Evidence map›Paper›PMID 40004049›Full record

ArticleInternational journal of molecular sciences2025

Novel Pathogenic Variant of the

Nikoletta Nagy, Ágnes Szalenko-Tőkés, Margit Pál, Barbara Anna Bokor, Roland Nagy, János András Jarabin, László Róvó, Márta Széll

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Article
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.

Nikoletta NagyDepartment of Medical Genetics, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0001-8576-7953
Ágnes Szalenko-TőkésDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Szeged, 6720 Szeged, Hungary.
Margit PálDepartment of Medical Genetics, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0003-3662-0837
Barbara Anna BokorDepartment of Medical Genetics, University of Szeged, 6720 Szeged, Hungary.ORCID 0009-0002-0824-1047
Roland NagyDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0003-1618-4724
János András JarabinDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Szeged, 6720 Szeged, Hungary.
László RóvóDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Szeged, 6720 Szeged, Hungary.
Márta SzéllDepartment of Medical Genetics, University of Szeged, 6720 Szeged, Hungary.

Funding

Government of Hungary EFOP-3.6.1-16-2016-00008Government of Hungary GINOP-2.3.2-15-2016-00039
6 · The paper itself

Abstract

Autosomal dominant non-syndromic hearing loss (ADNSHL) is a genetically heterogenic condition. The transformation/transcription domain associated protein (

Indexed as

Hearing Loss, SensorineuralAdultExome SequencingFemaleGenes, DominantGenetic Predisposition to DiseaseHeterozygoteHumansHungaryMaleMiddle AgedMutation, MissensePedigreehearing lossmissensenovelTRRAPvariantwhole exome sequencing

Identifiers

PMID40004049
PMCPMC11855266

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.