Power of deep, all-exon resequencing for discovery of human trait genes
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference45 articles.
1. Closing the Net on Common Disease Genes
2. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
3. Genome–wide association studies provide new insights into type 2 diabetes aetiology
4. Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
5. A Spectrum of PCSK9 Alleles Contributes to Plasma Levels of Low-Density Lipoprotein Cholesterol
Cited by 143 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. Identification of Rare Damaging Missense and Loss of Function Variants in GWAS Loci Using Genome Sequencing Data from Two Cohorts of Familial Late-Onset Alzheimer’s Disease;2023-12-18
2. Rare variant association on unrelated individuals in case–control studies using aggregation tests: existing methods and current limitations;Briefings in Bioinformatics;2023-09-22
3. Molecular Diagnosis of Genetic Diseases of the Kidney: Primer for Pediatric Nephrologists;Pediatric Kidney Disease;2023
4. Molecular characterization of vascular intestinal obstruction using whole-exome sequencing;Annals of Translational Medicine;2022-04
5. A robust association test with multiple genetic variants and covariates;Statistical Applications in Genetics and Molecular Biology;2022-01-01
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