Karina Lezirovitz (K Lezirovitz)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 17

Top Venues

Universidade de São Paulo Faculdade de Medicina Hospital das Clínicas

Universidade de Sao Paulo Campus da Capital (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universidade de São Paulo Faculdade de Medicina Hospital das Clínicas Jul 21 2009

Brazil

Research Associate :: Otolaryngology Lab/ LIM32

Education History

Universidade de Sao Paulo Campus da Capital

Brazil

PHD :: Instituto de Biociências

Universidade de Sao Paulo Campus da Capital

Brazil

BSC :: Instituto de Biociências

Publications

William Bertani-Torres, Karina Lezirovitz, Danillo Alencar-Coutinho, Eliete Pardono, Silvia Souza da Costa, Larissa do Nascimento Antunes, Judite de Oliveira, Paulo Alberto Otto, Véronique Pingault, Regina Célia Mingroni-Netto
Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants. Audiology research 14 (1) (2023)
William Bertani-Torres, Karina Lezirovitz, Danillo Alencar-Coutinho, Eliete Pardono, Silvia Souza da Costa, Larissa do Nascimento Antunes, Judite de Oliveira, Paulo Alberto Otto, Véronique Pingault, Regina Célia Mingroni-Netto
Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants. Audiology research 14 (1) (2023)
William Bertani-Torres, Karina Lezirovitz, Danillo Alencar-Coutinho, Eliete Pardono, Silvia Souza da Costa, Larissa do Nascimento Antunes, Judite de Oliveira, Paulo Alberto Otto, Véronique Pingault, Regina Célia Mingroni-Netto
Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants. Audiology research 14 (1) (2023)
Han Chen, Mehar Monga, Qinghua Fang, Loujin Slitin, Jakob Neef, Shashank S Chepurwar, Regina Célia Mingroni Netto, Karina Lezirovitz, Alfredo Tabith, Fritz Benseler, Nils Brose, Kathrin Kusch, Carolin Wichmann, Nicola Strenzke, Barbara Vona, Julia Preobraschenski, Tobias Moser
Ca2+-binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing. Protein & cell (2023)
Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima, Ana Carla Batissoco, Karina Lezirovitz
New Insights into the Identity of the DFNA58 Gene. Genes 13 (12) (2022)
Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima, Ana Carla Batissoco, Karina Lezirovitz
New Insights into the Identity of the DFNA58 Gene. Genes 13 (12) (2022)
Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima, Ana Carla Batissoco, Karina Lezirovitz
New Insights into the Identity of the DFNA58 Gene. Genes 13 (12) (2022)
Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima, Ana Carla Batissoco, Karina Lezirovitz
New Insights into the Identity of the DFNA58 Gene. Genes 13 (12) (2022)
Larissa Reis do Nascimento, Gleiciele Alice Vieira-Silva, João Paulo Fumio Whitaker Kitajima, Ana Carla Batissoco, Karina Lezirovitz
New Insights into the Identity of the DFNA58 Gene. Genes 13 (12) (2022)
André S Bueno, Kelly Nunes, Alex M M Dias, Leandro U Alves, Beatriz C A Mendes, Juliana Sampaio-Silva, Jeroen Smits, Helger G Yntema, Diogo Meyer, Karina Lezirovitz, Regina Célia Mingroni Netto
Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss. European journal of human genetics : EJHG (2021)
Ana Carla Batissoco, Vinicius Pedroso-Campos, Eliete Pardono, Juliana Sampaio-Silva, Cindy Yukimi Sonoda, Gleiciele Alice Vieira-Silva, Estefany Uchoa da Silva de Oliveira Longati, Diego César Batista Mariano, Ana Cristina Hiromi Hoshino, Tsuji Robinson Koji, Rafaela Jesus-Santos, Osorio Lopes Abath Neto, Ricardo Ferreira Bento, Jeanne Oiticica, Karina Lezirovitz
Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss. Human genetics (2021)
Ana Carla Batissoco, Karina Lezirovitz, D B Zanatta, C R M L Hemza, L R Vasques, Bryan E Strauss, Regina Célia Mingroni Netto, Luciana Amaral Haddad, Ricardo Ferreira Bento, Jeanne Oiticica
Cochlea cell-specific marker expression upon in vitro Hes1 knockdown. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 54 (7) (2021)
Karina Lezirovitz, Regina Célia Mingroni-Netto
Genetic etiology of non-syndromic hearing loss in Latin America. Human genetics (2021)
Janaína C Rodrigues, André Luís Lacerda Bachi, Gleiciele A V Silva, Marcelo Rossi, Jônatas do Bussador Amaral, Karina Lezirovitz, Rubens de Brito
New Insights on the Effect of TNF Alpha Blockade by Gene Silencing in Noise-Induced Hearing Loss. International journal of molecular sciences 21 (8) (2020)
Vitor G L Dantas, Manmeet H Raval, Angela Ballesteros, Runjia Cui, Laura K Gunther, Guilherme L Yamamoto, Leandro Ucela Alves, André Silva Bueno, Karina Lezirovitz, Sulene Pirana, Beatriz C A Mendes, Christopher M Yengo, Bechara Kachar, Regina C Mingroni-Netto
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific reports 8 (1) (2018)
Alex Marcel Moreira Dias, Karina Lezirovitz, Fernanda Stávale Nicastro, Beatriz C A Mendes, Regina Célia Mingroni-Netto
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of human genetics 64 (3) (2018)
Juliana Sampaio-Silva, Ana Carla Batissoco, Rafaela Jesus-Santos, Osório Abath-Neto, Luciano Cesar Scarpelli, Patricia Yoshie Nishimura, Layla Testa Galindo, Ricardo Ferreira Bento, Jeanne Oiticica, Karina Lezirovitz
Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family. Annals of human genetics 82 (1) (2017)

Karina Lezirovitz.css-eqlu8i{font-size:small;padding-left:4px;} (K Lezirovitz)

Publication Activity (10 Years)

Top Topics

Top Venues

Karina Lezirovitz (K Lezirovitz)