Evidence map›Paper›PMID 36281520›Full record

ArticleAnnals of laboratory medicine2023

The First Korean Case of VEXAS Syndrome Caused by a

Jihoon G Yoon, Seungbok Lee, Sheehyun Kim, Man Jin Kim, Yoon Hwan Chang, Jin Kyun Park, Dong-Yeop Shin, Jangsup Moon

Abstract readCase ReportsLetter
In one paragraph

Article in Annals of laboratory medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Clinical features in VEXAS syndrome: a systematic review.Rheumatology (Oxford, England) · 2025
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jihoon G YoonDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-4401-7803
Seungbok LeeDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-3145-8714
Sheehyun KimDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-4347-4420
Man Jin KimDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-9345-6976
Yoon Hwan ChangDepartment of Laboratory Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-9010-5281
Jin Kyun ParkDivision of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0003-2167-9393
Dong-Yeop ShinDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0003-1753-8846
Jangsup MoonDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0003-1282-4528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationSyndromeHumansRepublic of Korea

Identifiers

PMID36281520
PMCPMC9618899

What OpenQuestion holds

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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.