Publications by authors named "Yi-Qing Yang"

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Comment on "Accelerated biological aging and postoperative acute kidney injury in surgical patients: a retrospective multicentre cohort analysis of 94,006 cases".
YiQing Yang, Jing Hu

Int J Surg· December 2025

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A new KLF13 loss-of-function mutation responsible for sporadic dilated cardiomyopathy.
Xiang Tang, Yin Wang, Chen-Xi Yang, Zun-Ping Ke, Fang Yuan, Yi-Qing Yang

Mol Biol Rep· November 2025

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Globally patterned locus coeruleus-norepinephrine neuron-pericyte coupling orchestrates brain-wide vascular dynamics.
Le Sun, Xiao-Lan Peng, Hua-Xing Zi, Zhen-Kun Zhang, Yu-Chen Gong, Yi-Qing Yang

Neuron· November 2025

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Discovery of as a New Gene Predisposing to Dilated Cardiomyopathy.
Zun-Ping Ke, Jia-Ning Gu, Chen-Xi Yang, Xue-Lin Li, Su Zou, Yi-Qing Yang

Diagnostics (Basel)· August 2025

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Identification and Functional Characterization of a Novel Mutation Predisposing to Coffin-Siris Syndromic Congenital Heart Disease.
Zi Yan, Bin-Bin Dong, Yan-Jie Li, Chen-Xi Yang, Ying-Jia Xu, Yi-Qing Yang

Children (Basel)· May 2025

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Chromosomal Location and Identification of as a New Gene Responsible for Familial Bicuspid Aortic Valve.
Yan-Jie Li, Su Zou, Yi-Zhe Bian, Xing-Yuan Liu, Chen-Xi Yang, Yi-Qing Yang

Diagnostics (Basel)· March 2025

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Identification and Functional Investigation of as a Novel Gene Underpinning Familial Atrial Fibrillation.
Wei-Feng Jiang, Yu-Min Sun, Xing-Biao Qiu, Shao-Hui Wu, Yuan-Yuan Ding, Chen-Xi Yang, Yi-Qing Yang

Diagnostics (Basel)· October 2024

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Discovery and functional investigation of as a new causative gene for human congenital heart disease.
Zhi Wang, Xing-Yuan Liu, Chen-Xi Yang, Hui-Min Zhou, Yan-Jie Li, Yi-Qing Yang

Am J Transl Res· May 2024

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Empagliflozin ameliorates vascular calcification in diabetic mice through inhibiting Bhlhe40-dependent NLRP3 inflammasome activation.
Xiao-Xue Li, Zheng-Dong Chen, Xue-Jiao Sun, Yi-Qing Yang, Hong Jin

Acta Pharmacol Sin· April 2024

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Somatic mutation contributes to tetralogy of Fallot.
Pradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, Xing-Yuan Liu, Jia-Ning Gu, Chen-Xi Yang, Yi-Qing Yang

Exp Ther Med· February 2024

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Discovery of as a new gene underpinning congenital heart defects.
Bin-Bin Dong, Yan-Jie Li, Xing-Yuan Liu, Ri-Tai Huang, Chen-Xi Yang, Yi-Qing Yang

Am J Transl Res· January 2024

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Discovery of as a Novel Gene Underlying Atrial Fibrillation.
Ning Li, Yan-Jie Li, Xiao-Juan Guo, Shao-Hui Wu, Wei-Feng Jiang, Yi-Qing Yang

Biology (Basel)· August 2023

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VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.
Hong-Yu Shi, Meng-Shi Xie, Yu-Han Guo, Chen-Xi Yang, Jia-Ning Gu, Yi-Qing Yang

Eur J Med Genet· March 2023

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mA demethylase ALKBH5 attenuates doxorubicin-induced cardiotoxicity via posttranscriptional stabilization of Rasal3.
Ri-Feng Gao, Kun Yang, Ya-Nan Qu, Xiang Wei, Jia-Ran Shi, Yi-Qing Yang

iScience· March 2023

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Increased gestational palmitic acid predisposes offspring to congenital heart disease.
Yang Lv, Ri-Feng Gao, Chen-Xi Yang, Ying-Jia Xu, Yi-Qing Yang

Cell Rep Med· March 2023

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A novel GJA5 variant associated with increased risk of essential hypertension.
Juan Wang, Xue-Cheng Wang, Zhao-Hua Gu, Guang-Wei Ren, Xiao-Hong Zhao, Yi-Qing Yang

Am J Transl Res· February 2023

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Discovery of (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias.
Yan-Jie Li, Juan Wang, Willy G Ye, Xing-Yuan Liu, Li Li, Yi-Qing Yang

Biology (Basel)· February 2023

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SMAD4 loss-of-function mutation predisposes to congenital heart disease.
Yin Wang, Ying-Jia Xu, Chen-Xi Yang, Ri-Tai Huang, Song Xue, Yi-Qing Yang

Eur J Med Genet· January 2023

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Identification of as a Novel Gene Contributing to Dilated Cardiomyopathy.
Jia-Ning Gu, Chen-Xi Yang, Yuan-Yuan Ding, Qi Qiao, Ruo-Min Di, Ling Yang, Yi-Qing Yang

Diagnostics (Basel)· January 2023

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KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
Yu-Han Guo, Jun Wang, Xiao-Juan Guo, Ri-Feng Gao, Chen-Xi Yang, Yi-Qing Yang

J Am Heart Assoc· November 2022

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Identification of as a New Gene Predisposing to Congenital Heart Disease.
Hong-Yu Shi, Meng-Shi Xie, Chen-Xi Yang, Ri-Tai Huang, Song Xue, Yi-Qing Yang

Diagnostics (Basel)· August 2022

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A novel mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve.
Pradhan Abhinav, Gao-Feng Zhang, Cui-Mei Zhao, Ying-Jia Xu, Juan Wang, Yi-Qing Yang

Exp Ther Med· April 2022

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A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus.
Zun-Ping Ke, Gao-Feng Zhang, Yu-Han Guo, Yu-Min Sun, Jun Wang, Yi-Qing Yang

Genet Mol Biol· March 2022

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SOX7 loss-of-function variation as a cause of familial congenital heart disease.
Ri-Tai Huang, Yu-Han Guo, Chen-Xi Yang, Jia-Ning Gu, Xing-Biao Qiu, Yi-Qing Yang

Am J Transl Res· March 2022

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Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions.
Yu-Han Guo, Yi-Qing Yang

Biology (Basel)· March 2022

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