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Cited by 920

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Common Genetic Variation and Human Traits

Goldstein, David B.·2009·New England Journal of Medicine

Abstract

The human genome has been cracked wide open in recent years and is spilling many of its secrets. More than 100 genomewide association studies have been conducted for scores of human diseases, identifying hundreds of polymorphisms that are widely seen to influence disease risk. After many years in which the study of complex human traits was mired in false claims and methodologic inconsistencies, genomics has brought not only comprehensive representation of common variation but also welcome rigor in the interpretation of statistical evidence. Researchers now know how to properly account for most of the multiple hypothesis testing involved in mining . . .

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Metadata

Authors
Goldstein, D. B.
Venue
New England Journal of Medicine
Published
2009-04-23
Volume
360
Issue
17
Pages
1696-1698
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W1987493079
Cited by
920
References
1
FWCI
94.64
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Common Genetic Variation and Human Traits. https://app.cochat.ai/papers/10.1056/nejmp0806284
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Goldstein, D. B. (2009). Common Genetic Variation and Human Traits. New England Journal of Medicine. https://doi.org/10.1056/nejmp0806284

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.