S. B. Laurent

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Amélie Piton, J Gauthier, Fadi F. Hamdan et al. · Molecular Psychiatry · 2010 · 315 citations

Systematic Resequencing, X-chromosome Synaptic Genes, Genetic Disorder +8

<i>CCM1</i> mutation screen of sporadic cases with cerebral cavernous malformations

D. J. Verlaan, S. B. Laurent, Ulrich Sure et al. · Neurology · 2004 · 47 citations

Neurological Disorder, Vascular Malformation, Pathology +16

CCM3 mutations are uncommon in cerebral cavernous malformations

D. J. Verlaan, Julie Roussel, S. B. Laurent et al. · Neurology · 2005 · 45 citations

No <i>CCM2</i> mutations in a cohort of 31 sporadic cases

D. J. Verlaan, S. B. Laurent, Guy A. Rouleau et al. · Neurology · 2004 · 23 citations

Autism spectrum disorders associated with X chromosome markers in French-Canadian males

J Gauthier, Ridha Joober, Marie‐Pierre Dubé et al. · Molecular Psychiatry · 2005 · 23 citations · Full text

Autism Spectrum Disorders, Syndromic Autism, Genetic Disorder +6