Found: 20
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Evidence for two independent prostate cancer risk–associated loci in the HNF1B gene at 17q12.
- Published in:
- Nature Genetics, 2008, v. 40, n. 10, p. 1153, doi. 10.1038/ng.214
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- Publication type:
- Article
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.
- Published in:
- Nature Genetics, 2002, v. 32, n. 2, p. 321, doi. 10.1038/ng994
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- Publication type:
- Article
Identification of New Differentially Methylated Genes That Have Potential Functional Consequences in Prostate Cancer.
- Published in:
- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0048455
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- Publication type:
- Article
Positive results in association studies are associated with departure from Hardy-Weinberg equilibrium: hint for genotyping error?
- Published in:
- Human Genetics, 2002, v. 111, n. 6, p. 573, doi. 10.1007/s00439-002-0819-y
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- Publication type:
- Article
Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk.
- Published in:
- Human Genetics, 2002, v. 110, n. 2, p. 122, doi. 10.1007/s00439-001-0662-6
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- Publication type:
- Article
Association Between Two Unlinked Loci at 8q24 and Prostate Cancer Risk Among European Americans.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2007, v. 99, n. 20, p. 1525, doi. 10.1093/jnci/djm169
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- Publication type:
- Article
Sequence Variants in Toll-Like Receptor Gene Cluster (TLR6-TLR1-TLR10) and Prostate Cancer Risk.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2005, v. 97, n. 7, p. 525, doi. 10.1093/jnci/dji070
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- Publication type:
- Article
Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk.
- Published in:
- International Journal of Cancer, 2003, v. 106, n. 3, p. 375, doi. 10.1002/ijc.11249
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- Publication type:
- Article
Inherited genetic markers discovered to date are able to identify a significant number of men at considerably elevated risk for prostate cancer.
- Published in:
- Prostate, 2011, v. 71, n. 4, p. 421, doi. 10.1002/pros.21256
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- Publication type:
- Article
DNA copy number alterations in prostate cancers: A combined analysis of published CGH studies.
- Published in:
- Prostate, 2007, v. 67, n. 7, p. 692, doi. 10.1002/pros.20543
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- Publication type:
- Article
Germline copy number polymorphisms involving larger than 100 kb are uncommon in normal subjects.
- Published in:
- Prostate, 2007, v. 67, n. 3, p. 227, doi. 10.1002/pros.20441
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- Publication type:
- Article
A comprehensive association study for genes in inflammation pathway provides support for their roles in prostate cancer risk in the CAPS studyS. Lilly Zheng and Wennuan Liu contributed equally to the study.
- Published in:
- Prostate, 2006, v. 66, n. 14, p. 1556, doi. 10.1002/pros.20496
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- Publication type:
- Article
Meta-analysis of association of rare mutations and common sequence variants in the MSR1 gene and prostate cancer risk.
- Published in:
- Prostate, 2006, v. 66, n. 7, p. 728, doi. 10.1002/pros.20396
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- Publication type:
- Article
Serum levels of phytanic acid are associated with prostate cancer risk.
- Published in:
- Prostate, 2005, v. 63, n. 3, p. 209, doi. 10.1002/pros.20233
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- Publication type:
- Article
Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer.
- Published in:
- Prostate, 2003, v. 56, n. 1, p. 37, doi. 10.1002/pros.10225
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- Publication type:
- Article
Multiple genomic alterations on 21q22 predict various TMPRSS2/ERG fusion transcripts in human prostate cancers.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 11, p. 972, doi. 10.1002/gcc.20482
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- Publication type:
- Article
Comprehensive assessment of DNA copy number alterations in human prostate cancers using Affymetrix 100K SNP mapping array.
- Published in:
- Genes, Chromosomes & Cancer, 2006, v. 45, n. 11, p. 1018, doi. 10.1002/gcc.20369
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- Publication type:
- Article
Randomized trial finds that prostate cancer genetic risk score feedback targets prostate-specific antigen screening among at-risk men.
- Published in:
- 2016
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- Publication type:
- journal article
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1368, doi. 10.1093/hmg/ddp035
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- Publication type:
- Article
A support vector machine approach for detecting gene-gene interaction.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 2, p. 152, doi. 10.1002/gepi.20272
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- Publication type:
- Article