Author

Supriya Behl

McGill UniversityORCID 0000-0002-6672-4824Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anne‐Marie Mes‐MassoniD· 1 shared Caitlin T. FierhelleriD· 1 shared Celia M.T. GreenwoodiD· 1 shared Corinne Serruya· 1 shared Deepak SubramanianiD· 1 shared Diane Michele ProvencheriD· 1 shared Eleanor FewingsiD· 1 shared Hubert Fleury· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anne‐Marie Mes‐MassonORCID

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Author profile →

1 paper

Recent·Most cited

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