eMERGE is a national network organized and funded by the National Human Genome Research Institute (NHGRI) that combines DNA biorepositories with electronic medical record (EMR) systems for large scale, high-throughput genetic research in support of implementing genomic medicine.
Many factors contribute to risk of a disease. Some of these factors are internal, like genetics, and others are external, like where someone lives. Over the last several years researchers have discovered that in addition to one gene being associated with a given disease (monogenic factors), many genes across your genome can contribute to the development of a disease (polygenic factors). To learn more about elements that contribute to risk a disease, click here.
Latest News
RFI: Updated Genomic Data Sharing Policy
January 1, 2026 4:31 PM
NIH Notice: Updated Biosketch and OS Format
January 1, 2026 4:30 PM
NIH Loan Repayment Program (LRP) Update
August 8, 2025 3:24 PM
ELSI Revised NOFOs
April 4, 2025 2:34 PM
DEADLINE EXTENDED, Now April 14th: NCI/AcademyHealth Visiting Scholars Program
March 3, 2025 9:41 PM
Inviting Feedback on the Framework for the NIH Strategic Plan for Disability Health Research FY26-FY30
January 1, 2025 7:38 PM
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Recent Publications
Tragante V, Sulem P, Thorleifsson G, Frigge ML, Holm H, et al. Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels. Hypertension (Dallas, Tex. : 1979). 2026 Jul 9;.
Abe TA, Lancaster MC, Roden DM. Association of Common Ancestry-Enriched Variants With Cardiomyopathy and Arrhythmias. Circulation. 2026 Jun 16;153(24):1915-1927.
Lewis ACF, Clayton EW, Bangash H, Bland HT, Sabatello M, et al. Navigating data sharing in research. American journal of human genetics. 2026 Jun 4;113(6):1159-1167.
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