|
Prostate carcinoma
|
|
0.720 |
GeneticVariation
|
GWASCAT |
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.
|
26034056 |
2015 |
|
Malignant neoplasm of prostate
|
|
0.720 |
GeneticVariation
|
GWASDB |
Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.
|
23555315 |
2013 |
|
Prostate carcinoma
|
|
0.720 |
GeneticVariation
|
BEFREE |
Three of the 23 genetic variants explored were nominally associated with prostate cancer progression; rs9364554 (P = 0.041) on chromosome 6q25 and rs10896449 (P = 0.029) on chromosome 11q13 among patients treated with curative intent; and rs4054823 (P = 0.008) on chromosome 17p12 among patients on surveillance.
|
21520160 |
2012 |
|
Malignant neoplasm of prostate
|
|
0.720 |
GeneticVariation
|
BEFREE |
Three of the 23 genetic variants explored were nominally associated with prostate cancer progression; rs9364554 (P = 0.041) on chromosome 6q25 and rs10896449 (P = 0.029) on chromosome 11q13 among patients treated with curative intent; and rs4054823 (P = 0.008) on chromosome 17p12 among patients on surveillance.
|
21520160 |
2012 |
|
Malignant neoplasm of prostate
|
|
0.720 |
GeneticVariation
|
BEFREE |
We found evidence of prostate cancer association for the previously implicated SNPs including rs10896449, which we termed locus 1.
|
19505914 |
2009 |
|
Prostate carcinoma
|
|
0.720 |
GeneticVariation
|
BEFREE |
We found evidence of prostate cancer association for the previously implicated SNPs including rs10896449, which we termed locus 1.
|
19505914 |
2009 |
|
Malignant neoplasm of prostate
|
|
0.720 |
GeneticVariation
|
GWASDB |
Multiple loci identified in a genome-wide association study of prostate cancer.
|
18264096 |
2008 |
|
Malignant neoplasm of prostate
|
|
0.720 |
GeneticVariation
|
GWASDB |
Multiple newly identified loci associated with prostate cancer susceptibility.
|
18264097 |
2008 |
|
Prostate carcinoma
|
|
0.720 |
GeneticVariation
|
GWASCAT |
Multiple loci identified in a genome-wide association study of prostate cancer.
|
18264096 |
2008 |
|
Nasopharyngeal carcinoma
|
|
0.700 |
GeneticVariation
|
GWASDB |
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
|
20512145 |
2010 |
|
Malignant neoplasm of breast
|
|
0.010 |
GeneticVariation
|
BEFREE |
Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13).
|
23573233 |
2013 |
|
Breast Carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13).
|
23573233 |
2013 |
|
Malignant Neoplasms
|
|
0.010 |
GeneticVariation
|
BEFREE |
As part of the Cancer Genetic Markers of Susceptibility (CGEMS) Initiative, the region flanking the most significant marker, rs10896449, was fine mapped in 10 272 cases and 9123 controls of European origin (10 studies) using 120 common single nucleotide polymorphisms (SNPs) selected by a two-staged tagging strategy using HapMap SNPs.
|
21531787 |
2011 |
|
Primary malignant neoplasm
|
|
0.010 |
GeneticVariation
|
BEFREE |
As part of the Cancer Genetic Markers of Susceptibility (CGEMS) Initiative, the region flanking the most significant marker, rs10896449, was fine mapped in 10 272 cases and 9123 controls of European origin (10 studies) using 120 common single nucleotide polymorphisms (SNPs) selected by a two-staged tagging strategy using HapMap SNPs.
|
21531787 |
2011 |