Giovana Tardin Torrezan

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

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

Mev Dominguez–Valentin, Saskia Haupt, Toni T. Seppälä et al. · EClinicalMedicine · 2023 · 91 citations · Full text

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients

Felipe Cavalcanti Carneiro da Silva, Bianca CG Lisboa, Márcia CP Figueiredo et al. · BMC Medical Genetics · 2014 · 86 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

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

Pål Møller, Toni T. Seppälä, James G. Dowty et al. · Hereditary Cancer in Clinical Practice · 2022 · 52 citations · Full text