Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation

Por Gu, Jian-Yun, Xu, Jia-Hong, Yu, Hong, Yang, Yi-Qing
Publicado em 2012

Mutation spectrum of GATA4 associated with congenital atrial septal defects

Por Yang, Yi-Qing, Wang, Juan, Liu, Xing-Yuan, Chen, Xiao-Zhong, Zhang, Wei, Wang, Xiao-Zhou
Publicado em 2013

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

Por Wei, Dong, Bao, Han, Liu, Xing-Yuan, Zhou, Ning, Wang, Qian, Li, Ruo-Gu, Xu, Ying-Jia, Yang, Yi-Qing
Publicado em 2012

Novel GATA4 mutations in patients with congenital ventricular septal defects

Por Yang, Yi-Qing, Wang, Juan, Liu, Xing-Yuan, Chen, Xiao-Zhong, Zhang, Wei, Wang, Xiao-Zhou, Liu, Xu, Fang, Wei-Yi
Publicado em 2012

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

Por Xie, Wen-Hui, Chang, Cheng, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Fang, Wei-Yi, Liu, Xu, Yang, Yi-Qing
Publicado em 2013

PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

Por Qiu, Xing-Biao, Xu, Ying-Jia, Li, Ruo-Gu, Xu, Lei, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Qu, Xin-Kai
Publicado em 2014

Association of angiotensin-converting enzyme gene I/D and CYP11B2 gene −344T/C polymorphisms with lone atrial fibrillation and its recurrence after catheter ablation

Por ZHANG, XIAN-LING, WU, LI-QUN, LIU, XU, YANG, YI-QING, TAN, HONG-WEI, WANG, XIN-HUA, ZHOU, LI, JIANG, WEI-FENG, LI, ZHENG
Publicado em 2012

Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease

Por Wang, Juan, Xin, Yuan-Feng, Xu, Wen-Jun, Liu, Zhong-Min, Qiu, Xing-Biao, Qu, Xin-Kai, Xu, Lei, Li, Xin, Yang, Yi-Qing
Publicado em 2013

Genes Underlying Positive Influence of Prenatal Environmental Enrichment and Negative Influence of Prenatal Earthquake Simulation and Corrective Influence of Chinese Herbal Medicin...

Por Zhang, Xian Geng, Zhang, Hui, Lin, Lin, Yang, Yi Qing, Deng, Ting Ting, Liu, Qin, Liang, Xiao Li, Wang, Mi Qu, Peng, De Zhong
Publicado em 2014

Necroptosis, a novel type of programmed cell death, contributes to early neural cells damage after spinal cord injury in adult mice

Por Liu, Ming, Wu, Wei, Li, Hua, Li, Song, Huang, Li-tian, Yang, Yi-qing, Sun, Qing, Wang, Chun-xi, Yu, Zhuang, Hang, Chun-hua
Publicado no J Spinal Cord Med (2015)

MEF2C loss-of-function mutation contributes to congenital heart defects

Por Qiao, Xiao-Hui, Wang, Fei, Zhang, Xian-Ling, Huang, Ri-Tai, Xue, Song, Wang, Juan, Qiu, Xing-Biao, Liu, Xing-Yuan, Yang, Yi-Qing
Publicado no Int J Med Sci (2017)

Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot

Por Wang, Juan, Luo, Xue-Jiao, Xin, Yuan-Feng, Liu, Yi, Liu, Zhong-Min, Wang, Qian, Li, Ruo-Gu, Fang, Wei-Yi, Wang, Xiao-Zhou, Yang, Yi-Qing
Publicado em 2012

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

Por 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
Publicado no PLoS One (2015)

PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

Por Yuan, Fang, Zhao, Lan, Wang, Juan, Zhang, Wei, Li, Xin, Qiu, Xing-Biao, Li, Ruo-Gu, Xu, Ying-Jia, Xu, Lei, Qu, Xing-Kai, Fang, Wei-Yi, Yang, Yi-Qing
Publicado em 2013

TBX1 loss-of-function mutation contributes to congenital conotruncal defects

Por Zhang, Min, Li, Fu-Xing, Liu, Xing-Yuan, Hou, Jing-Yi, Ni, Shi-Hong, Wang, Juan, Zhao, Cui-Mei, Zhang, Wei, Kong, Ye, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Publicado no Exp Ther Med (2018)

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation

Por Wang, Zhan-Cheng, Ji, Wen-Hui, Ruan, Chang-Wu, Liu, Xing-Yuan, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Liu, Xu, Huang, Ru-Tai, Xue, Song, Yang, Yi-Qing
Publicado no Int J Med Sci (2016)

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

Por 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
Publicado no G3 (Bethesda) (2016)

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Por Huang, Ri-Tai, Wang, Juan, Xue, Song, Qiu, Xing-Biao, Shi, Hong-Yu, Li, Ruo-Gu, Qu, Xin-Kai, Yang, Xiao-Xiao, Liu, Hua, Li, Ning, Li, Yan-Jie, Xu, Ying-Jia, Yang, Yi-Qing
Publicado no Int J Med Sci (2017)

Mutational Spectrum of the NKX2-5 Gene in Patients with Lone Atrial Fibrillation

Por Yu, Hong, Xu, Jia-Hong, Song, Hao-Ming, Zhao, Lan, Xu, Wen-Jun, Wang, Juan, Li, Ruo-Gu, Xu, Lei, Jiang, Wei-Feng, Qiu, Xing-Biao, Jiang, Jin-Qi, Qu, Xin-Kai, Liu, Xu, Fang, Wei-Yi, Jiang, Jin-Fa, Yang, Yi-Qing
Publicado em 2014