Item Type | Name |
Concept
|
Autoimmune Diseases
|
Concept
|
Coronary Artery Disease
|
Concept
|
Disease
|
Concept
|
Disease Susceptibility
|
Concept
|
Models, Genetic
|
Concept
|
Models, Molecular
|
Concept
|
Models, Theoretical
|
Concept
|
Models, Statistical
|
Concept
|
Logistic Models
|
Concept
|
Proportional Hazards Models
|
Concept
|
Disease Progression
|
Concept
|
Disease-Free Survival
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Rare Diseases
|
Academic Article
|
Robust gene expression and mutation analyses of RNA-sequencing of formalin-fixed diagnostic tumor samples.
|
Academic Article
|
Assessment of data transformations for model-based clustering of RNA-Seq data.
|
Academic Article
|
Subject level clustering using a negative binomial model for small transcriptomic studies.
|
Academic Article
|
Bayseian genomic models for the incorporation of pathway topology knowledge into association studies.
|
Academic Article
|
Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.
|
Academic Article
|
Integrative genomic analysis identifies epigenetic marks that mediate genetic risk for epithelial ovarian cancer.
|
Academic Article
|
Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants.
|
Academic Article
|
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
|
Academic Article
|
Variation in NF-?B signaling pathways and survival in invasive epithelial ovarian cancer.
|
Academic Article
|
Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome.
|
Academic Article
|
Methylation of leukocyte DNA and ovarian cancer: relationships with disease status and outcome.
|
Academic Article
|
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
|
Academic Article
|
Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk.
|
Academic Article
|
Genetic variation in platinating agent and taxane pathway genes as predictors of outcome and toxicity in advanced non-small-cell lung cancer.
|
Academic Article
|
Evidence for a time-dependent association between FOLR1 expression and survival from ovarian carcinoma: implications for clinical testing. An Ovarian Tumour Tissue Analysis consortium study.
|
Academic Article
|
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk.
|
Academic Article
|
Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study.
|
Academic Article
|
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
|
Academic Article
|
Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk.
|
Academic Article
|
Obesity and survival among women with ovarian cancer: results from the Ovarian Cancer Association Consortium.
|
Academic Article
|
Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk.
|
Academic Article
|
Shared genetics underlying epidemiological association between endometriosis and ovarian cancer.
|
Academic Article
|
Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population.
|
Academic Article
|
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
|
Academic Article
|
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer.
|
Academic Article
|
Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer.
|
Academic Article
|
Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk.
|
Academic Article
|
Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer.
|
Academic Article
|
Prior oral contraceptive use in ovarian cancer patients: assessing associations with overall and progression-free survival.
|
Academic Article
|
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer.
|
Academic Article
|
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
|
Academic Article
|
Clinical and Emergent Biomarkers and Their Relationship to the Prognosis of Ovarian Cancer.
|
Academic Article
|
PPM1D Mosaic Truncating Variants in Ovarian Cancer Cases May Be Treatment-Related Somatic Mutations.
|
Academic Article
|
A targeted genetic association study of epithelial ovarian cancer susceptibility.
|
Academic Article
|
The association between socioeconomic status and tumour stage at diagnosis of ovarian cancer: A pooled analysis of 18 case-control studies.
|
Academic Article
|
Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.
|
Academic Article
|
Five endometrial cancer risk loci identified through genome-wide association analysis.
|
Academic Article
|
Chronic Recreational Physical Inactivity and Epithelial Ovarian Cancer Risk: Evidence from the Ovarian Cancer Association Consortium.
|
Academic Article
|
Expression signature distinguishing two tumour transcriptome classes associated with progression-free survival among rare histological types of epithelial ovarian cancer.
|
Academic Article
|
Recreational physical inactivity and mortality in women with invasive epithelial ovarian cancer: evidence from the Ovarian Cancer Association Consortium.
|
Academic Article
|
Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk.
|
Academic Article
|
Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study.
|
Academic Article
|
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer.
|
Academic Article
|
Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer.
|
Academic Article
|
Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study.
|
Academic Article
|
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
|
Academic Article
|
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
|
Academic Article
|
Risk Prediction for Epithelial Ovarian Cancer in 11 United States-Based Case-Control Studies: Incorporation of Epidemiologic Risk Factors and 17 Confirmed Genetic Loci.
|
Academic Article
|
HNF1B variants associate with promoter methylation and regulate gene networks activated in prostate and ovarian cancer.
|
Academic Article
|
Drug discovery using clinical outcome-based Connectivity Mapping: application to ovarian cancer.
|
Academic Article
|
Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration.
|
Academic Article
|
Cigarette smoking is associated with adverse survival among women with ovarian cancer: Results from a pooled analysis of 19 studies.
|
Academic Article
|
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
|
Academic Article
|
An integrative approach to assess X-chromosome inactivation using allele-specific expression with applications to epithelial ovarian cancer.
|
Academic Article
|
Mediation analysis of alcohol consumption, DNA methylation, and epithelial ovarian cancer.
|
Academic Article
|
Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study.
|
Academic Article
|
Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.
|
Academic Article
|
Identification of nine new susceptibility loci for endometrial cancer.
|
Academic Article
|
rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology.
|
Academic Article
|
Lenalidomide-based response-adapted therapy for older adults without high risk myeloma.
|
Academic Article
|
Statistical genomics in rare cancer.
|
Academic Article
|
Nonlinear mixed-effects models for modeling in vitro drug response data to determine problematic cancer cell lines.
|
Academic Article
|
Patterns and predictors of genetic referral among ovarian cancer patients at a National Cancer Institute-Comprehensive Cancer Center.
|
Academic Article
|
An evolutionary framework for treating pediatric sarcomas.
|
Academic Article
|
Oxidized mitochondrial DNA released after inflammasome activation is a disease biomarker for myelodysplastic syndromes.
|
Academic Article
|
Prospective Analyses of Sedentary Behavior in Relation to Risk of Ovarian Cancer.
|
Academic Article
|
Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer.
|
Academic Article
|
Predictors of residual disease after debulking surgery in advanced stage ovarian cancer.
|
Academic Article
|
Modeling phenotypic heterogeneity towards evolutionarily inspired osteosarcoma therapy.
|
Academic Article
|
Spatial transcriptomics analysis identifies a unique tumor-promoting function of the meningeal stroma in melanoma leptomeningeal disease.
|
Academic Article
|
Diagnostic tools in linkage analysis for quantitative traits.
|
Academic Article
|
Imputation methods for missing data for polygenic models.
|
Academic Article
|
Missing phenotype data imputation in pedigree data analysis.
|
Academic Article
|
Host genetic variation contributes to phenotypic diversity in myeloproliferative disorders.
|
Academic Article
|
Interacting alleles of the coinhibitory immunoreceptor genes cytotoxic T-lymphocyte antigen 4 and programmed cell-death 1 influence risk and features of primary biliary cirrhosis.
|
Academic Article
|
Model selection and Bayesian methods in statistical genetics: summary of group 11 contributions to Genetic Analysis Workshop 15.
|
Academic Article
|
Human phenylethanolamine N-methyltransferase genetic polymorphisms and exercise-induced epinephrine release.
|
Academic Article
|
Toll-like receptor polymorphisms and age-related macular degeneration.
|
Academic Article
|
Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data.
|
Academic Article
|
Density of common complex ocular traits in the aging eye: analysis of secondary traits in genome-wide association studies.
|
Academic Article
|
Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic.
|
Academic Article
|
Bayesian variable and model selection methods for genetic association studies.
|
Academic Article
|
Primary biliary cirrhosis is associated with a genetic variant in the 3' flanking region of the CTLA4 gene.
|
Academic Article
|
Evaluation of clustering and genotype distribution for replication in genome wide association studies: the age-related eye disease study.
|
Academic Article
|
Methods for analysis in pharmacogenomics: lessons from the Pharmacogenetics Research Network Analysis Group.
|
Academic Article
|
Genome-wide linkage analysis for uric acid in families enriched for hypertension.
|
Academic Article
|
Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
|
Academic Article
|
Polymorphisms in TCEAL7 and risk of epithelial ovarian cancer.
|
Academic Article
|
Polymorphisms in NF-kappaB inhibitors and risk of epithelial ovarian cancer.
|
Academic Article
|
A Bayesian hierarchical nonlinear model for assessing the association between genetic variation and drug cytotoxicity.
|
Academic Article
|
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
|
Academic Article
|
Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis.
|
Academic Article
|
ESR1/SYNE1 polymorphism and invasive epithelial ovarian cancer risk: an Ovarian Cancer Association Consortium study.
|
Academic Article
|
Inherited determinants of ovarian cancer survival.
|
Academic Article
|
Risk of ovarian cancer and inherited variants in relapse-associated genes.
|
Academic Article
|
Polymorphism in the GALNT1 gene and epithelial ovarian cancer in non-Hispanic white women: the Ovarian Cancer Association Consortium.
|
Academic Article
|
Variation at 8q24 and 9p24 and risk of epithelial ovarian cancer.
|
Academic Article
|
Familial aggregation of irritable bowel syndrome: a family case-control study.
|
Academic Article
|
Conference Scene: Lessons learned from the 5th Statistical Analysis Workshop of the Pharmacogenetics Research Network.
|
Academic Article
|
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.
|
Academic Article
|
Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.
|
Academic Article
|
Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association Consortium.
|
Academic Article
|
Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies.
|
Academic Article
|
Progesterone receptor gene polymorphisms and risk of endometriosis: results from an international collaborative effort.
|
Academic Article
|
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.
|
Academic Article
|
Common variants at 19p13 are associated with susceptibility to ovarian cancer.
|
Academic Article
|
Multivariate models to detect genomic signatures for a class of drugs: application to thiopurines pharmacogenomics.
|
Academic Article
|
Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study.
|
Academic Article
|
Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study.
|
Academic Article
|
The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing.
|
Academic Article
|
Mycophenolic acid response biomarkers: a cell line model system-based genome-wide screen.
|
Academic Article
|
Prostate cancer susceptibility polymorphism rs2660753 is not associated with invasive ovarian cancer.
|
Academic Article
|
Xenobiotic-Metabolizing gene polymorphisms and ovarian cancer risk.
|
Academic Article
|
LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.
|
Academic Article
|
Gene set analysis of SNP data: benefits, challenges, and future directions.
|
Academic Article
|
MicroRNA processing and binding site polymorphisms are not replicated in the Ovarian Cancer Association Consortium.
|
Academic Article
|
Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium.
|
Academic Article
|
A latent model for prioritization of SNPs for functional studies.
|
Academic Article
|
Associations of high-grade glioma with glioma risk alleles and histories of allergy and smoking.
|
Academic Article
|
Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development.
|
Academic Article
|
Use of the gamma method for self-contained gene-set analysis of SNP data.
|
Academic Article
|
Ovarian cancer risk associated with inherited inflammation-related variants.
|
Academic Article
|
Gene set analysis of survival following ovarian cancer implicates macrolide binding and intracellular signaling genes.
|
Academic Article
|
A Bayesian integrative genomic model for pathway analysis of complex traits.
|
Academic Article
|
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.
|
Academic Article
|
Genome-wide gene-set analysis for identification of pathways associated with alcohol dependence.
|
Academic Article
|
Simultaneous analysis of multiple data types in pharmacogenomic studies using weighted sparse canonical correlation analysis.
|
Academic Article
|
A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation.
|
Academic Article
|
ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium.
|
Academic Article
|
Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.
|
Academic Article
|
Survival is associated with genetic variation in inflammatory pathway genes among patients with resected and unresected pancreatic cancer.
|
Academic Article
|
Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.
|
Academic Article
|
Inherited variants in regulatory T cell genes and outcome of ovarian cancer.
|
Academic Article
|
Cigarette smoking and risk of ovarian cancer: a pooled analysis of 21 case-control studies.
|
Academic Article
|
Combined and interactive effects of environmental and GWAS-identified risk factors in ovarian cancer.
|
Academic Article
|
Analysis of over 10,000 Cases finds no association between previously reported candidate polymorphisms and ovarian cancer outcome.
|
Academic Article
|
Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.
|
Academic Article
|
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
|
Academic Article
|
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
|
Academic Article
|
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
|
Academic Article
|
Kernel canonical correlation analysis for assessing gene-gene interactions and application to ovarian cancer.
|
Academic Article
|
ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas.
|