Detecting Rare Variant Effects Using Extreme Phenotype Sampling in Sequencing Association Studies
Author:
Affiliation:
1. Department of Biostatistics; Harvard School of Public Health; Boston Massachusetts
Publisher
Wiley
Subject
Genetics(clinical),Epidemiology
Reference37 articles.
1. Statistical analysis strategies for association studies involving rare variants;Bansal;Nat Rev Genet,2010
2. Comparison of statistical tests for disease association with rare variants;Basu;Genet Epidemiol,2011
3. Exome sequencing: the expert view;Biesecker;Genome Biol,2011
4. Linkage disequilibrium mapping of quantitative-trait Loci by selective genotyping;Chen;Am J Hum Genet,2005
5. Uncovering the roles of rare variants in common disease through whole-genome sequencing;Cirulli;Nat Rev Genet,2010
Cited by 114 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. Extreme phenotype sampling and next generation sequencing to identify genetic variants associated with tacrolimus in African American kidney transplant recipients;The Pharmacogenomics Journal;2024-08-23
2. Low-frequency inherited complement receptor variants are associated with purpura fulminans;Blood Journal;2023-12-14
3. Risk of Tertiary, Quaternary, and Quinary Proliferative Vitreoretinopathy;Ophthalmology Retina;2023-06
4. Evaluation of Designs and Estimation Methods Under Response-Dependent Two-Phase Sampling for Genetic Association Studies;Statistics in Biosciences;2023-04-02
5. Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia;Hematology;2023-03-20
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