Adaptive clustering and adaptive weighting methods to detect disease associated rare variants
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2012143.pdf
Reference44 articles.
1. Pritchard JK : Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 2001; 69: 124–137.
2. Pritchard JK, Cox NJ : The allelic architecture of human disease genes: common disease-common variant...or not? Hum Mol Genet 2002; 11: 2417–2423.
3. Weiss KM, Terwilliger JD : How many diseases does it take to map a gene with SNPs? Nat Genet 2000; 26: 151–157.
4. Stratton MR, Rahman N : The emerging landscape of breast cancer susceptibility. Nat Genet 2008; 40: 17–22.
5. Walsh T, King MC : Ten genes for inherited breast cancer. Cancer Cell 2007; 11: 103–105.
Cited by 13 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. Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application;Mitochondrion;2024-11
2. Association analysis of mitochondrial DNA heteroplasmic variants: methods and application;2024-01-13
3. An adaptive test for meta‐analysis of rare variant association studies;Genetic Epidemiology;2019-12-12
4. A general statistic to test an optimally weighted combination of common and/or rare variants;Genetic Epidemiology;2019-09-09
5. Rare variant association testing for multicategory phenotype;Genetic Epidemiology;2019-05-13
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