The Path to Personalized Medicine
Open accessAbstract
M ajor investments in basic science have created an opportunity for significant progress in clinical medicine.Researchers have discovered hundreds of genes that harbor variations contributing
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Development and application of fair approaches will be critical for implementation of unbiased and interpretable models for Precision Medicine.
“The development and application of fair approaches will be critical for the implementation of unbiased and interpretable models for Precision Medicine106,116.”
From Sex and gender differences and biases in artificial intelligence for biomedicine and healthcare (2020) · cites this paper as [116]
The increasing interest in personalized medicine has come on the back of GWAS studies, under the rationale that patient risk can be prognosticated with increasing precision as more is learned about the roles of genes in disease.
“However, the increasing interest in personalized medicine has really come on the back of GWAS studies, under the rationale that patient risk can be prognosticated with increasing precision as more is learned about the roles of genes in disease [228].”
From Personality and Longevity: Knowns, Unknowns, and Implications for Public Health and Personalized Medicine (2011) · cites this paper as [228]
Interest in individual differences in health risk and treatment response has gained great traction over the last decade under the rubric of personalized medicine.
“Interest in individual differences in health risk and treatment response has gained great traction over the last decade under the rubric of personalized medicine [228].”
From Personality and Longevity: Knowns, Unknowns, and Implications for Public Health and Personalized Medicine (2011) · cites this paper as [228]
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- Authors
- Hamburg, M. A., & Collins, F. S.
- Affiliations
- National Institutes of Health (US)
- ORCID
- Collins, Francis S.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2010-07-22
- Volume
- 363
- Issue
- 4
- Pages
- 301-304
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2093065590
- Cited by
- 1,970
- References
- 0
- Citations by year
- 2026: 55 · 2025: 93 · 2024: 114 · 2023: 91 · 2022: 106 · 2021: 113 · 2020: 134 · 2019: 125 · 2018: 113 · 2017: 148 · 2016: 149 · 2015: 177 · 2014: 153 · 2013: 128 · 2012: 125
- FWCI
- 127.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- DigitalGeorgetown (Georgetown University Library) (submittedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- personalized medicine, genetic variation, genetic susceptibility, clinical translation, basic research
- MeSH terms
- Cooperative Behavior, Drug Evaluation, Preclinical, Genetic Testing, Health Policy, Humans, National Institutes of Health (U.S.), Pharmacogenetics, Registries, United States, United States Food and Drug Administration, Diagnostic Techniques and Procedures, Government Regulation, Rare Diseases, Translational Research, Biomedical, Precision Medicine
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