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

Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP

Bone(2022)10.1016/j.bone.2022.116516Source: DataRank Database

Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP is a research paper published in Bone (2022). On theSindex it has a DataRank of 0. It has been cited 5 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access5 citations

Download PDF

Cite:

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 (3 grants)Impact (FWCI 0.67)OA: greenTopics (63)IDs (PubMed, PMC, OpenAlex)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 (7)

Karissa Ludwig ORCID,Francis H. Glorieux ORCID,Brendan Lee ORCID,V. Reid Sutton ORCID,Jean-Marc Retrouvey

Live enrichment

PubMed:35970273 PMC:PMC10408670 OpenAlex:https://openalex.org/W4291152240

National Institutes of Health

Grant: 1U54AR068069-08

NIAMS NIH HHS

Grant: U54 AR068069

National Institutes of Health

Grant: 3U54AR068069-08S1

DIVERSITY SUPPLEMENT: BRITTLE BONE DISORDERS CONSORTIUM OF THE RARE DISEASE CLINICAL RESEARCH NETWORK

FWCI

0.67

Citation Percentile

0.7%

Citation Trend

2024

2025

2026

greenLicense: Elsevier TDM

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10408670/pdf/nihms-1913501.pdf

publisherhttps://api.elsevier.com/content/article/PII:S8756328222001934?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S8756328222001934?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/10408670

Fields of Study

Connective tissue disorders researchBone and Dental Protein StudiesBone health and treatments0301 basic medicine03 medical and health sciences0302 clinical medicineAmino AcidsAnimalsChildDiphosphonatesExtracellular Matrix ProteinsFemaleHumansInfantMalocclusionMiceMolecular ChaperonesMutationOsteogenesis ImperfectaPhenotypeRNA Splice SitesSkull

MeSH Terms

Amino AcidsAnimalsChildDiphosphonatesFemaleHumansInfantMalocclusionMutationOsteogenesis ImperfectaPhenotypeSkullExtracellular Matrix ProteinsMolecular ChaperonesRNA Splice SitesMice

Keywords

Dentinogenesis imperfectaMedicineOsteogenesis imperfectaCraniofacialMalocclusionMaxillaDentistryOrthodonticsAnatomyPlatybasiaCrtapExtracellular Matrix ProteinsDiphosphonatesSkullInfantMicePhenotypeMutationAnimalsHumansFemaleRNA Splice SitesAmino AcidsChildMolecular Chaperones

Sustainable Development Goals

SDG 0: No poverty