ArticleGenes2019
The Prevalence and Clinical Characteristics of
Open access · goldAbstract read
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 29 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 23% of its field
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.
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.
Who cites it
29 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.
- Delayed hearing loss in congenital cytomegalovirus infection: systematic review and meta-analysis.Brazilian journal of otorhinolaryngologyPooled it
- TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.Journal of molecular medicine (Berlin, Germany) · 2026Article
- Genetic Diagnosis and Discovery Enabled by Large Language Models.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Article
- A novel splicing variant in TECTA associated with prelingual autosomal dominant nonsyndromic hearing loss via dominant-negative effect.Human molecular genetics · 2025Article
- ThemedRxiv : the preprint server for health sciences · 2025Article
- Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approach.Cell reports. Medicine · 2025Article
- Microvilli control the morphogenesis of the tectorial membrane extracellular matrix.Developmental cell · 2025Article
- Rational design of a Lfng-enhancer AAV construct drives specific and efficient gene expression in inner ear supporting cells.Hearing research · 2025Article
- NovelGenes · 2025Article
- From genomic discovery to application in age-related hearing loss: a global bibliometric and cross-ethnic analysis.Frontiers in aging neuroscience · 2025Article
- Tectorial membrane: structure, function, and its implications for hearing loss.Frontiers in neurology · 2025Review
- Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.The journal of international advanced otology · 2024Article
- Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia.Croatian medical journal · 2024Article
- Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue.International journal of molecular sciences · 2024Article
- Microvilli regulate the release modes of alpha-tectorin to organize the domain-specific matrix architecture of the tectorial membrane.bioRxiv : the preprint server for biology · 2024Article
- A NovelLife (Basel, Switzerland) · 2023Article
- Behavioral characterization of the cochlear amplifier lesion due to loss of function of stereocilin (STRC) in human subjects.Hearing research · 2023Article
- Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report.Croatian medical journal · 2023Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
18 authors at 14 institutions in 1 country.
Rika YasukawaDepartment of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan. yasukawar@shinshu-u.ac.jp.
Hideaki MotekiDepartment of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan. moteki@shinshu-u.ac.jp.
Shin-Ya NishioDepartment of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan. nishio@shinshu-u.ac.jp.ORCID 0000-0001-6640-2297
Kotaro IshikawaDepartment of Otolaryngology, National Rehabilitation Center for Persons with Disabilities, 4-1 Namiki, Tokorozawa 359-8555, Japan. ishikawa-kotaro@rehab.go.jp.
Satoko AbeDepartment of Otorhinolaryngology, Toranomon Hospital, 2-2-2 Toranomon, Tokyo 105-0001, Japan. abe3387@ybb.ne.jp.
Yohei HonkuraDepartment of Otolaryngology-Head and Neck Surgery, Tohoku University School of Medicine, 1-1 Seiryomachi, Sendai 980-0872, Japan. y-honkura@ktb.biglobe.ne.jp.
Misako HyogoDepartment of Otolaryngology-Head and Neck Surgery, Kyoto Prefectural University of Medicine, 465 Kagii-cho, Kyoto 602-8566, Japan. mihyogo@koto.kpu-m.ac.jp.
Ryota MihashiDepartment of Otolaryngology-Head and Neck Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830-0011, Japan. mihashi_ryouta@med.kurume-u.ac.jp.
Tetsuo IkezonoDepartment of Otorhinolaryngology, Saitama Medical University, 38 Morohongo, Moroyama 350-0451, Japan. ikez@saitama-med.ac.jp.
Tomoko ShintaniDepartment of Microbiology, Sapporo Medical University School of Medicine, South-1, West-17, Sapporo 060-8556, Japan. shinto211@gmail.com.
Noriko OgasawaraDepartment of Microbiology, Sapporo Medical University School of Medicine, South-1, West-17, Sapporo 060-8556, Japan. ogasawara.n@sapmed.ac.jp.
Kyoko ShiraiDepartment of Otorhinolaryngology-Head and Neck Surgery, Tokyo Medical University, 6-7-1 Nishi-shinjuku, Tokyo 160-0023, Japan. anko.anko25@gmail.com.
Hiroshi YoshihashiDepartment of Medical Genetics, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Tokyo 183-8561, Japan. hiroshi_yoshihashi@tmhp.jp.
Takashi IshinoDepartment of Otorhinolaryngology, Head and Neck Surgery, Hiroshima University Hospital, 1-2-3 Kasumi, Hiroshima 734-0037, Japan. tishino@hiroshima-u.ac.jp.
Koshi OtsukiDepartment of Otolaryngology, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1295, Japan. kotsuki@fmu.ac.jp.
Tsukasa ItoDepartment of Otolaryngology, Head and Neck Surgery, Yamagata University Faculty of Medicine, 2-2-2 Iida-nishi, Yamagata 990-9585, Japan. tuito@med.id.yamagata-u.ac.jp.ORCID 0000-0002-4237-3564
Kazuma SugaharaDepartment of Otolaryngology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube City 755-8505, Japan. kazuma@yamaguchi-u.ac.jp.
Shin-Ichi UsamiDepartment of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan. usami@shinshu-u.ac.jp.ORCID 0000-0002-5068-6122
Shinshu University · JPSapporo Medical University · JPFukushima Medical University · JPHiroshima University Hospital · JPKurume University · JPKyoto Prefectural University of Medicine · JPNational Rehabilitation Center for Persons with Disabilities · JPSaitama Medical University · JPTohoku University · JPTokyo Medical University · JPTokyo Metropolitan Children's Medical Center · JPToranomon Hospital · JPYamagata University · JPYamaguchi University · JP
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
AdolescentAdultAgedAged, 80 and overAsian PeopleChildChild, PreschoolExtracellular Matrix ProteinsFemaleGPI-Linked ProteinsHearing Loss, SensorineuralHigh-Throughput Nucleotide SequencingHumansInfantInfant, NewbornJapanExtracellular Matrix ProteinsGPI-Linked ProteinsTECTA protein, humanautosomal dominantDFNA8/12genotype-phenotype correlationhaplotype analysishearing progressionnon-syndromic hearing lossprevalenceTECTA
Identifiers
What OpenQuestion holds
Textmetadata
LicenceCC BY
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.