Leveling the Playing Field in Homozygosity Mapping Using Map Distances-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Leveling the Playing Field in Homozygosity Mapping Using Map Distances

Published:2015-07-15 Issue:5 Volume:79 Page:366-372
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Li Yi¹,Cagirici Halise Busra²,Horpaopan Sukanya³,Ott Jurg⁴⁵,Imai Atsuko⁶,Majewski Jacek⁷,Lathrop Mark⁷

Affiliation:

1. School of Statistics; Shanxi University of Finance and Economics; Taiyuan Shanxi China

2. Department of Biomedical Sciences and Engineering; Koc University; Sariyer Istanbul Turkey

3. Department of Anatomy; Faculty of Medical Science; Naresuan University; Phitsanulok 65000 Thailand

4. Chinese Academy of Sciences; Institute of Psychology; Beijing China

5. Laboratory of Statistical Genetics; Rockefeller University; NY USA

6. Department of Cardiovascular Medicine; Osaka University Graduate School of Medicine; Osaka Japan

7. McGill University and Genome Québec Innovation Centre; Montreal Canada

Funder

Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12125/fullpdf

Reference33 articles.

1. Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1;Basel-Vanagaite;Am J Hum Genet,2012

2. Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects;Bloch-Zupan;Am J Hum Genet,2011

3. Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome;Burns;Neurology,2014

4. A selective sweep on a deleterious mutation in CPT1A in Arctic populations;Clemente;Am J Hum Genet,2014

5. A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in children;Fahiminiya;Hum Mol Genet,2014

Cited by 1 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. Heterozygosity mapping for human dominant trait variants;Human Mutation;2019-04-24

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