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Cited by 904

The DOI matches its Crossref record; 96 of the 96 references it cites were found in a registry or an index.

Pharmacogenomics in the clinic

Open access
Relling, Mary V., Evans, William E.·2015·Nature

Abstract

After decades of discovery, inherited variations have been identified in approximately 20 genes that affect about 80 medications and are actionable in the clinic. And some somatically acquired genetic variants direct the choice of 'targeted' anticancer drugs for individual patients. Current efforts that focus on the processes required to appropriately act on pharmacogenomic variability in the clinic are moving away from discovery and towards implementation of an evidenced-based strategy for improving the use of medications, thereby providing a cornerstone for precision medicine.

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Crossref · 10.1038/nature15817

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Metadata

Authors
Relling, M. V., & Evans, W. E.
Venue
Nature
Published
2015-10
Volume
526
Issue
7573
Pages
343-350
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W1896195310
Cited by
904
References
96
FWCI
77.65
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Pharmacogenomics in the clinic. https://app.cochat.ai/papers/10.1038/nature15817
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Relling, M. V., & Evans, W. E. (2015). Pharmacogenomics in the clinic. Nature. https://doi.org/10.1038/nature15817

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.