Association between Variant Y402H in Age-Related Macular Degeneration (AMD) Susceptibility Gene CFH and Treatment Response of AMD: A Meta-Analysis

por Chen, Han, Yu, Ke-Da, Xu, Ge-Zhi
Publicado 2012

Association of adjuvant aromatase inhibitor with cataract risk in postmenopausal women with breast cancer

por Chen, Han, Shao, Zhi-Ming, Yu, Ke-Da, Xu, Ge-Zhi
Publicado 2020

Expression of CCL2 and its receptor in activation and migration of microglia and monocytes induced by photoreceptor apoptosis

por Feng, ChaoYi, Wang, Xin, Liu, TianJin, Zhang, Meng, Xu, GeZhi, Ni, YingQin
Publicado 2017

Interaction of two functional genetic variants LOXL1 rs1048661 and VEGFA rs3025039 on the risk of age-related macular degeneration in Chinese women

por Chen, Han, Mo, Miao, Liu, Guang-Yu, Gong, Yang-Ming, Yu, Ke-Da, Xu, Ge-Zhi
Publicado 2020

Effect of Phosphorylated-Extracellular Regulated Kinase 1/2 Inhibitor on Retina from Light-induced Photoreceptor Degeneration

por Ding, Xin-Yi, Gu, Rui-Ping, Tang, Wen-Yi, Shu, Qin-Meng, Xu, Ge-Zhi, Zhang, Meng
Publicado 2018

Pediatric Infectious Endophthalmitis: A 271-case Retrospective Study at a Single Center in China

por Zhang, Meng, Xu, Ge-Zhi, Jiang, Rui, Ni, Ying-Qin, Wang, Ke-Yan, Gu, Rui-Ping, Ding, Xin-Yi
Publicado 2016

CCR2 overexpression promotes the efficient recruitment of retinal microglia in vitro

por Jiang, Xiao-shuang, Ni, Ying-qin, Liu, Tian-jin, Zhang, Meng, Ren, Hui, Jiang, Rui, Huang, Xin, Xu, Ge-zhi
Publicado 2012

Mutation Analysis of the RPGR Gene in a Chinese Cohort

por Liu, Hong-Li, Gao, Feng-Guan, Wang, Dan-Dan, Hu, Fang-Yuan, Xu, Ping, Chang, Qing, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2022

Downregulation of circRNA DMNT3B contributes to diabetic retinal vascular dysfunction through targeting miR-20b-5p and BAMBI

por Zhu, Ke, Hu, Xin, Chen, Han, Li, Fang, Yin, Ning, Liu, Ai-Lin, Shan, Kun, Qin, Yao-Wu, Huang, Xin, Chang, Qing, Xu, Ge-Zhi, Wang, Zhongfeng
Publicado 2019

Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses

por Gao, Feng-Juan, Tian, Guo-Hong, Hu, Fang-Yuan, Wang, Dan-Dan, Li, Jian-Kang, Chang, Qing, Chen, Fang, Xu, Ge-Zhi, Liu, Wei, Wu, Ji-Hong
Publicado 2020

Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort

por Gao, Feng-Juan, Wang, Dan-Dan, Hu, Fang-Yuan, Xu, Ping, Chang, Qing, Li, Jian-Kang, Liu, Wei, Zhang, Sheng-Hai, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2021

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

por Gao, Feng‐Juan, Dong, Jian‐Hong, Wang, Dan‐Dan, Chen, Fang, Hu, Fang‐Yuan, Chang, Qing, Xu, Ping, Liu, Wei, Li, Jian‐Kang, Huang, Ying, Wu, Ji‐Hong, Xu, Ge‐Zhi
Publicado 2020

Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family

por Qi, Yu-He, Gao, Feng-Juan, Hu, Fang-Yuan, Zhang, Sheng-Hai, Chen, Jun-Yi, Huang, Wan-Jing, Tian, Guo-Hong, Wang, Min, Gan, De-Kang, Wu, Ji-Hong, Xu, Ge-Zhi
Publicado 2017

Expanding the clinical and genetic spectrum of Heimler syndrome

por Gao, Feng-Juan, Hu, Fang-Yuan, Xu, Ping, Qi, Yu-He, Li, Jian-Kang, Zhang, Yong-Jin, Chen, Fang, Chang, Qing, Song, Fang, Shen, Si-Mai, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2019

Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy

por Huang, Xiao-Yan, Zhuang, Hong, Wu, Ji-Hong, Li, Jian-Kang, Hu, Fang-Yuan, Zheng, Yu, Tellier, Laurent Christian Asker M., Zhang, Sheng-Hai, Gao, Feng-Juan, Zhang, Jian-Guo, Xu, Ge-Zhi
Publicado 2017

Clinical and Genetic Characteristics of Chinese Patients with Occult Macular Dystrophy

por Wang, Dan-Dan, Gao, Feng-Juan, Li, Jian-Kang, Chen, Fang, Hu, Fang-Yuan, Xu, Ge-Zhi, Zhang, Jian-Guo, Sun, Hao-Xiang, Zhang, Sheng-Hai, Xu, Ping, Tian, Guo-Hong, Wu, Ji-Hong
Publicado 2020

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

por Gao, Feng-Juan, Wang, Dan-Dan, Li, Jian-Kang, Hu, Fang-Yuan, Xu, Ping, Chen, Fang, Qi, Yu-He, Liu, Wei, Li, Wei, Zhang, Sheng-Hai, Chang, Qing, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2021

Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

por Gao, Feng-Juan, Wang, Dan-Dan, Chen, Fang, Sun, Hao-Xiang, Hu, Fang-Yuan, Xu, Ping, Li, Jiankang, Liu, Wei, Qi, Yu-He, Li, Wei, Wang, Ming, Zhang, Shenghai, Xu, Ge-Zhi, Chang, Qing, Wu, Ji-Hong
Publicado 2021

ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

por Hu, Fang-Yuan, Li, Jian-kang, Gao, Feng-Juan, Qi, Yu-He, Xu, Ping, Zhang, Yong-Jin, Wang, Dan-Dan, Wang, Lu-Sheng, Li, Wei, Wang, Min, Chen, Fang, Shen, Si-Mai, Xu, Ge-Zhi, Zhang, Sheng-Hai, Chang, Qing, Wu, Ji-Hong
Publicado 2019