Jacques Motté

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

Vincent des Portes, Jean Marc Pinard, Pierre Billuart et al. · Cell · 1998 · 738 citations · Full text

Life Sciences, Genetics, Neuroscience +17

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

Gaëtan Lesca, Gabrielle Rudolf, Nadine Bruneau et al. · Nature Genetics · 2013 · 441 citations

Medicine, Neurology, Neuroscience +17

Levodopa-responsive dystonia

Alexandra Dürr, Roger Gil, Marie Vidailhet et al. · Brain · 2000 · 191 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The three stages of epilepsy in patients with <i>CDKL5</i> mutations

Nadia Bahi‐Buisson, Anna Kamińska, Nathalie Boddaert et al. · Epilepsia · 2008 · 190 citations

Medicine, Genetics, Neurology +16

Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism

Gaëtan Lesca, Gabrielle Rudolf, Audrey Labalme et al. · Epilepsia · 2012 · 188 citations

Medicine, Genetics, Neuroscience +17