Claude Cancès

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

Key clinical features to identify girls with CDKL5 mutations

Nadia Bahi‐Buisson, Juliette Nectoux, Haydeé Rosas‐Vargas et al. · Brain · 2008 · 285 citations

Cdkl5-associated Encephalopathy, Developmental Anomaly, Mendelian Disorder +12

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

Marc Bitoun, Jorge A. Bevilacqua, Bernard Prudhon et al. · Annals of Neurology · 2007 · 148 citations · Full text

Mutation in <i>POLR3K</i> causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation

Imen Dorboz, Hélène Dumay‐Odelot, K. Boussaid et al. · Neurology Genetics · 2018 · 86 citations · Full text

Reading abilities and cognitive functions of children with epilepsy: Influence of epileptic syndrome

Yves Chaix, V. Laguitton, Valérie Lauwers‐Cancès et al. · Brain and Development · 2005 · 71 citations

Neuropsychological Functioning, Cognitive Science, Child Literacy +10