Detalhe da pesquisa
1.
Validation of a prostate cancer polygenic risk score.
Prostate
; 80(15): 1314-1321, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33258481
2.
Germline mutations in PPFIBP2 are associated with lethal prostate cancer.
Prostate
; 78(16): 1222-1228, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30043417
3.
Genetic factors influencing prostate cancer risk in Norwegian men.
Prostate
; 78(3): 186-192, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29181843
4.
A comprehensive evaluation of CHEK2 germline mutations in men with prostate cancer.
Prostate
; 78(8): 607-615, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29520813
5.
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
6.
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
Nat Genet
; 39(5): 631-7, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17401366
7.
Germline mutations in HOXB13 and prostate-cancer risk.
N Engl J Med
; 366(2): 141-9, 2012 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-22236224
8.
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
9.
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
10.
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
11.
Inherited genetic variant predisposes to aggressive but not indolent prostate cancer.
Proc Natl Acad Sci U S A
; 107(5): 2136-40, 2010 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20080650
12.
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.
Nat Genet
; 32(2): 321-5, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12244320
13.
Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.
Prostate
; 72(4): 410-26, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21748754
14.
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
Hum Genet
; 131(7): 1095-103, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22198737
15.
Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families.
BMC Med Genet
; 13: 46, 2012 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22712434
16.
Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk.
Carcinogenesis
; 32(11): 1655-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21856995
17.
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
Hum Mol Genet
; 18(7): 1368-75, 2009 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19153072
18.
Association of CASP8 D302H polymorphism with reduced risk of aggressive prostate carcinoma.
Prostate
; 70(6): 646-53, 2010 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20033885
19.
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses.
Prostate
; 70(7): 735-44, 2010 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20333727
20.
STAT: Spinal Cord Compression.
Clin J Oncol Nurs
; 24(5): 592, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32945805