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

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia ( HDR ) Syndrome

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64299Source: DataRank Database

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia ( HDR ) Syndrome is a research paper published in American Journal of Medical Genetics Part A (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

omim

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 (1 grants)Impact (FWCI 0.00)OA: hybridTopics (29)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 (9)

Amanda V. Karam,Julia Shalen ORCID,David E. Tunkel ORCID,Belina Y. Yi ORCID,Kelsey S. Guthrie

Live enrichment

PubMed:41190486 PMC:PMC13034561 OpenAlex:https://openalex.org/W4415914067

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Grant: K08AR081405

FWCI

0.00

Citation Percentile

0.2%

hybridLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.64299

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.64299

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.64299

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/ajmg.a.64299

journalhttps://doi.org/10.1002/ajmg.a.64299

Fields of Study

Congenital heart defects researchGenomics and Rare DiseasesCongenital Heart Disease Studies

MeSH Terms

Exome SequencingArthritis, JuvenileChildFemaleHearing Loss, SensorineuralHumansHypoparathyroidismNephrosisPhenotypeGenetic Predisposition to DiseaseGATA3 Transcription Factor

Keywords

GATA3Lupus nephritisFrameshift mutationRenal dysplasiaExome sequencingJuvenile rheumatoid arthritisPhenotypeAutoimmune diseaseSensorineural hearing lossAutoimmunityHearing lossPsoriasisJuvenile Idiopathic ArthritisHdr SyndromeBarakat Syndrome

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia ( HDR ) Syndrome

FAIR Checklist

Authors (9)

Funding (1 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)