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

Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease

Genes(2021)10.3390/genes12060922Source: DataRank Database

Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease is a research paper published in Genes (2021). On theSindex it has a DataRank of 0. It has been cited 17 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access17 citations

Download PDF

Cite:

Linked data & code

gen doi

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 1.97)OA: goldTopics (40)IDs (PubMed, PMC, OpenAlex)Annotations (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 (11)

Cambria I. Wethey,Melissa T. Cuevas,Anna M. Monley ORCID,Erin E. Baschal ORCID,Morgan R. Bland

Live enrichment

PubMed:34208743 PMC:PMC8235452 OpenAlex:https://openalex.org/W3168196462

National Institutes of Health

Grant: R01AR068292

FWCI

1.97

Citation Percentile

0.9%

Citation Trend

2022

2023

2024

2025

goldLicense: cc-by

journalhttps://www.mdpi.com/2073-4425/12/6/922/pdf?version=1623979985

publisherhttps://www.mdpi.com/2073-4425/12/6/922/pdf?version=1623979985

publisherhttps://www.mdpi.com/2073-4425/12/6/922/pdf

journalhttps://doi.org/10.3390/genes12060922

repositoryhttps://pubmed.ncbi.nlm.nih.gov/34208743

Fields of Study

Connective tissue disorders researchGenetic factors in colorectal cancerTGF-β signaling in diseasesCytoskeletonExtracellular MatrixHumansMultifactorial InheritancePedigreePolymorphism, GeneticQuantitative Trait LociScoliosisExome Sequencing

MeSH Terms

Exome SequencingCytoskeletonExtracellular MatrixHumansPedigreePolymorphism, GeneticScoliosisMultifactorial InheritanceQuantitative Trait Loci

Keywords

Exome sequencingBiologyGeneticsGeneExomeGenome-wide association studyDiseaseMutationSingle-nucleotide polymorphismGenotypeMedicinePathologyCytoskeletonSpineExtracellular matrixVariantsIdiopathic ScoliosisMusculoskeletal DiseasePolygenic

Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease

FAIR Checklist

Authors (11)

Funding (1 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)