ISSN: 1381-6810

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Ophthalmic Genetics Q2 Unclaimed

Taylor and Francis Ltd. United Kingdom

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Ophthalmic Genetics is a journal indexed in SJR in Genetics (clinical) and Ophthalmology with an H index of 45. It has a price of 2040 €. It has an SJR impact factor of 0,509 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,509.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Ophthalmology (Q2) Pediatrics, Perinatology and Child Health (Q2) Genetics (clinical) (Q3)

Price

2040 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,509

SJR Impact factor

45

H Index

116

Total Docs (Last Year)

369

Total Docs (3 years)

3097

Total Refs

481

Total Cites (3 years)

337

Citable Docs (3 years)

1.24

Cites/Doc (2 years)

26.7

Ref/Doc

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American Journal of Medical Genetics, Part C: Seminars in Medical Genetics Q2
American Journal of Medical Genetics - Seminars in Medical Genetics Q2

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Aims and Scope

Best articles by citations

Phenotype in two families with RP3 associated with RPGR mutations

Aicardi Syndrome in a Genotypic Male

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

Congenital Achromatopsia and Macular Atrophy Caused by a Novel RecessivePDE6CMutation (p.E591K)

Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)

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

Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

Corneoscleral transplantation in congenital corneal staphyloma and Peters' anomaly

Molecular basis of Peters anomaly in Saudi Arabia

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma

Juvenile xanthogranuloma of the corneoscleral limbus: report of two cases

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Congenital Bilateral Retinal Detachment in Two Siblings with Osteoporosis-Pseudoglioma Syndrome

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

Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): A case-series

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

Ocular manifestations of autosomal recessive Alport syndrome

Estrogen-related Polymorphisms in Estonian Patients with Age-related Cataract

Central retinal vein occlusion as the initial manifestation of LHON / MELAS overlap syndrome with mitochondrial DNA G13513A mutation - Case report and literature review

Ocular manifestations of mosaic trisomy 22: A case report and review of the literature

An Unusual Cause of Pseudopapillary Oedema: Hyperphosphatemic Hyperostosis Syndrome