Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies

Published:2017-10 Issue:4 Volume:101 Page:539-551
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Benner Christian,Havulinna Aki S.,Järvelin Marjo-Riitta,Salomaa Veikko,Ripatti Samuli,Pirinen Matti

Funder

National Institute for Health and Welfare

Academy of Finland

Finnish Foundation for Cardiovascular Research

University of Oulu

Oulu University Hospital

Ministry of Health and Social Affairs

Regional Institute of Occupational Health

Doctoral Programme in Population Health

Academy of Finland Center of Excellence for Complex Disease Genetics

EU FP7 project ENGAGE

BioSHaRE

Biocentrum Helsinki

Sigrid Jusélius Foundation

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference53 articles.

1. Partitioning heritability by functional annotation using genome-wide association summary statistics;Finucane;Nat. Genet.,2015

2. Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data;Shi;Am. J. Hum. Genet.,2016

3. An atlas of genetic correlations across human diseases and traits;Bulik-Sullivan;Nat. Genet.,2015

4. Transethnic Genetic-Correlation Estimates from Summary Statistics;Brown;Am. J. Hum. Genet.,2016

5. JEPEG: a summary statistics based tool for gene-level joint testing of functional variants;Lee;Bioinformatics,2015

Cited by 205 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. Fine-mapping the CYP2A6 regional association with nicotine metabolism among African American smokers;Molecular Psychiatry;2024-08-31

2. Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases;Nature Genetics;2024-08-26

3. Early to Middle Pleistocene transition shapes the evolution of human-specific mutations associated with height and basal metabolic rate;2024-06-28

4. On blockwise and reference panel-based estimators for genetic data prediction in high dimensions;The Annals of Statistics;2024-06-01

5. Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants;2024-05-20

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