One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient Matchmaking.

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Title: One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient Matchmaking.
Authors: Osmond M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Price EM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Buske OJ; PhenoTips, Toronto, Canada., Frew M; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Couse M; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Hartley T; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Klamann C; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Le HGBH; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Xu J; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., So D; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Jain A; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Lu K; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Mo K; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Wyllie H; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Wall E; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Driver HG; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Cheung WA; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA., Cohen ASA; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri Kansas City School of Medicine, Kansas City, Missouri, USA.; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA., Farrow EG; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri Kansas City School of Medicine, Kansas City, Missouri, USA.; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA., Thiffault I; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri Kansas City School of Medicine, Kansas City, Missouri, USA.; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA., Consortium CRC; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada., Turinsky AL; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada., Pastinen T; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.; University of Missouri Kansas City School of Medicine, Kansas City, Missouri, USA.; Children's Mercy Research Institute, Kansas City, Missouri, USA., Brudno M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; PhenoTips, Toronto, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.; UHN DATA Team, University Health Network, Toronto, Canada.; Department of Computer Science, University of Toronto, Toronto, Canada.; Vector Institute, Toronto, Canada., Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.
Source: Human mutation [Hum Mutat] 2025 Oct 08; Vol. 2025, pp. 5941599. Date of Electronic Publication: 2025 Oct 08 (Print Publication: 2025).
Publication Type: Journal Article
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1098-1004
DOI:10.1155/humu/5941599