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1 - 10 of 32
Event
NSIGHT explores the implications, challenges and opportunities associated with the possible use of genomic sequence information during the newborn period.
Event
The Journeys in Human Genetics and Genomics Colloquium is part of a training partnership between ASHG and NHGRI to showcase the depth and breadth of exciting scientific, clinical, and societal elements of human genetics and genomics at an introductory level as well as to illustrate the myriad associated career opportunities.
… Society of Human Genetics (ASHG) and the National Human Genome Research Institute (NHGRI). The goal of the colloquium …
News Release
Research studies are now using polygenic risk scores to determine a person’s inherited risk for certain diseases, but there are inconsistencies in how these scores are calculated. NHGRI has published guidelines in Nature for how these scores should be reported.
… new approach will be used as a framework for publishing studies on polygenic risk scores. … Scientists and healthcare … the research teams, funded primarily by the National Human Genome Research Institute (NHGRI), have  published a 22-item … studies. This framework — created by NHGRI’s Clinical Genome Resource's (ClinGen) Complex Disease Working Group …
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.
… Hall 3:00 p.m. — 4:45 p.m Complex Traits Sequencing-based genome-wide association study of triglycerides in East Africans Board No. …
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. 
… Pediatric Genetics Education. PB2385 Edmond Wonkam Tingang Genome-Wide Sequencing Implicates Monogenic Disruption of Vascular … - 4:15 p.m. Faith Pangilinan Performance of a genome-wide association study of neural tube defects allows an unbiased …
News Release
NIH will support research that incorporates DNA sequence information into electronic medical records.
… into EMRs The grants, administered by the National Human Genome Research Institute (NHGRI), represent the third phase … patient electronic health records, and along with genome-wide testing, explore the roles of variants in a number of … conditions and disorders. In addition, their wide-ranging studies include evaluating the cost-effectiveness of genetic …
Archive
… Genome-Wide Association Studies for the Rest of Us: Adding Genome-Wide Association to …
Event
On June 17-18, 2021, NHGRI hosts a workshop, Multi-Omics in Health and Disease: Current Applications, Challenges and Future Directions.
… Design and Sample Collection Tuuli Lappalainen, New York Genome Center 3:25 - 3:45 p.m. Presentation 3 - Data … Session 3 : Application of Multi-omics to Observational Studies Moderator: Joannella Morales, NHGRI 1:10 - 1:25 p.m. … Discussion - Application of Multi-omics to Observational Studies  Moderator: Jonathan Haines, Case Western Reserve …
News Release
NIH will fund grants totaling $38 million over five years to develop methods that will improve the way that polygenic risk scores can be used to predict disease in diverse communities.
… with and without a particular disease. The National Human Genome Research Institute (NHGRI), part of NIH, will fund six …
Event
On March 12-16, 2024, the National Human Genome Research Institute (NHGRI) will participate in the 2024 ACMG Annual Clinical Genetics Meeting - an annual medical and scientific conference continues to provide groundbreaking research and the latest advances in medical genetics, genomics and personalized medicine.
… R. Rodney Howell Symposium: Looking Beyond the Lamppost: Genome-first Approaches Using EHR-linked Biobanks … Platform … Category March 14, 2024, 4:15 – 5:45 p.m MTCC-718 Phenome-wide Studies of Hereditary Transthyretin Amyloidosis in the … data sharing P836  A Framework and Implementation of the Association of Professors of Human and Medical Genetics …