Cristina S. Sabato

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

Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital

Edenir Inêz Palmero, Henrique C.R. Galvão, Gabriela Carvalho Fernandes et al. · Genetics and Molecular Biology · 2016 · 26 citations · Full text

Reproductive Genetic Counseling, Family Medicine, Oncogenetics Service +14

TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling

Camila Matzenbacher Bittar, Igor Araújo Vieira, Cristina S. Sabato et al. · Familial Cancer · 2019 · 26 citations

Engineering, Genetic Disorder, Uncertain Significance +8

Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome

André Escremim de Paula, Henrique de Campos Reis Galvão, Murilo Bonatelli et al. · Cancer Genetics · 2021 · 13 citations

Molecular Characterization, Genetic Testing, Mendelian Disorder +9