verified SJR 0,487 · Q2 • database Scopus / SJR & Web of Science indexed

United Kingdom · Taylor and Francis Ltd.

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Ophthalmic Genetics

Ophthalmic Genetics is a journal indexed in SJR in Genetics (clinical) and Ophthalmology with an H index of 47. It has a price of 2040 €. It has an SJR impact factor of 0,487 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,487.

ISSN: 1381-6810

Publisher: Taylor and Francis Ltd.

Category: Genetics (clinical)

Indexation: verifiedScopus / SJR verifiedWeb of Science

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schedule CountryOfPapers database fields

SJR Impact Factor trending_up

0,487 Q2

H-index 47

Acceptance rate pie_chart

32%

Source Acceptance_Rate

Time to publication hourglass_top

NPD

Field NPD

Publication cost (APC) payments

2.040 € Subscription

Non-OA path 0 €

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

SJR Impact

0,487

H-index

Docs (year)

123

Docs 3y

354

Total refs

3454

Cites 3y

411

Citable 3y

330

Cites/Doc 2y

1.02

Ref/Doc

28.08

Immediate OA

2040 €

Embargoed OA

NPD

Non OA / Submission

0 €

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Best articles by citations

Aicardi Syndrome in a Genotypic Male

Z-2 aldose reductase allele and diabetic retinopathy in India

Cataract and Glaucoma Development in Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease)

Book Review

Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son

Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesis

Asymmetric choroidal hypopigmentation in a Son and mother with Waardenburg syndrome type I

Association ofSOD2Polymorphisms with Primary Open Angle Glaucoma in a Chinese Population

Association of EFEMP1 with malattia leventinese and age-related macular degeneration: a mini-review

Association between diabetic retinopathy and interleukin-related gene polymorphisms: A machine learning aided meta-analysis

Are Duane syndrome and infantile esotropia allelic?

An Unusual Cause of Pseudopapillary Oedema: Hyperphosphatemic Hyperostosis Syndrome

SHOW MORE ARTICLES

Allelic variants in the MYOC/TIGR gene in patients with primary open-angle, exfoliative glaucoma and unaffected controls

3D Orbital Reconstruction in a Patient with Microphthalmos and a Large Orbital Cyst - A Case Report

Addendum to ABCR is a major retinal gene: a mini review

Activity of topotecan in retinoblastoma

Abstracts

Abnormal retinal architecture in a 33-week-old fetus with LCA and a homozygous C330Y mutation in RPE65

A rare homozygous rhodopsin splice-site mutation: the issue of when and whether to offer presymptomatic testing

A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy

A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophy

A novel nonsense mutation in Rhodopsin gene in two Indonesian Families with Autosomal Recessive Retinitis Pigmentosa

A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generations

A novel mutation disrupting the cytoplasmic domain of CRB1 in a large consanguineous family of Palestinian origin affected with Leber congenital amaurosis

FAQs

Ophthalmic Genetics has an SJR of 0,487 (best quartile Q2) in the CountryOfPapers database.

Immediate OA APC is 2040 EUR. Non-OA / submission fee is 0 EUR.

The acceptance rate recorded for Ophthalmic Genetics is 32%.

Ophthalmic Genetics

Metrics

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Researcher reviews

Best articles by citations

FAQs

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