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.
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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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NHGRI 2025 Training Meeting
December 12, 2024 10:27 PM
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Zhao K, Hsu CC, Pershad Y, Vlasschaert C, Bick AG. Interleukin-17 receptor-A signalling: atheroprotective role in JAK2 clonal haematopoiesis. European heart journal. 2025 Sep 23;.
Halvorsen M, Wang S, Miller-Fleming T, Yu D, Crowley J, et al. Persistent Tic Disorders Are Associated With 17q12 Duplications. Research square. 2025 Aug 19;.
Smit RAJ, Wade KH, Hui Q, Arias JD, Loos RJF, et al. Polygenic prediction of body mass index and obesity through the life course and across ancestries. Nature medicine. 2025 Sep;31(9):3151-3168.
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