Scale for the assessment and rating of ataxia: development of a new clinical scale T Schmitz-Hubsch, ST Du Montcel, L Baliko, J Berciano, S Boesch, ... Neurology 66 (11), 1717-1720, 2006 | 1858 | 2006 |
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1370 | 2018 |
HLA-A* 3101 and carbamazepine-induced hypersensitivity reactions in Europeans M McCormack, A Alfirevic, S Bourgeois, JJ Farrell, D Kasperavičiūtė, ... New England Journal of Medicine 364 (12), 1134-1143, 2011 | 1083 | 2011 |
Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ... Nature 520 (7546), 224-229, 2015 | 839 | 2015 |
Identification of common variants associated with human hippocampal and intracranial volumes JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ... Nature genetics 44 (5), 552-561, 2012 | 700 | 2012 |
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ... Brain imaging and behavior 8, 153-182, 2014 | 663 | 2014 |
The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 585 | 2020 |
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study CD Whelan, A Altmann, JA Botía, N Jahanshad, DP Hibar, J Absil, ... Brain 141 (2), 391-408, 2018 | 415 | 2018 |
Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin SK Tate, C Depondt, SM Sisodiya, GL Cavalleri, S Schorge, N Soranzo, ... Proceedings of the National Academy of Sciences 102 (15), 5507-5512, 2005 | 406 | 2005 |
Novel genetic loci associated with hippocampal volume DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ... Nature communications 8 (1), 13624, 2017 | 303 | 2017 |
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms T Schmitz-Hubsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, ... Neurology 71 (13), 982-989, 2008 | 299 | 2008 |
Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ... The American Journal of Human Genetics 86 (5), 707-718, 2010 | 279 | 2010 |
Genetic architecture of subcortical brain structures in 38,851 individuals CL Satizabal, HHH Adams, DP Hibar, CC White, MJ Knol, JL Stein, ... Nature genetics 51 (11), 1624-1636, 2019 | 251 | 2019 |
Novel genetic loci underlying human intracranial volume identified through genome-wide association HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Rentería, ... Nature neuroscience 19 (12), 1569-1582, 2016 | 247 | 2016 |
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ... Nature neuroscience 19 (3), 420-431, 2016 | 238 | 2016 |
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping ME Weale, C Depondt, SJ Macdonald, A Smith, P San Lai, SD Shorvon, ... The American Journal of Human Genetics 73 (3), 551-565, 2003 | 233 | 2003 |
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 230 | 2019 |
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study GL Cavalleri, ME Weale, KV Shianna, R Singh, JM Lynch, B Grinton, ... The Lancet Neurology 6 (11), 970-980, 2007 | 229 | 2007 |
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study H Jacobi, P Bauer, P Giunti, R Labrum, MG Sweeney, P Charles, A Duerr, ... Neurology 77 (11), 1035-1041, 2011 | 228 | 2011 |
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy MG Ricos, BL Hodgson, T Pippucci, A Saidin, YS Ong, SE Heron, ... Annals of neurology 79 (1), 120-131, 2016 | 211 | 2016 |