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

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study

Gene(2024)10.1016/j.gene.2024.148797Source: DataRank Database

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study is a research paper published in Gene (2024). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 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 (6 grants)Impact (FWCI 0.00)OA: greenTopics (48)IDs (PubMed, 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)

Christopher S. von Bartheld ORCID,Andrea B. Agarwal ORCID,Hans Vasquez-Gross,Sorath Noorani Siddiqui,Maleeha Azam ORCID

Live enrichment

PubMed:39068999 OpenAlex:https://openalex.org/W4401009023

National Institutes of Health

Grant: GM103554

National Institutes of Health

Grant: GM104944

National Institutes of Health

Grant: GM103440

NIGMS NIH HHS

Grant: P20 GM103440

NIGMS NIH HHS

Grant: P20 GM103554

NIGMS NIH HHS

Grant: U54 GM104944

FWCI

0.00

Citation Percentile

0.2%

greenLicense: http://www.elsevier.com/open-access/userlicense/1.0/

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11774097/pdf/nihms-2047558.pdf

publisherhttps://api.elsevier.com/content/article/PII:S0378111924006784?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0378111924006784?httpAccept=text/plain

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11774097/

Fields of Study

Ophthalmology and Eye DisordersVestibular and auditory disordersOcular Disorders and TreatmentsAdolescentAdultChildChild, PreschoolFemaleHumansMaleEsotropiaExotropiaGenetic Association StudiesGenetic Predisposition to DiseaseHaplotypesPakistanPolymorphism, Single NucleotideStrabismusWnt2 Protein

MeSH Terms

AdolescentAdultChildChild, PreschoolEsotropiaExotropiaFemaleHaplotypesHumansMalePakistanStrabismusGenetic Predisposition to DiseasePolymorphism, Single NucleotideWnt2 ProteinGenetic Association Studies

Keywords

BiologyStrabismusGeneticsSingle-nucleotide polymorphismCandidate geneGeneGenetic associationGenotypeAnatomyCase control association studyEsotropiaExotropiaSNPs

Sustainable Development Goals

SDG 0: Zero hunger