about
sameAs
Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear familyDetectable 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 cancerPancreatic Cancer GeneticsEpidemiology and Inherited Predisposition for Sporadic Pancreatic AdenocarcinomaFemale chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeGenetic polymorphisms in the 9p21 region associated with risk of multiple cancersTERT gene harbors multiple variants associated with pancreatic cancer susceptibilityAn integrated transcriptome and epigenome analysis identifies a novel candidate gene for pancreatic cancerWinner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level DataGenome-wide association study of survival in patients with pancreatic adenocarcinomaAssociation Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk.The BARD1 Cys557Ser variant and breast cancer risk in IcelandEvaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cellsVariants associated with susceptibility to pancreatic cancer and melanoma do not reciprocally affect riskPolymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).Family history of cancer and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium.Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancerGenome-wide association study identifies multiple susceptibility loci for pancreatic cancer.Identification of phosphorylated residues that affect the activity of the mitotic kinase Aurora-A.Variant ABO blood group alleles, secretor status, and risk of pancreatic cancer: results from the pancreatic cancer cohort consortium.The risk allele of SNP rs3803662 and the mRNA level of its closest genes TOX3 and LOC643714 predict adverse outcome for breast cancer patientsTranscriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1A.DNA methylation levels at chromosome 8q24 in peripheral blood are associated with 8q24 cancer susceptibility lociCharacterization of SNPs associated with prostate cancer in men of Ashkenazic descent from the set of GWAS identified SNPs: impact of cancer family history and cumulative SNP risk predictionLarge-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study.Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels.Two susceptibility loci identified for prostate cancer aggressiveness.Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancerCommon variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.Assessing disease risk in genome-wide association studies using family history.
P50
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Laufey T. Amundadottir
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2000-01-01T00:00:00Z