Gene4HL: an integrated genetic database for hearing loss

S Huang, G Zhao, J Wu, K Li, Q Wang, Y Fu… - Frontiers in …, 2021 - frontiersin.org
Hearing loss (HL) is one of the most common disabilities in the world. In industrialized
countries, HL occurs in 1–2/1,000 newborns, and approximately 60% of HL is caused by …

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice

C Liu, Y Huang, Y Zhang, H Ding, L Yu, A Wang… - International Journal of …, 2022 - Elsevier
Background Hearing loss (HL) is a prevalent sensorineural disorder, and is among the most
etiologically heterogeneous disorders. With the advent of next-generation sequencing …

[HTML][HTML] Genetic information and precision medicine in hearing loss

DY Oh, BY Choi - Clinical and Experimental …, 2020 - synapse.koreamed.org
Hearing loss (HL) is the most common sensory disorder, affecting at least one in 500 people
in developed countries, and has the highest incidence rate of any congenital sensory organ …

[图书][B] Unravelling the Genetic Bases of Hearing Loss: Functional Characterisation of Pathogenic Variants and Novel Candidate Genes Identified by Whole-Exome …

C Chiereghin - 2019 - search.proquest.com
Open Research Online oro.open.ac.uk Page 1 Open Research Online The Open University’s
repository of research publications and other research outputs Unravelling the Genetic Bases …

Genetics of hearing loss: syndromic

T Koffler, K Ushakov, KB Avraham - Otolaryngologic Clinics of …, 2015 - oto.theclinics.com
Hearing loss (HL) is the most prevalent sensory impairment in both childhood and
adulthood. 1, 2 According to the last update of the World Health Organization (WHO) …

Genetics of hearing loss

J Rudman, XZ Liu - The Hearing Journal, 2019 - journals.lww.com
Hearing loss (HL), as a broad diagnostic term, affects upwards of 360 million people
worldwide. 1 However, the etiologic diversity of HL proves to be a challenge to efficient …

Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review.

M Koohiyan - International Journal of Pediatric Otorhinolaryngology, 2019 - europepmc.org
Background Hereditary hearing loss (HL) as a common disorder is genetically
heterogeneous, which poses a challenge for clinical and molecular diagnosis. Next …

Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss

YB Xiang, CY Xu, YZ Xu, HZ Li, LL Zhou… - … Genetics & Genomic …, 2020 - Wiley Online Library
Background Hearing loss (HL) is a common sensory disorder in humans characterized by
extreme clinical and genetic heterogeneity. In recent years, next‐generation sequencing …

Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss

I Miyanohara, J Ohori, M Tabuchi, S Nishio… - Genes, 2024 - mdpi.com
Hearing loss (HL) is a common and multi-complex etiological deficit that can occur at any
age and can be caused by genetic variants, aging, toxic drugs, noise, injury, viral infection …

Systematic review of hearing loss genes in the African American population

CP Worden, A Jeyakumar - Otology & Neurotology, 2019 - journals.lww.com
Objective: Literature review of the genetic etiology of hearing loss (HL) in the African
American (AA) population. Data Sources: PubMed, EBSCO, and CINAHL were accessed …