Karine Boisvert

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

S. Scherer, A. C. Lionel, C. Marshall, 2014, Journal of Neurodevelopmental Disorders.

A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study

J. Simard, Y. Joly, H. Nabi, 2021, Cancers.

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

Marie-Pierre Dubé, Olaf Ansorge, Namrata Gupta, 2010, Nature Medicine.