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Guy Rouleau
Guy Rouleau
Montreal Neurological Institute-Hospital, McGill University
Adresse e-mail validée de mcgill.ca
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
DR Rosen, T Siddique, D Patterson, DA Figlewicz, P Sapp, A Hentati, ...
Nature 362 (6415), 59-62, 1993
86561993
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
TJ Kwiatkowski Jr, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
30132009
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
O Delattre, J Zucman, B Plougastel, C Desmaze, T Melot, M Peter, ...
Nature 359 (6391), 162-165, 1992
20771992
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ...
Nature genetics 40 (5), 572-574, 2008
17802008
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2
GA Rouleau, P Merel, M Lutchman, M Sanson, J Zucman, C Marineau, ...
Nature 363 (6429), 515-521, 1993
16551993
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
14962019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13472018
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
13382019
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
SM Pulst, A Nechiporuk, T Nechiporuk, S Gispert, XN Chen, ...
Nature genetics 14 (3), 269-276, 1996
12961996
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10032019
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
9842015
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
B Brais, JP Bouchard, YG Xie, DL Rochefort, N Chrétien, FMS Tomé, ...
Nature genetics 18 (2), 164-167, 1998
9371998
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
S Hadano, CK Hand, H Osuga, Y Yanagisawa, A Otomo, RS Devon, ...
Nature genetics 29 (2), 166-173, 2001
8562001
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy
P Cossette, L Liu, K Brisebois, H Dong, A Lortie, M Vanasse, ...
Nature genetics 31 (2), 184-189, 2002
8002002
Von Hippel–Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma
BR Seizinger, GA Rouleau, LJ Ozelius, AH Lane, GE Farmer, JM Lamiell, ...
Nature 332 (6161), 268-269, 1988
7861988
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7762009
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
J Winkelmann, B Schormair, P Lichtner, S Ripke, L Xiong, S Jalilzadeh, ...
Nature genetics 39 (8), 1000-1006, 2007
7672007
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
7512013
Risk factors for suicide completion in major depression: a case-control study of impulsive and aggressive behaviors in men
A Dumais, AD Lesage, M Alda, G Rouleau, M Dumont, N Chawky, M Roy, ...
American Journal of Psychiatry 162 (11), 2116-2124, 2005
7362005
The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane
AH Chishti, AC Kim, SM Marfatia, M Lutchman, M Hanspal, H Jindal, ...
Trends in biochemical sciences 23 (8), 281-282, 1998
6921998
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