Detalhe da pesquisa
1.
Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19.
Cell
; 174(3): 564-575.e18, 2018 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30033362
2.
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk.
Am J Hum Genet
; 109(5): 900-908, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35353984
3.
Familial recurrence risk with varying amount of family history.
Genet Epidemiol
; 43(4): 440-448, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30740785
4.
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
5.
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
Acta Neuropathol
; 137(6): 879-899, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30739198
6.
Identification of missing variants by combining multiple analytic pipelines.
BMC Bioinformatics
; 19(1): 139, 2018 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29661148
7.
FIRE: functional inference of genetic variants that regulate gene expression.
Bioinformatics
; 33(24): 3895-3901, 2017 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28961785
8.
Germline miRNA DNA variants and the risk of colorectal cancer by subtype.
Genes Chromosomes Cancer
; 56(3): 177-184, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636879
9.
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.
Hum Mol Genet
; 24(19): 5589-602, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26025378
10.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
; 135(8): 923-38, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262462
11.
Prediction of individual genetic risk to prostate cancer using a polygenic score.
Prostate
; 75(13): 1467-74, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26177737
12.
Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.
Hum Genet
; 134(4): 439-50, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25715684
13.
Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data.
Genet Epidemiol
; 37(5): 409-18, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23650101
14.
Mutational landscape of candidate genes in familial prostate cancer.
Prostate
; 74(14): 1371-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25111073
15.
Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.
Hum Genet
; 133(3): 347-56, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24162621
16.
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Blood
; 120(4): 843-6, 2012 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-22700719
17.
Using the gene ontology to scan multilevel gene sets for associations in genome wide association studies.
Genet Epidemiol
; 36(1): 3-16, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22161999
18.
Detecting genomic clustering of risk variants from sequence data: cases versus controls.
Hum Genet
; 132(11): 1301-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23842950
19.
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).
Hum Genet
; 132(1): 5-14, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23064873
20.
No association of germline alteration of MSR1 with prostate cancer risk.
Nat Genet
; 35(2): 128-9, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12958598