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Alvaro Gallego-Martinez
Alvaro Gallego-Martinez
Otology and Otoneurology - Genomics of Vestibular disorders - Universidad de Granada
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Titel
Zitiert von
Zitiert von
Jahr
Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere’s disease
C Martín-Sierra, A Gallego-Martinez, T Requena, L Frejo, ...
European Journal of Human Genetics 25 (2), 200-207, 2017
842017
Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease
L Frejo, A Gallego-Martinez, T Requena, E Martin-Sanz, JC Amor-Dorado, ...
Scientific reports 8 (1), 5974, 2018
772018
A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease
C Martín-Sierra, T Requena, L Frejo, SD Price, A Gallego-Martinez, ...
Human molecular genetics 25 (16), 3407-3415, 2016
772016
Differential proinflammatory signature in vestibular migraine and meniere disease
M Flook, L Frejo, A Gallego-Martinez, E Martin-Sanz, M Rossi-Izquierdo, ...
Frontiers in Immunology 10, 1229, 2019
722019
Burden of rare variants in the OTOG gene in familial Meniere’s disease
P Roman-Naranjo, A Gallego-Martinez, A Soto-Varela, I Aran, ...
Ear and hearing 41 (6), 1598-1605, 2020
622020
Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere’s disease
L Frejo, T Requena, S Okawa, A Gallego-Martinez, M Martinez-Bueno, ...
Frontiers in Immunology 8, 1739, 2017
622017
Genetic architecture of Meniere’s disease
A Gallego-Martinez, JA Lopez-Escamez
Hearing Research 397, 107872, 2020
542020
CSVS, a crowdsourcing database of the Spanish population genetic variability
M Peña-Chilet, G Roldán, J Perez-Florido, FM Ortuno, R Carmona, ...
Nucleic acids research 49 (D1), D1130-D1137, 2021
452021
Excess of rare missense variants in hearing loss genes in sporadic Meniere disease
A Gallego-Martinez, T Requena, P Roman-Naranjo, JA Lopez-Escamez
Frontiers in genetics 10, 423463, 2019
452019
Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI
W Schlee, S Schoisswohl, S Staudinger, A Schiller, A Lehner, B Langguth, ...
Progress in brain research 260, 441-451, 2021
442021
Genetic contribution to vestibular diseases
A Gallego-Martinez, JM Espinosa-Sanchez, JA Lopez-Escamez
Journal of neurology 265 (Suppl 1), 29-34, 2018
322018
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study
S Amanat, A Gallego-Martinez, J Sollini, P Perez-Carpena, ...
EBioMedicine 66, 2021
312021
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere’s disease
A Gallego-Martinez, T Requena, P Roman-Naranjo, P May, ...
Journal of Medical Genetics 57 (2), 82-88, 2020
312020
Genetics of vestibular syndromes
P Roman-Naranjo, A Gallego-Martinez, JAL Escamez
Current opinion in neurology 31 (1), 105-110, 2018
262018
Identification of potential Meniere's disease targets in the adult stria vascularis
S Gu, R Olszewski, L Nelson, A Gallego-Martinez, JA Lopez-Escamez, ...
Frontiers in Neurology 12, 630561, 2021
252021
Clinical and functional characterization of a missense ELF2 variant in a CANVAS family
H Ahmad, T Requena, L Frejo, M Cobo, A Gallego-Martinez, F Martin, ...
Frontiers in genetics 9, 330919, 2018
212018
Defective α‐tectorin may involve tectorial membrane in familial Meniere disease
P Roman‐Naranjo, AM Parra‐Perez, A Escalera‐Balsera, A Soto‐Varela, ...
Clinical and Translational Medicine 12 (6), 2022
172022
Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial
S Schoisswohl, B Langguth, M Schecklmann, A Bernal-Robledano, ...
Trials 22, 1-16, 2021
162021
DNA methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic Meniere disease
M Flook, A Escalera-Balsera, A Gallego-Martinez, JM Espinosa-Sanchez, ...
Biomedicines 9 (11), 1530, 2021
142021
A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets
T Requena, A Gallego-Martinez, JA Lopez-Escamez
Human Genomics 11, 1-11, 2017
142017
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