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Mouse screen reveals multiple new genes underlying mouse and human hearing loss

PLoS biology, 2019-04, Vol.17 (4), p.e3000194-e3000194

2019

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The Mouse as a Model for Age-Related Hearing Loss - A Mini-Review

Gerontology (Basel), 2015-01, Vol.61 (2), p.149-157

2015

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Differential regulation of mammalian and avian ATOH1 by E2F1 and its implication for hair cell regeneration in the inner ear

Scientific reports, 2021-09, Vol.11 (1), p.19368-19368, Article 19368

2021

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Age-Related Hearing Loss

Cold Spring Harbor perspectives in biology, 2019-08, Vol.9 (8), p.a033217

2019

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Targeted deletion of the RNA-binding protein Caprin1 leads to progressive hearing loss and impairs recovery from noise exposure in mice

Scientific reports, 2022-02, Vol.12 (1), p.2444-16, Article 2444

2022

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Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank

Scientific reports, 2021-03, Vol.11 (1), p.6470-6470, Article 6470

2021

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Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

BMC medical genomics, 2018-09, Vol.11 (1), p.77-77, Article 77

2018

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Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear

PLoS genetics, 2017-03, Vol.13 (3), p.e1006692-e1006692

2017

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Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice

Neurobiology of aging, 2013-08, Vol.34 (8), p.2077.e1-2077.e9

2013

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Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort

NeuroImage clinical, 2021-01, Vol.32, p.102823-102823, Article 102823

2021

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Regulation of the orphan nuclear receptor Nr2f2 by the DFNA15 deafness gene Pou4f3

PloS one, 2014-11, Vol.9 (11), p.e112247-e112247

2014

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GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank

American journal of human genetics, 2019-10, Vol.105 (4), p.788-802

2019

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An emerging role for stress granules in neurodegenerative disease and hearing loss

Hearing research, 2022-12, Vol.426, p.108634-108634, Article 108634

2022

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The ototoxic drug cisplatin localises to stress granules altering their dynamics and composition

Journal of cell science, 2023-07, Vol.136 (14)

2023

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High-frequency audiometry reveals high prevalence of aminoglycoside ototoxicity in children with cystic fibrosis

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.248-254

2015

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A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential

Hearing research, 2024-09, Vol.451, p.109091, Article 109091

2024

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The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss

International journal of audiology, 2013-02, Vol.52 (2), p.124-133

2013

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The Epidemiology of Otosclerosis in a British Cohort

Otology & neurotology, 2019-01, Vol.40 (1), p.22-30

2019

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Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank

European journal of human genetics : EJHG, 2020-08, Vol.28 (8), p.1056-1065

2020

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Drug-induced Stress Granule Formation Protects Sensory Hair Cells in Mouse Cochlear Explants During Ototoxicity

Scientific reports, 2019-08, Vol.9 (1), p.12501-9, Article 12501

2019

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Mutations and altered expression of SERPINF1 in patients with familial otosclerosis

Human molecular genetics, 2016-06, Vol.25 (12), p.2393-2403

2016

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Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population

Human genetics, 2018-05, Vol.137 (5), p.357-363

2018

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S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

Scientific reports, 2016-07, Vol.6 (1), p.28964, Article 28964

2016

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Correction: Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank

European journal of human genetics : EJHG, 2021-03, Vol.30 (10), p.1195-1195

2021

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The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity

Molecular and Cellular Biology, 2003-11, Vol.23 (22), p.7957-7964

2003

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Mouse screen reveals multiple new genes underlying mouse and human hearing loss

The Mouse as a Model for Age-Related Hearing Loss - A Mini-Review

Differential regulation of mammalian and avian ATOH1 by E2F1 and its implication for hair cell regeneration in the inner ear

Age-Related Hearing Loss

Targeted deletion of the RNA-binding protein Caprin1 leads to progressive hearing loss and impairs recovery from noise exposure in mice

Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear

Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice

Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort

Regulation of the orphan nuclear receptor Nr2f2 by the DFNA15 deafness gene Pou4f3

GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank

An emerging role for stress granules in neurodegenerative disease and hearing loss

The ototoxic drug cisplatin localises to stress granules altering their dynamics and composition

High-frequency audiometry reveals high prevalence of aminoglycoside ototoxicity in children with cystic fibrosis

A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss

The Epidemiology of Otosclerosis in a British Cohort

Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank

Drug-induced Stress Granule Formation Protects Sensory Hair Cells in Mouse Cochlear Explants During Ototoxicity

Mutations and altered expression of SERPINF1 in patients with familial otosclerosis

Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

Correction: Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank

The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity

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