2017 | Diagnostic application of clinical exome sequencing in Leber congenital amaurosis
| MOLECULAR VISION |
2019 | Diagnostic value of ganglion cell-inner plexiform layer for early detection of ethambutol-induced optic neuropathy | BRITISH JOURNAL OF OPHTHALMOLOGY |
2021 | DYNC2H1 variants cause Leber congenital amaurosis without syndromic features | CLINICAL GENETICS |
2016 | Ecchordosis physaliphora presenting with abducens nerve palsy | JOURNAL OF AAPOS |
2023 | Efficacy of part-time patching in preventing recurrence after bilateral lateral rectus recession in children with intermittent exotropia
| BMC OPHTHALMOLOGY |
2023 | Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia | AMERICAN JOURNAL OF MEDICAL GENETICS PART A |
2019 | Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation in a Patient with Hermansky-Pudlak Syndrome and Progressive Pulmonary Fibrosis
| Acute and Critical Care |
2022 | Factors Associated With Abducens Nerve Palsy in Patients Undergoing Surgery for Petroclival Meningiomas | JOURNAL OF NEURO-OPHTHALMOLOGY |
2022 | Factors Related to Axial Length Elongation in Myopic Children Who Received 0.05% Atropine Treatment | JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS |
2020 | Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis
| STEM CELL RESEARCH |
2019 | Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient
| STEM CELL RESEARCH |
2021 | Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1
| GENES |
2022 | Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy
| FRONTIERS IN NEUROLOGY |
2021 | Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients | OPHTHALMOLOGY RETINA |
2022 | Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study
| OPHTHALMOLOGY |
2023 | Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans
| GENES |
2021 | In Silico identification of a common mobile element insertion in exon 4 of RP1
| SCIENTIFIC REPORTS |
2013 | Linezolid-Associated Optic Neuropathy in a Patient With Drug-Resistant Tuberculosis | JOURNAL OF NEURO-OPHTHALMOLOGY |
2015 | Longitudinal analysis of retinal nerve fiber layer and ganglion cell-inner plexiform layer thickness in ethambutol-induced optic neuropathy | GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY |
2018 | Low dose versus conventional dose of intravitreal bevacizumab injection for retinopathy of prematurity: a case series with paired-eye comparison | ACTA OPHTHALMOLOGICA |
2019 | Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome
| JAMA OPHTHALMOLOGY |
2021 | Nationwide population-based incidence and etiologies of pediatric and adult Horner syndrome | JOURNAL OF NEUROLOGY |
2011 | Negative refraction power causes underestimation of peripapillary retinal nerve fibre layer thickness in spectral-domain optical coherence tomography | BRITISH JOURNAL OF OPHTHALMOLOGY |
2023 | Neuro-Ophthalmic Adverse Events of COVID-21 Infection and Vaccines: A Nationwide Cohort Study
| INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE |
2022 | Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus
| TRANSLATIONAL VISION SCIENCE & TECHNOLOGY |
2016 | Obstructive Sleep Apnea in Patients with Branch Retinal Vein Occlusion: A Preliminary Study
| Korean Journal of Ophthalmology |
2015 | Ocular alignment after bilateral lateral rectus recession in exotropic children with cerebral palsy | BRITISH JOURNAL OF OPHTHALMOLOGY |
2015 | Ophthalmological manifestations in patients with Leigh syndrome | BRITISH JOURNAL OF OPHTHALMOLOGY |
2018 | Ophthalmoplegia in Mitochondrial Disease
| YONSEI MEDICAL JOURNAL |
2016 | Optic Atrophy in a Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration. | JOURNAL OF NEURO-OPHTHALMOLOGY |
2021 | Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
| Korean Journal of Ophthalmology |
2020 | Population-based Incidence of Pediatric and Adult Optic Neuritis and the Risk of Multiple Sclerosis | OPHTHALMOLOGY |
2022 | Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort
| GENES |
2017 | Protective effect of idebenone on ethambutol-induced optic neuropathy in R28 cells and mice
| Dissertation |
2017 | Protective effect of idebenone on ethambutol-induced optic neuropathy in R28 cells and mice
| Dissertation |
2017 | Protective effects of biodegradable collagen implants on thinned sclera after strabismus surgery: a paired-eye study | JOURNAL OF AAPOS |
2023 | PTPN23 Neurodevelopmental Disorder Presenting With Optic Atrophy and Spasmus Nutans-Like Nystagmus | JOURNAL OF NEURO-OPHTHALMOLOGY |
2014 | Real stereopsis test using a three-dimensional display with Tridef software.
| YONSEI MEDICAL JOURNAL |
2012 | Recurrent bilateral retinal vasculitis as a manifestation of post-streptococcal uveitis syndrome
| Korean Journal of Ophthalmology |
2019 | Refractive Outcomes of 4-Year-old Children after Intravitreal Anti-vascular Endothelial Growth Factor versus Laser Photocoagulation for Retinopathy of Prematurity
| Korean Journal of Ophthalmology |
2016 | Restoration of Retinally Induced Aniseikonia in Patients with Epiretinal Membrane after Early Vitrectomy | RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES |
2016 | Retinal Artery Occlusion and the Risk of Stroke Development: Twelve-Year Nationwide Cohort Study | STROKE |
2017 | Retinal microstructures are altered in patients with idiopathic infantile nystagmus | GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY |
2016 | Retinal Nerve Fiber Layer Thickness is Decreased in Patients With Hematologic Malignancy. | JOURNAL OF GLAUCOMA |
2023 | Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model
| INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES |
2021 | Retinitis Pigmentosa with Epiretinal Neovascularization at the Macula | OPHTHALMOLOGY RETINA |
2020 | Risk factors associated with poor outcome after medial rectus resection for recurrent intermittent exotropia | GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY |
2016 | Risk factors for consecutive exotropia after esotropia surgery | JAPANESE JOURNAL OF OPHTHALMOLOGY |
2024 | Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea | NEUROLOGICAL SCIENCES |
2021 | RP2 Rod-Cone Dystrophy Causes Spasmus Nutans-Like Nystagmus | JOURNAL OF NEURO-OPHTHALMOLOGY |
2021 | Short Stature With Optic Atrophy and Cone Dystrophy | JAMA OPHTHALMOLOGY |
2020 | SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
| HUMAN MOLECULAR GENETICS |
2015 | Strabismus surgery and long-term visual outcomes in patients with preadolescent onset ocular myasthenia gravis | GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY |
2017 | Stroke risk among adult patients with third, fourth or sixth cranial nerve palsy: a Nationwide Cohort Study | ACTA OPHTHALMOLOGICA |
2014 | Surgical management of long-standing antielevation syndrome after unilateral anterior transposition of the inferior oblique muscle. | JOURNAL OF AAPOS |
2019 | Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome | Ophthalmic Genetics |
2023 | The importance of genome sequencing: unraveling SSBP1 variant missed by exome sequencing | OPHTHALMIC GENETICS |
2017 | Transient neonatal myasthenia gravis due to a mother with ocular onset of anti-muscle specific kinase myasthenia gravis | NEUROMUSCULAR DISORDERS |
2021 | TUBB3 M323V Syndrome Presents with Infantile Nystagmus
| GENES |
2024 | Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of PRDM13 causing North Carolina macular dystrophy in Korea
| MOLECULAR VISION |