Alvaro Gallego-Martinez
Alvaro Gallego-Martinez
Otology and Otoneurology - Genomics of Vestibular disorders - GENYO
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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
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
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
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, 76, 2019
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), 1-11, 2018
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
Genetic contribution to vestibular diseases
A Gallego-Martinez, JM Espinosa-Sanchez, JA Lopez-Escamez
Journal of neurology 265 (1), 29-34, 2018
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
Genetic architecture of Meniere’s disease
A Gallego-Martinez, JA Lopez-Escamez
Hearing research 397, 107872, 2020
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
Genetics of vestibular syndromes
P Roman-Naranjo, A Gallego-Martinez, JA Lopez Escamez
Current opinion in neurology 31 (1), 105-110, 2018
CSVS, a crowdsourcing database of the Spanish population genetic variability
M Peña-Chilet, G Roldán, J Perez-Florido, FM Ortuño, R Carmona, ...
Nucleic Acids Research 49 (D1), D1130-D1137, 2021
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, 85, 2018
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), 1-11, 2017
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, 441-451, 2021
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, 103309, 2021
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, 2021
Genetic inheritance and its contribution to tinnitus
S Amanat, A Gallego-Martinez, JA Lopez-Escamez
Springer, Berlin, Heidelberg, 2020
Bioinformatic integration of molecular networks and major pathways involved in mice cochlear and vestibular supporting cells
T Requena, A Gallego-Martinez, JA Lopez-Escamez
Frontiers in molecular neuroscience 11, 108, 2018
Rare Variants in the OTOG Gene Are a Frequent Cause of Familial Meniere’s Disease
P Roman-Naranjo, A Gallego-Martinez, A Soto-Varela, I Aran, ...
bioRxiv, 771527, 2019
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