Faculty profile
Jean McGowan-Jordan
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Read how they describe their research on their University of Ottawa profile.
Latest papers
TAF15::ZNF384 Mixed Phenotype Acute Leukemia With Complex Karyotype: Case Report With B-ALL Induction, Blinatumomab Bridging to Allogeneic Transplant and Literature Review.
Clinical case reports · 2025
Familial inheritance of 14q terminal deletion syndrome and review of the literature.
European journal of medical genetics · 2025
Genome Mapping Nomenclature.
Cytogenetic and genome research · 2023
Latest funding
- $23,654
Engaging patients with rare diseases in research to improve their care
CIHR · 2016 · Principal investigator
25 publications.
TAF15::ZNF384 Mixed Phenotype Acute Leukemia With Complex Karyotype: Case Report With B-ALL Induction, Blinatumomab Bridging to Allogeneic Transplant and Literature Review.
Blain S, Empringham B, Mahdi T, Hedley BD, McGowan-Jordan J, Padmore R
Familial inheritance of 14q terminal deletion syndrome and review of the literature.
Vincent KM, Prince B, McGowan-Jordan J, Carter MT
Genome Mapping Nomenclature.
Moore S, McGowan-Jordan J, Smith AC, Rack K, Koehler U, Stevens-Kroef M, Barseghyan H, Kanagal-Shamanna R, Hastings R, ISCN Standing Committee
Addenda to ISCN 2020.
Hastings R, McGowan-Jordan J, Moore S, ISCN Standing Committee
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
Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr.
McGowan-Jordan J, Hastings R, Moore S
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
Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.
Ghani M, Nfonsam L, Pranckeviciene E, Daoud H, Potter R, Chisholm C, Harper PE, Schaffer A, Little L, Sinclair-Bourque E, McGowan-Jordan J, Smith A, Bronicki L, Jarinova O
Atypical Hepatic Mesenchymal Hamartoma: Histologic Appearance, Immunophenotype, and Molecular Findings.
El Demellawy D, Lee JY, McDonell L, Dyment DA, Knisely AS, McGowan-Jordan J, Ngan B, Finegold M, Kapur RP, Nasr A
Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory.
Nfonsam L, Ordorica S, Ghani M, Potter R, Schaffer A, Daoud H, Vasli N, Chisholm C, Sinclair-Bourque E, McGowan-Jordan J, Smith AC, Jarinova O, Bronicki L
Engaging patients with rare diseases in research to improve their care
Principal investigators: Boycott, Kym M; McGowan-Jordan, Jean; Graham, Gail E
Keywords: Genetics; Patient Engagement; Quality Improvement; Rare Disease; Research Priorities
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Lucas Bronicki and Olga Jarinova: 11 shared papers
- Jean McGowan-Jordan and Olga Jarinova: 6 shared papers
- Melanie Lacaria and Pranesh Chakraborty: 4 shared papers
- Jean McGowan-Jordan and Dina El Demellawy: 4 shared papers
- Jean McGowan-Jordan and Lucas Bronicki: 3 shared papers
- Ming-Sound Tsao and Jean McGowan-Jordan: 2 shared papers
- Jean McGowan-Jordan and Mélanie Beaulieu Bergeron: 2 shared papers
- Elizabeth McCready and Jean McGowan-Jordan: 1 shared paper
- Elizabeth McCready and Olga Jarinova: 1 shared paper
- Melanie Lacaria and Jean McGowan-Jordan: 1 shared paper
- Melanie Lacaria and Dina El Demellawy: 1 shared paper
- Dennis Bulman and Jean McGowan-Jordan: 1 shared paper
- Dennis Bulman and Olga Jarinova: 1 shared paper
- Mark Basik and Jean McGowan-Jordan: 1 shared paper
- Pranesh Chakraborty and Jean McGowan-Jordan: 1 shared paper
- Pranesh Chakraborty and Christina Honeywell: 1 shared paper
- Jean McGowan-Jordan and Christina Honeywell: 1 shared paper
- Dina El Demellawy and Mélanie Beaulieu Bergeron: 1 shared paper
- Lucas Bronicki and Mélanie Beaulieu Bergeron: 1 shared paper
- Pathology and Laboratory Medicine
- Pediatrics
- Department of Laboratory Medicine and Pathobiology
- Family Medicine
- Pathology & Molecular Medicine
- Social Studies of Medicine
- Institute for Stem Cell Research
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.
Olga Jarinova
Pathology and Laboratory Medicine
6 shared papers, latest 2020
Dina El Demellawy
Pathology and Laboratory Medicine
4 shared papers, latest 2022
Lucas Bronicki
Pathology and Laboratory Medicine
3 shared papers, latest 2020
Mélanie Beaulieu Bergeron
Pathology and Laboratory Medicine
2 shared papers, latest 2022
Ming-Sound Tsao
Department of Laboratory Medicine and Pathobiology
2 shared papers, latest 2018
Christina Honeywell
Family Medicine
1 shared papers, latest 2012
Elizabeth McCready
Pathology & Molecular Medicine
1 shared papers, latest 2011
Melanie Lacaria
Institute for Stem Cell Research
1 shared papers, latest 2017
Dennis Bulman
Pediatrics
1 shared papers, latest 2012
Mark Basik
Social Studies of Medicine
1 shared papers, latest 2008
Pranesh Chakraborty
Pediatrics
1 shared papers, latest 2016
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Profile data last refreshed on September 25, 2026 from the university directory, publication records and CIHR, NSERC and SSHRC funding.