Defective α‐tectorin may involve tectorial membrane in familial Meniere disease von Roman‐Naranjo, Pablo, Parra‐Perez, Alberto M., Escalera‐Balsera, Alba, Soto‐Varela, Andres, Gallego‐Martinez, Alvaro, Aran, Ismael, Perez‐Fernandez, Nicolas, Bächinger, David, Eckhard, Andreas H., Gonzalez‐Aguado, Rocio, Frejo, Lidia, Lopez‐Escamez, Jose A.

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Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease von Frejo, Lidia, Gallego-Martinez, Alvaro, Requena, Teresa, Martin-Sanz, Eduardo, Amor-Dorado, Juan Carlos, Soto-Varela, Andres, Santos-Perez, Sofia, Espinosa-Sanchez, Juan Manuel, Batuecas-Caletrio, Angel, Aran, Ismael, Fraile, Jesus, Rossi-Izquierdo, Marcos, Lopez-Escamez, Jose Antonio

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Differential Proinflammatory Signature in Vestibular Migraine and Meniere Disease von Flook, Marisa, Frejo, Lidia, Gallego-Martinez, Alvaro, Martin-Sanz, Eduardo, Rossi-Izquierdo, Marcos, Amor-Dorado, Juan Carlos, Soto-Varela, Andres, Santos-Perez, Sofia, Batuecas-Caletrio, Angel, Espinosa-Sanchez, Juan Manuel, Pérez-Carpena, Patricia, Martinez-Martinez, Marta, Aran, Ismael, Lopez-Escamez, Jose Antonio

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Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis von Gu, Shoujun, Olszewski, Rafal, Nelson, Lacey, Gallego-Martinez, Alvaro, Antonio Lopez-Escamez, Jose, Hoa, Michael

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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study von Amanat, Sana, Gallego-Martinez, Alvaro, Sollini, Joseph, Perez-Carpena, Patricia, Espinosa-Sanchez, Juan M., Aran, Ismael, Soto-Varela, Andres, Batuecas‐Caletrio, Angel, Canlon, Barbara, May, Patrick, Cederroth, Christopher R., Lopez-Escamez, Jose A.

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Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease von Gallego-Martinez, Alvaro, Requena, Teresa, Roman-Naranjo, Pablo, Lopez-Escamez, Jose A

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Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease von Lamolda, Mar, Frejo, Lidia, Gallego-Martinez, Alvaro, Lopez-Escamez, Jose A

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A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets von Requena, Teresa, Gallego-Martinez, Alvaro, Lopez-Escamez, Jose A

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DNA Methylation Signature in Mononuclear Cells and Proinflammatory Cytokines May Define Molecular Subtypes in Sporadic Meniere Disease von Flook, Marisa, Escalera-Balsera, Alba, Gallego-Martinez, Alvaro, Espinosa-Sanchez, Juan Manuel, Aran, Ismael, Soto-Varela, Andres, Lopez-Escamez, Jose Antonio

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Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus von Gallego-Martinez, Alvaro, Escalera-Balsera, Alba, Trpchevska, Natalia, Robles-Bolivar, Paula, Roman-Naranjo, Pablo, Frejo, Lidia, Perez-Carpena, Patricia, Bulla, Jan, Gallus, Silvano, Canlon, Barbara, Cederroth, Christopher R., Lopez-Escamez, Jose A.

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family von Ahmad, Hena, Requena, Teresa, Frejo, Lidia, Cobo, Marien, Gallego-Martinez, Alvaro, Martin, Francisco, Lopez-Escamez, Jose A, Bronstein, Adolfo M

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Bioinformatic Integration of Molecular Networks and Major Pathways Involved in Mice Cochlear and Vestibular Supporting Cells von Requena, Teresa, Gallego-Martinez, Alvaro, Lopez-Escamez, Jose A

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A Systematic Review on the Genetic Contribution to Tinnitus von Perez-Carpena, Patricia, Lopez-Escamez, Jose A., Gallego-Martinez, Álvaro

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Genetic architecture of Meniere’s disease von Gallego-Martinez, Alvaro, Lopez-Escamez, Jose A.

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Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease von Frejo, Lidia, Requena, Teresa, Okawa, Satoshi, Gallego-Martinez, Alvaro, Martinez-Bueno, Manuel, Aran, Ismael, Batuecas-Caletrio, Angel, Benitez-Rosario, Jesus, Espinosa-Sanchez, Juan M, Fraile-Rodrigo, Jesus José, García-Arumi, Ana María, González-Aguado, Rocío, Marques, Pedro, Martin-Sanz, Eduardo, Perez-Fernandez, Nicolas, Pérez-Vázquez, Paz, Perez-Garrigues, Herminio, Santos-Perez, Sofía, Soto-Varela, Andres, Tapia, Maria C, Trinidad-Ruiz, Gabriel, Del Sol, Antonio, Alarcon Riquelme, Marta E, Lopez-Escamez, Jose A

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An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population von Parra-Perez, Alberto M., Gallego-Martinez, Alvaro, Lopez-Escamez, Jose A.

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A crowdsourcing database for the copy-number variation of the Spanish population von López-López, Daniel, Roldán, Gema, Fernández-Rueda, Jose L, Bostelmann, Gerrit, Carmona, Rosario, Aquino, Virginia, Perez-Florido, Javier, Ortuño, Francisco, Pita, Guillermo, Núñez-Torres, Rocío, González-Neira, Anna, Peña-Chilet, María, Dopazo, Joaquin

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Genetics of vestibular syndromes von Roman-Naranjo, Pablo, Gallego-Martinez, Alvaro, Lopez Escamez, Jose A

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Genetic contribution to vestibular diseases von Gallego-Martinez, Alvaro, Espinosa-Sanchez, Juan Manuel, Lopez-Escamez, Jose Antonio

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Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease von Martín-Sierra, Carmen, Gallego-Martinez, Alvaro, Requena, Teresa, Frejo, Lidia, Batuecas-Caletrío, Angel, Lopez-Escamez, Jose A

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