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.
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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
Inviting Feedback on the Framework for the NIH Strategic Plan for Disability Health Research FY26-FY30
January 1, 2025 7:38 PM
CTSA Collaborative & Innovative Acceleration (CCIA) Award NOFO and Notice for TA webinar
January 1, 2025 7:37 PM
NHGRI 2025 Training Meeting
December 12, 2024 10:27 PM
Funding Announcement: RFA-HG-25-005
November 11, 2024 2:36 PM
FY25 Bioethics NOSI is Live
October 10, 2024 7:32 PM
NOSI: Administrative supplements to active NIH awards to support replication studies using independent contract resources (NOT-RM-24-013)
October 10, 2024 3:28 PM
Recent Publications
Naderian M, Kullo IJ. Genetic risk disclosure and behavioural change: not so fast. European journal of preventive cardiology. 2025 Feb 5;.
Hui D, Dudek S, Kiryluk K, Walunas TL, Ritchie MD, et al. Risk factors affecting polygenic score performance across diverse cohorts. eLife. 2025 Jan 24;12.
Fejzo M, Wang X, Zöllner J, Pujol-Gualdo N, Mancuso N, et al. Multi-ancestry GWAS of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity. Research square. 2024 Dec 16;.