FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Shiqiang Li

Research Profile

Living Beings

Concepts & Ideas

Physiology

Geographic Areas

China

Procedures

Chemicals & Drugs

Disorders

Phenomena

Polymorphism, Single-Stranded Conformational

Co-author Network

Publications

TOP 3
Li Huang; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Screening for variants in 20 genes in 130 unrelated patients with cone-rod dystrophy.
Li Huang; Xiaoyun Jia; Lin Li; Shiqiang Li; Wenmin Sun; Panfeng Wang; Xueshan Xiao; Yang Gao; Xiangming Guo; Qingjiong Zhang
Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophy.
Yabin Chen; Xiangming Guo; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Qingjiong Zhang
Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Shiqiang Li (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Li Huang; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Screening for variants in 20 genes in 130 unrelated patients with cone-rod dystrophy.
Molecular medicine reports 2013;7(6):1779-85.
2013: Li Huang; Xiaoyun Jia; Lin Li; Shiqiang Li; Wenmin Sun; Panfeng Wang; Xueshan Xiao; Yang Gao; Xiangming Guo; Qingjiong Zhang
Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophy.
Neuroscience letters 2013;541():179-83.
2013: Yabin Chen; Xiangming Guo; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Qingjiong Zhang
Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy.
Molecular vision 2013;19():292-302.
2012: Li Huang; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
CRX variants in cone-rod dystrophy and mutation overview.
Biochemical and biophysical research communications 2012;426(4):498-503.
2012: Panfeng Wang; Xueshan Xiao; Xiangming Guo; Shiqiang Li; Wenmin Sun; Qingjiong Zhang
PAX6 mutations identified in 4 of 35 families with microcornea.
Investigative ophthalmology & visual science 2012;53(10):6338-42.
2012: Qin Wang; Yang Gao; Xiangming Guo; Shiqiang Li; Qingjiong Zhang
Mutation screening of TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness.
International journal of molecular medicine 2012;30(3):521-6.
2012: Huiqin Yang; Xiangming Guo; Shiqiang Li; Xueshan Xiao; Qingjiong Zhang
Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie disease.
Current eye research 2012;37(8):726-9.
2012: Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation.
Ophthalmic genetics 2012;33(2):119-21.
2012: Xueshan Xiao; Xiangming Guo; Shiqiang Li; Qingjiong Zhang
A novel locus for autosomal dominant congenital motor nystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692.
Human genetics 2012;131(5):697-702.
2012: Juan Wang; Panfeng Wang; Xueshan Xiao; Yang Gao; Shiqiang Li; Qingjiong Zhang
High myopia is not associated with single nucleotide polymorphisms in the COL2A1 gene in the Chinese population.
Molecular medicine reports 2012;5(1):133-7.
2011: Panfeng Wang; Xueshan Xiao; Xiangming Guo; Shiqiang Li; Qingjiong Zhang
KIF21A novel deletion and recurrent mutation in patients with congenital fibrosis of the extraocular muscles-1.
International journal of molecular medicine 2011;28(6):973-5.
2011: Xueshan Xiao; Guiying Mai; Shiqiang Li; Xiangming Guo; Qingjiong Zhang
Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy.
Biochemical and biophysical research communications 2011;409(2):181-6.
2011: Boyu Lu; Wenmin Sun; Panfeng Wang; Xueshan Xiao; Yang Gao; Xiangming Guo; Xiaoyun Jia; Dan Jiang; Shiqiang Li; Qingjiong Zhang
Replication study supports CTNND2 as a susceptibility gene for high myopia.
Investigative ophthalmology & visual science 2011;52(11):8258-61.
2011: Wenmin Sun; Xueshan Xiao; Xiangming Guo; Shiqiang Li; Qingjiong Zhang
Mutation analysis of 12 genes in Chinese families with congenital cataracts.
Molecular vision 2011;17():2197-206.
2011: Xiaohui Zhang; Xiangming Guo; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Qingjiong Zhang
Mutation spectrum of PAX6 in Chinese patients with aniridia.
Molecular vision 2011;17():2139-47.
2011: Wenmin Sun; Xueshan Xiao; Xiangming Guo; Shiqiang Li; Qingjiong Zhang
Mutational screening of six genes in Chinese patients with congenital cataract and microcornea.
Molecular vision 2011;17():1508-13.
2011: Lin Li; Xueshan Xiao; Shiqiang Li; Xiaoyun Jia; Panfeng Wang; Xiangming Guo; Xiaodong Jiao; Qingjiong Zhang; J Fielding Hejtmancik
Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis.
PloS one 2011;6(5):e19458.
2011: Huiqin Yang; Xueshan Xiao; Shiqiang Li; Guiying Mai; Qingjiong Zhang
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes.
Molecular vision 2011;17():1128-35.
2010: Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.
Biochemical and biophysical research communications 2010;403(2):237-41.
2010: Xiangming Guo; Xueshan Xiao; Shiqiang Li; Panfeng Wang; Xiaoyun Jia; Qingjiong Zhang
Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterization.
Archives of ophthalmology 2010;128(11):1473-9.
2010: Shiqiang Li; Xueshan Xiao; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosa.
Biochemical and biophysical research communications 2010;401(1):42-7.
2010: Juan Wang; Shiqiang Li; Xueshan Xiao; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1.
Molecular vision 2010;16():1146-53.
2010: Xiaoyun Jia; Xiangming Guo; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly.
Molecular vision 2010;16():676-81.
2010: Yanli Ji; Juan Wang; Xueshan Xiao; Shiqiang Li; Xiangming Guo; Qingjiong Zhang
Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa.
Current eye research 2010;35(1):73-9.
2009: Panfeng Wang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Xiaodong Jiao; Xiangming Guo; Qingjiong Zhang
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes.
Investigative ophthalmology & visual science 2009;50(4):1546-51.
2009: Xiaohui Zhang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Panfeng Wang; Huangxuan Shen; Xiangming Guo; Qingjiong Zhang
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma.
Molecular vision 2009;15():2911-8.
2009: Xiaoyu Xu; Shiqiang Li; Xueshan Xiao; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
Sequence variations of GRM6 in patients with high myopia.
Molecular vision 2009;15():2094-100.
2009: Panfeng Wang; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
An evaluation of OPTC and EPYC as candidate genes for high myopia.
Molecular vision 2009;15():2045-9.
2009: Yanhong Cong; Xiangming Guo; Xing Liu; Dan Cao; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Shaohua Fang; Qingjiong Zhang
Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gene with PACG in southern China.
Molecular vision 2009;15():1412-7.
2009: Mei Yang; Xiangming Guo; Xing Liu; Huangxuan Shen; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Shaohua Fang; Qingjiong Zhang
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma.
Molecular vision 2009;15():432-7.
2009: Zhikuan Yang; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.
Molecular vision 2009;15():312-8.
2009: Panfeng Wang; Zhikuan Yang; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Evaluation of MFRP as a candidate gene for high hyperopia.
Molecular vision 2009;15():181-6.
2008: Yanli Ji; A-Mei Zhang; Xiaoyun Jia; Ya-Ping Zhang; Xueshan Xiao; Shiqiang Li; Xiangming Guo; Hans-Jürgen Bandelt; Qingjiong Zhang; Yong-Gang Yao
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
American journal of human genetics 2008;83(6):760-8.
2008: Shaohua Fang; Xiangming Guo; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.
Molecular vision 2008;14():1974-82.
2007: Qingjiong Zhang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Xiangming Guo
The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals.
Investigative ophthalmology & visual science 2007;48(2):530-3.
2007: Qingjiong Zhang; Xueshan Xiao; Shiqiang Li; Xiangming Guo
FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.
Molecular vision 2007;13():1375-8.
2007: Qingjiong Zhang; Xueshan Xiao; Shiqiang Li; Xiaoyun Jia; Zhikuan Yang; Shizhou Huang; Rafael C Caruso; Tianqin Guan; Yuri V Sergeev; Xiangming Guo; J Fielding Hejtmancik
Mutations in NYX of individuals with high myopia, but without night blindness.
Molecular vision 2007;13():330-6.
2007: Qingjiong Zhang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Xiangming Guo
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1.
Journal of human genetics 2007;52(5):469-72.
2006: Xiaoyun Jia; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.
Journal of human genetics 2006;51(10):851-6.
2006: Xiangming Guo; Huangxuan Shen; Xueshan Xiao; Qilin Dai; Shiqiang Li; Xiaoyun Jia; J Fielding Hejtmancik; Qingjiong Zhang
Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1.
Journal of human genetics 2006;51(8):695-700.
2006: Panfeng Wang; Xiangming Guo; Xiaoyun Jia; Shiqiang Li; Xueshan Xiao; Qingjiong Zhang
Novel mutations of the PAX6 gene identified in Chinese patients with aniridia.
Molecular vision 2006;12():644-8.
2006: Xueshan Xiao; Xiaoyun Jia; Xiangming Guo; Shiqiang Li; Zhikuan Yang; Qingjiong Zhang
CSNB1 in Chinese families associated with novel mutations in NYX.
Journal of human genetics 2006;51(7):634-40.
2006: Xiangming Guo; Shiqiang Li; Xiaoyun Jia; Xueshan Xiao; Panfeng Wang; Qingjiong Zhang
Linkage analysis of two families with X-linked recessive congenital motor nystagmus.
Journal of human genetics 2006;51(1):76-80.
2005: Qingjiong Zhang; Xiangming Guo; Xueshan Xiao; Xiaoyun Jia; Shiqiang Li; J Fielding Hejtmancik
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.
Molecular vision 2005;11():554-60.