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Journal of Geriatric Cardiology : JGC|January 21, 2016
Efficacy and safety of a novel multi-electrode radiofrequency ablation catheter for renal sympathetic denervation in pigsQian Gan, Xin-Kai Qu, Kai-Zheng Gong, et al.G3 (Bethesda, Md.)|February 12, 2016
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary StenosisYu-Min Sun, Jun Wang, Xing-Biao Qiu, et al.International Journal of Medical Sciences|November 17, 2018
A SHOX2 loss-of-function mutation underlying familial atrial fibrillationNing Li, Zhang-Sheng Wang, Xin-Hua Wang, et al.Molecular Medicine Reports|April 2, 2016
TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndromeDong-Feng Guo, Ruo-Gu Li, Fang Yuan, et al.International Journal of Medical Sciences|February 27, 2016
Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial FibrillationZhan-Cheng Wang, Wen-Hui Ji, Chang-Wu Ruan, et al.Pediatric Cardiology|November 9, 2014
A novel NKX2.6 mutation associated with congenital ventricular septal defectJuan Wang, Jian-Hui Mao, Ke-Ke Ding, et al.Journal of the American Heart Association|November 30, 2021
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial FibrillationXiao-Juan Guo, Xing-Biao Qiu, Jun Wang, et al.American Journal of Translational Research|June 17, 2024
Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart diseaseZhi Wang, Xing-Yuan Liu, Chen-Xi Yang, et al.Biology|September 28, 2023
Discovery of TBX20 as a Novel Gene Underlying Atrial FibrillationNing Li, Yan-Jie Li, Xiao-Juan Guo, et al.International Heart Journal|July 11, 2017
Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated CardiomyopathyJia-Hong Xu, Jian-Yun Gu, Yu-Han Guo, et al.Pageof 9