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저는 지금 현재 세브란스병원 사시 소아안과 파트 부교수로 재직중입니다.
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약력 소개
- 1998. 한성과학고등학교 졸업
- 2003. 1-3. Johns Hopkins Hospital, Sidney Kimmel Comprehensive Cancer Center. 교환학생
- 2004. 연세대학교 의과대학 우수졸업 (Magna cum laude)
- 2005. 연세대학교 신촌 세브란스 병원 인턴
- 2006. ECFMG (0-658-118-5) 미국의사국사면허 취득, USMLE Step 3 State License to Maryland Pass.
- 2009. 17사단 군의관 만기 전역
- 2012. 신촌세브란스병원 안과 전공의 수료 및 안과전문의
- 2013. 안과 임상 강사 (clinical fellow in pediatric ophthalmology and strabismus)
- 2014. 안과 임상연구조교수
- 2015. 안과 조교수 (사시 소아안과)
- 2016. 강남세브란스병원 안과 조교수
- 2022. 강남세브란스병원 안과 부교수
- 2023. Harvard University, Mass Eye and Ear, Ocular Genomics Institute 연수 (Boston, USA)
Publication
- Original Articles
1. Min JS, Kim TI, Jun I, Stulting RD, Rho C, Han SB, Kim H, Choi J, Han J, Kim EK. Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in TGFBI: Phenotype, Genotype, and Treatment. Genes (Basel). 2025 Jan 11;16(1):76.
2. Surl D, Seo Y, Han J. Trends in myopia prevalence among late adolescents in South Korea: a population-level study and future projections up to 2050. BMJ Open Ophthalmol. 2024 Dec 11;9(1):e001748. (corresponding author)
3. Surl D, Lee H, Han J. Concentric Macular Rings Sign in a Patient with Variant Turner Syndrome. Ophthalmology. 2024 Nov 20 [Online ahead of print]. (corresponding author)
4. Sangermano R, Gupta P, Price C, Han J, Navarro J, Condroyer C, Place EM, Antonio A, Mukai S, Zanlonghi X, Sahel JA, DiTroia S, O’Heir E, Duncan JL, Pierce EA, Zeitz C, Audo I, Huckfeldt RM, Bujakowska KM. Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration. NPJ Genom Med. 2024 Nov 8;9(1):58.
5. Kim M, Seo Y, Surl D, Han J. Nanophthalmos with foveal hypoplasia and wrinkling of macular mound caused by novel biallelic RPSS56 variants. Korean J Ophthamol. 2024 Oct 22 [Online ahead of print]. (corresponding author)
6. Moon CE, Lee JK, Kim H, Kwon JM, Kang Y, Han J, Ji YW, Seo Y. Proteomic analysis of CD29+ Muller cells reveals metabolic reprogramming in rabbit myopia model. Sci Rep 2024 Oct 14;14(1):24072.
7. Surl D, Won D, Lee ST, Lee CS, Lee J, Lim HT, Chung SA, Song WK, Kim M, Kim SS, Shin S, Choi JR, Sangermano R, Byeon SH, Bujakowska KM,* Han J*. Clinician-Driven Reanalysis of Exome Sequencing Data From Patients With Inherited Retinal Diseases. JAMA Netw Open. 2024 May 1;7(5):e2414198. (*co-corresponding author)
8. Seo Y, Han J, Kim MJ, Cha NR, Kim J. Comprehensive evaluation of ocular complications in atopic dermatitis: insights from a contemporary cohort study in Korean population. Int J Dermatol. 2024 May;63(5):624-631.
9. Min YG, Moon Y, Kwon YN, Lee BJ, Park KA, Han JY, Han J, Lee HJ, Baek SH, Kim BJ, Kim JS, Park KS, Kim NH, Kim M, Nam TS, Oh SI, Jung JH, Sung JJ, Jang MJ, Kim SJ, Kim SM. Prognostic factors of first-onset optic neuritis based on diagnostic criteria and antibody status: a multicentre analysis of 427 eyes. J Neurol Neurosurg Psychiatry. 2024 Jul 15;95(8):753-760.
10. Seo Y, Joo K, Lee J, Diaz A, Jang S, Cherry TJ, Bujakowska KM, Han J,* Woo SJ,* Small KW. Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of PRDM13 causing North Carolina macular dystrophy in Korea. Mol Vis. 2024 Feb 19;30:58-66. (*co-corresponding author)
11. Han JY, Han J, Han SH. Efficacy of part-time patching in preventing recurrence after bilateral lateral rectus recession in children with intermittent exotropia. BMC Ophthalmol 2023 Dec 14;23(1):510.
12. Han JY, Kim S, Han J, Kim SS, Han SH, Lee SW, Kim YJ. Neuro-Ophthalmic Adverse Events of COVID-19 Infection and Vaccines: A Nationwide Cohort Study. Invest Ophthalmol Vis Sci. 2023 Nov 1;64(14):37.
13. Joo H, Lee CS, Joe S, Han J, Kim HK, Cho H. Bickerstaff’s brainstem encephalitis: a rare case of neurological complication in Ulcerative Colitis. BMC Neurol. 2023;23(1):386.
14. Moon Y, Park KA, Han J, Hwang JM, Kim SJ, Han SH, Lee BJ, Kang MC, Goh YH, Lim BC, Yang HK, Jung JH. Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea. Neuro Sci 2024 Mar;45(3):1173-1183.
15. Jung YH, Kwak JJ, Joo K, Lee HJ, Park KH, Kim MS, Lee EK, Byeon SH, Lee CS, Han J, Lee J, Yoon CK, Woo SJ. Clinical and genetic features of Korean with retinitis pigmentosa associated with mutations with rhodopsin. Front Genet 2023;14:1240067.
16. Jo WG, Lee CS, Han J. Clinical and Genetic Findings in Korean Patients with Choroideremia. Koran J Ophthalmol. 2023;37(4):285-291.
17. Kim DG, Joo K, Han J, Choi M, Kim SW, Park KH, Park SJ, Lee CS, Byeon SH, Woo SJ. Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans. Genes (Basel). 2023;14(5):1057.
18. Han JY, Han J, Han SH. Correlation between lateral rectus muscle recession and myopic progression in children with intermittent exotropia. Sci Rep 2023;13(1):7200.
19. Han J, Joo K, Kim US, Woo SJ, Lee EK, Lee JY, Park TK, Kim SJ, Byeon SH. Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee. Korean J Ophthalmol. 2023;37(2):166-186.
20. Choi YJ, Joo K, Lim HT, Kim SS, Han J*, Woo SJ*. Clinical and Genetic Features of Korean Patients with Achromatopsia. Genes (Basel). 2023 Feb 18;14(2):519. (*co-corresponding author)
21. Moon CE, Ji YW, Lee JK, Han K, Kim H, Byeon SH, Han S, Han J, Seo Y. Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model. Int J Mol Sci. 2023 Jan 9;24(2):1286
22. Seo Y, Lim HT, Lee BJ, Han J. Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia. Am J Med Genet A. 2023 Feb;191(2):582-585. (corresponding author)
23. Cho H, Seo Y, Han SH, Han J. Factors Related to Axial Length Elongation in Myopic Children Who Received 0.05% Atropine Treatment. J Ocul Pharmacol Ther 2022;38(10):703-708. (corresponding author)
24. Park KA, Yang HK, Han J*, Kim SJ*, Park SE, Lee HJ, Han SH, Oh SY, Hwang JM. Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study. J Ophthalmol 2022;4281772. (*co-corresponding author)
25. Seo Y, Kim TY, Won D, Shin S, Choi JR, Lee ST, Lee BJ, Lim HT, Han SH*, Han J*. . Front Neurol;13:978532. (*co-corresponding author)
26. Jun JW, Seo Y, Han SH, Han J. The importance of genome sequencing: unravelling SSBP1 variant missed by exome sequencing. Ophthalmic Genet 2023 Jun;44(3):286-290 (corresponding author)
27. Kim HR, Han J, Kim YJ, Kang HG, Byeon SH, Kim SS, Lee CS. Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy. Genes (Basel). 2022;13(7):1197
28. Lee J, Jeong H, Won D, Shin S, Lee ST, Choi JR, Byeon SH, Kuht HJ, Thomas MG*, Han J*. Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus. Transl Vis Sci Technol. 2022;11(6):25. (*co-corresponding author)
29. Seo Y, Kim TY, Won D, Choi JR, Seo GH, Lee ST, Han J. PTPN23 Neurodevelopmental Disorder Presenting With Optic Atrophy and Spasmus Nutans-Like Nystagmus. J Neuroophthalmol. 2023 Dec 14;23(1):510. (corresponding author)
30. Kuht HJ, Maconachie G, Han J, Kessel L, Van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi JH, Tobin MD, Sheth BMedSci V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arvelier B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Genotype and Phenotypic Spectrum of Foveal Hypoplasia. Ophthalmology. 2022;129(6):708-718.
31. Moon D, Park HW, Surl D, Won D, Lee ST, Shin S, Choi JR, Han J. Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort. Genes (Basel). 2021 Dec 23;13(1):27. (corresponding author)
32. Yoo J, Lim SH, Jung IH, Park HH, Han J, Hong CK. Factors Associated With Abducens Nerve Palsy in Patients Undergoing Surgery for Petroclival Meningiomas. J Neuroophthalmol. 2022;42(1):e209-e216.
33. Choi SI, Woo SJ, Oh BL, Han J, Lim HT, Lee BJ, Joo K, Park JY, Jang JH, So MK, Kim SJ. Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1. Genes (Basel). 2021 Oct 5;12(10):1578.
34. Jurkute N, Bertacchi M, Arno G, Tocco C, Kim US, Kruszewski AM, Avery AM, Bedoukian EC, Han J, Ahn SJ, Pontikos N, Acheson J, Davagnanam I, Bowman R, Kaliakasos M, Gradham A, Wakeling E, Oluonye N, Reddy MA, Clark E, Rosser E, Amanti-Bonneau P, Charif M, Lenaers G, Meunier I, Defoort S, Vincent-Delorme C, Robson AG, Holder GE, Jeanjean L, Martinez-Monseny A, Vidal-Santacana M, Dominici C, Gaggioli C, Giordano N, Caleo M, Liu GT, Genomic England Research Consortium, Webster AR, Studer M, Yu-Wai-Man P. Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model. Brain Commun. 2021 Jul 20;3(3):fcab162.
35. Han J, Kim TY, Kim M. Coats-like Exudative Vitreoretinopathy in NMNAT1 Leber Congenital Amaurosis. Ophthalmol Retina. 2021 Jul;5(7):624.
36. Won D, Hwang JY, Shim Y, Byeon SH, Lee J, Lee CS, Kim M, Lim HT, Choi JR, Lee ST*, Han J*. In Silico identification of a common mobile element insertion in exon 4 of RP1. Sci Rep. 2021 Jun 28;11(1):13381. (*co-corresponding author)
37. Cho H, Lyoo CH, Park SE, Seo Y, Han SH, Han J. Optical coherence tomography findings facilitate the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay. Korean J Ophthalmol. 2021 Aug;35(4):330-331. (corresponding author)
38. Seo Y, Kim SS, Han J. Short Stature With Optic Atrophy and Cone Dystrophy. JAMA Ophthalmol. 2021 Aug 1; 139(8):910-911. (corresponding author)
39. Kim HM, Joo K, Han J,* Woo SJ.* Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients. Genes (Basel). 2021 May 21;12(6):789. (*co-corresponding author)
40. Jin S, Park SE, Won D, Lee ST, Han SH, Han J. TUBB3 M323V Syndrome Presents with Infantile Nystagmus. Genes (Basel). 2021 Apr 15;12(4):575. (corresponding author)
41. Lee J, Han J, Byeon SH. Retinitis Pigmentosa with Epiretinal Neovascularization at the Macula. Ophthalmol Retina. 2021 Apr;5(4):329.
42. Lee J, Lee H, Lee YM, Kuht HJ, Thomas MG, Kim SJ, Lee ST, Han J. DYNC2H1 variants cause Leber congenital amaurosis without syndromic features. Clin Genet. 2021;100(1):11-113. (corresponding author)
43. Murakami Y, Koyanagi Y, Fukushima M, Yoshimura M, Fujiwara K, Akiyama M, Momozawa Y, Ueno S, Terasaki H, Oishi A, Miyata M, Ikeda H, Tsujikawa A, Mizobuchi K, Hayashi T, Fujinami K, Tsunoda K, Park JY, Han J, Kim M, Lee CS, Kim SJ, Park TK, Joo K, Woo SJ, Ikeda Y, Sonoda KH. Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients. Ophthalmol Retina. 2021 Dec;5(12):1269-1279.
44. Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Clinical utility gene card for FRMD7-related infantile nystagmus. Eur J Hum Genet. 2021 Oct;29(10):1584-1588.
45. Han J, Park SY, Lee JY. Nationwide population-based incidence and etiologies of pediatric and adult Horner syndrome. J Neurol. 2021 Apr;268(4):1276-1283.
46. Lee J, Suh Y, Jeong H, Kim GH, Byeon SH, Han J,* Lim HT*. Aberrant expression of PAX6 gene associated with classical aniridia: identification and functional characterization of novel noncoding mutations. J Hum Genet. 2021 Mar;66(3):333-338.(*co-corresponding author)
47. Han SY, Han J, Lee JB, Han SH. Comparison of surgical outcomes between lateral rectus recession and medial rectus advancement for postoperative consecutive exotropia. Medicine (Baltimore). 2020 Sep 4;99(36):e21401.
48. Kuht HJ,* Han J,* Maconachie GDE,* Park SE, Lee ST, McLean R, Sheth V, Hisaund M, Dawar B, Sylvius N, Mahmood U, Prodlock FA, Gottob I, Lim HT, Thomas MG. SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. Hum Mol Genet. 2020 Nov 4;29(18):2989-3002 (*co-first author)
49. Han JY, Yoon S, Brown NS, Han SH, Han J. Accuracy of the Hand-held Wavefront Aberrometer in Measurement of Refractive Error. Korean J Ophthalmol. 2020;34(3):227-234. (corresponding author)
50. Surl D, Shin S, Lee ST, Choi JR, Lee J, Byeon SH, Han SH, Lim HT,* Han J.* Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis. Mol Vis. 2020 Feb 24;26:26-35. (*co-corresponding author)
51. Park H, Han J, Lee Y, Kwak S, Koo SK. Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis. Stem Cell Res. 2020 Mar;43:101725.
52. Yoo TK, Han SH, Han J. RP2 Rod-Cone Dystrophy Causes Spasmus Nutans-Like Nystagmus. J Neuroophthalmol. 2021 Mar 1;41(1):e91-93. (corresponding author)
53. Lee JY,* Han J,* Yang M, Oh SY. Population-based Incidence of Pediatric and Adult Optic Neuritis and the Risk of Multiple Sclerosis. Ophthalmology. 2020;127(3):417-425. (co-first author)
54. Moon Y, Kim US, Han J, Ahn H, Lim HT. Clinical and Optic Disc Characteristics of Patients Showing Visual Recovery in Leber Hereditary Optic Neuropathy. J Neuroophthalmol. 2020;40(1):15-21.
55. Lee JS, Han J, Han SH. Risk factors associated with poor outcome after medial rectus resection for recurrent intermittent exotropia. Graefes Arch Clin Exp Ophthalmol. 2020;258(2):445-450.
56. Park H, Han J, Lee Y, Kwak S, Koo SK. Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient. Stem Cell Res. 2019;41:101648.
57. Lee ST, Han J. Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome. JAMA Ophthalmol. 2019;137(12):1465-1466. (corresponding author)
58. Park SE, Lee JS, Lee ST, Kim HT, Han SH, Han J. Targeted panel sequencing identifies a novel NR2F1 mutation in a patients with Bosch-Boonstra-Schaaf optic atrophy syndrome. Ophthalmic Genet. 2019;40(4):359-361. (corresponding author)
59. Kang HG, Kim TY, Han J, Han SH. Refractive Outcomes of 4-Year-old Children after Intravitreal Anti-vascular Endothelial Growth Factor versus Laser Photocoagulation for Retinopathy of Prematurity. Korean J Ophthalmol. 2019 Jun;33(3):272-278.
60. Sim W, Kim SY, Han J, Rim HT, Lee JG, Paik HC, Park MS. Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation in a Patient with Hermansky-Pudlak syndrome and Progressive Pulmonary Fibrosis. Acute Crit Care. 2019;34(1):95-98.
61. Lee SJ, Na JH, Han J, Lee YM. Ophthalmoplegia in Mitochondrial Disease. Yonsei Med J. 2018 Dec;59(10):1190-96.
62. Han J, Yang JY, Lee SC. A Young Woman With Acute Visual Loss. JAMA Ophthalmol. 2018 Sep 1;136(9):1066-1067.
63. Lee JY,* Han J,* Seo JG, Park KA, Oh SY. Diagnostic value of ganglion cell-inner plexiform layer for early detection of ethambutol-induced optic neuropathy. Br J Ophthalmol. 2019 Mar;103(3):379-384. (*co-first author)
64. Lee DH, Han J, Han SH, Lee SC, Kim M. Vitreous hemorrhage and rhegmatogenous retinal detachment that developed after botulinum toxin injection to the extraocular muscle: case report. BMC Ophthalmol. 2017 Dec 13;17(1):249.
65. Rim JH,* Lee ST,* Gee HY, Lee BJ, Choi JR, Park HW, Han SH, Han J. Accuracy of next-generation sequencing for molecular diagnosis in patients with infantile nystagmus syndrome. JAMA Ophthalmol. 2017 Dec 1;135(12):1376-1385. (corresponding author)
66. Yoo TK, Han SH, Han J. Protective effect of biodegradable collagen implants on thinned sclera after strabismus surgery: a paired-eye study. J AAPOS. 2017 Dec;21(6):467-471. (corresponding author)
67. Han J,* Rim JH,* Hwang IS, Kim J, Shin S, Lee ST, Choi JR. Diagnostic application of clinical exome sequencing in Leber congenital amaurosis. Mol Vis. 2017 Sep 20;23:649-59. (*co-first author)
68. Rim HT,* Han J,* Choi YS, Lee T, Kim SS. Stroke risk among adult patients with third, fourth, and sixth cranial nerve palsy: a Nationwide Cohort Study. Acta Ophthalmol. 2017 Nov;95(7):e656-e661 (*co-first author)
69. Han J, Lee T, Lee JB, Han SH. Retinal microstructures are altered in patients with idiopathic infantile nystagmus. Graefes Arch Clin Exp Ophthalmol. 2017 Aug;255(8):1661-1668.
70. Lee JY, Min JH, Han SH, Han J. Transient neonatal myasthenia gravis due to a mother with ocular onset of anti-muscle specific kinase myasthenia gravis. Neuromuscul Disord. 2017 Jul;27(7):655-657. (corresponding author)
71. Han J, Kang M, Han SH. Anterior nasal transposition of the inferior oblique muscle can cause antielevation syndrome. J AAPOS. 2016 Oct;20(5):453-5.
72. Han SY, Han J, Rhiu S, Lee JB, Han SH. Risk factors for consecutive exotropia after esotropia surgery. Jpn J Ophthalmol. 2016 Jul;60(4):333-40.
73. Ahn SS, Han J. Ecchordosis physaliphora presenting with abducens nerve palsy. J AAPOS. 2016 Jun;20(3):266-8. (corresponding author)
74. Kwon HJ, Kang EC, Lee J, Han J, Song WK. Obstructive Sleep Apnea in Patients with Branch Retinal Vein Occlusion: A Preliminary Study. Korean J Ophthalmol. 2016 Apr;30(2):121-6.
75. Han J, Kim SE, Lee SC, Lee CS. Low dose versus conventional dose of intravitreal bevacizumab injection for retinopathy of prematurity: a case series with paired-eye comparison. Acta Ophthalmol. 2018 Jun;96(4):e475-478.
76. Rim TH, Han J, Choi YS, Hwang SS, Lee CS, Lee SC, Kim SS. Retinal Artery Occlusion and the Risk of Stroke Development: Twelve-Year Nationwide Cohort Study. Stroke. 2016 Feb;47(2):376-82.
77. Han J, Kim DW, Lee CH, Han SH. Temporal optic atrophy in a patient with atypical pantothenate kinase-associated neurodegeneration. J Neuroophthalmol. 2016 Jun;36(2):182-6.
78. Han J,* Han SH,* Kim JH, Koh HJ. Restoration of retinally induced aniseikonia in patients with epiretinal membrane after early vitrectomy. Retina. 2016 Feb;36(2):311-20. (*co-first author)
79. Han J,* Byeon MK,* Lee J, Han SY, Lee JB, Han SH. Longitudinal analysis of retinal nerve fiber layer and ganglion cell-inner plexiform layer thickness in ethambutol-induced optic neuropathy. Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2293-9 (*co-first author)
80. Han J, Kim JH, Yoo H, Han SH, Hong S, Seong GJ, Kim CY. Retinal Nerve Fiber Layer Thickness is Decreased in Patients With Hematologic Malignancy. J Glaucoma. 2016 Mar;25(3):e175-81.
81. Han SY, Han J, Han SH, Lee JB, Rhiu S. Ocular alignment after bilateral lateral rectus recession in exotropic children with cerebral palsy. Br J Ophthalmol. 2015 Jun;99(6):757-61.
82. Han J, Han SY, Han SH, Lee JB. Strabismus surgery and long-term visual outcomes in patients with preadolescent onset ocular myasthenia gravis. Graefes Arch Clin Exp Ophthalmol. 2015 Jan;253(1):157-63.
83. Han J,* Lee YM,* Kim SM, Han SY, Lee JB, Han SH. Ophthalmological manifestations in patients with Leigh syndrome. Br J Ophthalmol. 2015 Apr;99(4):528-35. (*co-first author)
84. Han J, Han SY, Lee SK, Lee JB, Han SH. Real stereopsis test using a three-dimensional display with Tridef software. Yonsei Med J. 2014 Nov;55(6):1672-7.
85. Han J, Hong S, Lee S, Kim JK, Lee HK, Han SH. Changes in fusional vergence amplitudes after laser refractive surgery for moderate myopia. J Cataract Refract Surg. 2014 Oct;40(10):1670-5.
86. Han J, Han SY, Lee JB, Han SH. Surgical management of long-standing antielevation syndrome after unilateral anterior transposition of the inferior oblique muscle. J AAPOS. 2014 June;18(3):232-4.
87. Ryu IH, Han J, Lee HK, Kim JK, Han SH. Changes in the accommodation-convergence relationship after the Artisan phakic intraocular lens implantation for myopic patients. Korean J Ophthalmol. 2014 Apr;28(2):150-4.
88. Han J, Lee KS, Rhiu S, Lee JB, Han SH. Linezolid-associated optic neuropathy in a patient with drug-resistant tuberculosis. J Neuroophthalmol. 2013 Sep;33(3):316-8.
89. Han J, Lee SC, Song WK. Recurrent bilateral retinal vasculitis as a manifestation of post-streptococcal uveitis syndrome. Korean J Ophthalmol. 2012 Aug;26(4): 309-11.
90. Lee J, Kim NR, Kim H, Han J, Lee ES, Seong GJ, Kim CY. Negative refraction power causes underestimation of peripapillary retinal nerve fibre layer thickness in spectral-domain optical coherence tomography. Br J Ophthalmol. 2011 Sep;95(9):1284-9.