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Neural activity underlying tinnitus generation: Results from PET and fMRI

Hearing research, 2009-09, Vol.255 (1), p.1-13

2009

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Unilateral tinnitus: changes in connectivity and response lateralization measured with FMRI

PloS one, 2014-10, Vol.9 (10), p.e110704-e110704

2014

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Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant

Human genetics, 2022-04, Vol.141 (3-4), p.465-484

2022

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Mechanisms of adaptation in human auditory cortex

Journal of neurophysiology, 2013-08, Vol.110 (4), p.973-983

2013

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Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38

Genes, 2023-02, Vol.14 (2), p.457

2023

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Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant

Human genetics, 2022-04, Vol.141 (3-4), p.991-991

2022

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Functional imaging of unilateral tinnitus using fMRI

Acta oto-laryngologica, 2008-01, Vol.128 (4), p.415-421

2008

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Neural correlates of human somatosensory integration in tinnitus

Hearing research, 2010-08, Vol.267 (1-2), p.78-88

2010

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Cortical Tonotopic Map Changes in Humans Are Larger in Hearing Loss Than in Additional Tinnitus

The Journal of neuroscience, 2020-04, Vol.40 (16), p.3178-3185

2020

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Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis

Biomolecules (Basel, Switzerland), 2022-01, Vol.12 (2), p.220

2022

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Remote Cochlear Implant Assessments: Validity and Stability in Self-Administered Smartphone-Based Testing

Ear and hearing, 2024-01, Vol.45 (1), p.239

2024

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Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands

Journal of medical genetics, 2023-11, Vol.60 (11), p.1061-1066

2023

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Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants

Human genetics, 2022-11, Vol.141 (11), p.1723-1738

2022

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Long-Term Outcomes of Cochlear Implantation in Usher Syndrome

Ear and hearing, 2024-09

2024

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Computational Audiology: New Approaches to Advance Hearing Health Care in the Digital Age

Ear and hearing, 2021-11, Vol.42 (6), p.1499-1507

2021

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Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing

Developmental cell, 2021-05, Vol.56 (10), p.1526-1540.e7

2021

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A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

Journal of medical genetics, 2021-02, Vol.58 (2), p.96-104

2021

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Treatment-related hearing loss in weekly versus triweekly cisplatin chemoradiation for head and neck cancer

European archives of oto-rhino-laryngology, 2024-09

2024

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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

Human genetics, 2019-01, Vol.138 (1), p.61-72

2019

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A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype

Otology & neurotology, 2021-04, Vol.42 (4), p.e399-e407

2021

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Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre study

Journal of otolaryngology-head and neck surgery, 2023-12, Vol.52 (1), p.82-82, Article 82

2023

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A diffusion tensor imaging study on the auditory system and tinnitus

The open neuroimaging journal, 2010-06, Vol.4, p.16-25

2010

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Demographic, clinical and antibody characteristics of patients with digital ulcers in systemic sclerosis: data from the DUO Registry

Annals of the rheumatic diseases, 2012-05, Vol.71 (5), p.718-721

2012

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Medium intensity oral anticoagulants versus aspirin after cerebral ischaemia of arterial origin (ESPRIT): a randomised controlled trial

Lancet neurology, 2007-02, Vol.6 (2), p.115-124

Algra, A, Prof

2007

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Spondylodiscitis in ankylosing spondylitis, inflammation or trauma : a description of six cases

Scandinavian journal of rheumatology, 1996, Vol.25 (1), p.52-57

1996

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Neural activity underlying tinnitus generation: Results from PET and fMRI

Unilateral tinnitus: changes in connectivity and response lateralization measured with FMRI

Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant

Mechanisms of adaptation in human auditory cortex

Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38

Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant

Functional imaging of unilateral tinnitus using fMRI

Neural correlates of human somatosensory integration in tinnitus

Cortical Tonotopic Map Changes in Humans Are Larger in Hearing Loss Than in Additional Tinnitus

Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis

Remote Cochlear Implant Assessments: Validity and Stability in Self-Administered Smartphone-Based Testing

Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands

Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants

Long-Term Outcomes of Cochlear Implantation in Usher Syndrome

Computational Audiology: New Approaches to Advance Hearing Health Care in the Digital Age

Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

Treatment-related hearing loss in weekly versus triweekly cisplatin chemoradiation for head and neck cancer

De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype

Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre study

A diffusion tensor imaging study on the auditory system and tinnitus

Demographic, clinical and antibody characteristics of patients with digital ulcers in systemic sclerosis: data from the DUO Registry

Medium intensity oral anticoagulants versus aspirin after cerebral ischaemia of arterial origin (ESPRIT): a randomised controlled trial

Spondylodiscitis in ankylosing spondylitis, inflammation or trauma : a description of six cases

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