Novel CHM mutations identified in Chinese families with Choroideremia

by Cai, Xue-Bi, Huang, Xiu-Feng, Tong, Yi, Lu, Qin-Kang, Jin, Zi-Bing
Published 2016

Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa

by Wu, Juan, Chen, Lijia, Tam, Oi Sin, Huang, Xiu-Feng, Pang, Chi-Pui, Jin, Zi-Bing
Published 2014

Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells

by Zhang, Yilan, Ge, Xianglian, Yang, Fayu, Zhang, Liping, Zheng, Jiayong, Tan, Xuefang, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Published 2014

‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration

by Ran, Xia, Cai, Wei-Jun, Huang, Xiu-Feng, Liu, Qi, Lu, Fan, Qu, Jia, Wu, Jinyu, Jin, Zi-Bing
Published 2014

Identification of a Novel GJA8 (Cx50) Point Mutation Causes Human Dominant Congenital Cataracts

by Ge, Xiang-Lian, Zhang, Yilan, Wu, Yaming, LV, Jineng, Zhang, Wei, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Published 2014

Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families

by Lin, Bing, Cai, Xue-Bi, Zheng, Zhi-Li, Huang, Xiu-Feng, Liu, Xiao-Ling, Qu, Jia, Jin, Zi-Bing
Published 2016

CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome

by Dai, Ma-Li, Huang, Xiu-Feng, Wang, Qing-Feng, Cai, Wei-Jun, Jin, Zi-Bing, Wang, Yuqin
Published 2016

‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration

by Ran, Xia, Cai, Wei-Jun, Huang, Xiu-Feng, Liu, Qi, Lu, Fan, Qu, Jia, Wu, Jinyu, Jin, Zi-Bing
Published 2014

Identification of Three Novel Mutations in the FRMD7 Gene for X-linked Idiopathic Congenital Nystagmus

by Zhang, Xiao, Ge, Xianglian, Yu, Ying, Zhang, Yilan, Wu, Yaming, Luan, Yin, Sun, Ji, Qu, Jia, Jin, Zi-Bing, Gu, Feng
Published 2014

SLC7A14 linked to autosomal recessive retinitis pigmentosa

by Jin, Zi-Bing, Huang, Xiu-Feng, Lv, Ji-Neng, Xiang, Lue, Li, Dong-Qing, Chen, Jiangfei, Huang, Changjiang, Wu, Jinyu, Lu, Fan, Qu, Jia
Published 2014

Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing

by Zhang, Xiao, Ge, Xianglian, Shi, Wei, Huang, Ping, Min, Qingjie, Li, Minghan, Yu, Xinping, Wu, Yaming, Zhao, Guangyu, Tong, Yi, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Published 2014

Comprehensive Molecular Diagnosis of Bardet-Biedl Syndrome by High-Throughput Targeted Exome Sequencing

by Xing, Dong-Jun, Zhang, Hong-Xing, Huang, Na, Wu, Kun-Chao, Huang, Xiu-Feng, Huang, Fang, Tong, Yi, Pang, Chi-Pui, Qu, Jia, Jin, Zi-Bing
Published 2014

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

by Huang, Xiu-Feng, Xiang, Ping, Chen, Jie, Xing, Dong-Jun, Huang, Na, Min, Qingjie, Gu, Feng, Tong, Yi, Pang, Chi-Pui, Qu, Jia, Jin, Zi-Bing
Published 2013

The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing

by Lin, Zhong, Mao, Guang Yun, Vasudevan, Balamurali, Jin, Zi Bing, Ciuffreda, Kenneth J., Jhanji, Vishal, Zhou, Hong Jia, Wang, Ning Li, Liang, Yuan Bo
Published 2015

Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia

by Li, Fen-Fen, Huang, Xiu-Feng, Chen, Jie, Yu, Xu-Dong, Zheng, Mei-Qin, Lu, Fan, Jin, Zi-Bing, Gan, De-Kang
Published 2015

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family

by Zhang, Liping, Shi, Wei, Song, Liming, Zhang, Xiao, Cheng, Lulu, Wang, Yanfang, Ge, Xianglian, Li, Wei, Zhang, Wei, Min, Qingjie, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Published 2014

Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus

by Zhao, Hui, Huang, Xiu-Feng, Zheng, Zhi-Li, Deng, Wen-Li, Lei, Xin-Lan, Xing, Dong-Jun, Ye, Liang, Xu, Su-Zhong, Chen, Jie, Zhang, Fang, Yu, Xin-Ping, Jin, Zi-Bing
Published 2016

A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

by Zhang, Liyun, Xiang, Lue, Liu, Yiwen, Venkatraman, Prahatha, Chong, Leelyn, Cho, Jin, Bonilla, Sylvia, Jin, Zi-Bing, Pang, Chi Pui, Ko, Kam Ming, Ma, Ping, Zhang, Mingzhi, Leung, Yuk Fai
Published 2016

Correction: A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

by Zhang, Liyun, Xiang, Lue, Liu, Yiwen, Venkatraman, Prahatha, Chong, Leelyn, Cho, Jin, Bonilla, Sylvia, Jin, Zi-Bing, Pang, Chi Pui, Ko, Kam Ming, Ma, Ping, Zhang, Mingzhi, Leung, Yuk Fai
Published 2016