Paula Robles-Bolívar

This study challenges the traditional view of Meniere's disease by showing that endolymphatic hydrops is associated with epithelial hyperplasia rather than fluid pressure, suggesting a compensatory cellular response.

The paper identifies rare PRKRA variants in individuals with tinnitus and mild cognitive impairment, linking them to early cognitive decline and suggesting a potential role in disease mechanisms.

This study compares the genetic burden of missense and loss-of-function variants in familial and sporadic Meniere disease, finding divergent genetic architectures and shared enriched genes.

The paper identifies a rare GJD3 haplotype associated with familial Meniere Disease, showing it disrupts connexin assembly and affects inner ear function.