Jean‐Pierre Bouchard

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion et al. · Nature Genetics · 2008 · 1.5K citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Mendelian Disorder +10

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

Bernard Brais, Jean‐Pierre Bouchard, Ya‐Gang Xie et al. · Nature Genetics · 1998 · 796 citations · Full text

Systems Biology, Genetic Disorder, Short Gcg Expansions +7

A full genome search in multiple sclerosis

George C. Ebers, Kim Kukay, Dennis E. Bulman et al. · Nature Genetics · 1996 · 662 citations

Medicine, Genetics, Complex Disease +5

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

James C. Engert, Pierre Bérubé, Jocelyne Mercier et al. · Nature Genetics · 2000 · 434 citations

Genetic Disorder, Genetics, New Gene +7

Task-specific physical therapy for optimization of gait recovery in acute stroke patients

Carol L. Richards, Francine Malouin, Sharon Wood-Dauphinée et al. · Archives of Physical Medicine and Rehabilitation · 1993 · 347 citations

Gait Analysis, Task-specific Physical Therapy, Neurological Rehabilitation +16