ArticleGenes2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of
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In one paragraph
Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
What it found
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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.
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Who cites it
19 citing papers in PubMed, 39 citations in OpenAlex.
- Cervical vestibular-evoked myogenic potentials mediate the association between vestibular endolymphatic hydrops and clinical outcomes in acute low-tone sensorineural hearing loss.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026Article
- SDrecall: a sensitive approach for variant detection in segmental duplications.Genome biology · 2026Article
- Prevalence and Clinical Characteristics ofGenes · 2025Article
- The known structural variations in hearing loss and their diagnostic approaches: a comprehensive review.Molecular biology reports · 2025Review
- NovelGenes · 2025Article
- Intrauterine phenotype, genetic analysis, and pregnancy follow-up of fetuses with the 16p12.2 microdeletion.Frontiers in genetics · 2025Article
- A 250-kb Microdeletion Identified in Chromosome 16 Is Associated With Non-Syndromic Sensorineural Hearing Loss in a South Indian Consanguineous Family.Journal of audiology & otology · 2025Article
- Genetic predisposition to immune dysregulation and extracellular matrix remodeling in cardiac arrhythmia reveals potential mediation byFrontiers in cell and developmental biology · 2025Article
- Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis.International journal of molecular sciences · 2024Article
- Generation of human induced pluripotent stem cell lines derived from patients of cystic biliary atresia.Human cell · 2024Article
- Comprehensive genetic screening for vascular Ehlers-Danlos syndrome through an amplification-based next-generation sequencing system.American journal of medical genetics. Part A · 2023Article
- Searching for the Molecular Basis of Partial Deafness.International journal of molecular sciences · 2022Article
- Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.BMC medical genomics · 2022Article
- Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings.Human genetics · 2022Review
- The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.Human genetics · 2022Review
- Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss.Scientific reports · 2021Article
- A MissenseBioMed research international · 2021Article
- Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.Molecular genetics & genomic medicine · 2020Article
- The Importance of Early Genetic Diagnostics of Hearing Loss in Children.Medicina (Kaunas, Lithuania) · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors at 7 institutions in 1 country.
Kenjiro SugiyamaDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. ksugiyama@shinshu-u.ac.jp.
Hideaki MotekiDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. moteki@shinshu-u.ac.jp.
Shin-Ichiro KitajiriDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. kitajiri@shinshu-u.ac.jp.
Tomohiro KitanoDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. tomokitano@shinshu-u.ac.jp.
Shin-Ya NishioDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. nishio@shinshu-u.ac.jp.
Tomomi YamaguchiDepartment of Medical Genetics, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. t_yamaguchi@shinshu-u.ac.jp.
Keiko WakuiDepartment of Medical Genetics, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. kwakui@shinshu-u.ac.jp.
Satoko AbeDepartment of Otorhinolaryngology, Toranomon Hospital, 2-2-2 Toranomon, Minato-ku, Tokyo 105-8470, Japan. abe3387@ybb.ne.jp.
Akiko OzakiDepartment of Otorhinolaryngology-Head and Neck Surgery, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. oto108@osaka-med.ac.jp.
Remi MotegiDepartment of Otorhinolaryngology, Juntendo University, 2-1-1 Hongo, Bunkyo-ku 113-8421, Japan. Rmotegi@juntendo.
Hirooki MatsuiDepartment of Otolaryngology, Head and Neck Surgery, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata-shi, Yamagata 990-9585, Japan. matsuihirooki@gmail.com.
Masato TeraokaDepartment of Otolaryngology, Head and Neck Surgery, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, Ehime 791-0295, Japan. mteraoka@m.ehime-u.ac.jp.
Yumiko KobayashiDepartment of Otolaryngology-Head & Neck Surgery, Iwate Medical University, 19-1 Uchimaru, Morioka, Iwate 020-8505, Japan. ymkobaya@iwate-med.ac.jp.
Tomoki KoshoDepartment of Medical Genetics, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.
Shin-Ichi UsamiDepartment of Otorhinolaryngology, School of Medicine, Shinshu University, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. usami@shinshu-u.ac.jp.
Shinshu University · JPEhime University · JPIwate Medical University · JPJuntendo University · JPOsaka Medical and Pharmaceutical University · JPToranomon Hospital · JPYamagata University · JP
Funding
No grant is acknowledged in the PubMed record.
Abstract
The
Indexed as
Gene FrequencyAdolescentAdultAudiometryChildChild, PreschoolDNA Copy Number VariationsFemaleGPI-Linked ProteinsHearing LossHumansInfantMalePolymorphism, Single NucleotideGPI-Linked ProteinsOTOA protein, humancopy number variationsDFNB22hearing lossOTOA
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What OpenQuestion holds
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LicenceCC BY
Read underepoch 390
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.