Pamela Lachance‐Touchette

Genetically encoded impairment of neuronal <scp>KCC</scp> 2 cotransporter function in human idiopathic generalized epilepsy

Kristopher T. Kahle, Nancy D. Merner, Perrine Friedel et al. · EMBO Reports · 2014 · 187 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Cotransporter Function +10

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

Recurrent mutations in<i><scp>DNAJC5</scp></i>cause autosomal dominant Kufs disease

Maxime Cadieux‐Dion, E. Andermann, Pamela Lachance‐Touchette et al. · Clinical Genetics · 2012 · 68 citations

Screening of <i>GABRB3</i> in French‐Canadian families with idiopathic generalized epilepsy

Pamela Lachance‐Touchette, Caroline P. Martin, Chantal Poulin et al. · Epilepsia · 2010 · 28 citations · Full text

Mutation Burden of Rare Variants in Schizophrenia Candidate Genes

Simon Girard, Patrick A. Dion, Cynthia V. Bourassa et al. · PLoS ONE · 2015 · 19 citations · Full text