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An agenda for personalized medicine

Ng, Pauline C., Murray, Sarah S., Levy, Samuel, Venter, J. Craig·2009·Nature

DOI 10.1038/461724a

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Authors: Ng, P. C., Murray, S. S., Levy, S., & Venter, J. C.
Affiliations: J. Craig Venter Institute (US)
ORCID: Ng, Pauline C.
Murray, Sarah S.
Venter, J. Craig
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2009-10
Volume: 461
Issue: 7265
Pages: 724-726
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/461724a
OpenAlex: W2006204029
Cited by: 330
References: 20
Citations by year: 2026: 1 · 2025: 1 · 2024: 3 · 2023: 6 · 2022: 6 · 2021: 5 · 2020: 12 · 2019: 13 · 2018: 23 · 2017: 7 · 2016: 11 · 2015: 23 · 2014: 29 · 2013: 32 · 2012: 48
FWCI: 34.80
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
RePEc: Research Papers in Economics (submittedVersion)
DigitalGeorgetown (Georgetown University Library) (submittedVersion)
Topics: Health Sciences › Nursing › Issues, ethics and legal aspects › Biomedical Ethics and Regulation
Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
Keywords: personalized medicine, direct-to-consumer genetic testing, prediction accuracy, consumer genomics
MeSH terms: Ethnicity, False Negative Reactions, Female, Gene Frequency, Genetic Counseling, Genetic Markers, Genetic Testing, Genetics, Medical, Genotype, Humans, Male, Pharmacogenetics, Prospective Studies, Reproducibility of Results, Health Behavior, Genome, Human, Odds Ratio, Practice Guidelines as Topic, Sequence Analysis, DNA, Genetic Predisposition to Disease, Genome-Wide Association Study

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