A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations-Reference-Cited by-同舟云学术

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

Published:2013-05-26 Issue:7 Volume:45 Page:818-821
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Hu Zhibin,Shi Yongyong,Mo Xuming,Xu Jing,Zhao Bijun,Lin Yuan,Yang Shiwei,Xu Zhengfeng,Dai Juncheng,Pan Shandong,Da Min,Wang Xiaowei,Qian Bo,Wen Yang,Wen Juan,Xing Jinliang,Guo Xuejiang,Xia Yankai,Ma Hongxia,Jin Guangfu,Yu Shiqiang,Liu Jiayin,Zhou Zuomin,Wang Xinru,Chen Yijiang,Sha Jiahao,Shen Hongbing

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2636.pdf

Reference46 articles.

1. Hoffman, J.I. & Kaplan, S. The incidence of congenital heart disease. J. Am. Coll. Cardiol. 39, 1890–1900 (2002).

2. Bruneau, B.G. The developmental genetics of congenital heart disease. Nature 451, 943–948 (2008).

3. Krebs, L.T. et al. Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 14, 1343–1352 (2000).

4. Wang, J., Greene, S.B. & Martin, J.F. BMP signaling in congenital heart disease: new developments and future directions. Birth Defects Res. A Clin. Mol. Teratol. 91, 441–448 (2011).

5. Anderson, L.M. & Gibbons, G.H. Notch: a mastermind of vascular morphogenesis. J. Clin. Invest. 117, 299–302 (2007).

Cited by 77 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. Genome-wide association studies of Down syndrome associated congenital heart defects;2024-09-06

2. From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies;Current Problems in Cardiology;2024-09

3. Human Genetics of Ventricular Septal Defect;Advances in Experimental Medicine and Biology;2024

4. A gene‐based association test of interactions for maternal–fetal genotypes identifies genes associated with nonsyndromic congenital heart defects;Genetic Epidemiology;2023-06-21

5. Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls;Egyptian Journal of Medical Human Genetics;2023-04-03