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注意缺陷多动障碍的遗传学

Genetics of attention deficit hyperactivity disorder.

作者信息

Mick Eric, Faraone Stephen V

机构信息

Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Warren 705, 55 Fruit Street, Boston, MA 02114-2622, USA.

出版信息

Child Adolesc Psychiatr Clin N Am. 2008 Apr;17(2):261-84, vii-viii. doi: 10.1016/j.chc.2007.11.011.

Abstract

Results of behavioral genetic and molecular genetic studies have converged to suggest that both genetic and nongenetic factors contribute to the development of attention deficit hyperactivity disorder (ADHD). Family, twin, and adoption studies provide compelling evidence that genes play a strong role in mediating susceptibility to ADHD. In contrast to a handful of genome-wide scans conducted thus far, many candidate gene studies of ADHD have produced substantial evidence implicating several genes in the etiology of the disorder. Yet, even these associations are small and consistent with the idea that the genetic vulnerability to ADHD is mediated by many genes of small effects. These small effects emphasize the need for future candidate gene studies to implement strategies that will provide enough statistical power to detect such small effects.

摘要

行为遗传学和分子遗传学研究结果趋于一致,表明遗传因素和非遗传因素均对注意力缺陷多动障碍(ADHD)的发展有影响。家族、双胞胎和收养研究提供了有力证据,证明基因在介导ADHD易感性方面发挥着重要作用。与迄今为止进行的少数全基因组扫描不同,许多ADHD候选基因研究已产生大量证据,表明几种基因与该疾病的病因有关。然而,即使这些关联也很小,这与ADHD的遗传易感性由许多小效应基因介导的观点一致。这些小效应强调了未来候选基因研究需要实施能够提供足够统计效力以检测此类小效应的策略。

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