Journal Report

Ophthalmic Genetics

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Journal Information
Journal Title
Ophthalmic Genetics
Publisher
Taylor and Francis Ltd.
ISSN
1381-6810
E-ISSN
1744-5094
Database
SCOPUS
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Coats-like vasculopathy in the setting of PRPH2-associated multifocal macular pattern dystrophy
Michael Miltich, Emily H. Jung, Jesus Vidaurri-Martinez et al.
2026-11-4 Pages 1-6
DOI: 10.1080/13816810.2026.2754043
Identification of a novel homozygous variant in the <i>MKKS</i> gene in a consanguineous Afghan family with Bardet-Biedl syndrome living in Iran
Hourieh Kalhor, Sadid Hooshmandi, Mohammad Ghofrani
2026-11-4 Pages 1-6
DOI: 10.1080/13816810.2026.2738872
Xp22.13 duplication causing Nance–Horan syndrome: case report
Enrico Giuliano, Hannah L. Scanga, Ken K. Nischal
2026-10-30 Pages 1-4
DOI: 10.1080/13816810.2026.2749854
Association of CFH rs1061170 (Y402H), C2 rs9332739 (E318D), and C3 rs2230199 (R102G) gene polymorphism with age-related macular degeneration: an integrative systematic review, meta-analysis, and in-silico approach
Sabana B, Aishwarya Thanigai Arasu, Sabarinath Ravichandar et al.
2026-10-30 Pages 1-22
DOI: 10.1080/13816810.2026.2749870
Evaluation of corneal and lens densitometry using Scheimpflug tomography in neurofibromatosis type 1 patients without clinical ocular involvement
Ali Osman Gündogan, Ekrem Kadıoğlu, Zeynep Kaya et al.
2026-10-30 Pages 1-8
DOI: 10.1080/13816810.2026.2749855
NMNAT1 early-onset retinal dystrophy (EORD) caused by a novel 5‘UTR splice donor variant
Paula C. Morales, Cesar Estrada-Puente, Rachel D’Cunha et al.
2026-10-30 Pages 1-6
DOI: 10.1080/13816810.2026.2740645
Geographic disparities in the distribution of ISGEDR-affiliated ocular genetics physicians relative to retinitis pigmentosa burden
Neil Dogra, Jacob Perkins, Alex V. Levin
2026-10-21 Pages 1-6
DOI: 10.1080/13816810.2026.2749857
Co-occurrence of retinoblastoma and oculocutaneous albinism in a Mexican patient: a case report
Jose de Jesus Perez Becerra, Gladys Hassel Calderon Camacho, Juan Antonio Ramirez Corona et al.
2026-10-21 Pages 1-4
DOI: 10.1080/13816810.2026.2749845
Phenotypic variability of a dominant CRX mutation and molecular insights into pathogenesis
Isabella V. Y. Gomes, Chi Sun, Xiaodong Zhang et al.
2026-10-18 Pages 1-9
DOI: 10.1080/13816810.2026.2743837
Retinitis Pigmentosa and erythrocytic microcytosis related to hypomorphic variants in the <i>TRNT1</i> gene
Rhea Suribhatla, Saoud Al-Khuzaei, Penny Clouston et al.
2026-10-4 Pages 1-4
DOI: 10.1080/13816810.2026.2670419
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Printed: November 7, 2026 17:33