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
FOXC1-related Axenfeld–Rieger spectrum secondary to 6p25 deletion with concomitant distal 13q duplication arising from a maternal balanced t(6;13) translocation
Julie Pegu, Ria Sachdeva, Nivedita Rathore et al.
2026-11-11 Pages 1-4
DOI: 10.1080/13816810.2026.2759311
Pediatric <i>TTLL5</i> -related retinopathy and a recurrent deletion in the United Arab Emirates
Arif O. Khan
2026-11-9 Pages 1-5
DOI: 10.1080/13816810.2026.2758858
Choroidal neovascularization in a 16-year-old female carrier of a CHM mutation
Edward Barayev, Gad Dotan, Amir Sternfeld et al.
2026-11-9 Pages 1-3
DOI: 10.1080/13816810.2026.2760460
Waardenburg–anophthalmia syndrome associated with an SMOC1 start- loss variant: a case report
Neelam Pawar, Sruthi Krishna, Meenakshi Ravindran
2026-11-9 Pages 1-4
DOI: 10.1080/13816810.2026.2743066
Capturing the full spectrum of systemic comorbidities in LHON patients requires a prospective study design
Josef Finsterer
2026-11-9 Pages 1-1
DOI: 10.1080/13816810.2026.2756339
Suspected SCALP syndrome (sebaceous nevus, CNS malformations, aplasia cutis congenita, limbal dermoid, and pigmented nevus) and the spectrum of mosaic RASopathies: ophthalmic and systemic manifestations in a paediatric cohort
Aiswarya Sasi, Bhoomika Sharma, Lokesh Lingappa et al.
2026-11-9 Pages 1-14
DOI: 10.1080/13816810.2026.2758263
The effects of blunt ocular trauma in patients with inherited retinal disease: a multicenter case series
Lily C. Farrell, Justin C. Muste, Demet Tekin et al.
2026-11-8 Pages 1-11
DOI: 10.1080/13816810.2026.2758258
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
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Printed: November 12, 2026 15:54