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Journal of Human Genetics|September 15, 2006
Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathyXiaoyun Jia, Shiqiang Li, Xueshan Xiao, et al.Current Eye Research|May 9, 2012
Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie diseaseHuiqin Yang, Shiqiang Li, Xueshan Xiao, et al.Molecular Vision|August 26, 2011
Mutation analysis of 12 genes in Chinese families with congenital cataractsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.Journal of Human Genetics|March 14, 2007
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, et al.Biochemical and Biophysical Research Communications|September 14, 2010
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosaShiqiang Li, Xueshan Xiao, Panfeng Wang, et al.Molecular Vision|November 11, 2016
X-linked heterozygous mutations in <i>ARR3</i> cause female-limited early onset high myopiaXueshan Xiao, Shiqiang Li, Xiaoyun Jia, 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.Molecular Vision|January 27, 2009
Evaluation of MFRP as a candidate gene for high hyperopiaPanfeng Wang, Zhikuan Yang, Shiqiang Li, et al.Molecular Vision|November 4, 2008
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinismShaohua Fang, Xiangming Guo, Xiaoyun Jia, et al.Pageof 22