Imputation of behavioral candidate gene repeat variants in 486,551 publicly-available UK Biobank individuals-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Imputation of behavioral candidate gene repeat variants in 486,551 publicly-available UK Biobank individuals

Published:2019-02-05 Issue:6 Volume:27 Page:963-969
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Border Richard,Smolen Andrew,Corley Robin P.,Stallings Michael C.,Brown Sandra A.^ORCID,Conger Rand D.,Derringer Jaime,Donnellan M. Brent,Haberstick Brett C.,Hewitt John K.,Hopfer Christian,Krauter Ken,McQueen Matthew B.,Wall Tamara L.,Keller Matthew C.^ORCID,Evans Luke M.^ORCID

Funder

Institute for Behavioral Genetics, University of Colorado Boulder

U.S. Department of Health & Human Services | NIH | National Institute of Mental Health

U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse

U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/s41431-019-0349-x.pdf

Reference42 articles.

1. McInnes LA, Freimer NB. Mapping genes for psychiatric disorders and behavioral traits. Curr Opin Genet Dev. 1995;5:376–81.

2. Ramamoorthy S, Bauman AL, Moore KR, et al. Antidepressant and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization. Proc Natl Acad Sci USA. 1993;90:2542–6.

3. Sabol SZ, Hu S, Hamer D. A functional polymorphism in the monoamine oxidase A gene promoter. Hum Genet. 1998;103:273–9.

4. Tol HHM Van, Wu CM, Guan H-C, et al. Multiple dopamine D4 receptor variants in the human population. Nature. 1992;358:149–52.

5. Vandenbergh DJ, Persico AM, Hawkins AL, et al. Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR. Genomics. 1992;14:1104–6.

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cross-ancestry genetic architecture and prediction for cholesterol traits;Human Genetics;2024-03-27

2. A method for an unbiased estimate of cross-ancestry genetic correlation using individual-level data;Nature Communications;2023-02-09

3. Cross-ancestry genetic architecture and prediction for cholesterol traits;2023-02-02

4. Genome-wide gene-gene interaction of the 5-HTTLPR promoter polymorphism emphasizes the important role of neuroplasticity in depression;Progress in Neuro-Psychopharmacology and Biological Psychiatry;2022-12

5. MAOA‐LPR polymorphism and math anxiety: A marker of genetic susceptibility to social influences in girls?;Annals of the New York Academy of Sciences;2022-06-28

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3