Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy

por Shen, Ren-Juan, Wang, Jun-Gang, Li, Yang, Jin, Zi-Bing
Publicado 2021

Global spectrum of USH2A mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy

por Su, Bing-Nan, Shen, Ren-Juan, Liu, Zhuo-Lin, Li, Yang, Jin, Zi-Bing
Publicado 2022

Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3

por Li, Yan-Ping, Shen, Ren-Juan, Cheng, You-Min, Zhao, Qingqing, Jin, Kangxin, Jin, Zi-Bing, Zhang, Shaodan
Publicado 2023

Second hit impels oncogenesis of retinoblastoma in patient-induced pluripotent stem cell-derived retinal organoids: direct evidence for Knudson's theory

por Li, Yan-Ping, Wang, Ya-Ting, Wang, Wen, Zhang, Xiao, Shen, Ren-Juan, Jin, Kangxin, Jin, Li-Wen, Jin, Zi-Bing
Publicado 2022

Slc7a14 Is Indispensable in Zebrafish Retinas

por Zhuang, You-Yuan, Xiang, Lue, Wen, Xin-Ran, Shen, Ren-Juan, Zhao, Ning, Zheng, Si-Si, Han, Ru-Yi, Qu, Jia, Lu, Fan, Jin, Zi-Bing
Publicado 2019

Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China

por Liu, Yang, Zhang, Jin-Jin, Piao, Shun-Yu, Shen, Ren-Juan, Ma, Ya, Xue, Zhong-Qi, Zhang, Wen, Liu, Juan, Jin, Zi-Bing, Zhuang, Wen-Juan
Publicado 2021

Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort

por Xu, Ke, Chen, De-Fu, Chang, Haoyu, Shen, Ren-Juan, Gao, Hua, Wang, Xiao-Fang, Feng, Zhuo-Kun, Zhang, Xiaohui, Xie, Yue, Li, Yang, Jin, Zi-Bing
Publicado 2021

Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals

por Chen, Shihao, Li, Xing-Yong, Jin, Jia-Jia, Shen, Ren-Juan, Mao, Jian-Yang, Cheng, Fei-Fei, Chen, Zhen-Ji, Linardaki, Emmanouela, Voulgaraki, Stavroula, Aslanides, Ioannis M., Jin, Zi-Bing
Publicado 2021

Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus

por Wang, Xiao-Fang, Chen, Hui, Huang, Peng-Juan, Feng, Zhuo-Kun, Hua, Zi-Qi, Feng, Xiang, Han, Fang, Xu, Xiao-Tao, Shen, Ren-Juan, Li, Yang, Jin, Zi-Bing, Yu, Huan-Yun
Publicado 2021

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations

por Wu, Kun-Chao, Lv, Ji-Neng, Yang, Hui, Yang, Feng-Mei, Lin, Rui, Lin, Qiang, Shen, Ren-Juan, Wang, Jun-Bin, Duan, Wen-Hua, Hu, Min, Zhang, Jun, He, Zhan-Long, Jin, Zi-Bing
Publicado 2020

Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction

por Giffen, Kimberlee P., Li, Yi, Liu, Huizhan, Zhao, Xiao-Chang, Zhang, Chang-Jun, Shen, Ren-Juan, Wang, Tianying, Janesick, Amanda, Chen, Bo-Bei, Gong, Shu-Sheng, Kachar, Bechara, Jin, Zi-Bing, He, David Z.
Publicado 2022