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Paper Details

matchbox: An open-source tool for patient matching via the Matchmaker Exchange.
Hum Mutat
19
2018
Rare disease, novel gene, patient, patients, rare, rare disease
Access to Information, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Information Dissemination, Information Storage and Retrieval, Patient Selection, Phenotype, Rare Diseases, Software, Web Browser
Author NameAffiliation
Harindra ArachchiCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Harindra ArachchiThe Broad Institute of MIT and Harvard
Harindra ArachchiCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Harindra ArachchiThe Broad Institute of MIT and Harvard
Monica H WojcikCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Monica H WojcikBoston Children's Hospital, Harvard Medical School
Ben WeisburdCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Ben WeisburdCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Julius O B JacobsenWilliam Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London
Elise ValkanasCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Samantha BaxterCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Samantha BaxterCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Alicia B ByrneCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Alicia B Byrne
Alicia B ByrneSchool of Pharmacy and Medical Sciences, University of South Australia
Anne O'Donnell-LuriaCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Anne O'Donnell-LuriaBoston Children's Hospital, Harvard Medical School
Anne O'Donnell-LuriaCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Anne O'Donnell-LuriaBoston Children's Hospital, Harvard Medical School
Melissa A HaendelOregon Clinical and Translational Research Institute, Oregon Health & Science University
Melissa A HaendelLinus Pauling Institute, Oregon State University
Melissa A HaendelOregon Clinical and Translational Research Institute, Oregon Health & Science University
Melissa A HaendelLinus Pauling Institute, Oregon State University
Damian SmedleyWilliam Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London
Daniel G MacArthurCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Daniel G MacArthurCenter for Genomic Medicine, Massachusetts General Hospital
Daniel G MacArthurThe Broad Institute of MIT and Harvard
Daniel G MacArthurCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Daniel G MacArthurThe Broad Institute of MIT and Harvard
Daniel G MacArthurCenter for Genomic Medicine, Massachusetts General Hospital
Anthony A PhilippakisThe Broad Institute of MIT and Harvard
Anthony A PhilippakisThe Broad Institute of MIT and Harvard
Heidi L RehmCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Heidi L RehmThe Broad Institute of MIT and Harvard
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
Heidi L RehmCenter for Mendelian Genomics, The Broad Institute of MIT and Harvard
Heidi L RehmThe Broad Institute of MIT and Harvard
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
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