• 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

相似文献

1
Most reported genetic associations with general intelligence are probably false positives.大多数与一般智力相关的遗传关联可能都是假阳性。
Psychol Sci. 2012;23(11):1314-23. doi: 10.1177/0956797611435528. Epub 2012 Sep 24.
2
Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.利用混合DNA和50万个单核苷酸多态性微阵列对一般认知能力进行全基因组数量性状位点关联扫描。
Genes Brain Behav. 2008 Jun;7(4):435-46. doi: 10.1111/j.1601-183X.2007.00368.x. Epub 2008 Jan 22.
3
Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936.认知能力候选基因的复制研究:1936年洛锡安出生队列研究
Genes Brain Behav. 2009 Mar;8(2):238-47. doi: 10.1111/j.1601-183X.2008.00470.x. Epub 2008 Dec 10.
4
Toward Robust Functional Neuroimaging Genetics of Cognition.走向认知功能神经影像学遗传学的稳健研究。
J Neurosci. 2019 Oct 30;39(44):8778-8787. doi: 10.1523/JNEUROSCI.0888-19.2019. Epub 2019 Sep 30.
5
Genetical background of intelligence.智力的遗传背景。
Postepy Hig Med Dosw (Online). 2016 Jun 13;70(0):590-8. doi: 10.5604/17322693.1204943.
6
Association between the CHRM2 gene and intelligence in a sample of 304 Dutch families.在304个荷兰家庭样本中CHRM2基因与智力之间的关联。
Genes Brain Behav. 2006 Nov;5(8):577-84. doi: 10.1111/j.1601-183X.2006.00211.x.
7
Overlap between genetic variants associated with schizophrenia spectrum disorders and intelligence quotient: a systematic review.与精神分裂症谱系障碍和智商相关的遗传变异重叠:系统综述。
J Psychiatry Neurosci. 2022 Nov 22;47(6):E393-E408. doi: 10.1503/jpn.220026. Print 2022 Nov-Dec.
8
A three-stage genome-wide association study of general cognitive ability: hunting the small effects.一项关于一般认知能力的三阶段全基因组关联研究:寻找小效应。
Behav Genet. 2010 Nov;40(6):759-67. doi: 10.1007/s10519-010-9350-4. Epub 2010 Mar 21.
9
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics.在一个大型欧洲血统样本中,14个候选基因与精神分裂症无显著关联:对精神科遗传学的启示。
Am J Psychiatry. 2008 Apr;165(4):497-506. doi: 10.1176/appi.ajp.2007.07101573. Epub 2008 Jan 15.
10
Functional gene group analysis indicates no role for heterotrimeric G proteins in cognitive ability.功能基因组分析表明异源三聚体G蛋白在认知能力方面没有作用。
PLoS One. 2014 Mar 13;9(3):e91690. doi: 10.1371/journal.pone.0091690. eCollection 2014.

引用本文的文献

1
Association of Polymorphism and Cognitive Function: An Observational Study in the Chinese Adults.基因多态性与认知功能的关联:一项针对中国成年人的观察性研究。
Alpha Psychiatry. 2025 Feb 28;26(1):38719. doi: 10.31083/AP38719. eCollection 2025 Feb.
2
The Genetics of Intelligence.智力的遗传学
Dtsch Arztebl Int. 2025 Jan 24;122(2):38-42. doi: 10.3238/arztebl.m2024.0236.
3
mi-Mic: a novel multi-layer statistical test for microbiota-disease associations.mi-Mic:一种用于微生物组-疾病关联的新型多层统计检验方法。
Genome Biol. 2024 May 1;25(1):113. doi: 10.1186/s13059-024-03256-0.
4
Genome-wide association study in 404,302 individuals identifies 7 significant loci for reaction time variability.在 404,302 个人中进行全基因组关联研究,确定了 7 个与反应时变异性相关的显著位点。
Mol Psychiatry. 2023 Sep;28(9):4011-4019. doi: 10.1038/s41380-023-02292-9. Epub 2023 Oct 20.
5
Multivariate prediction of cognitive performance from the sleep electroencephalogram.从睡眠脑电图多变量预测认知表现。
Neuroimage. 2023 Oct 1;279:120319. doi: 10.1016/j.neuroimage.2023.120319. Epub 2023 Aug 12.
6
The next 10 years of behavioural genomic research.行为基因组学研究的未来十年。
JCPP Adv. 2022 Nov 4;2(4):e12112. doi: 10.1002/jcv2.12112. eCollection 2022 Dec.
7
A multi-faceted role of dual-state dopamine signaling in working memory, attentional control, and intelligence.双态多巴胺信号在工作记忆、注意力控制和智力方面的多方面作用。
Front Behav Neurosci. 2023 Feb 16;17:1060786. doi: 10.3389/fnbeh.2023.1060786. eCollection 2023.
8
Celebrating a Century of Research in Behavioral Genetics.庆祝行为遗传学研究的一个世纪。
Behav Genet. 2023 Mar;53(2):75-84. doi: 10.1007/s10519-023-10132-3. Epub 2023 Jan 20.
9
The relationship between temperament, polygenic score for intelligence and cognition: A population-based study of middle-aged adults.气质、智力多基因评分与认知的关系:一项基于人群的中年成年人研究。
Genes Brain Behav. 2022 Apr;21(4):e12798. doi: 10.1111/gbb.12798. Epub 2022 Feb 16.
10
The Genome-Wide Study of Human Social Behavior and Its Application in Sociology.人类社会行为的全基因组研究及其在社会学中的应用
Front Sociol. 2019 Jun 26;4:53. doi: 10.3389/fsoc.2019.00053. eCollection 2019.

本文引用的文献

1
The Promises and Pitfalls of Genoeconomics*.基因经济学的前景与陷阱*
Annu Rev Econom. 2012 Jul 1;4:627-662. doi: 10.1146/annurev-economics-080511-110939. Epub 2012 Jun 18.
2
Molecular Genetics and Economics.分子遗传学与经济学
J Econ Perspect. 2011 Fall;25(4):57-82. doi: 10.1257/jep.25.4.57.
3
Genome-wide association studies establish that human intelligence is highly heritable and polygenic.全基因组关联研究表明,人类智力具有高度遗传性和多基因性。
Mol Psychiatry. 2011 Oct;16(10):996-1005. doi: 10.1038/mp.2011.85. Epub 2011 Aug 9.
4
The false-positive to false-negative ratio in epidemiologic studies.流行病学研究中的假阳性与假阴性比值。
Epidemiology. 2011 Jul;22(4):450-6. doi: 10.1097/EDE.0b013e31821b506e.
5
From GWAS to biology: lessons from FTO.从 GWAS 到生物学:FTO 的启示。
Ann N Y Acad Sci. 2011 Mar;1220:162-71. doi: 10.1111/j.1749-6632.2010.05903.x.
6
Rare copy number deletions predict individual variation in intelligence.罕见的拷贝数缺失可预测个体智力的差异。
PLoS One. 2011 Jan 26;6(1):e16339. doi: 10.1371/journal.pone.0016339.
7
A commentary on 'common SNPs explain a large proportion of the heritability for human height' by Yang et al. (2010).对杨等人(2010年)所著《常见单核苷酸多态性解释了人类身高遗传力的很大一部分》的一篇评论。
Twin Res Hum Genet. 2010 Dec;13(6):517-24. doi: 10.1375/twin.13.6.517.
8
Hundreds of variants clustered in genomic loci and biological pathways affect human height.数以百计的变异体聚集在基因组位置和生物途径中,影响人类身高。
Nature. 2010 Oct 14;467(7317):832-8. doi: 10.1038/nature09410. Epub 2010 Sep 29.
9
Common SNPs explain a large proportion of the heritability for human height.常见的单核苷酸多态性解释了人类身高遗传的很大一部分。
Nat Genet. 2010 Jul;42(7):565-9. doi: 10.1038/ng.608. Epub 2010 Jun 20.
10
Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies.在 100 项全基因组关联研究中复制常见疾病和表型的过去候选基因座。
Eur J Hum Genet. 2010 Jul;18(7):832-7. doi: 10.1038/ejhg.2010.26. Epub 2010 Mar 17.

大多数与一般智力相关的遗传关联可能都是假阳性。

Most reported genetic associations with general intelligence are probably false positives.

机构信息

Department of Psychology, Union College, Schenectady, NY 12308, USA.

出版信息

Psychol Sci. 2012;23(11):1314-23. doi: 10.1177/0956797611435528. Epub 2012 Sep 24.

DOI:10.1177/0956797611435528
PMID:23012269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3498585/
Abstract

General intelligence (g) and virtually all other behavioral traits are heritable. Associations between g and specific single-nucleotide polymorphisms (SNPs) in several candidate genes involved in brain function have been reported. We sought to replicate published associations between g and 12 specific genetic variants (in the genes DTNBP1, CTSD, DRD2, ANKK1, CHRM2, SSADH, COMT, BDNF, CHRNA4, DISC1, APOE, and SNAP25) using data sets from three independent, well-characterized longitudinal studies with samples of 5,571, 1,759, and 2,441 individuals. Of 32 independent tests across all three data sets, only 1 was nominally significant. By contrast, power analyses showed that we should have expected 10 to 15 significant associations, given reasonable assumptions for genotype effect sizes. For positive controls, we confirmed accepted genetic associations for Alzheimer's disease and body mass index, and we used SNP-based calculations of genetic relatedness to replicate previous estimates that about half of the variance in g is accounted for by common genetic variation among individuals. We conclude that the molecular genetics of psychology and social science requires approaches that go beyond the examination of candidate genes.

摘要

普遍智力(g)和几乎所有其他行为特征都是可遗传的。已经报道了 g 与参与大脑功能的几个候选基因中的特定单核苷酸多态性(SNP)之间的关联。我们试图使用来自三个独立的、特征良好的纵向研究的数据来复制 g 与 12 种特定遗传变异体(在 DTNBP1、CTSD、DRD2、ANKK1、CHRM2、SSADH、COMT、BDNF、CHRNA4、DISC1、APOE 和 SNAP25 基因中)之间的已发表关联,这些研究样本分别为 5571、1759 和 2441 人。在所有三个数据集的 32 个独立测试中,只有 1 个具有名义上的显著性。相比之下,根据基因型效应大小的合理假设,功效分析表明,我们本应预期会有 10 到 15 个显著关联。对于阳性对照,我们确认了阿尔茨海默病和体重指数的公认遗传关联,我们还使用基于 SNP 的遗传相关性计算来复制先前的估计,即 g 的大约一半变异是由个体之间的常见遗传变异引起的。我们得出的结论是,心理学和社会科学的分子遗传学需要超越候选基因检验的方法。