Alvaro Gallego-Martinez
Epigenetics and Gene Expression · CABIMER
Biography
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Bioinformatics, hearing loss, tinnitus, meniere disease, genomics, vestibular disorders, epigenetics, cancer evolution, transcriptomics, single cell |
Profile
| Institution | CABIMER |
| Position | Postdoc |
| Home page | https://scholar.google.es/citations?hl=es&user=NnBP1C0AAAAJ |
| Contact email | alvaro.gallego@cabimer.es |
| ORCID | 0000-0002-6068-8965 |
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| BCB Committee | Junior Hub |
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Research
Research topics
OmicsComputational MethodsTranscriptomicsRNA Sequencing (RNA-seq)Data AnalysisArtificial IntelligenceMachine Learning in BiologyBioinformatics Software and ToolsData VisualizationGenomicsGenome SequencingGenome Assembly
View all (41 more)
Large language modelsFunctional genomicsFunctional annotationFunction predictionStructural bioinformaticsMolecular flexibilityExpression ProfilingSystems BiologyGenomic AnnotationVariant callingEpigenomicsDNA methylation3D chromatin structureIntegrative AnalysisRegulatory biologyStatistical Methods for BiologyFrequentist analysisMolecular evolutionSequence analysisSequence AlignmentPhylogenetic AnalysisMutation Analysis and designChromatin accessibilityExperimental designMappingPathway analysisMultivariate statisticsNetwork BiologyStructure-function relationshipSingle-cell omicsSingle-cell (scRNA-seq)Structure predictionMolecular Interactions/DockingBayesian statisticsNon-parametric statisticsDeep Learning in BiologyProtein/Nucleic Acid designSpatial transcriptomicsSequence error correctionKnowledge graphsHistone structure and regulation
Research lines
None
Publications 31 entries
- Different Contribution of Missense and Loss‐of‐Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease Article · 21 Sep 2025
- A Neuron-Like Cellular Model for Severe Tinnitus Associated with Rare Variations in the ANK2 Gene Article · 15 Jan 2025
- Trends in the diagnosis of paediatric sensorineural hearing loss: a scoping review of gene panels, exome and genome sequencing Article · 10 Dec 2024
- An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population Article · Mar 2024
- Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease Article · 23 Feb 2024
View all (26 more)
- Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease Article · 22 Dec 2023
- Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease Article · 23 Mar 2023
- Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus Article · 30 Nov 2022
- A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss Article · 7 Sep 2022
- Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial Article · 4 Dec 2021
- DNA Methylation Signature in Mononuclear Cells and Proinflammatory Cytokines May Define Molecular Subtypes in Sporadic Meniere Disease Article · 25 Oct 2021
- Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study Article · Apr 2021
- Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis Article · 5 Feb 2021
- Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI Book / chapter · 2021
- Genetic architecture of Meniere's disease Article · Nov 2020
- CSVS, a crowdsourcing database of the Spanish population genetic variability Article · 29 Sep 2020
- Clinical and molecular genetics of Meniere disease Article · 1 Aug 2020
- Burden of rare variants in the OTOG Gene in familial meniere's disease Article · 2 Apr 2020
- Genetic Inheritance and Its Contribution to Tinnitus Book / chapter · 2020
- Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere’s disease Article · 7 Sep 2019
- Differential proinflammatory signature in vestibular migraine and meniere disease Article · 4 Jun 2019
- Excess of Rare Missence Variants in Hearing Loss Genes in Sporadic Meniere Disease Article · 15 Feb 2019
- Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease Article · 13 Apr 2018
- Bioinformatic integration of molecular networks and major pathways involved in mice cochlear and vestibular supporting cells Article · 5 Apr 2018
- Genetic contribution to vestibular diseases Article · 26 Mar 2018
- Clinical and functional characterization of a missense ELF2 variant in a CANVAS family Article · 23 Mar 2018
- Genetics of vestibular syndromes Article · Feb 2018
- Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease Article · 13 Dec 2017
- A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets Article · 22 May 2017
- Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease Article · 23 Nov 2016
- A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease Article · 21 Jun 2016