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Congenital corneal opacities as a new feature in an unusual case of White-Sutton syndrome

Journal of American Association for Pediatric Ophthalmology and Strabismus(2022)10.1016/j.jaapos.2022.05.007Source: DataRank Database

Congenital corneal opacities as a new feature in an unusual case of White-Sutton syndrome is a research paper published in Journal of American Association for Pediatric Ophthalmology and Strabismus (2022). On theSindex it has a DataRank of 0. It has been cited 4 times.

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0DataRank · unranked

Scored on demand from live citation data

4 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.67)OA: closedTopics (36)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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Authors (2)

Ta Chen Chang ORCID,Maria Fernanda Villalba ORCID

Live enrichment

PubMed:35948257 OpenAlex:https://openalex.org/W4290374821

Research to Prevent Blindness

Grant: GR004596

Glaucoma Research Foundation

Grant: 2021 RPB / AAO

National Institutes of Health

Grant: P30EY014801

FWCI

0.67

Citation Percentile

0.7%

Citation Trend

2023

2024

2025

closedLicense: http://www.elsevier.com/open-access/userlicense/1.0/

publisherhttps://api.elsevier.com/content/article/PII:S1091853122001434?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1091853122001434?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.jaapos.2022.05.007

repositoryhttps://pubmed.ncbi.nlm.nih.gov/35948257

Fields of Study

Connective tissue disorders researchGenetic and Kidney Cyst DiseasesGenomics and Rare DiseasesFemaleHumansMutationIntellectual DisabilityMicrocephalyEye AbnormalitiesCorneal OpacityTransposases

MeSH Terms

Corneal OpacityEye AbnormalitiesFemaleHumansIntellectual DisabilityMicrocephalyMutationTransposases

Keywords

MedicinePatent foramen ovaleCorneal opacityExome sequencingWhite (mutation)StrabismusFacial dysmorphismOphthalmologyMicrocephalyExomeDermatologyPediatricsCorneaGeneticsSurgeryMutationBiology

Sustainable Development Goals

SDG 0: No poverty

Congenital corneal opacities as a new feature in an unusual case of White-Sutton syndrome

FAIR Checklist

Authors (2)

Funding (3 grants)

Impact

Open Access

Topics