Caroline Meloche

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

Anna Fassio, Lysanne Patry, Sonia Congia et al. · Human Molecular Genetics · 2011 · 233 citations · Full text

Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord

Alexandre Montpetit, Stéphanie Côté, Edna Brustein et al. · PLoS Genetics · 2008 · 170 citations · Full text

Genetics, Novel Neurocutaneous Syndrome, Genomic Mechanism +20

Expanding the Clinical Phenotype Associated With<i>ELOVL4</i>Mutation

Maxime Cadieux‐Dion, Maude Turcotte-Gauthier, Anne Noreau et al. · JAMA Neurology · 2014 · 128 citations

Novel α1 and γ2 GABA_A receptor subunit mutations in families with idiopathic generalized epilepsy

Pamela Lachance‐Touchette, Patricia M.G.E. Brown, Caroline Meloche et al. · European Journal of Neuroscience · 2011 · 110 citations

Neurogenomics, Genetics, Genetic Epidemiology +18

Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001

Thai Hoa Tran, Sylvie Langlois, Caroline Meloche et al. · Blood Advances · 2021 · 78 citations · Full text