Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report von Li, Yuanyuan, Chen, Yuxue, Sun, Yang, Li, Shouxin, Dong, Lingli, Li, Zongzhe, Shen, Guifen

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A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency von Cui, Guanglin, MD, PhD, Li, Zongzhe, MD, Li, Rui, MD, PhD, Huang, Jin, MD, Wang, Haoran, MD, Zhang, Lina, MD, Ding, Hu, MD, PhD, Wang, Dao Wen, MD, PhD

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Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke von Cui, Guanglin, Wang, Haoran, Li, Rui, Zhang, Lina, Li, Zongzhe, Wang, Yan, Hui, Rutai, Ding, Hu, Wang, Dao Wen

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Numerical simulation and experimental study of gas cyclone–liquid jet separator for fine particle separation von Wang, Liwang, Chen, Erwen, Ma, Liang, Yang, Zhanghuang, Li, Zongzhe, Yang, Weihui, Wang, Hualin, Chang, Yulong

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Aortic root aortopathy in bicuspid aortic valve associated with high genetic risk von Ma, Mingjia, Li, Zongzhe, Mohamed, Mohamed Abdulkadir, Liu, Ligang, Wei, Xiang

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Effects of Shuanghuanglian oral liquids on patients with COVID-19: a randomized, open-label, parallel-controlled, multicenter clinical trial von Ni, Li, Wen, Zheng, Hu, Xiaowen, Tang, Wei, Wang, Haisheng, Zhou, Ling, Wu, Lujin, Wang, Hong, Xu, Chang, Xu, Xizhen, Xiao, Zhichao, Li, Zongzhe, Li, Chene, Liu, Yujian, Duan, Jialin, Chen, Chen, Li, Dan, Zhang, Runhua, Li, Jinliang, Yi, Yongxiang, Huang, Wei, Chen, Yanyan, Zhao, Jianping, Zuo, Jianping, Weng, Jianping, Jiang, Hualiang, Wang, Dao Wen

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The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA von Wang, James Jiqi, Yu, Bo, Li, Zongzhe

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COL5A1 Variants Cause Aortic Dissection by Activating TGF‐β‐Signaling Pathway von Chen, Peng, Yu, Bo, Li, Zongzhe, Chen, Yanghui, Sun, Yang, Wang, Dao Wen

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MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway von Chen, Peng, Li, Zongzhe, Nie, Jiali, Wang, Hong, Yu, Bo, Wen, Zheng, Sun, Yang, Shi, Xiaolu, Jin, Li, Wang, Dao-Wen

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RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy von Dai, Jiaqi, Li, Zongzhe, Huang, Wei, Chen, Peng, Sun, Yang, Wang, Hong, Wu, Dongyang, Chen, Yanghui, Li, Chenze, Xiao, Lei, Liu, Hao, Wei, Haoran, Li, Rui, Duan, Quanlu, Peng, Liyuan, Song, Xiuli, Yu, Ting, Wang, Yan, Wang, Dao Wen

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Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report von Li, Xianqing, Li, Zongzhe, Chen, Peng, Wang, Yan, Wang, Dao Wen, Wang, Dao Wu

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Rare Variants and Polymorphisms of FBN1 Gene May Increase the Risk of Non-Syndromic Aortic Dissection von Pan, Meichen, Li, Lianjie, Li, Zehao, Chen, Shu, Li, Zongzhe, Wang, Yuning, He, Henghui, Lin, Lihua, Wang, Haihao, Liu, Qian

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Erratum to: MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway von Chen, Peng, Li, Zongzhe, Nie, Jiali, Wang, Hong, Yu, Bo, Wen, Zheng, Sun, Yang, Shi, Xiaolu, Jin, Li, Wang, Dao-Wen

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Machine learning modeling identifies hypertrophic cardiomyopathy subtypes with genetic signature von Dai, Jiaqi, Wang, Tao, Xu, Ke, Sun, Yang, Li, Zongzhe, Chen, Peng, Wang, Hong, Wu, Dongyang, Chen, Yanghui, Xiao, Lei, Liu, Hao, Wei, Haoran, Li, Rui, Peng, Liyuan, Yu, Ting, Wang, Yan, Sun, Zhongsheng, Wang, Dao Wen

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Case Report: A Novel LAMP2 Splice-Altering Mutation Causes Cardiac-Only Danon Disease von Li, Zongzhe, Ma, Fei, Li, Rui, Xiao, Zhichao, Zeng, Hesong, Wang, Dao Wen

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Identification of COL3A1 variants associated with sporadic thoracic aortic dissection: a case--control study von Chen, Yanghui, Sun, Yang, Li, Zongzhe, Li, Chenze, Xiao, Lei, Dai, Jiaqi, Li, Shiyang, Liu, Hao, Hu, Dong, Wu, Dongyang, Hu, Senlin, Yu, Bo, Chen, Peng, Xu, Ping, Kong, Wei, Wang, Dao Wen

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Object Tracking With Structured Metric Learning von Zhao, Xiaolin, Xu, Zhuofan, Zhao, Boxin, Chen, Xiaolong, Li, Zongzhe

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Comparison of High-Resolution Melting Analysis, TaqMan Allelic Discrimination Assay, and Sanger Sequencing for Clopidogrel Efficacy Genotyping in Routine Molecular Diagnostics von Zhang, Lina, Cui, Guanglin, Li, Zongzhe, Wang, Haoran, Ding, Hu, Wang, Dao Wen

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The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia von Dai, Jiaqi, Li, Ke, Huang, Man, Sun, Yang, Liu, Hao, Li, Zongzhe, Chen, Peng, Wang, Hong, Wu, Dongyang, Chen, Yanghui, Xiao, Lei, Wei, Haoran, Li, Rui, Peng, Liyuan, Yu, Ting, Wang, Yan, Wang, Dao Wen

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Growth of Metal Organic Frameworks on the Surface of Individual Cellulose Nanocrystals von Cho, Kyoungil, Li, Zongzhe, MacLachlan, Mark J.

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