Author

Hubert Fleury

Centre Hospitalier de l’Université de Montréal

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· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:statistical model· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anne‐Marie Mes‐MassoniD· 1 shared Benjamin J. T. Dodd· 1 shared Benjamin NebenfuehriD· 1 shared Bruce Proctor· 1 shared Caitlin T. FierhelleriD· 1 shared Celia M.T. GreenwoodiD· 1 shared Clara M. Stiefel· 1 shared Colin SempeckiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anne‐Marie Mes‐MassonORCID

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Author profile →

2 papers

Recent·Most cited

The APE2 nuclease is essential for DNA double strand break repairby microhomology-mediated end-joining.

Hubert Fleury, Myles K. MacEachern, Clara M. Stiefel, Roopesh Anand, Colin Sempeck, Benjamin Nebenfuehr, Kelper Maurer-Alcalá, Kerri A. Ball, Bruce Proctor, Ondrej Beláň, Erin Taylor, Raquel Ortega, Benjamin J. T. Dodd, Laila Weatherly, Djelika Dansoko, , Nausica Arnoult

This study identifies APE2 nuclease as a critical factor for MMEJ repair, showing its role in telomere fusion and DNA repair reporter assays.

Molecular Cell · Apr 11, 2023Peer-reviewedMolecular Biology

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