Jinu Han

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2014-2023
Publications (10 Years): 24

Top Topics

Children With Cerebral Palsy

Botulinum Toxin

Top Venues

International journal of molecular sciences

The British journal of ophthalmology

Ophthalmic genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, Kyusun Han, Hyunjin Kim, Seok Ho Byeon, Suenghan Han, Jinu Han, Yuri Seo
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model. International journal of molecular sciences 24 (2) (2023)
Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, Kyusun Han, Hyunjin Kim, Seok Ho Byeon, Suenghan Han, Jinu Han, Yuri Seo
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model. International journal of molecular sciences 24 (2) (2023)
Yong Je Choi, Kwangsic Joo, Hyun-Taek Lim, Sung Soo Kim, Jinu Han, Se Joon Woo
Clinical and Genetic Features of Korean Patients with Achromatopsia. Genes 14 (2) (2023)
Dong Geun Kim, Kwangsic Joo, Jinu Han, Mihyun Choi, Seong-Woo Kim, Kyu Hyung Park, Sang Jun Park, Christopher Seungkyu Lee, Suk Ho Byeon, Se Joon Woo
Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans. Genes 14 (5) (2023)
Yong Je Choi, Kwangsic Joo, Hyun-Taek Lim, Sung Soo Kim, Jinu Han, Se Joon Woo
Clinical and Genetic Features of Korean Patients with Achromatopsia. Genes 14 (2) (2023)
Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, Kyusun Han, Hyunjin Kim, Seok Ho Byeon, Suenghan Han, Jinu Han, Yuri Seo
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model. International journal of molecular sciences 24 (2) (2023)
Yeji Moon, Kyung-Ah Park, Jinu Han, Jeong-Min Hwang, Seong Joon Kim, Sueng-Han Han, Byung Joo Lee, Min Chae Kang, Yong Hyu Goh, Byung Chan Lim, Hee Kyung Yang, Jae Ho Jung
Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, Kyusun Han, Hyunjin Kim, Seok Ho Byeon, Suenghan Han, Jinu Han, Yuri Seo
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model. International journal of molecular sciences 24 (2) (2023)
Yong Je Choi, Kwangsic Joo, Hyun-Taek Lim, Sung Soo Kim, Jinu Han, Se Joon Woo
Clinical and Genetic Features of Korean Patients with Achromatopsia. Genes 14 (2) (2023)
Kyung-Ah Park, Hee Kyung Yang, Jinu Han, Seong Joon Kim, Sung Eun Park, Haeng-Jin Lee, Sueng-Han Han, Sei Yeul Oh, Jeong-Min Hwang
Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study. Journal of ophthalmology 2022 (2022)
Hyuna Cho, Yuri Seo, Sueng-Han Han, Jinu Han
Factors Related to Axial Length Elongation in Myopic Children Who Received 0.05% Atropine Treatment. Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics 38 (10) (2022)
Yuri Seo, Hyun Taek Lim, Byung Joo Lee, Jinu Han
Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia. American journal of medical genetics. Part A (2022)
Hae Rang Kim, Jinu Han, Yong Joon Kim, Hyun Goo Kang, Suk Ho Byeon, Sung Soo Kim, Christopher Seungkyu Lee
Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy. Genes 13 (7) (2022)
Jae Won Jun, Yuri Seo, Sueng-Han Han, Jinu Han
The importance of genome sequencing: unraveling SSBP1 variant missed by exome sequencing. Ophthalmic genetics (2022)
Junwon Lee, Hyun Joo Lee, Young-Mock Lee, Helen J Kuht, Mervyn G Thomas, Sang Jin Kim, Seung-Tae Lee, Jinu Han
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features. Clinical genetics 100 (1) (2021)
Soohwa Jin, Sung-Eun Park, Dongju Won, Seung-Tae Lee, Sueng-Han Han, Jinu Han
TUBB3 M323V Syndrome Presents with Infantile Nystagmus. Genes 12 (4) (2021)
Basu Dawar, Helen J Kuht, Jinu Han, Gail D E Maconachie, Mervyn G Thomas
Clinical utility gene card for FRMD7-related infantile nystagmus. European journal of human genetics : EJHG 29 (10) (2021)
Dabin Moon, Hye Won Park, Dongheon Surl, Dongju Won, Seung-Tae Lee, Saeam Shin, Jong Rak Choi, Jinu Han
Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort. Genes 13 (1) (2021)
Hyeong-Min Kim, Kwangsic Joo, Jinu Han, Se Joon Woo
Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients. Genes 12 (6) (2021)
Soon-Il Choi, Se Joon Woo, Baek-Lok Oh, Jinu Han, Hyun-Taek Lim, Byung-Joo Lee, Kwangsic Joo, Jun-Young Park, Ja-Hyun Jang, Min-Kyung So, Sang-Jin Kim
Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1. Genes 12 (10) (2021)
Neringa Jurkute, Michele Bertacchi, Gavin Arno, Chiara Tocco, Ungsoo Samuel Kim, Adam M Kruszewski, Robert A Avery, Emma C Bedoukian, Jinu Han, Sung Jun Ahn, Nikolas Pontikos, James Acheson, Indran Davagnanam, Richard Bowman, Marios Kaliakatsos, Alice Gardham, Emma Wakeling, Ngozi Oluonye, Maddy Ashwin Reddy, Elaine Clark, Elisabeth Rosser, Patrizia Amati-Bonneau, Majida Charif, Guy Lenaers, Isabelle Meunier, Sabine Defoort, Catherine Vincent-Delorme, Anthony G Robson, Graham E Holder, Luc Jeanjean, Antonio Martinez-Monseny, Mariona Vidal-Santacana, Chloé Dominici, Cedric Gaggioli, Nadia Giordano, Matteo Caleo, Grant T Liu, null null, Andrew R Webster, Michèle Studer, Patrick Yu-Wai-Man
Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model. Brain communications 3 (3) (2021)
Junwon Lee, Yoonjong Suh, Han Jeong, Gu-Hwan Kim, Suk Ho Byeon, Jinu Han, Hyun-Taek Lim
Aberrant expression of PAX6 gene associated with classical aniridia: identification and functional characterization of novel noncoding mutations. Journal of human genetics 66 (3) (2020)
Sung Eun Park, Jihei Sara Lee, Seung-Tae Lee, Hye Young Kim, Sueng-Han Han, Jinu Han
Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome. Ophthalmic genetics 40 (4) (2019)
Wooho Sim, Song Yee Kim, Jinu Han, Tyler Hyung Taek Rim, Jin Gu Lee, Hyo Chae Paik, Moo Suk Park
Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation in a Patient with Hermansky-Pudlak Syndrome and Progressive Pulmonary Fibrosis. Acute and critical care 34 (1) (2019)
Jinu Han, Young-Mock Lee, Sang Myung Kim, So Young Han, Jong Bok Lee, Sueng-Han Han
Ophthalmological manifestations in patients with Leigh syndrome. The British journal of ophthalmology 99 (4) (2014)
So Young Han, Jinu Han, Jong Bok Lee, Soolienah Rhiu
Ocular alignment after bilateral lateral rectus recession in exotropic children with cerebral palsy. The British journal of ophthalmology 99 (6) (2014)