Qingjiong Zhang

Overview

Best Publications

• Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.

  Anren Li;Xiaodong Jiao;Francis L. Munier;Daniel F. Schorderet

  279
  Citations

• Functions of the intermediate filament cytoskeleton in the eye lens

  Shuhua Song;Andrew Landsbury;Ralf Dahm;Yizhi Liu

  182
  Citations

• 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;A-Mei Zhang;Xiaoyun Jia;Ya-Ping Zhang

  180
  Citations

• Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing

  Yan Xu;Liping Guan;Tao Shen;Jianguo Zhang

  173
  Citations

• A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

  Qingjiong Zhang;Xiangming Guo;Xueshan Xiao;Xiaoyun Jia

  165
  Citations

• Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population

  Yi Shi;Jia Qu;Dingding Zhang;Peiquan Zhao

  157
  Citations

• Novel locus for X linked recessive high myopia maps to Xq23–q25 but outside MYP1

  Q Zhang;X Guo;X Xiao;X Jia

  145
  Citations

• Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene

  Qingjiong Zhang;Qingjiong Zhang;Fareeha Zulfiqar;Xueshan Xiao;S. Amer Riazuddin;S. Amer Riazuddin

  143
  Citations

• Mutations in βB3-crystallin associated with autosomal recessive cataract in two pakistani families

  S. Amer Riazuddin;Afshan Yasmeen;Wenliang Yao;Yuri V. Sergeev

  136
  Citations

• Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis

  Lin Li;Lin Li;Xueshan Xiao;Shiqiang Li;Xiaoyun Jia

  130
  Citations

• 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;Shiqiang Li

  127
  Citations

• Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy

  Xiaoyun Jia;Shiqiang Li;Xueshan Xiao;Xiangming Guo

  123
  Citations

• An overview of myopia genetics

  Xue-Bi Cai;Shou-Ren Shen;De-Fu Chen;Qingjiong Zhang

  113
  Citations

• 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

  109
  Citations

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

  Chen Y;Zhang Q;Shen T;Xiao X

  99
  Citations

• Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy.

  Xueshan Xiao;Guiying Mai;Shiqiang Li;Xiangming Guo

  92
  Citations

• Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

  Zi-Bing Jin;Jinyu Wu;Xiu-Feng Huang;Chun-Yun Feng

  90
  Citations

• Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia.

  Qin Wang;Panfeng Wang;Shiqiang Li;Xueshan Xiao

  83
  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;Xiaoyun Jia

  79
  Citations

• Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.

  Zhikuan Yang;Xueshan Xiao;Shiqiang Li;Qingjiong Zhang

  78
  Citations