A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome

por Alves, Leandro Ucela, Pardono, Eliete, Otto, Paulo A., Mingroni Netto, Regina Célia
Publicado 2015

Haplotypes of single cancer driver genes and their local ancestry in a highly admixed long-lived population of Northeast Brazil

por Galisa, Steffany Larissa Galdino, Jacob, Priscila Lima, de Farias, Allysson Allan, Lemes, Renan Barbosa, Alves, Leandro Ucela, Nóbrega, Júlia Cristina Leite, Zatz, Mayana, Santos, Silvana, Weller, Mathias
Publicado 2022

NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

por Salazar-Silva, R, Dantas, Vitor Lima Goes, Alves, Leandro Ucela, Batissoco, Ana Carla, Oiticica, Jeanne, Lawrence, Elizabeth A, Kawafi, Abdelwahab, Yang, Yushi, Nicastro, Fernanda Stávale, Novaes, Beatriz Caiuby, Hammond, Chrissy, Kague, Erika, Mingroni-Netto, R C
Publicado 2020

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