Detalhe da pesquisa
1.
Epigenetic activation of SOX11 is associated with recurrence and progression of ductal carcinoma in situ to invasive breast cancer.
Br J Cancer
; 2024 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38760444
2.
Dose-escalated simultaneous integrated boost radiotherapy in early breast cancer (IMPORT HIGH): a multicentre, phase 3, non-inferiority, open-label, randomised controlled trial.
Lancet
; 401(10394): 2124-2137, 2023 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37302395
3.
Genetic susceptibility to radiation-induced breast cancer after Hodgkin lymphoma.
Blood
; 133(10): 1130-1139, 2019 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573632
4.
Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years.
Breast Cancer Res
; 21(1): 58, 2019 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31060593
5.
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.
Am J Hum Genet
; 99(4): 903-911, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27640304
6.
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression.
Hum Mol Genet
; 25(17): 3863-3876, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27402876
7.
MED12, TERT promoter and RBM15 mutations in primary and recurrent phyllodes tumours.
Br J Cancer
; 118(2): 277-284, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29315289
8.
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
Am J Hum Genet
; 97(1): 22-34, 2015 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26073781
9.
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Am J Hum Genet
; 96(1): 5-20, 2015 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25529635
10.
Partial-breast radiotherapy after breast conservation surgery for patients with early breast cancer (UK IMPORT LOW trial): 5-year results from a multicentre, randomised, controlled, phase 3, non-inferiority trial.
Lancet
; 390(10099): 1048-1060, 2017 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28779963
11.
SOX11 promotes invasive growth and ductal carcinoma in situ progression.
J Pathol
; 243(2): 193-207, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28707729
12.
PIK3CA mutations are common in lobular carcinoma in situ, but are not a biomarker of progression.
Breast Cancer Res
; 19(1): 7, 2017 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28095868
13.
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.
Hum Mol Genet
; 24(1): 285-98, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25168388
14.
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.
Genet Med
; 19(5): 599-603, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27711073
15.
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
J Med Genet
; 53(12): 800-811, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27595995
16.
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium.
Hum Genet
; 135(1): 137-54, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26621531
17.
Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Am J Hum Genet
; 93(6): 1046-60, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24290378
18.
Mutation detection in saliva from oral cancer patients.
Oral Oncol
; 151: 106717, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38412584
19.
Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer.
Nat Genet
; 54(6): 850-860, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35681052
20.
Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?
Cancers (Basel)
; 13(10)2021 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34069208