Zi-Bing Jin

Beijing Institute of Ophthalmology, Capital Medical University

Affiliated withCapital Medical University

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2024

Other Publications

Article	Year
Molecular diagnosis of putative Stargardt disease by capture next generation sequencing. PloS one\| PubMed ID: 24763286	2014
'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration. Database : the journal of biological databases and curation\| PubMed ID: 24939193	2014
A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family. Scientific reports\| PubMed ID: 25374051	2014
The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing. PloS one\| PubMed ID: 26421841	2015
Molecular genetic analysis and phenotypic characteristics of a consanguineous family with glycogen storage disease type Ia. Molecular medicine reports\| PubMed ID: 27511118	2016
ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy. Human genetics\| PubMed ID: 32440726	2020
Emerging roles of non-coding RNAs in retinal diseases: A review. Clinical & experimental ophthalmology\| PubMed ID: 32519377	2020
Bioenergetic Crosstalk between Mesenchymal Stem Cells and various Ocular Cells through the intercellular trafficking of Mitochondria. Theranostics\| PubMed ID: 32641991	2020
COCO enhances the efficiency of photoreceptor precursor differentiation in early human embryonic stem cell-derived retinal organoids. Stem cell research & therapy\| PubMed ID: 32831148	2020
Generation of Nonhuman Primate Model of Cone Dysfunction through AAV-Mediated Ablation. Molecular therapy. Methods & clinical development\| PubMed ID: 32953936	2020
Towards stem cell-based neuronal regeneration for glaucoma. Progress in brain research\| PubMed ID: 32988476	2020
The road to restore vision with photoreceptor regeneration. Experimental eye research\| PubMed ID: 33010290	2021
Generation of three human iPSC lines from a retinitis pigmentosa family with SLC7A14 mutation. Stem cell research\| PubMed ID: 33207307	2020
Abundant Neural circRNA Cdr1as Is Not Indispensable for Retina Maintenance. Frontiers in cell and developmental biology\| PubMed ID: 33240875	2020
Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 33318192	2020
Patient iPSC-derived retinal organoids: Observable retinal diseases in-a-dish. Histology and histopathology\| PubMed ID: 33491763	2021
Eyes on coronavirus. Stem cell research\| PubMed ID: 33535156	2021
Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa. Frontiers in cell and developmental biology\| PubMed ID: 33598457	2020
Transplantation of GMP-grade human iPSC-derived retinal pigment epithelial cells in rodent model: the first pre-clinical study for safety and efficacy in China. Annals of translational medicine\| PubMed ID: 33708872	2021
Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus. Frontiers in cell and developmental biology\| PubMed ID: 33732697	2021
Circular RNAs in the Central Nervous System. Frontiers in molecular biosciences\| PubMed ID: 33816552	2021
Modeling retinitis pigmentosa through patient-derived retinal organoids. STAR protocols\| PubMed ID: 33899019	2021
Modeling human retinoblastoma using embryonic stem cell-derived retinal organoids. STAR protocols\| PubMed ID: 33899024	2021
Investigation of Macular Choroidal Thickness and Blood Flow Change by Optical Coherence Tomography Angiography After Posterior Scleral Reinforcement. Frontiers in medicine\| PubMed ID: 34017847	2021
Conversion of mouse embryonic fibroblasts into neural crest cells and functional corneal endothelia by defined small molecules. Science advances\| PubMed ID: 34088673	2021
Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy. Orphanet journal of rare diseases\| PubMed ID: 34130719	2021
Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals. Frontiers in cell and developmental biology\| PubMed ID: 34136477	2021
Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis. Annals of the rheumatic diseases\| PubMed ID: 34161253	2021
Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort. Frontiers in cell and developmental biology\| PubMed ID: 34178978	2021
Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China. Frontiers in cell and developmental biology\| PubMed ID: 34222226	2021
Stem Cell-Based Regeneration and Restoration for Retinal Ganglion Cell: Recent Advancements and Current Challenges. Biomolecules\| PubMed ID: 34356611	2021
The association of myopia progression with the morphological changes of optic disc and β-peripapillary atrophy in primary school students. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie\| PubMed ID: 34357418	2022
miR-183 and miR-96 orchestrate both glucose and fat utilization in skeletal muscle. EMBO reports\| PubMed ID: 34358402	2021
Retinal Degeneration Caused by Ago2 Disruption. Investigative ophthalmology & visual science\| PubMed ID: 34529004	2021
Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy. Frontiers in cell and developmental biology\| PubMed ID: 34676220	2021
Retinal organoids as models for development and diseases. Cell regeneration (London, England)\| PubMed ID: 34719743	2021
Clinical Features and Natural History in a Cohort of Chinese Patients with RPE65-Associated Inherited Retinal Dystrophy. Journal of clinical medicine\| PubMed ID: 34830511	2021
Implantable collamer lens versus small incision lenticule extraction for high myopia correction: A systematic review and meta-analysis. BMC ophthalmology\| PubMed ID: 34961514	2021
The Impact of Study-at-Home During the COVID-19 Pandemic on Myopia Progression in Chinese Children. Frontiers in public health\| PubMed ID: 35071149	2021
Requirements for human-induced pluripotent stem cells. Cell proliferation\| PubMed ID: 35083805	2022
Association Between Color Vision Deficiency and Myopia in Chinese Children Over a Five-Year Period. Investigative ophthalmology & visual science\| PubMed ID: 35103751	2022
miR-182 targeting reprograms tumor-associated macrophages and limits breast cancer progression. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 35105806	2022
New loci for refractive errors and ocular biometric parameters in young Chinese Han adults. Science China. Life sciences\| PubMed ID: 35301706	2022
CLEC3B is a novel causative gene for macular-retinal dystrophy. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 35331648	2022
MLL5 is involved in retinal photoreceptor maturation through facilitating CRX-mediated photoreceptor gene transactivation. iScience\| PubMed ID: 35359806	2022
Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction. Science advances\| PubMed ID: 35394837	2022
Functional microglia derived from human pluripotent stem cells empower retinal organ. Science China. Life sciences\| PubMed ID: 35451725	2022
Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract. Frontiers in cell and developmental biology\| PubMed ID: 35531093	2022
Therapeutic Effects of Human Pluripotent Stem Cell-Derived Mesenchymal Stem Cells on a Murine Model of Acute Type-2-Dominated Airway Inflammation. Stem cell reviews and reports\| PubMed ID: 35622293	2022
Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations. Investigative ophthalmology & visual science\| PubMed ID: 35657619	2022
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American journal of human genetics\| PubMed ID: 35931049	2022
Global spectrum of mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy. Frontiers in aging neuroscience\| PubMed ID: 36034145	2022
Effects and Prognosis of Cataract Surgery in Patients with Retinitis Pigmentosa. Ophthalmology and therapy\| PubMed ID: 36057888	2022
Microglial hexokinase 2 deficiency increases ATP generation through lipid metabolism leading to β-amyloid clearance. Nature metabolism\| PubMed ID: 36203054	2022
A saturated map of common genetic variants associated with human height. Nature\| PubMed ID: 36224396	2022
Author Correction: Microglial hexokinase 2 deficiency increases ATP generation through lipid metabolism leading to β-amyloid clearance. Nature metabolism\| PubMed ID: 36241712	2022
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome biology\| PubMed ID: 36575460	2022
Mechanosensitive channel Piezo1 is an essential regulator in cell cycle progression of optic nerve head astrocytes. Glia\| PubMed ID: 36598105	2023
Second hit impels oncogenesis of retinoblastoma in patient-induced pluripotent stem cell-derived retinal organoids: direct evidence for Knudson's theory. PNAS nexus\| PubMed ID: 36714839	2022
SLAMF7/STAT6 Pathway Inhibits Innate Immune Response in Late-Stage Human Keratitis: A Comparative Transcriptome Analysis. Microorganisms\| PubMed ID: 36838330	2023
Time-Course Transcriptomic Analysis Reveals the Crucial Roles of PANoptosis in Fungal Keratitis. Investigative ophthalmology & visual science\| PubMed ID: 36867131	2023
Prevalence and Characteristics of Myopia in Adult Rhesus Macaques in Southwest China. Translational vision science & technology\| PubMed ID: 36947048	2023
Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China. Molecular genetics and genomics : MGG\| PubMed ID: 36964802	2023
Immunomodulatory properties of mesenchymal stem cells: A potential therapeutic strategy for allergic rhinitis. Allergy\| PubMed ID: 36975714	2023
IMI-Management and Investigation of High Myopia in Infants and Young Children. Investigative ophthalmology & visual science\| PubMed ID: 37126360	2023
Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome type 2 caused by biallelic variants in the USH2A gene. Stem cell research\| PubMed ID: 37126974	2023
A rational consideration of the genomic instability of human-induced pluripotent stem cells for clinical applications. Science China. Life sciences\| PubMed ID: 37296348	2023
Retinal organoid and gene editing for basic and translational research. Vision research\| PubMed ID: 37307693	2023
Six-month repeated irradiation of 650 nm low-level red light reduces the risk of myopia in children: a randomized controlled trial. International ophthalmology\| PubMed ID: 37318667	2023
Evaluation of Limbal Stem Cells in Patients With Type 2 Diabetes: An In Vivo Confocal Microscopy Study. Cornea\| PubMed ID: 37399570	2024
Implementing a digital comprehensive myopia prevention and control strategy for children and adolescents in China: a cost-effectiveness analysis. The Lancet regional health. Western Pacific\| PubMed ID: 37520278	2023
REG1A protects retinal photoreceptors from blue light damage. Annals of the New York Academy of Sciences\| PubMed ID: 37531162	2023
Deep phenotyping of 11,880 highlanders reveals novel adaptive traits in native Tibetans. iScience\| PubMed ID: 37680474	2023
Clinical Features of Fundus Tessellation and Its Relationship with Myopia: A Systematic Review and Meta-analysis. Ophthalmology and therapy\| PubMed ID: 37733224	2023
Comprehensive Genetic Analysis Unraveled the Missing Heritability and a Founder Variant of BEST1 in a Chinese Cohort With Autosomal Recessive Bestrophinopathy. Investigative ophthalmology & visual science\| PubMed ID: 37747403	2023
Extracellular Vesicle MicroRNAs From Corneal Stromal Stem Cell Enhance Stemness of Limbal Epithelial Stem Cells by Targeting the Notch Pathway. Investigative ophthalmology & visual science\| PubMed ID: 37768272	2023
Comprehensive genetic analysis reveals the mutational landscape of ABCA4-associated retinal dystrophy in a Chinese cohort. Gene\| PubMed ID: 37774808	2024
The Evolution and Visual Prognosis of Glial Proliferation with Different Grades after Macular Hole Surgery: An Optical Coherence Tomography-Based Study. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde\| PubMed ID: 37788659	2023
Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3. Heliyon\| PubMed ID: 37809982	2023
Acute onset of decreased vision after violently vomiting: A case report. European journal of ophthalmology\| PubMed ID: 37844619	2024
Bietti's crystalline dystrophy: genotyping and deep qualitative and quantitative phenotyping in preparation for clinical trials. The British journal of ophthalmology\| PubMed ID: 37963713	2024
Genetic detection of two novel LRP5 pathogenic variants in patients with familial exudative vitreoretinopathy. BMC ophthalmology\| PubMed ID: 38030997	2023
CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids. Stem cell research & therapy\| PubMed ID: 38049871	2023
Fundus Tessellated Density of Pathologic Myopia. Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)\| PubMed ID: 38079255	2023
Timp1 Deletion Induces Anxiety-like Behavior in Mice. Neuroscience bulletin\| PubMed ID: 38113013	2024
Initiation of China Alliance of Research in High Myopia (CHARM): protocol for an AI-based multimodal high myopia research biobank. BMJ open\| PubMed ID: 38151272	2023
RNA fusion in human retinal development. eLife\| PubMed ID: 38165397	2024
Rationale and protocol paper for the Asia Pacific Network for inherited eye diseases. Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)\| PubMed ID: 38233300	2024
Foveal Microstructure and Visual Outcomes after Pars Plana Vitrectomy in Patients with Different Types of Epiretinal Membrane Foveoschisis. Ophthalmic research\| PubMed ID: 38246146	2024
Closure Grading and Visual Outcome in Patients with Large Idiopathic Macular Holes: A Spectral-Domain Optical Coherence Tomography Observation. Ophthalmic research\| PubMed ID: 38253044	2024
Enhanced innate responses in microglia derived from retinoblastoma patient-specific iPSCs. Glia\| PubMed ID: 38258347	2024
Turning point of organoid transplantation: first-in-human trial of iPSC-derived retinal organoid grafting in patients with retinitis pigmentosa. Science China. Life sciences\| PubMed ID: 38332215	2024
A Novel Grading System for Diffuse Chorioretinal Atrophy in Pathologic Myopia. Ophthalmology and therapy\| PubMed ID: 38441856	2024
Modeling autosomal dominant retinitis pigmentosa by using patient-specific retinal organoids with a class-3 RHO mutation. Experimental eye research\| PubMed ID: 38479725	2024
Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature communications\| PubMed ID: 38548728	2024
Daily Low-Level Red Light for Spherical Equivalent Error and Axial Length in Children With Myopia: A Randomized Clinical Trial. JAMA ophthalmology\| PubMed ID: 38662345	2024
Effects of fluorescent protein tdTomato on mouse retina. Experimental eye research\| PubMed ID: 38663720	2024
Patient-derived induced pluripotent stem cells with a mutation exhibit cell junction abnormalities and aberrant cellular differentiation potential. World journal of stem cells\| PubMed ID: 38817331	2024
Parallel comparison of ocular metrics in non-human primates with high myopia by LS900, ultrasonography and MRI-based 3D reconstruction. Experimental eye research\| PubMed ID: 39029552	2024
Deep Learning-Enabled Vasculometry Depicts Phased Lesion Patterns in High Myopia Progression. Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)\| PubMed ID: 39053733	2024
Trio-based whole-exome sequencing of 200 Chinese patients with keratoconus. Experimental eye research\| PubMed ID: 39326774	2024
ROCK inhibitor enhances mitochondrial transfer via tunneling nanotubes in retinal pigment epithelium. Theranostics\| PubMed ID: 39346535	2024