1.Comprehensive Mutation Analysis by Whole-Exome Sequencing in 41 Chinese Families With Leber Congenital Amaurosis

Chen, YB, Zhang, QY,     More...

Chen, YB, Zhang, QY, Shen, T, Xiao, XS, Li, SQ, Guan, LP, Zhang, JG, Zhu, ZH, Yin, Y, Wang, PF, Guo, XM, Wang, J, Zhang, QJ     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2013, Volume 54, Issue 6, Pages 4351-4357

收錄情况： WOS

WOS核心合集引用: 83  2024影響因子:  4.7  发表年影響因子:  3.661 

2.Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1

Li, JL, Gao, B, Guan     More...

Li, JL, Gao, B, Guan, LP, Xiao, XS, Zhang, JG, Li, SQ, Jiang, H, Jia, XY, Yang, JH, Guo, XM, Yin, Y, Wang, J, Zhang, QJ     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2015, Volume 56, Issue 6, Pages 4150-4155

收錄情况： WOS

WOS核心合集引用: 45  2024影響因子:  4.7  发表年影響因子:  3.427