Author

Geneviève Gagnon

McGill UniversityORCID 0009-0003-5747-7918Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Approach:matrix factorization· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Claude BhéreriD· 3 shared Daniel TaliuniD· 3 shared Justin PelletieriD· 3 shared Dariel Ashton‐BeaucageiD· 2 shared Jean‐Christophe GrenieriD· 2 shared John David RiouxiD· 2 shared Julie HussiniD· 2 shared Philippe M. CampeauiD· 2 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Claude BhérerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedFeb 3, 2026

A multi-ancestry genetic reference for the Quebec population

Peyton McClelland, Georgette Femerling, Rose Laflamme…·Guillaume Lettre

The paper constructs a genetic reference panel for the Quebec population using whole-genome sequencing and GWAS to improve phenotype-genotype association discovery.

8 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintOct 30, 2025

An Elevated Birth Prevalence of Fraser Syndrome in Quebec Linked To A Founder Pathogenic Variant

Geneviève Gagnon, Justin Pelletier, Dariel Ashton‐Beaucage…·Claude Bhérer

The paper estimates an elevated birth prevalence of Fraser syndrome in Quebec's French-Canadian population and identifies a founder pathogenic variant.

DOI 10.1101/2025.10.30.25336922

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 11, 2025

Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases

Claude Bhérer, Jean‐Christophe Grenier, Justin Pelletier…·John David Rioux

The paper identifies enriched coding variants in a French-Canadian founder population and explores their association with inflammatory bowel diseases.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky