Author

Dariel Ashton‐Beaucage

McGill UniversityORCID 0000-0001-6987-5487Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Claude BhéreriD· 2 shared Daniel TaliuniD· 2 shared Geneviève GagnoniD· 2 shared John David RiouxiD· 2 shared Justin PelletieriD· 2 shared Philippe M. CampeauiD· 2 shared Alain BittoniD· 1 shared Aspasia Karalis· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Claude BhérerORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

Geneviève Gagnon, Justin Pelletier, Dariel Ashton‐Beaucage, Mohadese Sayahian Dekhordi, Vincent Chapdelaine, Marie‐Ange Delrue, Aspasia Karalis, Daniel Taliun, John David Rioux, Philippe M. Campeau, Claude Bhérer

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

medRxiv · Oct 30, 2025 · PreprintGenetic & Genomic Medicine

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, Gabrielle Boucher, Geneviève Gagnon, Philippe Goyette, Dariel Ashton‐Beaucage, Christine R. Stevens, Robert J. Battat, Alain Bitton, Philippe M. Campeau, Catherine Laprise, Hailiang Huang, Mark J. Daly, Daniel Taliun, , John David Rioux

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

medRxiv · Jul 11, 2025 · PreprintGenetic & Genomic Medicine