ÁLVARO
GALLEGO MARTÍNEZ
PROFESOR SUSTITUTO (LOSU)
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaCentro de Investigación Biomédica en Red sobre Enfermedades Raras -ko ikertzaileekin lankidetzan egindako argitalpenak (9)
2024
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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
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An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population
Human Genetics, Vol. 143, Núm. 3, pp. 423-435
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Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease
Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131
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Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease
Genes, Vol. 15, Núm. 1
2023
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A crowdsourcing database for the copy-number variation of the Spanish population
Human Genomics, Vol. 17, Núm. 1
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Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease
Cells, Vol. 12, Núm. 7
2022
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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
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Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
npj Genomic Medicine, Vol. 7, Núm. 1
2021
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CSVS, a crowdsourcing database of the Spanish population genetic variability
Nucleic acids research, Vol. 49, Núm. D1, pp. D1130-D1137