Publications by authors named "Ismael Aran"

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Whole genome DNA methylation profiles define Meniere's disease subclusters.
Vibha Patil, Pablo Cruz-Granados, Francisca E Cara, Juan Carlos Amor-Dorado, Ismael Aran

J Mol Med (Berl)· October 2025

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An ultra-rare missense variant in the KIF1B gene linked to autoinflammatory Menière's disease.
Pablo Cruz-Granados, Giselle Bianco-Bortoletto, Ismael Aran, Victoria Rivero de Jesus, Jose A Lopez-Escamez

NPJ Genom Med· May 2025

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Numerical Simulations of the Epley Maneuver With Clinical Implications.
Ismael Arán-Tapia, Andrés Soto-Varela, Vicente Pérez-Muñuzuri, Sofía Santos-Pérez, Ismael Arán

Ear Hear· June 2024

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Numerical simulations to determine the stimulation of the crista ampullaris during the Head Impulse Test.
Ismael Arán-Tapia, Andrés Soto-Varela, Vicente Pérez-Muñuzuri, Sofía Santos-Pérez, Ismael Arán

Comput Biol Med· September 2023

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Defective α-tectorin may involve tectorial membrane in familial Meniere disease.
Pablo Roman-Naranjo, Alberto M Parra-Perez, Alba Escalera-Balsera, Andres Soto-Varela, Alvaro Gallego-Martinez, Ismael Aran

Clin Transl Med· June 2022

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DNA Methylation Signature in Mononuclear Cells and Proinflammatory Cytokines May Define Molecular Subtypes in Sporadic Meniere Disease.
Marisa Flook, Alba Escalera-Balsera, Alvaro Gallego-Martinez, Juan Manuel Espinosa-Sanchez, Ismael Aran

Biomedicines· October 2021

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Clinical and Cytokine Profile in Patients with Early and Late Onset Meniere Disease.
Maria-Del-Carmen Moleon, Estrella Martinez-Gomez, Marisa Flook, Andreina Peralta-Leal, Juan Antonio Gallego, Ismael Aran

J Clin Med· September 2021

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Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.
Pablo Roman-Naranjo, Alvaro Gallego-Martinez, Andrés Soto-Varela, Ismael Aran, Maria Del Carmen Moleon

Ear Hear· July 2021

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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study.
Sana Amanat, Alvaro Gallego-Martinez, Joseph Sollini, Patricia Perez-Carpena, Juan M Espinosa-Sanchez, Ismael Aran

EBioMedicine· April 2021

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Differential Proinflammatory Signature in Vestibular Migraine and Meniere Disease.
Marisa Flook, Lidia Frejo, Alvaro Gallego-Martinez, Eduardo Martin-Sanz, Marcos Rossi-Izquierdo, Ismael Aran

Front Immunol· October 2020

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Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.
Lidia Frejo, Alvaro Gallego-Martinez, Teresa Requena, Eduardo Martin-Sanz, Juan Carlos Amor-Dorado, Ismael Aran

Sci Rep· April 2018

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Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.
Lidia Frejo, Teresa Requena, Satoshi Okawa, Alvaro Gallego-Martinez, Manuel Martinez-Bueno, Ismael Aran

Front Immunol· December 2017

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Clinical Subgroups in Bilateral Meniere Disease.
Lidia Frejo, Andres Soto-Varela, Sofía Santos-Perez, Ismael Aran, Angel Batuecas-Caletrio

Front Neurol· October 2016

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Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.
Sonia Cabrera, Elena Sanchez, Teresa Requena, Manuel Martinez-Bueno, Jesus Benitez, Ismael Aran

PLoS One· July 2015

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Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
Teresa Requena, Irene Gazquez, Antonia Moreno, Angel Batuecas, Ismael Aran

Immunogenetics· May 2013

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Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
Irene Gázquez, Antonia Moreno, Teresa Requena, Jeff Ohmen, Sofia Santos-Perez, Ismael Aran

Eur Arch Otorhinolaryngol· March 2013

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High prevalence of systemic autoimmune diseases in patients with Menière's disease.
Irene Gazquez, Andres Soto-Varela, Ismael Aran, Sofia Santos, Angel Batuecas

PLoS One· February 2012

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MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease.
Irene Gazquez, Antonia Moreno, Ismael Aran, Andres Soto-Varela, Sofia Santos

Otol Neurotol· February 2012

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Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.
Irene Gazquez, Jose A Lopez-Escamez, Antonia Moreno, Colleen A Campbell, Nicole C Meyer, Ismael Aran

DNA Cell Biol· September 2011

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Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study.
José A Lopez-Escamez, Pablo Saenz-Lopez, Irene Gazquez, Antonia Moreno, Carlos Gonzalez-Oller, Ismael Aran

BMC Med Genet· January 2011

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Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease.
Jose A Lopez-Escamez, Antonia Moreno, Monica Bernal, Herminio Perez-Garrigues, Sofia Santos-Perez, Ismael Aran

Acta Otolaryngol· November 2009

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Time course of episodes of definitive vertigo in Meniere's disease.
Herminio Perez-Garrigues, Jose A Lopez-Escamez, Paz Perez, Ricardo Sanz, Miguel Orts, Ismael Aran

Arch Otolaryngol Head Neck Surg· November 2008

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HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.
Jose A Lopez-Escamez, Jose R Vilchez, Andres Soto-Varela, Sofia Santos-Perez, Herminio Perez-Garrigues, Ismael Aran

Otol Neurotol· October 2007

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