Evidence map›Paper›PMID 30576380›Full record

ArticlePloS one2018

Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.

Jargalkhuu Erdenechuluun, Yin-Hung Lin, Khongorzul Ganbat, Delgermaa Bataakhuu, Zaya Makhbal, Cheng-Yu Tsai, Yi-Hsin Lin, Yen-Hui Chan, Chuan-Jen Hsu, Wei-Chung Hsu and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Different Rates of theDiagnostics (Basel, Switzerland) · 2021
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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 4 institutions in 2 countries.

Jargalkhuu ErdenechuluunDepartment of Otolaryngology, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia.
Yin-Hung LinDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Khongorzul GanbatThe EMJJ Otolaryngology Hospital, Ulaanbaatar, Mongolia.
Delgermaa BataakhuuDepartment of Otolaryngology, National Center for Maternal and Child Health, Ulaanbaatar, Mongolia.
Zaya MakhbalDepartment of Otolaryngology, National Center for Maternal and Child Health, Ulaanbaatar, Mongolia.
Cheng-Yu TsaiDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Yi-Hsin LinDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Yen-Hui ChanDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Chuan-Jen HsuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Wei-Chung HsuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.
Pei-Lung ChenGraduate Institute of Medical Genomics and Proteomics, National Taiwan University College of Medicine, Taipei, Taiwan.
Chen-Chi WuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0000-0002-5047-2204
National Taiwan University · TWNational Taiwan University Hospital · TWNational Center for Communicable Diseases · MNMongolian National University of Medical Sciences · MN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic factors are an important cause of idiopathic sensorineural hearing impairment (SNHI). From the epidemiological perspective, mutations of three deafness genes: GJB2, SLC26A4, and MT-RNR1, are much more prevalent than those of other genes worldwide. However, mutation spectra of common deafness genes differ remarkably across different populations. Here, we performed comprehensive genetic examination and haplotype analyses in 188 unrelated Mongolian families with idiopathic SNHI, and compared their mutation spectra and haplotypes to those of other European and Asian cohorts. We confirmed genetic diagnoses in 18 (9.6%) of the 188 families, including 13 with bi-allelic GJB2 mutations, three with bi-allelic SLC26A4 mutations, and two with homoplasmic MT-RNR1 m.1555A>G mutation. Moreover, mono-allelic mutations were identified in 17 families (9.0%), including 14 with mono-allelic GJB2 mutations and three with mono-allelic SLC26A4 mutations. Interestingly, three GJB2 mutations prevalent in other populations, including c.35delG in Caucasians, c.235delC in East Asians, and c.-23+1G>A in Southwest and South Asians, were simultaneously detected in Mongolian patients. Haplotype analyses further confirmed founder effects for each of the three mutations, indicating that each mutation derived from its ancestral origin independently. By demonstrating the unique spectra of deafness-associated mutations, our findings may have important clinical and scientific implications for refining the molecular diagnostics of SNHI in Mongolian patients, and for elucidating the genetic relationships among Eurasian populations.

Indexed as

AllelesAsian PeopleConnexin 26ConnexinsDeafnessGenetic Predisposition to DiseaseHaplotypesHearing Loss, SensorineuralHumansMongoliaMutationSulfate TransportersConnexin 26ConnexinsGJB2 protein, humanSLC26A4 protein, humanSulfate Transporters

Identifiers

PMID30576380
PMCPMC6303056
OpenAlexW2905983326

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LicenceCC BY
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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.