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- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genome Technology Program1
- Impact of Genomic Variation on Function (IGVF) Consortium1
- Clinical Genome (ClinGen) Resource1
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Event
On May 19-20, 2016, the National Human Genome Research Institute (NHGRI) hosted a two-day workshop where participants were asked to weigh the benefits and risks of sharing aggregate genomic data with secondary users.
Event
On October 25-29, 2022, the National Human Genome Research Institute (NHGRI) will participate in the ASHG Annual Meeting - the world's largest human genetics and genomics meeting and exposition.
… 8:00 p.m. Mendelian Phenotypes Human brains with Tay Sachs disease exhibit altered transcriptomes during fetal … of secondary genomic findings: Experiences of sickle cell disease research participants Board No. PB2224 Jameson Floyd … in two hereditary prostate cancer cohorts reveals rare risk-associated Board No. PB1123 Georgea Foley Convention …
FAQ
Questions and answers to help applicants responding to the Pre-Application Webinar for the Building Partnerships and Broadening Perspectives to Advance ELSI Research (BBAER) Program RFA-HG-24-026.
… Awarded BBAER Sites are expected to implement their needs assessments plan and submit a summary of findings to NHGRI …
FAQ
Questions and answers to help applicants responding to the ML/AI Tools to Advance Genomic Translational Research (MAGen) notice of funding opportunities (NOFOs): RFA-HG-24-004 and RFA-HG-24-005.
… how individuals with pathogenic genetic variants manifest disease—the goal of this NOFO—but applicants should clearly … predicting penetrance relate to how individuals manifest disease and identify genomic and non-genomic factors that … of the NOFO?  Clinical expertise in the proposed disease should be integrated at all stages so the developed …
FAQ
On October 10, 2024, NHGRI hosted a pre-application webinar for the Population Genomic Screening in Primary Care NOFOs: RFA-HG-24-021, RFA-HG-24-022, and RFA-HG-24-023. These FAQs contain questions answered during that webinar.
… selecting for or excluding anyone who might be at risk. Final procedures will be determined by Steering …
News Release
Cari Young and Julie Nadel join NHGRI as public policy and education fellows.
… likes to address scientific questions and think about new disease models from a genetics perspective. Julie received …
FAQ
Frequently asked questions from the September 23, 2024 pre-application webinar the NHGRI ELSI Program hosted.
News Release
NHGRI researchers will present four platform talks and 55 posters to highlight the institute's diverse portfolio at the 65th annual meeting of ASHG.
… 9. Danielle M. Karyadi: Whole exome sequencing in 75 high-risk families identifies eight previously unknown prostate … screen to diagnose rare genetic disorders and unravel disease mechanisms. (Clinical Genetic Testing) 2187T. … associated with parkinsonism in patients with Gaucher disease and GBA1 mutation carriers. (Metabolic Disorders) …
News Release
NHGRI hosted a CRISPR "Ask Me Anything" with Jennifer Doudna, Ph.D., reaching 10.5 million people worldwide.
… This is what researchers are testing out for Sickle Cell Disease. The team received two questions from Congresswoman … provide affordable options for patients with genetic disease. Many folks had questions about the misunderstandings … - to use CRISPR to impact the course of any particular disease, we'd need to have a really strong understanding of …
News Release
Genome: Unlocking Life's Code exhibition is going on tour after having completed a 14-month engagement at the Smithsonian's National Museum of Natural History.
… DNA interactive, search for the right medicine for a given disease. An interactive puzzle allows visitors to learn how genetic, environmental and random factors influence risk for a particular disease.  Connections: Natural World and Genomic Journey: …