Evidence map›Paper›PMID 39336818›Full record

ArticleGenes2024

Genetic Basis of Hearing Loss in Mongolian Patients: A Next-Generation Sequencing Study.

Bayasgalan Gombojav, Jargalkhuu Erdenechuluun, Zaya Makhbal, Narandalai Danshiitsoodol, Erkhembulgan Purevdorj, Maralgoo Jargalmaa, Tserendulam Batsaikhan, Pei-Hsuan Lin, Yue-Sheng Lu, Ming-Yu Lo and 3 more

Abstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. A UniqueInternational journal of molecular sciences · 2026
    Article
  2. 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.

Bayasgalan GombojavDepartment of Epidemiology and Biostatistics, School of Public Health, Mongolian National University of Medical Sciences, Ulaanbaatar 14210, Mongolia.
Jargalkhuu ErdenechuluunDepartment of Otolaryngology, School of Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar 14170, Mongolia.
Zaya MakhbalThe EMJJ Otolaryngology Hospital, Ulaanbaatar 14210, Mongolia.
Narandalai DanshiitsoodolHealthy Twin Registry of Mongolia, Ulaanbaatar 14210, Mongolia.ORCID 0000-0002-9524-3667
Erkhembulgan PurevdorjHealthy Twin Registry of Mongolia, Ulaanbaatar 14210, Mongolia.
Maralgoo JargalmaaThe EMJJ Otolaryngology Hospital, Ulaanbaatar 14210, Mongolia.
Tserendulam BatsaikhanDepartment of Otolaryngology, School of Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar 14170, Mongolia.
Pei-Hsuan LinDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.
Yue-Sheng LuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.
Ming-Yu LoDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.
Hsin-Yi TsengDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.
Cheng-Yu TsaiDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.ORCID 0000-0001-6150-4577
Chen-Chi WuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100225, Taiwan.ORCID 0000-0002-5047-2204

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectiveThe genetic landscape of sensorineural hearing impairment (SNHI) varies across populations. In Mongolia, previous studies have shown a lower prevalence of

methodsWe utilized the next-generation sequencing for investigating the causative mutations in 99 Mongolian patients with SNHI.

resultsWe identified pathogenic variants in 53 of the 99 SNHI patients (54%), with

conclusionsOur findings expand the understanding of the genetic landscape of SNHI in Mongolia and highlight the importance of considering population-specific variations in genetic testing and counseling for SNHI.

Indexed as

Hearing Loss, SensorineuralHigh-Throughput Nucleotide SequencingMutationSulfate TransportersAdolescentAdultChildChild, PreschoolConnexin 26FemaleHumansMaleMiddle AgedMongoliaYoung AdultConnexin 26GJB2 protein, humanSLC26A4 protein, humanSulfate Transportersgenetic etiology 3hearing loss 1SLC26A4 2

Identifiers

PMID39336818
PMCPMC11431586

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Registered trials

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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.