Jinu I. Han
Yongin, Republic of Korea
Last Updated: 09/26/2026
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Found 107 publications
Genome-wide association and multi-omics functional screens reveal the genetic architecture of foveal development.
Journal: medRxiv : the preprint server for health sciences
Published: June 22, 2026
A Dosage-Dependent Dominant-Negative Mechanism of SLC45A2(W74R) in Autosomal Dominant Oculocutaneous Albinism Revealed by Zebrafish Modeling.
Journal: Translational vision science & technology
Published: February 18, 2026
Timing of height growth peaks and axial elongation in atropine-treated myopic children.
Journal: BMC ophthalmology
Published: February 03, 2026
Etiological characteristics, clinical manifestations, and prognosis of patients with endogenous endophthalmitis in 2024: a single-center retrospective cohort study
Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
Published: January 06, 2026
Genetic Architecture of Myopia and Its Implications for Risk Stratification and Prognosis.
Journal: Diagnostics (Basel, Switzerland)
Published: December 30, 2025
Myopia Management Consensus Statement in South Korean Children 2025 by the Korean Myopia Society for the Korean Association for Pediatric Ophthalmology and Strabismus.
Journal: Korean journal of ophthalmology : KJO
Published: November 21, 2025
Structure-function relationship between handheld photopic negative response and macular GCIPL thickness in chronic optic neuropathy.
Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: October 29, 2025
Unilateral Medial Rectus Recession Can Produce Incomitance in Patients with Acute Acquired Comitant Esotropia: A Case Series.
Journal: Korean journal of ophthalmology : KJO
Published: September 09, 2025
Clinical Features According to the Type of Intermittent Exotropia: Korean Intermittent Exotropia Multicenter Study.
Journal: Epidemiologia (Basel, Switzerland)
Published: August 01, 2025
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.
Journal: Research square
Published: June 05, 2025
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.
Journal: NPJ genomic medicine
Published: April 22, 2025
Last Updated: 09/26/2026