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Vision Sciences Society Annual Meeting Abstract July 2025

Neural mechanisms of social contingency perception in communicative interactions: an fMRI study

Ting Zhang; Rui Wang; Yi Jiang

Journal of Vision. 2025; 25(9):2371. https://doi.org/10.1167/jov.25.9.2371

ARVO Annual Meeting Abstract June 2025

Genetic confirmation and clinical characterization of P3H2-associated inherited eye disease

Qingjiong Zhang; Yi Jiang; Shiqiang Li; Xueshan Xiao

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):4357.

ARVO Annual Meeting Abstract June 2025

Clinical and genetic landscape of congenital cataract: systematic insights into 39 genes

Dongwei Guo; Yi Jiang; yuxi zheng; Shiqiang Li; Guangming Jin; Xueshan Xiao; Xiaoyun Jia; Wenmin Sun; Danying Zheng; James Fielding Hejtmancik; Qingjiong Zhang

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):1358.

ARVO Annual Meeting Abstract June 2025

Comprehensive reanalysis of a large cohort of unsolved hereditary optic atrophy: insight from novel causative genes

yuxi zheng; Xiaoyun Jia; Shiqiang Li; Yi Jiang; Dongwei Guo; Xueshan Xiao; James Fielding Hejtmancik; Wenmin Sun; Qingjiong Zhang

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):3204.

ARVO Annual Meeting Abstract June 2025

Clinical and genetic risk factors identified in 29 of 89 probands with amblyopia and/or anisometropia associated with low-to moderate myopia in children

Yi Jiang; yuxi zheng; Dongwei Guo; Xiaoyun Jia; Shiqiang Li; Xueshan Xiao; Wenmin Sun; Qingjiong Zhang

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):2822.

ARVO Annual Meeting Abstract June 2025

Anti-Vascular Endothelial Growth Factor as a Treatment Method for Pseudophakic Cystoid Macular Edema

Justin Tan; Yi Jiang; Jasmine Lam

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):2604.

ARVO Annual Meeting Abstract June 2025

Assessment of the Quality of Information on Glaucoma Treatment Available on Social Media Platforms by Large Language Models

Asha Bulusu; Paul Cotran; Amer Alwreikat; Ying Jiang; Michael Cooper; Ashwin Philip Verghese; David J Ramsey

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):3910.

Cornea April 2025

Prox1 Protein in Corneal Limbal Lymphatic Vessels Maintains Limbal Stem Cell Stemness and Regulates Corneal Injury Repair

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An Wang; Zongyuan Li; Yilin Jiang; Mingxiong Chen; Hanrui Yu; Zhao Li; Shengshu Sun; Ge Bai; Qun Wang; Yifei Huang; Liqiang Wang
TAGS: alkalies, burns, cornea, corneal injuries, limbal stem cells, lymphatic vessels, prospero-related homeobox 1 protein, recovery of function, epithelium, rna, messenger
Invest. Ophthalmol. Vis. Sci.. 2025; 66(4):81. https://doi.org/10.1167/iovs.66.4.81

Includes: Supplemental Content

Retina January 2025

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype

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Yingwei Wang; Pangfeng Wang; Zhen Yi; Jiamin Ouyang; Yi Jiang; Shiqiang Li; Xiaoyun Jia; Xueshan Xiao; James Fielding Hejtmancik; Wenmin Sun; Qingjiong Zhang
TAGS: abca4 gene, introns, phenotype
Invest. Ophthalmol. Vis. Sci.. 2025; 66(1):65. https://doi.org/10.1167/iovs.66.1.65

Includes: Supplemental Content

Genetics August 2024

The Systemic Genotype-Phenotype Characterization of PAX6 -Related Eye Disease in 164 Chinese Families

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Yi Jiang; Zhen Yi; Yuxi Zheng; Jiamin Ouyang; Dongwei Guo; Shiqiang Li; Xueshan Xiao; Panfeng Wang; Wenmin Sun; Qingjiong Zhang
TAGS: pax6 transcription factor, phenotype, family, eye, eye diseases, cohort studies, genotype, chinese (other dialects), chinese people
Invest. Ophthalmol. Vis. Sci.. 2024; 65(10):46. https://doi.org/10.1167/iovs.65.10.46

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2024

COL2A1 -associated Stickler syndrome in Chinese children: clinical and genetic risk factors underlying the serious consequence

Yi Jiang; Qingjiong Zhang

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3843.

Genetics January 2024

Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families

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Dongwei Guo; Shiqiang Li; Xueshan Xiao; Yi Jiang; Yingwei Wang; Guangming Jin; Junwen Wang; Jiamin Ouyang; Xiaoyun Jia; Wenmin Sun; Panfeng Wang; Danying Zheng; Qingjiong Zhang
TAGS: cohort studies, ectopia lentis, family, fibrillin-1, genetics, genes, genotype, phenotype
Invest. Ophthalmol. Vis. Sci.. 2024; 65(1):20. https://doi.org/10.1167/iovs.65.1.20

Includes: Supplemental Content

Genetics April 2023

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism

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Yingwei Wang; Wenmin Sun; Xueshan Xiao; Yi Jiang; Jiamin Ouyang; Junwen Wang; Zhen Yi; Shiqiang Li; Xiaoyun Jia; Panfeng Wang; J. Fielding Hejtmancik; Qingjiong Zhang
TAGS: haplotypes, myopia, retinal cone, genes, mosaicism, family
Invest. Ophthalmol. Vis. Sci.. 2023; 64(4):29. https://doi.org/10.1167/iovs.64.4.29

Includes: Supplemental Content

Genetics March 2023

The Genetic Confirmation and Clinical Characterization of LOXL3 -Associated MYP28: A Common Type of Recessive Extreme High Myopia

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Yi Jiang; Lin Zhou; Yingwei Wang; Jiamin Ouyang; Shiqiang Li; Xueshan Xiao; Xiaoyun Jia; Junwen Wang; Zhen Yi; Wenmin Sun; Xiaodong Jiao; Panfeng Wang; J. Fielding Hejtmancik; Qingjiong Zhang
TAGS: genetics, myopia
Invest. Ophthalmol. Vis. Sci.. 2023; 64(3):24. https://doi.org/10.1167/iovs.64.3.24

Includes: Supplemental Content

Biochemistry and Molecular Biology March 2023

Missense Mutations in MAB21L1 : Causation of Novel Autosomal Dominant Ocular BAMD Syndrome

PDF

Panfeng Wang; Pengsen Wu; Junwen Wang; Yiyan Zeng; Yi Jiang; Yingwei Wang; Shiqiang Li; Xueshan Xiao; Qingjiong Zhang
TAGS: missense mutation, phenotype, syndrome, family
Invest. Ophthalmol. Vis. Sci.. 2023; 64(3):19. https://doi.org/10.1167/iovs.64.3.19

Includes: Supplemental Content

Retina August 2022

Dependence of Retinal Pigment Epithelium Integrity on the NRF2–Heme Oxygenase-1 Axis

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Yida Jiang; Li-Juan Duan; Jingbo Pi; Yun-Zheng Le; Guo-Hua Fong
TAGS: body tissue, heme, mice, oxidative stress, oxygenases, painful bladder syndrome, personal integrity, retinal pigment cell, retinal pigment epithelium, eye
Invest. Ophthalmol. Vis. Sci.. 2022; 63(9):30. https://doi.org/10.1167/iovs.63.9.30

Includes: Supplemental Content

Genetics August 2022

Clinical and Genetic Analysis of RDH12 -Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod Dystrophy

PDF

Junwen Wang; Yingwei Wang; Shiqiang Li; Xueshan Xiao; Zhen Yi; Yi Jiang; Xueqing Li; Xiaoyun Jia; Panfeng Wang; Chenjin Jin; Wenmin Sun; Qingjiong Zhang
TAGS: alleles, family, retinal diseases, retinitis pigmentosa, genetic analysis, chinese (other dialects), phenotype, chinese people
Invest. Ophthalmol. Vis. Sci.. 2022; 63(9):24. https://doi.org/10.1167/iovs.63.9.24

Includes: Supplemental Content

Biochemistry and Molecular Biology July 2022

Hypoxia-Induced Scleral HIF-2α Upregulation Contributes to Rises in MMP-2 Expression and Myopia Development in Mice

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Wenjing Wu; Yongchao Su; Changxi Hu; Huixin Tao; Ying Jiang; Guandong Zhu; Jiadi Zhu; Ying Zhai; Jia Qu; Xiangtian Zhou; Fei Zhao
TAGS: gelatinase a, hypoxia, mice, myopia, sclera, up-regulation (physiology)
Invest. Ophthalmol. Vis. Sci.. 2022; 63(8):2. https://doi.org/10.1167/iovs.63.8.2

ARVO Annual Meeting Abstract June 2022

In-Situ Repair of Corneal Stroma using A Light-Curable Hydrogel from Porcine Corneal Extracellular Matrix

Ali R Djalilian; Ghasem Yazdanpanah; Xiang Shen; Tara Thanh Nguyen; Khandaker Anwar; Oju Jeon; Yizhou Jiang; Mohammad Pachenari; Yayue Pan; Tolou Shokuhfar; Mark Rosenblatt; Eben Alsberg

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2639.

Genetics May 2022

Different Phenotypes Represent Advancing Stages of ABCA4 -Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center

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Yingwei Wang; Wenmin Sun; Jing Zhou; Xueqing Li; Yi Jiang; Shiqiang Li; Xiaoyun Jia; Xueshan Xiao; Jiamin Ouyang; Yueye Wang; Lin Zhou; Yuxi Long; Mengchu Liu; Yongyu Li; Zhen Yi; Panfeng Wang; Qingjiong Zhang
TAGS: abca4 gene, chinese (other dialects), chinese people, longitudinal studies, phenotype, retinal diseases, family
Invest. Ophthalmol. Vis. Sci.. 2022; 63(5):28. https://doi.org/10.1167/iovs.63.5.28

Includes: Supplemental Content

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Neural mechanisms of social contingency perception in communicative interactions: an fMRI study

Genetic confirmation and clinical characterization of P3H2-associated inherited eye disease

Clinical and genetic landscape of congenital cataract: systematic insights into 39 genes

Comprehensive reanalysis of a large cohort of unsolved hereditary optic atrophy: insight from novel causative genes

Clinical and genetic risk factors identified in 29 of 89 probands with amblyopia and/or anisometropia associated with low-to moderate myopia in children

Anti-Vascular Endothelial Growth Factor as a Treatment Method for Pseudophakic Cystoid Macular Edema

Assessment of the Quality of Information on Glaucoma Treatment Available on Social Media Platforms by Large Language Models

Prox1 Protein in Corneal Limbal Lymphatic Vessels Maintains Limbal Stem Cell Stemness and Regulates Corneal Injury Repair

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype

The Systemic Genotype-Phenotype Characterization of PAX6 -Related Eye Disease in 164 Chinese Families

COL2A1 -associated Stickler syndrome in Chinese children: clinical and genetic risk factors underlying the serious consequence

Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism

The Genetic Confirmation and Clinical Characterization of LOXL3 -Associated MYP28: A Common Type of Recessive Extreme High Myopia

Missense Mutations in MAB21L1 : Causation of Novel Autosomal Dominant Ocular BAMD Syndrome

Dependence of Retinal Pigment Epithelium Integrity on the NRF2–Heme Oxygenase-1 Axis

Clinical and Genetic Analysis of RDH12 -Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod Dystrophy

Hypoxia-Induced Scleral HIF-2α Upregulation Contributes to Rises in MMP-2 Expression and Myopia Development in Mice

In-Situ Repair of Corneal Stroma using A Light-Curable Hydrogel from Porcine Corneal Extracellular Matrix

Different Phenotypes Represent Advancing Stages of ABCA4 -Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center

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