Marjanka K Schmidt

cancer researcher

Marjanka K Schmidt is …
instance of (P31):
humanQ5

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P6178Dimensions author ID015226066562.99
P496ORCID iD0000-0002-2228-429X

P108employerLeiden UniversityQ156598
Antoni van LeeuwenhoekziekenhuisQ2536586
P734family nameSchmidtQ15240355
SchmidtQ15240355
SchmidtQ15240355
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q3601638611q13 is a susceptibility locus for hormone receptor positive breast cancer
Q3587156719p13.1 is a triple-negative-specific breast cancer susceptibility locus
Q338488952q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
Q371698739q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium
Q35973982A Randomised Controlled Trial of Consent Procedures for the Use of Residual Tissues for Medical Research: Preferences of and Implications for Patients, Research and Clinical Practice.
Q57250674A common coding variant in CASP8 is associated with breast cancer risk
Q35755874A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Q37619303A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium
Q44809185A method to reduce the invasiveness of fetal catheterization in the cow.
Q92711687A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Q46484925A novel method for transuterine identification of piglets
Q35870483A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients
Q37599352A role for XRCC2 gene polymorphisms in breast cancer risk and survival
Q57305942A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Q37424001A trial of consent procedures for future research with clinically derived biological samples
Q33328665ATBF1 and NQO1 as candidate targets for allelic loss at chromosome arm 16q in breast cancer: absence of somatic ATBF1 mutations and no role for the C609T NQO1 polymorphism
Q61970237Abstract 3274: SNP-SNP interaction analyses of NQO1 and NF-κB signaling pathway genes on breast cancer survival and treatment outcome
Q40241119Accuracy of the online prognostication tools PREDICT and Adjuvant! for early-stage breast cancer patients younger than 50 years.
Q39437211Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
Q30779634Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases
Q40329088An association study of established breast cancer reproductive and lifestyle risk factors with tumour subtype defined by the prognostic 70-gene expression signature (MammaPrint®).
Q33327370An information-theoretic analysis of genetics, gender and age in cancer patients
Q36073563An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
Q35681656Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis
Q57937919Assessment of PD-L1 expression across breast cancer molecular subtypes, in relation to mutation rate, BRCA1-like status, tumor-infiltrating immune cells and survival
Q97070156Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers
Q35218520Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy
Q45979098Association analysis identifies 65 new breast cancer risk loci.
Q37292963Association of ESR1 gene tagging SNPs with breast cancer risk
Q37684672Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Q37268494Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry
Q114182713Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Q99609984Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer
Q54582432Association of the germline TP53 R72P and MDM2 SNP309 variants with breast cancer survival in specific breast tumor subgroups.
Q35022847Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
Q35523236Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
Q35532898Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium
Q57056093Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Q37002955BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Q38400720Biobanks and the return of results to donors
Q36295142Biomarkers in Breast Cancer - An Update
Q52192129Birth and prematurity influence intestinal function in the newborn pig.
Q50545166Bisection of bovine morulae and blastocysts from superovulated Danish dairy cows.
Q56835471Blood Chemistry, Nutrient Metabolism, and Organ Weights in Fetal and Newborn Calves Derived from In Vitro-Produced Bovine Embryos1
Q41617470Body dimensions and birth and organ weights of calves derived from in vitro produced embryos cultured with or without serum and oviduct epithelium cells
Q46115524Body mass index and breast cancer survival: a Mendelian randomization analysis
Q100457582Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Q61970254Breast Cancer Survival and Tumor Characteristics in Premenopausal Women Carrying theCHEK2*1100delCGermline Mutation
Q40258706Breast Cancer Survival of BRCA1/BRCA2 Mutation Carriers in a Hospital-Based Cohort of Young Women.
Q34327945Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
Q102073773Breast cancer risk factors and their effects on survival: a Mendelian randomisation study
Q35940158Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Q61970255Breast tumors induced by high-dose radiation display similar genetic profiles
Q36449203CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer
Q51392341CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women.
Q37524058CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populations
Q35006280Calibration and discriminatory accuracy of prognosis calculation for breast cancer with the online Adjuvant! program: a hospital-based retrospective cohort study.
Q34963894Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Q30491311Cause-specific Mortality in a Population-based Cohort of 9799 Women Treated for Ductal Carcinoma In Situ
Q37395510Chemotherapy for 70-Year-Old Women with Breast Cancer in Germany: A Survey by the German Breast Group
Q55711192Clinical outcome for BRCA1 and BRCA2 mutation carriers after contralateral prophylactic mastectomy.
Q42462630Clinical relevance of the putative stem cell marker p63 in breast cancer
Q52672618Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey.
Q88446209Clinicopathological Risk Factors for an Invasive Breast Cancer Recurrence after Ductal Carcinoma In Situ-A Nested Case-Control Study
Q52234383Coculture of bovine demiembryos prior to freezing
Q34250074Combination of osteopontin and activated leukocyte cell adhesion molecule as potent prognostic discriminators in HER2- and ER-negative breast cancer
Q44798882Combined ACTH and glucocorticoid treatment improves survival and organ maturation in premature newborn calves
Q94486442Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Q33627208Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients
Q35891162Common breast cancer susceptibility loci are associated with triple-negative breast cancer
Q35794653Common germline polymorphisms associated with breast cancer-specific survival
Q34379032Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Q31082788Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q103740231Comprehensive trends in incidence, treatment, survival and mortality of first primary invasive breast cancer stratified by age, stage and receptor subtype in the Netherlands between 1989-2017
Q34181322Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer
Q92097678Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey
Q57278898Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q30660858Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer
Q37685729DNA mismatch repair gene MSH6 implicated in determining age at natural menopause
Q30980437Data management and data analysis techniques in pharmacoepidemiological studies using a pre-planned multi-database approach: a systematic literature review.
Q30861409Determinants of weight and length of Indonesian neonates.
Q36246468Diabetes and Breast Cancer Subtypes.
Q52245657Differential cleavage rates and sex determination in bovine embryos.
Q27851413Do MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium
Q55110745E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium.
Q42493389Ease of calving, blood chemistry, insulin and bovine growth hormone of newborn calves derived from embryos produced in vitro in culture systems with serum and co-culture or with PVA.
Q46832322Elective cesarean delivery affects gut maturation and delays microbial colonization but does not increase necrotizing enterocolitis in preterm pigs
Q61970226Erratum to: Subsequent risk of ipsilateral and contralateral invasive breast cancer after treatment for ductal carcinoma in situ: incidence and the effect of radiotherapy in a population-based cohort of 10,090 women
Q57250672Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk
Q51766497Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation.
Q35477949Evaluation of the Dutch BRCA1/2 clinical genetic center referral criteria in an unselected early breast cancer population
Q35653910Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk
Q28246059Evidence of alternative promoters directing isoform-specific expression of human endothelin-converting enzyme-1 mRNA in cultured endothelial cells
Q36720821Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors
Q35064451Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
Q37342144Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
Q35916745Exceptions to the rule of informed consent for research with an intervention
Q46247419Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer cases
Q48222563Experimental endotoxemia induces leukocyte adherence and plasma extravasation within the rat pial microcirculation.
Q37307305Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1,828 bilateral breast cancers and 7,030 controls
Q37236216Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).
Q36111237Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus
Q35524465Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Q61230414Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes
Q92480972Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Q39844032Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Q36248936Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk
Q34903062Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Q37367871Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Q34979715Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium
Q114182808Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Q36124728Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Q36742577Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
Q56835462GLP-2 stimulates intestinal growth in premature TPN-fed pigs by suppressing proteolysis and apoptosis
Q40137431Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium
Q61970256Genetic determinants of breast cancer characteristics and outcome in women under 50 years of age
Q37739048Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Q35925620Genetic predisposition to ductal carcinoma in situ of the breast
Q35151684Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Q54338212Genetic variants in TGFβ-1 and PAI-1 as possible risk factors for cardiovascular disease after radiotherapy for breast cancer.
Q35179897Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
Q34378972Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Q36422109Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium
Q30000080Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Q28388497Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Q36842233Genome-wide association analysis identifies three new breast cancer susceptibility loci
Q35996692Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Q63681757Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Q24622610Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Q95329367Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Q64040390Genome-wide association study of germline variants and breast cancer-specific mortality
Q59566871Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility
Q96432094Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
Q114182677Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
Q34158129Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome
Q36276540Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Q36547888Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers
Q44386662High in vitro development after somatic cell nuclear transfer and trichostatin A treatment of reconstructed porcine embryos
Q37121271High-throughput automated scoring of Ki67 in breast cancer tissue microarrays from the Breast Cancer Association Consortium
Q35102646Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Q36720814Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk
Q36859142Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Q36086247Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Q34038964Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions
Q36014067Identification of novel genetic markers of breast cancer survival
Q46103372Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Q57210017Imaging features and safety and efficacy of endovascular stroke treatment: a meta-analysis of individual patient-level data
Q49259778Immunohistochemical localization of estrogen receptor-alpha in sex ducts and gonads of newborn piglets.
Q38677974Impact of Age at Primary Breast Cancer on Contralateral Breast Cancer Risk in BRCA1/2 Mutation Carriers
Q52875534Impact of trastuzumab treatment beyond disease progression for advanced/metastatic breast cancer on survival - results from a prospective, observational study in Germany.
Q114184688Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Q51053686Independent prognostic value of screen detection in invasive breast cancer.
Q45897710Inferior survival for young patients with contralateral compared to unilateral breast cancer: a nationwide population-based study in the Netherlands
Q35104068Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
Q34898735Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors
Q37699105Invited review: the preterm pig as a model in pediatric gastroenterology
Q47190168Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium
Q57191573Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair
Q28267893Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Q29416989Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Q37534934Long-term impact of the 70-gene signature on breast cancer outcome
Q46340590Long-term outcome prediction by clinicopathological risk classification algorithms in node-negative breast cancer--comparison between Adjuvant!, St Gallen, and a novel risk algorithm used in the prospective randomized Node-Negative-Breast Cancer-3 (
Q35119701Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium
Q37692442Lower mitotic activity in BRCA1/2-associated primary breast cancers occurring after risk-reducing salpingo-oophorectomy
Q43884136Macromolecule absorption and cortisol secretion in newborn calves derived from in vitro produced embryos
Q37583102Mammographic screening detects low-risk tumor biology breast cancers
Q46327439Maternal endometrial oedema may increase perinatal mortality of cloned and transgenic piglets
Q114182490Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Q34497352MicroRNA related polymorphisms and breast cancer risk
Q34123806Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls
Q36897003Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Q37356243Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
Q30374367No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Q37079859No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
Q36388124No peri- and postnatal effects on calves born after transfer of in vitro produced embryos vitrified by the open pulled straw (OPS) method
Q38422696Obtaining 'fresh' consent for genetic research with biological samples archived 10 years ago.
Q38424053Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment
Q33651520Optimized outcome prediction in breast cancer by combining the 70-gene signature with clinical risk prediction algorithms
Q50862667Outcome of BRCA1- compared with BRCA2-associated ovarian cancer: a nationwide study in the Netherlands.
Q67995402Oviduct epithelial cell co-culture of early porcine embryos
Q52171861Ovulation and embryonic developmental rate following hCG-stimulation in sows.
Q28584533PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Q47143943PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.
Q36184231PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2.
Q52897434PREPARE trial: a randomized phase III trial comparing preoperative, dose-dense, dose-intensified chemotherapy with epirubicin, paclitaxel and CMF versus a standard-dosed epirubicin/cyclophosphamide followed by paclitaxel ± darbepoetin alfa in primar
Q52897474PREPARE trial: a randomized phase III trial comparing preoperative, dose-dense, dose-intensified chemotherapy with epirubicin, paclitaxel, and CMF versus a standard-dosed epirubicin-cyclophosphamide followed by paclitaxel with or without darbepoetin
Q34289136Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Q112572520Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes
Q37307937Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium
Q52867263Pazopanib (GW786034) and cyclophosphamide in patients with platinum-resistant, recurrent, pre-treated ovarian cancer - Results of the PACOVAR-trial.
Q33382867Pegylated liposomal doxorubicin (CAELYX) in patients with advanced ovarian cancer: results of a German multicenter observational study
Q36873786Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium
Q96577047Personalized early detection and prevention of breast cancer: ENVISION consensus statement
Q40077453Piglets born from handmade cloning, an innovative cloning method without micromanipulation
Q62583133Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Q36066735Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
Q47814471Postmortem findings in cloned and transgenic piglets dead before weaning
Q92055460Prediction and clinical utility of a contralateral breast cancer risk model
Q42551975Prediction of benefit from chemotherapy in ER-positive/HER2-negative breast cancer--a problem still to be solved
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q91832507Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts
Q91521771Predictors of an Invasive Breast Cancer Recurrence after DCIS: A Systematic Review and Meta-analyses
Q46233703Proceedings of the 7th Biannual International Symposium on Nasopharyngeal Carcinoma 2015: Yogyakarta, Indonesia. 4-6 June 2015.
Q33519812Prognostic impact of thymidine phosphorylase expression in breast cancer--comparison of microarray and immunohistochemical data
Q37350137Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups
Q55508030Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Q96816951Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement
Q90242034Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Q36009422RAD51B in Familial Breast Cancer
Q31049054Randomised double-blind trial of the effect of vitamin A supplementation of Indonesian pregnant women on morbidity and growth of their infants during the first year of life.
Q29583867Rare and low-frequency coding variants alter human adult height
Q114182625Rare germline copy number variants (CNVs) and breast cancer risk
Q35155449Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
Q33429468Regulatory aspects of genetic research with residual human tissue: effective and efficient data coding
Q45951126Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.
Q34201814Risk Factors for Endometriosis in a German Case-Control Study
Q59567394Risk estimations and treatment decisions in early stage breast cancer: Agreement among oncologists and the impact of the 70-gene signature
Q46789413Role of urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor type 1 (PAI-1) for prognosis in endometrial cancer
Q36545934SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival
Q69402030Sex determination of bovine embryos based on embryonic cleavage rates
Q69402032Sex determination of bovine embryos using H-Y antibodies
Q61118451Shared heritability and functional enrichment across six solid cancers
Q64004349Shared heritability and functional enrichment across six solid cancers
Q41612727Simplified cryopreservation of porcine cloned blastocysts
Q34209206Skin-reducing Mastectomy with Primary Implant Reconstruction
Q30423124Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types
Q36131718Subsequent risk of ipsilateral and contralateral invasive breast cancer after treatment for ductal carcinoma in situ: incidence and the effect of radiotherapy in a population-based cohort of 10,090 women
Q33593016Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies
Q33566957TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer
Q46607547Ten-year Results of Intense Dose-dense chemotherapy show superior survival compared to a conventional schedule in High-risk Primary Breast Cancer: Final results of AGO Phase III iddEPC trial
Q44255432Ten-year analysis of the prospective multicentre Chemo-N0 trial validates American Society of Clinical Oncology (ASCO)-recommended biomarkers uPA and PAI-1 for therapy decision making in node-negative breast cancer patients
Q59567583The 70-gene prognosis-signature predicts disease outcome in breast cancer patients with 1–3 positive lymph nodes in an independent validation study
Q61970242The BIO-PIN paradigm: 'access to' or 'return of' results?
Q49817640The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.
Q91178389The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Q35974884The Impact of the Overall Radiotherapy Time on Clinical Outcome of Patients with Nasopharyngeal Carcinoma; A Retrospective Study
Q35781316The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients
Q52229674The freezability of biopsied bovine embryos.
Q37690088The method of detection of ductal carcinoma in situ has no therapeutic implications: results of a population-based cohort study
Q36142060The role of genetic breast cancer susceptibility variants as prognostic factors
Q45222336The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li-Fraumeni syndrome and related phenotypes
Q89961489Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Q35937961Treatment with insulin (analogues) and breast cancer risk in diabetics; a systematic review and meta-analysis of in vitro, animal and human evidence
Q38942058Trends in breast cancer incidence among women with type-2 diabetes in British general practice.
Q54432641Tumour tissue: who is in control?
Q92994868Two truncating variants in FANCC and breast cancer risk
Q35038355Use of insulin and insulin analogs and risk of cancer - systematic review and meta-analysis of observational studies.
Q33646542Use of metformin and survival of diabetic women with breast cancer
Q90169993Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation
Q43818515Vitamin A and iron supplementation of Indonesian pregnant women benefits vitamin A status of their infants
Q35224593Worse breast cancer prognosis of BRCA1/BRCA2 mutation carriers: what's the evidence? A systematic review with meta-analysis
Q56775683[Consent for the secondary use of human residual tissue: the patient is best served by an 'opting-out' procedure]
Q57129628[Gene expression classifiers in the prognosis of breast cancer]
Q61970257[Genetic research with stored human tissue: a coding procedure with optimal use of information and protection of privacy]
Q56783042[Secondary use of human tissue: consent and better information required]
Q37414133rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

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