Publications

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D
Ambalavanan A, Girard SL, Ahn K, Zhou S, Dionne-Laporte A, Spiegelman D, Bourassa CV, Gauthier J, Hamdan FF, Xiong L et al..  2016.  De novo variants in sporadic cases of childhood onset schizophrenia.. Eur J Hum Genet. 24(6):944-8.
E
Benedet AL, Labbe A, Lemay P, Zimmer ER, Pascoal TA, Leuzy A, Mathotaarachchi S, Mohades S, Shin M, Dionne-Laporte A et al..  2015.  Epistasis analysis links immune cascades and cerebral amyloidosis.. J Neuroinflammation. 12:227.
Ambalavanan A, Chaumette B, Zhou S, Xie P, He Q, Spiegelman D, Dionne-Laporte A, Bourassa CV, Therrien M, Rochefort D et al..  2018.  Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.. Am J Med Genet B Neuropsychiatr Genet.
M
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Oliveira RDe Barros, Turecki G, Dion PA et al..  2019.  Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.. PLoS One. 14(11):e0225186.