GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits-Reference-Cited by-同舟云学术

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits

Published:2018-05-16 Issue:W1 Volume:46 Page:W114-W120
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Huang Dandan¹²,Yi Xianfu³,Zhang Shijie¹,Zheng Zhanye¹,Wang Panwen⁴,Xuan Chenghao²,Sham Pak Chung⁵⁶⁷,Wang Junwen⁴⁸^ORCID,Li Mulin Jun¹

Affiliation:

1. Department of Pharmacology, Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China

2. Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China

3. School of Biomedical Engineering, Tianjin Medical University, Tianjin, China

4. Department of Health Sciences Research & Center for Individualized Medicine, Mayo Clinic, Scottsdale, USA

5. Center for Genomic Sciences, The University of Hong Kong, Hong Kong SAR, China

6. Departments of Psychiatry, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China

7. State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong SAR, China

8. Department of Biomedical Informatics, Arizona State University, Scottsdale, USA

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/46/W1/W114/25110167/gky407.pdf

Reference57 articles.

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2. Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression;Li;Brief. Bioinformatics,2015

3. Beyond GWASs: illuminating the dark road from association to function;Edwards;Am. J. Hum. Genet.,2013

4. An expanded view of complex traits: from polygenic to omnigenic;Boyle;Cell,2017

5. Chromatin marks identify critical cell types for fine mapping complex trait variants;Trynka;Nat. Genet.,2013

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