An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nn.4632.pdf
Reference78 articles.
1. Welter, D. et al. The NHGRI GWAS Catalog, a curated resource of SNP-trait associations. Nucleic Acids Res. 42, D1001–D1006 (2014).
2. Alexander, R.P., Fang, G., Rozowsky, J., Snyder, M. & Gerstein, M.B. Annotating non-coding regions of the genome. Nat. Rev. Genet. 11, 559–571 (2010).
3. Goldstein, D.B. Common genetic variation and human traits. N. Engl. J. Med. 360, 1696–1698 (2009).
4. Pickrell, J.K. et al. Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature 464, 768–772 (2010).
5. Lappalainen, T. et al. Transcriptome and genome sequencing uncovers functional variation in humans. Nature 501, 506–511 (2013).
Cited by 379 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. Extensive co-regulation of neighboring genes complicates the use of eQTLs in target gene prioritization;Human Genetics and Genomics Advances;2024-10
2. CD33 and SHP-1/PTPN6 Interaction in Alzheimer’s Disease;Genes;2024-09-13
3. Accurate identification of genes associated with brain disorders by integrating heterogeneous genomic data into a Bayesian framework;eBioMedicine;2024-09
4. Identification of a specific APOE transcript and functional elements associated with Alzheimer’s disease;Molecular Neurodegeneration;2024-08-29
5. Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state;Nature Communications;2024-08-08
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