This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Ottawa directory, so their courses and email address may be missing. Find their university profile.
Latest papers
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient Matchmaking.
Human mutation · 2025
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery.
Human mutation · 2022
Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study.
Fetal diagnosis and therapy · 2017
Latest funding
- $100,000
Care4Rare-SOLVE
CIHR · 2020 · Principal investigator
- $1,225,000
Finding of Rare Disease Genes in Canada (FORGE CANADA)
CIHR · 2010 · Co-investigator
3 publications.
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient Matchmaking.
Osmond M, Price EM, Buske OJ, Frew M, Couse M, Hartley T, Klamann C, Le HGBH, Xu J, So D, Jain A, Lu K, Mo K, Wyllie H, Wall E, Driver HG, Cheung WA, Cohen ASA, Farrow EG, Thiffault I, Consortium CRC, Turinsky AL, Pastinen T, Brudno M, Boycott KM
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery.
Driver HG, Hartley T, Price EM, Turinsky AL, Buske OJ, Osmond M, Ramani AK, Kirby E, Kernohan KD, Couse M, Elrick H, Lu K, Mashouri P, Mohan A, So D, Klamann C, Le HGBH, Herscovich A, Marshall CR, Statia A, Canada Consortium CR, Knoppers BM, Brudno M, Boycott KM
Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study.
Xi Y, Arbabi A, McNaughton AJM, Hamilton A, Hull D, Perras H, Chiu T, Morrison S, Goldsmith C, Creede E, Anger GJ, Honeywell C, Cloutier M, Macchio N, Kiss C, Liu X, Crocker S, Davies GA, Brudno M, Armour CM
Care4Rare-SOLVE
Principal investigators: Boycott, Kym M; Brudno, Michael
Keywords: 1-Sided Match Making; Data Federation; Rare Disease
Finding of Rare Disease Genes in Canada (FORGE CANADA)
Principal investigators: Boycott, Kym M; Friedman, Jan M; Michaud, Jacques L
Keywords: Gene Identification; Mendelian Disorders; Rare Disease
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
- Computer Science
- Family Medicine
- Other
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.
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