Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
Prevalence of the HOXB13 G84E prostate cancer risk allele in men treated with radical prostatectomy.
BJU Int
; 113(5): 830-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24148311
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
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
14.
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
15.
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
16.
Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.
Prostate
; 69(11): 1195-205, 2009 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19434657
17.
Association of prostate cancer risk variants with clinicopathologic characteristics of the disease.
Clin Cancer Res
; 14(18): 5819-24, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18794092
18.
Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations.
Prostate
; 68(12): 1257-62, 2008 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18491292
19.
Germ-line mutation of NKX3.1 cosegregates with hereditary prostate cancer and alters the homeodomain structure and function.
Cancer Res
; 66(1): 69-77, 2006 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16397218
20.
A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer risk.
Cancer Res
; 65(4): 1213-22, 2005 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15735005