Human genetic variation and its contribution to complex traits

被引:707
|
作者
Frazer, Kelly A. [1 ]
Murray, Sarah S.
Schork, Nicholas J.
Topol, Eric J.
机构
[1] Scripps Translat Sci Inst, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ASSOCIATION; COPY-NUMBER VARIATION; PROSTATE-CANCER RISK; STRUCTURAL VARIATION; SUSCEPTIBILITY LOCI; COMMON VARIANT; RARE VARIANTS; LINKAGE DISEQUILIBRIUM; POPULATION-GENETICS; SKIN PIGMENTATION;
D O I
10.1038/nrg2554
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The last few years have seen extensive efforts to catalogue human genetic variation and correlate it with phenotypic differences. Most common SNPs have now been assessed in genome-wide studies for statistical associations with many complex traits, including many important common diseases. Although these studies have provided new biological insights, only a limited amount of the heritable component of any complex trait has been identified and it remains a challenge to elucidate the functional link between associated variants and phenotypic traits. Technological advances, such as the ability to detect rare and structural variants, and a clear understanding of the challenges in linking different types of variation with phenotype, will be essential for future progress.
引用
收藏
页码:241 / 251
页数:11
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