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Molecular Medicine Reports|April 9, 2013
Screening for variants in 20 genes in 130 unrelated patients with cone-rod dystrophyLi Huang, Shiqiang Li, Xueshan Xiao, et al.The British Journal of Ophthalmology|June 22, 2021
Biallelic variants in <i>CPAMD8</i> are associated with primary open-angle glaucoma and primary angle-closure glaucomaXueqing Li, Wenmin Sun, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|December 9, 2008
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genesPanfeng Wang, Shiqiang Li, Xueshan Xiao, et al.Clinical Genetics|August 22, 2022
Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafishJiamin Ouyang, Shiqiang Li, Wenmin Sun, et al.Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|December 14, 2011
Common variants in chromosome 4q25 are associated with myopia in Chinese adultsYang Gao, Panfeng Wang, Shiqiang Li, et al.International Journal of Molecular Medicine|January 17, 2012
Novel RS1 mutations associated with X-linked juvenile retinoschisisJunhui Yi, Shiqiang Li, Xiaoyun Jia, et al.Molecular Vision|May 26, 2021
Heterozygous <i>GJA1</i> variants with ocular phenotype: Missense in domain but truncation out of domainXueqing Li, Xueshan Xiao, Shiqiang Li, et al.Human Genetics|April 6, 2020
Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large familiesWenmin Sun, Shiqiang Li, Xiaoyun Jia, et al.Journal of Human Genetics|August 24, 2012
Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1Lin Li, Xueshan Xiao, Changxian Yi, et al.International Journal of Molecular Medicine|August 28, 2015
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucomaXiaobo Huang, Xueshan Xiao, Xiaoyun Jia, et al.Pageof 17