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Molecular Vision|July 30, 2005
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612Qingjiong Zhang, Xiangming Guo, Xueshan Xiao, et al.
Molecular Vision|December 1, 2004
Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese familyQingjiong Zhang, Xiangming Guo, Xueshan Xiao, et al.
Molecular Vision|February 13, 2013
Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathyYabin Chen, Xiaoyun Jia, Panfeng Wang, et al.
Experimental Eye Research|December 21, 2020
Spectrum-frequency and genotype-phenotype analysis of rhodopsin variantsHualei Luo, Xueshan Xiao, Shiqiang Li, et al.
Molecular Medicine Reports|September 6, 2012
Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degenerationJunhui Yi, Shiqiang Li, Xiaoyun Jia, et al.
American Journal of Medical Genetics. Part A|January 20, 2026
Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature ReviewYijun Dong, Xueshan Xiao, Shiqiang Li, et al.
Frontiers in Genetics|November 8, 2021
Genotype-Phenotype Analysis of <i>RPGR</i> Variations: Reporting of 62 Chinese Families and a Literature ReviewJunxing Yang, Lin Zhou, Jiamin Ouyang, et al.
Acta Ophthalmologica|February 9, 2022
Landscape of pathogenic variants in six pre-mRNA processing factor genes for retinitis pigmentosa based on large in-house data sets and database comparisonsJunwen Wang, Xueshan Xiao, Shiqiang Li, et al.
Biochemical and Biophysical Research Communications|September 11, 2012
CRX variants in cone-rod dystrophy and mutation overviewLi Huang, Xueshan Xiao, Shiqiang Li, et al.
American Journal of Ophthalmology|December 21, 2020
Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 MutationsYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.
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