Evidence map›Paper›PMID 42279121›Full record

ReviewJournal of clinical medicine2026

The Genetic Causes of Auditory Neuropathy: A Systematic Review.

Nathania Yong, Michelle Cao, Erin Anderson, Lilian Downie, Gary Rance, Jinzi Bai, Karen Liddle, Antonia Howard, Libby Smith, Valerie Sung and 1 more

Registry-linked trialAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Journal of clinical medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07778641 (Genetic Study of OTOF- Related Auditory Neuropathy Spectrum Disorder), which is not on this 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.

NCT07778641 not yet recruitingnot on this map

Genetic Study of OTOF- Related Auditory Neuropathy Spectrum Disorder

Typeobservational_patient_registrySponsorSohag UniversityRan2026 to 2027Enrolled30ConditionsAuditory Neuropathy Spectrum Disorder, Auditory NeuropathyArmsWhole exome sequencing.
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

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

11 authors.

Nathania YongMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-9459-7052
Michelle CaoMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Erin AndersonMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Lilian DownieMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Gary RanceDepartment of Audiology and Speech Pathology, The University of Melbourne, Parkville, VIC 3010, Australia.
Jinzi BaiMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0009-0007-3559-4776
Karen LiddleChild Health Research Centre, The University of Queensland, South Brisbane, QLD 4101, Australia.ORCID 0000-0003-1948-5872
Antonia HowardMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Libby SmithMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0009-0008-4346-4928
Valerie SungMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Jing WangMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-5701-476X

Funding

National Health and Medical Research Council GNT2033683
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

auditory neuropathydiagnostic yieldgeneticshearing lossnext-generation sequencingOTOF

Identifiers

PMID42279121
PMCPMC13258488

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.