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Journal Articles (6)
Meeting Abstract (3)

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Investigative Ophthalmology & Visual Science (7)
Journal of Vision (1)
Translational Vision Science & Technology (1)

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Biochemistry and Molecular Biology (4)
ARVO Annual Meeting Abstract (2)
Genetics (1)
Special Issue (1)
Vision Sciences Society Annual Meeting Abstract (1)

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Eye Anatomy and Disorders (6)
Genetics (5)
Biochemistry and Molecular Biology (4)
Translational Research (1)

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mitochondria (5)
mutation (5)
optic atrophy, hereditary, leber (5)
chinese people (4)
dna, mitochondrial (4)
proband (3)
cell lines (2)
chinese (other dialects) (2)
incidence (2)
carrying (1)

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ARVO Annual Meeting Abstract June 2024

Abnormal Facial Perception in Adult amblyopia: Evidence from Behavioral Experiments

Xiaolu Ming; Gantian Huang; Meng Liao; ping jiang; Longqian Liu

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5210.

Vision Sciences Society Annual Meeting Abstract September 2021

Comparison of fMRI Experimental Paradigm for Decoding Color Constancy

Mei Kuang; Zong-Yi Zhan; Ping Jiang; Xin-Yu Du; Shao-Bing Gao (Corresponding Author)

Journal of Vision. 2021; 21(9):2272. https://doi.org/10.1167/jov.21.9.2272

Biochemistry and Molecular Biology June 2021

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations

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Xiaofen Jin; Juanjuan Zhang; Qiuzi Yi; Feilong Meng; Jialing Yu; Yanchun Ji; Jun Q. Mo; Yi Tong; Pingping Jiang; Min-Xin Guan
TAGS: mitochondria, mutation, optic atrophy, hereditary, leber, cell lines, proteins, western blotting
Invest. Ophthalmol. Vis. Sci.. 2021; 62(7):22. https://doi.org/10.1167/iovs.62.7.22

Includes: Supplemental Content

Special Issue July 2020

Ophthalmologist-Level Classification of Fundus Disease With Deep Neural Networks

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Ping Jiang; Quansheng Dou; Li Shi
TAGS: disorder classification, ophthalmologists, taxonomic classification, training, inference, datasets
Trans. Vis. Sci. Tech.. 2020; 9(2):39. https://doi.org/10.1167/tvst.9.2.39

ARVO Annual Meeting Abstract September 2016

Incidence and spectrum of MT- ND 1 mutations in Chinese subjects with Leber’s hereditary optic neuropathy

Yanchun Ji; Pingping Jiang; Min-Xin Guan

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6583.

Biochemistry and Molecular Biology May 2016

Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy

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Yanchun Ji; Min Liang; Juanjuan Zhang; Ling Zhu; Zengjun Zhang; Runing Fu; Xiaoling Liu; Minglian Zhang; Qun Fu; Fuxin Zhao; Yi Tong; Yanhong Sun; Pingping Jiang; Min-Xin Guan
TAGS: chinese people, mutation, optic atrophy, hereditary, leber, proband, mitochondria, dna, mitochondrial, incidence, carrying
Invest. Ophthalmol. Vis. Sci.. 2016; 57(6):2377-2389. https://doi.org/10.1167/iovs.16-19243

Includes: Supplemental Content

Genetics July 2015

Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy

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Pingping Jiang; Min Liang; Juanjuan Zhang; Yinglong Gao; Zheyun He; Han Yu; Fuxin Zhao; Yanchun Ji; Xiaoling Liu; Minglian Zhang; Qun Fu; Yi Tong; Yanhong Sun; Xiangtian Zhou; Taosheng Huang; Jia Qu; Min-Xin Guan
TAGS: chinese people, mutation, optic atrophy, hereditary, leber, proband, mitochondria, dna, mitochondrial, prevalence
Invest. Ophthalmol. Vis. Sci.. 2015; 56(8):4778-4788. https://doi.org/10.1167/iovs.14-16158

Includes: Supplemental Content

Biochemistry and Molecular Biology March 2014

Frequency and Spectrum of Mitochondrial ND6 Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy

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Min Liang; Pingping Jiang; Feng Li; Juanjuan Zhang; Yanchun Ji; Yiqun He; Meifen Xu; Jinping Zhu; Xiangjuan Meng; Fuxin Zhao; Yi Tong; Xiaoling Liu; Yanhong Sun; Xiangtian Zhou; Jun Qin Mo; Jia Qu; Min-Xin Guan
TAGS: chinese (other dialects), chinese people, mitochondria, mutation, optic atrophy, hereditary, leber, proband, incidence, dna, mitochondrial
Invest. Ophthalmol. Vis. Sci.. 2014; 55(3):1321-1331. https://doi.org/10.1167/iovs.13-13011

Includes: Supplemental Content

Biochemistry and Molecular Biology July 2012

Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families

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Xiangtian Zhou; Yaping Qian; Juanjuan Zhang; Yi Tong; Pingping Jiang; Min Liang; Xianning Dai; Huihui Zhou; Fuxin Zhao; Yanchun Ji; Jun Qin Mo; Jia Qu; Min-Xin Guan
TAGS: cell lines, chinese (other dialects), chinese people, dna, mitochondrial, family, genes, mitochondria, mutation, optic atrophy, hereditary, leber, genetic pedigree
Invest. Ophthalmol. Vis. Sci.. 2012; 53(8):4586-4594. https://doi.org/10.1167/iovs.11-9109

Includes: Supplemental Content

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Investigative Ophthalmology & Visual Science
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