François Rivier

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

Christel Depienne, Delphine Bouteiller, Boris Keren et al. · PLoS Genetics · 2009 · 368 citations · Full text

Mainly Affects Females, Dravet Syndrome, Mendelian Disorder +15

Cytochrome Oxidase, Acetylcholinesterase, and NADPH-Diaphorase Staining in Human Supratemporal and Insular Cortex: Evidence for Multiple Auditory Areas

François Rivier, Stéphanie Clarke · NeuroImage · 1997 · 309 citations

Auditory Imagery, Auditory Modeling, Neurophysiology +15

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

Christophe Béroud, Sylvie Tuffery‐Giraud, Masafumi Matsuo et al. · Human Mutation · 2006 · 192 citations

Artificial Dmd Protein, Genetics, Molecular Biology +16

Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans

Jack J. Collier, Claire Guissart, Monika Oláhová et al. · New England Journal of Medicine · 2021 · 185 citations · Full text

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q

Michel Guipponi, François Rivier, Federico Vigevano et al. · Human Molecular Genetics · 1997 · 166 citations · Full text