Guy Rouleau
Guy Rouleau
Montreal Neurological Institute and Hospital
Verified email at
TitleCited byYear
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
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
TJ Kwiatkowski, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
O Delattre, J Zucman, BÚ Plougastel, C Desmaze, T Melot, M Peter, ...
Nature 359 (6391), 162-165, 1992
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
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
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, 2008
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
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
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
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
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
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
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
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, 1998
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
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22
GA Rouleau, W Wertelecki, JL Haines, WJ Hobbs, JA Trofatter, ...
Nature 329 (6136), 246-248, 1987
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
Variation in genome-wide mutation rates within and between human families
DF Conrad, JEM Keebler, MA DePristo, SJ Lindsay, Y Zhang, F Casals, ...
Nature genetics 43 (7), 712, 2011
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
DA Figlewicz, A Krizus, MG Martinoli, V Meininger, M Dib, GA Rouleau, ...
Human molecular genetics 3 (10), 1757-1761, 1994
Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment
A Pramatarova, J Laganière, J Roussel, K Brisebois, GA Rouleau
Journal of Neuroscience 21 (10), 3369-3374, 2001
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