Alvaro Gallego-Martinez

12PUBLICATIONS
25CO-AUTHORS
Wireless communication systems and technologies (incl. microwave and millimetrewave)Medical infection agents (incl. prions)Neural engineeringGene expression (incl. microarray and other genome-wide approaches)Epidemiological modelling
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Publications (12)

|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

|Jan 15, 2025
A Neuron-Like Cellular Model for Severe Tinnitus Associated with Rare Variations in the ANK2 Gene.

Mar Lamolda, Lidia Frejo, Juan Martin-Lagos

|Dec 11, 2024
Trends in the diagnosis of paediatric sensorineural hearing loss: a scoping review of gene panels, exome and genome sequencing.

Adela Serrano-Herrera, Jose Antonio Lopez-Escamez, Alvaro Gallego-Martinez

|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

|Feb 23, 2024
Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease.

Marisa Flook, Elena Rojano, Alvaro Gallego-Martinez

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