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Paper Details

The Matchmaker Exchange: a platform for rare disease gene discovery.
Hum Mutat
338
2015
MME, genome, patients, rare, rare disease
Database Management Systems, Databases, Genetic, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Information Dissemination, Rare Diseases, Software
Author NameAffiliation
Anthony A PhilippakisThe Broad Institute of Harvard and MIT
Anthony A PhilippakisHarvard Medical School
Anthony A PhilippakisBrigham & Women's Hospital
Anthony A PhilippakisThe Broad Institute of Harvard and MIT
Anthony A PhilippakisBrigham & Women's Hospital
Anthony A PhilippakisHarvard Medical School
Danielle R Azzariti
Sergi Beltran
Anthony J BrookesUniversity of Leicester
Anthony J BrookesUniversity of Leicester
Catherine A BrownsteinHarvard Medical School
Catherine A BrownsteinDivision of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital
Catherine A BrownsteinHarvard Medical School
Catherine A BrownsteinDivision of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital
Michael BrudnoUniversity of Toronto
Michael BrudnoThe Hospital for Sick Children
Michael BrudnoThe Hospital for Sick Children
Han G BrunnerRadboud University Medical Center
Han G BrunnerMaastricht University Medical Center
Orion J BuskeUniversity of Toronto
Orion J BuskeThe Hospital for Sick Children
Orion J BuskeThe Hospital for Sick Children
Orion J BuskeUniversity of Toronto
Orion J BuskeThe Hospital for Sick Children
Orion J BuskeThe Hospital for Sick Children
Knox Carey
Cassie DollGoogle Inc
Sergiu DumitriuThe Hospital for Sick Children
Stephanie O M DykeMcGill University
Johan T den DunnenHuman and Clinical Genetics, Leiden University Medical Center
Helen V FirthCambridge University Hospitals NHS Foundation Trust
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Marta GirdeaUniversity of Toronto
Marta GirdeaThe Hospital for Sick Children
Michael A Gonzalez
Melissa A HaendelDepartment of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Melissa A HaendelDepartment of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Ada HamoshMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University
Ingrid A HolmHarvard Medical School
Ingrid A HolmDivision of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital
Ingrid A HolmHarvard Medical School
Ingrid A HolmDivision of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital
Lijia HuangThe Children's Hospital of Eastern Ontario Research Institute
Matthew E HurlesWellcome Trust Sanger Institute
Matthew E HurlesWellcome Trust Sanger Institute
Ben HuttonWellcome Trust Sanger Institute
Joel B KrierHarvard Medical School
Joel B KrierBrigham and Women's Hospital
Andriy MisyuraThe Hospital for Sick Children
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