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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Recent Publications
Henechowicz TL, Coleman PL, Gustavson DE, Mekki YN, Gordon RL, et al. Polygenic Associations between Motor Behaviour, Neuromotor Traits, and Active Music Engagement in Four Cohorts. bioRxiv : the preprint server for biology. 2025 Mar 30;.
Zhong X, Jia G, Yin Z, Cheng K, Cox NJ. Longitudinal Analysis of Electronic Health Records Reveals Medical Conditions Associated with Subsequent Alzheimer's Disease Development. medRxiv : the preprint server for health sciences. 2025 Mar 24;.
Middha P, Thummalapalli R, Quandt Z, Balaratnam K, Ziv E, et al. Germline prediction of immune checkpoint inhibitor discontinuation for immune-related adverse events. Journal for immunotherapy of cancer. 2025 Mar 28;13(3).
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