Detalhe da pesquisa
1.
Author Correction: The evolutionary history of lethal metastatic prostate cancer.
Nature
; 584(7820): E18, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32728210
2.
Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men.
Hum Mol Genet
; 32(3): 489-495, 2023 01 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36018819
3.
Evaluating Germline Testing Panels in Southern African Males With Advanced Prostate Cancer.
J Natl Compr Canc Netw
; 21(3): 289-296.e3, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36898365
4.
Prostate cancer risk in men of differing genetic ancestry and approaches to disease screening and management in these groups.
Br J Cancer
; 126(10): 1366-1373, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34923574
5.
The BARCODE1 Pilot: a feasibility study of using germline single nucleotide polymorphisms to target prostate cancer screening.
BJU Int
; 129(3): 325-336, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34214236
6.
African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer.
Int J Cancer
; 148(1): 99-105, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32930425
7.
Marital status and prostate cancer incidence: a pooled analysis of 12 case-control studies from the PRACTICAL consortium.
Eur J Epidemiol
; 36(9): 913-925, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275018
8.
The evolutionary history of lethal metastatic prostate cancer.
Nature
; 520(7547): 353-357, 2015 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-25830880
9.
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
10.
Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data.
PLoS Genet
; 13(9): e1007001, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28945760
11.
Polygenic risk-tailored screening for prostate cancer: A benefit-harm and cost-effectiveness modelling study.
PLoS Med
; 16(12): e1002998, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31860675
12.
Correction: Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
; 120(8): 867, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30837682
13.
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Am J Hum Genet
; 99(4): 877-885, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666373
14.
AA9int: SNP interaction pattern search using non-hierarchical additive model set.
Bioinformatics
; 34(24): 4141-4150, 2018 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29878078
15.
gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.
Genet Epidemiol
; 41(4): 297-308, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211093
16.
Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status.
Hum Mol Genet
; 25(24): 5490-5499, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27798103
17.
Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
; 119(1): 96-104, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29915322
18.
Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium.
Br J Cancer
; 118(6): e16, 2018 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29438364
19.
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
; 118(6): e9, 2018 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29438362
20.
SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns.
Bioinformatics
; 33(6): 822-833, 2017 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28039167