UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test
Author:
Funder
National Institutes of Health
NIH
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank;Van Hout;bioRxiv,2019
2. The UK Biobank resource with deep phenotyping and genomic data;Bycroft;Nature,2018
3. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study;Dewey;Science,2016
4. Unravelling the human genome-phenome relationship using phenome-wide association studies;Bush;Nat. Rev. Genet.,2016
5. A fast and accurate algorithm to test for binary phenotypes and its application to PheWAS;Dey;Am. J. Hum. Genet.,2017
Cited by 62 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. Rare coding variant analysis for human diseases across biobanks and ancestries;Nature Genetics;2024-08-29
2. Bootstrap Evaluation of Association Matrices (BEAM) for Integrating Multiple Omics Profiles with Multiple Outcomes;2024-08-03
3. Analysis of variants in untranslated and promoter regions and breast cancer risk using whole genome sequencing data;2024-07-05
4. Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease;iScience;2024-07
5. Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease;Nature Genetics;2024-06-10
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