Evidence map›Paper›PMID 39062633›Full record

ArticleGenes2024

Stefan J Rietmann, Noëlle Cochet-Faivre, Helene Dropsy, Vidhya Jagannathan, Lucie Chevallier, Tosso Leeb

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Stefan J RietmannInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.ORCID 0009-0004-0932-552X
Noëlle Cochet-FaivreUnité de Dermatologie, CHUV-Animaux de Compagnie, Ecole Nationale Vétérinaire d'Alfort, 94700 Maisons-Alfort, France.
Helene DropsyUnité de Dermatologie, CHUV-Animaux de Compagnie, Ecole Nationale Vétérinaire d'Alfort, 94700 Maisons-Alfort, France.
Vidhya JagannathanInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
Lucie ChevallierU955-IMRB, Team 10-Biology of the Neuromuscular System, INSERM, UPEC, Ecole Nationale Vétérinaire d'Alfort, 94700 Maisons-Alfort, France.ORCID 0000-0001-8602-1993
Tosso LeebInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.ORCID 0000-0003-0553-4880

Funding

Swiss National Science Foundation 310030_200354
6 · The paper itself

Abstract

Hypohidrotic ectodermal dysplasia is a developmental defect characterized by sparse or absent hair, missing or malformed teeth and defects in eccrine glands. Loss-of-function variants in the X-chromosomal

Indexed as

Ectodermal Dysplasia 1, AnhidroticEctodysplasinsMutation, MissenseAnimalsCat DiseasesCatsMaleWhole Genome SequencingEctodysplasinsanimal modeldermatologydevelopmentFelis catusprecision medicineskinWGSX-linked

Identifiers

PMID39062633
PMCPMC11276485

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.