Natalia Campacci

发表

Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome

R. Reis, M. Melendez, H. Galvão, 2022, Cancers.

New insights on familial colorectal cancer type X syndrome

R. Reis, M. Melendez, A. Evangelista, 2022, Scientific Reports.

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

R. Reis, C. Scapulatempo-Neto, G. Berardinelli, 2021, Cancer genetics.

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

J. Ragoussis, F. Couch, P. Tonin, 2020, Human mutation.

The Brazilian TP53 mutation (R337H) and sarcomas

R. Reis, D. O. Vidal, S. Serrano, 2020, PloS one.

Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer

R. Reis, M. Melendez, André L Carvalho, 2017, Cancer medicine.

The germline mutational landscape of BRCA1 and BRCA2 in Brazil

R. Reis, M. A. Moreira, H. Seuánez, 2018, Scientific Reports.

Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population

C. Scapulatempo-Neto, M. Melendez, A. Evangelista, 2018, Oncotarget.

Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer

P. Ashton-Prolla, R. Giugliani, L. Schüler-Faccini, 2020, Genetics and molecular biology.

Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients

D. Carraro, A. Evangelista, G. Torrezan, 2020, Frontiers in Oncology.

The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?

J. Goldim, H. Galvão, E. Palmero, 2024, Frontiers in psychology.