Mai T. Pham

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.

MDAtlas provides an open-access multiomics database for Meniere Disease, integrating genomic, transcriptomic, and epigenomic data to support research on disease mechanisms and biomarkers.

The paper introduces a new method for differential splicing detection that incorporates exon-junction reads, improving statistical power while controlling false discovery rates.

The paper identifies rare missense variants in OTOP2 and MYO7A genes in a South Korean Meniere disease cohort, suggesting their potential pathogenic roles.