A, De Meyer GR, De Milito A, De Santi M, de Souza W, De Tata V, De
Zio D, Debnath J, Dechant R, Decuypere JP, Deegan S, Dehay B, Del Bello B, Del
Re DP, Delage-Mourroux R, Delbridge LM, Deldicque L, Delorme-Axford E, Deng Y,
Dengjel J, Denizot M, Dent P, Der CJ, Deretic V, Derrien B, Deutsch E, Devarenne
TP, Devenish RJ, Di Bartolomeo S, Di Daniele N, Di Domenico F, Di Nardo A, Di
Paola S, Di Pietro A, Di Renzo L, DiAntonio A, Díaz-Araya G, Díaz-Laviada I,
Diaz-Meco MT, Diaz-Nido J, Dickey CA, Dickson RC, Diederich M, Digard P, Dikic
I, Dinesh-Kumar SP, Ding C, Ding WX, Ding Z, Dini L, Distler JH, Diwan A,
Djavaheri-Mergny M, Dmytruk K, Dobson RC, Doetsch V, Dokladny K, Dokudovskaya S,
Donadelli M, Dong XC, Dong X, Dong Z, Donohue TM Jr, Doran KS, D'Orazi G, Dorn
GW 2nd, Dosenko V, Dridi S, Drucker L, Du J, Du LL, Du L, du Toit A, Dua P, Duan
L, Duann P, Dubey VK, Duchen MR, Duchosal MA, Duez H, Dugail I, Dumit VI, Duncan
MC, Dunlop EA, Dunn WA Jr, Dupont N, Dupuis L, Durán RV, Durcan TM, Duvezin-
Caubet S, Duvvuri U, Eapen V, Ebrahimi-Fakhari D, Echard A, Eckhart L, Edelstein
CL, Edinger AL, Eichinger L, Eisenberg T, Eisenberg-Lerner A, Eissa NT, El-Deiry
WS, El-Khoury V, Elazar Z, Eldar-Finkelman H, Elliott CJ, Emanuele E, Emmenegger
U, Engedal N, Engelbrecht AM, Engelender S, Enserink JM, Erdmann R, Erenpreisa
J, Eri R, Eriksen JL, Erman A, Escalante R, Eskelinen EL, Espert L, Esteban-
Martínez L, Evans TJ, Fabri M, Fabrias G, Fabrizi C, Facchiano A, Færgeman NJ,
Faggioni A, Fairlie WD, Fan C, Fan D, Fan J, Fang S, Fanto M, Fanzani A, Farkas
T, Faure M, Favier FB, Fearnhead H, Federici M, Fei E, Felizardo TC, Feng H,
Feng Y, Feng Y, Ferguson TA, Fernández ÁF, Fernandez-Barrena MG, Fernandez-Checa
JC, Fernández-López A, Fernandez-Zapico ME, Feron O, Ferraro E, Ferreira-Halder
CV, Fesus L, Feuer R, Fiesel FC, Filippi-Chiela EC, Filomeni G, Fimia GM,
Fingert JH, Finkbeiner S, Finkel T, Fiorito F, Fisher PB, Flajolet M, Flamigni
F, Florey O, Florio S, Floto RA, Folini M, Follo C, Fon EA, Fornai F, Fortunato
F, Fraldi A, Franco R, Francois A, François A, Frankel LB, Fraser ID, Frey N,
Freyssenet DG, Frezza C, Friedman SL, Frigo DE, Fu D, Fuentes JM, Fueyo J,
Fujitani Y, Fujiwara Y, Fujiya M, Fukuda M, Fulda S, Fusco C, Gabryel B, Gaestel
M, Gailly P, Gajewska M, Galadari S, Galili G, Galindo I, Galindo MF,
Galliciotti G, Galluzzi L, Galluzzi L, Galy V, Gammoh N, Gandy S, Ganesan AK,
Ganesan S, Ganley IG, Gannagé M, Gao FB, Gao F, Gao JX, García Nannig L, García
Véscovi E, Garcia-Macía M, Garcia-Ruiz C, Garg AD, Garg PK, Gargini R, Gassen
NC, Gatica D, Gatti E, Gavard J, Gavathiotis E, Ge L, Ge P, Ge S, Gean PW,
Gelmetti V, Genazzani AA, Geng J, Genschik P, Gerner L, Gestwicki JE, Gewirtz
DA, Ghavami S, Ghigo E, Ghosh D, Giammarioli AM, Giampieri F, Giampietri C,
Giatromanolaki A, Gibbings DJ, Gibellini L, Gibson SB, Ginet V, Giordano A,
Giorgini F, Giovannetti E, Girardin SE, Gispert S, Giuliano S, Gladson CL,
Glavic A, Gleave M, Godefroy N, Gogal RM Jr, Gokulan K, Goldman GH, Goletti D,
Goligorsky MS, Gomes AV, Gomes LC, Gomez H, Gomez-Manzano C, Gómez-Sánchez R,
Gonçalves DA, Goncu E, Gong Q, Gongora C, Gonzalez CB, Gonzalez-Alegre P,
Gonzalez-Cabo P, González-Polo RA, Goping IS, Gorbea C, Gorbunov NV, Goring DR,
Gorman AM, Gorski SM, Goruppi S, Goto-Yamada S, Gotor C, Gottlieb RA, Gozes I,
Gozuacik D, Graba Y, Graef M, Granato GE, Grant GD, Grant S, Gravina GL, Green
DR, Greenhough A, Greenwood MT, Grimaldi B, Gros F, Grose C, Groulx JF, Gruber
F, Grumati P, Grune T, Guan JL, Guan KL, Guerra B, Guillen C, Gulshan K, Gunst
J, Guo C, Guo L, Guo M, Guo W, Guo XG, Gust AA, Gustafsson ÅB, Gutierrez E,
Gutierrez MG, Gwak HS, Haas A, Haber JE, Hadano S, Hagedorn M, Hahn DR, Halayko
AJ, Hamacher-Brady A, Hamada K, Hamai A, Hamann A, Hamasaki M, Hamer I, Hamid Q,
Hammond EM, Han F, Han W, Handa JT, Hanover JA, Hansen M, Harada M, Harhaji-
Trajkovic L, Harper JW, Harrath AH, Harris AL, Harris J, Hasler U, Hasselblatt
P, Hasui K, Hawley RG, Hawley TS, He C, He CY, He F, He G, He RR, He XH, He YW,
He YY, Heath JK, Hébert MJ, Heinzen RA, Helgason GV, Hensel M, Henske EP, Her C,
Herman PK, Hernández A, Hernandez C, Hernández-Tiedra S, Hetz C, Hiesinger PR,
Higaki K, Hilfiker S, Hill BG, Hill JA, Hill WD, Hino K, Hofius D, Hofman P,
Höglinger GU, Höhfeld J, Holz MK, Hong Y, Hood DA, Hoozemans JJ, Hoppe T, Hsu C,
Hsu CY, Hsu LC, Hu D, Hu G, Hu HM, Hu H, Hu MC, Hu YC, Hu ZW, Hua F, Hua Y,
Huang C, Huang HL, Huang KH, Huang KY, Huang S, Huang S, Huang WP, Huang YR,
Huang Y, Huang Y, Huber TB, Huebbe P, Huh WK, Hulmi JJ, Hur GM, Hurley JH, Husak
Z, Hussain SN, Hussain S, Hwang JJ, Hwang S, Hwang TI, Ichihara A, Imai Y,
Imbriano C, Inomata M, Into T, Iovane V, Iovanna JL, Iozzo RV, Ip NY, Irazoqui
JE, Iribarren P, Isaka Y, Isakovic AJ, Ischiropoulos H, Isenberg JS, Ishaq M,
Ishida H, Ishii I, Ishmael JE, Isidoro C, Isobe K, Isono E, Issazadeh-Navikas S,
Itahana K, Itakura E, Ivanov AI, Iyer AK, Izquierdo JM, Izumi Y, Izzo V,
Jäättelä M, Jaber N, Jackson DJ, Jackson WT, Jacob TG, Jacques TS, Jagannath C,
Jain A, Jana NR, Jang BK, Jani A, Janji B, Jannig PR, Jansson PJ, Jean S,
Jendrach M, Jeon JH, Jessen N, Jeung EB, Jia K, Jia L, Jiang H, Jiang H, Jiang
L, Jiang T, Jiang X, Jiang X, Jiang X, Jiang Y, Jiang Y, Jiménez A, Jin C, Jin
H, Jin L, Jin M, Jin S, Jinwal UK, Jo EK, Johansen T, Johnson DE, Johnson GV,
Johnson JD, Jonasch E, Jones C, Joosten LA, Jordan J, Joseph AM, Joseph B,
Joubert AM, Ju D, Ju J, Juan HF, Juenemann K, Juhász G, Jung HS, Jung JU, Jung
YK, Jungbluth H, Justice MJ, Jutten B, Kaakoush NO, Kaarniranta K, Kaasik A,
Kabuta T, Kaeffer B, Kågedal K, Kahana A, Kajimura S, Kakhlon O, Kalia M,
Kalvakolanu DV, Kamada Y, Kambas K, Kaminskyy VO, Kampinga HH, Kandouz M, Kang
C, Kang R, Kang TC, Kanki T, Kanneganti TD, Kanno H, Kanthasamy AG, Kantorow M,
Kaparakis-Liaskos M, Kapuy O, Karantza V, Karim MR, Karmakar P, Kaser A, Kaushik
S, Kawula T, Kaynar AM, Ke PY, Ke ZJ, Kehrl JH, Keller KE, Kemper JK, Kenworthy
AK, Kepp O, Kern A, Kesari S, Kessel D, Ketteler R, Kettelhut Ido C, Khambu B,
Khan MM, Khandelwal VK, Khare S, Kiang JG, Kiger AA, Kihara A, Kim AL, Kim CH,
Kim DR, Kim DH, Kim EK, Kim HY, Kim HR, Kim JS, Kim JH, Kim JC, Kim JH, Kim KW,
Kim MD, Kim MM, Kim PK, Kim SW, Kim SY, Kim YS, Kim Y, Kimchi A, Kimmelman AC,
Kimura T, King JS, Kirkegaard K, Kirkin V, Kirshenbaum LA, Kishi S, Kitajima Y,
Kitamoto K, Kitaoka Y, Kitazato K, Kley RA, Klimecki WT, Klinkenberg M, Klucken
J, Knævelsrud H, Knecht E, Knuppertz L, Ko JL, Kobayashi S, Koch JC, Koechlin-
Ramonatxo C, Koenig U, Koh YH, Köhler K, Kohlwein SD, Koike M, Komatsu M,
Kominami E, Kong D, Kong HJ, Konstantakou EG, Kopp BT, Korcsmaros T, Korhonen L,
Korolchuk VI, Koshkina NV, Kou Y, Koukourakis MI, Koumenis C, Kovács AL, Kovács
T, Kovacs WJ, Koya D, Kraft C, Krainc D, Kramer H, Kravic-Stevovic T, Krek W,
Kretz-Remy C, Krick R, Krishnamurthy M, Kriston-Vizi J, Kroemer G, Kruer MC,
Kruger R, Ktistakis NT, Kuchitsu K, Kuhn C, Kumar AP, Kumar A, Kumar A, Kumar D,
Kumar D, Kumar R, Kumar S, Kundu M, Kung HJ, Kuno A, Kuo SH, Kuret J, Kurz T,
Kwok T, Kwon TK, Kwon YT, Kyrmizi I, La Spada AR, Lafont F, Lahm T, Lakkaraju A,
Lam T, Lamark T, Lancel S, Landowski TH, Lane DJ, Lane JD, Lanzi C, Lapaquette
P, Lapierre LR, Laporte J, Laukkarinen J, Laurie GW, Lavandero S, Lavie L,
LaVoie MJ, Law BY, Law HK, Law KB, Layfield R, Lazo PA, Le Cam L, Le Roch KG, Le
Stunff H, Leardkamolkarn V, Lecuit M, Lee BH, Lee CH, Lee EF, Lee GM, Lee HJ,
Lee H, Lee JK, Lee J, Lee JH, Lee JH, Lee M, Lee MS, Lee PJ, Lee SW, Lee SJ, Lee
SJ, Lee SY, Lee SH, Lee SS, Lee SJ, Lee S, Lee YR, Lee YJ, Lee YH, Leeuwenburgh
C, Lefort S, Legouis R, Lei J, Lei QY, Leib DA, Leibowitz G, Lekli I, Lemaire
SD, Lemasters JJ, Lemberg MK, Lemoine A, Leng S, Lenz G, Lenzi P, Lerman LO,
Lettieri Barbato D, Leu JI, Leung HY, Levine B, Lewis PA, Lezoualc'h F, Li C, Li
F, Li FJ, Li J, Li K, Li L, Li M, Li M, Li Q, Li R, Li S, Li W, Li W, Li X, Li
Y, Lian J, Liang C, Liang Q, Liao Y, Liberal J, Liberski PP, Lie P, Lieberman
AP, Lim HJ, Lim KL, Lim K, Lima RT, Lin CS, Lin CF, Lin F, Lin F, Lin FC, Lin K,
Lin KH, Lin PH, Lin T, Lin WW, Lin YS, Lin Y, Linden R, Lindholm D, Lindqvist
LM, Lingor P, Linkermann A, Liotta LA, Lipinski MM, Lira VA, Lisanti MP, Liton
PB, Liu B, Liu C, Liu CF, Liu F, Liu HJ, Liu J, Liu JJ, Liu JL, Liu K, Liu L,
Liu L, Liu Q, Liu RY, Liu S, Liu S, Liu W, Liu XD, Liu X, Liu XH, Liu X, Liu X,
Liu X, Liu Y, Liu Y, Liu Z, Liu Z, Liuzzi JP, Lizard G, Ljujic M, Lodhi IJ,
Logue SE, Lokeshwar BL, Long YC, Lonial S, Loos B, López-Otín C, López-Vicario
C, Lorente M, Lorenzi PL, Lõrincz P, Los M, Lotze MT, Lovat PE, Lu B, Lu B, Lu
J, Lu Q, Lu SM, Lu S, Lu Y, Luciano F, Luckhart S, Lucocq JM, Ludovico P, Lugea
A, Lukacs NW, Lum JJ, Lund AH, Luo H, Luo J, Luo S, Luparello C, Lyons T, Ma J,
Ma Y, Ma Y, Ma Z, Machado J, Machado-Santelli GM, Macian F, MacIntosh GC,
MacKeigan JP, Macleod KF, MacMicking JD, MacMillan-Crow LA, Madeo F, Madesh M,
Madrigal-Matute J, Maeda A, Maeda T, Maegawa G, Maellaro E, Maes H, Magariños M,
Maiese K, Maiti TK, Maiuri L, Maiuri MC, Maki CG, Malli R, Malorni W, Maloyan A,
Mami-Chouaib F, Man N, Mancias JD, Mandelkow EM, Mandell MA, Manfredi AA, Manié
SN, Manzoni C, Mao K, Mao Z, Mao ZW, Marambaud P, Marconi AM, Marelja Z, Marfe
G, Margeta M, Margittai E, Mari M, Mariani FV, Marin C, Marinelli S, Mariño G,
Markovic I, Marquez R, Martelli AM, Martens S, Martin KR, Martin SJ, Martin S,
Martin-Acebes MA, Martín-Sanz P, Martinand-Mari C, Martinet W, Martinez J,
Martinez-Lopez N, Martinez-Outschoorn U, Martínez-Velázquez M, Martinez-Vicente
M, Martins WK, Mashima H, Mastrianni JA, Matarese G, Matarrese P, Mateo R,
Matoba S, Matsumoto N, Matsushita T, Matsuura A, Matsuzawa T, Mattson MP, Matus
S, Maugeri N, Mauvezin C, Mayer A, Maysinger D, Mazzolini GD, McBrayer MK,
McCall K, McCormick C, McInerney GM, McIver SC, McKenna S, McMahon JJ, McNeish
IA, Mechta-Grigoriou F, Medema JP, Medina DL, Megyeri K, Mehrpour M, Mehta JL,
Mei Y, Meier UC, Meijer AJ, Meléndez A, Melino G, Melino S, de Melo EJ, Mena MA,
Meneghini MD, Menendez JA, Menezes R, Meng L, Meng LH, Meng S, Menghini R, Menko
AS, Menna-Barreto RF, Menon MB, Meraz-Ríos MA, Merla G, Merlini L, Merlot AM,
Meryk A, Meschini S, Meyer JN, Mi MT, Miao CY, Micale L, Michaeli S, Michiels C,
Migliaccio AR, Mihailidou AS, Mijaljica D, Mikoshiba K, Milan E, Miller-Fleming
L, Mills GB, Mills IG, Minakaki G, Minassian BA, Ming XF, Minibayeva F, Minina
EA, Mintern JD, Minucci S, Miranda-Vizuete A, Mitchell CH, Miyamoto S, Miyazawa
K, Mizushima N, Mnich K, Mograbi B, Mohseni S, Moita LF, Molinari M, Molinari M,
Møller AB, Mollereau B, Mollinedo F, Mongillo M, Monick MM, Montagnaro S,
Montell C, Moore DJ, Moore MN, Mora-Rodriguez R, Moreira PI, Morel E, Morelli
MB, Moreno S, Morgan MJ, Moris A, Moriyasu Y, Morrison JL, Morrison LA, Morselli
E, Moscat J, Moseley PL, Mostowy S, Motori E, Mottet D, Mottram JC, Moussa CE,
Mpakou VE, Mukhtar H, Mulcahy Levy JM, Muller S, Muñoz-Moreno R, Muñoz-Pinedo C,
Münz C, Murphy ME, Murray JT, Murthy A, Mysorekar IU, Nabi IR, Nabissi M, Nader
GA, Nagahara Y, Nagai Y, Nagata K, Nagelkerke A, Nagy P, Naidu SR, Nair S,
Nakano H, Nakatogawa H, Nanjundan M, Napolitano G, Naqvi NI, Nardacci R,
Narendra DP, Narita M, Nascimbeni AC, Natarajan R, Navegantes LC, Nawrocki ST,
Nazarko TY, Nazarko VY, Neill T, Neri LM, Netea MG, Netea-Maier RT, Neves BM,
Ney PA, Nezis IP, Nguyen HT, Nguyen HP, Nicot AS, Nilsen H, Nilsson P, Nishimura
M, Nishino I, Niso-Santano M, Niu H, Nixon RA, Njar VC, Noda T, Noegel AA, Nolte
EM, Norberg E, Norga KK, Noureini SK, Notomi S, Notterpek L, Nowikovsky K,
Nukina N, Nürnberger T, O'Donnell VB, O'Donovan T, O'Dwyer PJ, Oehme I, Oeste
CL, Ogawa M, Ogretmen B, Ogura Y, Oh YJ, Ohmuraya M, Ohshima T, Ojha R, Okamoto
K, Okazaki T, Oliver FJ, Ollinger K, Olsson S, Orban DP, Ordonez P, Orhon I,
Orosz L, O'Rourke EJ, Orozco H, Ortega AL, Ortona E, Osellame LD, Oshima J,
Oshima S, Osiewacz HD, Otomo T, Otsu K, Ou JH, Outeiro TF, Ouyang DY, Ouyang H,
Overholtzer M, Ozbun MA, Ozdinler PH, Ozpolat B, Pacelli C, Paganetti P, Page G,
Pages G, Pagnini U, Pajak B, Pak SC, Pakos-Zebrucka K, Pakpour N, Palková Z,
Palladino F, Pallauf K, Pallet N, Palmieri M, Paludan SR, Palumbo C, Palumbo S,
Pampliega O, Pan H, Pan W, Panaretakis T, Pandey A, Pantazopoulou A, Papackova
Z, Papademetrio DL, Papassideri I, Papini A, Parajuli N, Pardo J, Parekh VV,
Parenti G, Park JI, Park J, Park OK, Parker R, Parlato R, Parys JB, Parzych KR,
Pasquet JM, Pasquier B, Pasumarthi KB, Patschan D, Patterson C, Pattingre S,
Pattison S, Pause A, Pavenstädt H, Pavone F, Pedrozo Z, Peña FJ, Peñalva MA,
Pende M, Peng J, Penna F, Penninger JM, Pensalfini A, Pepe S, Pereira GJ,
Pereira PC, Pérez-de la Cruz V, Pérez-Pérez ME, Pérez-Rodríguez D, Pérez-Sala D,
Perier C, Perl A, Perlmutter DH, Perrotta I, Pervaiz S, Pesonen M, Pessin JE,
Peters GJ, Petersen M, Petrache I, Petrof BJ, Petrovski G, Phang JM, Piacentini
M, Pierdominici M, Pierre P, Pierrefite-Carle V, Pietrocola F, Pimentel-Muiños
FX, Pinar M, Pineda B, Pinkas-Kramarski R, Pinti M, Pinton P, Piperdi B, Piret
JM, Platanias LC, Platta HW, Plowey ED, Pöggeler S, Poirot M, Polčic P, Poletti
A, Poon AH, Popelka H, Popova B, Poprawa I, Poulose SM, Poulton J, Powers SK,
Powers T, Pozuelo-Rubio M, Prak K, Prange R, Prescott M, Priault M, Prince S,
Proia RL, Proikas-Cezanne T, Prokisch H, Promponas VJ, Przyklenk K, Puertollano
R, Pugazhenthi S, Puglielli L, Pujol A, Puyal J, Pyeon D, Qi X, Qian WB, Qin ZH,
Qiu Y, Qu Z, Quadrilatero J, Quinn F, Raben N, Rabinowich H, Radogna F, Ragusa
MJ, Rahmani M, Raina K, Ramanadham S, Ramesh R, Rami A, Randall-Demllo S, Randow
F, Rao H, Rao VA, Rasmussen BB, Rasse TM, Ratovitski EA, Rautou PE, Ray SK,
Razani B, Reed BH, Reggiori F, Rehm M, Reichert AS, Rein T, Reiner DJ, Reits E,
Ren J, Ren X, Renna M, Reusch JE, Revuelta JL, Reyes L, Rezaie AR, Richards RI,
Richardson DR, Richetta C, Riehle MA, Rihn BH, Rikihisa Y, Riley BE, Rimbach G,
Rippo MR, Ritis K, Rizzi F, Rizzo E, Roach PJ, Robbins J, Roberge M, Roca G,
Roccheri MC, Rocha S, Rodrigues CM, Rodríguez CI, de Cordoba SR, Rodriguez-Muela
N, Roelofs J, Rogov VV, Rohn TT, Rohrer B, Romanelli D, Romani L, Romano PS,
Roncero MI, Rosa JL, Rosello A, Rosen KV, Rosenstiel P, Rost-Roszkowska M, Roth
KA, Roué G, Rouis M, Rouschop KM, Ruan DT, Ruano D, Rubinsztein DC, Rucker EB
3rd, Rudich A, Rudolf E, Rudolf R, Ruegg MA, Ruiz-Roldan C, Ruparelia AA,
Rusmini P, Russ DW, Russo GL, Russo G, Russo R, Rusten TE, Ryabovol V, Ryan KM,
Ryter SW, Sabatini DM, Sacher M, Sachse C, Sack MN, Sadoshima J, Saftig P, Sagi-
Eisenberg R, Sahni S, Saikumar P, Saito T, Saitoh T, Sakakura K, Sakoh-
Nakatogawa M, Sakuraba Y, Salazar-Roa M, Salomoni P, Saluja AK, Salvaterra PM,
Salvioli R, Samali A, Sanchez AM, Sánchez-Alcázar JA, Sanchez-Prieto R, Sandri
M, Sanjuan MA, Santaguida S, Santambrogio L, Santoni G, Dos Santos CN, Saran S,
Sardiello M, Sargent G, Sarkar P, Sarkar S, Sarrias MR, Sarwal MM, Sasakawa C,
Sasaki M, Sass M, Sato K, Sato M, Satriano J, Savaraj N, Saveljeva S, Schaefer
L, Schaible UE, Scharl M, Schatzl HM, Schekman R, Scheper W, Schiavi A, Schipper
HM, Schmeisser H, Schmidt J, Schmitz I, Schneider BE, Schneider EM, Schneider
JL, Schon EA, Schönenberger MJ, Schönthal AH, Schorderet DF, Schröder B, Schuck
S, Schulze RJ, Schwarten M, Schwarz TL, Sciarretta S, Scotto K, Scovassi AI,
Screaton RA, Screen M, Seca H, Sedej S, Segatori L, Segev N, Seglen PO, Seguí-
Simarro JM, Segura-Aguilar J, Seki E, Sell C, Seiliez I, Semenkovich CF, Semenza
GL, Sen U, Serra AL, Serrano-Puebla A, Sesaki H, Setoguchi T, Settembre C,
Shacka JJ, Shajahan-Haq AN, Shapiro IM, Sharma S, She H, Shen CK, Shen CC, Shen
HM, Shen S, Shen W, Sheng R, Sheng X, Sheng ZH, Shepherd TG, Shi J, Shi Q, Shi
Q, Shi Y, Shibutani S, Shibuya K, Shidoji Y, Shieh JJ, Shih CM, Shimada Y,
Shimizu S, Shin DW, Shinohara ML, Shintani M, Shintani T, Shioi T, Shirabe K,
Shiri-Sverdlov R, Shirihai O, Shore GC, Shu CW, Shukla D, Sibirny AA, Sica V,
Sigurdson CJ, Sigurdsson EM, Sijwali PS, Sikorska B, Silveira WA, Silvente-
Poirot S, Silverman GA, Simak J, Simmet T, Simon AK, Simon HU, Simone C, Simons
M, Simonsen A, Singh R, Singh SV, Singh SK, Sinha D, Sinha S, Sinicrope FA,
Sirko A, Sirohi K, Sishi BJ, Sittler A, Siu PM, Sivridis E, Skwarska A, Slack R,
Slaninová I, Slavov N, Smaili SS, Smalley KS, Smith DR, Soenen SJ, Soleimanpour
SA, Solhaug A, Somasundaram K, Son JH, Sonawane A, Song C, Song F, Song HK, Song
JX, Song W, Soo KY, Sood AK, Soong TW, Soontornniyomkij V, Sorice M, Sotgia F,
Soto-Pantoja DR, Sotthibundhu A, Sousa MJ, Spaink HP, Span PN, Spang A, Sparks
JD, Speck PG, Spector SA, Spies CD, Springer W, Clair DS, Stacchiotti A, Staels
B, Stang MT, Starczynowski DT, Starokadomskyy P, Steegborn C, Steele JW,
Stefanis L, Steffan J, Stellrecht CM, Stenmark H, Stepkowski TM, Stern ST,
Stevens C, Stockwell BR, Stoka V, Storchova Z, Stork B, Stratoulias V,
Stravopodis DJ, Strnad P, Strohecker AM, Ström AL, Stromhaug P, Stulik J, Su YX,
Su Z, Subauste CS, Subramaniam S, Sue CM, Suh SW, Sui X, Sukseree S, Sulzer D,
Sun FL, Sun J, Sun J, Sun SY, Sun Y, Sun Y, Sun Y, Sundaramoorthy V, Sung J,
Suzuki H, Suzuki K, Suzuki N, Suzuki T, Suzuki YJ, Swanson MS, Swanton C, Swärd
K, Swarup G, Sweeney ST, Sylvester PW, Szatmari Z, Szegezdi E, Szlosarek PW,
Taegtmeyer H, Tafani M, Taillebourg E, Tait SW, Takacs-Vellai K, Takahashi Y,
Takáts S, Takemura G, Takigawa N, Talbot NJ, Tamagno E, Tamburini J, Tan CP, Tan
L, Tan ML, Tan M, Tan YJ, Tanaka K, Tanaka M, Tang D, Tang D, Tang G, Tanida I,
Tanji K, Tannous BA, Tapia JA, Tasset-Cuevas I, Tatar M, Tavassoly I,
Tavernarakis N, Taylor A, Taylor GS, Taylor GA, Taylor JP, Taylor MJ, Tchetina
EV, Tee AR, Teixeira-Clerc F, Telang S, Tencomnao T, Teng BB, Teng RJ, Terro F,
Tettamanti G, Theiss AL, Theron AE, Thomas KJ, Thomé MP, Thomes PG, Thorburn A,
Thorner J, Thum T, Thumm M, Thurston TL, Tian L, Till A, Ting JP, Titorenko VI,
Toker L, Toldo S, Tooze SA, Topisirovic I, Torgersen ML, Torosantucci L,
Torriglia A, Torrisi MR, Tournier C, Towns R, Trajkovic V, Travassos LH, Triola
G, Tripathi DN, Trisciuoglio D, Troncoso R, Trougakos IP, Truttmann AC, Tsai KJ,
Tschan MP, Tseng YH, Tsukuba T, Tsung A, Tsvetkov AS, Tu S, Tuan HY, Tucci M,
Tumbarello DA, Turk B, Turk V, Turner RF, Tveita AA, Tyagi SC, Ubukata M,
Uchiyama Y, Udelnow A, Ueno T, Umekawa M, Umemiya-Shirafuji R, Underwood BR,
Ungermann C, Ureshino RP, Ushioda R, Uversky VN, Uzcátegui NL, Vaccari T,
Vaccaro MI, Váchová L, Vakifahmetoglu-Norberg H, Valdor R, Valente EM, Vallette
F, Valverde AM, Van den Berghe G, Van Den Bosch L, van den Brink GR, van der
Goot FG, van der Klei IJ, van der Laan LJ, van Doorn WG, van Egmond M, van Golen
KL, Van Kaer L, van Lookeren Campagne M, Vandenabeele P, Vandenberghe W,
Vanhorebeek I, Varela-Nieto I, Vasconcelos MH, Vasko R, Vavvas DG, Vega-Naredo
I, Velasco G, Velentzas AD, Velentzas PD, Vellai T, Vellenga E, Vendelbo MH,
Venkatachalam K, Ventura N, Ventura S, Veras PS, Verdier M, Vertessy BG, Viale
A, Vidal M, Vieira HL, Vierstra RD, Vigneswaran N, Vij N, Vila M, Villar M,
Villar VH, Villarroya J, Vindis C, Viola G, Viscomi MT, Vitale G, Vogl DT,
Voitsekhovskaja OV, von Haefen C, von Schwarzenberg K, Voth DE, Vouret-Craviari
V, Vuori K, Vyas JM, Waeber C, Walker CL, Walker MJ, Walter J, Wan L, Wan X,
Wang B, Wang C, Wang CY, Wang C, Wang C, Wang C, Wang D, Wang F, Wang F, Wang G,
Wang HJ, Wang H, Wang HG, Wang H, Wang HD, Wang J, Wang J, Wang M, Wang MQ, Wang
PY, Wang P, Wang RC, Wang S, Wang TF, Wang X, Wang XJ, Wang XW, Wang X, Wang X,
Wang Y, Wang Y, Wang Y, Wang YJ, Wang Y, Wang Y, Wang YT, Wang Y, Wang ZN,
Wappner P, Ward C, Ward DM, Warnes G, Watada H, Watanabe Y, Watase K, Weaver TE,
Weekes CD, Wei J, Weide T, Weihl CC, Weindl G, Weis SN, Wen L, Wen X, Wen Y,
Westermann B, Weyand CM, White AR, White E, Whitton JL, Whitworth AJ, Wiels J,
Wild F, Wildenberg ME, Wileman T, Wilkinson DS, Wilkinson S, Willbold D,
Williams C, Williams K, Williamson PR, Winklhofer KF, Witkin SS, Wohlgemuth SE,
Wollert T, Wolvetang EJ, Wong E, Wong GW, Wong RW, Wong VK, Woodcock EA, Wright
KL, Wu C, Wu D, Wu GS, Wu J, Wu J, Wu M, Wu M, Wu S, Wu WK, Wu Y, Wu Z, Xavier
CP, Xavier RJ, Xia GX, Xia T, Xia W, Xia Y, Xiao H, Xiao J, Xiao S, Xiao W, Xie
CM, Xie Z, Xie Z, Xilouri M, Xiong Y, Xu C, Xu C, Xu F, Xu H, Xu H, Xu J, Xu J,
Xu J, Xu L, Xu X, Xu Y, Xu Y, Xu ZX, Xu Z, Xue Y, Yamada T, Yamamoto A, Yamanaka
K, Yamashina S, Yamashiro S, Yan B, Yan B, Yan X, Yan Z, Yanagi Y, Yang DS, Yang
JM, Yang L, Yang M, Yang PM, Yang P, Yang Q, Yang W, Yang WY, Yang X, Yang Y,
Yang Y, Yang Z, Yang Z, Yao MC, Yao PJ, Yao X, Yao Z, Yao Z, Yasui LS, Ye M,
Yedvobnick B, Yeganeh B, Yeh ES, Yeyati PL, Yi F, Yi L, Yin XM, Yip CK, Yoo YM,
Yoo YH, Yoon SY, Yoshida K, Yoshimori T, Young KH, Yu H, Yu JJ, Yu JT, Yu J, Yu
L, Yu WH, Yu XF, Yu Z, Yuan J, Yuan ZM, Yue BY, Yue J, Yue Z, Zacks DN,
Zacksenhaus E, Zaffaroni N, Zaglia T, Zakeri Z, Zecchini V, Zeng J, Zeng M, Zeng
Q, Zervos AS, Zhang DD, Zhang F, Zhang G, Zhang GC, Zhang H, Zhang H, Zhang H,
Zhang H, Zhang J, Zhang J, Zhang J, Zhang J, Zhang JP, Zhang L, Zhang L, Zhang
L, Zhang L, Zhang MY, Zhang X, Zhang XD, Zhang Y, Zhang Y, Zhang Y, Zhang Y,
Zhang Y, Zhao M, Zhao WL, Zhao X, Zhao YG, Zhao Y, Zhao Y, Zhao YX, Zhao Z, Zhao
ZJ, Zheng D, Zheng XL, Zheng X, Zhivotovsky B, Zhong Q, Zhou GZ, Zhou G, Zhou H,
Zhou SF, Zhou XJ, Zhu H, Zhu H, Zhu WG, Zhu W, Zhu XF, Zhu Y, Zhuang SM, Zhuang
X, Ziparo E, Zois CE, Zoladek T, Zong WX, Zorzano A, Zughaier SM. Guidelines for
the use and interpretation of assays for monitoring autophagy (3rd edition).
Autophagy. 2016;12(1):1-222. doi: 10.1080/15548627.2015.1100356. Erratum in:
Autophagy. 2016;12(2):443. Selliez, Iban [corrected to Seiliez, Iban]. PMID:
26799652; PMCID: PMC4835977.
508: Benini R, Roth R, Khoja Z, Avoli M, Wintermark P. Does angiogenesis play a
role in the establishment of mesial temporal lobe epilepsy? Int J Dev Neurosci.
2016 Apr;49:31-6. doi: 10.1016/j.ijdevneu.2016.01.001. Epub 2016 Jan 7. PMID:
26773167; PMCID: PMC4878886.
509: Morrissy AS, Garzia L, Shih DJ, Zuyderduyn S, Huang X, Skowron P, Remke M,
Cavalli FM, Ramaswamy V, Lindsay PE, Jelveh S, Donovan LK, Wang X, Luu B, Zayne
K, Li Y, Mayoh C, Thiessen N, Mercier E, Mungall KL, Ma Y, Tse K, Zeng T,
Shumansky K, Roth AJ, Shah S, Farooq H, Kijima N, Holgado BL, Lee JJ, Matan-
Lithwick S, Liu J, Mack SC, Manno A, Michealraj KA, Nor C, Peacock J, Qin L,
Reimand J, Rolider A, Thompson YY, Wu X, Pugh T, Ally A, Bilenky M, Butterfield
YS, Carlsen R, Cheng Y, Chuah E, Corbett RD, Dhalla N, He A, Lee D, Li HI, Long
W, Mayo M, Plettner P, Qian JQ, Schein JE, Tam A, Wong T, Birol I, Zhao Y, Faria
CC, Pimentel J, Nunes S, Shalaby T, Grotzer M, Pollack IF, Hamilton RL, Li XN,
Bendel AE, Fults DW, Walter AW, Kumabe T, Tominaga T, Collins VP, Cho YJ,
Hoffman C, Lyden D, Wisoff JH, Garvin JH Jr, Stearns DS, Massimi L, Schüller U,
Sterba J, Zitterbart K, Puget S, Ayrault O, Dunn SE, Tirapelli DP, Carlotti CG,
Wheeler H, Hallahan AR, Ingram W, MacDonald TJ, Olson JJ, Van Meir EG, Lee JY,
Wang KC, Kim SK, Cho BK, Pietsch T, Fleischhack G, Tippelt S, Ra YS, Bailey S,
Lindsey JC, Clifford SC, Eberhart CG, Cooper MK, Packer RJ, Massimino M, Garre
ML, Bartels U, Tabori U, Hawkins CE, Dirks P, Bouffet E, Rutka JT, Wechsler-Reya
RJ, Weiss WA, Collier LS, Dupuy AJ, Korshunov A, Jones DT, Kool M, Northcott PA,
Pfister SM, Largaespada DA, Mungall AJ, Moore RA, Jabado N, Bader GD, Jones SJ,
Malkin D, Marra MA, Taylor MD. Divergent clonal selection dominates
medulloblastoma at recurrence. Nature. 2016 Jan 21;529(7586):351-7. doi:
10.1038/nature16478. Epub 2016 Jan 13. PMID: 26760213; PMCID: PMC4936195.
510: Citerio G, Cypel M, Dobb GJ, Dominguez-Gil B, Frontera JA, Greer DM, Manara
AR, Shemie SD, Smith M, Valenza F, Wijdicks EFM. Organ donation in adults: a
critical care perspective. Intensive Care Med. 2016 Mar;42(3):305-315. doi:
10.1007/s00134-015-4191-5. Epub 2016 Jan 11. PMID: 26754754.
511: Mutch WA, Ellis MJ, Ryner LN, Graham MR, Dufault B, Gregson B, Hall T,
Bunge M, Essig M, Fisher JA, Duffin J, Mikulis DJ; Canada North Concussion
Network, and; University Health Network Cerebrovascular Reactivity Research
Group. Brain magnetic resonance imaging CO2 stress testing in adolescent
postconcussion syndrome. J Neurosurg. 2016 Sep;125(3):648-60. doi:
10.3171/2015.6.JNS15972. Epub 2015 Dec 18. PMID: 26684777.
512: Choquet K, Tétreault M, Yang S, La Piana R, Dicaire MJ, Vanstone MR,
Mathieu J, Bouchard JP, Rioux MF, Rouleau GA; Care4Rare Canada Consortium,
Boycott KM, Majewski J, Brais B. SPG7 mutations explain a significant proportion
of French Canadian spastic ataxia cases. Eur J Hum Genet. 2016
Jul;24(7):1016-21. doi: 10.1038/ejhg.2015.240. Epub 2015 Dec 2. PMID: 26626314;
PMCID: PMC5070891.
513: Steinbok P, Gopalakrishnan CV, Hengel AR, Vitali AM, Poskitt K, Hawkins C,
Drake J, Lamberti-Pasculli M, Ajani O, Hader W, Mehta V, McNeely PD, McDonald
PJ, Ranger A, Vassilyadi M, Atkinson J, Ryall S, Eisenstat DD, Hukin J.
Pediatric thalamic tumors in the MRI era: a Canadian perspective. Childs Nerv
Syst. 2016 Feb;32(2):269-80. doi: 10.1007/s00381-015-2968-z. Epub 2015 Nov 23.
PMID: 26597682.
514: Block KI, Gyllenhaal C, Lowe L, Amedei A, Amin ARMR, Amin A, Aquilano K,
Arbiser J, Arreola A, Arzumanyan A, Ashraf SS, Azmi AS, Benencia F, Bhakta D,
Bilsland A, Bishayee A, Blain SW, Block PB, Boosani CS, Carey TE, Carnero A,
Carotenuto M, Casey SC, Chakrabarti M, Chaturvedi R, Chen GZ, Chen H, Chen S,
Chen YC, Choi BK, Ciriolo MR, Coley HM, Collins AR, Connell M, Crawford S,
Curran CS, Dabrosin C, Damia G, Dasgupta S, DeBerardinis RJ, Decker WK, Dhawan
P, Diehl AME, Dong JT, Dou QP, Drew JE, Elkord E, El-Rayes B, Feitelson MA,
Felsher DW, Ferguson LR, Fimognari C, Firestone GL, Frezza C, Fujii H, Fuster
MM, Generali D, Georgakilas AG, Gieseler F, Gilbertson M, Green MF, Grue B, Guha
G, Halicka D, Helferich WG, Heneberg P, Hentosh P, Hirschey MD, Hofseth LJ,
Holcombe RF, Honoki K, Hsu HY, Huang GS, Jensen LD, Jiang WG, Jones LW,
Karpowicz PA, Keith WN, Kerkar SP, Khan GN, Khatami M, Ko YH, Kucuk O,
Kulathinal RJ, Kumar NB, Kwon BS, Le A, Lea MA, Lee HY, Lichtor T, Lin LT,
Locasale JW, Lokeshwar BL, Longo VD, Lyssiotis CA, MacKenzie KL, Malhotra M,
Marino M, Martinez-Chantar ML, Matheu A, Maxwell C, McDonnell E, Meeker AK,
Mehrmohamadi M, Mehta K, Michelotti GA, Mohammad RM, Mohammed SI, Morre DJ,
Muralidhar V, Muqbil I, Murphy MP, Nagaraju GP, Nahta R, Niccolai E, Nowsheen S,
Panis C, Pantano F, Parslow VR, Pawelec G, Pedersen PL, Poore B, Poudyal D,
Prakash S, Prince M, Raffaghello L, Rathmell JC, Rathmell WK, Ray SK, Reichrath
J, Rezazadeh S, Ribatti D, Ricciardiello L, Robey RB, Rodier F, Rupasinghe HPV,
Russo GL, Ryan EP, Samadi AK, Sanchez-Garcia I, Sanders AJ, Santini D, Sarkar M,
Sasada T, Saxena NK, Shackelford RE, Shantha Kumara HMC, Sharma D, Shin DM,
Sidransky D, Siegelin MD, Signori E, Singh N, Sivanand S, Sliva D, Smythe C,
Spagnuolo C, Stafforini DM, Stagg J, Subbarayan PR, Sundin T, Talib WH, Thompson
SK, Tran PT, Ungefroren H, Vander Heiden MG, Venkateswaran V, Vinay DS,
Vlachostergios PJ, Wang Z, Wellen KE, Whelan RL, Yang ES, Yang H, Yang X, Yaswen
P, Yedjou C, Yin X, Zhu J, Zollo M. Designing a broad-spectrum integrative
approach for cancer prevention and treatment. Semin Cancer Biol. 2015 Dec;35
Suppl(Suppl):S276-S304. doi: 10.1016/j.semcancer.2015.09.007. PMID: 26590477;
PMCID: PMC4819002.
515: Hankinson TC, Dudley RW, Torok MR, Patibandla MR, Dorris K, Poonia S,
Wilkinson CC, Bruny JL, Handler MH, Liu AK. Short-term mortality following
surgical procedures for the diagnosis of pediatric brain tumors: outcome
analysis in 5533 children from SEER, 2004-2011. J Neurosurg Pediatr. 2016
Mar;17(3):289-97. doi: 10.3171/2015.7.PEDS15224. Epub 2015 Nov 20. PMID:
26588456.
516: Garfinkle J, Wintermark P, Shevell MI, Oskoui M; Canadian Cerebral Palsy
Registry. Cerebral palsy after neonatal encephalopathy: do neonates with
suspected asphyxia have worse outcomes? Dev Med Child Neurol. 2016
Feb;58(2):189-94. doi: 10.1111/dmcn.12953. Epub 2015 Nov 11. PMID: 26555029.
517: Ba OL, Caremel R, Aharony S, Loutochin O, Barbe M, Jacques L, Tuite G,
Ruggieri M, Campeau L, Corcos J. Évaluation de l'efficacité d'une technique de
réinnervation vésicale dans un modèle de chat paraplégique : résultats d'une
étude pilote. Prog Urol. 2015 Nov;25(13):847. French. doi:
10.1016/j.purol.2015.08.263. PMID: 26544457.
518: Biardeau X, Biardeau X, Lam van Ba O, Caremel R, Aharony S, Lotouchin O,
Barbe M, Tuite G, Jacques L, Ruggieri M, Campeau L, Corcos J. « Rerouting »
nerveux lombo-sacré pour la restauration de la vidange vésicale dans un modèle
félin traumatisé médullaire : étude pilote. Prog Urol. 2015 Nov;25(13):847.
French. doi: 10.1016/j.purol.2015.08.262. PMID: 26544456.
519: Merner ND, Chandler MR, Bourassa C, Liang B, Khanna AR, Dion P, Rouleau GA,
Kahle KT. Regulatory domain or CpG site variation in SLC12A5, encoding the
chloride transporter KCC2, in human autism and schizophrenia. Front Cell
Neurosci. 2015 Oct 12;9:386. doi: 10.3389/fncel.2015.00386. PMID: 26528127;
PMCID: PMC4600830.
520: Srour M, Hamdan FF, McKnight D, Davis E, Mandel H, Schwartzentruber J,
Martin B, Patry L, Nassif C, Dionne-Laporte A, Ospina LH, Lemyre E, Massicotte
C, Laframboise R, Maranda B, Labuda D, Décarie JC, Rypens F, Goldsher D, Fallet-
Bianco C, Soucy JF, Laberge AM, Maftei C; Care4Rare Canada Consortium, Boycott
K, Brais B, Boucher RM, Rouleau GA, Katsanis N, Majewski J, Elpeleg O, Kukolich
MK, Shalev S, Michaud JL. Joubert Syndrome in French Canadians and
Identification of Mutations in CEP104. Am J Hum Genet. 2015 Nov 5;97(5):744-53.
doi: 10.1016/j.ajhg.2015.09.009. Epub 2015 Oct 17. PMID: 26477546; PMCID:
PMC4667103.
521: Quah PL, Chan YH, Aris IM, Pang WW, Toh JY, Tint MT, Broekman BF, Saw SM,
Kwek K, Godfrey KM, Gluckman PD, Chong YS, Meaney MJ, Yap FK, van Dam RM, Lee
YS, Chong MF; GUSTO Study Group. Prospective associations of appetitive traits
at 3 and 12 months of age with body mass index and weight gain in the first 2
years of life. BMC Pediatr. 2015 Oct 12;15:153. doi: 10.1186/s12887-015-0467-8.
PMID: 26459321; PMCID: PMC4603814.
522: Alzahrani A, Alsowayan O, Farmer JP, Capolicchio JP, Jednak R, El-Sherbiny
M. Comprehensive analysis of the clinical and urodynamic outcomes of secondary
tethered spinal cord before and after spinal cord untethering. J Pediatr Urol.
2016 Apr;12(2):101.e1-6. doi: 10.1016/j.jpurol.2015.08.011. Epub 2015 Sep 26.
PMID: 26454453.
523: Guerrini R, Duchowny M, Jayakar P, Krsek P, Kahane P, Tassi L, Melani F,
Polster T, Andre VM, Cepeda C, Krueger DA, Cross JH, Spreafico R, Cosottini M,
Gotman J, Chassoux F, Ryvlin P, Bartolomei F, Bernasconi A, Stefan H, Miller I,
Devaux B, Najm I, Giordano F, Vonck K, Barba C, Blumcke I. Diagnostic methods
and treatment options for focal cortical dysplasia. Epilepsia. 2015
Nov;56(11):1669-86. doi: 10.1111/epi.13200. Epub 2015 Oct 5. PMID: 26434565.
524: Zhou Y, Aris IM, Tan SS, Cai S, Tint MT, Krishnaswamy G, Meaney MJ, Godfrey
KM, Kwek K, Gluckman PD, Chong YS, Yap F, Lek N, Gooley JJ, Lee YS. Sleep
duration and growth outcomes across the first two years of life in the GUSTO
study. Sleep Med. 2015 Oct;16(10):1281-6. doi: 10.1016/j.sleep.2015.07.006. Epub
2015 Jul 17. PMID: 26429758.
525: Fontebasso AM, Shirinian M, Khuong-Quang DA, Bechet D, Gayden T, Kool M, De
Jay N, Jacob K, Gerges N, Hutter B, Şeker-Cin H, Witt H, Montpetit A, Brunet S,
Lepage P, Bourret G, Klekner A, Bognár L, Hauser P, Garami M, Farmer JP, Montes
JL, Atkinson J, Lambert S, Kwan T, Korshunov A, Tabori U, Collins VP, Albrecht
S, Faury D, Pfister SM, Paulus W, Hasselblatt M, Jones DT, Jabado N. Non-random
aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with
older age. Oncotarget. 2015 Oct 13;6(31):31844-56. doi:
10.18632/oncotarget.5571. PMID: 26378811; PMCID: PMC4741644.
526: Keezer MR, Simard-Tremblay E, Veilleux M. The Diagnostic Accuracy of
Prolonged Ambulatory Versus Routine EEG. Clin EEG Neurosci. 2016
Apr;47(2):157-61. doi: 10.1177/1550059415607108. Epub 2015 Sep 15. PMID:
26376916.
527: Wolf NI, Bernard G. Mutations in RNF216 do not cause 4H syndrome.
Parkinsonism Relat Disord. 2015 Nov;21(11):1387-8. doi:
10.1016/j.parkreldis.2015.09.014. Epub 2015 Sep 4. PMID: 26365775.
528: Sawyer SL, Hartley T, Dyment DA, Beaulieu CL, Schwartzentruber J, Smith A,
Bedford HM, Bernard G, Bernier FP, Brais B, Bulman DE, Warman Chardon J,
Chitayat D, Deladoëy J, Fernandez BA, Frosk P, Geraghty MT, Gerull B, Gibson W,
Gow RM, Graham GE, Green JS, Heon E, Horvath G, Innes AM, Jabado N, Kim RH,
Koenekoop RK, Khan A, Lehmann OJ, Mendoza-Londono R, Michaud JL, Nikkel SM,
Penney LS, Polychronakos C, Richer J, Rouleau GA, Samuels ME, Siu VM,
Suchowersky O, Tarnopolsky MA, Yoon G, Zahir FR; FORGE Canada Consortium;
Care4Rare Canada Consortium, Majewski J, Boycott KM. Utility of whole-exome
sequencing for those near the end of the diagnostic odyssey: time to address
gaps in care. Clin Genet. 2016 Mar;89(3):275-84. doi: 10.1111/cge.12654. Epub
2015 Sep 22. PMID: 26283276; PMCID: PMC5053223.
529: Rektor I, Schachter SC, Arya R, Arzy S, Braakman H, Brodie MJ, Brugger P,
Chang BS, Guekht A, Hermann B, Hesdorffer DC, Jones-Gotman M, Kanner AM, Garcia-
Larrea L, Mareš P, Mula M, Neufeld M, Risse GL, Ryvlin P, Seeck M, Tomson T,
Korczyn AD. Third International Congress on Epilepsy, Brain, and Mind: Part 2.
Epilepsy Behav. 2015 Sep;50:138-59. doi: 10.1016/j.yebeh.2015.07.014. Epub 2015
Aug 8. PMID: 26264466.
530: Noreau A, La Piana R, Marcoux C; FORGE Canada, Dion PA, Brais B, Bernard G,
Rouleau GA. Novel SIL1 mutations cause cerebellar ataxia and atrophy in a
French-Canadian family. Neurogenetics. 2015 Oct;16(4):315-8. doi:
10.1007/s10048-015-0455-z. Epub 2015 Aug 11. PMID: 26260654.
531: Jung S, Polosa A, Lachapelle P, Wintermark P. Visual Impairments Following
Term Neonatal Encephalopathy: Do Retinal Impairments Also Play a Role? Invest
Ophthalmol Vis Sci. 2015 Aug;56(9):5182-93. doi: 10.1167/iovs.15-16407. PMID:
26244294.
532: Hubermann L, Boychuck Z, Shevell M, Majnemer A. Age at Referral of Children
for Initial Diagnosis of Cerebral Palsy and Rehabilitation: Current Practices. J
Child Neurol. 2016 Mar;31(3):364-9. doi: 10.1177/0883073815596610. Epub 2015 Aug
3. PMID: 26239493.
533: Labidi M, Lavoie P, Lapointe G, Obaid S, Weil AG, Bojanowski MW, Turmel A.
Predicting success of endoscopic third ventriculostomy: validation of the ETV
Success Score in a mixed population of adult and pediatric patients. J
Neurosurg. 2015 Dec;123(6):1447-55. doi: 10.3171/2014.12.JNS141240. Epub 2015
Jul 24. PMID: 26207604.
534: Jansen AC, Robitaille Y, Honavar M, Mullatti N, Leventer RJ, Andermann E,
Andermann F, Squier W. The histopathology of polymicrogyria: a series of 71
brain autopsy studies. Dev Med Child Neurol. 2016 Jan;58(1):39-48. doi:
10.1111/dmcn.12840. Epub 2015 Jul 14. PMID: 26179148.
535: Thiffault I, Wolf NI, Forget D, Guerrero K, Tran LT, Choquet K, Lavallée-
Adam M, Poitras C, Brais B, Yoon G, Sztriha L, Webster RI, Timmann D, van de
Warrenburg BP, Seeger J, Zimmermann A, Máté A, Goizet C, Fung E, van der Knaap
MS, Fribourg S, Vanderver A, Simons C, Taft RJ, Yates JR 3rd, Coulombe B,
Bernard G. Recessive mutations in POLR1C cause a leukodystrophy by impairing
biogenesis of RNA polymerase III. Nat Commun. 2015 Jul 7;6:7623. doi:
10.1038/ncomms8623. PMID: 26151409; PMCID: PMC4506509.
536: Valdés PA, Jacobs V, Harris BT, Wilson BC, Leblond F, Paulsen KD, Roberts
DW. Quantitative fluorescence using 5-aminolevulinic acid-induced protoporphyrin
IX biomarker as a surgical adjunct in low-grade glioma surgery. J Neurosurg.
2015 Sep;123(3):771-80. doi: 10.3171/2014.12.JNS14391. Epub 2015 Jul 3. PMID:
26140489; PMCID: PMC4646619.
537: Rahman Z, Wong CH, Dexter M, Olsson G, Wong M, Gebsky V, Nahar N, Wood A,
Byth K, King M, Bleasel AB. Epilepsy in patients with primary brain tumors: The
impact on mood, cognition, and HRQOL. Epilepsy Behav. 2015 Jul;48:88-95. doi:
10.1016/j.yebeh.2015.03.016. Epub 2015 Jun 29. PMID: 26136184.
538: Kevelam SH, Taube JR, van Spaendonk RM, Bertini E, Sperle K, Tarnopolsky M,
Tonduti D, Valente EM, Travaglini L, Sistermans EA, Bernard G, Catsman-
Berrevoets CE, van Karnebeek CD, Østergaard JR, Friederich RL, Fawzi Elsaid M,
Schieving JH, Tarailo-Graovac M, Orcesi S, Steenweg ME, van Berkel CG, Waisfisz
Q, Abbink TE, van der Knaap MS, Hobson GM, Wolf NI. Altered PLP1 splicing causes
hypomyelination of early myelinating structures. Ann Clin Transl Neurol. 2015
Jun;2(6):648-61. doi: 10.1002/acn3.203. Epub 2015 May 1. PMID: 26125040; PMCID:
PMC4479525.
539: Fallah A, Rodgers SD, Weil AG, Vadera S, Mansouri A, Connolly MB, Major P,
Ma T, Devinsky O, Weiner HL, Gonzalez-Martinez JA, Bingaman WE, Najm I, Gupta A,
Ragheb J, Bhatia S, Steinbok P, Witiw CD, Widjaja E, Snead OC, Rutka JT.
Resective Epilepsy Surgery for Tuberous Sclerosis in Children: Determining
Predictors of Seizure Outcomes in a Multicenter Retrospective Cohort Study.
Neurosurgery. 2015 Oct;77(4):517-24; discussion 524. doi:
10.1227/NEU.0000000000000875. PMID: 26120800.
540: Goodson WH 3rd, Lowe L, Carpenter DO, Gilbertson M, Manaf Ali A, Lopez de
Cerain Salsamendi A, Lasfar A, Carnero A, Azqueta A, Amedei A, Charles AK,
Collins AR, Ward A, Salzberg AC, Colacci A, Olsen AK, Berg A, Barclay BJ, Zhou
BP, Blanco-Aparicio C, Baglole CJ, Dong C, Mondello C, Hsu CW, Naus CC, Yedjou
C, Curran CS, Laird DW, Koch DC, Carlin DJ, Felsher DW, Roy D, Brown DG,
Ratovitski E, Ryan EP, Corsini E, Rojas E, Moon EY, Laconi E, Marongiu F, Al-
Mulla F, Chiaradonna F, Darroudi F, Martin FL, Van Schooten FJ, Goldberg GS,
Wagemaker G, Nangami GN, Calaf GM, Williams G, Wolf GT, Koppen G, Brunborg G,
Lyerly HK, Krishnan H, Ab Hamid H, Yasaei H, Sone H, Kondoh H, Salem HK, Hsu HY,
Park HH, Koturbash I, Miousse IR, Scovassi AI, Klaunig JE, Vondráček J, Raju J,
Roman J, Wise JP Sr, Whitfield JR, Woodrick J, Christopher JA, Ochieng J,
Martinez-Leal JF, Weisz J, Kravchenko J, Sun J, Prudhomme KR, Narayanan KB,
Cohen-Solal KA, Moorwood K, Gonzalez L, Soucek L, Jian L, D'Abronzo LS, Lin LT,
Li L, Gulliver L, McCawley LJ, Memeo L, Vermeulen L, Leyns L, Zhang L, Valverde
M, Khatami M, Romano MF, Chapellier M, Williams MA, Wade M, Manjili MH, Lleonart
ME, Xia M, Gonzalez MJ, Karamouzis MV, Kirsch-Volders M, Vaccari M, Kuemmerle
NB, Singh N, Cruickshanks N, Kleinstreuer N, van Larebeke N, Ahmed N, Ogunkua O,
Krishnakumar PK, Vadgama P, Marignani PA, Ghosh PM, Ostrosky-Wegman P, Thompson
PA, Dent P, Heneberg P, Darbre P, Sing Leung P, Nangia-Makker P, Cheng QS, Robey
RB, Al-Temaimi R, Roy R, Andrade-Vieira R, Sinha RK, Mehta R, Vento R, Di Fiore
R, Ponce-Cusi R, Dornetshuber-Fleiss R, Nahta R, Castellino RC, Palorini R, Abd
Hamid R, Langie SA, Eltom SE, Brooks SA, Ryeom S, Wise SS, Bay SN, Harris SA,
Papagerakis S, Romano S, Pavanello S, Eriksson S, Forte S, Casey SC, Luanpitpong
S, Lee TJ, Otsuki T, Chen T, Massfelder T, Sanderson T, Guarnieri T, Hultman T,
Dormoy V, Odero-Marah V, Sabbisetti V, Maguer-Satta V, Rathmell WK, Engström W,
Decker WK, Bisson WH, Rojanasakul Y, Luqmani Y, Chen Z, Hu Z. Assessing the
carcinogenic potential of low-dose exposures to chemical mixtures in the
environment: the challenge ahead. Carcinogenesis. 2015 Jun;36 Suppl 1(Suppl
1):S254-96. doi: 10.1093/carcin/bgv039. Erratum in: Carcinogenesis. 2016
Mar;37(3):344. PMID: 26106142; PMCID: PMC4480130.
541: Gutierrez M, Thiffault I, Guerrero K, Martos-Moreno GÁ, Tran LT, Benko W,
van der Knaap MS, van Spaendonk RM, Wolf NI, Bernard G. Large exonic deletions
in POLR3B gene cause POLR3-related leukodystrophy. Orphanet J Rare Dis. 2015 Jun
5;10:69. doi: 10.1186/s13023-015-0279-9. PMID: 26045207; PMCID: PMC4520020.
542: Perreault S Sp1, Lober RM, Davis C, Stave C, Partap S Sp2, Fisher PG.
Sports and childhood brain tumors: Can I play? Neurooncol Pract. 2014
Dec;1(4):158-165. doi: 10.1093/nop/npu020. Epub 2014 Sep 1. PMID: 26034627;
PMCID: PMC4369718.
543: Mack SC, Agnihotri S, Bertrand KC, Wang X, Shih DJ, Witt H, Hill N, Zayne
K, Barszczyk M, Ramaswamy V, Remke M, Thompson Y, Ryzhova M, Massimi L,
Grajkowska W, Lach B, Gupta N, Weiss WA, Guha A, Hawkins C, Croul S, Rutka JT,
Pfister SM, Korshunov A, Pekmezci M, Tihan T, Philips JJ, Jabado N, Zadeh G,
Taylor MD. Spinal Myxopapillary Ependymomas Demonstrate a Warburg Phenotype.
Clin Cancer Res. 2015 Aug 15;21(16):3750-8. doi: 10.1158/1078-0432.CCR-14-2650.
Epub 2015 May 8. PMID: 25957288; PMCID: PMC4537825.
544: Kepp O, Senovilla L, Vitale I, Vacchelli E, Adjemian S, Agostinis P, Apetoh
L, Aranda F, Barnaba V, Bloy N, Bracci L, Breckpot K, Brough D, Buqué A, Castro
MG, Cirone M, Colombo MI, Cremer I, Demaria S, Dini L, Eliopoulos AG, Faggioni
A, Formenti SC, Fučíková J, Gabriele L, Gaipl US, Galon J, Garg A, Ghiringhelli
F, Giese NA, Guo ZS, Hemminki A, Herrmann M, Hodge JW, Holdenrieder S,
Honeychurch J, Hu HM, Huang X, Illidge TM, Kono K, Korbelik M, Krysko DV, Loi S,
Lowenstein PR, Lugli E, Ma Y, Madeo F, Manfredi AA, Martins I, Mavilio D, Menger
L, Merendino N, Michaud M, Mignot G, Mossman KL, Multhoff G, Oehler R, Palombo
F, Panaretakis T, Pol J, Proietti E, Ricci JE, Riganti C, Rovere-Querini P,
Rubartelli A, Sistigu A, Smyth MJ, Sonnemann J, Spisek R, Stagg J, Sukkurwala
AQ, Tartour E, Thorburn A, Thorne SH, Vandenabeele P, Velotti F, Workenhe ST,
Yang H, Zong WX, Zitvogel L, Kroemer G, Galluzzi L. Consensus guidelines for the
detection of immunogenic cell death. Oncoimmunology. 2014 Dec 13;3(9):e955691.
doi: 10.4161/21624011.2014.955691. PMID: 25941621; PMCID: PMC4292729.
545: Sun J, Zheng J, Tang L, Healy J, Sinnett D, Dai YE. Association between
CEBPE Variant and Childhood Acute Leukemia Risk: Evidence from a Meta-Analysis
of 22 Studies. PLoS One. 2015 May 4;10(5):e0125657. doi:
10.1371/journal.pone.0125657. PMID: 25938438; PMCID: PMC4418706.
546: Srour M, Hamdan FF, Gan-Or Z, Labuda D, Nassif C, Oskoui M, Gana-Weisz M,
Orr-Urtreger A, Rouleau GA, Michaud JL. A homozygous mutation in SLC1A4 in
siblings with severe intellectual disability and microcephaly. Clin Genet. 2015
Jul;88(1):e1-4. doi: 10.1111/cge.12605. Epub 2015 May 28. PMID: 25930971.
547: Oskoui M. Disentangling racial and ethnic disparities in cerebral palsy.
Dev Med Child Neurol. 2015 Sep;57(9):791-2. doi: 10.1111/dmcn.12772. Epub 2015
Apr 21. PMID: 25900384.
548: Torchia J, Picard D, Lafay-Cousin L, Hawkins CE, Kim SK, Letourneau L, Ra
YS, Ho KC, Chan TS, Sin-Chan P, Dunham CP, Yip S, Ng HK, Lu JQ, Albrecht S,
Pimentel J, Chan JA, Somers GR, Zielenska M, Faria CC, Roque L, Baskin B, Birks
D, Foreman N, Strother D, Klekner A, Garami M, Hauser P, Hortobágyi T, Bognár L,
Wilson B, Hukin J, Carret AS, Van Meter TE, Nakamura H, Toledano H, Fried I,
Fults D, Wataya T, Fryer C, Eisenstat DD, Scheineman K, Johnston D, Michaud J,
Zelcer S, Hammond R, Ramsay DA, Fleming AJ, Lulla RR, Fangusaro JR, Sirachainan
N, Larbcharoensub N, Hongeng S, Barakzai MA, Montpetit A, Stephens D, Grundy RG,
Schüller U, Nicolaides T, Tihan T, Phillips J, Taylor MD, Rutka JT, Dirks P,
Bader GD, Warmuth-Metz M, Rutkowski S, Pietsch T, Judkins AR, Jabado N, Bouffet
E, Huang A. Molecular subgroups of atypical teratoid rhabdoid tumours in
children: an integrated genomic and clinicopathological analysis. Lancet Oncol.
2015 May;16(5):569-82. doi: 10.1016/S1470-2045(15)70114-2. Epub 2015 Apr 14.
PMID: 25882982.
549: Dudley RWR, Smith C, Dishop M, Mirsky D, Handler MH, Rao S. A cervical
spine mass caused by Onchocerca lupi. Lancet. 2015 Oct 3;386(10001):1372. doi:
10.1016/S0140-6736(14)62255-8. Epub 2015 Apr 3. PMID: 25843892.
550: Kang PB, Morrison L, Iannaccone ST, Graham RJ, Bönnemann CG, Rutkowski A,
Hornyak J, Wang CH, North K, Oskoui M, Getchius TS, Cox JA, Hagen EE, Gronseth
G, Griggs RC; Guideline Development Subcommittee of the American Academy of
Neurology and the Practice Issues Review Panel of the American Association of
Neuromuscular & Electrodiagnostic Medicine. Evidence-based guideline summary:
evaluation, diagnosis, and management of congenital muscular dystrophy: Report
of the Guideline Development Subcommittee of the American Academy of Neurology
and the Practice Issues Review Panel of the American Association of
Neuromuscular & Electrodiagnostic Medicine. Neurology. 2015 Mar
31;84(13):1369-78. doi: 10.1212/WNL.0000000000001416. PMID: 25825463; PMCID:
PMC4388744.
551: Garfinkle J, Sant'Anna GM, Rosenblatt B, Majnemer A, Wintermark P, Shevell
MI. Somatosensory evoked potentials in neonates with hypoxic-ischemic
encephalopathy treated with hypothermia. Eur J Paediatr Neurol. 2015
Jul;19(4):423-8. doi: 10.1016/j.ejpn.2015.03.001. Epub 2015 Mar 7. PMID:
25814390.
552: Jobling RK, Assoum M, Gakh O, Blaser S, Raiman JA, Mignot C, Roze E, Dürr
A, Brice A, Lévy N, Prasad C, Paton T, Paterson AD, Roslin NM, Marshall CR,
Desvignes JP, Roëckel-Trevisiol N, Scherer SW, Rouleau GA, Mégarbané A, Isaya G,
Delague V, Yoon G. PMPCA mutations cause abnormal mitochondrial protein
processing in patients with non-progressive cerebellar ataxia. Brain. 2015
Jun;138(Pt 6):1505-17. doi: 10.1093/brain/awv057. Epub 2015 Mar 25. PMID:
25808372; PMCID: PMC4542620.
553: Gardiner C, Harrison P, Belting M, Böing A, Campello E, Carter BS, Collier
ME, Coumans F, Ettelaie C, van Es N, Hochberg FH, Mackman N, Rennert RC, Thaler
J, Rak J, Nieuwland R. Extracellular vesicles, tissue factor, cancer and
thrombosis - discussion themes of the ISEV 2014 Educational Day. J Extracell
Vesicles. 2015 Mar 13;4:26901. doi: 10.3402/jev.v4.26901. PMID: 25773446; PMCID:
PMC4359985.
554: Picard M, Azuelos I, Jung B, Giordano C, Matecki S, Hussain S, White K, Li
T, Liang F, Benedetti A, Gentil BJ, Burelle Y, Petrof BJ. Mechanical ventilation
triggers abnormal mitochondrial dynamics and morphology in the diaphragm. J Appl
Physiol (1985). 2015 May 1;118(9):1161-71. doi: 10.1152/japplphysiol.00873.2014.
Epub 2015 Mar 12. PMID: 25767033.
555: Bourque PR, Chardon JW, Massie R. Autoimmune peripheral neuropathies. Clin
Chim Acta. 2015 Sep 20;449:37-42. doi: 10.1016/j.cca.2015.02.039. Epub 2015 Mar
4. PMID: 25748038.
556: Pinchefsky E, Dubrovsky AS, Friedman D, Shevell M. Part I--Evaluation of
pediatric post-traumatic headaches. Pediatr Neurol. 2015 Mar;52(3):263-9. doi:
10.1016/j.pediatrneurol.2014.10.013. Epub 2014 Oct 16. PMID: 25701185.
557: Helman G, Van Haren K, Bonkowsky JL, Bernard G, Pizzino A, Braverman N,
Suhr D, Patterson MC, Ali Fatemi S, Leonard J, van der Knaap MS, Back SA,
Damiani S, Goldman SA, Takanohashi A, Petryniak M, Rowitch D, Messing A, Wrabetz
L, Schiffmann R, Eichler F, Escolar ML, Vanderver A; GLIA Consortium. Disease
specific therapies in leukodystrophies and leukoencephalopathies. Mol Genet
Metab. 2015 Apr;114(4):527-36. doi: 10.1016/j.ymgme.2015.01.014. Epub 2015 Feb
7. PMID: 25684057; PMCID: PMC4390468.
558: Gomez-Amaya SM, Barbe MF, de Groat WC, Brown JM, Tuite GF, Corcos J, Fecho
SB, Braverman AS, Ruggieri MR Sr. Neural reconstruction methods of restoring
bladder function. Nat Rev Urol. 2015 Feb;12(2):100-18. doi:
10.1038/nrurol.2015.4. PMID: 25666987; PMCID: PMC4324509.
559: Parikh S, Bernard G, Leventer RJ, van der Knaap MS, van Hove J, Pizzino A,
McNeill NH, Helman G, Simons C, Schmidt JL, Rizzo WB, Patterson MC, Taft RJ,
Vanderver A; GLIA Consortium. A clinical approach to the diagnosis of patients
with leukodystrophies and genetic leukoencephelopathies. Mol Genet Metab. 2015
Apr;114(4):501-515. doi: 10.1016/j.ymgme.2014.12.434. Epub 2014 Dec 29. PMID:
25655951; PMCID: PMC4390485.
560: Cai S, Pang WW, Low YL, Sim LW, Sam SC, Bruntraeger MB, Wong EQ, Fok D,
Broekman BF, Singh L, Richmond J, Agarwal P, Qiu A, Saw SM, Yap F, Godfrey KM,
Gluckman PD, Chong YS, Meaney MJ, Kramer MS, Rifkin-Graboi A; GUSTO Study Group.
Infant feeding effects on early neurocognitive development in Asian children. Am
J Clin Nutr. 2015 Feb;101(2):326-36. doi: 10.3945/ajcn.114.095414. Epub 2014 Dec
10. PMID: 25646330.
561: Chen D, Gaborieau V, Zhao Y, Chabrier A, Wang H, Waterboer T, Zaridze D,
Lissowska J, Rudnai P, Fabianova E, Bencko V, Janout V, Foretova L, Mates IN,
Szeszenia-Dabrowska N, Boffetta P, Pawlita M, Lathrop M, Gyllensten U, Brennan
P, McKay JD. A systematic investigation of the contribution of genetic variation
within the MHC region to HPV seropositivity. Hum Mol Genet. 2015 May
1;24(9):2681-8. doi: 10.1093/hmg/ddv015. Epub 2015 Jan 23. PMID: 25616963.
562: Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad
N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ,
Bernard M, Bohlken MM, Boks MP, Bralten J, Brown AA, Chakravarty MM, Chen Q,
Ching CR, Cuellar-Partida G, den Braber A, Giddaluru S, Goldman AL, Grimm O,
Guadalupe T, Hass J, Woldehawariat G, Holmes AJ, Hoogman M, Janowitz D, Jia T,
Kim S, Klein M, Kraemer B, Lee PH, Olde Loohuis LM, Luciano M, Macare C, Mather
KA, Mattheisen M, Milaneschi Y, Nho K, Papmeyer M, Ramasamy A, Risacher SL,
Roiz-Santiañez R, Rose EJ, Salami A, Sämann PG, Schmaal L, Schork AJ, Shin J,
Strike LT, Teumer A, van Donkelaar MM, van Eijk KR, Walters RK, Westlye LT,
Whelan CD, Winkler AM, Zwiers MP, Alhusaini S, Athanasiu L, Ehrlich S, Hakobjan
MM, Hartberg CB, Haukvik UK, Heister AJ, Hoehn D, Kasperaviciute D, Liewald DC,
Lopez LM, Makkinje RR, Matarin M, Naber MA, McKay DR, Needham M, Nugent AC, Pütz
B, Royle NA, Shen L, Sprooten E, Trabzuni D, van der Marel SS, van Hulzen KJ,
Walton E, Wolf C, Almasy L, Ames D, Arepalli S, Assareh AA, Bastin ME, Brodaty
H, Bulayeva KB, Carless MA, Cichon S, Corvin A, Curran JE, Czisch M, de
Zubicaray GI, Dillman A, Duggirala R, Dyer TD, Erk S, Fedko IO, Ferrucci L,
Foroud TM, Fox PT, Fukunaga M, Gibbs JR, Göring HH, Green RC, Guelfi S, Hansell
NK, Hartman CA, Hegenscheid K, Heinz A, Hernandez DG, Heslenfeld DJ, Hoekstra
PJ, Holsboer F, Homuth G, Hottenga JJ, Ikeda M, Jack CR Jr, Jenkinson M, Johnson
R, Kanai R, Keil M, Kent JW Jr, Kochunov P, Kwok JB, Lawrie SM, Liu X, Longo DL,
McMahon KL, Meisenzahl E, Melle I, Mohnke S, Montgomery GW, Mostert JC,
Mühleisen TW, Nalls MA, Nichols TE, Nilsson LG, Nöthen MM, Ohi K, Olvera RL,
Perez-Iglesias R, Pike GB, Potkin SG, Reinvang I, Reppermund S, Rietschel M,
Romanczuk-Seiferth N, Rosen GD, Rujescu D, Schnell K, Schofield PR, Smith C,
Steen VM, Sussmann JE, Thalamuthu A, Toga AW, Traynor BJ, Troncoso J, Turner JA,
Valdés Hernández MC, van 't Ent D, van der Brug M, van der Wee NJ, van Tol MJ,
Veltman DJ, Wassink TH, Westman E, Zielke RH, Zonderman AB, Ashbrook DG, Hager
R, Lu L, McMahon FJ, Morris DW, Williams RW, Brunner HG, Buckner RL, Buitelaar
JK, Cahn W, Calhoun VD, Cavalleri GL, Crespo-Facorro B, Dale AM, Davies GE,
Delanty N, Depondt C, Djurovic S, Drevets WC, Espeseth T, Gollub RL, Ho BC,
Hoffmann W, Hosten N, Kahn RS, Le Hellard S, Meyer-Lindenberg A, Müller-Myhsok
B, Nauck M, Nyberg L, Pandolfo M, Penninx BW, Roffman JL, Sisodiya SM, Smoller
JW, van Bokhoven H, van Haren NE, Völzke H, Walter H, Weiner MW, Wen W, White T,
Agartz I, Andreassen OA, Blangero J, Boomsma DI, Brouwer RM, Cannon DM, Cookson
MR, de Geus EJ, Deary IJ, Donohoe G, Fernández G, Fisher SE, Francks C, Glahn
DC, Grabe HJ, Gruber O, Hardy J, Hashimoto R, Hulshoff Pol HE, Jönsson EG,
Kloszewska I, Lovestone S, Mattay VS, Mecocci P, McDonald C, McIntosh AM, Ophoff
RA, Paus T, Pausova Z, Ryten M, Sachdev PS, Saykin AJ, Simmons A, Singleton A,
Soininen H, Wardlaw JM, Weale ME, Weinberger DR, Adams HH, Launer LJ, Seiler S,
Schmidt R, Chauhan G, Satizabal CL, Becker JT, Yanek L, van der Lee SJ, Ebling
M, Fischl B, Longstreth WT Jr, Greve D, Schmidt H, Nyquist P, Vinke LN, van
Duijn CM, Xue L, Mazoyer B, Bis JC, Gudnason V, Seshadri S, Ikram MA;
Alzheimer’s Disease Neuroimaging Initiative; CHARGE Consortium; EPIGEN; IMAGEN;
SYS, Martin NG, Wright MJ, Schumann G, Franke B, Thompson PM, Medland SE. Common
genetic variants influence human subcortical brain structures. Nature. 2015 Apr
9;520(7546):224-9. doi: 10.1038/nature14101. Epub 2015 Jan 21. PMID: 25607358;
PMCID: PMC4393366.
563: Van Haren K, Bonkowsky JL, Bernard G, Murphy JL, Pizzino A, Helman G, Suhr
D, Waggoner J, Hobson D, Vanderver A, Patterson MC; GLIA Consortium. Consensus
statement on preventive and symptomatic care of leukodystrophy patients. Mol
Genet Metab. 2015 Apr;114(4):516-26. doi: 10.1016/j.ymgme.2014.12.433. Epub 2014
Dec 27. PMID: 25577286.
564: Chyu MC, Austin T, Calisir F, Chanjaplammootil S, Davis MJ, Favela J, Gan
H, Gefen A, Haddas R, Hahn-Goldberg S, Hornero R, Huang YL, Jensen Ø, Jiang Z,
Katsanis JS, Lee JA, Lewis G, Lovell NH, Luebbers HT, Morales GG, Matis T,
Matthews JT, Mazur L, Ng EY, Oommen KJ, Ormand K, Rohde T, Sánchez-Morillo D,
Sanz-Calcedo JG, Sawan M, Shen CL, Shieh JS, Su CT, Sun L, Sun M, Sun Y, Tewolde
SN, Williams EA, Yan C, Zhang J, Zhang YT. Healthcare Engineering Defined: A
White Paper. J Healthc Eng. 2015;6(4):635-47. doi: 10.1260/2040-2295.6.4.635.
PMID: 27010831.
565: Broekman BF, Wang C, Li Y, Rifkin-Graboi A, Saw SM, Chong YS, Kwek K,
Gluckman PD, Fortier MV, Meaney MJ, Qiu A; GUSTO Study Group. Gestational age
and neonatal brain microstructure in term born infants: a birth cohort study.
PLoS One. 2014 Dec 23;9(12):e115229. doi: 10.1371/journal.pone.0115229. PMID:
25535959; PMCID: PMC4275243.
566: Gilardino MS, Karunanayake M, Al-Humsi T, Izadpanah A, Al-Ajmi H, Marcoux
J, Atkinson J, Farmer JP. A comparison and cost analysis of cranioplasty
techniques: autologous bone versus custom computer-generated implants. J
Craniofac Surg. 2015 Jan;26(1):113-7. doi: 10.1097/SCS.0000000000001305. PMID:
25534061.
567: Ahn JJ, O'Mahony J, Moshkova M, Hanwell HE, Singh H, Zhang MA, Marrie RA,
Bar-Or A, Sadovnick DA, Dunn SE, Banwell BL. Puberty in females enhances the
risk of an outcome of multiple sclerosis in children and the development of
central nervous system autoimmunity in mice. Mult Scler. 2015 May;21(6):735-48.
doi: 10.1177/1352458514551453. Epub 2014 Dec 22. PMID: 25533291.
568: Pinchefsky E, Dubrovsky AS, Friedman D, Shevell M. Part II--Management of
pediatric post-traumatic headaches. Pediatr Neurol. 2015 Mar;52(3):270-80. doi:
10.1016/j.pediatrneurol.2014.10.015. Epub 2014 Oct 16. PMID: 25499091.
569: Dai YE, Tang L, Healy J, Sinnett D. Contribution of polymorphisms in IKZF1
gene to childhood acute leukemia: a meta-analysis of 33 case-control studies.
PLoS One. 2014 Nov 25;9(11):e113748. doi: 10.1371/journal.pone.0113748. PMID:
25423013; PMCID: PMC4244140.
570: La Piana R, Vanasse M, Brais B, Bernard G. Myelination Delay and Allan-
Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene. J Child
Neurol. 2015 Sep;30(10):1371-4. doi: 10.1177/0883073814555189. Epub 2014 Nov 7.
PMID: 25380603.
571: La Piana R, Tran LT, Guerrero K, Brais B, Levesque S, Sébire G, Riou E,
Bernard G. Spastic paraparesis and marked improvement of leukoencephalopathy in
Aicardi-Goutières syndrome. Neuropediatrics. 2014 Dec;45(6):406-10. doi:
10.1055/s-0034-1393710. Epub 2014 Oct 24. PMID: 25343331.
572: Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M,
Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S,
Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van
der Knaap MS, Bernard G; 4H Research Group. Clinical spectrum of 4H
leukodystrophy caused by POLR3A and POLR3B mutations. Neurology. 2014 Nov
18;83(21):1898-905. doi: 10.1212/WNL.0000000000001002. Epub 2014 Oct 22. PMID:
25339210; PMCID: PMC4248461.
573: Winkler-Schwartz A, Garfinkle J, Shevell MI. Autism spectrum disorder in a
term birth neonatal intensive care unit population. Pediatr Neurol. 2014
Dec;51(6):776-80. doi: 10.1016/j.pediatrneurol.2014.07.009. Epub 2014 Jul 16.
PMID: 25303867.
574: Donald KA, Kakooza AM, Wammanda RD, Mallewa M, Samia P, Babakir H, Bearden
D, Majnemer A, Fehlings D, Shevell M, Chugani H, Wilmshurst JM. Pediatric
Cerebral Palsy in Africa: Where Are We? J Child Neurol. 2015 Jul;30(8):963-71.
doi: 10.1177/0883073814549245. Epub 2014 Oct 7. PMID: 25296926.
575: Armstrong-Wells J, Donnelly M, Post MD, Manco-Johnson MJ, Winn VD, Sébire
G. Inflammatory predictors of neurologic disability after preterm premature
rupture of membranes. Am J Obstet Gynecol. 2015 Feb;212(2):212.e1-9. doi:
10.1016/j.ajog.2014.09.016. Epub 2014 Sep 16. PMID: 25223243; PMCID: PMC4312536.
576: Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill
RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E,
Dan B, Parrini E, Guerrini R, Scheffer IE, Berkovic SF, Leventer RJ, Shen Y, Wu
BL, Barkovich AJ, Sahin M, Chang BS, Bamshad M, Nickerson DA, Shendure J, Poduri
A, Yu TW, Walsh CA. Somatic mutations in cerebral cortical malformations. N Engl
J Med. 2014 Aug 21;371(8):733-43. doi: 10.1056/NEJMoa1314432. PMID: 25140959;
PMCID: PMC4274952.
577: Finkel RS, McDermott MP, Kaufmann P, Darras BT, Chung WK, Sproule DM, Kang
PB, Foley AR, Yang ML, Martens WB, Oskoui M, Glanzman AM, Flickinger J, Montes
J, Dunaway S, O'Hagen J, Quigley J, Riley S, Benton M, Ryan PA, Montgomery M,
Marra J, Gooch C, De Vivo DC. Observational study of spinal muscular atrophy
type I and implications for clinical trials. Neurology. 2014 Aug 26;83(9):810-7.
doi: 10.1212/WNL.0000000000000741. Epub 2014 Jul 30. PMID: 25080519; PMCID:
PMC4155049.
578: Robinson MÈ, Rossignol E, Brais B, Rouleau G, Arbour JF, Bernard G.
Vanishing white matter disease in French-Canadian patients from Quebec. Pediatr
Neurol. 2014 Aug;51(2):225-32. doi: 10.1016/j.pediatrneurol.2014.05.006. Epub
2014 May 14. PMID: 25079571.
579: Fasano A, Bologna M, Iezzi E, Pavone L, Srour M, Di Biasio F, Grillea G,
Rouleau GA, Levert A, Sebastiano F, Colonnese C, Berardelli A. Congenital Mirror
Movements in a New Italian Family. Mov Disord Clin Pract. 2014 Jul
28;1(3):180-187. doi: 10.1002/mdc3.12066. PMID: 30713853; PMCID: PMC6353446.
580: Gauvin M, Lina JM, Lachapelle P. Advance in ERG analysis: from peak time
and amplitude to frequency, power, and energy. Biomed Res Int. 2014;2014:246096.
doi: 10.1155/2014/246096. Epub 2014 Jul 1. PMID: 25061605; PMCID: PMC4100345.
581: Zhang JY, Oskoui M, Shevell M. A population-based study of communication
impairment in cerebral palsy. J Child Neurol. 2015 Mar;30(3):277-84. doi:
10.1177/0883073814538497. Epub 2014 Jul 22. PMID: 25051968.
582: Koenekoop RK, Sui R, Sallum J, van den Born LI, Ajlan R, Khan A, den
Hollander AI, Cremers FP, Mendola JD, Bittner AK, Dagnelie G, Schuchard RA,
Saperstein DA. Oral 9-cis retinoid for childhood blindness due to Leber
congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b
trial. Lancet. 2014 Oct 25;384(9953):1513-20. doi:
10.1016/S0140-6736(14)60153-7. Epub 2014 Jul 13. PMID: 25030840.
583: Zeidman LA, Ziller MG, Shevell M. Gerstmann, Sträussler, and Scheinker: the
persecution of the men behind the syndrome. Neurology. 2014 Jul 15;83(3):272-7.
doi: 10.1212/WNL.0000000000000606. PMID: 25024443.
584: Kashani A, Thiffault I, Dilenge ME, Saint-Martin C, Guerrero K, Tran LT,
Shoubridge E, van der Knaap MS, Braverman N, Bernard G. A homozygous mutation in
the NDUFS1 gene presents with a mild cavitating leukoencephalopathy.
Neurogenetics. 2014 Aug;15(3):161-4. doi: 10.1007/s10048-014-0412-2. Epub 2014
Jun 21. PMID: 24952175.
585: Kahle KT, Merner ND, Friedel P, Silayeva L, Liang B, Khanna A, Shang Y,
Lachance-Touchette P, Bourassa C, Levert A, Dion PA, Walcott B, Spiegelman D,
Dionne-Laporte A, Hodgkinson A, Awadalla P, Nikbakht H, Majewski J, Cossette P,
Deeb TZ, Moss SJ, Medina I, Rouleau GA. Genetically encoded impairment of
neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.
EMBO Rep. 2014 Jul;15(7):766-74. doi: 10.15252/embr.201438840. Epub 2014 Jun 13.
PMID: 24928908; PMCID: PMC4196980.
586: Vargus-Adams JN, Majnemer A. International Classification of Functioning,
Disability and Health (ICF) as a framework for change: revolutionizing
rehabilitation. J Child Neurol. 2014 Aug;29(8):1030-5. doi:
10.1177/0883073814533595. Epub 2014 May 21. PMID: 24850572.
587: Perreault S, Ramaswamy V, Achrol AS, Chao K, Liu TT, Shih D, Remke M,
Schubert S, Bouffet E, Fisher PG, Partap S, Vogel H, Taylor MD, Cho YJ, Yeom KW.
MRI surrogates for molecular subgroups of medulloblastoma. AJNR Am J
Neuroradiol. 2014 Jul;35(7):1263-9. doi: 10.3174/ajnr.A3990. Epub 2014 May 15.
PMID: 24831600; PMCID: PMC4819007.
588: Jadavji NM, Bahous RH, Deng L, Malysheva O, Grand'maison M, Bedell BJ,
Caudill MA, Rozen R. Mouse model for deficiency of methionine synthase reductase
exhibits short-term memory impairment and disturbances in brain choline
metabolism. Biochem J. 2014 Jul 15;461(2):205-12. doi: 10.1042/BJ20131568. PMID:
24800750.
589: Fontebasso AM, Papillon-Cavanagh S, Schwartzentruber J, Nikbakht H, Gerges
N, Fiset PO, Bechet D, Faury D, De Jay N, Ramkissoon LA, Corcoran A, Jones DT,
Sturm D, Johann P, Tomita T, Goldman S, Nagib M, Bendel A, Goumnerova L, Bowers
DC, Leonard JR, Rubin JB, Alden T, Browd S, Geyer JR, Leary S, Jallo G, Cohen K,
Gupta N, Prados MD, Carret AS, Ellezam B, Crevier L, Klekner A, Bognar L, Hauser
P, Garami M, Myseros J, Dong Z, Siegel PM, Malkin H, Ligon AH, Albrecht S,
Pfister SM, Ligon KL, Majewski J, Jabado N, Kieran MW. Recurrent somatic
mutations in ACVR1 in pediatric midline high-grade astrocytoma. Nat Genet. 2014
May;46(5):462-6. doi: 10.1038/ng.2950. Epub 2014 Apr 6. PMID: 24705250; PMCID:
PMC4282994.
590: Dubrovsky AS, Friedman D, Kocilowicz H. Pediatric post-traumatic headaches
and peripheral nerve blocks of the scalp: a case series and patient satisfaction
survey. Headache. 2014 May;54(5):878-87. doi: 10.1111/head.12334. Epub 2014 Apr
2. PMID: 24697265.
591: Kool M, Jones DT, Jäger N, Northcott PA, Pugh TJ, Hovestadt V, Piro RM,
Esparza LA, Markant SL, Remke M, Milde T, Bourdeaut F, Ryzhova M, Sturm D, Pfaff
E, Stark S, Hutter S, Seker-Cin H, Johann P, Bender S, Schmidt C, Rausch T, Shih
D, Reimand J, Sieber L, Wittmann A, Linke L, Witt H, Weber UD, Zapatka M, König
R, Beroukhim R, Bergthold G, van Sluis P, Volckmann R, Koster J, Versteeg R,
Schmidt S, Wolf S, Lawerenz C, Bartholomae CC, von Kalle C, Unterberg A, Herold-
Mende C, Hofer S, Kulozik AE, von Deimling A, Scheurlen W, Felsberg J,
Reifenberger G, Hasselblatt M, Crawford JR, Grant GA, Jabado N, Perry A, Cowdrey
C, Croul S, Zadeh G, Korbel JO, Doz F, Delattre O, Bader GD, McCabe MG, Collins
VP, Kieran MW, Cho YJ, Pomeroy SL, Witt O, Brors B, Taylor MD, Schüller U,
Korshunov A, Eils R, Wechsler-Reya RJ, Lichter P, Pfister SM; ICGC PedBrain
Tumor Project. Genome sequencing of SHH medulloblastoma predicts genotype-
related response to smoothened inhibition. Cancer Cell. 2014 Mar
17;25(3):393-405. doi: 10.1016/j.ccr.2014.02.004. PMID: 24651015; PMCID:
PMC4493053.
592: Racine E, Bell E, Yan A, Andrew G, Bell LE, Clarke M, Dubljevic V,
Goldowitz D, Janvier A, McLachlan K, Muhajarine N, Nicholas D, Oskoui M,
Rasmussen C, Rasmussen LA, Roberts W, Shevell M, Wade L, Yager JY. Ethics
challenges of transition from paediatric to adult health care services for young
adults with neurodevelopmental disabilities. Paediatr Child Health. 2014
Feb;19(2):65-8. doi: 10.1093/pch/19.2.65. PMID: 24596475; PMCID: PMC3941669.
593: Mack SC, Witt H, Piro RM, Gu L, Zuyderduyn S, Stütz AM, Wang X, Gallo M,
Garzia L, Zayne K, Zhang X, Ramaswamy V, Jäger N, Jones DT, Sill M, Pugh TJ,
Ryzhova M, Wani KM, Shih DJ, Head R, Remke M, Bailey SD, Zichner T, Faria CC,
Barszczyk M, Stark S, Seker-Cin H, Hutter S, Johann P, Bender S, Hovestadt V,
Tzaridis T, Dubuc AM, Northcott PA, Peacock J, Bertrand KC, Agnihotri S, Cavalli
FM, Clarke I, Nethery-Brokx K, Creasy CL, Verma SK, Koster J, Wu X, Yao Y, Milde
T, Sin-Chan P, Zuccaro J, Lau L, Pereira S, Castelo-Branco P, Hirst M, Marra MA,
Roberts SS, Fults D, Massimi L, Cho YJ, Van Meter T, Grajkowska W, Lach B,
Kulozik AE, von Deimling A, Witt O, Scherer SW, Fan X, Muraszko KM, Kool M,
Pomeroy SL, Gupta N, Phillips J, Huang A, Tabori U, Hawkins C, Malkin D,
Kongkham PN, Weiss WA, Jabado N, Rutka JT, Bouffet E, Korbel JO, Lupien M,
Aldape KD, Bader GD, Eils R, Lichter P, Dirks PB, Pfister SM, Korshunov A,
Taylor MD. Epigenomic alterations define lethal CIMP-positive ependymomas of
infancy. Nature. 2014 Feb 27;506(7489):445-50. doi: 10.1038/nature13108. Epub
2014 Feb 19. PMID: 24553142; PMCID: PMC4174313.
594: van Karnebeek CD, Shevell M, Zschocke J, Moeschler JB, Stockler S. The
metabolic evaluation of the child with an intellectual developmental disorder:
diagnostic algorithm for identification of treatable causes and new digital
resource. Mol Genet Metab. 2014 Apr;111(4):428-38. doi:
10.1016/j.ymgme.2014.01.011. Epub 2014 Jan 24. PMID: 24518794.
595: Smith ML, Olds J, Snyder T, Elliott I, Lach L, Whiting S. A follow-up study
of cognitive function in young adults who had resective epilepsy surgery in
childhood. Epilepsy Behav. 2014 Mar;32:79-83. doi: 10.1016/j.yebeh.2014.01.006.
Epub 2014 Feb 7. PMID: 24508594.
596: Theeler BJ, Ellezam B, Sadighi ZS, Mehta V, Tran MD, Adesina AM, Bruner JM,
Puduvalli VK. Adult pilocytic astrocytomas: clinical features and molecular
analysis. Neuro Oncol. 2014 Jun;16(6):841-7. doi: 10.1093/neuonc/not246. Epub
2014 Jan 26. PMID: 24470550; PMCID: PMC4022218.
597: LeBlanc AC, Ramcharitar J, Afonso V, Hamel E, Bennett DA, Pakavathkumar P,
Albrecht S. Caspase-6 activity in the CA1 region of the hippocampus induces age-
dependent memory impairment. Cell Death Differ. 2014 May;21(5):696-706. doi:
10.1038/cdd.2013.194. Epub 2014 Jan 10. PMID: 24413155; PMCID: PMC3978300.
598: Owen M, Shevell M, Donofrio M, Majnemer A, McCarter R, Vezina G, Bouyssi-
Kobar M, Evangelou I, Freeman D, Weisenfeld N, Limperopoulos C. Brain volume and
neurobehavior in newborns with complex congenital heart defects. J Pediatr. 2014
May;164(5):1121-1127.e1. doi: 10.1016/j.jpeds.2013.11.033. Epub 2013 Dec 22.
PMID: 24367983; PMCID: PMC4474232.
599: Kleinman CL, Gerges N, Papillon-Cavanagh S, Sin-Chan P, Pramatarova A,
Quang DA, Adoue V, Busche S, Caron M, Djambazian H, Bemmo A, Fontebasso AM,
Spence T, Schwartzentruber J, Albrecht S, Hauser P, Garami M, Klekner A, Bognar
L, Montes JL, Staffa A, Montpetit A, Berube P, Zakrzewska M, Zakrzewski K,
Liberski PP, Dong Z, Siegel PM, Duchaine T, Perotti C, Fleming A, Faury D, Remke
M, Gallo M, Dirks P, Taylor MD, Sladek R, Pastinen T, Chan JA, Huang A, Majewski
J, Jabado N. Fusion of TTYH1 with the C19MC microRNA cluster drives expression
of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR. Nat Genet.
2014 Jan;46(1):39-44. doi: 10.1038/ng.2849. Epub 2013 Dec 8. PMID: 24316981.
600: Yu C, Ramgopal S, Libenson M, Abdelmoumen I, Powell C, Remy K, Madsen JR,
Rotenberg A, Loddenkemper T. Outcomes of vagal nerve stimulation in a pediatric
population: a single center experience. Seizure. 2014 Feb;23(2):105-11. doi:
10.1016/j.seizure.2013.10.002. Epub 2013 Oct 17. PMID: 24309238.
601: Aris IM, Soh SE, Tint MT, Liang S, Chinnadurai A, Saw SM, Rajadurai VS,
Kwek K, Meaney MJ, Godfrey KM, Gluckman PD, Yap FK, Chong YS, Lee YS. Effect of
maternal glycemia on neonatal adiposity in a multiethnic Asian birth cohort. J
Clin Endocrinol Metab. 2014 Jan;99(1):240-7. doi: 10.1210/jc.2013-2738. Epub
2013 Dec 20. PMID: 24243635.
602: Bizik G, Picard M, Nijjar R, Tourjman V, McEwen BS, Lupien SJ, Juster RP.
Allostatic load as a tool for monitoring physiological dysregulations and
comorbidities in patients with severe mental illnesses. Harv Rev Psychiatry.
2013 Nov-Dec;21(6):296-313. doi: 10.1097/HRP.0000000000000012. PMID: 24201821.
603: Synofzik M, Bernard G, Lindig T, Gburek-Augustat J. Teaching neuroimages:
hypomyelinating leukodystrophy with hypodontia due to POLR3B: look into a
leukodystrophy's mouth. Neurology. 2013 Nov 5;81(19):e145. doi:
10.1212/01.wnl.0000435300.64776.7e. PMID: 24190003; PMCID: PMC3812106.
604: Verhey LH, Signori A, Arnold DL, Bar-Or A, Sadovnick AD, Marrie RA, Banwell
B, Sormani MP. Clinical and MRI activity as determinants of sample size for
pediatric multiple sclerosis trials. Neurology. 2013 Oct 1;81(14):1215-21. doi:
10.1212/WNL.0b013e3182a6cb9b. Epub 2013 Aug 21. PMID: 23966255; PMCID:
PMC3795606.
605: Poliachik SL, Poliakov AV, Jansen LA, McDaniel SS, Wray CD, Kuratani J,
Saneto RP, Ojemann JG, Novotny EJ Jr. Tissue localization during resective
epilepsy surgery. Neurosurg Focus. 2013 Jun;34(6):E8. doi:
10.3171/2013.3.FOCUS1360. PMID: 23724842.
606: Dudley RW, Parolin M, Gagnon B, Saluja R, Yap R, Montpetit K, Ruck J,
Poulin C, Cantin MA, Benaroch TE, Farmer JP. Long-term functional benefits of
selective dorsal rhizotomy for spastic cerebral palsy. J Neurosurg Pediatr. 2013
Aug;12(2):142-50. doi: 10.3171/2013.4.PEDS12539. Epub 2013 May 28. PMID:
23713680.
607: Baird R, Guilbault MP, Tessier R, Ansermino JM. A systematic review and
meta-analysis of caudal blockade versus alternative analgesic strategies for
pediatric inguinal hernia repair. J Pediatr Surg. 2013 May;48(5):1077-85. doi:
10.1016/j.jpedsurg.2013.02.030. PMID: 23701786.
608: Garfinkle J, Sant'Anna GM, Wintermark P, Ali N, Morneault L, Koclas L,
Shevell MI. Cooling in the real world: therapeutic hypothermia in hypoxic-
ischemic encephalopathy. Eur J Paediatr Neurol. 2013 Sep;17(5):492-7. doi:
10.1016/j.ejpn.2013.03.006. Epub 2013 Apr 18. PMID: 23603010.
609: Zou Y, Chiu H, Zinovyeva A, Ambros V, Chuang CF, Chang C. Developmental
decline in neuronal regeneration by the progressive change of two intrinsic
timers. Science. 2013 Apr 19;340(6130):372-376. doi: 10.1126/science.1231321.
PMID: 23599497; PMCID: PMC4074024.
610: Dufresne D, Hamdan FF, Rosenfeld JA, Torchia B, Rosenblatt B, Michaud JL,
Srour M. Homozygous deletion of Tenascin-R in a patient with intellectual
disability. J Med Genet. 2012 Jul;49(7):451-4. doi:
10.1136/jmedgenet-2012-100831. Epub 2012 Jun 22. PMID: 22730557; PMCID:
PMC3395313.
611: Bretholz A, Doan Q, Cheng A, Lauder G. A presurvey and postsurvey of a web-
and simulation-based course of ultrasound-guided nerve blocks for pediatric
emergency medicine. Pediatr Emerg Care. 2012 Jun;28(6):506-9. doi:
10.1097/PEC.0b013e3182586f42. PMID: 22653464.
612: Shevell M. A Canadian paradox: Tommy Douglas and eugenics. Can J Neurol
Sci. 2012 Jan;39(1):35-9. doi: 10.1017/s0317167100012658. PMID: 22384493.
613: Martin K, Baird R, Farmer JP, Emil S, Laberge JM, Shaw K, Puligandla P. The
use of laparoscopy in ventriculoperitoneal shunt revisions. J Pediatr Surg. 2011
Nov;46(11):2146-50. doi: 10.1016/j.jpedsurg.2011.07.001. PMID: 22075347.
614: Shevell MI. A brief synopsis of the "why, what, and how" of teaching ethics
to pediatric neurology trainees. Semin Pediatr Neurol. 2011 Jun;18(2):79-80.
doi: 10.1016/j.spen.2011.05.009. PMID: 22036484.
615: Garfinkle J, Andermann F, Shevell MI. Neurolathyrism in vapniarka: medical
heroism in a concentration Camp. Can J Neurol Sci. 2011 Nov;38(6):839-44. doi:
10.1017/s0317167100012403. PMID: 22030420.
616: Bernard G, Chouery E, Putorti ML, Tétreault M, Takanohashi A, Carosso G,
Clément I, Boespflug-Tanguy O, Rodriguez D, Delague V, Abou Ghoch J, Jalkh N,
Dorboz I, Fribourg S, Teichmann M, Megarbane A, Schiffmann R, Vanderver A, Brais
B. Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III
cause a recessive hypomyelinating leukodystrophy. Am J Hum Genet. 2011 Sep
9;89(3):415-23. doi: 10.1016/j.ajhg.2011.07.014. Erratum in: Am J Hum Genet.
2012 Nov 2;91(5):972. PMID: 21855841; PMCID: PMC3169829.
617: Hasan A, Palumbo M, Atkinson J, Carret AS, Farmer JP, Montes J, Albrecht S,
Saint-Martin C, Freeman CR. Treatment-related morbidity in atypical
teratoid/rhabdoid tumor: multifocal necrotizing leukoencephalopathy. Pediatr
Neurosurg. 2011;47(1):7-14. doi: 10.1159/000323412. Epub 2011 May 26. PMID:
21613772.
618: Garfinkle J, Shevell MI. Predictors of outcome in term infants with
neonatal seizures subsequent to intrapartum asphyxia. J Child Neurol. 2011
Apr;26(4):453-9. doi: 10.1177/0883073810382907. Epub 2011 Jan 26. PMID:
21270469.
619: Garon ML, Rufiange M, Hamilton R, McCulloch DL, Lachapelle P. Asymmetrical
growth of the photopic hill during the light adaptation effect. Doc Ophthalmol.
2010 Dec;121(3):177-87. doi: 10.1007/s10633-010-9243-0. Epub 2010 Aug 15. PMID:
20711798.
620: Limperopoulos C. Extreme prematurity, cerebellar injury, and autism. Semin
Pediatr Neurol. 2010 Mar;17(1):25-9. doi: 10.1016/j.spen.2010.01.003. PMID:
20434689.
621: Self L, Shevell MI; REPACQ Consortium. A registry-based assessment of
cerebral palsy and cerebral malformations. J Child Neurol. 2010
Nov;25(11):1313-8. doi: 10.1177/0883073810362759. Epub 2010 Mar 11. PMID:
20223748.
622: Shevell MI. The terms diplegia and quadriplegia should not be abandoned.
Dev Med Child Neurol. 2010 Jun;52(6):508-9. doi:
10.1111/j.1469-8749.2009.03566.x. Epub 2009 Dec 18. PMID: 20030685.
623: Al-Macki N, Miller SP, Hall N, Shevell M. The spectrum of abnormal
neurologic outcomes subsequent to term intrapartum asphyxia. Pediatr Neurol.
2009 Dec;41(6):399-405. doi: 10.1016/j.pediatrneurol.2009.06.001. PMID:
19931160.
624: Shamji MF, Vassilyadi M, Lam CH, Montes JL, Farmer JP. Congenital tumors of
the central nervous system: the MCH experience. Pediatr Neurosurg.
2009;45(5):368-74. doi: 10.1159/000257526. Epub 2009 Nov 11. PMID: 19907201.
625: Frigon C, Loetwiriyakul W, Ranger M, Otis A. An acute pain service improves
postoperative pain management for children undergoing selective dorsal
rhizotomy. Paediatr Anaesth. 2009 Dec;19(12):1213-9. doi:
10.1111/j.1460-9592.2009.03184.x. Epub 2009 Oct 23. PMID: 19863740.
626: Shevell MI. Current understandings and challenges in the management of
cerebral palsy. Minerva Pediatr. 2009 Aug;61(4):399-413. PMID: 19752849.
627: Shevell MI. Present conceptualization of early childhood neurodevelopmental
disabilities. J Child Neurol. 2010 Jan;25(1):120-6. doi:
10.1177/0883073809336122. Epub 2009 Sep 8. PMID: 19738235.
628: Sloan ME, Simard-Tremblay E, Shevell MI. Features of a subset of children
with complex partial epilepsy requiring combination therapy for effective
seizure control. J Child Neurol. 2010 Jan;25(1):43-7. doi:
10.1177/0883073809336126. Epub 2009 Jun 3. PMID: 19494358.
629: Ryckman J, Laberge JM, Puligandla PS. Paraplegia after chest wall resection
for primitive neuroectodermal tumor. Semin Pediatr Surg. 2009 May;18(2):113-5.
doi: 10.1053/j.sempedsurg.2009.02.010. PMID: 19349002.
630: Shevell M. The tripartite origins of the tonic neck reflex: Gesell,
Gerstmann, and Magnus. Neurology. 2009 Mar 3;72(9):850-3. doi:
10.1212/01.wnl.0000343961.35429.09. PMID: 19255413.
631: Bernard G, Shevell M. The wobbly child: an approach to inherited ataxias.
Semin Pediatr Neurol. 2008 Dec;15(4):194-208. doi: 10.1016/j.spen.2008.10.011.
PMID: 19073328.
632: Venkateswaran S, Shevell M. The case against routine electroencephalography
in specific language impairment. Pediatrics. 2008 Oct;122(4):e911-6. doi:
10.1542/peds.2008-0257. Epub 2008 Sep 15. PMID: 18794194.
633: Frigon C, Sedeek K, Poulin C, Brown K, Farmer JP. Does ketamine affect
intraoperative electrophysiological monitoring in children undergoing selective
posterior rhizotomy? Paediatr Anaesth. 2008 Sep;18(9):831-7. doi:
10.1111/j.1460-9592.2008.02687.x. PMID: 18768043.
634: Crevier L, Mercier C. L'organisation de la transition enfant à adulte en
neurochirurgie pédiatrique au Canada [The organization of the transition from
childhood to adulthood in pediatric neurosurgery in Canada]. Neurochirurgie.
2008 Oct;54(5):583-6. French. doi: 10.1016/j.neuchi.2008.07.006. Epub 2008 Aug
26. PMID: 18752813.
635: Nadler B, Shevell MI. Childhood absence epilepsy requiring more than one
medication for seizure control. Can J Neurol Sci. 2008 Jul;35(3):297-300. PMID:
18714796.
636: Webster RI, Erdos C, Evans K, Majnemer A, Saigal G, Kehayia E,
Thordardottir E, Evans A, Shevell MI. Neurological and magnetic resonance
imaging findings in children with developmental language impairment. J Child
Neurol. 2008 Aug;23(8):870-7. doi: 10.1177/0883073808315620. PMID: 18660471.
637: Ang C, Hauerstock D, Guiot MC, Kasymjanova G, Roberge D, Kavan P, Muanza T.
Characteristics and outcomes of medulloblastoma in adults. Pediatr Blood Cancer.
2008 Nov;51(5):603-7. doi: 10.1002/pbc.21588. PMID: 18649371.
638: Bernard G, Riou E, Rosenblatt B, Dilenge ME, Poulin C. Simultaneous
Guillain-Barré syndrome and acute disseminated encephalomyelitis in the
pediatric population. J Child Neurol. 2008 Jul;23(7):752-7. doi:
10.1177/0883073808314360. Epub 2008 Mar 19. PMID: 18354151.
639: Bernard G, Shevell MI. Channelopathies: a review. Pediatr Neurol. 2008
Feb;38(2):73-85. doi: 10.1016/j.pediatrneurol.2007.09.007. PMID: 18206787.
640: Racine J, Behn D, Lachapelle P. Structural and functional maturation of the
retina of the albino Hartley guinea pig. Doc Ophthalmol. 2008 Jul;117(1):13-26.
doi: 10.1007/s10633-007-9098-1. Epub 2007 Nov 22. PMID: 18034273.
641: Farmer JP, Sabbagh AJ. Selective dorsal rhizotomies in the treatment of
spasticity related to cerebral palsy. Childs Nerv Syst. 2007 Sep;23(9):991-1002.
doi: 10.1007/s00381-007-0398-2. Epub 2007 Jul 21. PMID: 17643249.
642: Shevell M. Office evaluation of the child with developmental delay. Semin
Pediatr Neurol. 2006 Dec;13(4):256-61. doi: 10.1016/j.spen.2006.09.006. PMID:
17178355.
643: Frigon C, Mai R, Valois-Gomez T, Desparmet J. Bowel hematoma following an
iliohypogastric-ilioinguinal nerve block. Paediatr Anaesth. 2006
Sep;16(9):993-6. doi: 10.1111/j.1460-9592.2006.01909.x. PMID: 16918666.
644: Srour M, Mazer B, Shevell MI. Analysis of clinical features predicting
etiologic yield in the assessment of global developmental delay. Pediatrics.
2006 Jul;118(1):139-45. doi: 10.1542/peds.2005-2702. PMID: 16818559.
645: Majnemer A, Limperopoulos C, Shevell M, Rohlicek C, Rosenblatt B,
Tchervenkov C. Health and well-being of children with congenital cardiac
malformations, and their families, following open-heart surgery. Cardiol Young.
2006 Apr;16(2):157-64. doi: 10.1017/S1047951106000096. PMID: 16553978.
646: Oskoui M, Webster RI, Zhang X, Shevell MI. Factors predictive of outcome in
childhood epilepsy. J Child Neurol. 2005 Nov;20(11):898-904. doi:
10.1177/08830738050200110701. PMID: 16417860.
647: Mittal S, Montes JL, Farmer JP, Rosenblatt B, Dubeau F, Andermann F, Poulin
N, Olivier A. Long-term outcome after surgical treatment of temporal lobe
epilepsy in children. J Neurosurg. 2005 Nov;103(5 Suppl):401-12. doi:
10.3171/ped.2005.103.5.0401. PMID: 16302611.
648: Shevell M, Majnemer A, Platt RW, Webster R, Birnbaum R. Developmental and
functional outcomes in children with global developmental delay or developmental
language impairment. Dev Med Child Neurol. 2005 Oct;47(10):678-83. doi:
10.1017/S0012162205001386. PMID: 16174311.
649: Oskoui M, Shevell MI. Profile of pediatric hemiparesis. J Child Neurol.
2005 Jun;20(6):471-6. doi: 10.1177/088307380502000601. PMID: 15996394.
650: Shevell MI, Majnemer A, Webster RI, Platt RW, Birnbaum R. Outcomes at
school age of preschool children with developmental language impairment. Pediatr
Neurol. 2005 Apr;32(4):264-9. doi: 10.1016/j.pediatrneurol.2004.12.008. PMID:
15797183.
651: Shevell MI. The "Bermuda triangle" of neonatal neurology: cerebral palsy,
neonatal encephalopathy, and intrapartum asphyxia. Semin Pediatr Neurol. 2004
Mar;11(1):24-30. doi: 10.1016/j.spen.2004.01.005. PMID: 15132251.
652: Shevell MI. The ethics of case reports. Paediatr Child Health. 2004
Feb;9(2):83-4. doi: 10.1093/pch/9.2.83. PMID: 19654984; PMCID: PMC2720465.
653: Racine J, Behn D, Simard E, Lachapelle P. Spontaneous occurrence of a
potentially night blinding disorder in guinea pigs. Doc Ophthalmol. 2003
Jul;107(1):59-69. doi: 10.1023/a:1024435911882. PMID: 12906123.
654: Behn D, Doke A, Racine J, Casanova C, Chemtob S, Lachapelle P. Dark
adaptation is faster in pigmented than albino rats. Doc Ophthalmol. 2003
Mar;106(2):153-9. doi: 10.1023/a:1022511918823. PMID: 12678280.
655: Al-Twajri WA, Shevell MI. Atypical benign epilepsy of childhood with
rolandic spikes: features of a subset requiring more than one medication for
seizure control. J Child Neurol. 2002 Dec;17(12):901-4. PMID: 12593463.
656: Shevell MI. Clinical and diagnostic profile of agenesis of the corpus
callosum. J Child Neurol. 2002 Dec;17(12):896-900. PMID: 12593462.
657: Shevell M. Hallervorden and history. N Engl J Med. 2003 Jan 2;348(1):3-4.
doi: 10.1056/NEJMp020158. PMID: 12510036.
658: Mittal S, Farmer JP, Al-Atassi B, Montpetit K, Gervais N, Poulin C,
Benaroch TE, Cantin MA. Functional performance following selective posterior
rhizotomy: long-term results determined using a validated evaluative measure. J
Neurosurg. 2002 Sep;97(3):510-8. doi: 10.3171/jns.2002.97.3.0510. PMID:
12296632.
659: Farmer JP, Khan S, Khan A, Ortenberg J, Freeman C, O'Gorman AM, Montes J.
Neurofibromatosis type 1 and the pediatric neurosurgeon: a 20-year institutional
review. Pediatr Neurosurg. 2002 Sep;37(3):122-36. doi: 10.1159/000064398. PMID:
12187057.
660: Mittal S, Farmer JP, Al-Atassi B, Gibis J, Kennedy E, Galli C, Courchesnes
G, Poulin C, Cantin MA, Benaroch TE. Long-term functional outcome after
selective posterior rhizotomy. J Neurosurg. 2002 Aug;97(2):315-25. doi:
10.3171/jns.2002.97.2.0315. PMID: 12186459.
661: Al-Twaijri WA, Shevell MI. A novel chronic childhood sensory predominant
neuropathy. Pediatr Neurol. 2002 Jul;27(1):49-52. doi:
10.1016/s0887-8994(02)00376-4. PMID: 12160974.
662: Limperopoulos C, Majnemer A, Shevell MI, Rohlicek C, Rosenblatt B,
Tchervenkov C, Darwish HZ. Predictors of developmental disabilities after open
heart surgery in young children with congenital heart defects. J Pediatr. 2002
Jul;141(1):51-8. doi: 10.1067/mpd.2002.125227. PMID: 12091851.
663: Dembinska O, Rojas LM, Chemtob S, Lachapelle P. Evidence for a brief period
of enhanced oxygen susceptibility in the rat model of oxygen-induced
retinopathy. Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2481-90. PMID: 12091454.
664: Al-Twaijri WA, Shevell MI. Pediatric migraine equivalents: occurrence and
clinical features in practice. Pediatr Neurol. 2002 May;26(5):365-8. doi:
10.1016/s0887-8994(01)00416-7. PMID: 12057796.
665: Mittal S, Farmer JP, Al-Atassi B, Montpetit K, Gervais N, Poulin C, Cantin
MA, Benaroch TE. Impact of selective posterior rhizotomy on fine motor skills.
Long-term results using a validated evaluative measure. Pediatr Neurosurg. 2002
Mar;36(3):133-41. doi: 10.1159/000048368. PMID: 11919447.
666: Nguyen TN, Polomeno RC, Farmer JP, Montes JL. Ophthalmic complications of
slit-ventricle syndrome in children. Ophthalmology. 2002 Mar;109(3):520-4;
discussion 524-5. doi: 10.1016/s0161-6420(01)00985-x. PMID: 11874754.
667: Majnemer A, Desrosiers J, Gauthier J, Dutil E, Robichaud L, Rousseau J,
Hébert L. Involvement of occupational therapy departments in research: a
provincial survey. Can J Occup Ther. 2001 Dec;68(5):272-9. doi:
10.1177/000841740106800503. PMID: 11765666.
668: Mittal S, Farmer JP, Poulin C, Silver K. Reliability of intraoperative
electrophysiological monitoring in selective posterior rhizotomy. J Neurosurg.
2001 Jul;95(1):67-75. doi: 10.3171/jns.2001.95.1.0067. PMID: 11453400.
669: Shevell MI, Majnemer A, Rosenbaum P, Abrahamowicz M. Etiologic
determination of childhood developmental delay. Brain Dev. 2001
Jul;23(4):228-35. doi: 10.1016/s0387-7604(01)00212-1. PMID: 11377001.
670: Farmer JP, Montes JL, Freeman CR, Meagher-Villemure K, Bond MC, O'Gorman
AM. Brainstem Gliomas. A 10-year institutional review. Pediatr Neurosurg. 2001
Apr;34(4):206-14. doi: 10.1159/000056021. PMID: 11359114.
671: Mittal S, Farmer JP, Rosenblatt B, Andermann F, Montes JL, Villemure JG.
Intractable epilepsy after a functional hemispherectomy: important lessons from
an unusual case. Case report. J Neurosurg. 2001 Mar;94(3):510-4. doi:
10.3171/jns.2001.94.3.0510. PMID: 11235958.
672: Rousseau S, Lachapelle P. The electroretinogram recorded at the onset of
dark-adaptation: understanding the origin of the scotopic oscillatory
potentials. Doc Ophthalmol. 1999;99(2):135-50. doi: 10.1023/a:1002679932462.
PMID: 11097118.
673: Limperopoulos C, Majnemer A, Shevell MI, Rosenblatt B, Rohlicek C,
Tchervenkov C. Neurodevelopmental status of newborns and infants with congenital
heart defects before and after open heart surgery. J Pediatr. 2000
Nov;137(5):638-45. doi: 10.1067/mpd.2000.109152. PMID: 11060529.
674: Shevell M. Confronting the past: Contemporary German paediatric response to
medical practice in the Third Reich. Paediatr Child Health. 2000 Nov;5(8):451-2.
doi: 10.1093/pch/5.8.451. PMID: 20177554; PMCID: PMC2819958.
675: Miller SP, Shevell MI, Patenaude Y, O'Gorman AM. Neuromotor spectrum of
periventricular leukomalacia in children born at term. Pediatr Neurol. 2000
Aug;23(2):155-9. doi: 10.1016/s0887-8994(00)00172-7. PMID: 11020641.
676: Modha A, Vassilyadi M, George A, Kuehn S, Hsu E, Ventureyra EC.
Medulloblastoma in children--the Ottawa experience. Childs Nerv Syst. 2000
Jun;16(6):341-50. doi: 10.1007/s003810050529. PMID: 10933229.
677: Miller SP, O'Gorman AM, Shevell MI. Recurrent artery of Heubner infarction
in infancy. Dev Med Child Neurol. 2000 May;42(5):344-6. doi:
10.1017/s0012162200000608. PMID: 10855656.
678: Vernet O, Montes JL, Farmer JP, Blundell JE, Bertrand G, Freeman CR. Long
term results of multimodality treatment of craniopharyngioma in children. J Clin
Neurosci. 1999 May;6(3):199-203. doi: 10.1054/jocn.1998.0041. PMID: 10835167.
679: Painson JC, Veldhuis JD, Tannenbaum GS. Single exposure to testosterone in
adulthood rapidly induces regularity in the growth hormone release process. Am J
Physiol Endocrinol Metab. 2000 May;278(5):E933-40. doi:
10.1152/ajpendo.2000.278.5.E933. PMID: 10780951.
680: Rousseau S, Lachapelle P. Transient enhancing of cone electroretinograms
following exposure to brighter photopic backgrounds. Vision Res.
2000;40(8):1013-8. doi: 10.1016/s0042-6989(99)00245-x. PMID: 10720670.
681: Rilliet B, de Paul Djientcheu V, Vernet O, Montes J, Farmer JP, Bertrand G.
Craniopharyngiomas, results in children and adolescents operated through a
transsphenoidal approach compared with an intracranial approach. Front Radiat
Ther Oncol. 1999;33:114-22. doi: 10.1159/000061228. PMID: 10549482.
682: Majnemer A, Limperopoulos C. Developmental progress of children with
congenital heart defects requiring open heart surgery. Semin Pediatr Neurol.
1999 Mar;6(1):12-9. doi: 10.1016/s1071-9091(99)80042-4. PMID: 10098225.
683: Majnemer A, Mazer B. Neurologic evaluation of the newborn infant:
definition and psychometric properties. Dev Med Child Neurol. 1998
Oct;40(10):708-15. doi: 10.1111/j.1469-8749.1998.tb12332.x. PMID: 9851241.
684: Wagner C, Caplan SR, Tannenbaum GS. Genesis of the ultradian rhythm of GH
secretion: a new model unifying experimental observations in rats. Am J Physiol.
1998 Dec;275(6):E1046-54. doi: 10.1152/ajpendo.1998.275.6.E1046. PMID: 9843748.
685: Houle AM, Vernet O, Jednak R, Pippi Salle JL, Farmer JP. Bladder function
before and after selective dorsal rhizotomy in children with cerebral palsy. J
Urol. 1998 Sep;160(3 Pt 2):1088-91. doi: 10.1097/00005392-199809020-00032. PMID:
9719282.
686: Shevell MI. Clinical ethics and developmental delay. Semin Pediatr Neurol.
1998 Mar;5(1):70-5. doi: 10.1016/s1071-9091(98)80021-1. PMID: 9548644.
687: Shevell MI. The evaluation of the child with a global developmental delay.
Semin Pediatr Neurol. 1998 Mar;5(1):21-6. doi: 10.1016/s1071-9091(98)80014-4.
PMID: 9548637.
688: Shevell MI. Neurology's witness to history: part II. Leo Alexander's
contributions to the Nuremberg Code (1946 to 1947). Neurology. 1998
Jan;50(1):274-8. doi: 10.1212/wnl.50.1.274. PMID: 9443492.
689: Roy S, Martel J, Tenenhouse HS. Growth hormone normalizes renal
1,25-dihydroxyvitamin D3-24-hydroxylase gene expression but not Na+-phosphate
cotransporter (Npt2) mRNA in phosphate-deprived Hyp mice. J Bone Miner Res. 1997
Oct;12(10):1672-80. doi: 10.1359/jbmr.1997.12.10.1672. PMID: 9333128.
690: Ludemann JP, Tewfik TL, Meagher-Villemure K, Bernard C. Congenital
mesenchymoma transgressing the cribriform plate. J Otolaryngol. 1997
Aug;26(4):270-2. PMID: 9263898.
691: Lam CH, Montes J, Farmer JP, O'Gorman AM, Meagher-Villemure K. Traumatic
aneurysm from shaken baby syndrome: case report. Neurosurgery. 1996
Dec;39(6):1252-5. doi: 10.1097/00006123-199612000-00041. PMID: 8938784.
692: Feindel W. Neurosurgery at the Montreal Neurological Institute and McGill
University Hospitals. Neurosurgery. 1996 Oct;39(4):830-9. doi:
10.1097/00006123-199610000-00038. PMID: 8880779.
693: Vernet O, Farmer JP, Houle AM, Montes JL. Impact of urodynamic studies on
the surgical management of spinal cord tethering. J Neurosurg. 1996
Oct;85(4):555-9. doi: 10.3171/jns.1996.85.4.0555. PMID: 8814155.
694: Lacroix M, Farmer JP, Meagher-Villemure K, Rosenblatt B, Montes JL. Cauda
equina histiocytosis X. Pediatr Neurol. 1996 Apr;14(3):231-5. doi:
10.1016/0887-8994(96)00081-1. PMID: 8736408.
695: Vernet O, Montes JL, O'Gorman AM, Baruchel S, Farmer JP.
Encephaloduroarterio-synangiosis in a child with sickle cell anemia and moyamoya
disease. Pediatr Neurol. 1996 Apr;14(3):226-30. doi:
10.1016/0887-8994(96)00045-8. PMID: 8736407.
696: Robb P. Personal reminiscences: the development of neurology at the
Montreal Children's Hospital. Pediatr Neurol. 1996 Apr;14(3):185-8. doi:
10.1016/0887-8994(96)00061-6. PMID: 8736400.
697: Vernet O, Farmer JP, Montes JL. Comparison of syringopleural and
syringosubarachnoid shunting in the treatment of syringomyelia in children. J
Neurosurg. 1996 Apr;84(4):624-8. doi: 10.3171/jns.1996.84.4.0624. PMID: 8613854.
698: Vernet O, Farmer JP, Lambert R, Montes JL. Radionuclide shuntogram: adjunct
to manage hydrocephalic patients. J Nucl Med. 1996 Mar;37(3):406-10. PMID:
8772632.
699: Côté A, Porras H, Meehan B. Age-dependent vulnerability to carotid
chemodenervation in piglets. J Appl Physiol (1985). 1996 Jan;80(1):323-31. doi:
10.1152/jappl.1996.80.1.323. PMID: 8847323.
700: Vernet O, Farmer JP, Meagher-Villemure K, Montes JL. Supratentorial ectopic
ependymoma. Can J Neurol Sci. 1995 Nov;22(4):316-9. doi:
10.1017/s0317167100039561. PMID: 8599779.
701: Vassilyadi M, Farmer JP, Montes JL. Negative-pressure hydrocephalus. J
Neurosurg. 1995 Sep;83(3):486-90. doi: 10.3171/jns.1995.83.3.0486. PMID:
7666227.
702: Majnemer A, Shevell MI. Diagnostic yield of the neurologic assessment of
the developmentally delayed child. J Pediatr. 1995 Aug;127(2):193-9. doi:
10.1016/s0022-3476(95)70294-6. PMID: 7543566.
703: Lam CH, Farmer JP, Meagher-Villemure K, Montes JL. Masson's vegetant
haemangio-endothelioma. Pediatr Neurosurg. 1995;23(2):93-6. doi:
10.1159/000120943. PMID: 8555102.
704: Montes JL, Rosenblatt B, Farmer JP, O'Gorman AM, Andermann F, Watters GV,
Meagher-Villemure K. Lesionectomy of MRI detected lesions in children with
epilepsy. Pediatr Neurosurg. 1995;22(4):167-73. doi: 10.1159/000120897. PMID:
7619716.
705: Ross IB, Shevell MI, Montes JL, Rosenblatt B, Watters GV, Farmer JP,
O'Gorman AM. Encephaloduroarteriosynangiosis (EDAS) for the treatment of
childhood moyamoya disease. Pediatr Neurol. 1994 May;10(3):199-204. doi:
10.1016/0887-8994(94)90023-x. PMID: 8060421.
706: Montes JL, Clarke DB, Farmer JP. Stereotactic transtentorial hiatus
ventriculoperitoneal shunting for the sequestered fourth ventricle. Technical
note. J Neurosurg. 1994 Apr;80(4):759-61. doi: 10.3171/jns.1994.80.4.0759. PMID:
8151361.
707: Clarke DB, Farmer JP, Montes JL, Watters GV, Rouleau G. Newborn apnea
caused by a neurofibroma at the craniocervical junction. Can J Neurol Sci. 1994
Feb;21(1):64-6. doi: 10.1017/s0317167100048800. PMID: 8180909.
708: Baltuch GH, Farmer JP, Meagher-Villemure K, O'Gorman AM, Montes JL.
Ganglioglioma presenting as a vascular lesion in a 10-year-old boy. Case report.
J Neurosurg. 1993 Dec;79(6):920-3. doi: 10.3171/jns.1993.79.6.0920. PMID:
8246060.
709: Shevell MI, Silver K, Watters GV, Rosenblatt B. Transient oculosympathetic
paresis (group II Raeder paratrigeminal neuralgia) of childhood: migraine
variant. Pediatr Neurol. 1993 Jul-Aug;9(4):289-92. doi:
10.1016/0887-8994(93)90065-k. PMID: 8216541.
710: Giroux M, Farmer JP, Meagher-Villemure KM, O'Gorman AM, Montes JL.
Intraventricular central neurocytoma. Can J Neurol Sci. 1992 Aug;19(3):392-6.
PMID: 1393851.
711: Trasler JM, Alcivar AA, Awoniyi CA, Santulli R, Zirkin BR, Hecht NB.
Temporal gene expression is restored concomitantly with germ cells in the
experimentally regressed rat testis. Endocrinology. 1992 Jul;131(1):297-304.
doi: 10.1210/endo.131.1.1612009. PMID: 1612009.
712: Munz M, Farmer JP, Auger L, O'Gorman AM, Schloss MD. Otitis media and CNS
complications. J Otolaryngol. 1992 Jun;21(3):224-6. PMID: 1404577.
713: Wiesel S, Bevan JC, Samuel J, Donati F. Vecuronium neuromuscular blockade
in a child with mitochondrial myopathy. Anesth Analg. 1991 May;72(5):696-9. doi:
10.1213/00000539-199105000-00020. PMID: 1673325.
714: Benoit J, Lachapelle P. Temporal relationship between ERG components and
geniculate unit activity in rabbit. Vision Res. 1990;30(6):797-806. doi:
10.1016/0042-6989(90)90048-p. PMID: 2385920.
715: Gardner DJ, O'Gorman AM, Blundell JE. Intraspinal epidermoid tumour: late
complication of lumbar puncture. CMAJ. 1989 Aug 1;141(3):223-5. PMID: 2752348;
PMCID: PMC1269411.
716: Tenenhouse HS, Klugerman AH, Gurd W, Lapointe M, Tannenbaum GS. Pituitary
involvement in renal adaptation to phosphate deprivation. Am J Physiol. 1988
Sep;255(3 Pt 2):R373-8. doi: 10.1152/ajprenal.1988.255.3.F373. PMID: 3414832.