Cornelis P. Lanting - Publications

Performance Results and Timing of Cochlear Implantation in Patients With DFNA9 (p.Pro51Ser).

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: October 28, 2025

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: Journal of medical genetics

Published: January 05, 2023

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

Journal: Biomolecules

Published: December 19, 2021

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

Journal: Human genetics

Published: November 23, 2021

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

Journal: Human genetics

Published: October 05, 2021

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

Journal: Human genetics

Published: May 30, 2021

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

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: March 12, 2021