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Paper Details

The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.
Am J Hum Genet
146
2015
HPO, Human, Mendelian diseases, common diseases, human, rare disease, risk alleles
Gene Ontology, Genetic Diseases, Inborn, Humans, MEDLINE, Models, Biological, Phenotype, Terminology as Topic
Author NameAffiliation
Tudor GrozaUniversity of Queensland, Australia Garvan Institute of Medical Research
Tudor GrozaUniversity of Queensland, Australia Garvan Institute of Medical Research
Sebastian K??hlerInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Sebastian K??hlerInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Dawid MoldenhauerInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin, Germany University of Applied Sciences
Nicole VasilevskyOregon Health & Science University
Nicole VasilevskyOregon Health & Science University
Gareth BaynamUniversity of Western Australia, Australia Institute for Immunology and Infectious Diseases, Murdoch University, Public Health and Clinical Services Division, King Edward Memorial Hospital, Australia Telethon Kids Institute
Gareth BaynamUniversity of Western Australia, Australia Institute for Immunology and Infectious Diseases, Murdoch University, Public Health and Clinical Services Division, King Edward Memorial Hospital, Australia Telethon Kids Institute
Tomasz ZemojtelInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin, Germany Institute of Bioorganic Chemistry, Polish Academy of Sciences
Lynn M SchrimlUniversity of Maryland, USA Institute for Genome Sciences
Warren A KibbeCenter for Biomedical Informatics and Information Technology, National Cancer Institute, 9609 Medical Center Drive
Warren A KibbeCenter for Biomedical Informatics and Information Technology, National Cancer Institute, 9609 Medical Center Drive
Paul N SchofieldUniversity of Cambridge
Paul N SchofieldUniversity of Cambridge
Tim BeckUniversity of Leicester
Drashtti VasantEuropean Bioinformatics Institute
Anthony J BrookesUniversity of Leicester
Anthony J BrookesUniversity of Leicester
Andreas ZanklGarvan Institute of Medical Research, The Children's Hospital at Westmead, Sydney Medical School, University of Sydney
Nicole L WashingtonLawrence Berkeley National Laboratory
Nicole L WashingtonLawrence Berkeley National Laboratory
Christopher J MungallLawrence Berkeley National Laboratory
Christopher J MungallLawrence Berkeley National Laboratory
Suzanna E LewisLawrence Berkeley National Laboratory
Suzanna E LewisLawrence Berkeley National Laboratory
Melissa A HaendelOregon Health & Science University
Melissa A HaendelOregon Health & Science University
Helen ParkinsonEuropean Bioinformatics Institute
Helen ParkinsonEuropean Bioinformatics Institute
Peter N RobinsonInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin, Germany Max Planck Institute for Molecular Genetics, Germany Berlin Brandenburg Center for Regenerative Therapies, Freie Universitat Berlin
Peter N RobinsonInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin, Germany Max Planck Institute for Molecular Genetics, Germany Berlin Brandenburg Center for Regenerative Therapies, Freie Universitat Berlin
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