Impact Factor
2.61
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.19
184 total citations
h5-index
16
h5 depth signal
Cited share
55.8%
92 of 165
Total citations
184
Citation footprint
Metric signal
1.05
External metric anchor
Self-citation
4.3%
8 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
372
China
125
United Kingdom
96
India
66
Australia
64
Citing Fields of Research
Ophthalmology
1,062
Genetics & Genomics
233
Cytogenetics
157
Congenital Disorders
102
Brain Neurological Disorders
49
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
2,191
Articles tracked across the journal lifetime
Indexed publication set
165
92 cited publications
Last 12 months
137
11.4 publications/month
Open access share
21.9%
30 OA publications in the last year
Leading citing country
United States
372 citing publications
Leading citing field
Ophthalmology
1,062 citing publications
Latest tracked publication
18 October 2026
10 recent records available
Coverage & Indexing History
v15n1, Mar. 1994-
v15n1, Mar. 1994-
Active Coverage
Research Focus & Classification
Indexed Subjects
Ophthalmology
Issuing & Sponsoring Bodies
Contributor
International Society for Genetic Eye Disease
Contributor
Ophthalmic Genetics Study Club
Contributor
International Society of Pediatric Ophthalmology
Broad Categories
Genetics, Medical
Ophthalmology
MeSH Descriptors
Eye Diseases
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1080/13816810.2026.2743837
Open DOI
Phenotypic variability of a dominant CRX mutation and molecular insights into pathogenesis
02
DOI 10.1080/13816810.2026.2670419
Open DOI
Retinitis Pigmentosa and erythrocytic microcytosis related to hypomorphic variants in the TRNT1 gene
1. Retinitis pigmentosa (RP) is an inherited retinal dystrophy characterized by nyctalopia, visual field constriction, and progressive retinal degeneration. Typical phenotypic features include bone...
03
DOI 10.1080/13816810.2026.2738873
Open DOI
Late onset retinoblastoma in a child with 13 q deletion syndrome
04
DOI 10.1080/13816810.2026.2738871
Open DOI
Patient- and caregiver-reported outcomes in Bardet-Biedl syndrome: a scoping review
05
DOI 10.1080/13816810.2026.2738870
Open DOI
Anterior segment dysgenesis with bilateral acorea and microphthalmia associated with compound heterozygous FOXE3 pathogenic variants: outcomes after optical iridectomy
1. Microcoria and acorea are rare congenital ocular anomalies characterized by an abnormally small pupil and complete absence of a pupillary opening, respectively (1–3). These conditions represent ...
06
DOI 10.1080/13816810.2026.2738874
Open DOI
Norrie disease with asymmetric retinal severity associated with novel NDP variants
07
DOI 10.1080/13816810.2026.2738880
Open DOI
An unusual segmental retinal venous abnormality detected during retinopathy of prematurity screening in an infant with a PAX2 variant
Congenital abnormalities of retinal venous development are rare and may be difficult to distinguish from prematurity-related vascular changes when detected during retinopathy of prematurity screening. In premature infants, atypical poste...
08
DOI 10.1080/13816810.2026.2727546
Open DOI
Treatment outcomes of extra-ocular retinoblastoma after multimodal therapy: a prospective study
1. Retinoblastoma (RB) is the most common primary malignant intraocular tumor of childhood (1). Although potentially curable, outcomes vary widely due to socioeconomic and healthcare disparities. A...
09
DOI 10.1080/13816810.2026.2731375
Open DOI
Congenital microcephaly and bilateral chorioretinal atrophy associated with a KIF11 nonsense variant
1. Kinesin family member 11 (KIF11) encodes kinesin-like protein KIF11, a microtubule-associated motor protein that plays an essential role in mitotic spindle formation, centrosome separation, and ...
10
DOI 10.1080/13816810.2026.2736738
Open DOI
Could thiamine supplementation delay the progression of retinal dystrophy in Rogers syndrome?
1. Thiamine-responsive megaloblastic anemia (TRMA) syndrome (OMIM 249270), also known as Rogers syndrome, is a rare autosomal recessive disorder characterized by a triad of diabetes mellitus, megal...
Bibliographical & Catalog Notes
Imprint varies.
Also issued online.
Official publication of the International Society for Genetic Eye Disease, the Ophthalmic Genetics Study Club and the International Society of Paediatric Ophthalmology.
Vol. 15, no. 1 (MAR 1994)19940721 Notice published Printed on acid-free paper