Evidence map›Paper›PMID 38676816›Full record

ArticleJournal of clinical immunology2024

Functional Validation of a COPA Mutation Broadens the Spectrum of COPA Syndrome.

Robin Kechiche, Clémence David, Joseph A Marsh, Géraldine Labouret, Marie-Louise Frémond

Abstract readLetterCase Reports
PubMed Publisher
In one paragraph

Article in Journal of clinical immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Genetic Familial Interstitial Lung Disease.Clinics in chest medicine · 2025
    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

5 authors.

Robin Kechiche *Laboratory of Neurogenetics and Neuroinflammation Imagine Institute, INSERM UMR1163, Paris, France.
Clémence David *Laboratory of Neurogenetics and Neuroinflammation Imagine Institute, INSERM UMR1163, Paris, France.
Joseph A MarshMRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Géraldine Labouret *Pediatric Pulmonology Department, University Hospital for Children, Toulouse, France.
Marie-Louise Frémond *Laboratory of Neurogenetics and Neuroinflammation Imagine Institute, INSERM UMR1163, Paris, France. marie-louise.fremond@aphp.fr.

Funding

Fondation pour la Recherche Médicale FDM202106013329
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Immunologic Deficiency SyndromesFemaleHumansMaleMutation

Identifiers

PMID38676816

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.