“Matching” consent to purpose: The example of the Matchmaker Exchange-Reference-Cited by-同舟云学术

“Matching” consent to purpose: The example of the Matchmaker Exchange

Published:2017-07-12 Issue:10 Volume:38 Page:1281-1285
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Dyke Stephanie O. M.¹^ORCID,Knoppers Bartha M.¹,Hamosh Ada²,Firth Helen V.³,Hurles Matthew³,Brudno Michael⁴⁵,Boycott Kym M.⁶^ORCID,Philippakis Anthony A.⁷,Rehm Heidi L.⁷⁸^ORCID

Affiliation:

1. Centre of Genomics and Policy; Faculty of Medicine; McGill University; Montreal Quebec Canada

2. McKusick-Nathans Institute of Genetic Medicine; Johns Hopkins University; Baltimore Maryland

3. Wellcome Trust Sanger Institute; Wellcome Genome Campus; Hinxton Cambridge UK

4. Department of Computer Science; University of Toronto; Toronto Ontario Canada

5. Centre for Computational Medicine; Hospital for Sick Children; Toronto Ontario Canada

6. Children's Hospital of Eastern Ontario Research Institute; University of Ottawa; Ontario Canada

7. Broad Institute of MIT and Harvard; Cambridge Massachusetts

8. Department of Pathology; Brigham & Women's Hospital and Harvard Medical School; Boston Massachusetts

Funder

Canadian Institutes of Health Research

Government of Canada

Ministère de l’Économie

Ontario Genomics Institute

Ontario Research Fund

Children's Hospital of Eastern Ontario Foundation

Canada Research Chair in Law and Medicine

National Institutes of Health

Baylor-Hopkins Center for Mendelian Genomics

Wellcome Trust

Care4Rare Canada Consortium

Genome Quebec, Genome Canada, the Government of Canada, and the Ministère de l’Économie, Innovation et Exportation du Quèbec

Genome Canada, the Canadian Institutes of Health Research, the Ontario Genomics Institute, Ontario Research Fund, Genome Quebec, and Children’s Hospital of Eastern Ontario Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

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3. International cooperation to enable the diagnosis of all rare genetic diseases;Boycott;American Journal of Human Genetics,2017

4. PhenomeCentral: A portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases;Buske;Human Mutation,2015a

5. The Matchmaker Exchange API: Automating patient matching through the exchange of structured phenotypic and genotypic profiles;Buske;Human Mutation,2015b

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