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Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63596Source: DataRank Database

Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing is a research paper published in American Journal of Medical Genetics Part A (2024). On theSindex it has a DataRank of 0. It has been cited 6 times.

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Open Access6 citations

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omim go refseq

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 1.19)OA: hybridTopics (28)IDs (PubMed, PMC, OpenAlex)Annotations (3)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)

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Authors (18)

Lindsay V. Clark ORCID,Erdal Coşgun ORCID,Kimberly A. Aldinger ORCID,Andrew E. Timms ORCID,Lely A. Quina ORCID

Live enrichment

PubMed:38895864 PMC:PMC11706325 OpenAlex:https://openalex.org/W4399810303

NHLBI NIH HHS

Grant: R01 HL126523

NHLBI NIH HHS

Grant: P01 HL090554

Seattle Children's Research Institute

Aaron Matthew SIDS Research Guild

Seattle Children's Research Institute

FWCI

1.19

Citation Percentile

0.8%

Citation Trend

2025

2026

hybridLicense: cc-by-nc-nd

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.63596

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.a.63596

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63596

journalhttps://doi.org/10.1002/ajmg.a.63596

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38895864

Fields of Study

Neuroscience of respiration and sleepMitochondrial Function and PathologyNeonatal Respiratory Health Research

MeSH Terms

Whole Genome SequencingAdultFemaleGene FrequencyHumansInfantInfant, NewbornMaleSudden Infant DeathGenetic VariationGenetic Predisposition to Disease

Keywords

GeneGeneticsBiologySudden infant death syndromeAlleleGenomeMedicineROSArrhythmiaCardiomyopathySidsSudepWgsSuid

Sustainable Development Goals

SDG 0: Good health and well-being

Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing

FAIR Checklist

Authors (18)

Funding (5 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)