Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.

Human genetics - 1 Apr 2022

Usami Shin-Ichi, Nishio Shin-Ya

Abstract excerpt

Etiological studies have shown genetic disorders to be a major cause of sensorineural hearing loss, but there are a limited number of comprehensive etiological reports based on genetic analysis. In the present study, the same platform using a diagnostic DNA panel carrying 63 deafness genes and the same filtering algorithm were applied to 10,047 samples obtained from social health insurance-based genetic testing...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child, Preschool
Share to Deafness
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss

Share to Hearing Loss, Sensorineural

Share to Insurance, Health

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 34599366
DOI: 10.1007/s00439-021-02371-3
PMCID: PMC9035015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.PMID 34599366Read ↗

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.Semantic proximity Read ↗

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.Semantic proximity Read ↗

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.Semantic proximity Read ↗

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approachSemantic proximity Read ↗

Molecular diagnosis of hereditary deafness and application of stepwise testing strategy.Semantic proximity Read ↗

Genetic background in late-onset sensorineural hearing loss patients.Semantic proximity Read ↗

Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss.Semantic proximity Read ↗

Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.Semantic proximity Read ↗

Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing lossSemantic proximity Read ↗

Next-Generation Sequencing Facilitates Genetic Diagnosis And Improves The Management Of Patients With Hearing Loss In Clinical PracticeSemantic proximity Read ↗

Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.Semantic proximity Read ↗

Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.