血管性痴呆的遗传学。

IF 0.7 Q3 Medicine Minerva Psichiatrica Pub Date : 2010-03-01
Melissa E Murray, James F Meschia, Dennis W Dickson, Owen A Ross
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引用次数: 0

摘要

基因研究正在改变我们诊断、评估和治疗病人的方式。全基因组关联研究时代有望发现异质性疾病的共同风险变异,而以往的小规模关联研究总体上是失败的。然而,随着我们进入后关联时代,人们对包括血管疾病在内的一些疾病缺乏具有重大影响的风险因素感到一定程度的失望。血管性疾病本质上是偶发性的,但也有家族遗传因素。本综述将重点讨论血管性痴呆症、血管性疾病的遗传风险因素,并强调新技术如何克服全基因组关联的局限性,找出影响疾病风险的基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetics of Vascular Dementia.

Genetic studies are transforming the way we diagnose, evaluate and treat patients. The era of genome-wide association studies promised to discover common risk variants in heterogeneous disorders where previous small-scale association studies had on the whole failed. However, as we enter the post-association era a degree of disappoint is felt regarding the lack of risk factors with large effect for a number of disorders including vascular disease. Vascular disorders are sporadic by nature, though a familial component has been observed. This review will focus on vascular dementia, the genetic risk factors for vascular disorders and highlight how new technologies may overcome the limitations of genome-wide association and nominate those genes that influence disease risk.

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来源期刊
Minerva Psichiatrica
Minerva Psichiatrica PSYCHIATRY-
CiteScore
1.10
自引率
0.00%
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0
期刊介绍: The journal Minerva Psichiatrica publishes scientific papers on psychiatry, psycology and psycopharmacology. Manuscripts may be submitted in the form of editorials, original articles, review articles, case reports, therapeutical notes, special articles and letters to the Editor. Manuscripts are expected to comply with the instructions to authors which conform to the Uniform Requirements for Manuscripts Submitted to Biomedical Editors by the International Committee of Medical Journal Editors (www.icmje.org). Articles not conforming to international standards will not be considered for acceptance.
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