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Current Eye Research|June 26, 2018
Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger SyndromeXun Wang, Xing Liu, Liqin Huang, et al.
Molecular Vision|March 10, 2016
Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopiaJiali Li, Bei Gao, Xueshan Xiao, et al.
Molecular Vision|December 24, 2011
Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studiesQin Wang, Yang Gao, Panfeng Wang, et al.
International Journal of Molecular Sciences|March 11, 2023
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the LiteratureDi Zhu, Junwen Wang, Yingwei Wang, et al.
Molecular Vision|December 1, 2004
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutationQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Investigative Ophthalmology & Visual Science|December 20, 2014
Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencingDan Jiang, Jiali Li, Xueshan Xiao, et al.
Experimental Eye Research|August 16, 2022
Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisonsYingwei Wang, Yi Jiang, Xueqing Li, et al.
Molecular Vision|January 9, 2010
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or colobomaXiaohui Zhang, Shiqiang Li, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|May 15, 2014
Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucomaXiaobo Huang, Miaoling Li, Xiangming Guo, et al.
American Journal of Ophthalmology|September 28, 2021
Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11Junxing Yang, Xueshan Xiao, Shiqiang Li, et al.
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