Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.14.28Source: DataRank Database

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype is a research paper published in Investigative Ophthalmology & Visual Science (2025). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Download PDF

Cite:

Linked data & code

refseq

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 0.00)OA: goldTopics (36)IDs (PubMed, PMC, OpenAlex)Annotations (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (10)

James G. Bellingham ORCID,Fabiana Louise Motta ORCID,Neringa Jurkutė ORCID,Salmo Raskin ORCID,Fabiana Ramos ORCID

Live enrichment

PubMed:41230902 PMC:PMC12617670 OpenAlex:https://openalex.org/W4416187897

NEI NIH HHS

Grant: R01 EY025718

Wellcome Trust

Grant: 206619/Z/17/Z

NEI NIH HHS

Grant: R01 EY015518

NIGMS NIH HHS

Grant: P20 GM139769

Wellcome Trust

FWCI

0.00

Citation Percentile

0.2%

goldLicense: cc-by-nc-nd

journalhttps://iovs.arvojournals.org/arvo/content_public/journal/iovs/938735/i1552-5783-66-14-28_1762955544.13607.pdf

publisherhttps://iovs.arvojournals.org/arvo/content_public/journal/iovs/938735/i1552-5783-66-14-28_1762955544.13607.pdf

publisherhttp://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.66.14.28

journalhttps://doi.org/10.1167/iovs.66.14.28

repositoryhttps://pubmed.ncbi.nlm.nih.gov/41230902

Fields of Study

Connexins and lens biologyIntraocular Surgery and LensesOcular Disorders and TreatmentsHumansCataractIntronsMaleFemalePhenotypePedigreeRNA SplicingMembrane ProteinsMutationChildExome SequencingDNA Mutational AnalysisCataract, Autosomal Dominant

MeSH Terms

Exome SequencingCataractChildDNA Mutational AnalysisFemaleHumansIntronsMaleMembrane ProteinsMutationPedigreePhenotypeRNA Splicing

Keywords

RNA splicingIntronPhenotypeMechanism (biology)ExonLens (geology)

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype

FAIR Checklist

Authors (10)

Funding (6 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)