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    Chapter

    Genetic Contribution to Tinnitus and Tinnitus Disorder

    Tinnitus is a subjective perception of sound reported in almost 15% of the global population. Tinnitus can be found associated with hearing loss, hyperacusis, noise exposure, and several comorbidities such as ...

    Christopher R. Cederroth, Natalia Trpchevska, Sana Amanat in Textbook of Tinnitus (2024)

  2. Article

    Open Access

    Screening for Circulating Inflammatory Proteins Does Not Reveal Plasma Biomarkers of Constant Tinnitus

    Tinnitus would benefit from an objective biomarker. The goal of this study is to identify plasma biomarkers of constant and chronic tinnitus among selected circulating inflammatory proteins.

    Christopher R. Cederroth, Mun-Gwan Hong in Journal of the Association for Research in… (2023)

  3. Article

    Open Access

    Low Evidence for Tinnitus Risk Factors: A Systematic Review and Meta-analysis

    Identifying risk factors for tinnitus could facilitate not only the recommendations for prevention measures, but also identifying potential pathways for new interventions. This study reports the first comprehe...

    Roshni Biswas, Eleni Genitsaridi in Journal of the Association for Research in… (2023)

  4. Article

    Open Access

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

    Tinnitus is the phantom percept of an internal non-verbal set of noises and tones. It is reported by 15% of the population and it is usually associated with hearing and/or brain disorders. The role of structur...

    Alvaro Gallego-Martinez, Alba Escalera-Balsera, Natalia Trpchevska in npj Genomic Medicine (2022)

  5. No Access

    Article

    A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences

    Complex chromosome translocations are structural chromosomal rearrangements involving three or more chromosomes and more than two breakpoints. A complex chromosome rearrangement was detected in a phenotypicall...

    Natalia Trpchevska, Ivanka Dimova in Journal of Assisted Reproduction and Genet… (2017)