Genetic association studies of complex neurological diseases

被引:20
作者
Abou-Sleiman, P. M.
Hanna, M. G.
Wood, N. W.
机构
[1] Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
[2] Ctr Neuromuscular Dis, Inst Neurol, London, England
基金
英国医学研究理事会;
关键词
D O I
10.1136/jnnp.2005.082024
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Genetic association studies offer a powerful approach to identify the multiple variants of small effect that modulate susceptibility to common, complex disease. They, however, have a poor reputation, mainly because of the consistent lack of replication of all but a few. Thousands of genetic studies have been carried out on multifactorial diseases in the past 30 years, yielding only about 50 variants that can be considered to be true positives. Although the positive studies show proof of principle, the multitude of negative studies indicate fundamental problems in the design and execution of association studies. Here, we discuss some of the more pertinent study design and data analysis issues which can affect the outcome of genetic association studies.
引用
收藏
页码:1302 / 1304
页数:3
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