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Estimating the genetic variance of major depressive disorder due to all single nucleotide polymorphisms

机译:估计由于所有单核苷酸多态性导致的主要抑郁症的遗传变异

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摘要

Genome-wide association studies of psychiatric disorders have been criticized for their lack of explaining a considerable proportion of the heritability established in twin and family studies. Genome-wide association studies of major depressive disorder in particular have so far been unsuccessful in detecting genome-wide significant single nucleotide polymorphisms (SNPs). Using two recently proposed methods designed to estimate the heritability of a phenotype that is attributable to genome-wide SNPs, we show that SNPs on current platforms contain substantial information concerning the additive genetic variance of major depressive disorder. To assess the consistency of these two methods, we analyzed four other complex phenotypes from different domains. The pattern of results is consistent with estimates of heritability obtained in twin studies carried out in the same population.
机译:精神疾病的全基因组关联研究因缺乏解释双胞胎和家庭研究建立的遗传力比例而受到批评。迄今为止,特别是主要抑郁症的全基因组关联研究在检测全基因组范围内的重要单核苷酸多态性(SNP)方面尚不成功。使用设计用于估计可归因于全基因组SNP的表型的遗传力的两个最近提出的方法,我们表明当前平台上的SNP包含有关主要抑郁症加性遗传方差的大量信息。为了评估这两种方法的一致性,我们分析了来自不同域的四种其他复杂表型。结果的模式与在同一人群中进行的双胞胎研究中获得的遗传力估计值一致。

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