Neurobiology and Development
Bally BP, Farmer WT, Jones EV, Jessa S, Kacerovsky JB, Mayran A, Peng H, Lefebvre JL, Drouin J, Hayer A, Ernst C, Murai KK, Human iPSC-Derived Down Syndrome Astrocytes Display Genome-Wide Perturbations in Gene Expression, an Altered Adhesion Profile, and Increased Cellular Dynamics. - Human Molecular Genetics 2020 Jan 15
Ferent J, Constable S, Gigante ED, Yam PT, Mariani LE, Legué E, Liem Jr. KF, Caspary T*, Charron F*. The ciliary protein Arl13b functions outside of the primary cilium in Shh mediated axon guidance. Cell Reports Volume 29, Issue 11, 10 December 2019, Pages 3356-3366.e3 *These authors contributed equally, co-corresponding authors.
Accogli A#, Calabretta S#, St-Onge J, Boudrahem-Addour N, Dionne-Laporte A, Joset P, Azzarello-Burri S, Rauch A, Krier J, Fieg E, Pallais JC, Undiagnosed Diseases Network, McConkie-Rosell A, McDonald M, Freedman SF, Rivière J-B, Lafond-Lapalme J, Simpson BN, Hopkin RJ, Trimouille A, Van-Gils J, Begtrup A, McWalter K, Severino M, Rouleau GA, Yam PT, Charron F*, Srour M*. De novo pathogenic variants in N-cadherin cause ACOG, a syndromic neurodevelopmental disorder with agenesis of the corpus callosum and axon pathfinding, cardiac, ocular and genital defects. American Journal of Human Genetics Volume 105, Issue 4, 3 October 2019, Pages 854-868 # Equal contribution * Co-corresponding authors
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