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1.
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
; 24(1): 119-129, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34906479
2.
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Hum Mutat
; 42(3): 290-299, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33326660
3.
Genetic cancer risk assessment: A screenshot of the psychosocial profile of women at risk for hereditary breast and ovarian cancer syndrome.
Psychooncology
; 29(4): 681-687, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31984583
4.
BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry.
Hum Mutat
; 40(10): 1781-1796, 2019 10.
Article
in English
| MEDLINE | ID: mdl-31112363
5.
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
; 24(10): 2208, 2022 Oct.
Article
in English
| MEDLINE | ID: mdl-36205748
6.
Association of polymorphisms with a family history of cancer and the presence of germline mutations in the BRCA1/BRCA2 genes.
Hered Cancer Clin Pract
; 14: 2, 2016.
Article
in English
| MEDLINE | ID: mdl-26770289
7.
Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital.
Genet Mol Biol
; 39(2): 168-77, 2016 May 13.
Article
in English
| MEDLINE | ID: mdl-27192127
8.
Tumor protein 53 mutations and inherited cancer: beyond Li-Fraumeni syndrome.
Curr Opin Oncol
; 22(1): 64-9, 2010 Jan.
Article
in English
| MEDLINE | ID: mdl-19952748
9.
XAF1 as a modifier of p53 function and cancer susceptibility.
Sci Adv
; 6(26): eaba3231, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32637605
10.
Development and validation of a simple questionnaire for the identification of hereditary breast cancer in primary care.
BMC Cancer
; 9: 283, 2009 Aug 14.
Article
in English
| MEDLINE | ID: mdl-19682358
11.
Genotype-phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol.
Cancer Med
; 8(5): 2114-2122, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30897307
12.
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study.
Endocr Connect
; 8(3): 289-298, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-30763276
13.
Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
Front Genet
; 9: 161, 2018.
Article
in English
| MEDLINE | ID: mdl-29868112
14.
Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group.
JCO Precis Oncol
; 22018.
Article
in English
| MEDLINE | ID: mdl-31517176
15.
Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.
Cancer Med
; 6(12): 3014-3024, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-29055968
16.
Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry.
Oncotarget
; 7(49): 80465-80481, 2016 Dec 06.
Article
in English
| MEDLINE | ID: mdl-27741520
17.
Sequencing technology status of BRCA1/2 testing in Latin American Countries.
NPJ Genom Med
; 5: 22, 2020.
Article
in English
| MEDLINE | ID: mdl-32550004
18.
Optimization of a pentaplex panel for MSI analysis without control DNA in a Brazilian population: correlation with ancestry markers.
Eur J Hum Genet
; 22(7): 875-80, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24193342
19.
Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil.
PLoS One
; 9(6): e99893, 2014.
Article
in English
| MEDLINE | ID: mdl-24936644
20.
Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil.
Genet Mol Biol
; 32(3): 447-55, 2009 Jul.
Article
in English
| MEDLINE | ID: mdl-21637504