Author

Corinne Serruya

McGill University Health Centre

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 3 Research Focus:differential expression· 2 Research Focus:variant calling· 1

Frequent Co-Authors

Anne‐Marie Mes‐MassoniD· 3 shared Caitlin T. FierhelleriD· 3 shared Celia M.T. GreenwoodiD· 3 shared Diane Michele ProvencheriD· 3 shared Jiannis RagoussisiD· 3 shared Patricia N. ToniniD· 3 shared Timothée ReviliD· 3 shared Wejdan M. AleneziiD· 3 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Anne‐Marie Mes‐MassonORCID

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3 papers

Recent·Most cited

Genetic and molecular analyses of candidate germline BRIP1/FANCJ variants implicated in breast and ovarian cancer

Wejdan M. Alenezi, Larissa Milano, Caitlin T. Fierheller, Corinne Serruya, Timothée Revil, Kathleen Klein Oros, J. J. Bruce, Dan Spiegelman, Trevor J. Pugh, Anne‐Marie Mes‐Masson, Diane Michele Provencher, William David Foulkes, Zaki El Haffaf, Guy Armand Rouleau, Luigi Bouchard, , Patricia N. Tonin

The paper investigates five BRIP1/FANCJ variants for their clinical relevance in breast and ovarian cancer, finding three likely damaging variants associated with cellular sensitivity to chemotherapy drugs.

International Journal of Molecular Sciences · Jan 20, 2026Peer-reviewedGenetic & Genomic Medicine

The germline DNA repair gene landscape in BRCA1 and BRCA2 implicated hereditary breast cancer families

Wejdan M. Alenezi, Neil Recio, Caitlin T. Fierheller, Corinne Serruya, Timothée Revil, Anne‐Marie Mes‐Masson, Diane Michele Provencher, Celia M.T. Greenwood, Jiannis Ragoussis, Patricia N. Tonin

The paper analyzes germline DNA repair gene variants in BRCA1 and BRCA2 families to assess the prevalence of damaging variants in DNA repair genes beyond established breast cancer predisposing genes.

medRxiv · Jun 24, 2025 · PreprintGenetic & Genomic Medicine

The genetic analysis of a founder Northern American population of European descent identifies FANCI as a candidate familial ovarian cancer risk gene

Caitlin T. Fierheller, Laure Guitton-Sert, Wejdan M. Alenezi, Timothée Revil, Kathleen Klein Oros, Yuandi Gao, Karine Bédard, Suzanna L. Arcand, Corinne Serruya, Supriya Behl, Liliane Meunier, Hubert Fleury, Eleanor Fewings, Deepak Subramanian, Javad Nadaf, , Patricia N. Tonin

This paper identifies FANCI c.1813C>T as a candidate familial ovarian cancer risk allele in a French Canadian population with founder effects.

Genome Medicine · Dec 1, 2021Peer-reviewedGenetic & Genomic Medicine