Cited by 330Biomedical Ethics and RegulationGenomics and Rare DiseasesPharmacogenetics and Drug Metabolism

An agenda for personalized medicine

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

Integrity signals

Registry

Crossref · 10.1038/461724a

Cites

20 of 20 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cites

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Cited by

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Authors
Ng, P. C., Murray, S. S., Levy, S., & Venter, J. C.
Affiliations
J. Craig Venter Institute (US)
Venue
Nature
Published
2009-10
Volume
461
Issue
7265
Pages
724-726
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
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
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DigitalGeorgetown (Georgetown University Library) (submittedVersion)
Topics
  • Health Sciences › Medicine › Physiology › 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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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