Hospital Universitario Virgen de las Nieves-ko ikertzaileekin lankidetzan egindako argitalpenak (24)

2024

  1. 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

  2. Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease

    Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131

  3. Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease

    Genes, Vol. 15, Núm. 1

2023

  1. The statistical analysis plan for the unification of treatments and interventions for tinnitus patients randomized clinical trial (UNITI-RCT)

    Trials, Vol. 24, Núm. 1

2022

  1. 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

  2. Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus

    npj Genomic Medicine, Vol. 7, Núm. 1

2021

  1. Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

    EBioMedicine, Vol. 66

  2. CSVS, a crowdsourcing database of the Spanish population genetic variability

    Nucleic acids research, Vol. 49, Núm. D1, pp. D1130-D1137

  3. Dna methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic meniere disease

    Biomedicines, Vol. 9, Núm. 11

  4. Genetic Inheritance and Its Contribution to Tinnitus

    Current Topics in Behavioral Neurosciences (Springer Science and Business Media Deutschland GmbH), pp. 29-47

  5. Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis

    Frontiers in Neurology, Vol. 12

  6. 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

  7. 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

  1. Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease

    Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605

  2. Clinical and molecular genetics of Meniere disease

    Medizinische Genetik, Vol. 32, Núm. 2, pp. 141-148

  3. 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

  4. Genetic architecture of Meniere's disease

    Hearing Research, Vol. 397

2019

  1. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

  2. Excess of Rare Missence Variants in Hearing Loss Genes in Sporadic Meniere Disease

    Frontiers in Genetics, Vol. 10, Núm. FEB

2018

  1. Genetic contribution to vestibular diseases

    Journal of Neurology, Vol. 265, pp. 29-34