Evidence map›Paper›PMID 33690815›Full record

ArticleBlood2021

Novel somatic mutations in UBA1 as a cause of VEXAS syndrome.

James A Poulter, Jason C Collins, Catherine Cargo, Ruth M De Tute, Paul Evans, Daniela Ospina Cardona, David T Bowen, Joanna R Cunnington, Elaine Baguley, Mark Quinn and 5 more

Open access · bronzeAbstract readComment
In one paragraph

Article in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 4 pooled it
30.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

119 citing papers in PubMed, 4 syntheses or guidelines pooled it, 227 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Article
  8. SomaticBlood neoplasia · 2026
    Article
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  10. Review
  11. Article
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59 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 2 countries.

James A PoulterLeeds Institute of Rheumatic and Musculoskeletal Medicine and.ORCID 0000-0003-2048-5693
Jason C CollinsNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-7653-0070
Catherine CargoHaematological Malignancy Diagnostic Service, St James's University Hospital, Leeds, United Kingdom.
Ruth M De TuteHaematological Malignancy Diagnostic Service, St James's University Hospital, Leeds, United Kingdom.
Paul EvansHaematological Malignancy Diagnostic Service, St James's University Hospital, Leeds, United Kingdom.
Daniela Ospina CardonaNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD.
David T BowenDepartment of Haematology, Leeds Teaching Hospitals, Leeds, United Kingdom.
Joanna R CunningtonDepartment of Rheumatology, Hull University Teaching Hospitals, Hull, United Kingdom.
Elaine BaguleyDepartment of Rheumatology, Hull University Teaching Hospitals, Hull, United Kingdom.
Mark QuinnDepartment of Rheumatology, York Teaching Hospital NHS Foundation Trust, York, United Kingdom; and.
Michael GreenDepartment of Rheumatology, York Teaching Hospital NHS Foundation Trust, York, United Kingdom; and.
Dennis McGonagleLeeds Institute of Rheumatic and Musculoskeletal Medicine and.
David B BeckNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD.
Achim WernerNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD.ORCID 0000-0003-1051-8447
Sinisa SavicLeeds Institute of Rheumatic and Musculoskeletal Medicine and.ORCID 0000-0001-7910-0554
National Institutes of Health · USSt James's University Hospital · GBUniversity of Leeds · GBUniversity of Hull · GBYork Teaching Hospital NHS Foundation Trust · GBLeeds Teaching Hospitals NHS Trust · GB

Funding

Genetic Analysis of Complex Inflammatory DisordersZIAHG200371 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI KASTNER, DANIEL · 2011 to 2024
$18.8M
Ubiquitin-dependent cell-fate decisions during human development and diseaseZIADE000749 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI WERNER, ACHIM · 2018 to 2025
$14.1M
Medical Research Council MR/T02044X/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Ubiquitin-Activating EnzymesHumansMutationSyndromeUbiquitin-Activating Enzymes

Identifiers

PMID33690815
PMCPMC8462400
OpenAlexW3134290526

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.