New approaches to investigating heterogeneity in complex traits

被引:28
作者
Bomprezzi, R
Kovanen, PE
Martin, R
机构
[1] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[3] NINDS, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1136/jmg.40.8.553
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Great advances in the field of genetics have been made in the last few years. However, resolving the complexity that underlies the susceptibility to many polygenic human diseases remains a major challenge to researchers. The fast increase in availability of genetic data and the better understanding of the clinical and pathological heterogeneity of many autoimmune diseases such as multiple sclerosis, but also Parkinson's disease, Alzheimer's disease, and many more, have changed our views on their pathogenesis and diagnosis, and begins to influence clinical management. At the same time, more powerful methods that allow the analysis of large numbers of genes and proteins simultaneously open opportunities to examine their complex interactions. Using multiple sclerosis as a prototype, we review here how new methodologies such as gene expression profiling can be exploited to gain insight into complex trait diseases.
引用
收藏
页码:553 / 559
页数:7
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