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Qingjiong Zhang

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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.

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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.
2013: Zhixue Li; Zirong Chen; Daming Deng; Huocong Huang; Guorong Jin; Liang Tian; Juan Wang; Lizi Wu; Qingjiong Zhang; Youran Zou; Huangxuan Shen
Overexpression of Six1 leads to retardation of myogenic differentiation in C2C12 myoblasts.
Molecular biology reports 2013;40(1):217-23.
2012: Lin Li; Xueshan Xiao; Changxian Yi; Xiangming Guo; James Fielding Hejtmancik; Xiaodong Jiao; Qingjiong Zhang
Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.
Journal of human genetics 2012;57(12):756-9.
2012: Junhui Yi; Xiangming Guo; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Qingjiong Zhang
Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degeneration.
Molecular medicine reports 2012;6(5):1045-9.
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: Zirong Chen; Yumei Gu; Chengbin Hu; Guorong Jin; Shuibin Lin; Xiumei Lin; Lizi Wu; Qingjiong Zhang; Yujuan Zhu; Huangxuan Shen
DNA methyltransferase inhibitor CDA-II inhibits myogenic differentiation.
Biochemical and biophysical research communications 2012;422(3):522-6.
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: Junhui Yi; Xiangming Guo; Xiaoyun Jia; Shiqiang Li; Panfeng Wang; Xueshan Xiao; Qingjiong Zhang
Novel RS1 mutations associated with X-linked juvenile retinoschisis.
International journal of molecular medicine 2012;29(4):644-8.
2012: Rui Bi; Xiaoyun Jia; A-Mei Zhang; Qingjiong Zhang; Yong-Gang Yao
Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy.
Molecular vision 2012;18():3087-94.
2012: Xiaodong Jiao; Anren Li; Shiqiang Li; Panfeng Wang; Qingjiong Zhang; Xiangming Guo; J Fielding Hejtmancik
Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia.
Molecular vision 2012;18():2633-46.
2012: A-Mei Zhang; Qingjiong Zhang; Xiangming Guo; Xiaoyun Jia; Yong-Gang Yao
Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
Journal of translational medicine 2012;10():43.
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: A-Mei Zhang; Qingjiong Zhang; Rui Bi; Xiangming Guo; Xiaoyun Jia; Qing-Peng Kong; Shiqiang Li; Antonio Salas; Panfeng Wang; Xueshan Xiao; Yong-Gang Yao
Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients.
PloS one 2011;6(11):e27750.
2011: A-Mei Zhang; Qingjiong Zhang; Wen Zhang; Xin-Ying Zhuang; Hans-Jürgen Bandelt; Xiaoyun Jia; Shiqiang Li; Dong Wang; Dandan Yu; Yong-Gang Yao
Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A?
PloS one 2011;6(10):e26511.
2011: Heather Dehlin Scoma; Geetha Yadav; Qingjiong Zhang; Joseph Fogerty; Monica Humby; Joseph C Besharse
The de-ubiquitinylating enzyme, USP2, is associated with the circadian clockwork and regulates its sensitivity to light.
PloS one 2011;6(9):e25382.
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: Xueshan Xiao; Xiangming Guo; Xiaoyun Jia; Lin Li; Shiqiang Li; Wei Li; Wenmin Sun; Panfeng Wang; Qingjiong Zhang
Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP.
Molecular vision 2011;17():2049-55.
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: A-Mei Zhang; Xiaoyun Jia; Qingjiong Zhang; Yong-Gang Yao
No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A.
Human genetics 2010;128(4):465-8.
2010: Yang Zou; Xiaoyun Jia; A-Mei Zhang; Wen-Zhi Wang; Shiqiang Li; Xiangming Guo; Qing-Peng Kong; Qingjiong Zhang; Yong-Gang Yao
The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations.
Biochemical and biophysical research communications 2010;399(2):179-85.
2010: Dandan Yu; Xiaoyun Jia; A-Mei Zhang; Xiangming Guo; Ya-Ping Zhang; Qingjiong Zhang; Yong-Gang Yao
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.
Neurogenetics 2010;11(3):349-56.
2010: Dandan Yu; Xiaoyun Jia; A-Mei Zhang; Shiqiang Li; Yang Zou; Qingjiong Zhang; Yong-Gang Yao
Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
PloS one 2010;5(10):e13426.
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; Xiaoyun Jia; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese.
Molecular vision 2010;16():416-24.
2010: Qin Wang; Panfeng Wang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Xiangming Guo; Qing-Peng Kong; Yong-Gang Yao; Qingjiong Zhang
Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia.
Molecular vision 2010;16():303-9.
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: A-Mei Zhang; Yang Zou; Xiangming Guo; Xiaoyun Jia; Qingjiong Zhang; Yong-Gang Yao
Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
Biochemical and biophysical research communications 2009;386(2):392-5.
2009: Xueshan Xiao; Qingjiong Zhang
Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutation.
American journal of medical genetics. Part A 2009;149A(8):1786-8.
2009: Shuhua Song; Andrew Landsbury; Ralf Dahm; Yizhi Liu; Qingjiong Zhang; Roy A Quinlan
Functions of the intermediate filament cytoskeleton in the eye lens.
The Journal of clinical investigation 2009;119(7):1837-48.
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: A-Mei Zhang; Xiaoyun Jia; Yong-Gang Yao; Qingjiong Zhang
Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy.
Biochemical and biophysical research communications 2008;376(1):221-4.
2008: Hua-Wei Wang; Xiaoyun Jia; Yanli Ji; Qing-Peng Kong; Qingjiong Zhang; Yong-Gang Yao; Ya-Ping Zhang
Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.
Mutation research 2008;643(1-2):48-53.
2008: Panfeng Wang; Xiaoling Liang; Junhui Yi; Qingjiong Zhang
Novel SOX2 mutation associated with ocular coloboma in a Chinese family.
Archives of ophthalmology 2008;126(5):709-13.
2008: Zhikuan Yang; Qingjiong Zhang; Jian Ge; Zhiqun Tan
Protective effects of tetramethylpyrazine on rat retinal cell cultures.
Neurochemistry international 2008;52(6):1176-87.
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.
2008: Tuo Li; Xueshan Xiao; Shiqiang Li; Yiqiao Xing; Xiangming Guo; Qingjiong Zhang
Evaluation of EGR1 as a candidate gene for high myopia.
Molecular vision 2008;14():1309-12.
2007: Yanli Ji; Xiaoyun Jia; Qingjiong Zhang; Yong-Gang Yao
mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
Biochemical and biophysical research communications 2007;364(2):238-42.
2007: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
Human genetics 2007;122(3-4):293-9.
2007: Panfeng Wang; Xiangming Guo; Qingjiong Zhang
Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2007;245(9):1401-2.
2007: Ming Der Perng; Qingjiong Zhang; Roy A Quinlan
Insights into the beaded filament of the eye lens.
Experimental cell research 2007;313(10):2180-8.
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.
2007: Juan Wang; Jinling Liu; Qingjiong Zhang
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Molecular vision 2007;13():108-13.
2006: Xinguo Deng; Qingjiong Zhang; Shixing Hu; Yang Gao; Liu Yan
[Pharmacokinetics of puerarin in the aqueous humor and vitreous of rabbit eye following systemic administration].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 2006;22(4):275-9.
2006: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Wenliang Yao; Shouling Li; Xiaodong Jiao; Amber Shahzadi; MUHAMMAD AMER; Muhammad Iqbal; Tayyab Hussnain; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
Molecular vision 2006;12():1283-91.
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; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
Human genetics 2005;118(3-4):356-65.
2005: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Yuri V Sergeev; Zaheeruddin A Qazi; Tayyab Husnain; Raphael Caruso; Sheikh Riazuddin; Paul Sieving; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Investigative ophthalmology & visual science 2005;46(7):2264-70.
2005: Sheikh Amer Riazuddin; Afshan Yasmeen; Wenliang Yao; Yuri V Sergeev; Qingjiong Zhang; Fareeha Zulfiqar; Assad Riaz; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
Investigative ophthalmology & visual science 2005;46(6):2100-6.
2005: Sheikh Amer Riazuddin; Afshan Yasmeen; Qingjiong Zhang; Wenliang Yao; Muhammad Farooq Sabar; Zahoor Ahmed; Sheikh Riazuddin; J Fielding Hejtmancik
A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
Investigative ophthalmology & visual science 2005;46(2):623-6.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Afshan Yasmeen; Peter K Rogan; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
Molecular vision 2005;11():977-85.
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.
2004: Qingjiong Zhang; Xiangming Guo; Xueshan Xiao; Junhui Yi; Xiaoyun Jia; J Fielding Hejtmancik
Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
Molecular vision 2004;10():890-900.
2004: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Zahoor Ahmad; Sheikh Riazuddin; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
Molecular vision 2004;10():884-9.
2004: Anren Li; Xiaodong Jiao; Francis L Munier; Daniel F Schorderet; Wenliang Yao; Fumino Iwata; Mutsuko Hayakawa; Atsushi Kanai; Muh Shy Chen; Richard Alan Lewis; John R Heckenlively; Richard G Weleber; Elias Traboulsi; Qingjiong Zhang; Xueshan Xiao; Muriel I Kaiser-Kupfer; Yuri V Sergeev; J Fielding Hejtmancik
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
American journal of human genetics 2004;74(5):817-26.
2002: Dajiang Li; Qingjiong Zhang
[Transcription changes of alpha A-crystallins gene during the development of retinal degeneration in Rd, Rds and C3H mouse].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 2002;18(2):115-8.
2001: Qingjiong Zhang; Xiangming Guo; Xiaoyun Jia; Xueshan Xiao; Li Guo; Shaozhen Li
[Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2001;18(6):441-3.
2001: Guanguang Feng; Haitao Li; Yuzhen Yi; Jianliang Zheng; Qingjiong Zhang; X Wang; C Du
[Study on the dynamic changes of retinoblastoma gene of SO-Rb50 cell line].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 2001;17(2):111-3.
2001: Huangxuan Shen; Qingjiong Zhang; Z Kuang; Xueshan Xiao; R Li
[Cloning the differentially expressed genes in the retina of rds mouse during the development of retinitis pigmentosa].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2001;18(2):114-7.
2001: Xiulan Zhang; Qiang Yu; Qingjiong Zhang; Changxian Yi
Clinical analysis of Leber's hereditary optic neuropathy harboring mtDNA mutation at nt11778.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 2001;17(1):31-4.
2000: Qingjiong Zhang; Xueshan Xiao; Huangxuan Shen; Shaozhen Li; Futian Jiang
Correlation of gene structure and psychophysical measurement in red-green color vision deficiency in Chinese.
Japanese journal of ophthalmology 2000;44(6):596-600.
2000: Yingjun Chen; Qingjiong Zhang
Spatio-temporate expression of P53, Bcl-2 and Fas in the retina of RD, Rds and C3H mice.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 2000;16(3):158-62.
1999: Huangxuan Shen; Qingjiong Zhang; Xueshan Xiao; Shaozhen Li; Li Guo; Futian Jiang
[Analysis of fusion points in hybrid genes and gene deletion for congenital red-green color vision defects].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 1999;16(5):290-2.
1999: Huangxuan Shen; Qingjiong Zhang; Xueshan Xiao; Shaozhen Li; X Guo; X Jia; Li Guo
Differential gene expression in retina of myopic chicken eyes using mRNA differential display.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1999;15(3):137-40, 152.
1999: L Zheng; S Liu; Li-xia Deng; Qingjiong Zhang
[Using the method of two-color fluorescence in situ hybridization to detect aneuploidy of human sperms].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 1999;16(2):116-8.
1999: Y Hu; Qingjiong Zhang
[Genetic polymorphisms of CYP1A1 and susceptibility of lung cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 1999;16(1):26-8.
1998: F Zhang; Qingjiong Zhang; Huangxuan Shen; Shaozhen Li; Xueshan Xiao
[Analysis of rhodopsin and peripherin/RDS genes in Chinese patients with retinitis pigmentosa].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1998;14(4):210-4.
1998: Huangxuan Shen; Qingjiong Zhang; Xueshan Xiao; Shaozhen Li; Li Guo; Futian Jiang
Color vision defects with variation in the exon 5 of red and green pigment genes.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1998;14(3):130-3.
1997: Hui Zhang; H Ye; C Zhang; Fanbo Zeng; X Huang; Qingjiong Zhang; Zhen Li; B Du
Experimental studies on extremely low frequency pulsed magnetic field inhibiting sarcoma and enhancing cellular immune functions.
Science in China. Series C, Life sciences / Chinese Academy of Sciences 1997;40(4):392-7.
1997: Qingjiong Zhang; K Minoda; R Zeng; Zhongyao Wu; Xueshan Xiao; Shaozhen Li; F Zhang
Exon-by-exon screening for RB germline mutations using Heteroduplex-SSCP analysis.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1997;13(1):5-11.
1996: Qingjiong Zhang; K Minoda
Detection of RB germline mutations using exon-by-exon heteroduplex analysis compared with SSCP.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1996;12(3):151-7.
1996: Qingjiong Zhang; K Minoda
Single 5'green-3'red hybrid gene in protanopia.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1996;12(1):5-9.
1994: R Zeng; X Jiang; Qingjiong Zhang; B Hu; Y Chen
Preliminary report of molecular detection of retinoblastoma gene mutations.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1994;10(1):1-5.
1992: Qingjiong Zhang; W Mao; Q Ma; R Zeng; Lezheng Wu; De-zheng Wu; Y Chen
Detection of gene alteration for color vision defects by polymerase chain reaction.
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1992;8(1):8-11.
1992: Qingjiong Zhang; W Mao; Q Ma; R Zeng; Lezheng Wu; De-zheng Wu; Y Chen
Molecular basis of congenital color vision defects in Chinese patients.
Japanese journal of ophthalmology 1992;36(4):479-87.
1990: Qingjiong Zhang; W Mao; Q Ma; R Zeng; Lezheng Wu; De-zheng Wu; Y Chen
[Visual pigment genes for color vision defects].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1990;6(3-4):51-7.
1990: Qingjiong Zhang; W Mao; Q Ma; R Zeng; Lezheng Wu; Dezheng Wu; Y Chen
[Visual pigment genes for color vision defects].
Yan ke xue bao = Eye science / "Yan ke xue bao" bian ji bu 1990;6(3-4):51-7.