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

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.

The journal of international advanced otology - 29 Jul 2024

Zhuri Drenushe, Sezginer Guler Hazal, Yalcintepe Sinem, Demir Selma, Atli Engin, Ikbal Atli Emine, Gurkan Hakan

Abstract excerpt

Hearing loss is a widespread condition throughout the world. It may affect patients from newborns to the elderly. There are too many reasons for hearing loss, including congenital hearing loss, virus infections, age-related situations, and traumatic situations, which may be related to the immune-mediated system. Fifty percent of hearing loss is related to genetic mutations and defects; genetic causes are highly...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Hearing Loss

Share to High-Throughput Nucleotide Sequencing

Share to Infant

Share to Infant, Newborn

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 39161163
DOI: 10.5152/iao.2024.22919
PMCID: PMC11363168

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

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.PMID 39161163Read ↗

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

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

Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.Semantic proximity Read ↗

Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical PracticeSemantic proximity Read ↗

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.Semantic proximity Read ↗

Next-generation sequencing for genetic testing of hearing loss populations.Semantic proximity Read ↗

Whole-exome sequencing and its impact in hereditary hearing loss.Semantic proximity Read ↗

The role of next generation sequencing in predicting hearing loss.Semantic proximity Read ↗

Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center: An Eight-year Study.Semantic proximity Read ↗

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

Molecular diagnostics for hereditary hearing loss in children.Semantic proximity Read ↗

Implementing next-generation sequencing for diagnosis and management of hereditary hearing impairment: a comprehensive review.Semantic proximity Read ↗

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