GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve
Li, Ruo-Gu, Xu, Ying-Jia, Wang, Juan, Liu, Xing-Yuan, Yuan, Fang, Huang, Ri-Tai, Xue, Song, Li, Li, Liu, Hua, Li, Yan-Jie, Qu, Xin-Kai, Shi, Hong-Yu, Zhang, Min, Qiu, Xing-Biao, Yang, Yi-Qing
Published in The American journal of cardiology (15.02.2018)
Published in The American journal of cardiology (15.02.2018)
Get full text
Journal Article
Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease
Li, Ruo-Gu, Xu, Ying-Jia, Ye, Willy G., Li, Yan-Jie, Chen, Honghong, Qiu, Xing-Biao, Yang, Yi-Qing, Bai, Donglin
Published in Heart rhythm (01.05.2021)
Published in Heart rhythm (01.05.2021)
Get full text
Journal Article
GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot
Yang, Yi-Qing, Gharibeh, Lara, Li, Ruo-Gu, Xin, Yuan-Feng, Wang, Juan, Liu, Zhong-Min, Qiu, Xing-Biao, Xu, Ying-Jia, Xu, Lei, Qu, Xin-Kai, Liu, Xu, Fang, Wei-Yi, Huang, Ri-Tai, Xue, Song, Nemer, Georges
Published in Human mutation (01.12.2013)
Published in Human mutation (01.12.2013)
Get full text
Journal Article
ISL1 loss-of-function mutation contributes to congenital heart defects
Ma, Lan, Wang, Juan, Li, Li, Qiao, Qi, Di, Ruo-Min, Li, Xiu-Mei, Xu, Ying-Jia, Zhang, Min, Li, Ruo-Gu, Qiu, Xing-Biao, Li, Xun, Yang, Yi-Qing
Published in Heart and vessels (01.04.2019)
Published in Heart and vessels (01.04.2019)
Get full text
Journal Article
Nuclear receptor corepressor 1 represses cardiac hypertrophy
Li, Chao, Sun, Xue‐Nan, Chen, Bo‐Yan, Zeng, Meng‐Ru, Du, Lin‐Juan, Liu, Ting, Gu, Hui‐Hui, Liu, Yuan, Li, Yu‐Lin, Zhou, Lu‐Jun, Zheng, Xiao‐Jun, Zhang, Yu‐Yao, Zhang, Wu‐Chang, Liu, Yan, Shi, Chaoji, Shao, Shuai, Shi, Xue‐Rui, Yi, Yi, Liu, Xu, Wang, Jun, Auwerx, Johan, Wang, Zhao V, Jia, Feng, Li, Ruo‐Gu, Duan, Sheng‐Zhong
Published in EMBO molecular medicine (07.11.2019)
Published in EMBO molecular medicine (07.11.2019)
Get full text
Journal Article
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
Zhao, Cui-Mei, Peng, Lu-Ying, Li, Li, Liu, Xing-Yuan, Wang, Juan, Zhang, Xian-Ling, Yuan, Fang, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing
Published in PloS one (20.04.2015)
Published in PloS one (20.04.2015)
Get full text
Journal Article
A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve
Qu, Xin-Kai, MD, Qiu, Xing-Biao, MD, Yuan, Fang, MD, Wang, Juan, MD, Zhao, Cui-Mei, MD, Liu, Xing-Yuan, MD, Zhang, Xian-Ling, MD, Li, Ruo-Gu, MD, Xu, Ying-Jia, MD, Hou, Xu-Min, MD, Fang, Wei-Yi, MD, Liu, Xu, MD, Yang, Yi-Qing, MD
Published in The American journal of cardiology (15.12.2014)
Published in The American journal of cardiology (15.12.2014)
Get full text
Journal Article
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy
Qiao, Qi, Zhao, Cui-Mei, Yang, Chen-Xi, Gu, Jia-Ning, Guo, Yu-Han, Zhang, Min, Li, Ruo-Gu, Qiu, Xing-Biao, Xu, Ying-Jia, Yang, Yi-Qing
Published in Clinical chemistry and laboratory medicine (27.04.2021)
Published in Clinical chemistry and laboratory medicine (27.04.2021)
Get full text
Journal Article
CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy
Qiu, Xing-Biao, Qu, Xin-Kai, Li, Ruo-Gu, Liu, Hua, Xu, Ying-Jia, Zhang, Min, Shi, Hong-Yu, Hou, Xu-Min, Liu, Xu, Yuan, Fang, Sun, Yu-Min, Wang, Jun, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Published in Clinical chemistry and laboratory medicine (2017)
Published in Clinical chemistry and laboratory medicine (2017)
Get full text
Journal Article
Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication
Sun, Yiguo, Yang, Yi-Qing, Gong, Xiang-Qun, Wang, Xin-Hua, Li, Ruo-Gu, Tan, Hong-Wei, Liu, Xu, Fang, Wei-Yi, Bai, Donglin
Published in Human mutation (01.04.2013)
Published in Human mutation (01.04.2013)
Get full text
Journal Article
TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy
Zhang, Xian-Ling, Qiu, Xing-Biao, Yuan, Fang, Wang, Juan, Zhao, Cui-Mei, Li, Ruo-Gu, Xu, Lei, Xu, Ying-Jia, Shi, Hong-Yu, Hou, Xu-Min, Qu, Xin-Kai, Xu, Ya-Wei, Yang, Yi-Qing
Published in Biochemical and biophysical research communications (01.03.2015)
Published in Biochemical and biophysical research communications (01.03.2015)
Get full text
Journal Article
A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle
Wang, Zhi, Song, Hao-Ming, Wang, Fei, Zhao, Cui-Mei, Huang, Ri-Tai, Xue, Song, Li, Ruo-Gu, Qiu, Xing-Biao, Xu, Ying-Jia, Liu, Xing-Yuan, Yang, Yi-Qing
Published in International Heart Journal (27.09.2019)
Published in International Heart Journal (27.09.2019)
Get full text
Journal Article
Microbiota in Gut, Oral Cavity, and Mitral Valves Are Associated With Rheumatic Heart Disease
Shi, Xue-Rui, Chen, Bo-Yan, Lin, Wen-Zhen, Li, Yu-Lin, Wang, Yong-Li, Liu, Yan, Huang, Jing-Juan, Zhang, Wei-Wei, Ma, Xiao-Xin, Shao, Shuai, Li, Ruo-Gu, Duan, Sheng-Zhong
Published in Frontiers in cellular and infection microbiology (09.03.2021)
Published in Frontiers in cellular and infection microbiology (09.03.2021)
Get full text
Journal Article
NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve
Wang, Juan, Abhinav, Pradhan, Xu, Ying-Jia, Li, Ruo-Gu, Zhang, Min, Qiu, Xing-Biao, Di, Ruo-Min, Qiao, Qi, Li, Xiu-Mei, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Published in International journal of molecular medicine (01.04.2019)
Published in International journal of molecular medicine (01.04.2019)
Get full text
Journal Article
MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy
Yuan, Fang, Qiu, Zhao-Hui, Wang, Xing-Hua, Sun, Yu-Min, Wang, Jun, Li, Ruo-Gu, Liu, Hua, Zhang, Min, Shi, Hong-Yu, Zhao, Liang, Jiang, Wei-Feng, Liu, Xu, Qiu, Xing-Biao, Qu, Xin-Kai, Yang, Yi-Qing
Published in Clinical chemistry and laboratory medicine (23.02.2018)
Published in Clinical chemistry and laboratory medicine (23.02.2018)
Get full text
Journal Article
GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy
Li, Ruo-Gu, Li, Li, Qiu, Xing-Biao, Yuan, Fang, Xu, Lei, Li, Xin, Xu, Ying-Jia, Jiang, Wei-Feng, Jiang, Jin-Qi, Liu, Xu, Fang, Wei-Yi, Zhang, Min, Peng, Lu-Ying, Qu, Xin-Kai, Yang, Yi-Qing
Published in Biochemical and biophysical research communications (04.10.2013)
Published in Biochemical and biophysical research communications (04.10.2013)
Get full text
Journal Article
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect
Qiao, Xiao-Hui, Wang, Qian, Wang, Juan, Liu, Xing-Yuan, Xu, Ying-Jia, Huang, Ri-Tai, Xue, Song, Li, Yan-Jie, Zhang, Min, Qu, Xin-Kai, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing
Published in European journal of medical genetics (01.04.2018)
Published in European journal of medical genetics (01.04.2018)
Get full text
Journal Article
Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy
Xu, Jia-Hong, Gu, Jian-Yun, Guo, Yu-Han, Zhang, Hong, Qiu, Xing-Biao, Li, Ruo-Gu, Shi, Hong-Yu, Liu, Hua, Yang, Xiao-Xiao, Xu, Ying-Jia, Qu, Xin-Kai, Yang, Yi-Qing
Published in International Heart Journal (01.01.2017)
Published in International Heart Journal (01.01.2017)
Get full text
Journal Article
HAND2 loss-of-function mutation causes familial dilated cardiomyopathy
Liu, Hua, Xu, Ying-Jia, Li, Ruo-Gu, Wang, Zhang-Sheng, Zhang, Min, Qu, Xin-Kai, Qiao, Qi, Li, Xiu-Mei, Di, Ruo-Min, Qiu, Xing-Biao, Yang, Yi-Qing
Published in European journal of medical genetics (01.09.2019)
Published in European journal of medical genetics (01.09.2019)
Get full text
Journal Article
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis
Sun, Yu-Min, Wang, Jun, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Qu, Xin-Kai, Shi, Hong-Yu, Hou, Xu-Min, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Published in G3 : genes - genomes - genetics (01.04.2016)
Published in G3 : genes - genomes - genetics (01.04.2016)
Get full text
Journal Article