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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
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
On February 9-10, 2021, NHGRI will host it's 13th Genomic Medicine Meeting - Genomic Medicine XIII: Developing a Clinical Genomic Informatics Research Agenda.
… Bias in Algorithm Development: Can Implementation of Genetic Information in Clinical Informatics Decision Making … search of lost variants: How EHR integration can improve genetic medicine Presenter: Lisa A. Bastarache, M.S.  … to improve the detection, treatment and reporting of genetic disorders in clinical settings. The objectives of …
Event
NHGRI sponsored its 12th Genomic Medicine meeting, Genomic Medicine XII: Genomics and Risk Prediction on May 6-7, 2019.
… other information sources that should be integrated with genetic variant information in predicting risk Identify …
Archive
… Genetic Association Information Network (GAIN) … Archive …
Archive
… Epidemiology for Researchers Performing Genetic/Genomic Studies … Archive …
News Release
NIH will support research that incorporates DNA sequence information into electronic medical records.
… immune system. They will use DNA sequencing to examine the genetic make-up of 2,500 individuals and combine this … for disease-causing variants in the LDLR gene, the leading genetic cause of premature coronary artery disease, and … studies include evaluating the cost-effectiveness of genetic testing, characterizing the genetics of pain and …
Event
The Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG) will hold its 11th annual meeting online on February 16, 2022.
… Physicians’ knowledge, beliefs, and use of race and human genetic variation: new measures and insights . BMC Health …
Archive
… Characterizing and Displaying Genetic Variants for Clinical Action Workshop … Archive …
Event
On August 31 - September 1, 2022, the National Human Genome Research Institute (NHGRI) will sponsor its 14th Genomic Medicine meeting, Genomic Medicine XIV: Genomic Learning Healthcare Systems. Â
… Practice (15 min) Rizwan Hamid  Scalable Solutions for Genetic Counseling (15 min) Cynthia A. James  Genomic …
News Release
NIH programs are establishing which genes and genomic variants play a role in human disease, enabling use in medicine and research.
…  A healthcare provider consults with a patient about her genetic test results. Image Credit: Darryl Leja, NHGRI … epilepsy and RASopathies; the latter is a group of rare genetic conditions that include Noonan syndrome, …