Search details
1.
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
Br J Cancer
; 128(12): 2283-2294, 2023 06.
Article
in English
| MEDLINE | ID: mdl-37076566
2.
Association analysis identifies 65 new breast cancer risk loci.
Nature
; 551(7678): 92-94, 2017 11 02.
Article
in English
| MEDLINE | ID: mdl-29059683
3.
VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis.
Bioinformatics
; 33(9): 1389-1391, 2017 05 01.
Article
in English
| MEDLINE | ID: mdl-28453673
4.
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Breast Cancer Res Treat
; 161(1): 117-134, 2017 01.
Article
in English
| MEDLINE | ID: mdl-27796716
5.
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
PLoS Genet
; 10(4): e1004256, 2014 04.
Article
in English
| MEDLINE | ID: mdl-24698998
6.
Genetic predisposition to ductal carcinoma in situ of the breast.
Breast Cancer Res
; 18(1): 22, 2016 Feb 17.
Article
in English
| MEDLINE | ID: mdl-26884359
7.
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
PLoS Genet
; 9(3): e1003173, 2013.
Article
in English
| MEDLINE | ID: mdl-23544012
8.
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
PLoS Genet
; 9(3): e1003212, 2013.
Article
in English
| MEDLINE | ID: mdl-23544013
9.
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
Breast Cancer Res
; 17: 61, 2015 Apr 25.
Article
in English
| MEDLINE | ID: mdl-25925750
10.
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.
Breast Cancer Res
; 15(3): 402, 2013 Jun 21.
Article
in English
| MEDLINE | ID: mdl-23809231
11.
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
Hum Mol Genet
; 20(16): 3304-21, 2011 Aug 15.
Article
in English
| MEDLINE | ID: mdl-21593217
12.
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.
Hum Mol Genet
; 20(23): 4732-47, 2011 Dec 01.
Article
in English
| MEDLINE | ID: mdl-21890493
13.
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Nat Genet
; 55(9): 1435-1439, 2023 09.
Article
in English
| MEDLINE | ID: mdl-37592023
14.
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
Hum Mutat
; 33(4): 690-702, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22253144
15.
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Breast Cancer Res
; 14(1): R33, 2012 Feb 20.
Article
in English
| MEDLINE | ID: mdl-22348646
16.
CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival.
Cancers (Basel)
; 14(2)2022 Jan 12.
Article
in English
| MEDLINE | ID: mdl-35053516
17.
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.
Cancers (Basel)
; 14(14)2022 Jul 11.
Article
in English
| MEDLINE | ID: mdl-35884425
18.
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
NPJ Breast Cancer
; 7(1): 52, 2021 May 12.
Article
in English
| MEDLINE | ID: mdl-33980861
19.
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer.
NPJ Breast Cancer
; 6: 44, 2020.
Article
in English
| MEDLINE | ID: mdl-32964118
20.
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Nat Genet
; 52(1): 56-73, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31911677