List of works - Henricus Kunst

A Comparison of Surgical Treatments for Superior Semicircular Canal Dehiscence: A Systematic Review

scientific article

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

scientific article published on 06 July 2020

A Retrospective Cohort Study on the Influence of Comorbidity on Soft Tissue Reactions, Revision Surgery, and Implant Loss in Bone-anchored Hearing Implants

scientific article

A new bone-anchored hearing implant: short-term retrospective data on implant survival and subjective benefit

scientific article

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

scientific article

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2

scientific journal article

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family

scientific article

Auditory brainstem response prior to MRI compared to standalone MRI in the detection of vestibular schwannoma: A modelling study

scientific article published in 2021

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1

scientific article

Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment

scientific article published on 12 January 2017

Causes of permanent childhood hearing impairment ⬇️

scientific article published on February 1, 2011

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

scientific article published on 21 November 2017

Cochlear Implantation in Patients With Usher Syndrome Type IIa Increases Performance and Quality of Life

scientific article published on 11 May 2017

Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11.

scientific article published on 17 April 2017

Congenital oval or round window anomaly with or without abnormal facial nerve course: surgical results for 15 ears

scientific article published on July 2012

Diagnosing necrotizing external otitis on CT and MRI: assessment of pattern of extension

scientific article published in 2021

Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans

scientific article

External ear anomalies and hearing impairment in Noonan Syndrome

scientific article published on April 2015

Feasibility of a wait-and-scan period as initial management strategy for head and neck paraganglioma.

scientific article

Gamma Knife radiosurgery for treatment of growing vestibular schwannomas in patients with neurofibromatosis Type 2: a matched cohort study with sporadic vestibular schwannomas.

scientific article published on 27 January 2017

Gamma Knife radiosurgery for vestibular schwannomas: evaluation of tumor control and its predictors in a large patient cohort in The Netherlands

scientific article published on 02 October 2015

Genetics of hereditary head and neck paragangliomas

scientific article

Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations

scientific article published on 23 July 2011

Genotype-specific abnormalities in mitochondrial function associate with distinct profiles of energy metabolism and catecholamine content in pheochromocytoma and paraganglioma.

scientific article published on 30 May 2013

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.

scientific article published on 12 May 2018

Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment

scientific article

Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors.

scientific article published on 12 October 2015

Insufficient evidence for a role of SERPINF1 in otosclerosis

scientific article published on 09 April 2019

Intrafamilial variable hearing loss in TRPV4 induced spinal muscular atrophy

scientific article

Karyotype-specific ear and hearing problems in young adults with Turner syndrome and the effect of oxandrolone treatment

scientific article published in October 2014

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

scientific article published on 14 January 2017

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse

scientific article published on 28 June 2018

Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome.

scientific article published on 26 March 2015

Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction

scientific article

Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment

scientific article

Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment

scientific article

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease

scientific article

Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrum

scientific article

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome

scientific article published on June 2016

Phenotypes of Two Dutch DFNA3 Families with Mutations in GJB2 ⬇️

scientific article published on March 1, 2011

Potential savings in the diagnosis of vestibular schwannoma

scientific article published on 18 August 2017

Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in <i>TMC1</i> ⬇️

scientific article published on June 26, 2010

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

scientific article

Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations

scientific article published in June 2011

Pulsatile Tinnitus: Differential Diagnosis and Radiological Work-Up

scientific article

Retreatment of vestibular schwannoma with Gamma Knife radiosurgery: clinical outcome, tumor control, and review of literature

scientific article published on 6 October 2017

Risk factors for complications in cochlear implant surgery

scientific article published on 10 February 2018

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

scientific article

SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma ⬇️

scientific article published on January 11, 2011

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

scientific article

Similar phenotypes caused by mutations in OTOG and OTOGL.

scientific article

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands

scientific article published on 21 December 2016

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients

scientific article

The phenotype of SDHB germline mutation carriers: a nationwide study

scientific article published on 10 May 2017

List of works by Henricus Kunst

A Comparison of Surgical Treatments for Superior Semicircular Canal Dehiscence: A Systematic Review

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

A Retrospective Cohort Study on the Influence of Comorbidity on Soft Tissue Reactions, Revision Surgery, and Implant Loss in Bone-anchored Hearing Implants

A new bone-anchored hearing implant: short-term retrospective data on implant survival and subjective benefit

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family

Auditory brainstem response prior to MRI compared to standalone MRI in the detection of vestibular schwannoma: A modelling study

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1

Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment

Causes of permanent childhood hearing impairment ⬇️

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

Cochlear Implantation in Patients With Usher Syndrome Type IIa Increases Performance and Quality of Life

Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11.

Congenital oval or round window anomaly with or without abnormal facial nerve course: surgical results for 15 ears

Diagnosing necrotizing external otitis on CT and MRI: assessment of pattern of extension

Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans

External ear anomalies and hearing impairment in Noonan Syndrome

Feasibility of a wait-and-scan period as initial management strategy for head and neck paraganglioma.

Gamma Knife radiosurgery for treatment of growing vestibular schwannomas in patients with neurofibromatosis Type 2: a matched cohort study with sporadic vestibular schwannomas.

Gamma Knife radiosurgery for vestibular schwannomas: evaluation of tumor control and its predictors in a large patient cohort in The Netherlands

Genetics of hereditary head and neck paragangliomas

Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations

Genotype-specific abnormalities in mitochondrial function associate with distinct profiles of energy metabolism and catecholamine content in pheochromocytoma and paraganglioma.

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.

Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment

Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors.

Insufficient evidence for a role of SERPINF1 in otosclerosis

Intrafamilial variable hearing loss in TRPV4 induced spinal muscular atrophy

Karyotype-specific ear and hearing problems in young adults with Turner syndrome and the effect of oxandrolone treatment

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse

Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome.

Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction

Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment

Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease

Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrum

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome

Phenotypes of Two Dutch DFNA3 Families with Mutations in GJB2 ⬇️

Potential savings in the diagnosis of vestibular schwannoma

Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in &lt;i&gt;TMC1&lt;/i&gt; ⬇️

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations

Pulsatile Tinnitus: Differential Diagnosis and Radiological Work-Up

Retreatment of vestibular schwannoma with Gamma Knife radiosurgery: clinical outcome, tumor control, and review of literature

Risk factors for complications in cochlear implant surgery

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma ⬇️

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

Similar phenotypes caused by mutations in OTOG and OTOGL.

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients

The phenotype of SDHB germline mutation carriers: a nationwide study

Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in <i>TMC1</i> ⬇️