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Paper Details

International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.
Am J Hum Genet
233
2017
Author NameAffiliation
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Ana RathInstitut National de la Sante et de la Recherche Medicale US14
Ana RathInstitut National de la Sante et de la Recherche Medicale US14
Jessica X ChongUniversity of Washington
Jessica X ChongUniversity of Washington
Taila HartleyChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Fowzan S AlkurayaKing Faisal Research Center
Gareth Baynam
Gareth Baynam
Anthony J BrookesUniversity of Leicester
Anthony J BrookesUniversity of Leicester
Michael BrudnoUniversity of Toronto
Angel CarracedoGalician Foundation of Genomic Medicine and University of Santiago de Compostela
Johan T den DunnenDepartments of Human Genetics and Clinical Genetics, Leiden University Medical Center
Stephanie O M DykeMcGill University
Xavier EstivillSidra Medical and Research Center
Xavier EstivillSidra Medical and Research Center
Jack Goldblatt
Stephen C GroftNational Center for Advancing Translational Sciences, National Institutes of Health
Ivo GutCenter for Genomic Regulation, Barcelona Institute of Science and Technology, Universitat Pompeu Fabra
Ada HamoshMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Philip HieterUniversity of British Columbia
Matthew E HurlesWellcome Trust Sanger Institute
Matthew E HurlesWellcome Trust Sanger Institute
Petra KaufmannNational Center for Advancing Translational Sciences, National Institutes of Health
Bartha Maria KnoppersMcGill University
Jeffrey P KrischerUniversity of South Florida Health Informatics Institute
Gert MatthijsCenter for Human Genetics, University of Leuven
Gert MatthijsCenter for Human Genetics, University of Leuven
Annie OlryInstitut National de la Sante et de la Recherche Medicale US14
Justin PaschallWellcome Trust Sanger Institute
Justin PaschallWellcome Trust Sanger Institute
Anthony A PhilippakisBroad Institute of MIT and Harvard
Anthony A PhilippakisBroad Institute of MIT and Harvard
Heidi L RehmBroad Institute of MIT and Harvard
Heidi L RehmBroad Institute of MIT and Harvard
Peter N RobinsonInstitut fur Medizinische Genetik und Humangenetik, Charite Universitatsmdizin Berlin
Peter N RobinsonInstitut fur Medizinische Genetik und Humangenetik, Charite Universitatsmdizin Berlin
Pak C ShamUniversity of Hong Kong
Domenica TaruscioNational Centre for Rare Diseases, Istituto Superiore di Sanita
Han G BrunnerRadboud University Medical Center, the Netherlands Maastricht University Medical Center
Michael J BamshadUniversity of Washington, Seattle Children's Hospital
Michael J BamshadUniversity of Washington, Seattle Children's Hospital
Hanns Lochm??llerJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University
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