Mathieu Langlois

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.

E. Fombonne, J. Lacaille, M. Krebs, 2010, American journal of human genetics.

Mutation Burden of Rare Variants in Schizophrenia Candidate Genes

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

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay

E. Lemyre, M. Srour, G. Mathonnet, 2014, BMC Medical Genomics.

A prospective study of the impact of AGTR1 A1166C on the effects of candesartan in patients with heart failure.

J. Rouleau, A. Ducharme, J. Tardif, 2018, Pharmacogenomics.