TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosisEdor Kabashi, Guy A. Rouleau, Vincent Meininger et al.|Nature Genetics|2008Cited by 1.5k
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Grace Yoon, Guy A. Rouleau et al.|Neurology Genetics|2016Cited by 98
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorderZiv Gan‐Or, Guy A. Rouleau, Cynthia V. Bourassa et al.|Neurobiology of Aging|2016Cited by 15