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Molecular Vision|November 22, 2012
Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopiaXiaodong Jiao, Panfeng Wang, Shiqiang Li, et al.
Chemical Biology & Drug Design|December 21, 2006
Radiolabeling and in vitro and in vivo characterization of [18F]FB-[R(8,15,21), L17]-VIP as a PET imaging agent for tumor overexpressed VIP receptorsDengfeng Cheng, Duanzhi Yin, Gucai Li, 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.
Current Eye Research|June 26, 2018
Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger SyndromeXun Wang, Xing Liu, Liqin Huang, et al.
Molecular Vision|March 10, 2016
Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopiaJiali Li, Bei Gao, Xueshan Xiao, et al.
Plos One|October 27, 2010
Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>CDandan Yu, Xiaoyun Jia, A-Mei Zhang, et al.
Journal of Medical Genetics|December 22, 2018
Biallelic mutations in <i>USP45,</i> encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosisZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Investigative Ophthalmology & Visual Science|January 15, 2015
Evaluation of 12 myopia-associated genes in Chinese patients with high myopiaJiali Li, Dan Jiang, Xueshan Xiao, et al.
Human Molecular Genetics|January 29, 2019
CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projectionJiamin Ouyang, Wenmin Sun, Xueshan Xiao, et al.
Photodiagnosis and Photodynamic Therapy|March 7, 2025
The influence of malnutrition-sarcopenia syndrome on chorioretinal microvasculature using optical coherence tomography angiographyYitong Cheng, Jiawei Wang, Shanshan Li, et al.
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