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Molecular Reproduction and Development|July 6, 2004
Identification and analysis of stage-specific expression of lysosome-associated protein transmembrane 4alpha gene during development of preimplantation rabbit nuclear transfer embryoWeidong Yu, Xin He, Guisheng Liu, et al.
Molecular Vision|May 10, 2011
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypesHuiqin Yang, Xueshan Xiao, Shiqiang Li, 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.
Biochemical and Biophysical Research Communications|November 16, 2010
mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese populationXiaoyun Jia, Shiqiang Li, Panfeng Wang, et al.
Experimental Eye Research|February 18, 2018
Frequent mutations of RetNet genes in eoHM: Further confirmation in 325 probands and comparison with late-onset high myopia based on exome sequencingLin Zhou, Xueshan Xiao, Shiqiang Li, et al.
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