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A Genomewide Scan for Intelligence Identifies Quantitative Trait Loci on 2q and 6p

机译:全基因组情报扫描可识别2q和6p上的数量性状位点

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摘要

Between 40% and 80% of the variation in human intelligence (IQ) is attributable to genetic factors. Except for many rare mutations resulting in severe cognitive dysfunction, attempts to identify these factors have not been successful. We report a genomewide linkage scan involving 634 sibling pairs designed to identify chromosomal regions that explain variation in IQ. Model-free multipoint linkage analysis revealed evidence of a significant quantitative-trait locus for performance IQ at 2q24.1-31.1 (LOD score 4.42), which overlaps the 2q21-33 region that has repeatedly shown linkage to autism. A second region revealed suggestive linkage for both full-scale and verbal IQs on 6p25.3-22.3 (LOD score 3.20 for full-scale IQ and 2.33 for verbal IQ), overlapping marginally with the 6p22.3-21.31 region implicated in reading disability and dyslexia.
机译:人类智力(IQ)变异的40%至80%可归因于遗传因素。除了许多导致严重的认知功能障碍的罕见突变外,识别这些因素的尝试均未成功。我们报告了涉及634个同胞对的全基因组连锁扫描,旨在识别可解释IQ差异的染色体区域。无模型的多点连锁分析揭示了在2q24.1-31.1(LOD得分4.42)处表现IQ的重要数量特征位点的证据,该位点与反复显示自闭症连锁的2q21-33地区重叠。第二个区域显示在6p25.3-22.3上智商和智商都有暗示的联系(智商的LOD得分为3.20,智商的智商为2.33),与涉及阅读障碍的6p22.3-21.31区域略有重叠和阅读障碍。

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