Wenmin Sun

Detection of Mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 Families With Early-Onset High Myopia by Exome Sequencing

Dan Jiang, Jiali Li, Xueshan Xiao et al. · Investigative Ophthalmology & Visual Science · 2014 · 121 citations · Full text

Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes

Wenmin Sun, Li Huang, Yan Xu et al. · Investigative Ophthalmology & Visual Science · 2015 · 106 citations

Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands

Li Huang, Xueshan Xiao, Shiqiang Li et al. · Experimental Eye Research · 2016 · 67 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +9

Exome Sequencing of 18 Chinese Families with Congenital Cataracts: A New Sight of the NHS Gene

Wenmin Sun, Xueshan Xiao, Shiqiang Li et al. · PLoS ONE · 2014 · 61 citations · Full text

<b>Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening</b>

Jianjun Chen, Qiwei Wang, Patricia E. Cabrera et al. · Investigative Ophthalmology & Visual Science · 2017 · 56 citations · Full text