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AddAiraksinen, O(lavi)
AddAlhava, E.
AddAlhonen, L.
AddAtalay, M(ustafa)
AddCederberg, H.
AddDunkel, L(eo)
AddEskelinen, M(atti)
AddGiniatullin, R.
AddGröhn, O(lli)
AddHarno, K.
AddHartikainen, J(aana).
AddHartikainen, J(uha).
AddHarvima, I.
AddHiltunen, M(ikko)
AddJääskeläinen, J(uha) E.
AddJäkälä, P(ekka)
AddJänne, J.
AddJantunen, E(sa)
AddJärvinen, R.
AddJulkunen, P.
AddKaikkonen, M(inna) U.
AddKauhanen, J(ussi)
AddKivipelto, M(iia)
AddKoistinaho, M.
AddKoivisto, T(imo)
AddKokki, H.
AddKönönen, M.
AddKosma, V(eli)-M(atti)
AddKröger, H.
AddKurl, S(udhir)
AddKuusisto, J(ohanna)
AddLaakso, M(arkku)
AddLakka, T(imo) A.
AddLapinlampi, N(iina)
AddLaukkanen, J(ari) (UEF/KSSHP)
AddLevonen, A(nna)-L(iisa)
AddLindgren, A(ntti) E.
AddLöppönen, H(eikki)
AddMannermaa, A.
AddManninen, H.
AddMecklin, J(ukka)-P(ekka)
AddMoilanen, L(eena)
AddMönkkönen, J.
AddMykkänen, H.
AddNuutinen, J.
AddPaajanen, H.
AddPaananen, J.
AddPalvimo, J.J.
AddPelkonen, J(ukka)
AddPihlajamäki, J(ussi)
AddPihlajamäki, M.
AddPitkänen, A(sla)
AddPunnonen, K.
AddRaatikainen K
AddRauramaa, R.
AddRissanen, T.T.
AddRoine, R(isto) P.
AddRyynänen, O.P.
AddSaarikoski, S.
AddSchwab, U(rsula)
AddSivenius, J.
AddSoininen, H(ilkka)
AddSoininen, P(asi)
AddSorri, I.
AddStancakova, A(lena)
AddSulkava, R.
AddSund, R(eijo)
AddTammi, M.
AddTanila, H(eikki)
AddTiihonen, J(ari)
AddUusaro, A.
AddUusitupa, M.
AddVanninen, R.
AddVaskilampi, T.
AddViinamäki, H(eimo)
AddVirtanen, M(arianna)
AddVoutilainen, R(aimo)
AddVoutilainen, S(ari)
AddWahlfors, J.
AddWirth, T.
AddWong, G.
AddYlä-Herttuala, S(eppo)

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Breast cancer risk factors and survival by tumor subtype: pooled analyses from the Breast Cancer Association Consortium.Mannermaa, A.147 dayssaveRefWorks
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.Mannermaa, A.148 dayssaveRefWorks
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.Mannermaa, A.154 dayssaveRefWorks
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.Mannermaa, A.260 dayssaveRefWorks
Predicting breast cancer risk using interacting genetic and demographic factors and machine learning.Mannermaa, A.351 dayssaveRefWorks
MicroRNAs Associated With Biological Pathways of Left- and Right-sided Colorectal Cancer.Mannermaa, A.353 dayssaveRefWorks
High mutation burden of circulating cell-free DNA in early-stage breast cancer patients is associated with a poor relapse-free survival.Mannermaa, A.358 dayssaveRefWorks
Peritumor to tumor apparent diffusion coefficient ratio is associated with biologically more aggressive breast cancer features and correlates with the prognostication tools.Mannermaa, A.363 dayssaveRefWorks
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.Mannermaa, A.371 dayssaveRefWorks
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.Mannermaa, A.400 dayssaveRefWorks
Cellular hyaluronan is associated with a poor prognosis in renal cell carcinoma.Mannermaa, A.416 dayssaveRefWorks
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.Mannermaa, A.478 dayssaveRefWorks
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.Mannermaa, A.523 dayssaveRefWorks
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.Mannermaa, A.532 dayssaveRefWorks
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.Mannermaa, A.555 dayssaveRefWorks
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.Mannermaa, A.593 dayssaveRefWorks
Two truncating variants in FANCC and breast cancer risk.Mannermaa, A.663 dayssaveRefWorks
Nrf2 and SQSTM1/p62 jointly contribute to mesenchymal transition and invasion in glioblastoma.Mannermaa, A.669 dayssaveRefWorks
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.Mannermaa, A.799 dayssaveRefWorks
Genome-wide association study of germline variants and breast cancer-specific mortality.Mannermaa, A.852 dayssaveRefWorks
Shared heritability and functional enrichment across six solid cancers.Mannermaa, A.879 dayssaveRefWorks
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.Mannermaa, A.919 dayssaveRefWorks
Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls.Mannermaa, A.1023 dayssaveRefWorks
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.Mannermaa, A.1100 dayssaveRefWorks
E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium.Mannermaa, A.1153 dayssaveRefWorks
Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation.Mannermaa, A.1210 dayssaveRefWorks
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.Mannermaa, A.1219 dayssaveRefWorks
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.Mannermaa, A.1253 dayssaveRefWorks
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium.Mannermaa, A.1261 dayssaveRefWorks
PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.Mannermaa, A.1280 dayssaveRefWorks
Body mass index and breast cancer survival: a Mendelian randomization analysis.Mannermaa, A.1289 dayssaveRefWorks
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.Mannermaa, A.1323 dayssaveRefWorks
Association analysis identifies 65 new breast cancer risk loci.Mannermaa, A.1339 dayssaveRefWorks
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.Mannermaa, A.1339 dayssaveRefWorks
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.Mannermaa, A.1441 dayssaveRefWorks
Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium.Mannermaa, A.1451 dayssaveRefWorks
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.Mannermaa, A.1521 dayssaveRefWorks
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility.Mannermaa, A.1538 dayssaveRefWorks
BRCA2 hypomorphic missense variants confer moderate risks of breast cancer.Mannermaa, A.1565 dayssaveRefWorks
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer.Mannermaa, A.1595 dayssaveRefWorks
Genome-wide association study identifies novel breast cancer susceptibility loci.Mannermaa, A.1674 dayssaveRefWorks
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk.Mannermaa, A.1681 dayssaveRefWorks
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.Mannermaa, A.1698 dayssaveRefWorks
Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups.Mannermaa, A.1707 dayssaveRefWorks
Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium.Mannermaa, A.1720 dayssaveRefWorks
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.Mannermaa, A.1721 dayssaveRefWorks
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.Mannermaa, A.1738 dayssaveRefWorks
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.Mannermaa, A.1750 dayssaveRefWorks
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).Mannermaa, A.1750 dayssaveRefWorks
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.Mannermaa, A.1751 dayssaveRefWorks
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