Pablo Román-Naranjo

The paper identifies rare variants in the TECTA gene associated with familial Meniere disease and suggests their impact on tectorial membrane stability.

The paper identifies rare variants in the OTOG gene as a frequent cause of familial Meniere’s disease through exome sequencing and variant analysis.

This study identifies an excess of rare missense variants in SNHL genes in sporadic Meniere disease patients compared to controls.