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

Genome-Wide Detection of Allele Specific Copy Number Variation Associated with Insulin Resistance in African Americans from the HyperGEN Study

UNC Libraries(2020)10.17615/wrwb-1632Source: DataRank Database

Genome-Wide Detection of Allele Specific Copy Number Variation Associated with Insulin Resistance in African Americans from the HyperGEN Study is a research paper published in UNC Libraries (2020). 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 (4 grants)Impact (FWCI 0.00)OA: greenTopics (32)IDs (PubMed, OpenAlex)SDGs (2)

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 (14)

Nicholas M. Pajewski ORCID,Pankow, Jim,Treva Rice ORCID,Donna K. Arnett ORCID,Uli Broeckel

Live enrichment

PubMed:19162232 OpenAlex:https://openalex.org/W4298269359

National Institutes of Health

Grant: 5T32NS054584-03

UAB Pre and Post-Doctoral Training Program in Biostatistics

National Institutes of Health

Grant: 2R01HL055673-11A1

Hypergen: Genetics of Left Ventricular Hypertrophy

Wellcome Trust

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5T32HL079888-10

UAB Biostatistics Pre-doctoral Training Program

FWCI

0.00

Citation Percentile

0.2%

greenLicense: CC BY

repositoryhttps://doi.org/10.17615/wrwb-1632

https://doi.org/10.1371/journal.pone.0024052

https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0024052&type=printable

https://dx.doi.org/10.17615/wrwb-1632

https://pubmed.ncbi.nlm.nih.gov/21901158

Fields of Study

Genomic variations and chromosomal abnormalitiesEpigenetics and DNA MethylationGenetics and Neurodevelopmental Disorders0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

Copy-number variationGeneticsAlleleVariation (astronomy)BiologyGenomeGeneAdultMaleDNA Copy Number VariationsScienceQRFastingMiddle AgedPolymorphism, Single NucleotideWhite PeopleBlack or African AmericanHypertensionMedicineHumansFemaleInsulin ResistanceAllelesResearch ArticleGenome-Wide Association Study

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Zero hunger