about
Genome-wide association studies identify four ER negative-specific breast cancer risk lociNetwork-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer RiskGenome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairCandidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskGenome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer TypesPALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSLarge-scale genotyping identifies 41 new loci associated with breast cancer risk.Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic dataTP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerEvaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation CarriersGenome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy.Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarcheEvaluating genome-wide association study-identified breast cancer risk variants in African-American womenGenetic variation in mitotic regulatory pathway genes is associated with breast tumor gradeCommon non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association ConsortiumMicroRNA related polymorphisms and breast cancer risk.Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors.Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer riskInherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer.Genetic predisposition to in situ and invasive lobular carcinoma of the breast.Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study.Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapyAssociations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriersFine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.Identification of six new susceptibility loci for invasive epithelial ovarian cancer.An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriersCommon Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) RiskNovel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density MeasuresCis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancerCommon germline polymorphisms associated with breast cancer-specific survival.Genetic predisposition to ductal carcinoma in situ of the breastBreast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
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name
Joe Dennis
@ast
Joe Dennis
@en
Joe Dennis
@es
Joe Dennis
@nl
type
label
Joe Dennis
@ast
Joe Dennis
@en
Joe Dennis
@es
Joe Dennis
@nl
prefLabel
Joe Dennis
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Joe Dennis
@en
Joe Dennis
@es
Joe Dennis
@nl
P106
P31
P496
0000-0003-4591-1214