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- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genetic Architecture of Complex Traits1
- Genome Technology Program1
- 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) Consortium2
- Developmental Genotype-Tissue Expression (dGTEx)1
Event
On February 23, 2023, NHGRI and the Smithsonian National Museum of African American History and Culture (NMAAHC) continue their collaboration to present, "Historically Speaking: Next Generation of Black Leaders in Genetic Science."
News
To prevent an emerging genomic technology from contributing to health disparities, a scientific team funded by the National Institutes of Health has devised new ways to improve a genetic testing method called a polygenic risk score.
… disparities often stem from systemic discrimination, not genetics, these false results are a way that inequitable …
15 Ways Genomics Influences Our World
Genomics is revolutionizing health assessments before birth.
… Prenatal Genetic Diagnostic Tests Australia's Centre for Genetics Education - Overview of Prenatal Testing CBS News: … NLM - Genetic Testing Registry American Society of Human Genetics - Prenatal Cell-Free DNA Screening Infographics … Clinicians - A Guide to Genomic Test Results for Non-Genetics Providers American Society of Human Genetics - …
Media Advisory
On December 7, 2022, the National Human Genome Research Institute will host a webinar to discuss the key findings from a recently released Human Genetics & Genomics Workforce Survey Report.
… This past month, the American Society of Human Genetics (ASHG) released the Human Genetics and Genomics Workforce Survey Report, which lays a … to discuss the key findings from a recently released Human Genetics & Genomics Workforce Survey Report. The panelists …
News Release
By considering mixed genetic lineages, NHGRI researchers demonstrated that previously inferred links between a genomic variant that helps digest lactose and traits such as a person’s height and cholesterol level may not be valid.
… ancestry should be re-evaluated. “By reading population genetics papers, we realized that the pattern of genetic … catalogs of human genomic variation. By reading population genetics papers, we realized that the pattern of genetic …
Event
Join us on Wednesday, May 25, as scholars and scientists answer audience questions and address the complexities surrounding historical and present-day eugenics and scientific racism in the context of existing and developing genetic and genomic screening technologies.
Educational Resources
Carrier screening is a genetic test performed on people who display no symptoms for a genetic disorder but may be at risk for passing it on to their children.
News Release
NIH will award nearly $80 million to support the establishment of the Mendelian Genomics Research Consortium and the development of novel methods and approaches that help researchers identify the genetic causes of single-gene diseases.
Event
NHGRI hosted a webinar to provide an overview of the Investigator-Initiated Research on Genetic Counseling Processes and Practices Request for Applications (RFA-HG-20-048 and RFA-HG-20-049).