Personalized Medicine and the Power of Electronic Health Records
- PMID: 30901549
- PMCID: PMC6921466
- DOI: 10.1016/j.cell.2019.02.039
Personalized Medicine and the Power of Electronic Health Records
Abstract
Personalized medicine has largely been enabled by the integration of genomic and other data with electronic health records (EHRs) in the United States and elsewhere. Increased EHR adoption across various clinical settings and the establishment of EHR-linked population-based biobanks provide unprecedented opportunities for the types of translational and implementation research that drive personalized medicine. We review advances in the digitization of health information and the proliferation of genomic research in health systems and provide insights into emerging paths for the widespread implementation of personalized medicine.
Copyright © 2019 Elsevier Inc. All rights reserved.
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References
-
- Abul-Husn NS, Manickam K, Jones LK, Wright EA, Hartzel DN, Gonzaga-Jauregui C, O'Dushlaine C, Leader JB, Lester Kirchner H, Lindbuchler DM, et al. (2016). Genetic identification of familial hypercholesterolemia within a single U.S. health care system. Science 354. - PubMed
-
- Adler-Milstein J, and Jha AK (2017). HITECH Act Drove Large Gains In Hospital Electronic Health Record Adoption. Health Aff (Millwood) 36, 1416–1422. - PubMed
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