Jean Michel Pedespan

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

Karine Poirier, Nicolas Lebrun, Loïc Broix et al. · Nature Genetics · 2013 · 488 citations · Full text

Developmental Anomaly, Developmental Biology, Brain Development +9

Delineating <i>FOXG1</i> syndrome

Nancy Végas, Mara Cavallin, Camille Maillard et al. · Neurology Genetics · 2018 · 75 citations · Full text

From splitting GLUT1 deficiency syndromes to overlapping phenotypes

Marie Hully, Sandrine Vuillaumier‐Barrot, Christiane Le Bizec et al. · European Journal of Medical Genetics · 2015 · 69 citations

Autoimmune Disease, Genetic Disorder, Genetics +4

Callosotomy for intractable epilepsy: overall outcome.

Alain Rougier, Bernard Claverie, Jean Michel Pedespan et al. · PubMed · 1997 · 48 citations

Neuropsychology, Neurological Disorder, Clinical Neurology +18

Recurrent KIF2A mutations are responsible for classic lissencephaly

Mara Cavallin, Emilia K. Bijlsma, Adrienne El Morjani et al. · Neurogenetics · 2016 · 27 citations

Recurrent Kif2a Mutations, Mitophagy, Mendelian Disorder +5