A Novel Spatial Position Prediction Navigation System Makes Surgery More Accurate
Zhang, Lin-Sen, Liu, Shi-Qi, Xie, Xiao-Liang, Zhou, Xiao-Hu, Hou, Zeng-Guang, Wang, Chao-Nan, Qu, Xin-Kai, Han, Wen-Zheng, Ma, Xi-Yao, Song, Meng
Published in IEEE transactions on medical imaging (01.12.2023)
Published in IEEE transactions on medical imaging (01.12.2023)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy
XU, LEI, ZHAO, LAN, YUAN, FANG, JIANG, WEI-FENG, LIU, HUA, LI, RUO-GU, XU, YING-JIA, ZHANG, MIN, FANG, WEI-YI, QU, XIN-KAI, YANG, YI-QING, QIU, XING-BIAO
Published in International journal of molecular medicine (01.11.2014)
Published in International journal of molecular medicine (01.11.2014)
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ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy
Sun, Yu-Min, Wang, Jun, Xu, Ying-Jia, Wang, Xin-Hua, Yuan, Fang, Liu, Hua, Li, Ruo-Gu, Zhang, Min, Li, Yan-Jie, Shi, Hong-Yu, Zhao, Liang, Qiu, Xing-Biao, Qu, Xin-Kai, Yang, Yi-Qing
Published in Heart and vessels (01.07.2018)
Published in Heart and vessels (01.07.2018)
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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)
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Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation
Xie, Wen-Hui, Chang, Cheng, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Fang, Wei-Yi, Liu, Xu, Yang, Yi-Qing
Published in Clinics (São Paulo, Brazil) (01.06.2013)
Published in Clinics (São Paulo, Brazil) (01.06.2013)
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Impact of prior permanent pacemaker on long‐term clinical outcomes of patients undergoing percutaneous coronary intervention
Li, Yan‐Jie, Zhang, Wei‐Wei, Yang, Xiao‐Xiao, Li, Ning, Qiu, Xing‐Biao, Qu, Xin‐Kai, Fang, Wei‐Yi, Yang, Yi‐Qing, Li, Ruo‐Gu
Published in Clinical cardiology (Mahwah, N.J.) (01.04.2017)
Published in Clinical cardiology (Mahwah, N.J.) (01.04.2017)
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A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias
YUAN, FANG, QIU, XING-BIAO, LI, RUO-GU, QU, XIN-KAI, WANG, JUAN, XU, YING-JIA, LIU, XU, FANG, WEI-YI, YANG, YI-QING, LIAO, DE-NING
Published in International journal of molecular medicine (01.02.2015)
Published in International journal of molecular medicine (01.02.2015)
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Journal Article
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation
Qiu, Xing-Biao, Xu, Ying-Jia, Li, Ruo-Gu, Xu, Lei, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Qu, Xin-Kai
Published in Clinics (São Paulo, Brazil) (01.01.2014)
Published in Clinics (São Paulo, Brazil) (01.01.2014)
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GATA5 loss-of-function mutation in familial dilated cardiomyopathy
ZHANG, XIAN-LING, DAI, NENG, TANG, KAI, CHEN, YAN-QING, CHEN, WEI, WANG, JUAN, ZHAO, CUI-MEI, YUAN, FANG, QIU, XING-BIAO, QU, XIN-KAI, YANG, YI-QING, XU, YA-WEI
Published in International journal of molecular medicine (01.03.2015)
Published in International journal of molecular medicine (01.03.2015)
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Journal Article
NKX2-6 mutation predisposes to familial atrial fibrillation
WANG, JUN, ZHANG, DAI-FU, SUN, YU-MIN, LI, RUO-GU, QIU, XING-BIAO, QU, XIN-KAI, LIU, XU, FANG, WEI-YI, YANG, YI-QING
Published in International journal of molecular medicine (01.12.2014)
Published in International journal of molecular medicine (01.12.2014)
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