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The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4963 Subjects

机译:ATXN1和TRIM31基因与ADHD背景下的智力有关:来自一项总计4963名受试者的大型协作研究的证据

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摘要

Intelligence is a highly heritable trait for which it has proven difficult to identify the actual genes. In the past decade, five whole-genome linkage scans have suggested genomic regions important to human intelligence; however, so far none of the responsible genes or variants in those regions have been identified. Apart from these regions, a handful of candidate genes have been identified, although most of these are in need of replication. The recent growth in publicly available data sets that contain both whole genome association data and a wealth of phenotypic data, serves as an excellent resource for fine mapping and candidate gene replication. We used the publicly available data of 947 families participating in the International Multi-Centre ADHD Genetics (IMAGE) study to conduct an in silico fine mapping study of previously associated genomic locations, and to attempt replication of previously reported candidate genes for intelligence. Although this sample was ascertained for attention deficit/hyperactivity disorder (ADHD), intelligence quotient (IQ) scores were distributed normally. We tested 667 single nucleotide polymorphisms (SNPs) within 15 previously reported candidate genes for intelligence and 29451 SNPs in five genomic loci previously identified through whole genome linkage and association analyses. Significant SNPs were tested in four independent samples (4,357 subjects), one ascertained for ADHD, and three population-based samples. Associations between intelligence and SNPs in the ATXN1 and TRIM31 genes and in three genomic locations showed replicated association, but only in the samples ascertained for ADHD, suggesting that these genetic variants become particularly relevant to IQ on the background of a psychiatric disorder. © 2010 Wiley-Liss, Inc.
机译:智力是一种高度可遗传的特征,已证明难以鉴定出实际基因。在过去的十年中,五次全基因组连锁扫描表明了对人类智力重要的基因组区域。但是,到目前为止,尚未发现这些区域中的负责任基因或变异体。除这些区域外,还鉴定了少数候选基因,尽管其中大多数需要复制。包含完整的基因组关联数据和大量的表型数据的公共可用数据集最近的增长,为精细定位和候选基因复制提供了极好的资源。我们使用了参与国际多中心ADHD遗传学(IMAGE)研究的947个家庭的公开数据,对先前相关的基因组位置进行了计算机精细作图研究,并尝试复制先前报道的候选基因以提高智力。尽管确定了该样本的注意力缺陷/多动障碍(ADHD),但智商(IQ)得分呈正态分布。我们测试了先前报告的15个智力候选基因中的667个单核苷酸多态性(SNP),以及五个先前通过全基因组连锁和关联分析确定的基因组位点中的29451个SNP。在四个独立样本(4,357名受试者)中测试了重要的SNP,其中一个被确定为ADHD,另外三个则是基于人群的样本。 ATXN1和TRIM31基因以及三个基因组位置中的智商和SNP之间的关联显示出重复的关联,但仅在确定为ADHD的样品中,这表明这些遗传变异与精神疾病背景下的IQ密切相关。 ©2010 Wiley-Liss,Inc.

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