Lionel Carmant

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

Patrick Cossette, Lidong Liu, Katéri Brisebois et al. · Nature Genetics · 2002 · 653 citations

Medicine, Genetics, Neurology +14

Mutations in <i>SYNGAP1</i> in Autosomal Nonsyndromic Mental Retardation

Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman et al. · New England Journal of Medicine · 2009 · 351 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Stroke in children

Sylvain Lanthier, Lionel Carmant, Matthias David et al. · Neurology · 2000 · 338 citations

Medicine, Neurology, Pediatrics +11

Mutations in<i>SYNGAP1</i>Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

Martin H. Berryer, Fadi F. Hamdan, Laura L. Klitten et al. · Human Mutation · 2012 · 280 citations

Life Sciences, Genetics, Molecular Genetics +17

<i>KCNQ2</i> encephalopathy

J Gordon Millichap, Kristen Park, Tammy N. Tsuchida et al. · Neurology Genetics · 2016 · 242 citations · Full text

Medicine, Neurology, Pharmacology +14