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- Developmental Genotype-Tissue Expression (dGTEx)1
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genetic Architecture of Complex Traits1
- 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
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).
… an overview of the Investigator-Initiated Research on Genetic Counseling Processes and Practices Request for … … Online … Webinar for Investigator-Initiated Research on Genetic Counseling Processes and Practices Request for … an overview of the Investigator-Initiated Research on Genetic Counseling Processes and Practices Request for …
Event
On November 1-5, 2023, 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. The annual meeting provides a forum for the presentation and discussion of cutting-edge science in all areas of human genetics.
… Nicola Sugden Understanding ableism in abstracts for genetic and genomic autism research PB2437 Erin Mansell … study of neural tube defects allows an unbiased search for genetic contribution. PB2092 Ted Han Genome wide CRISPR … associated with canine body size. PB1092 Yixing Han Common Genetic Variants are Associated with Plasma and Skin …
About NHGRI
NHGRI is the driving force for advancing genomics research at the National Institutes of Health, the largest biomedical research agency in the world.
… Genome Project, Dna Sequencing, Human Genome Sequencing, Genetic Testing … NHGRI is the driving force for advancing …
Event
On January 25, 2023, the National Human Genome Research Institute will hold a roundtable on social and behavioral genomics.
… GWAS of educational attainment” by the Social Science Genetic Association Consortium Problems with Using … Lucas J. Matthews Social by Nature by Catherine Bliss Genetic ancestry testing among white nationalists: From identity …
Event
Annual scientific lecture honoring NHGRI's founding scientific director, Jeffrey M. Trent, Ph.D.
… and Genetics, part of NIH, delivered the lecture on the genetic susceptibility to cancer. … The seventh annual … Trent's research has provided important insights into the genetic basis of cancer. He is the author of more than 350 … patients. Dr. Trent continues to lead studies of the genetic basis of various complex diseases in humans, as well …
Event
NHGRI and George Mason University's Institute for Digital InnovAtion co-host the Computational Genomics Conference, on Wednesday, April 28, 2021.
… data science technologies are changing the landscape of genetic and genomic research. With resources like cloud … to investigate complex questions and work towards ensuring genetic and genomic advances benefit all. This workshop …
Event
NHGRI will host a director's research seminar by Matt Hurles, Director of the Wellcome Trust Sanger Institute on October 30, 2023.
… and leads a research group focused on deciphering the genetic causes of severe developmental disorders, and …
Event
On February 16, 2023, the National Human Genome Research Institute (NHGRI) held a follow-up working group consultation after the 14th Genomic Medicine meeting, Genomic Medicine XIV: Genomic Learning Healthcare Systems.
… of Alabama at Birmingham Heersink School of Medicine Our Genetic Testing Service is in the design phase, and we hope … UAB physician can use to ask for assistance in ordering genetic testing. The initial contact will be a Genetic Counseling Assistant (GCA). If the request is more …
Event
The Encyclopedia of DNA Elements (ENCODE) Consortium presented a half-day workshop on the accessibility & utilization of ENCODE data.
Event
The Excellence in Clinical Research Seminar Series is designed to facilitate clinical research in the rare disease space with a focus on aspects of regulatory medicine and clinical trials in Mendelian disorders.