Yoann Saillour

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 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

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

Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects

Karine Poirier, Yoann Saillour, Nadia Bahi‐Buisson et al. · Human Molecular Genetics · 2010 · 266 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (<i>TUBA1A</i>)

Karine Poirier, David A. Keays, Fiona Francis et al. · Human Mutation · 2007 · 236 citations

Life Sciences, Genetics, Neuroscience +15