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Genomewide Association Study Identifies Copy Number Variants Associated With Warfarin Dose Response and Risk of Venous Thromboembolism in African Americans

Clinical Pharmacology & Therapeutics(2022)10.1002/cpt.2820Source: DataRank Database

Genomewide Association Study Identifies Copy Number Variants Associated With Warfarin Dose Response and Risk of Venous Thromboembolism in African Americans is a research paper published in Clinical Pharmacology & Therapeutics (2022). On theSindex it has a DataRank of 0. It has been cited 3 times.

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Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 0.50)OA: greenTopics (30)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)

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Authors (7)

Cristina Alarcón ORCID,Larisa H. Cavallari ORCID,Edith A. Nutescu ORCID,Gemma L. Carvill ORCID,Minoli A. Perera ORCID

Live enrichment

PubMed:36507737 PMC:PMC11238476 OpenAlex:https://openalex.org/W4311159500

NHLBI NIH HHS

Grant: R01 HL136962

NHLBI NIH HHS

Grant: R21 HL106097

NIMHD NIH HHS

Grant: U54 MD010723

NCATS NIH HHS

Grant: KL2 TR002387

FWCI

0.50

Citation Percentile

0.7%

Citation Trend

2023

2025

greenLicense: http://onlinelibrary.wiley.com/termsAndConditions#vor

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11238476/pdf/nihms-1989364.pdf

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/cpt.2820

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/cpt.2820

publisherhttps://ascpt.onlinelibrary.wiley.com/doi/pdf/10.1002/cpt.2820

Fields of Study

Genetic Associations and EpidemiologyGenomic variations and chromosomal abnormalitiesPrenatal Screening and Diagnostics

MeSH Terms

AnticoagulantsBlack or African AmericanHumansWarfarinPolymorphism, Single NucleotideVenous ThromboembolismGenome-Wide Association StudyDNA Copy Number Variations

Keywords

WarfarinCopy-number variationVKORC1Odds ratioPharmacogenomicsPharmacogeneticsVitamin K epoxide reductaseSingle-nucleotide polymorphismAnticoagulantMedicineInternal medicineBioinformaticsBiologyGeneGeneticsPharmacologyGenomeGenotypeAtrial fibrillation

Sustainable Development Goals

SDG 0: Good health and well-being