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Chantal Depondt
Chantal Depondt
Professor of Neurology, Université Libre de Bruxelles
Verified email at erasme.ulb.ac.be
Title
Cited by
Cited by
Year
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
18492006
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13662018
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
10792011
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
8342015
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
6982012
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
6642014
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
5732020
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
4122018
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
4052005
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
2982017
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
2982008
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
2792010
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
2452016
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
2422019
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
2372016
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
2322003
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
2302019
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
2282007
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
2242011
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
2092016
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