Jean-Pierre Bouchard

The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum

Heidi Howard, David B. Mount, Daniel Rochefort et al. · Nature Genetics · 2002 · 278 citations

Medicine, Neurology, Neuroscience +16

Oculopharyngeal Muscular Dystrophy

Bernard Brais, Guy A. Rouleau, Jean-Pierre Bouchard et al. · Seminars in Neurology · 1999 · 178 citations

Medicine, Genetics, Molecular Genetics +16

South Africa: Challenges and successes of the COVID-19 lockdown

Nancy Stiegler, Jean-Pierre Bouchard · Annales Médico-psychologiques revue psychiatrique · 2020 · 166 citations · Full text

Social Sciences, Health Policy, Infectious Disease Control +14

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis

Hannah Kaneb, Andrew W. Folkmann, Véronique Belzil et al. · Human Molecular Genetics · 2014 · 130 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease

Sergiu C. Blumen, Bernard Brais, Amos D. Korczyn et al. · Annals of Neurology · 1999 · 98 citations

Medicine, Genetics, Neurology +17