Faculty profile
Mélanie Beaulieu Bergeron
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Read how they describe their research on their University of Ottawa profile.
Latest papers
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.
American journal of medical genetics. Part A · 2022
Porokeratotic eccrine ostial and dermal duct nevus associated with an 11 megabase 3p deletion.
Pediatric dermatology · 2022
ALU transposition induces familial hypertrophic cardiomyopathy.
Molecular genetics & genomic medicine · 2020
3 publications.
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.
Vincent KM, Stavropoulos DJ, Beaulieu-Bergeron M, Yang C, Jiang M, Zuijdwijk C, Dyment DA, Graham GE
Porokeratotic eccrine ostial and dermal duct nevus associated with an 11 megabase 3p deletion.
Castle AMR, Ramien ML, Kanigsberg N, El Demellawy D, McGowan-Jordan J, Beaulieu Bergeron M, Armour CM
ALU transposition induces familial hypertrophic cardiomyopathy.
Nfonsam L, Huang L, Carson N, McGowan-Jordan J, Beaulieu Bergeron M, Goobie S, Conacher S, McCarty D, Benson L, Hewson S, Zahavich L, Sinclair-Bourque E, Smith A, Potter R, Ghani M, Bronicki L, Jarinova O
Frequent collaborators
- Pathology and Laboratory Medicine
Co-authors at University of Ottawa, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Jean McGowan-Jordan
Pathology and Laboratory Medicine
2 shared papers, latest 2022
Olga Jarinova
Pathology and Laboratory Medicine
1 shared papers, latest 2020
Dina El Demellawy
Pathology and Laboratory Medicine
1 shared papers, latest 2022
Lucas Bronicki
Pathology and Laboratory Medicine
1 shared papers, latest 2020
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Profile data last refreshed on September 25, 2026 from the university directory, publication records and CIHR, NSERC and SSHRC funding.