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Molecular Vision|June 21, 2006
Novel mutations of the PAX6 gene identified in Chinese patients with aniridiaPanfeng Wang, Xiangming Guo, Xiaoyun Jia, et al.Ebiomedicine|May 27, 2020
Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosaZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.Plos One|January 13, 2017
Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic NeuropathyYadi Li, Jie Li, Xiaoyun Jia, et al.Molecular Vision|August 19, 2011
Mutation spectrum of PAX6 in Chinese patients with aniridiaXiaohui Zhang, Panfeng Wang, Shiqiang Li, et al.Journal of Human Genetics|October 22, 2005
Linkage analysis of two families with X-linked recessive congenital motor nystagmusXiangming Guo, Shiqiang Li, Xiaoyun Jia, et al.The British Journal of Ophthalmology|October 17, 2015
KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathyHuan Hu, Xueshan Xiao, Shiqiang Li, et al.JAMA Ophthalmology|June 7, 2014
Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patientsShiqiang Li, Li Huang, Xueshan Xiao, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|April 1, 2021
Systemic Genotype-Phenotype Analysis of MYOC Variants Based on Exome Sequencing and Literature ReviewXueqing Li, Xueshan Xiao, Shiqiang Li, et al.Molecular Vision|October 29, 2009
Sequence variations of GRM6 in patients with high myopiaXiaoyu Xu, Shiqiang Li, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|January 15, 2019
Germline Mutations in CTNNB1 Associated With Syndromic FEVR or Norrie DiseaseWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.Pageof 17