• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通才基因与学习障碍。

Generalist genes and learning disabilities.

作者信息

Plomin Robert, Kovas Yulia

机构信息

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom.

出版信息

Psychol Bull. 2005 Jul;131(4):592-617. doi: 10.1037/0033-2909.131.4.592.

DOI:10.1037/0033-2909.131.4.592
PMID:16060804
Abstract

The authors reviewed recent quantitative genetic research on learning disabilities that led to the conclusion that genetic diagnoses differ from traditional diagnoses in that the effects of relevant genes are largely general rather than specific. This research suggests that most genes associated with common learning disabilities--language impairment, reading disability, and mathematics disability--are generalists in 3 ways. First, genes that affect common learning disabilities are largely the same genes responsible for normal variation in learning abilities. Second, genes that affect any aspect of a learning disability affect other aspects of the disability. Third, genes that affect one learning disability are also likely to affect other learning disabilities. These quantitative genetic findings have far-reaching implications for molecular genetics and neuroscience as well as psychology.

摘要

作者回顾了近期关于学习障碍的定量遗传学研究,该研究得出结论:基因诊断与传统诊断不同,相关基因的影响在很大程度上是普遍的而非特定的。这项研究表明,与常见学习障碍(语言障碍、阅读障碍和数学障碍)相关的大多数基因在三个方面具有普遍性。首先,影响常见学习障碍的基因在很大程度上与导致学习能力正常变异的基因相同。其次,影响学习障碍任何一个方面的基因也会影响该障碍的其他方面。第三,影响一种学习障碍的基因也可能影响其他学习障碍。这些定量遗传学研究结果对分子遗传学、神经科学以及心理学都具有深远的影响。

相似文献

1
Generalist genes and learning disabilities.通才基因与学习障碍。
Psychol Bull. 2005 Jul;131(4):592-617. doi: 10.1037/0033-2909.131.4.592.
2
Genetics and educational psychology.遗传学与教育心理学。
Br J Educ Psychol. 2003 Mar;73(Pt 1):3-14. doi: 10.1348/000709903762869888.
3
Genetic factors contributing to learning and language delays and disabilities.导致学习及语言发育迟缓与障碍的遗传因素。
Child Adolesc Psychiatr Clin N Am. 2001 Apr;10(2):259-77, viii.
4
Human behavioural genetics of cognitive abilities and disabilities.认知能力与认知障碍的人类行为遗传学。
Bioessays. 1997 Dec;19(12):1117-24. doi: 10.1002/bies.950191211.
5
Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins.基因对早期单词识别能力与障碍的影响:一项针对7岁双胞胎的研究。
J Child Psychol Psychiatry. 2005 Apr;46(4):373-84. doi: 10.1111/j.1469-7610.2004.00358.x.
6
Specificity and characteristics of learning disabilities.学习障碍的特异性与特征
J Child Psychol Psychiatry. 2005 Oct;46(10):1108-15. doi: 10.1111/j.1469-7610.2004.00394.x.
7
Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.22q11.2缺失综合征患儿的数学学习障碍:综述
Dev Disabil Res Rev. 2009;15(1):4-10. doi: 10.1002/ddrr.44.
8
Overlap and specificity of genetic and environmental influences on mathematics and reading disability in 10-year-old twins.10岁双胞胎中基因和环境因素对数学及阅读障碍影响的重叠性与特异性
J Child Psychol Psychiatry. 2007 Sep;48(9):914-22. doi: 10.1111/j.1469-7610.2007.01748..x.
9
Modes of imprinted gene action in learning disability.学习障碍中印迹基因的作用模式。
J Intellect Disabil Res. 2006 May;50(Pt 5):318-25. doi: 10.1111/j.1365-2788.2006.00843.x.
10
Exploring the concept of alexithymia in the lives of people with learning disabilities.探索学习障碍者生活中的述情障碍概念。
J Intellect Disabil. 2005 Sep;9(3):229-39. doi: 10.1177/1744629505056696.

引用本文的文献

1
A comparative study of EEG functional and effective connectivity patterns in children with learning difficulties during reading and math tasks.学习困难儿童在阅读和数学任务期间脑电图功能和有效连接模式的比较研究。
Front Neurosci. 2025 Aug 18;19:1612884. doi: 10.3389/fnins.2025.1612884. eCollection 2025.
2
Interventions for children and adolescents with specific learning disability and co-occurring disorders.针对患有特定学习障碍及并发疾病的儿童和青少年的干预措施。
Pediatr Res. 2025 Jul 18. doi: 10.1038/s41390-025-04261-0.
3
Accessible Literacy for Emerging Communicators (ALEC): A Proposed Model and Case Application with Children on the Autism Spectrum.
新兴沟通者的无障碍读写能力(ALEC):一种针对自闭症谱系儿童的模型提议及案例应用
Perspect ASHA Spec Interest Groups. 2024;1:236-248. doi: 10.1044/2024_persp-24-00107.
4
The cognitive science of language diversity: achievements and challenges.语言多样性的认知科学:成就与挑战
Cogn Process. 2025 Feb 25. doi: 10.1007/s10339-025-01262-z.
5
Beyond the sum of their parts: A multi-dimensional approach to dyscalculia-dyslexia comorbidity integrating studies of the brain, behavior, and genetics.超越其各部分之和:一种整合大脑、行为和遗传学研究的计算障碍-阅读障碍共病的多维度研究方法。
Dev Cogn Neurosci. 2025 Apr;72:101510. doi: 10.1016/j.dcn.2025.101510. Epub 2025 Jan 10.
6
Comparing Serum AMH, InhB, Testosterone Levels and Finger Length Ratio (2D/4D) of Male Children with Specific Learning Disorder and Controls.比较患有特定学习障碍的男童与对照组的血清抗缪勒管激素(AMH)、抑制素B(InhB)、睾酮水平及指长比(2D/4D)。
Noro Psikiyatr Ars. 2024 Aug 9;67(3):221-227. doi: 10.29399/npa.28345. eCollection 2024.
7
Multi-polygenic score prediction of mathematics, reading, and language abilities independent of general cognitive ability.独立于一般认知能力的数学、阅读和语言能力的多基因评分预测
Mol Psychiatry. 2025 Feb;30(2):414-422. doi: 10.1038/s41380-024-02671-w. Epub 2024 Jul 31.
8
Evocative effects on the early caregiving environment of genetic factors underlying the development of intellectual and academic ability.遗传因素对智力和学术能力发展的早期教养环境的唤起效应。
Child Dev. 2024 Nov-Dec;95(6):2082-2101. doi: 10.1111/cdev.14142. Epub 2024 Jul 30.
9
Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion.在与 READ1 缺失相关的发育性阅读障碍中,对复杂大细胞刺激时腹侧额顶网络中的神经激活的改变。
Behav Brain Funct. 2024 Jun 26;20(1):16. doi: 10.1186/s12993-024-00241-2.
10
Exploring the genetic etiology across the continuum of the general psychopathology factor: a Swedish population-based family and twin study.探究一般精神病理学因素连续体的遗传病因学:一项基于瑞典人群的家庭和双胞胎研究。
Mol Psychiatry. 2024 Oct;29(10):2921-2928. doi: 10.1038/s41380-024-02552-2. Epub 2024 Apr 10.