Detalhe da pesquisa
1.
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
N Engl J Med
; 384(5): 428-439, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33471991
2.
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer.
BMC Cancer
; 23(1): 738, 2023 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37563628
3.
Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points-based ACMG/AMP approach.
Hum Mutat
; 43(12): 1921-1944, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35979650
4.
Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells.
Blood
; 129(8): 950-958, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-27899358
5.
BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer.
Breast Cancer Res Treat
; 168(1): 117-126, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29164420
6.
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility.
Genet Med
; 20(4): 452-457, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28837162
7.
Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells.
Proc Natl Acad Sci U S A
; 112(7): 2157-62, 2015 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-25646469
8.
Molecular and genetic diversity in the metastatic process of melanoma.
J Pathol
; 233(1): 39-50, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24399611
9.
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.
Breast Cancer Res
; 15(3): 402, 2013 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23809231
10.
Validation of the BOADICEA model for predicting the likelihood of carrying pathogenic variants in eight breast and ovarian cancer susceptibility genes.
Sci Rep
; 13(1): 8536, 2023 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37237042
11.
Androgen receptor htSNPs in relation to androgen levels and OC use in young women from high-risk breast cancer families.
Mol Genet Metab
; 102(1): 82-90, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20947401
12.
Precision Oncology of High-Grade Ovarian Cancer Defined through Targeted Sequencing.
Cancers (Basel)
; 13(20)2021 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34680387
13.
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
Hum Mutat
; 31(3): E1200-40, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20104584
14.
Oral contraceptives and postmenopausal hormones and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers and noncarriers: the WECARE Study.
Breast Cancer Res Treat
; 120(1): 175-83, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19597986
15.
Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer.
Breast Cancer Res Treat
; 123(2): 491-8, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20135344
16.
Reproductive factors and risk of contralateral breast cancer by BRCA1 and BRCA2 mutation status: results from the WECARE study.
Cancer Causes Control
; 21(6): 839-46, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20130978
17.
Author Correction: Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma.
Nat Commun
; 11(1): 1714, 2020 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32238805
18.
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
Hum Mutat
; 29(4): 555-64, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18330910
19.
Author Correction: Validation of the BOADICEA model for predicting the likelihood of carrying pathogenic variants in eight breast and ovarian cancer susceptibility genes.
Sci Rep
; 13(1): 15294, 2023 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37714994
20.
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Fam Cancer
; 16(2): 195-203, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27696107