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Clinical Utility of Molecular Tumor Board Review for Identification of Possible Germline Pathogenic Variants on Tumor Next-Generation Sequencing Reports

JCO Precision Oncology(2024)10.1200/po.24.00301Source: DataRank Database

Clinical Utility of Molecular Tumor Board Review for Identification of Possible Germline Pathogenic Variants on Tumor Next-Generation Sequencing Reports is a research paper published in JCO Precision Oncology (2024). On theSindex it has a DataRank of 0. It has been cited 4 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access4 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.72)OA: hybridTopics (47)IDs (PubMed, PMC, OpenAlex)

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 (9)

James P. Collard ORCID,Ning Li ORCID,Donglin Yan ORCID,Charles S. Dietrich ORCID,Rachel W. Miller ORCID

Live enrichment

PubMed:39259913 PMC:PMC11404756 OpenAlex:https://openalex.org/W4402434542

NCI NIH HHS

Grant: P30 CA177558

NCI NIH HHS

Grant: P30 CA014520

National Institutes of Health

Grant: 3P30CA177558-01S1

CTRP Supplement

FWCI

0.72

Citation Percentile

0.7%

Citation Trend

2024

2025

hybridLicense: cc-by-nc-nd

journalhttps://ascopubs.org/doi/pdfdirect/10.1200/PO.24.00301

publisherhttps://ascopubs.org/doi/pdfdirect/10.1200/PO.24.00301

journalhttps://doi.org/10.1200/po.24.00301

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39259913

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11404756

Fields of Study

Cancer Genomics and DiagnosticsGenomics and Rare DiseasesGenetic factors in colorectal cancer03 medical and health sciences0302 clinical medicineHumansHigh-Throughput Nucleotide SequencingMaleGerm-Line MutationFemaleNeoplasmsMiddle AgedGenetic TestingAdultAged

MeSH Terms

AdultAgedFemaleGenetic TestingHumansMaleMiddle AgedNeoplasmsGerm-Line MutationHigh-Throughput Nucleotide Sequencing

Keywords

GermlineReferralMedicineGenetic testingGenetic counselingInternal medicineOncologyGeneticsBioinformaticsBiologyFamily medicineGeneMaleAdultNeoplasmsHumansHigh-Throughput Nucleotide SequencingFemaleORIGINAL REPORTSMiddle AgedGerm-Line MutationAged