Articles choisis

• Human copy number variants are enriched in regions of low-mappability. Jean Monlong, Caroline Meloche, Guy Rouleau, Patrick Cossette, Simon Louis Girard, Guillaume Bourque. https://biorxiv.org/content/early/2015/12/11/03416

• De novo variants in sporadic cases of childhood onset schizophrenia. Ambalavanan A, Girard SL, Ahn K, Zhou S, […],Rapoport J, Rouleau GA. Eur J Hum Genet. 2015

• Mutation burden of rare variants in schizophrenia candidate genes.Girard SL¹, Dion PA², Bourassa CV³ […] Dubé MP⁸, Rouleau GA³. PLoS One. 2015 

• Genome-wide association study in FTD: divide to conquer. Girard SL and Rouleau GA. Lancet Neurol. 2014

• Exome sequencing identifies FUS mutations as a cause of essential tremor. Merner ND, Girard SL, Catoire H […] Dion PA, Rouleau GA. Am J Hum Genet. 2012

• Increased exonic de novo mutation rate in individuals with schizophrenia. Girard SL […] Krebs MO, Rouleau GA. Nat Genet. 2011 [PDF: ng.886]

• Where are the missing pieces of the schizophrenia genetics puzzle? Girard SL, Xiong L, Dion PA, Rouleau GA. Curr Opin Genet Dev. 2011