Evidence map›Paper›PMID 38352997›Full record

ArticleAmerican journal of medical genetics. Part A2024

Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.

Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 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
0.3field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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

12 authors at 6 institutions in 2 countries.

Duygu DumanJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0001-7583-0349
Memoona RamzanJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Asli SubasiogluDepartment of Medical Genetics, İzmir Katip Çelebi University, Ataturk Education and Research Hospital, İzmir, Turkey.
Ahmet MutluFaculty of Medicine, Department of Otorhinolaryngology, Istanbul Medeniyet University, Istanbul, Turkey.
LéShon PeartDr. John T. Macdonald Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Serhat SeyhanLaboratory of Genetics, Memorial Şişli Hospital, Istanbul, Turkey.
Shengru GuoJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Kadri IlaDepartment of Otorhinolaryngology, Umraniye Education and Research Hospital, Istanbul, Turkey.
Burhan BaltaDepartment of Medical Genetics, Kayseri Training and Research Hospital, Kayseri, Turkey.ORCID 0000-0003-2672-2493
Mahmut Tayyar KalciogluFaculty of Medicine, Department of Otorhinolaryngology, Istanbul Medeniyet University, Istanbul, Turkey.
Guney BademciJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0002-4052-8833
Mustafa TekinJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0002-3525-7960
University of Miami · USIstanbul Eye Hospital · TRIzmir Kâtip Çelebi University · TRKayseri Eğitim ve Araştırma Hastanesi · TRMemorial Sisli Hospital · TRÜmraniye Eğitim ve Araştırma Hastanesi · TR

Funding

A Collaborative Search for New Genes for Non-Syndromic DeafnessR01DC009645 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MUSTAFA TEKIN · 2010 to 2026
$11.8M
Genetic Studies of Inner Ear AnomaliesR01DC012836 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TEKIN, MUSTAFA · 2013 to 2017
$3.2M
NIDCD NIH HHS R01 DC009645NIH HHS R01DC009645NIH HHS R01DC012836
6 · The paper itself

Abstract

Autosomal dominant sensorineural hearing loss (ADSNHL) is a genetically heterogeneous disorder caused by pathogenic variants in various genes, including MYH14. However, the interpretation of pathogenicity for MYH14 variants remains a challenge due to incomplete penetrance and the lack of functional studies and large families. In this study, we performed exome sequencing in six unrelated families with ADSNHL and identified five MYH14 variants, including three novel variants. Two of the novel variants, c.571G > C (p.Asp191His) and c.571G > A (p.Asp191Asn), were classified as likely pathogenic using ACMG and Hearing Loss Expert panel guidelines. In silico modeling demonstrated that these variants, along with p.Gly1794Arg, can alter protein stability and interactions among neighboring molecules. Our findings suggest that MYH14 causative variants may be more contributory and emphasize the importance of considering this gene in patients with nonsyndromic mainly post-lingual severe form of hearing loss. However, further functional studies are needed to confirm the pathogenicity of these variants.

Indexed as

Exome SequencingHearing Loss, SensorineuralMyosin Heavy ChainsMyosin Type IIPedigreeAdolescentAdultChildFemaleGenes, DominantGenetic Predisposition to DiseaseHumansMaleMiddle AgedMutationMYH7b protein, humanMyosin Heavy ChainsMyosin Type IIgenehearing lossMYH14pathogenic variant

Identifiers

PMID38352997
PMCPMC11060900
OpenAlexW4391816251

What OpenQuestion holds

Textmetadata
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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.