Sáhlua Miguel Volc

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

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

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

Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome

Gabriel S. Macedo, Igor Araújo Vieira, Ana Paula Carneiro Brandalize et al. · Cancer Genetics · 2016 · 23 citations

Rare Germline Variant, Genetic Disorder, Genetics +8

Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with MSH2 Germline Pathogenic Variants

Nathália de Angelis de Carvalho, Bianca Naomi Niitsuma, Vanessa Nascimento Kozak et al. · Cancers · 2020 · 20 citations · Full text