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Investigative Ophthalmology & Visual Science|December 11, 2025
Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor MorphologyYingwei Wang, Shuhan Zhang, Yuxi Zheng, et al.
The British Journal of Ophthalmology|September 30, 2022
Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritanceYingwei Wang, Xueshan Xiao, Xueqing Li, et al.
Molecular Vision|March 30, 2007
Mutations in NYX of individuals with high myopia, but without night blindnessQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.
The British Journal of Ophthalmology|October 14, 2021
Clinical and genetic features of retinoschisis in 120 families with RS1 mutationsSainan Xiao, Wenmin Sun, Xueshan Xiao, et al.
American Journal of Human Genetics|November 26, 2008
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutationYanli Ji, A-Mei Zhang, Xiaoyun Jia, et al.
Investigative Ophthalmology & Visual Science|August 22, 2022
Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod DystrophyJunwen Wang, Yingwei Wang, Shiqiang Li, et al.
Plos One|November 24, 2011
Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patientsA-Mei Zhang, Xiaoyun Jia, Rui Bi, et al.
Investigative Ophthalmology & Visual Science|April 25, 2023
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic MechanismYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|May 11, 2013
Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosisYabin Chen, Qingyan Zhang, Tao Shen, et al.
Investigative Ophthalmology & Visual Science|June 27, 2015
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1Jiali Li, Bei Gao, Liping Guan, et al.
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