A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms

por Pereira, Tiago V, Mingroni-Netto, Regina C
Publicado 2011

A Cell Junctional Protein Network Associated with Connexin-26

por Batissoco, Ana C., Salazar-Silva, Rodrigo, Oiticica, Jeanne, Bento, Ricardo F., Mingroni-Netto, Regina C., Haddad, Luciana A.
Publicado 2018

Inbreeding estimates in human populations: Applying new approaches to an admixed Brazilian isolate

por Lemes, Renan B., Nunes, Kelly, Carnavalli, Juliana E. P., Kimura, Lilian, Mingroni-Netto, Regina C., Meyer, Diogo, Otto, Paulo A.
Publicado 2018

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

por Dantas, Vitor G.L., Lezirovitz, Karina, Yamamoto, Guilherme L., Moura de Souza, Carolina Fischinger, Ferreira, Simone Gomes, Mingroni-Netto, Regina C.
Publicado 2014

Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea

por Oiticica, Jeanne, Barboza-Junior, Luiz Carlos M, Batissoco, Ana Carla, Lezirovitz, Karina, Mingroni-Netto, Regina C, Haddad, Luciana A, Bento, Ricardo F
Publicado 2010

A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family

por Uehara, Daniela T, Freitas, Érika L, Alves, Leandro U, Mazzeu, Juliana F, Auricchio, Maria TBM, Tabith, Alfredo, Monteiro, Mário LR, Rosenberg, Carla, Mingroni-Netto, Regina C
Publicado 2015

Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss

por Dantas, Vitor G. L., Raval, Manmeet H., Ballesteros, Angela, Cui, Runjia, Gunther, Laura K., Yamamoto, Guilherme L., Alves, Leandro Ucela, Bueno, André Silva, Lezirovitz, Karina, Pirana, Sulene, Mendes, Beatriz C. A., Yengo, Christopher M., Kachar, Bechara, Mingroni-Netto, Regina C.
Publicado 2018