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

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics(2025)10.1111/cge.70118Source: DataRank Database

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions is a research paper published in Clinical Genetics (2025). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Free full text

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 (12 grants)Impact (FWCI 0.00)OA: hybridTopics (41)IDs (PubMed, OpenAlex)

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 (23)

Daniel E. McGinn,T. Blaine Crowley ORCID,Lydia Rockart,Audrey Green,Victoria Giunta ORCID

Live enrichment

PubMed:41360439 OpenAlex:https://openalex.org/W4417141835

National Institutes of Health

Grant: P01HD070454

National Institutes of Health

Grant: R01HL157157

National Institutes of Health

Grant: R01GM125757

National Institutes of Health

Grant: R01GM125757‐03

National Institutes of Health

Grant: U01MH101720

Canadian Institutes of Health Research

Grant: MOP‐313331

Canadian Institutes of Health Research

Grant: MOP‐111238

NHLBI NIH HHS

Grant: R01 HL084410

CIHR

Grant: MOP-313331

NICHD NIH HHS

Grant: P30 HD071593

NIH HHS

Grant: R01GM125757-03

CIHR

Grant: MOP-111238

FWCI

0.00

Citation Percentile

0.2%

hybridLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.70118

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.70118

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.70118

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1111/cge.70118

journalhttps://doi.org/10.1111/cge.70118

Fields of Study

Congenital heart defects researchCongenital Heart Disease StudiesGenomic variations and chromosomal abnormalitiesHumansHeart Defects, CongenitalFemaleMalePrevalenceChromosome DeletionChromosomes, Human, Pair 22Child, PreschoolInfantChildAdolescentAdult

MeSH Terms

AdolescentAdultChildChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22FemaleHeart Defects, CongenitalHumansInfantMalePrevalence

Keywords

Bicuspid aortic valveTruncus arteriosusHeart diseaseCardiomyopathyCohortTruncusHeart defectHaploinsufficiencyHypertrophic cardiomyopathy22q11.2 distal deletionchromosome abnormalitieschromosome deletioncongenital heart diseaseheart defects‐congenital