about
Detectable clonal mosaicism and its relationship to aging and cancerImputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Characterization of large structural genetic mosaicism in human autosomeAnalysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesA genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancerEpigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancerNetwork-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer RiskFemale chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeGermline mutations in shelterin complex genes are associated with familial gliomaThe Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International ConsortiumTERT gene harbors multiple variants associated with pancreatic cancer susceptibilityTargeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene ConsortiumGenome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer TypesGermline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancerPALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSGenome-wide association study of endometrial cancer in E2C2The obesity-associated polymorphisms FTO rs9939609 and MC4R rs17782313 and endometrial cancer risk in non-Hispanic white womenAssociation Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.A splicing variant of TERT identified by GWAS interacts with menopausal estrogen therapy in risk of ovarian cancerChronic Recreational Physical Inactivity and Epithelial Ovarian Cancer Risk: Evidence from the Ovarian Cancer Association ConsortiumAssessing the genetic architecture of epithelial ovarian cancer histological subtypes.No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium.Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data.Exome-wide association study of endometrial cancer in a multiethnic populationFunctional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148Proportion of cancer in a Middle eastern country attributable to established risk factorsGenome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.Maximizing resources to study an uncommon cancer: E2C2--Epidemiology of Endometrial Cancer Consortium.Variation in NF-κB signaling pathways and survival in invasive epithelial ovarian cancerPolymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.Phytoestrogen consumption from foods and supplements and epithelial ovarian cancer risk: a population-based case control study.Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers.Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutationCoffee and tea consumption and endometrial cancer risk in a population-based study in New Jersey.Cigar and pipe smoking, smokeless tobacco use and pancreatic cancer: an analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4)Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer
P50
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P50
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Sara H Olson
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Sara H Olson
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Sara H Olson
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Sara H Olson
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Sara H Olson
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type
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Sara H Olson
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Sara H Olson
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Sara Olson
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Sara H Olson
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Sara H Olson
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Sara H Olson
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Sara H Olson
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Sara H Olson
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P106
P21
P31
P496
0000-0003-0182-2754