Jose Antonio Lopez-Escamez (Prof)

Professor of Ménière’s disease and Neurosciences

The Kolling Institute, University of Sydney, Australia.

Latest Contribution

Schematic showing the structural role of otogelin, a large protein of 2929 amino acids located in the protein complex of the apical crown that anchors hair cell stereocilia to the tectorial membrane.

Genetic foundations of Ménière’s disease: changing the game

4 November 2025 | | ENTA - Vestibular Disorders, ENTA - Neurotology, ENTA - Audiology - Diagnostic, ENTA - Tinnitus

Sydney researchers reveal genetic roots of Ménière’s disease. Familial patterns and gene discoveries highlight autosomal inheritance in rare cases, transforming molecular insights. Ménière’s disease (MD) is a chronic disorder of the inner ear defined by clinical criteria of episodic vertigo...

Picture of ear

Genetics WG4. Improving diagnosis and drug development through the genetic understanding of tinnitus subtypes: a TINNET endeavour

1 January 2016 | | ENTA - Audiology - Adult, ENTA - Audiology - Diagnostic, ENTA - Tinnitus

Christopher R Cederroth and Jose Antonio Lopez-Escamez explain how progress is being made to investigate the contribution of genetic factors to tinnitus, including a subtype of ‘extreme’ tinnitus in Ménière’s disease. Genetics WG4 is working towards determining the genetic basis...