PATRICIA
PÉREZ CARPENA
DOCENTE INVITADA
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von Centro de Investigación Biomédica en Red sobre Enfermedades Raras (8)
2024
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A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss
Laryngoscope
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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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Cognitive Screening and Hearing Assessment in Patients With Chronic Tinnitus
Clinical and Experimental Otorhinolaryngology, Vol. 17, Núm. 1, pp. 15-25
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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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Phenotypic spectrum of tinnitus patients bearing rare ANK2 gene variants
European Archives of Oto-Rhino-Laryngology
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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
2022
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Balance Disorders Including Ménière’s Disease
Comprehensive Pharmacology (Elsevier), pp. 770-782
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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