Variant Spectrum of Formin Homology 2 Domain‐Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy

por Wu, Guixin, Ruan, Jieyun, Liu, Jie, Zhang, Channa, Kang, Lianming, Wang, Jizheng, Zou, Yubao, Song, Lei
Publicado 2021

TNNT2 Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in the Han Chinese Population

por Li, Xiaoping, Wang, Huan, Luo, Rong, Gu, Haiyong, Zhang, Channa, Zhang, Yu, Hui, Rutai, Wu, Xiushan, Hua, Wei
Publicado 2013

Prognostic value of neutrophil gelatinase-associated lipocalin and glycosylated hemoglobin for non-ST-segment elevation myocardial infarction patients with single concomitant chron...

por Peng, Wenhua, Zhang, Channa, Wang, Zhijun, Yang, Wenqi, Luo, He, Li, Xiaofeng, Fu, Dongliang, Yu, Changan, Zhou, Yifeng
Publicado 2019

Functional Haplotypes of the hTERT Gene, Leukocyte Telomere Length Shortening, and the Risk of Peripheral Arterial Disease

por Zhang, Weili, Chen, Yu, Yang, Xiaomin, Fan, Jingyao, Mi, Xuenan, Wang, Jizheng, Zhang, Channa, Hu, Frank B., Hui, Rutai
Publicado 2012

Prevalence and risk factors of abnormal left ventricular geometrical patterns in untreated hypertensive patients

por Li, Hui, Pei, Fei, Shao, Liying, Chen, Jingzhou, Sun, Kai, Zhang, Xinyu, Zhang, Channa, Liu, Jibing, Xiao, Chuanshi, Hui, Rutai
Publicado 2014

A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension

por Xiao, Xiao, Li, Rui, Wu, Cunjin, Yan, Yupeng, Yuan, Mengmeng, Cui, Bing, Zhang, Yu, Zhang, Channa, Zhang, Xiaoxia, Zhang, Weili, Hui, Rutai, Wang, Yibo
Publicado 2022

Correction: A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension

por Xiao, Xiao, Li, Rui, Wu, Cunjin, Yan, Yupeng, Yuan, Mengmeng, Cui, Bing, Zhang, Yu, Zhang, Channa, Zhang, Xiaoxia, Zhang, Weili, Hui, Rutai, Wang, Yibo
Publicado 2022