An evaluation of OPTC and EPYC as candidate genes for high myopia

Por Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2009

Mutational screening of six genes in Chinese patients with congenital cataract and microcornea

Por Sun, Wenmin, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2011

Mutation analysis of 12 genes in Chinese families with congenital cataracts

Por Sun, Wenmin, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2011

Exome Sequencing of 18 Chinese Families with Congenital Cataracts: A New Sight of the NHS Gene

Por Sun, Wenmin, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2014

Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis

Por Li, Jie, Jia, Xiaoyun, Li, Shiqiang, Fang, Shaohua, Guo, Xiangming
Publicado em 2014

X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia

Por Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Publicado no Mol Vis (2016)

Evaluation of EGR1 as a candidate gene for high myopia

Por Li, Tuo, Xiao, Xueshan, Li, Shiqiang, Xing, Yiqiao, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2008

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism

Por Fang, Shaohua, Guo, Xiangming, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Zhang, Qingjiong
Publicado em 2008

Evaluation of MFRP as a candidate gene for high hyperopia

Por Wang, Panfeng, Yang, Zhikuan, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2009

Investigation of the association between CALCRL polymorphisms and primary angle closure glaucoma

Por Cao, Dan, Liu, Xing, Guo, Xiangming, Cong, Yanhong, Huang, Jingjing, Mao, Zhen
Publicado em 2009

Sequence variations of GRM6 in patients with high myopia

Por Xu, Xiaoyu, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2009

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters’ anomaly

Por Jia, Xiuhua, Guo, Xiangming, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Zhang, Qingjiong
Publicado em 2010

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

Por Ji, Yanli, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2010

PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1

Por Wang, Juan, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2010

Mutation spectrum of PAX6 in Chinese patients with aniridia

Por Zhang, Xiaohui, Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2011

A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family

Por Xiao, Xueshan, Guo, Xiangming, Jia, Xiaoyun, Li, Shiqiang, Wang, Panfeng, Zhang, Qingjiong
Publicado em 2011

Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

Por Zhang, A-Mei, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong, Yao, Yong-Gang
Publicado em 2012

Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy

Por Yang, Huiqin, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado em 2012

Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis

Por Xin, Wei, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Publicado no PLoS One (2015)

Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy

Por Li, Yadi, Li, Jie, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming
Publicado no PLoS One (2017)