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Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutations

Leukemia(2025)10.1038/s41375-025-02775-4Source: DataRank Database

Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutations is a research paper published in Leukemia (2025). 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

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Enrichment:Funding (5 grants)Impact (FWCI 5.06)OA: hybridTopics (27)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 (10)

Amy K. Wang,Samuel J. Magaziner ORCID,Sachiko P. Keane,Manja Meggendorfer ORCID,Wolfgang Kern ORCID

Live enrichment

PubMed:41068485 PMC:PMC12634433 OpenAlex:https://openalex.org/W4414981656

EC | Horizon 2020 Framework Programme

Grant: 953407

Exploring cell-to-cell heterogeneity and exploiting epigenetic regulation for the interception of myeloid disease cells.

U.S. Department of Defense

Grant: BMFRP-IDA HT9425-23-1-0507

U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute

Grant: R00AR078205

Gabrielle's Angel Foundation for Cancer Research

Edward P. Evans Foundation

FWCI

5.06

Citation Percentile

1.0%

Citation Trend

2026

hybridLicense: cc-by

journalhttps://www.nature.com/articles/s41375-025-02775-4.pdf

publisherhttps://www.nature.com/articles/s41375-025-02775-4.pdf

publisherhttps://www.nature.com/articles/s41375-025-02775-4

journalhttps://doi.org/10.1038/s41375-025-02775-4

repositoryhttps://pubmed.ncbi.nlm.nih.gov/41068485

Fields of Study

Otitis Media and Relapsing PolychondritisCarbohydrate Chemistry and SynthesisImmunodeficiency and Autoimmune Disorders0303 health sciences03 medical and health sciences

MeSH Terms

FemaleHumansMaleMutationMyelodysplastic SyndromesSkin Diseases, GeneticUbiquitin-Activating Enzymes

Keywords

MutationSomatic cellPhenotypeDiseaseMyelodysplastic syndromesGeneGermline mutationHaematopoiesisHematologyMaleHumansSkin Diseases, GeneticFemaleUbiquitin-Activating EnzymesArticle