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Atomic-level investigation of KCNJ2 mutations associated with ventricular arrhythmic syndrome phenotypes

Scientific Reports(2025)10.1038/s41598-025-95062-2Source: DataRank Database

Atomic-level investigation of KCNJ2 mutations associated with ventricular arrhythmic syndrome phenotypes is a research paper published in Scientific Reports (2025). On theSindex it has a DataRank of 0. It has been cited 2 times.

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Open Access2 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (6 grants)Impact (FWCI 1.40)OA: goldTopics (47)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)

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Authors (7)

Corey L. Anderson ORCID,Louise Reilly ORCID,Ryan L. Woltz ORCID,Yusra Sajid Kiani ORCID,Nipavan Chiamvimonvat ORCID

Live enrichment

PubMed:40175568 PMC:PMC11965533 OpenAlex:https://openalex.org/W4409148268

National Institute of Health

Grant: NIH R01 HL163987

NIH

Grant: NIH R01 HL170521

NHLBI NIH HHS

Grant: R01 HL170521

NHLBI NIH HHS

Grant: R01 HL163987

The Heart Rhythm Society Postdoctoral Fellowship

Gary and Marie Weiner Professorship

FWCI

1.40

Citation Percentile

0.8%

Citation Trend

2026

goldLicense: cc-by-nc-nd

journalhttps://www.nature.com/articles/s41598-025-95062-2.pdf

publisherhttps://www.nature.com/articles/s41598-025-95062-2.pdf

publisherhttps://www.nature.com/articles/s41598-025-95062-2

journalhttps://doi.org/10.1038/s41598-025-95062-2

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40175568

Fields of Study

Cardiac electrophysiology and arrhythmiasIon channel regulation and functionCardiomyopathy and Myosin StudiesHumansPotassium Channels, Inwardly RectifyingPhenotypeAndersen SyndromeMutationMolecular Dynamics SimulationFemaleMaleArrhythmias, Cardiac

MeSH Terms

Arrhythmias, CardiacFemaleHumansMaleMutationPhenotypePotassium Channels, Inwardly RectifyingAndersen SyndromeMolecular Dynamics Simulation

Keywords

HomomericMutationPhenotypeMutagenesisMutantLong QT syndromeLoss functionGeneticsBiologyPotassium channelChannelopathyComputational biologyBiophysicsMedicineGeneNeuroscienceInternal medicineQT intervalMolecular modelingPCAMD simulationNormal Mode AnalysisInward Rectifier CurrentKcnj2Kir2.1Site-directed Mutagenesis Analysis

Atomic-level investigation of KCNJ2 mutations associated with ventricular arrhythmic syndrome phenotypes

FAIR Checklist

Authors (7)

Funding (6 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)