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The Human Variome Project

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Year: 2008
Type: article
Abstract: An ambitious plan to collect, curate, and make accessible information on genetic variations affecting human health is beginning to be realized.
Source: Science
DOI: 10.1126/science.1167363
Authors: Richard G. H. Cotton, Arleen D. Auerbach, Myles Axton, Carol Isaacson Barash, Samuel F. Berkovic, Anthony J. Brookes, John Burn, Garry Cutting, Johan T. den Dunnen, Paul Flicek, Nelson Freimer, Marc S. Greenblatt, Heather J. Howard, Michael Katz, Finlay A. Macrae, Donna Maglott, Gabriela Möslein, Sue Povey, Rajkumar S. Ramesar, Carolyn S. Richards, Daniela Seminara, Timothy D. Smith, María-Jesús Sobrido, Jan Helge Solbakk, Rudolph E. Tanzi, Sean V. Tavtigian, Graham R. Taylor, Joji Utsunomiya, Michael Watson
Institutions: Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Austin Health, University of California, Los Angeles, Instituto de Salud Carlos III, Centre for Biomedical Network Research on Rare Diseases, Fundación Pública Galega de Medicina Xenómica, Harvard University, Massachusetts General Hospital
Language: English

Topic: Genomics and Rare Diseases
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences

Open Access status: green

Funder: National Institute of Diabetes and Digestive and Kidney Diseases
Award: G3777803959
OpenAlex ID: W2145828552
FWCI: 4.393
Cites: 6
Cited by: 72
Related to: 10
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