ÁLVARO
GALLEGO MARTÍNEZ
PROFESOR SUSTITUTO (LOSU)
Hospital Universitario Virgen de las Nieves
Granada, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Universitario Virgen de las Nieves (24)
2024
-
A Systematic Review on the Genetic Contribution to Tinnitus
JARO - Journal of the Association for Research in Otolaryngology, Vol. 25, Núm. 1, pp. 13-33
-
Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease
Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131
-
Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease
Genes, Vol. 15, Núm. 1
2023
2022
-
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss
European Journal of Human Genetics, Vol. 30, Núm. 11, pp. 1301-1305
-
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
npj Genomic Medicine, Vol. 7, Núm. 1
2021
-
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study
EBioMedicine, Vol. 66
-
CSVS, a crowdsourcing database of the Spanish population genetic variability
Nucleic acids research, Vol. 49, Núm. D1, pp. D1130-D1137
-
Dna methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic meniere disease
Biomedicines, Vol. 9, Núm. 11
-
Genetic Inheritance and Its Contribution to Tinnitus
Current Topics in Behavioral Neurosciences (Springer Science and Business Media Deutschland GmbH), pp. 29-47
-
Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis
Frontiers in Neurology, Vol. 12
-
Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI
Progress in Brain Research (Elsevier B.V.), pp. 441-451
-
Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial
Trials, Vol. 22, Núm. 1
2020
-
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease
Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605
-
Clinical and molecular genetics of Meniere disease
Medizinische Genetik, Vol. 32, Núm. 2, pp. 141-148
-
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease
Journal of Medical Genetics, Vol. 57, Núm. 2, pp. 82-88
-
Genetic architecture of Meniere's disease
Hearing Research, Vol. 397
2019
-
Differential proinflammatory signature in vestibular migraine and meniere disease
Frontiers in Immunology, Vol. 10, Núm. JUN
-
Excess of Rare Missence Variants in Hearing Loss Genes in Sporadic Meniere Disease
Frontiers in Genetics, Vol. 10, Núm. FEB
2018
-
Genetic contribution to vestibular diseases
Journal of Neurology, Vol. 265, pp. 29-34