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

The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy

Journal of Neuromuscular Diseases(2024)10.3233/jnd-230129Source: DataRank Database

The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy is a research paper published in Journal of Neuromuscular Diseases (2024). On theSindex it has a DataRank of 0. It has been cited 4 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access4 citations

Download PDF

Cite:

Linked data & code

refsnp

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 0.65)OA: bronzeTopics (53)IDs (PubMed, PMC, OpenAlex)Annotations (1)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 (39)

Daniele Sabbatini ORCID,Aurora Fusto ORCID,Domenico Gorgoglione ORCID,Giovanni Umberto Borin,Martina Penzo

Live enrichment

PubMed:38363615 PMC:PMC10977446 OpenAlex:https://openalex.org/W4391884413

Telethon

Grant: GTB12001D

Telethon

Grant: GTB12001

National Institutes of Health

Grant: 5R01AR061875-03

Clinically Meaningful Outcomes for Duchenne Muscular Dystrophy Therapeutic Trials

FWCI

0.65

Citation Percentile

0.6%

Citation Trend

2024

2026

bronzeLicense: CC BY NC

journalhttps://content.iospress.com:443/download/journal-of-neuromuscular-diseases/jnd230129?id=journal-of-neuromuscular-diseases%2Fjnd230129

publisherhttps://content.iospress.com:443/download/journal-of-neuromuscular-diseases/jnd230129?id=journal-of-neuromuscular-diseases%2Fjnd230129

publisherhttps://journals.sagepub.com/doi/pdf/10.3233/JND-230129

publisherhttps://journals.sagepub.com/doi/full-xml/10.3233/JND-230129

journalhttps://doi.org/10.3233/jnd-230129

Fields of Study

Muscle Physiology and DisordersCardiomyopathy and Myosin StudiesAdipose Tissue and Metabolism03 medical and health sciences0303 health sciences

MeSH Terms

HaplotypesHumansCardiomyopathiesRetrospective StudiesStroke VolumeDystrophinVentricular Function, LeftProtein IsoformsMuscular Dystrophy, DuchenneLatent TGF-beta Binding Proteins

Keywords

DystrophinMedicineGeeDuchenne muscular dystrophyInternal medicineEjection fractionCardiologyDilated cardiomyopathyCardiomyopathyGeneralized estimating equationCohortGenotypeHeart failureEndocrinologyGeneBiologyGeneticsGlucocorticoid TreatmentGenetic ModifiersLtbp4Research ReportLeft610Ventricular Function, Leftdilated cardiomyopathy; Duchenne muscular dystrophy; genetic modifiers; glucocorticoid treatment; LTBP4Ventricular FunctionHumansProtein IsoformsMuscular DystrophyRetrospective Studies600Stroke VolumeDuchennedilated cardiomyopathy; Duchenne muscular dystrophy; genetic modifiers; glucocorticoid treatment; LTBP4;Muscular Dystrophy, DuchenneHaplotypesLatent TGF-beta Binding ProteinsCardiomyopathies

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being