Finding the missing heritability of complex diseases

Review

关键词: GENOME-WIDE ASSOCIATION;    DENSITY-LIPOPROTEIN CHOLESTEROL;    COPY-NUMBER VARIATION;    RARE VARIANTS;    SUSCEPTIBILITY LOCI;    BREAST-CANCER;    STRUCTURAL VARIATION;    MENTAL-RETARDATION;    CROHNS-DISEASE;    INCREASE RISK;   

DOI  :  10.1038/nature08494

来源: SCIE

【 摘 要 】

Genome-wide association studies have identified hundreds of genetic variants associated with complex human diseases and traits, and have provided valuable insights into their genetic architecture. Most variants identified so far confer relatively small increments in risk, and explain only a small proportion of familial clustering, leading many to question how the remaining, 'missing' heritability can be explained. Here we examine potential sources of missing heritability and propose research strategies, including and extending beyond current genome-wide association approaches, to illuminate the genetics of complex diseases and enhance its potential to enable effective disease prevention or treatment.

【 授权许可】

Free