期刊
TRENDS IN GENETICS
卷 24, 期 12, 页码 613-621出版社
ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tig.2008.09.004
关键词
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资金
- European Commission [HEALTH-F4-2007-201413]
- Medical Research Council [G0601261]
- Oxford NIHR Biomedical Research Centre
- Diabetes UK
- Wellcome Trust
- MRC [G0601261] Funding Source: UKRI
- Medical Research Council [G0601261] Funding Source: researchfish
Over the past two years, there has been a spectacular change in the capacity to identify common genetic variants that contribute to predisposition to complex multifactorial phenotypes such as type 2 diabetes (T2D). The principal advance has been the ability to undertake surveys of genome-wide association in large study samples. Through these and related efforts, similar to 20 common variants are now robustly implicated in T2D susceptibility. Current developments, for example in high-throughput resequencing, should help to provide a more comprehensive view of T2D susceptibility in the near future. Although additional investigation is needed to define the causal variants within these novel T2D-susceptibility regions, to understand disease mechanisms and to effect clinical translation, these findings are already highlighting the predominant contribution of defects in pancreatic beta-cell function to the development of T21D.
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