Abstract
Pharmacogenetics is the study of the role of inheritance in variation in drug response phenotypes. Those phenotypes can range from life-threatening adverse drugs reactions at one end of the spectrum to equally serious lack of therapeutic efficacy at the other. Over the past half century, pharmacogenetics has-like all of medical genetics-evolved from a discipline with a focus on monogenetic traits to become pharmacogenomics, with a genome-wide perspective. This article will briefly review recent examples of the application of genome-wide techniques to clinical pharmacogenomic studies and to pharmacogenomic model systems that vary from cell line-based model systems to yeast gene deletion libraries. Functional validation of candidate genes and the use of genome-wide techniques to gain mechanistic insights will be emphasized for the establishment of biological plausibility and as essential follow-up steps after the identification of candidate genes. © The Author 2008. Published by Oxford University Press. All rights reserved.
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CITATION STYLE
Wang, L., & Weinshilboum, R. M. (2008). Pharmacogenomics: Candidate gene identification, functional validation and mechanisms. Human Molecular Genetics, 17(R2). https://doi.org/10.1093/hmg/ddn270
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