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Issue Date	Title	Journal Title
2017	Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome	JAMA OPHTHALMOLOGY
2020	Copy Number Variations and Multiallelic Variants in Korean Patients With Leber Congenital Amaurosis	MOLECULAR VISION
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	TUBB3 M323V Syndrome Presents with Infantile Nystagmus	GENES