Evidence map›Paper›PMID 37108562›Full record

ArticleInternational journal of molecular sciences2023

Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients.

Margit Pál, Dóra Nagy, Alexandra Neller, Katalin Farkas, Dóra Leprán-Török, Nikoletta Nagy, Dalma Füstös, Roland Nagy, Adrienne Németh, Judit Szilvássy and 3 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 25% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Novel Pathogenic Variant of theInternational journal of molecular sciences · 2025
    Article
  4. 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

13 authors at 4 institutions in 2 countries.

Margit PálDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.ORCID 0000-0003-3662-0837
Dóra NagyDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.ORCID 0000-0002-6224-1972
Alexandra NellerDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Katalin FarkasDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Dóra Leprán-TörökDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Nikoletta NagyDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.ORCID 0000-0001-8576-7953
Dalma FüstösDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Roland NagyDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0003-1618-4724
Adrienne NémethDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Pécs, 7621 Pécs, Hungary.ORCID 0000-0001-9965-0609
Judit SzilvássyDepartment of Otorhinolaryngology and Head-Neck Surgery, University of Debrecen, 4032 Debrecen, Hungary.
László RovóDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.
József Géza KissDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0003-1332-3901
Márta SzéllDepartment of Medical Genetics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
University of Szeged · HUJohannes Kepler University of Linz · ATUniversity of Debrecen · HUUniversity of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hearing loss is the most prevalent sensory disorder worldwide. The majority of congenital nonsyndromic hearing loss (NSHL) cases are caused by hereditary factors. Previously, the majority of NSHL studies focused on the

Indexed as

Hearing LossConnexin 26ConnexinsDeafnessHumansHungaryMutationPilot ProjectsConnexin 26Connexinscochlear implantsgenetic hearing lossgenetic testing

Identifiers

PMID37108562
PMCPMC10138659
OpenAlexW4366287487

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.