Constellation, le dépôt institutionnel de l'Université du Québec à Chicoutimi

2013

Casals, Ferran, Hodgkinson, Alan, Hussin, Julie, Idaghdour, Youssef, Bruat, Vanessa, de Maillard, Thibault, Grenier, Jean-Christophe, Gbeha, Elias, Hamdan, Fadi F., Girard, Simon, Spinella, Jean-François, Larivière, Mathieu, Saillour, Virginie, Healy, Jasmine, Fernández, Isabel, Sinnett, Daniel, Michaud, Jacques L., Rouleau, Guy A., Haddad, Elie, Le Deist, Françoise et Awadalla, Philip. (2013). Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. PloS Genetics, 9, (9), e100381.

2022

Moreau, Claudia, Tremblay, Frédérique, Wolking, Stefan, Girard, Alexandre, Laprise, Catherine, Hamdan, Fadi F., Michaud, Jacques L., Minassian, Berge, Cossette, Patrick et Girard, Simon. (2022). Assessment of burden and segregation profiles of CNVs in patients with epilepsy. Annals of Clinical and Translational Neurology, 9, (7), p. 1050-1058.

2023

Girard, Alexandre, Moreau, Claudia, Michaud, Jacques L., Minassian, Berge, Cossette, Patrick et Girard, Simon L.. (2023). Unraveling the role of non-coding rare variants in epilepsy. PLOS ONE, 18, (9), e0291935.