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Downregulation of circRNA DMNT3B contributes to diabetic retinal vascular dysfunction through targeting miR-20b-5p and BAMBI

EBioMedicine, 2019-11, Vol.49, p.341-353

2019

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Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

British journal of ophthalmology, 2021-01, Vol.105 (1), p.87-92

2021

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Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy

British journal of ophthalmology, 2020-06, Vol.104 (6), p.846-851

2020

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Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

Acta ophthalmologica (Oxford, England), 2021-06, Vol.99 (4), p.e470-e479

2021

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Association between variant Y402H in age-related macular degeneration (AMD) susceptibility gene CFH and treatment response of AMD: a meta-analysis

PloS one, 2012-08, Vol.7 (8), p.e42464-e42464

2012

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Emergency Drug Procurement Planning Based on Big-Data Driven Morbidity Prediction

IEEE transactions on industrial informatics, 2019-12, Vol.15 (12), p.6379-6388

2019

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Expanding the clinical and genetic spectrum of Heimler syndrome

Orphanet journal of rare diseases, 2019-12, Vol.14 (1), p.290-290, Article 290

2019

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The electrotonic architecture of the retinal microvasculature: modulation by angiotensin II

The Journal of physiology, 2011-05, Vol.589 (9), p.2383-2399

2011

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Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

Orphanet journal of rare diseases, 2021-04, Vol.16 (1), p.174-174, Article 174

2021

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Neuroprotective effect of transcorneal electrical stimulation on light-induced photoreceptor degeneration

Experimental neurology, 2009-10, Vol.219 (2), p.439-452

2009

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ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

Frontiers in genetics, 2019-09, Vol.10, p.773-773

2019

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Mutation Analysis of the RPGR Gene in a Chinese Cohort

Frontiers in genetics, 2022-03, Vol.13, p.850122-850122

2022

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Pediatric Infectious Endophthalmitis： A 271-case Retrospective Study at a Single Center in China

Chinese medical journal, 2016-12, Vol.129 (24), p.2936-2943

2016

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A simple new technique for the induction of residual posterior vitreous cortex removal and membrane peeling

International journal of ophthalmology, 2021-04, Vol.14 (4), p.622-625

2021

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Effect of Phosphorylated-Extracellular Regulated Kinase 1/2 Inhibitor on Retina from Light-induced Photoreceptor Degeneration

Chinese medical journal, 2018-12, Vol.131 (23), p.2836-2843

2018

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Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 2019-11, Vol.126 (11), p.1549-1556

2019

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Long-term follow-up of vitrectomy in patients with pathologic myopic foveoschisis

International journal of ophthalmology, 2017-02

2017

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Neuroprotective Effects of Naloxone against Light-Induced Photoreceptor Degeneration through Inhibiting Retinal Microglial Activation

Investigative ophthalmology & visual science, 2008-06, Vol.49 (6), p.2589-2598

2008

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Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses

BMC ophthalmology, 2020-06, Vol.20 (1), p.212-212, Article 212

2020

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Generation and characterization of immortalized rat retinal microglial cell lines

Journal of neuroscience research, 2014-04, Vol.92 (4), p.424-431

2014

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Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family

Frontiers in genetics, 2017-08, Vol.8, p.107-107

2017

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Focal choroidal excavation complicated with choroidal neovascularization in young and middle aged patients

International journal of ophthalmology, 2019-06, Vol.12 (6)

2019

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Retinal displacement after closure of idiopathic macular hole

Asian Pacific journal of tropical medicine, 2018-02, Vol.11 (2), p.155-161

2018

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Ghrelin Attenuates Retinal Neuronal Autophagy and Apoptosis in an Experimental Rat Glaucoma Model

Investigative ophthalmology & visual science, 2017-12, Vol.58 (14), p.6113-6122

2017

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Digenic heterozygous mutations in EYS/LRP5 in a Chinese family with retinitis pigmentosa

International journal of ophthalmology, 2017-02

2017

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Downregulation of circRNA DMNT3B contributes to diabetic retinal vascular dysfunction through targeting miR-20b-5p and BAMBI

Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

Association between variant Y402H in age-related macular degeneration (AMD) susceptibility gene CFH and treatment response of AMD: a meta-analysis

Emergency Drug Procurement Planning Based on Big-Data Driven Morbidity Prediction

Expanding the clinical and genetic spectrum of Heimler syndrome

The electrotonic architecture of the retinal microvasculature: modulation by angiotensin II

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

Neuroprotective effect of transcorneal electrical stimulation on light-induced photoreceptor degeneration

ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

Mutation Analysis of the RPGR Gene in a Chinese Cohort

Pediatric Infectious Endophthalmitis： A 271-case Retrospective Study at a Single Center in China

A simple new technique for the induction of residual posterior vitreous cortex removal and membrane peeling

Effect of Phosphorylated-Extracellular Regulated Kinase 1/2 Inhibitor on Retina from Light-induced Photoreceptor Degeneration

Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa

Long-term follow-up of vitrectomy in patients with pathologic myopic foveoschisis

Neuroprotective Effects of Naloxone against Light-Induced Photoreceptor Degeneration through Inhibiting Retinal Microglial Activation

Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses

Generation and characterization of immortalized rat retinal microglial cell lines

Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family

Focal choroidal excavation complicated with choroidal neovascularization in young and middle aged patients

Retinal displacement after closure of idiopathic macular hole

Ghrelin Attenuates Retinal Neuronal Autophagy and Apoptosis in an Experimental Rat Glaucoma Model

Digenic heterozygous mutations in EYS/LRP5 in a Chinese family with retinitis pigmentosa

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