Evidence map›Paper›PMID 41944016›Full record

ArticleAllergy2026

Schnitzler Syndrome as an Autoinflammatory Disease Driven by B-Cell-Specific Somatic MYD88 Mutation.

Yuyi Zhou, Yoko Ueki, Naoya Iwata, Hiroshi Oue, Kentaro Kato, Mengyan Li, Kazushi Izawa, Tomoyasu Jo, Seishi Ogawa, Kenji Kabashima and 1 more

Abstract readLetter
In one paragraph

Article in Allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Yuyi ZhouDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yoko UekiDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Naoya IwataDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0009-0006-7291-8381
Hiroshi OueDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0009-0003-3090-0237
Kentaro KatoDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0009-0002-5104-9851
Mengyan LiDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kazushi IzawaDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0003-1080-0936
Tomoyasu JoDepartment of Hematology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0001-9381-0421
Seishi OgawaDepartment of Pathology and Tumour Biology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-7778-5374
Kenji KabashimaDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-0773-0554
Naotomo KambeDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0001-9610-4952

Funding

Japan Agency for Medical Research and Development JP24ek0109582Ministry of Health, Labour and Welfare
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

geneticsIgM gammopathySchnitzler syndrome

Identifiers

PMID41944016
PMCPMC13466152

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.