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<i>SLC12A2</i>: a new gene associated with autosomal dominant Non-Syndromic hearing loss in humans

scientific article published in 2020

Genetic Dissection of Temperament Personality Traits in Italian Isolates

artículo científico publicado en 2021

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability

artículo científico publicado en 2021

Hearing loss and brain abnormalities due to pathogenic mutations in <i>ADGRV1</i> gene: a case report

artículo científico publicado en 2020

Molecular testing for the study of non-syndromic hearing loss

scientific article published in 2020

Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss

artículo científico publicado en 2019

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.

artículo científico publicado en 2018

Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene

artículo científico publicado en 2021

TBL1Y: a new gene involved in syndromic hearing loss

article

The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population

scientific article published in 2023

There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss

artículo científico publicado en 2021

Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection

artículo científico publicado en 2018

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