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AddAla-Kokko, T(ero)
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AddEskelinen, S.
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AddHallman, M.
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AddHukkanen J(anne)
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AddJaakkola, M(aritta) S.
AddJaakola, V-P.
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AddKesäniemi, Y(rjö) A(ntero)
AddKettunen, J(ohannes)
AddKietzmann, T(homas).
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AddKnuuttila, M.
AddKoivukangas, J.
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Breast cancer risk factors and survival by tumor subtype: pooled analyses from the Breast Cancer Association Consortium.Winqvist, R(obert)106 dayssaveRefWorks
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.Winqvist, R(obert)107 dayssaveRefWorks
Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer.Winqvist, R(obert)158 dayssaveRefWorks
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.Winqvist, R(obert)219 dayssaveRefWorks
Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition.Winqvist, R(obert)236 dayssaveRefWorks
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.Winqvist, R(obert)359 dayssaveRefWorks
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.Winqvist, R(obert)437 dayssaveRefWorks
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.Winqvist, R(obert)482 dayssaveRefWorks
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Homologous recombination DNA repair defects in PALB2-associated breast cancers.Winqvist, R(obert)632 dayssaveRefWorks
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.Winqvist, R(obert)758 dayssaveRefWorks
Genome-wide association study of germline variants and breast cancer-specific mortality.Winqvist, R(obert)811 dayssaveRefWorks
Shared heritability and functional enrichment across six solid cancers.Winqvist, R(obert)838 dayssaveRefWorks
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.Winqvist, R(obert)878 dayssaveRefWorks
Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls.Winqvist, R(obert)982 dayssaveRefWorks
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The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.Winqvist, R(obert)1178 dayssaveRefWorks
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.Winqvist, R(obert)1212 dayssaveRefWorks
PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.Winqvist, R(obert)1239 dayssaveRefWorks
Body mass index and breast cancer survival: a Mendelian randomization analysis.Winqvist, R(obert)1248 dayssaveRefWorks
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.Winqvist, R(obert)1282 dayssaveRefWorks
Association analysis identifies 65 new breast cancer risk loci.Winqvist, R(obert)1298 dayssaveRefWorks
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.Winqvist, R(obert)1298 dayssaveRefWorks
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.Winqvist, R(obert)1400 dayssaveRefWorks
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.Winqvist, R(obert)1480 dayssaveRefWorks
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility.Winqvist, R(obert)1497 dayssaveRefWorks
BRCA2 hypomorphic missense variants confer moderate risks of breast cancer.Winqvist, R(obert)1524 dayssaveRefWorks
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk.Winqvist, R(obert)1640 dayssaveRefWorks
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.Winqvist, R(obert)1657 dayssaveRefWorks
Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium.Winqvist, R(obert)1679 dayssaveRefWorks
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.Winqvist, R(obert)1697 dayssaveRefWorks
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.Winqvist, R(obert)1709 dayssaveRefWorks
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).Winqvist, R(obert)1709 dayssaveRefWorks
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.Winqvist, R(obert)1710 dayssaveRefWorks
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.Winqvist, R(obert)1723 dayssaveRefWorks
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.Winqvist, R(obert)1724 dayssaveRefWorks
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome.Winqvist, R(obert)1727 dayssaveRefWorks
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.Winqvist, R(obert)1747 dayssaveRefWorks
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.Winqvist, R(obert)1759 dayssaveRefWorks
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression.Winqvist, R(obert)1766 dayssaveRefWorks
RAD51B in Familial Breast Cancer.Winqvist, R(obert)1834 dayssaveRefWorks
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.Winqvist, R(obert)1842 dayssaveRefWorks
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.Winqvist, R(obert)1851 dayssaveRefWorks
Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.Winqvist, R(obert)1862 dayssaveRefWorks
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.Winqvist, R(obert)1899 dayssaveRefWorks
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.Winqvist, R(obert)1902 dayssaveRefWorks
Genetic predisposition to ductal carcinoma in situ of the breast.Winqvist, R(obert)1912 dayssaveRefWorks
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