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6 p, 595.1 KB |
The Deep Genome Project
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Lloyd, K. C. Kent (University of California. Department of Surgery) ;
Adams, David J. (Wellcome Trust Sanger Institute (Regne Unit)) ;
Baynam, Gareth (Curtin University. Faculty of Science and Engineering) ;
Beaudet, Arthur L. (Baylor College of Medicine. Department of Molecular and Human Genetics) ;
Bosch i Tubert, Fàtima (Universitat Autònoma de Barcelona. Centre de Biotecnologia Animal i de Teràpia Gènica (CBATEG)) ;
Boycott, Kym M. (University of Ottawa. Children's Hospital of Eastern Ontario Research Institute) ;
Braun, Robert E. (The Jackson Laboratory) ;
Caulfield, Mark (Queen Mary University of London. William Harvey Research Institute) ;
Cohn, Ronald (The Hospital for Sick Children) ;
Dickinson, Mary E. (Baylor College of Medicine. Departments of Molecular Physiology and Biophysics) ;
Dobbie, Michael S. (The Australian National University) ;
Flenniken, Ann M. (Lunenfeld-Tanenbaum Research Institute. The Centre for Phenogenomics) ;
Flicek, Paul (European Bioinformatics Institute) ;
Galande, Sanjeev (Indian Institute of Science, Education and Research. National Facility for Gene Function in Health and Disease) ;
Gao, Xiang (Nanjing University. SKL of Pharmaceutical Biotechnology and Model Animal Research Center) ;
Grobler, Anne (North-West University. Preclinical Drug Development Platform) ;
Heaney, Jason D. (Baylor College of Medicine. Department of Molecular and Human Genetics) ;
Herault, Yann (Institut de Génétique, Biologie Moléculaire et Cellulaire) ;
De Angelis, Martin Hrabe (German Center for Diabetes Research) ;
Lupski, James R. (Baylor College of Medicine. Department of Molecular and Human Genetics) ;
Lyonnet, Stanislas (Institut Imagine (Paris, França)) ;
Mallon, Ann-Marie (Mammalian Genetics Unit and Mary Lyon Centre. Medical Research Council Harwell Institute) ;
Mammano, Fabio (Institute of Biochemistry and Cell Biology. Italian National Research Council) ;
MacRae, Calum A. (Brigham and Women's Hospital (Boston, Estats Units d'Amèrica)) ;
McInnes, Roderick (McGill University. Lady Davis Research Institute) ;
McKerlie, Colin (The Hospital for Sick Children) ;
Meehan, Terrence F. (European Bioinformatics Institute) ;
Murray, Stephen A. (The Jackson Laboratory) ;
Nutter, Lauryl M. J. (The Hospital for Sick Children) ;
Obata, Yuichi (BioResource Research Center) ;
Parkinson, Helen (Indian Institute of Science. National Facility for Gene Function in Health and Disease) ;
Pepper, Michael S. (University of Pretoria. Institute for Cellular and Molecular Medicine) ;
Sedlacek, Radislav (Czech Centre for Phenogenomics) ;
Seong, Je Kyung (Seoul National University. Korea Mouse Phenotyping Consortium) ;
Shiroishi, Toshihiko (BioResource Research Center) ;
Smedley, Damian (Queen Mary University of London) ;
Tocchini-Valentini, Glauco (Institute of Biochemistry and Cell Biology. Italian National Research Council) ;
Valle, David (The Johns Hopkins University School of Medicine. McKusick-Nathans Department of Genetic Medicine) ;
Wang, Chi-Kuang Leo (National Laboratory Animal Center. National Applied Research Laboratories) ;
Wells, Sara (Medical Research Council Harwell Institute) ;
White, Jacqueline (The Jackson Laboratory) ;
Wurst, Wolfgang (Ludwig Maximillian's Universitat Munchen. Deutsches Zentrum für Neurodegenerative Erkrankungen) ;
Xu, Ying (Medical College of Soochow University. Cambridge-Suda Genomic Resource Center) ;
Brown, Steve D. M. (Medical Research Council Harwell Institute)
2020 -  10.1186/s13059-020-1931-9
Genome biology, Vol. 21 (february 2020)
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10 p, 1.2 MB |
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
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Köhler, Sebastian (Monarch Initiative) ;
Carmody, Leigh (Jackson Laboratory for Genomic Medicine) ;
Vasilevsky, Nicole (Oregon Health and Science University) ;
Jacobsen, Julius O. B. (Queen Mary University of London) ;
Danis, Daniel (Jackson Laboratory for Genomic Medicine) ;
Gourdine, Jean-Philippe (Oregon Health and Science University) ;
Gargano, Michael A. (Jackson Laboratory for Genomic Medicine) ;
Harris, Nomi (Lawrence Berkeley National Laboratory) ;
Matentzoglu, Nicolas (European Bioinformatics Institute) ;
McMurry, Julie A. (Oregon State University) ;
Osumi-Sutherland, David (European Bioinformatics Institute) ;
Cipriani, Valentina (University College of London) ;
Balhoff, James P. (University of North Carolina at Chapel Hill) ;
Conlin, Tom (Oregon State University) ;
Blau, Hannah (Jackson Laboratory for Genomic Medicine) ;
Baynam, Gareth (Government of Western Australia) ;
Palmer, Richard (Curtin University (Perth, Australia)) ;
Gratian, Dylan (Government of Western Australia) ;
Dawkins, Hugh (Government of Western Australia) ;
Segal, Michael (SimulConsult) ;
Jansen, Anna (UZ Brussel) ;
Muaz, Ahmed (Darlinghurst) ;
Chang, Willie H. (Centre for Computational Medicine. Hospital for Sick Children. Department of Computer Science. University of Toronto) ;
Bergerson, Jenna (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Laulederkind, Stanley (Marquette University) ;
Yüksel, Z. (Bioscientia GmbH) ;
Beltran i Agulló, Sergi (Universitat Pompeu Fabra) ;
Freeman, Alexandra F. (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Sergouniotis, Panos (University of Manchester. Manchester Royal Eye Hospital) ;
Durkin, Daniel (Jackson Laboratory for Genomic Medicine) ;
Storm, Andrea L. (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Hanauer, Marc (INSERM) ;
Brudno, Michael (University of Toronto) ;
Bello, Susan (Jackson Laboratory) ;
Sincan, Murat (Sanford Health) ;
Rageth, Kayli (Sanford Health) ;
Wheeler, Matthew T. (Stanford University School of Medicine) ;
Oegema, Renske (University Medical Center) ;
Lourghi, Halima (INSERM) ;
Della Rocca, Maria G. (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Thompson, R. (Newcastle University) ;
Castellanos, Francisco (Jackson Laboratory for Genomic Medicine) ;
Priest, James (Stanford University School of Medicine) ;
Cunningham-Rundles, Charlotte (Mount Sinai School of Medicine) ;
Hegde, Ayushi (Jackson Laboratory for Genomic Medicine) ;
Lovering, Ruth Caroline (University College London) ;
Hajek, Catherine (Sanford Imagenetics. Sanford Health) ;
Olry, Annie (INSERM) ;
Notarangelo, Luigi (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Similuk, Morgan (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Zhang, Xingmin (Jackson Laboratory for Genomic Medicine) ;
Gómez-Andrés, David (Hospital Universitari Vall d'Hebron. Institut de Recerca) ;
Lochmüller, Hanns (Ottawa Hospital Research Institute) ;
Dollfus, Hélène (Strasbourg University Hospital) ;
Rosenzweig, Sergio (NIH Clinical Center) ;
Marwaha, Shruti (Stanford University School of Medicine) ;
Rath, Ana (INSERM) ;
Sullivan, Kathleen (University of Pennsylvania Perelman School of Medicine) ;
Smith, Cynthia (Jackson Laboratory) ;
Milner, Joshua D. (National Institute of Allergy and Infectious Diseases (Bethesda, Estats Units d'Amèrica)) ;
Leroux, Dorothée (Strasbourg University Hospital) ;
Boerkoel, Cornelius (Sanford Health) ;
Klion, Amy (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Carter, Melody C. (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ;
Groza, Tudor (Darlinghurst) ;
Smedley, Damian (Queen Mary University of London) ;
Haendel, Melissa Anne (Oregon State University) ;
Mungall, Christopher (Lawrence Berkeley National Laboratory) ;
Robinson, Peter N. (University of Connecticut) ;
Universitat Autònoma de Barcelona
The Human Phenotype Ontology (HPO) - a standardized vocabulary of phenotypic abnormalities associated with 7000+ diseases - is used by thousands of researchers, clinicians, informaticians and electronic health record systems around the world. [...]
2019 - 10.1093/nar/gky1105
Nucleic acids research, Vol. 47 Núm. D1 (august 2019) , p. D1018-D1027
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