Bringing genome-wide association findings into clinical use

被引:248
|
作者
Manolio, Teri A. [1 ]
机构
[1] NHGRI, Div Genom Med, Rockville, MD 20892 USA
基金
美国国家卫生研究院;
关键词
GENETIC RISK; COMMON VARIANTS; DISEASE; PREDICTION; LOCI; RARE; POLYMORPHISMS; MEDICINE; YOUNG; CLASSIFICATION;
D O I
10.1038/nrg3523
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide association studies (GWASs) have been heralded as a major advance in biomedical discovery, having identified similar to 2,000 robust associations with complex diseases since 2005. Despite this success, they have met considerable scepticism regarding their clinical applicability; this scepticism arises from such aspects as the modest effect sizes of associated variants and their unclear functional consequences. There are, however, promising examples of GWAS findings that will or that may soon be translated into clinical care. These examples include variants identified through GWASs that provide strongly predictive or prognostic information or that have important pharmacological implications; these examples may illustrate promising approaches to wider clinical application.
引用
收藏
页码:549 / 558
页数:10
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