J. Leblanc

First glance at the molecular etiology of hearing loss in French-Canadian families from Saguenay-Lac-Saint-Jean’s founder population

N. Braverman, J. Tardif, A. Pratte, 2021, Human Genetics.

Benefits of Newborn Screening for Vitamin D-Dependant Rickets Type 1A in a Founder Population

L. Bouchard, J. Leblanc, T. Cruz-Mariño, 2022, Frontiers in Endocrinology.

French-Canadian families from Saguenay-Lac-Saint-Jean: a new founder population for APECED

P. Caron, B. Ellezam, J. Mathieu, 2021, Endocrine.

First glance at the molecular etiology of hearing loss in French-Canadian families from Saguenay-Lac-Saint-Jean’s founder population

N. Braverman, J. Tardif, A. Pratte, 2021, Human Genetics.

Portrait of autosomal recessive diseases in the French‐Canadian founder population of Saguenay‐Lac‐Saint‐Jean

J. Tardif, L. Bouchard, A. Pratte, 2023, American journal of medical genetics. Part A.

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.

Influence of CYP2D6 activity on the disposition and cardiovascular toxicity of the antidepressant agent venlafaxine in humans.

J. Turgeon, M. Yessine, B A Hamelin, 1999, Pharmacogenetics.

American Society of Human Genetics Releases Apology for Misuse of Genetic Research

G. Mortier, P. Klinge, V. Sutton, 2023, American journal of medical genetics. Part A.