Henrique C.R. Galvão

Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification

Michael T. Parsons, Emma Tudini, Hongyan Li et al. · Human Mutation · 2019 · 148 citations · Full text

Genetics, Genetic Epidemiology, Pathology +25

The germline mutational landscape of BRCA1 and BRCA2 in Brazil

Edenir Inêz Palmero, Dirce Maria Carraro, Bárbara Alemar et al. · Scientific Reports · 2018 · 90 citations · Full text

Prevalence of <i>BRCA1/BRCA2</i> mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry

Gabriela Carvalho Fernandes, Rodrigo Augusto Depieri Michelli, Henrique C.R. Galvão et al. · Oncotarget · 2016 · 77 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

XAF1 as a modifier of p53 function and cancer susceptibility

Emília M. Pinto, Bonald C. Figueiredo, Wenan Chen et al. · Science Advances · 2020 · 52 citations · Full text