Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease by Alba Escalera-Balsera, Pablo Roman-Naranjo, Jose Antonio Lopez-Escamez

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

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

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

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Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction by Angelo Augusto M. Sumalde, Melissa A. Scholes, Olivia A. Kalmanson, Elizabeth A. Terhune, Lidia Frejo, Cambria I. Wethey, Pablo Roman-Naranjo, Patrick M. Carry, Samuel P. Gubbels, Jose A. Lopez-Escamez, Nancy Hadley-Miller, Regie Lyn P. Santos-Cortez

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