Evidence map›Paper›PMID 42639505›Full record

ArticleJournal of human immunity2026

Autosomal recessive OSMRβ deficiency: Connecting OSM and/or IL-31 with atopy.

Anne Puel, Jean-Laurent Casanova, Vivien Béziat

Abstract readComment
In one paragraph

Article in Journal of human immunity, 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

5 · Who and what money

Authors and funding

3 authors.

Anne PuelUniversité Paris Cité, Institut Imagine, Laboratory of human genetics of infectious diseases, Necker branch, INSERM UMR 1163, F-75015, Paris, France.ORCID https://orcid.org/0000-0003-2603-0323
Jean-Laurent CasanovaUniversité Paris Cité, Institut Imagine, Laboratory of human genetics of infectious diseases, Necker branch, INSERM UMR 1163, F-75015, Paris, France.ORCID https://orcid.org/0000-0002-7782-4169
Vivien BéziatUniversité Paris Cité, Institut Imagine, Laboratory of human genetics of infectious diseases, Necker branch, INSERM UMR 1163, F-75015, Paris, France.ORCID https://orcid.org/0000-0002-4020-824X

Funding

Genome-wide search for inborn errors of IL-17 immunity underlying chronic mucocutaneous candidiasisR01AI127564 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Jean-Laurent Casanova · 2017 to 2026
$4.8M
NIAID NIH HHS R01 AI127564
6 · The paper itself

Abstract

Hyper-IgE syndrome (HIES) is characterized by recurrent infections, severe eczema, impaired inflammation, and extrahematopoietic manifestations. Most patients carry dominant-negative

Identifiers

PMID42639505
PMCPMC13502130

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.