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Ophthalmic Genetics : Impact Factor & More

eISSN: 1744-5094pISSN: 1381-6810

Key Metrics

CiteScore
2.4
H-Index
44
Impact Factor
< 5
SJR
Q3Ophthalmology
SNIP
0.71
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Topics Covered on Ophthalmic Genetics

Ophthalmic Genetics Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher TAYLOR & FRANCIS INC
Language English
Frequency Quarterly
General Details
LanguageEnglish
FrequencyQuarterly
Publication Start Year1982
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Ophthalmic Genetics

Ophthalmological phenotype associated with biallelic CPAMD8 variants: first report in Mexican patients
  • 2 Apr 2026
  • Ophthalmic Genetics
Identification of a founder mutation in the PRPH2 gene in an isolated Pacific Island population
  • 1 Apr 2026
  • Ophthalmic Genetics
Isolated bull’s eye maculopathy in two siblings with biallelic TULP1 variants
  • 30 Mar 2026
  • Ophthalmic Genetics
A novel case of Heimler syndrome in a young child with compound heterozygous PEX26 mutations: clinical and genetic insights with literature review
  • 29 Mar 2026
  • Ophthalmic Genetics
Primary congenital glaucoma in a patient with Coffin-siris syndrome type 1 due to an ARID1B mutation: a novel association
  • 29 Mar 2026
  • Ophthalmic Genetics
Characterization of ARB in twins: in-trans frameshift and deep intronic BEST1 variants
  • 28 Mar 2026
  • Ophthalmic Genetics
Ophthalmological phenotype associated with biallelic CPAMD8 variants: first report in Mexican patients
  • 2 Apr 2026
  • Ophthalmic Genetics
Identification of a founder mutation in the PRPH2 gene in an isolated Pacific Island population
  • 1 Apr 2026
  • Ophthalmic Genetics
Isolated bull’s eye maculopathy in two siblings with biallelic TULP1 variants
  • 30 Mar 2026
  • Ophthalmic Genetics
A novel case of Heimler syndrome in a young child with compound heterozygous PEX26 mutations: clinical and genetic insights with literature review
  • 29 Mar 2026
  • Ophthalmic Genetics
Primary congenital glaucoma in a patient with Coffin-siris syndrome type 1 due to an ARID1B mutation: a novel association
  • 29 Mar 2026
  • Ophthalmic Genetics
Characterization of ARB in twins: in-trans frameshift and deep intronic BEST1 variants
  • 28 Mar 2026
  • Ophthalmic Genetics

FAQs on Ophthalmic Genetics