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.