Search Results - Jinu Han

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  1. 41
    Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort

    Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort by Moon, Dabin, Park, Hye Won, Surl, Dongheon, Won, Dongju, Lee, Seung-Tae, Shin, Saeam, Choi, Jong Rak, Han, Jinu

    Published in Genes
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  2. 42
    Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome

    Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome by Park, Sung Eun, Lee, Jihei Sara, Lee, Seung-Tae, Kim, Hye Young, Han, Sueng-Han, Han, Jinu

    Published in Ophthalmic genetics
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  3. 43
    A cross-sectional study of ophthalmologic examination findings in 5385 Koreans presenting with intermittent exotropia

    A cross-sectional study of ophthalmologic examination findings in 5385 Koreans presenting with intermittent exotropia by Kim, Dae Hee, Jung, Jae Ho, Choi, Mi Young, Hwang, Jeong-Min, Kim, Su Jin, Lee, Yeon-hee, Han, Sueng-Han, Choi, Dong Gyu

    Published in Scientific reports
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  4. 44
    Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy

    Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy by Kim, Hae Rang, Han, Jinu, Kim, Yong Joon, Kang, Hyun Goo, Byeon, Suk Ho, Kim, Sung Soo, Lee, Christopher Seungkyu

    Published in Genes
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  5. 45
    Author Correction: A cross-sectional study of ophthalmologic examination findings in 5385 Koreans presenting with intermittent exotropia

    Author Correction: A cross-sectional study of ophthalmologic examination findings in 5385 Koreans presenting with intermittent exotropia by Kim, Dae Hee, Jung, Jae Ho, Choi, Mi Young, Hwang, Jeong‑Min, Kim, Su Jin, Lee, Yeon‑hee, Han, Sueng‑Han, Choi, Dong Gyu

    Published in Scientific reports
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  6. 46
    Clinical and Genetic Features of Korean Patients with Achromatopsia

    Clinical and Genetic Features of Korean Patients with Achromatopsia by Choi, Yong Je, Joo, Kwangsic, Lim, Hyun Taek, Kim, Sung Soo, Han, Jinu, Woo, Se Joon

    Published in Genes
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  7. 47
    Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

    Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay by Cho, Hyuna, Lyoo, Chul Hyoung, Park, Sung Eun, Seo, Yuri, Han, Sueng-Han, Han, Jinu

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  8. 48
    Diagnostic application of clinical exome sequencing in Leber congenital amaurosis

    Diagnostic application of clinical exome sequencing in Leber congenital amaurosis by Han, Jinu, Rim, John Hoon, Hwang, In Sik, Kim, Jieun, Shin, Saeam, Lee, Seung-Tae, Choi, Jong Rak

    Published in Molecular vision
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  9. 49
    TUBB3 M323V Syndrome Presents with Infantile Nystagmus

    TUBB3 M323V Syndrome Presents with Infantile Nystagmus by Jin, Soohwa, Park, Sung-Eun, Won, Dongju, Lee, Seung-Tae, Han, Sueng-Han, Han, Jinu

    Published in Genes
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  10. 50
    Ophthalmoplegia in Mitochondrial Disease

    Ophthalmoplegia in Mitochondrial Disease by Lee, Sang Jun, Na, Ji Hoon, Han, Jinu, Lee, Young Mock

    Published in Yonsei medical journal
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  11. 51
    Refractive Outcomes of 4-Year-old Children after Intravitreal Anti-vascular Endothelial Growth Factor versus Laser Photocoagulation for Retinopathy of Prematurity

    Refractive Outcomes of 4-Year-old Children after Intravitreal Anti-vascular Endothelial Growth Factor versus Laser Photocoagulation for Retinopathy of Prematurity by Kang, Hyun Goo, Kim, Tae Young, Han, Jinu, Han, Sueng Han

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  12. 52
    DYNC2H1 variants cause Leber congenital amaurosis without syndromic features

    DYNC2H1 variants cause Leber congenital amaurosis without syndromic features by Lee, Junwon, Lee, Hyunjoo, Lee, Young‐Mock, Kuht, Helen J., Thomas, Mervyn G., Kim, Sang Jin, Lee, Seung‐Tae, Han, Jinu

    Published in Clinical genetics
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  13. 53
    Clinical and Genetic Findings in Korean Patients with Choroideremia

    Clinical and Genetic Findings in Korean Patients with Choroideremia by Woo Gyeong Jo, Christopher Seungkyu Lee, Jinu Han

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  14. 54
    Accuracy of the Hand-held Wavefront Aberrometer in Measurement of Refractive Error

    Accuracy of the Hand-held Wavefront Aberrometer in Measurement of Refractive Error by Han, Jae Yong, Yoon, Sangchul, Brown, Nicolas Scott, Han, Sueng-Han, Han, Jinu

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  15. 55
    Strabismus surgery and long-term visual outcomes in patients with preadolescent onset ocular myasthenia gravis

    Strabismus surgery and long-term visual outcomes in patients with preadolescent onset ocular myasthenia gravis by Han, Jinu, Han, So Young, Han, Sueng-Han, Lee, Jong Bok

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  16. 56
    Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans

    Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans by Kim, Dong Geun, Joo, Kwangsic, Han, Jinu, Choi, Mihyun, Kim, Seong-Woo, Park, Kyu Hyung, Park, Sang Jun, Lee, Christopher Seungkyu, Byeon, Suk Ho, Woo, Se Joon

    Published in Genes
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  17. 57
    Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus

    Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus by Lee, Junwon, Jeong, Han, Won, Dongju, Shin, Saeam, Lee, Seung-Tae, Choi, Jong Rak, Byeon, Suk Ho, Kuht, Helen J., Thomas, Mervyn G., Han, Jinu

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  18. 58
    Clinician-Driven Reanalysis of Exome Sequencing Data From Patients With Inherited Retinal Diseases

    Clinician-Driven Reanalysis of Exome Sequencing Data From Patients With Inherited Retinal Diseases by Surl, Dongheon, Won, Dongju, Lee, Seung-Tae, Lee, Christopher Seungkyu, Lee, Junwon, Lim, Hyun Taek, Chung, Seung Ah, Song, Won Kyung, Kim, Min, Kim, Sung Soo, Shin, Saeam, Choi, Jong Rak, Sangermano, Riccardo, Byeon, Suk Ho, Bujakowska, Kinga M, Han, Jinu

    Published in JAMA network open
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  19. 59
    Obstructive Sleep Apnea in Patients with Branch Retinal Vein Occlusion: A Preliminary Study

    Obstructive Sleep Apnea in Patients with Branch Retinal Vein Occlusion: A Preliminary Study by Kwon, Hee Jung, Kang, Eui Chun, Lee, Junwon, Han, Jinu, Song, Won Kyung

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  20. 60
    Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1

    Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1 by Choi, Soon-Il, Woo, Se-Joon, Oh, Baek-Lok, Han, Jinu, Lim, Hyun-Taek, Lee, Byung-Joo, Joo, Kwangsic, Park, Jun-Young, Jang, Ja-Hyun, So, Min-Kyung, Kim, Sang-Jin

    Published in Genes
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