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

Precision medicine in hearing loss.

Journal of genetics and genomics = Yi chuan xue bao - 20 Feb 2018

Rudman Jason R, Mei Christine, Bressler Sara E, Blanton Susan H, Liu Xue-Zhong

Abstract excerpt

Precision medicine (PM) proposes customized medical care based on a patient's unique genome, biomarkers, environment and behaviors. Hearing loss (HL) is the most common sensorineural disorder worldwide and is frequently caused by a single genetic mutation. With recent advances in PM tools such as genetic sequencing and data analysis, the field of HL is ideally positioned to adopt the strategies of PM. Here, we...

Read the complete abstract on PubMed

Topics

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

Share to Mutation
Share to Hearing, Cochlea, Tinnitus, Genetics
Share to Hearing Loss

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ear Surgery and Otitis Media

Share to Genomics

Share to Precision Medicine

Share to Translational Research, Biomedical

Source

Identifiers

PMID: 29500086
DOI: 10.1016/j.jgg.2018.02.004

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Precision medicine in hearing loss.PMID 29500086Read ↗

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

Genetics of Hearing Loss: Syndromic.Semantic proximity Read ↗

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

Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss.Semantic proximity Read ↗

Genetics of hearing loss: where are we standing now?Semantic proximity Read ↗

Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approachSemantic proximity Read ↗

Precision Medicine as a New Frontier in Speech-Language Pathology: How Applying Insights From Behavior Genomics Can Improve Outcomes in Communication DisordersSemantic proximity Read ↗

Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.Semantic proximity Read ↗

Hearing loss: mechanisms revealed by genetics and cell biology.Semantic proximity Read ↗

Comprehensive Genetic Profiling of Sensorineural Hearing Loss Using an Integrative Diagnostic ApproachSemantic proximity Read ↗

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