Alberto M Parra-Pérez

7PUBLICATIONS
19CO-AUTHORS
Medical infection agents (incl. prions)Medical bacteriologyEpidemiological modellingGene mappingNatural products and bioactive compounds
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Publications (7)

|Sep 24, 2025
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.

Alberto M Parra-Perez, Alvaro Gallego-Martinez, Alba Escalera-Balsera

|Jun 26, 2025
Replication of Missense OTOG Gene Variants in a Brazilian Patient with Menière's Disease.

Giselle Bianco-Bortoletto, Geovana Almeida-Carneiro, Helena Fabbri-Scallet

|Mar 23, 2024
An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population.

Alberto M Parra-Perez, Alvaro Gallego-Martinez, Jose A Lopez-Escamez

|Jan 23, 2024
Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease.

Alba Escalera-Balsera, Alberto M Parra-Perez, Alvaro Gallego-Martinez

|Sep 07, 2022
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss.

Paula Robles-Bolivar, David Bächinger, Alberto M Parra-Perez

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