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

New Phenotypic Features in FGFR1‐Related Osteoglophonic Dysplasia

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64092Source: DataRank Database

New Phenotypic Features in FGFR1‐Related Osteoglophonic Dysplasia is a research paper published in American Journal of Medical Genetics Part A (2025). On theSindex it has a DataRank of 0. It has been cited 2 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access2 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 0.84)OA: hybridTopics (46)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (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 (8)

Holly E. Babcock,Corey S. Gill,Jamie L. Fraser ORCID,Debra S. Regier ORCID,Rajdeep Kaur ORCID

Live enrichment

PubMed:40260920 PMC:PMC12339206 OpenAlex:https://openalex.org/W4409676495

National Institutes of Health

Grant: ZIA HD009024

FWCI

0.84

Citation Percentile

0.7%

Citation Trend

2026

hybridLicense: public-domain

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.64092

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.64092

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.64092

journalhttps://doi.org/10.1002/ajmg.a.64092

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40260920

Fields of Study

Fibroblast Growth Factor ResearchCraniofacial Disorders and TreatmentsConnective tissue disorders researchChild, PreschoolFemaleHumansMaleBone Diseases, DevelopmentalFibroblast Growth Factor-23MutationPhenotypeReceptor, Fibroblast Growth Factor, Type 1Child

MeSH Terms

Fibroblast Growth Factor-23Bone Diseases, DevelopmentalChildChild, PreschoolFemaleHumansInfantMaleMutationPhenotypeReceptor, Fibroblast Growth Factor, Type 1

Keywords

CraniosynostosisCraniofacialFibroblast growth factor receptor 1PhenotypeHypophosphatemiaDysplasiaShort statureCraniofacial abnormalityMedicineGeneticsBiologyAnatomyPathologyEndocrinologyGeneReceptorFibroblast growth factorSkeletal DysplasiaImpacted TeethFgfr1Nonossifying FibromasOsteoglophonic Dysplasia

Sustainable Development Goals

SDG 0: Good health and well-being