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Genes|April 3, 2021
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and CardiomyopathyNing Li, Ying-Jia Xu, Hong-Yu Shi, et al.Acta Pharmacologica Sinica|February 28, 2012
Plasma ghrelin levels are closely associated with severity and morphology of angiographically-detected coronary atherosclerosis in Chineses patients with diabetes mellitusMin Zhang, Wei-yi Fang, Fang Yuan, et al.Molecular Medicine Reports|January 8, 2013
Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillationHai-Feng Shi, Jie-Fu Yang, Qian Wang, et al.European Journal of Medical Genetics|April 1, 2021
SOX17 loss-of-function variation underlying familial congenital heart diseaseLan Zhao, Wei-Feng Jiang, Chen-Xi Yang, et al.Experimental and Therapeutic Medicine|January 26, 2024
Somatic GATA4 mutation contributes to tetralogy of FallotPradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, et al.European Journal of Medical Genetics|December 21, 2019
Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathyRuo-Min Di, Chen-Xi Yang, Cui-Mei Zhao, et al.Journal of Cardiovascular Translational Research|December 12, 2018
Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated CardiomyopathyYing-Jia Xu, Zhang-Sheng Wang, Chen-Xi Yang, et al.American Journal of Translational Research|April 15, 2022
SOX7 loss-of-function variation as a cause of familial congenital heart diseaseRi-Tai Huang, Yu-Han Guo, Chen-Xi Yang, et al.Diagnostics (Basel, Switzerland)|January 21, 2023
Identification of BMP10 as a Novel Gene Contributing to Dilated CardiomyopathyJia-Ning Gu, Chen-Xi Yang, Yuan-Yuan Ding, et al.International Journal of Molecular Medicine|December 16, 2014
A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmiasFang Yuan, Xing-Biao Qiu, Ruo-Gu Li, et al.Pageof 9