ArticleAnnals of family medicine
Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable.
Article in Annals of family medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
18 citing papers in PubMed.
- Process for mainstreaming genetic cascade testing into primary and tertiary health systems in familial hypercholesterolaemia (FH), an autosomal dominant, fully penetrant disorder.Family medicine and community health · 2025Article
- Review
- Anticipating the primary care role in genomic medicine: expectations of genetics health professionals.Journal of community genetics · 2021Article
- Barriers and strategies to integrate medical genetics and primary care in underserved populations: a scoping review.Journal of community genetics · 2021Article
- A stepwise approach to implementing pharmacogenetic testing in the primary care setting.Pharmacogenomics · 2019Article
- Bridging the gap in genetics: a progressive model for primary to specialist care.BMC medical education · 2019Article
- Primary care providers' lived experiences of genetics in practice.Journal of community genetics · 2019Article
- Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.Frontiers in genetics · 2019Article
- Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.Human molecular genetics · 2018Review
- Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach.Journal of community genetics · 2018Article
- Translating Biobank Science into Patient-Centered Language.Biopreservation and biobanking · 2018Article
- "I don't have to know why it snows, I just have to shovel it!": Addiction Recovery, Genetic Frameworks, and Biological Citizenship.BioSocieties · 2017Article
- Identifying "ownership" through role descriptions to support implementing universal colorectal cancer tumor screening for Lynch syndrome.Genetics in medicine : official journal of the American College of Medical Genetics · 2017Article
- Primary care providers' experiences with and perceptions of personalized genomic medicine.Canadian family physician Medecin de famille canadien · 2016Article
- Sociocultural variation in attitudes toward use of genetic information and participation in genetic research by race in the United States: implications for precision medicine.Journal of the American Medical Informatics Association : JAMIA · 2016Article
- The Future of Patient Engagement in the Governance of Shared Data.EGEMS (Washington, DC) · 2016Article
- A Use Case to Support Precision Medicine for Frequently Hospitalized Older Adults with Polypharmacy.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2016Article
- Potential utility of precision medicine for older adults with polypharmacy: a case series study.Pharmacogenomics and personalized medicine · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Genomic research has generated much new knowledge into mechanisms of human disease, with the potential to catalyze novel drug discovery and development, prenatal and neonatal screening, clinical pharmacogenomics, more sensitive risk prediction, and enhanced diagnostics. Genomic medicine, however, has been limited by critical evidence gaps, especially those related to clinical utility and applicability to diverse populations. Genomic medicine may have the greatest impact on health care if it is integrated into primary care, where most health care is received and where evidence supports the value of personalized medicine grounded in continuous healing relationships. Redesigned primary care is the most relevant setting for clinically useful genomic medicine research. Taking insights gained from the activities of the Institute of Medicine (IOM) Roundtable on Translating Genomic-Based Research for Health, we apply lessons learned from the patient-centered medical home national experience to implement genomic medicine in a patient-centered, learning health care system.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.