P. Lachance-Touchette

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

Michael R. Johnson, A. Uitterlinden, P. May, 2018, The Lancet Neurology.

Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease

F. Andermann, S. Berkovic, G. Rouleau, 2013, Clinical genetics.

Screening of GABRB3 in French‐Canadian families with idiopathic generalized epilepsy

L. Carmant, P. Cossette, M. Gravel, 2010, Epilepsia.

Mutation Burden of Rare Variants in Schizophrenia Candidate Genes

M. Krebs, M. Dubé, R. Joober, 2015, PloS one.

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

L. Carmant, P. Cossette, D. Bowie, 2011, The European journal of neuroscience.

Single-cell genetic expression of mutant GABAA receptors causing Human genetic epilepsy alters dendritic spine and GABAergic bouton formation in a mutation-specific manner

P. Cossette, G. Di Cristo, P. Lachance-Touchette, 2014, Front. Cell. Neurosci..

Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy

P. Awadalla, S. Moss, G. Rouleau, 2014, EMBO reports.