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Xiangming Guo · SciRah

Researcher profile · Semantic Scholar

Xiangming Guo

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Xiangming Guo — researcher profile on SciRah

h-index: 36
Works: 128
Citations: 3,668

Most-cited papers

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing
Yan Xu, L. Guan, T. Shen, Jian-Guo Zhang +9 more
2014Human Genetics178 citations
Semantic Scholar
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Yanli Ji, A-Mei Zhang, Xiao-yun Jia, Ya-Ping Zhang +6 more
2008American Journal of Human Genetics146 citations Open access
Semantic Scholar
Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis
Lin Li, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +5 more
2011PLoS ONE119 citations Open access
Semantic Scholar
Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.
Dan Jiang, Jia-Li Li, Xueshan Xiao, Shi-qiang Li +4 more
2014Investigative Ophthalmology and Visual Science108 citations Open access
Semantic Scholar
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, Xueshan Xiao +6 more
2015Investigative Ophthalmology and Visual Science98 citations Open access
Semantic Scholar
Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosis.
Yabin Chen, Qingyan Zhang, T. Shen, Xueshan Xiao +9 more
2013Investigative Ophthalmology and Visual Science95 citations Open access
Semantic Scholar
KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy
Huan Hu, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +2 more
2015British Journal of Ophthalmology77 citations Open access
Semantic Scholar
X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia
Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia, Xiangming Guo +1 more
2016Molecular Vision76 citations
Semantic Scholar
Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy.
Xueshan Xiao, Gui-Ying Mai, Shi-qiang Li, Xiangming Guo +1 more
2011Biochemical and Biophysical Research Communications - BBRC75 citations
Semantic Scholar
Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia
Qin Wang, Pan-Feng Wang, Shi-qiang Li, Xueshan Xiao +5 more
2010Molecular Vision68 citations
Semantic Scholar
Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands.
Li Huang, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +6 more
2016Experimental Eye Research67 citations
Semantic Scholar
Mutation analysis of 12 genes in Chinese families with congenital cataracts
Wenmin Sun, Xueshan Xiao, Shi-qiang Li, Xiangming Guo +1 more
2011Molecular Vision66 citations
Semantic Scholar
Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gene with PACG in southern China
Yanhong Cong, Xiangming Guo, Xing Liu, D. Cao +5 more
2009Molecular Vision65 citations
Semantic Scholar
Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.
Jia-Li Li, Dan Jiang, Xueshan Xiao, Shi-qiang Li +4 more
2015Investigative Ophthalmology and Visual Science64 citations Open access
Semantic Scholar
Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes
Li Huang, Qingyan Zhang, Shi-qiang Li, L. Guan +11 more
2013PLoS ONE64 citations Open access
Semantic Scholar
CRX variants in cone-rod dystrophy and mutation overview.
Li Huang, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +3 more
2012Biochemical and Biophysical Research Communications - BBRC60 citations
Semantic Scholar
Exome Sequencing of 18 Chinese Families with Congenital Cataracts: A New Sight of the NHS Gene
Wenmin Sun, Xueshan Xiao, Shi-qiang Li, Xiangming Guo +1 more
2014PLoS ONE59 citations Open access
Semantic Scholar
Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucoma.
Xiaobo Huang, Miao-Ling Li, Xiangming Guo, Shi-qiang Li +4 more
2014Investigative Ophthalmology and Visual Science57 citations Open access
Semantic Scholar
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
Jia-Li Li, Bei Gao, L. Guan, Xueshan Xiao +9 more
2015Investigative Ophthalmology and Visual Science53 citations
Semantic Scholar
Replication study supports CTNND2 as a susceptibility gene for high myopia.
Boyu Lu, Dan Jiang, Pan-Feng Wang, Yang Gao +6 more
2011Investigative Ophthalmology and Visual Science49 citations
Semantic Scholar
Mutations in NYX of individuals with high myopia, but without night blindness
Qing-Jiong Zhang, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +7 more
2007Molecular Vision49 citations
Semantic Scholar
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes.
Pan-Feng Wang, Shi-qiang Li, Xueshan Xiao, Xiao-yun Jia +3 more
2009Investigative Ophthalmology and Visual Science48 citations
Semantic Scholar
Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia
Jia-Li Li, Bei Gao, Xueshan Xiao, Shi-qiang Li +4 more
2016Molecular Vision47 citations
Semantic Scholar
Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients
A-Mei Zhang, Xiao-yun Jia, R. Bi, A. Salas +7 more
2011PLoS ONE47 citations Open access
Semantic Scholar
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese
Yanli Ji, Xiao-yun Jia, Shi-qiang Li, Xueshan Xiao +2 more
2010Molecular Vision47 citations
Semantic Scholar
Mutational screening of six genes in Chinese patients with congenital cataract and microcornea
Wenmin Sun, Xueshan Xiao, Shi-qiang Li, Xiangming Guo +1 more
2011Molecular Vision43 citations
Semantic Scholar
Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy
H. Yang, Shi-qiang Li, Xueshan Xiao, Pan-Feng Wang +2 more
2012Molecular Vision42 citations
Semantic Scholar
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma
Xiao-Hui Zhang, Shi-qiang Li, Xueshan Xiao, Xiao-yun Jia +4 more
2009Molecular Vision38 citations
Semantic Scholar
Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencing
Yan Xu, L. Guan, Xueshan Xiao, Jian-Guo Zhang +8 more
2015Molecular Vision37 citations
Semantic Scholar
Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterization.
Xiangming Guo, Xueshan Xiao, Shi-qiang Li, Pan-Feng Wang +2 more
2010A M A Archives of Ophthalmology37 citations Open access
Semantic Scholar
Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patients.
Shi-qiang Li, Li Huang, Xueshan Xiao, Xiao-yun Jia +2 more
2014JAMA ophthalmology36 citations
Semantic Scholar
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1
Qing-Jiong Zhang, Shi-qiang Li, Xueshan Xiao, Xiao-yun Jia +1 more
2007Journal of Human Genetics36 citations
Semantic Scholar
Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma
Dan Jiang, Zhikuan Yang, Shi-qiang Li, Xueshan Xiao +5 more
2013Molecular Vision35 citations
Semantic Scholar
The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations.
Yang Zou, Xiao-yun Jia, A-Mei Zhang, Wenjun Wang +5 more
2010Biochemical and Biophysical Research Communications - BBRC35 citations
Semantic Scholar
Sequence variations of GRM6 in patients with high myopia
Xiaoyu Xu, Shi-qiang Li, Xueshan Xiao, Pan-Feng Wang +2 more
2009Molecular Vision34 citations
Semantic Scholar
Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probands.
Yan Xu, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +6 more
2016Experimental Eye Research33 citations
Semantic Scholar
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma.
Xiaobo Huang, Xueshan Xiao, Xiao-yun Jia, Shi-qiang Li +4 more
2015International Journal of Molecular Medicine32 citations Open access
Semantic Scholar
Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa.
Shi-qiang Li, L. Guan, Shao-Hua Fang, Hui Jiang +8 more
2014International Journal of Molecular Medicine31 citations Open access
Semantic Scholar
PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1
Juan Wang, Shi-qiang Li, Xueshan Xiao, Pan-Feng Wang +2 more
2010Molecular Vision31 citations
Semantic Scholar
Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia
Xiao-Dong Jiao, Pan-Feng Wang, Shi-qiang Li, An-Ren Li +3 more
2012Molecular Vision30 citations
Semantic Scholar
Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis
Jie Li, Xiao-yun Jia, Shi-qiang Li, Shao-Hua Fang +1 more
2014Molecular Vision28 citations
Semantic Scholar
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosa.
Shi-qiang Li, Xueshan Xiao, Pan-Feng Wang, Xiangming Guo +1 more
2010Biochemical and Biophysical Research Communications - BBRC27 citations
Semantic Scholar
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy
Dandan Yu, Xiao-yun Jia, A-Mei Zhang, Xiangming Guo +3 more
2010Neurogenetics27 citations
Semantic Scholar
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma
Mei Yang, Xiangming Guo, Xing Liu, Huang-Xuan Shen +5 more
2009Molecular Vision27 citations
Semantic Scholar
A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family
Xueshan Xiao, Xiangming Guo, Xiao-yun Jia, Shi-qiang Li +2 more
2011Molecular Vision26 citations
Semantic Scholar
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism
Shao-Hua Fang, Xiangming Guo, Xiao-yun Jia, Xueshan Xiao +2 more
2008Molecular Vision26 citations
Semantic Scholar
Mutation spectrum of PAX6 in Chinese patients with aniridia
Xiao-Hui Zhang, Pan-Feng Wang, Shi-qiang Li, Xueshan Xiao +2 more
2011Molecular Vision25 citations
Semantic Scholar
Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis
W. Xin, Xueshan Xiao, Shi-qiang Li, Xiao-yun Jia +2 more
2015PLoS ONE24 citations Open access
Semantic Scholar
Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy
Ya-Di Li, J. Li, Xiao-yun Jia, Xueshan Xiao +2 more
2017PLoS ONE23 citations Open access
Semantic Scholar
Investigation of the association between CALCRL polymorphisms and primary angle closure glaucoma
D. Cao, Xing Liu, Xiangming Guo, Yanhong Cong +2 more
2009Molecular Vision23 citations
Semantic Scholar

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Shi-qiang Li — researcher profile on SciRah
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Qing-Jiong Zhang — researcher profile on SciRah
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Pan-Feng Wang — researcher profile on SciRah

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Ye Yin — researcher profile on SciRah

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Jun Wang — researcher profile on SciRah

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Li Huang — researcher profile on SciRah

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Xing Liu — researcher profile on SciRah