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Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy

Journal of Personalized Medicine(2022)10.3390/jpm12050733Source: DataRank Database

Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy is a research paper published in Journal of Personalized Medicine (2022). On theSindex it has a DataRank of 0. It has been cited 5 times.

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Open Access5 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (10 grants)Impact (FWCI 0.77)OA: goldTopics (28)IDs (PubMed, PMC, OpenAlex)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)

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Authors (10)

Edward G. Jones ORCID,Amy M. Berkman ORCID,Hanna J. Tadros ORCID,Jill A. Rosenfeld ORCID,Yaping Yang ORCID

Live enrichment

PubMed:35629155 PMC:PMC9145017 OpenAlex:https://openalex.org/W4225259889

National Institutes of Health

Grant: K08-HL136839

National Institutes of Health

Grant: R38-HL143612

NHLBI NIH HHS

Grant: K08 HL136839

NIH HHS

Grant: R01-HL149870

NHLBI NIH HHS

Grant: R38 HL143612

National Institutes of Health

Grant: 5K08HL136839-04

The Role of Junctophilin Type 2 in Cardiac Node Automaticity

National Institutes of Health

Grant: 5R38HL143612-03

Duke Resident Physician-Scientist Program- NHLBI

Children’s Cardiomyopathy Foundation

Derfner Foundation

American Academy of Pediatrics

FWCI

0.77

Citation Percentile

0.7%

Citation Trend

2023

2024

2025

goldLicense: cc-by

journalhttps://www.mdpi.com/2075-4426/12/5/733/pdf?version=1652317510

publisherhttps://www.mdpi.com/2075-4426/12/5/733/pdf?version=1652317510

publisherhttps://www.mdpi.com/2075-4426/12/5/733/pdf

journalhttps://doi.org/10.3390/jpm12050733

repositoryhttps://pubmed.ncbi.nlm.nih.gov/35629155

Fields of Study

Cardiomyopathy and Myosin StudiesCongenital heart defects researchWilliams Syndrome Research03 medical and health sciences0302 clinical medicine

Keywords

MYH7Hypertrophic cardiomyopathyMedicineCohortMedical geneticsGeneticsProbandCardiomyopathyPopulationExome sequencingExomeSudden cardiac deathBioinformaticsGeneInternal medicineBiologyMutationHeart failureGenetic TestingSecondary FindingMutation HotspotIncidentally Identified VariantArticle

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Reduced inequalities