Karine Poirier

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

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

David A. Keays, Guoling Tian, Karine Poirier et al. · Cell · 2007 · 444 citations · Full text

Life Sciences, Neurobiology, Neuroscience +14

Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Xavier H. Jaglin, Karine Poirier, Yoann Saillour et al. · Nature Genetics · 2009 · 372 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

Christel Depienne, Delphine Bouteiller, Boris Keren et al. · PLoS Genetics · 2009 · 371 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

Nadia Bahi‐Buisson, Karine Poirier, Franck J. Fourniol et al. · Brain · 2014 · 315 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17