Detalhe da pesquisa
1.
The SARS-CoV-2 protein NSP2 enhances microRNA-mediated translational repression.
J Cell Sci
; 136(19)2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37732428
2.
The topology of data: opportunities for cancer research.
Bioinformatics
; 37(19): 3091-3098, 2021 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34320632
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.
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma.
Blood
; 132(19): 2040-2052, 2018 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194254
5.
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Hum Mol Genet
; 24(10): 2966-84, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25652398
6.
Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C.
Genome Res
; 24(11): 1854-68, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25122612
7.
Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups.
Breast Cancer Res
; 18(1): 104, 2016 10 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27756439
8.
Genetic predisposition to ductal carcinoma in situ of the breast.
Breast Cancer Res
; 18(1): 22, 2016 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26884359
9.
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.
Hum Mol Genet
; 23(22): 6096-111, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24943594
10.
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
Nat Genet
; 39(5): 645-9, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17401363
11.
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
Nat Genet
; 39(7): 870-4, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17529973
12.
A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.
Nat Genet
; 38(10): 1173-7, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16998489
13.
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study.
Breast Cancer Res
; 16(3): R51, 2014 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24887515
14.
Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.
Genet Med
; 16(1): 19-24, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703681
15.
Genetic variants at chromosomes 2q35, 5p12, 6q25.1, 10q26.13, and 16q12.1 influence the risk of breast cancer in men.
PLoS Genet
; 7(9): e1002290, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21949660
16.
Large-scale fine mapping of the HNF1B locus and prostate cancer risk.
Hum Mol Genet
; 20(16): 3322-9, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21576123
17.
Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer.
Hum Mol Genet
; 20(14): 2869-78, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21531787
18.
Health diplomacy in action: The cancer legacy of the Good Friday Agreement.
J Cancer Policy
; 38: 100448, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37839622
19.
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.
Proc Natl Acad Sci U S A
; 106(19): 7933-8, 2009 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-19383797
20.
TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
Am J Hum Genet
; 82(2): 501-9, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18252230