M. Verstreken

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Hereditary Otovestibular Dysfunction and Ménière's Disease in a Large Belgian Family Is Caused by a Missense Mutation in the COCH Gene

P. van de Heyning, F. Wuyts, E. Fransen, 2001, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

G. Richardson, P. Heyning, P. Van de Heyning, 1998, Nature Genetics.

A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

C. Cremers, F. Cremers, F. Wuyts, 2001, Journal of medical genetics.

Osteogenesis imperfecta and hearing loss.

J. Claes, M. Verstreken, P. H. Van de Heyning, 1996, Acta oto-rhino-laryngologica Belgica.

DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System

Jason J. Corneveaux, M. Bitner-Glindzicz, G. Mortier, 2016, Human mutation.

Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2

K. Venken, E. Fransen, P. Govaerts, 2010, Genes and Immunity.

Involvement of T cell receptor Beta alterations in the development of otosclerosis linked to OTSC 2 Running title : T cell receptor Beta alterations in otosclerosis

Paul J Govaerts, Niels Hellings, Guy Van Camp, 2010 .

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

G. Richardson, W. Kimberling, P. Heyning, 1998, Nature Genetics.

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

G Van Camp, P Van de Heyning, C. Cremers, 1999, Human molecular genetics.

Mutations in the KCNQ 4 gene are responsible for autosomal dominant deafness in four DFNA 2 families

C. Cremers, P. Heyning, S. Bhasin, 1999 .

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

F. E. Offeciers, G. Richardson, P. Govaerts, 1998, Nature genetics.

Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea

E. Green, P. Van de Heyning, P. Willems, 1997, European journal of human genetics : EJHG.

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

F. E. Offeciers, K. Verhoeven, P. Govaerts, 1997, American journal of human genetics.

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

C. Morton, F. Wuyts, E. Fransen, 1999, Human molecular genetics.

Three Years of Vestibular Infant Screening in Infants With Sensorineural Hearing Loss.

L. Maes, F. Declau, I. Dhooge, 2022, Pediatrics.

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

C. Cremers, M. Burmeister, P. Willems, 1999, Journal of medical genetics.

Bilateral otospongiosis and a unilateral vestibular schwannoma in a patient with Myhre syndrome.

J. Casselman, B. De Foer, E. Offeciers, 2014, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Audiometric analysis of a Belgian family linked to the DFNA10 locus.

K. Verhoeven, F. Wuyts, F. Declau, 2000, The American journal of otology.

Otosclerosis: a genetically heterogeneous disease involving at least three different genes.

F. E. Offeciers, C. Cremers, F. Declau, 2002, Bone.

Stapedotomy with Microdrill or Carbon Dioxide Laser: Influence on Inner Ear Function

A. Zarowski, E. Offeciers, T. Somers, 2006, The Annals of otology, rhinology, and laryngology.

DFNA10/EYA4--the clinical picture.

C. Cremers, F. Declau, Richard J. H. Smith, 2002, Advances in oto-rhino-laryngology.

Enhancement of the otic capsule in active retrofenestral otosclerosis.

P. Parizel, A. D. De Schepper, F. Wuyts, 2004, Otology and Neurotology.

The MO-meatocanalplasty: long-term results in the narrow external auditory canal with recurrent otitis externa or the inability to wear a hearing aid

G. De Greve, A. Zarowski, J. van Dinther, 2021, European Archives of Oto-Rhino-Laryngology.

Transient depression of inner ear function after stapedotomy: skeeter versus CO(2) laser technique.

F. E. Offeciers, A. Zarowski, T. Somers, 2007, Advances in oto-rhino-laryngology.

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

C. Cremers, V. Tiranti, M. Zeviani, 1999, European Journal of Human Genetics.

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

T. Fagerheim, K. Verhoeven, Richard J. H. Smith, 2000, Human Genetics.

Clinical presentation of DFNA8-DFNA12.

F. E. Offeciers, K. Verhoeven, G. De Ceulaer, 2002, Advances in oto-rhino-laryngology.

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment

H. Kremer, F. Denoyelle, G. Girotto, 2023, Audiology research.

Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection.

A. Gilles, I. Dhooge, A. Boudewyns, 2022, JAMA otolaryngology-- head & neck surgery.