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

Genotype‐function‐phenotype correlations for SCN1A variants identified by clinical genetic testing

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.52297Source: DataRank Database

Genotype‐function‐phenotype correlations for SCN1A variants identified by clinical genetic testing is a research paper published in Annals of Clinical and Translational Neurology (2025). On theSindex it has a DataRank of 0. It has been cited 1 time.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access1 citations

Download PDF

Cite:

Linked data & code

refseq

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 3.20)OA: goldTopics (27)IDs (PubMed, PMC, OpenAlex)Annotations (1)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 H. Thompson ORCID,Dillon Scott,Tatiana V Abramova ORCID,Bethany Stieve,Abigail Freeman ORCID

Live enrichment

PubMed:39838578 PMC:PMC11920720 OpenAlex:https://openalex.org/W4406723363

National Center for Advancing Translational Sciences

Grant: UL1TR002373

National Institutes of Health

Grant: NS108874

Lily's Fund for Epilepsy Research

Grant: AAJ2532

NINDS NIH HHS

Grant: U54 NS108874

FWCI

3.20

Citation Percentile

0.9%

Citation Trend

2026

goldLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.52297

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.52297

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.52297

journalhttps://doi.org/10.1002/acn3.52297

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39838578

Fields of Study

Epilepsy research and treatmentGenomics and Rare DiseasesHereditary Neurological Disorders

MeSH Terms

AdolescentChildChild, PreschoolEpilepsyFemaleGenetic TestingHumansInfantInterneuronsMaleGenetic Association StudiesNAV1.1 Voltage-Gated Sodium Channel

Keywords

EpilepsyLoss functionGenetic testingMedicineClinical significancePhenotypeGenotypeGeneticsNeuroscienceBiologyGeneInternal medicine

Sustainable Development Goals

SDG 0: Good health and well-being

Genotype‐function‐phenotype correlations for SCN1A variants identified by clinical genetic testing

FAIR Checklist

Authors (7)

Funding (4 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)