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Chinese Journal of Ocular Fundus Diseases

Supervisor：China Association for Science and Technology Sponsor：Chinese Medical Association
Editor-in-chief：Li Xiaoxin
Publishing period： Monthly ISSN：1005-1015 CN：51-1434/R

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  • Chinese expert consensus on the standardized application of multi-luminance mobility test in clinical trials for inherited retinal dystrophy

    2025, 41(3): 169-177
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  • Clinical phenotype and genotype analysis of retinitis pigmentosa sine pigmento caused by BBS gene mutations

    2025, 41(3): 178-185
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  • Genotype-phenotype analysis of COL2A1 and COL11A1 de novo mutations leading to Stickler syndrome types 1 and 2

    2025, 41(3): 186-193
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  • Association between CHRM1 gene polymorphisms and genetic susceptibility to high myopia in the Han population of Henan province

    2025, 41(3): 194-199
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  • Analysis of genetic variations and clinical phenotypes in patients with early-onset high myopia associated with hereditary eye diseases

    2025, 41(3): 200-212
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  • Expression of inherited retinal disease related genes in human microglia

    2025, 41(3): 213-220
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  • Bibliometric analysis of gene therapy for retinitis pigmentosa in recent 20 years

    2025, 41(3): 221-230
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  • Research progress in research on Bestrophinopathies and mutations in BEST1 gene

    2025, 41(3): 239-248
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