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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.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.Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|July 2, 2026
Sensitive detection of prostate cancer antigen 3 (PCA3) in urine based upon CRISPR/Cas12a and gold nanorods (AuNRs)Wenjie Liao, Shiqiang Li, Shaoyong Wu, 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.Journal of Human Genetics|July 13, 2006
Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1Xiangming Guo, Huangxuan Shen, Xueshan Xiao, et al.Human Genetics|June 8, 2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, et al.Pageof 22