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11 - 20 of 585
About NHGRI
Organization
Established in 1989, NHGRI collaborates with the scientific and medical communities to catalyze genomic breakthroughs.
Event
2018 KOMP2-IMPC Annual Fall Meeting
The 2018 meeting focused on KOMP's collaborations with various human disease gene discovery programs.
Grantees
Research Funding
To accelerate genomics research, NHGRI funds and collaborates with scientists t government, public and private institutions
News Release
NIH creates Atlas of Human Malformation Syndromes in Diverse Populations
NHGRI researchers collaborated with physicians and medical geneticists worldwide to create the Atlas of Human Malformation Syndromes in Diverse Populations.
News Release
NIH and Alaska Native leaders identify how to achieve socially responsible genomics research
A 2018 workshop led by Alaska Native people provides a path towards collaborative, community-driven genomics research.
Profile
Neil Hanchard unravels the complexity of childhood diseases, aims to diversify genomics research
Dr. Hanchard talks about his journey into genetics research, his collaborations with international researchers, and the importance of determination in science.
News Release
Genetic carriers for sickle cell disease have higher risks of blood clots across diverse ancestries
NIH researchers and collaborators have found that that sickle cell trait is prevalent among diverse human populations.
Research Funding
Centers for Common Disease Genomics
A collaborative large-scale genome sequencing effort to identify rare risk and protective variants contributing to multiple common disease phenotypes.
News Release
President Gurib-Fakim of Mauritius Supports H3Africa Initiative
African scientists and collaborators gathered in Pointe aux Piments in Mauritius for the 9th Human Health and Heredity in Africa Consortium Meeting.
News Release
Williams-Beuren syndrome added to Atlas of Human Malformation Syndromes in Diverse Population
NHGRI researchers and their international collaborators have added Williams-Beuren syndrome to the Atlas of Human Malformation Syndromes in Diverse Populations.