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- Genome Technology Program5
- Impact of Genomic Variation on Function (IGVF) Consortium1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium1
- Ethical, Legal and Social Implications (ELSI) Research Program3
About NHGRI
Established in 1989, NHGRI collaborates with the scientific and medical communities to catalyze genomic breakthroughs.
Event
The 2018 meeting focused on KOMP's collaborations with various human disease gene discovery programs.
Grantees
To accelerate genomics research, NHGRI funds and collaborates with scientists t government, public and private institutions
News Release
NHGRI researchers collaborated with physicians and medical geneticists worldwide to create the Atlas of Human Malformation Syndromes in Diverse Populations.
News Release
A 2018 workshop led by Alaska Native people provides a path towards collaborative, community-driven genomics research.
Profile
Dr. Hanchard talks about his journey into genetics research, his collaborations with international researchers, and the importance of determination in science.
News Release
NIH researchers and collaborators have found that that sickle cell trait is prevalent among diverse human populations.
Research Funding
A collaborative large-scale genome sequencing effort to identify rare risk and protective variants contributing to multiple common disease phenotypes.
News Release
African scientists and collaborators gathered in Pointe aux Piments in Mauritius for the 9th Human Health and Heredity in Africa Consortium Meeting.
News Release
NHGRI researchers and their international collaborators have added Williams-Beuren syndrome to the Atlas of Human Malformation Syndromes in Diverse Populations.