Gaëlle Morin

The paper identifies rare founder variants in a population and develops a platform for variant prioritization, showing that some pathogenic variants may be missed by conventional methods.

This paper identifies a DM1-associated haplotype in all patients using haplotype-based methods, demonstrating its utility for carrier status inference without direct repeat sizing.

This study reveals fine-scale genetic structure in the Saguenay-Lac-Saint-Jean region using genotype data and genealogies, showing a genetic gradient and historical migration patterns.