A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
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Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"DNA methylation age of human tissues and cell typesEpigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancerGenomic/Epigenomic Alterations in Ovarian Carcinoma: Translational Insight into Clinical PracticeNetwork-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer RiskOvarian cancer screening--current status, future directionsGenetic risk prediction in complex diseaseDNA methylation changes in epithelial ovarian cancer histotypes.Targeted immune therapy of ovarian cancerContribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the PopulationClinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C statusA Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer.Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal CancerGenetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening TrialA genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.Common variants at 19p13 are associated with susceptibility to ovarian cancer.Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.Ovarian cancer epidemiology in the era of collaborative team science.Integration of Population-Level Genotype Data with Functional Annotation Reveals Over-Representation of Long Noncoding RNAs at Ovarian Cancer Susceptibility Loci.A splicing variant of TERT identified by GWAS interacts with menopausal estrogen therapy in risk of ovarian cancerAssessing the genetic architecture of epithelial ovarian cancer histological subtypes.Assessment of Multifactor Gene-Environment Interactions and Ovarian Cancer Risk: Candidate Genes, Obesity, and Hormone-Related Risk Factors.Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer.Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.Approaches to integrating germline and tumor genomic data in cancer research.Risk of ovarian cancer and inherited variants in relapse-associated genesGene expression profile for predicting survival in advanced-stage serous ovarian cancer across two independent datasets.Functional annotation signatures of disease susceptibility loci improve SNP association analysis.Aging effects on DNA methylation modules in human brain and blood tissue.Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population.Genome-wide investigation of regional blood-based DNA methylation adjusted for complete blood counts implicates BNC2 in ovarian cancer.Analyzing association of the XRCC3 gene polymorphism with ovarian cancer risk.CXCL12 expression by healthy and malignant ovarian epithelial cells.A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.Methylation of leukocyte DNA and ovarian cancer: relationships with disease status and outcome.Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium.Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: pooled analysis within the Ovarian Cancer Association Consortium.The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
P2860
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P2860
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@ast
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@en
type
label
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@ast
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@en
prefLabel
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@ast
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@en
P2093
P2860
P50
P921
P356
P1433
P1476
A genome-wide association stud ...... usceptibility locus on 9p22.2.
@en
P2093
Alice S Whittemore
Andrew Berchuck
Australian Cancer (Ovarian) Study
Brooke L Fridley
Bruce A J Ponder
Carole Pye
Catherine Phelan
Celeste Leigh Pearce
Claus Hogdall
P2860
P2888
P304
P356
10.1038/NG.424
P407
P50
P577
2009-08-02T00:00:00Z