Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications von He, Guo‐Wei, Maslen, Cheryl L., Chen, Huan‐Xin, Hou, Hai‐Tao, Bai, Xiao‐Yan, Wang, Xiu‐Li, Liu, Xiao‐Cheng, Lu, Wan‐Li, Chen, Xin‐Xin, Chen, Wei‐Dan, Xing, Quan‐Sheng, Wu, Qin, Wang, Jun, Yang, Qin

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Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects von Zheng, Si‐Qiang, Chen, Huan‐Xin, Liu, Xiao‐Cheng, Yang, Qin, He, Guo‐Wei

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Identification and functional analysis of genetic variants of ISL1 gene promoter in human atrial septal defects von Yin, Xiu‐Yun, Chen, Huan‐Xin, Chen, Zhuo, Yang, Qin, Han, Jun, He, Guo‐Wei

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Functional significance of novel variants of the MEF2C gene promoter in congenital ventricular septal defects von Zeng, Zhi‐Hua, Chen, Huan‐Xin, Liu, Xiao‐Cheng, Yang, Qin, He, Guo‐Wei

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Novel mutations of TCTN3/LTBP2 with cellular function changes in congenital heart disease associated with polydactyly von Chen, Huan‐Xin, Yang, Zi‐Yue, Hou, Hai‐Tao, Wang, Jun, Wang, Xiu‐Li, Yang, Qin, Liu, Lin, He, Guo‐Wei

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Metabolomics and Biomarkers for Paroxysmal and Persistent Atrial Fibrillation von Zhang, Li-Li, Lin, Wen-Hua, Di, Cheng-Ye, Hou, Hai-Tao, Chen, Huan-Xin, Zhou, Jie, Yang, Qin, He, Guo-Wei

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Identification and functional analysis of variants of MYH6 gene promoter in isolated ventricular septal defects von Zuo, Ji-Yang, Chen, Huan-Xin, Liu, Zhi-Gang, Yang, Qin, He, Guo-Wei

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Pathophysiological Role of Variants of the Promoter Region of CITED2 Gene in Sporadic Tetralogy of Fallot Patients with Cellular Function Verification von Chen, Zhuo, Chen, Huan-Xin, Hou, Hai-Tao, Yin, Xiu-Yun, Yang, Qin, He, Guo-Wei

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A multicenter, randomized controlled study on the efficacy of agomelatine in ameliorating anhedonia, reduced motivation, and circadian rhythm disruptions in patients with major dep... von Guo, Ping, Xu, Yong, Lv, Liang, Feng, Min, Fang, Yu, Huang, Wei-Quan, Cheng, Shan-Fei, Qian, Min-Cai, Yang, Shengliang, Wang, Shi-Kai, Chen, Huan-Xin

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Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis von Yin, Xiu-Yun, Chen, Huan-Xin, Chen, Zhuo, Yang, Qin, Han, Jun, He, Guo-Wei

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Metabolomics Analysis Identifies Differential Metabolites as Biomarkers for Acute Myocardial Infarction von Zhou, Jie, Hou, Hai-Tao, Song, Yu, Zhou, Xiao-Lin, Chen, Huan-Xin, Zhang, Li-Li, Xue, Hong-Mei, Yang, Qin, He, Guo-Wei

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Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation von Chen, Huan‐Xin, Hou, Hai‐Tao, Wang, Xiu‐Li, Wang, Jun, Yang, Qin, He, Guo‐Wei

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Rapid detection of PAH gene mutations in Chinese people von Zhang, Xin, Chen, Huan-Xin, Li, Chuan, Zhang, Gui, Liao, Sheng-Yun, Peng, Zhuo-Chun, Lai, Xiao-Ping, Wang, Ling-Li

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Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice von Yokoi, Fumiaki, Chen, Huan-Xin, Dang, Mai Tu, Cheetham, Chad C, Campbell, Susan L, Roper, Steven N, Sweatt, J David, Li, Yuqing

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Balance of Inhibitory and Excitatory Synaptic Activity Is Altered in Fast-Spiking Interneurons in Experimental Cortical Dysplasia von Zhou, Fu-Wen, Chen, Huan-Xin, Roper, Steven N

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Increased circulating levels of tumor necrosis factor-like cytokine 1A and decoy receptor 3 correlate with SYNTAX score in patients undergoing coronary surgery von Li, Xin-Ya, Hou, Hai-Tao, Chen, Huan-Xin, Wang, Zheng-Qing, He, Guo-Wei

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Functional integration of human neural precursor cells in mouse cortex von Zhou, Fu-Wen, Fortin, Jeff M, Chen, Huan-Xin, Martinez-Diaz, Hildabelis, Chang, Lung-Ji, Reynolds, Brent A, Roper, Steven N

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Genetic Variants of CITED2 Gene Promoter in Human Atrial Septal Defects: Case-Control Study and Cellular Functional Verification von Chen, Zhuo, Chen, Huan-Xin, Hou, Hai-Tao, Yin, Xiu-Yun, Yang, Qin, Han, Jun, He, Guo-Wei

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Hydrogen sulfide-mediated endothelial function and the interaction with eNOS and PDE5A activity in human internal mammary arteries von Yuan, Chao, Hou, Hai-Tao, Chen, Huan-Xin, Wang, Jun, Wang, Zheng-Qing, Chen, Tie-Nan, Novakovic, Aleksandra, Marinko, Marija, Yang, Qin, Liu, Zhi-Gang, He, Guo-Wei

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Variants of the promoter of MYH6 gene in congenital isolated and sporadic patent ductus arteriosus: case-control study and cellular functional analyses von Zuo, Ji-Yang, Chen, Huan-Xin, Yang, Qin, He, Guo-Wei

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