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AddAla-Kokko, T(ero)
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AddAntikainen, R.
AddAnttonen, V(uokko)
AddBiancari, F(austo)
AddBloigu, R(isto)
AddEskelinen, S.
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AddHakkola, J.
AddHallman, M.
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AddHukkanen J(anne)
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AddJaakkola, M(aritta) S.
AddJaakola, V-P.
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AddKeinänen-Kiukaanniemi, S(irkka)
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AddKesäniemi, Y(rjö) A(ntero)
AddKettunen, J(ohannes)
AddKietzmann, T(homas).
AddKivirikko, K.I.
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)260 dayssaveRefWorks
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PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.Winqvist, R(obert)1393 dayssaveRefWorks
Body mass index and breast cancer survival: a Mendelian randomization analysis.Winqvist, R(obert)1402 dayssaveRefWorks
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.Winqvist, R(obert)1436 dayssaveRefWorks
Association analysis identifies 65 new breast cancer risk loci.Winqvist, R(obert)1452 dayssaveRefWorks
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.Winqvist, R(obert)1452 dayssaveRefWorks
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.Winqvist, R(obert)1554 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)1634 dayssaveRefWorks
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility.Winqvist, R(obert)1652 dayssaveRefWorks
BRCA2 hypomorphic missense variants confer moderate risks of breast cancer.Winqvist, R(obert)1678 dayssaveRefWorks
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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)1811 dayssaveRefWorks
Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium.Winqvist, R(obert)1833 dayssaveRefWorks
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.Winqvist, R(obert)1851 dayssaveRefWorks
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.Winqvist, R(obert)1863 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)1863 dayssaveRefWorks
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.Winqvist, R(obert)1864 dayssaveRefWorks
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.Winqvist, R(obert)1878 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)1878 dayssaveRefWorks
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome.Winqvist, R(obert)1881 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)1902 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)1913 dayssaveRefWorks
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression.Winqvist, R(obert)1920 dayssaveRefWorks
RAD51B in Familial Breast Cancer.Winqvist, R(obert)1988 dayssaveRefWorks
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.Winqvist, R(obert)1997 dayssaveRefWorks
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.Winqvist, R(obert)2005 dayssaveRefWorks
Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.Winqvist, R(obert)2016 dayssaveRefWorks
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.Winqvist, R(obert)2053 dayssaveRefWorks
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.Winqvist, R(obert)2056 dayssaveRefWorks
Genetic predisposition to ductal carcinoma in situ of the breast.Winqvist, R(obert)2066 dayssaveRefWorks
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