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Optometry and Vision Science : Official Publication of the American Academy of Optometry|October 9, 2013
Cone-rod dysfunction is a sign of early-onset high myopiaPanfeng Wang, Xueshan Xiao, Li Huang, et al.
Molecular Vision|October 22, 2009
An evaluation of OPTC and EPYC as candidate genes for high myopiaPanfeng Wang, Shiqiang Li, Xueshan Xiao, et al.
International Journal of Molecular Medicine|February 19, 2014
Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screeningShiqiang Li, Tao Shen, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|January 26, 2007
The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individualsQingjiong Zhang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|June 21, 2011
Mutational screening of six genes in Chinese patients with congenital cataract and microcorneaWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Plos One|June 27, 2014
Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS geneWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 20, 2021
Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 InvolvementYi Jiang, Shiqiang Li, Xueshan Xiao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 10, 2010
Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterizationXiangming Guo, Xueshan Xiao, Shiqiang Li, et al.
Plos One|July 11, 2015
Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel AnalysisWei Xin, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|April 21, 2010
A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomalyXiuhua Jia, Xiangming Guo, Xiaoyun Jia, et al.
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