Bruna Durães de Figueiredo Barros

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

Giovana Tardin Torrezan, Elisa Napolitano Ferreira, Adriana Miti Nakahata et al. · Nature Communications · 2014 · 174 citations · Full text

Whole‐exome sequencing of non‐ <i>BRCA1/BRCA2</i> mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

Paula Silva Felicio, Rebeca Silveira Grasel, Natália Campacci et al. · Human Mutation · 2020 · 61 citations · Full text

Current Study, Cancer Risk, Whole‐exome Sequencing +15

Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors

Ana Cristina Victorino Krepischi, Mariana Maschietto, Elisa Napolitano Ferreira et al. · Molecular Cytogenetics · 2016 · 55 citations · Full text

BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation

Rafael Canfield Brianese, Kivvi Duarte de Mello Nakamura, Fernanda Gabriella dos Santos Ramos Almeida et al. · Breast Cancer Research and Treatment · 2017 · 53 citations

Recurrent Event, Breast Oncology, Somatic Variant +11

A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease

Elisa Napolitano Ferreira, Bruna Durães de Figueiredo Barros, Jorge Estefano de Souza et al. · Human Genomics · 2016 · 37 citations · Full text