Zi-Bing Jin

Molecular diagnosis of putative Stargardt disease by capture next generation sequencing.

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family.

The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing.

Molecular genetic analysis and phenotypic characteristics of a consanguineous family with glycogen storage disease type Ia.

ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy.

Emerging roles of non-coding RNAs in retinal diseases: A review.

Bioenergetic Crosstalk between Mesenchymal Stem Cells and various Ocular Cells through the intercellular trafficking of Mitochondria.

COCO enhances the efficiency of photoreceptor precursor differentiation in early human embryonic stem cell-derived retinal organoids.

Generation of Nonhuman Primate Model of Cone Dysfunction through AAV-Mediated Ablation.

Towards stem cell-based neuronal regeneration for glaucoma.

The road to restore vision with photoreceptor regeneration.

Generation of three human iPSC lines from a retinitis pigmentosa family with SLC7A14 mutation.

Abundant Neural circRNA Cdr1as Is Not Indispensable for Retina Maintenance.

Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin.

Patient iPSC-derived retinal organoids: Observable retinal diseases in-a-dish.

Eyes on coronavirus.

Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa.

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.

Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus.

Circular RNAs in the Central Nervous System.

Modeling retinitis pigmentosa through patient-derived retinal organoids.

Modeling human retinoblastoma using embryonic stem cell-derived retinal organoids.

Investigation of Macular Choroidal Thickness and Blood Flow Change by Optical Coherence Tomography Angiography After Posterior Scleral Reinforcement.

Conversion of mouse embryonic fibroblasts into neural crest cells and functional corneal endothelia by defined small molecules.

Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy.

Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals.

Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis.

Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort.

Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China.

Stem Cell-Based Regeneration and Restoration for Retinal Ganglion Cell: Recent Advancements and Current Challenges.

The association of myopia progression with the morphological changes of optic disc and β-peripapillary atrophy in primary school students.

miR-183 and miR-96 orchestrate both glucose and fat utilization in skeletal muscle.

Retinal Degeneration Caused by Ago2 Disruption.

Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy.

Retinal organoids as models for development and diseases.

Clinical Features and Natural History in a Cohort of Chinese Patients with RPE65-Associated Inherited Retinal Dystrophy.

Implantable collamer lens versus small incision lenticule extraction for high myopia correction: A systematic review and meta-analysis.

The Impact of Study-at-Home During the COVID-19 Pandemic on Myopia Progression in Chinese Children.

Requirements for human-induced pluripotent stem cells.

Association Between Color Vision Deficiency and Myopia in Chinese Children Over a Five-Year Period.

miR-182 targeting reprograms tumor-associated macrophages and limits breast cancer progression.

New loci for refractive errors and ocular biometric parameters in young Chinese Han adults.

CLEC3B is a novel causative gene for macular-retinal dystrophy.

MLL5 is involved in retinal photoreceptor maturation through facilitating CRX-mediated photoreceptor gene transactivation.

Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.

Functional microglia derived from human pluripotent stem cells empower retinal organ.

Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract.

Therapeutic Effects of Human Pluripotent Stem Cell-Derived Mesenchymal Stem Cells on a Murine Model of Acute Type-2-Dominated Airway Inflammation.

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations.

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Global spectrum of mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy.

Effects and Prognosis of Cataract Surgery in Patients with Retinitis Pigmentosa.

Microglial hexokinase 2 deficiency increases ATP generation through lipid metabolism leading to β-amyloid clearance.

A saturated map of common genetic variants associated with human height.

Author Correction: Microglial hexokinase 2 deficiency increases ATP generation through lipid metabolism leading to β-amyloid clearance.

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.

Mechanosensitive channel Piezo1 is an essential regulator in cell cycle progression of optic nerve head astrocytes.

Second hit impels oncogenesis of retinoblastoma in patient-induced pluripotent stem cell-derived retinal organoids: direct evidence for Knudson's theory.

SLAMF7/STAT6 Pathway Inhibits Innate Immune Response in Late-Stage Human Keratitis: A Comparative Transcriptome Analysis.

Time-Course Transcriptomic Analysis Reveals the Crucial Roles of PANoptosis in Fungal Keratitis.

Prevalence and Characteristics of Myopia in Adult Rhesus Macaques in Southwest China.

Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China.

Immunomodulatory properties of mesenchymal stem cells: A potential therapeutic strategy for allergic rhinitis.

IMI-Management and Investigation of High Myopia in Infants and Young Children.

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.

A rational consideration of the genomic instability of human-induced pluripotent stem cells for clinical applications.

Retinal organoid and gene editing for basic and translational research.

Six-month repeated irradiation of 650 nm low-level red light reduces the risk of myopia in children: a randomized controlled trial.

Evaluation of Limbal Stem Cells in Patients With Type 2 Diabetes: An In Vivo Confocal Microscopy Study.

Implementing a digital comprehensive myopia prevention and control strategy for children and adolescents in China: a cost-effectiveness analysis.

REG1A protects retinal photoreceptors from blue light damage.

Deep phenotyping of 11,880 highlanders reveals novel adaptive traits in native Tibetans.

Clinical Features of Fundus Tessellation and Its Relationship with Myopia: A Systematic Review and Meta-analysis.

Comprehensive Genetic Analysis Unraveled the Missing Heritability and a Founder Variant of BEST1 in a Chinese Cohort With Autosomal Recessive Bestrophinopathy.

Extracellular Vesicle MicroRNAs From Corneal Stromal Stem Cell Enhance Stemness of Limbal Epithelial Stem Cells by Targeting the Notch Pathway.

Comprehensive genetic analysis reveals the mutational landscape of ABCA4-associated retinal dystrophy in a Chinese cohort.

The Evolution and Visual Prognosis of Glial Proliferation with Different Grades after Macular Hole Surgery: An Optical Coherence Tomography-Based Study.

Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3.

Acute onset of decreased vision after violently vomiting: A case report.

Bietti's crystalline dystrophy: genotyping and deep qualitative and quantitative phenotyping in preparation for clinical trials.

Genetic detection of two novel LRP5 pathogenic variants in patients with familial exudative vitreoretinopathy.

CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids.

Fundus Tessellated Density of Pathologic Myopia.

Timp1 Deletion Induces Anxiety-like Behavior in Mice.

Initiation of China Alliance of Research in High Myopia (CHARM): protocol for an AI-based multimodal high myopia research biobank.

RNA fusion in human retinal development.

Rationale and protocol paper for the Asia Pacific Network for inherited eye diseases.

Foveal Microstructure and Visual Outcomes after Pars Plana Vitrectomy in Patients with Different Types of Epiretinal Membrane Foveoschisis.

Closure Grading and Visual Outcome in Patients with Large Idiopathic Macular Holes: A Spectral-Domain Optical Coherence Tomography Observation.

Enhanced innate responses in microglia derived from retinoblastoma patient-specific iPSCs.

Turning point of organoid transplantation: first-in-human trial of iPSC-derived retinal organoid grafting in patients with retinitis pigmentosa.

A Novel Grading System for Diffuse Chorioretinal Atrophy in Pathologic Myopia.

Modeling autosomal dominant retinitis pigmentosa by using patient-specific retinal organoids with a class-3 RHO mutation.

Genetic control of DNA methylation is largely shared across European and East Asian populations.

Daily Low-Level Red Light for Spherical Equivalent Error and Axial Length in Children With Myopia: A Randomized Clinical Trial.

Effects of fluorescent protein tdTomato on mouse retina.

Patient-derived induced pluripotent stem cells with a mutation exhibit cell junction abnormalities and aberrant cellular differentiation potential.

Parallel comparison of ocular metrics in non-human primates with high myopia by LS900, ultrasonography and MRI-based 3D reconstruction.

Deep Learning-Enabled Vasculometry Depicts Phased Lesion Patterns in High Myopia Progression.