Karina Lezirovitz

14PUBLICATIONS
35CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingOrganic chemical synthesisNeurogeneticsMiddle Eastern languages
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Publications (14)

|Jun 25, 2026
A Structural Variant in the 5' Regulatory Region of DIAPH3 Segregates with Postlingual Hearing Loss and Auditory Neuropathy in a Multigenerational Brazilian Family.

|Jun 03, 2026
Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

|Feb 23, 2024
Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants.

William Bertani-Torres, Karina Lezirovitz, Danillo Alencar-Coutinho

|Dec 09, 2023
Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing.

Han Chen, Mehar Monga, Qinghua Fang

|Dec 23, 2022
New Insights into the Identity of the DFNA58 Gene.

Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima

|Jan 15, 2022
Correction to: Genetic etiology of non-syndromic hearing loss in Latin America.

Karina Lezirovitz, Regina Célia Mingroni-Netto

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Frequent Collaborators

5 joint publications

Ana Carla Batissoco

4 joint publications

Ricardo Ferreira Bento

4 joint publications

Jeanne Oiticica

3 joint publications

Regina Célia Mingroni-Netto