Vincent des Portes

Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey et al. · The American Journal of Human Genetics · 2003 · 765 citations · Full text

Medicine, Neurology, Neuroscience +13

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

Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

Sébastien Jacquemont, Aurore Curie, Vincent des Portes et al. · Science Translational Medicine · 2011 · 611 citations

Life Sciences, Molecular Biology, Neuroscience +17

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

Pierre Billuart, T Bienvenu, Nathalie Ronce et al. · Nature · 1998 · 553 citations

Life Sciences, Genetics, Molecular Genetics +6

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 · 498 citations

Life Sciences, Genetics, Neuroscience +12