about
Shortened telomere length is associated with increased risk of cancer: a meta-analysisCYP2D6 gene variants: association with breast cancer specific survival in a cohort of breast cancer patients from the United Kingdom treated with adjuvant tamoxifenCommon variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs.Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.A gene (DLG2) located at 17q12-q21 encodes a new homologue of the Drosophila tumor suppressor dIg-APOT1 loss-of-function variants predispose to familial melanomaGenome-wide association studies identify four ER negative-specific breast cancer risk lociGenome-wide association study identifies novel breast cancer susceptibility lociInteractions between genes involved in the antioxidant defence system and breast cancer riskIdentification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal womenCommon genetic variation in candidate genes and susceptibility to subtypes of breast cancerRed-clover-derived isoflavones and mammographic breast density: a double-blind, randomized, placebo-controlled trial [ISRCTN42940165]Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control studyGenetic variation in the HSD17B1 gene and risk of prostate cancer.Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskDo MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium.Common polymorphisms in the prostaglandin pathway genes and their association with breast cancer susceptibility and survivalLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairHyaluronan-mediated motility receptor gene single nucleotide polymorphisms and risk of breast cancerCandidate 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 TypesGenetic variants in ER cofactor genes and endometrial cancer riskPALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSGenome-wide association study of endometrial cancer in E2C2Large-scale genotyping identifies 41 new loci associated with breast cancer risk.Genome-wide association study identifies three new melanoma susceptibility loci.A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.Genome-wide association study identifies a common variant associated with risk of endometrial cancer.Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.Rare and low-frequency coding variants alter human adult heightNo clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.Radiogenomics: radiobiology enters the era of big data and team science.Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients.Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancerAssociation between common variation in 120 candidate genes and breast cancer risk.The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study.Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design.
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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type
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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altLabel
Alison M Dunning
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Alison Margaret Dunning
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Alison Margaret Dunning
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Alison Margaret Dunning
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Dunning AM
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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Alison Dunning
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P106
P21
P31
P496
0000-0001-6651-7166
P6304
alison-dunning