Sebastien JanssensdeVarebeke

Genotype-Phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9) Part II: A Prospective Cross-Sectional Study of the Vestibular Phenotype in 111 Carriers

E. Fransen, R. Pennings, V. van Rompaey, 2021, Ear and hearing.

Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I—A Cross-sectional Study of Hearing Function in 111 Carriers

E. Fransen, R. Pennings, V. van Rompaey, 2021, Ear and hearing.

A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene

V. van Rompaey, V. Topsakal, G. Van Camp, 2019, European Archives of Oto-Rhino-Laryngology.

Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment

W. Wuyts, G. Van Camp, K. Ketelslagers, 2018, European Journal of Human Genetics.

Accelerated Cognitive Decline Associated With Hearing Loss and Bilateral Vestibulopathy: Insights From a Prospective Cross-Sectional Study Using the Repeatable Battery for the Assessment of Neuropsychological Status Adjusted for the Hearing Impaired in the DFNA9 Population

S. Engelborghs, P. Cras, A. Van Ombergen, 2022, Ear and hearing.

Pathogenic Variants in the COCH Gene That Lead to Hearing Loss and Vestibular Deficit: Update on DFNA9 and Introducing DFNB110

E. van Wijk, E. Fransen, R. Pennings, 2022, B-ENT.

A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene

V. van Rompaey, V. Topsakal, G. Van Camp, 2019, European Archives of Oto-Rhino-Laryngology.