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In this issue: entering the era of high-density genome-wide association studies.

机译:在本期中:进入高密度全基因组关联研究的时代。

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In a previous issue of The Journal of Clinical Psychiatry, my colleagues and I reviewed progress in the genetic, transcriptomic, and proteomic study of Alzheimer's disease (AD).1 In this issue, we report initial findings from the first genome-wide survey of more than 500,000 single nucleotide polymorphisms (SNPs) in late-onset AD cases and controls. This study provides empirical support for the unparalleled contribution of the apolipoprotein E (APOE) gene to the risk of late-onset AD, it demonstrates the promise of increasingly high-density genome-wide association studies in the discovery of previously elusive susceptibility genes for AD and other common phenotypes, and it underscores some of the methodological challenges that remain to be addressed in this important endeavor.
机译:在上一期的《临床精神病学杂志》中,我和我的同事回顾了阿尔茨海默氏病(AD)的基因,转录组和蛋白质组学研究的进展。1在本期中,我们报告了首次对全基因组进行的全基因组调查的初步发现在迟发性AD病例和对照中有超过500,000个单核苷酸多态性(SNP)。这项研究为载脂蛋白E(APOE)基因对迟发性AD风险的无与伦比的贡献提供了经验支持,它证明了在发现以前难以捉摸的AD易感性基因的过程中,越来越高的全基因组关联研究的前景以及其他常见的表型,它突显了这项重要工作中仍需解决的一些方法学挑战。

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