Detalhe da pesquisa
1.
Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain.
Am J Hum Genet
; 111(3): 584-593, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38417439
2.
Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance.
Am J Hum Genet
; 108(3): 458-468, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33609447
3.
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.
Am J Hum Genet
; 108(7): 1190-1203, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34146516
4.
Clinical effectiveness and safety of olaparib in BRCA-mutated, HER2-negative metastatic breast cancer in a real-world setting: final analysis of LUCY.
Breast Cancer Res Treat
; 204(2): 237-248, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38112922
5.
Disentangling the relationships of body mass index and circulating sex hormone concentrations in mammographic density using Mendelian randomization.
Breast Cancer Res Treat
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38653906
6.
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry.
Breast Cancer Res
; 25(1): 93, 2023 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37559094
7.
The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
Cancer
; 129(6): 901-907, 2023 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36571512
8.
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.
Am J Hum Genet
; 107(5): 837-848, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33022221
9.
Clinical outcomes and prognostic factors in triple-negative invasive lobular carcinoma of the breast.
Breast Cancer Res Treat
; 200(2): 217-224, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37210429
10.
Salicylates enhance CRM1 inhibitor antitumor activity by induction of S-phase arrest and impairment of DNA-damage repair.
Blood
; 137(4): 513-523, 2021 01 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33507295
11.
Summary of the experiences, knowledge, medical management, and family communication of monoallelic MUTYH carriers.
J Genet Couns
; 32(2): 342-350, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36245263
12.
Surveillance mammography after treatment for male breast cancer.
Breast Cancer Res Treat
; 194(3): 693-698, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35713802
13.
Tissue methylated DNA markers for sporadic pancreatic cancer are strongly associated with familial and genetically predisposed pancreatic cancer.
Pancreatology
; 22(6): 770-773, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35843766
14.
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study.
Br J Sports Med
; 56(20): 1157-1170, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328784
15.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33326660
16.
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.
Breast Cancer Res
; 23(1): 86, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34407845
17.
Germline genetic testing in breast cancer: Rationale for the testing of all women diagnosed by the age of 60 years and for risk-based testing of those older than 60 years.
Cancer
; 127(6): 828-833, 2021 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33146899
18.
Mendelian randomisation study of smoking exposure in relation to breast cancer risk.
Br J Cancer
; 125(8): 1135-1145, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34341517
19.
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.
Br J Cancer
; 124(4): 842-854, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495599
20.
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
Am J Hum Genet
; 102(2): 233-248, 2018 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29394989