human | Q5 |
P6178 | Dimensions author ID | 015226066562.99 |
P496 | ORCID iD | 0000-0002-2228-429X |
P108 | employer | Leiden University | Q156598 |
Antoni van Leeuwenhoekziekenhuis | Q2536586 | ||
P734 | family name | Schmidt | Q15240355 |
Schmidt | Q15240355 | ||
Schmidt | Q15240355 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | female | Q6581072 |
Q36016386 | 11q13 is a susceptibility locus for hormone receptor positive breast cancer |
Q35871567 | 19p13.1 is a triple-negative-specific breast cancer susceptibility locus |
Q33848895 | 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy |
Q37169873 | 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium |
Q35973982 | A 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. |
Q57250674 | A common coding variant in CASP8 is associated with breast cancer risk |
Q35755874 | A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer |
Q37619303 | A 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 |
Q44809185 | A method to reduce the invasiveness of fetal catheterization in the cow. |
Q92711687 | A network analysis to identify mediators of germline-driven differences in breast cancer prognosis |
Q46484925 | A novel method for transuterine identification of piglets |
Q35870483 | A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients |
Q37599352 | A role for XRCC2 gene polymorphisms in breast cancer risk and survival |
Q57305942 | A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer |
Q37424001 | A trial of consent procedures for future research with clinically derived biological samples |
Q33328665 | ATBF1 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 |
Q61970237 | Abstract 3274: SNP-SNP interaction analyses of NQO1 and NF-κB signaling pathway genes on breast cancer survival and treatment outcome |
Q40241119 | Accuracy of the online prognostication tools PREDICT and Adjuvant! for early-stage breast cancer patients younger than 50 years. |
Q39437211 | Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers |
Q30779634 | Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases |
Q40329088 | An association study of established breast cancer reproductive and lifestyle risk factors with tumour subtype defined by the prognostic 70-gene expression signature (MammaPrint®). |
Q33327370 | An information-theoretic analysis of genetics, gender and age in cancer patients |
Q36073563 | An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression |
Q35681656 | Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis |
Q57937919 | Assessment of PD-L1 expression across breast cancer molecular subtypes, in relation to mutation rate, BRCA1-like status, tumor-infiltrating immune cells and survival |
Q97070156 | Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers |
Q35218520 | Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy |
Q45979098 | Association analysis identifies 65 new breast cancer risk loci. |
Q37292963 | Association of ESR1 gene tagging SNPs with breast cancer risk |
Q37684672 | Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21. |
Q37268494 | Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry |
Q114182713 | Association 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 |
Q99609984 | Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer |
Q54582432 | Association of the germline TP53 R72P and MDM2 SNP309 variants with breast cancer survival in specific breast tumor subgroups. |
Q35022847 | Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies |
Q35523236 | Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers |
Q35532898 | Associations 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 |
Q57056093 | Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis |
Q37002955 | BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers |
Q38400720 | Biobanks and the return of results to donors |
Q36295142 | Biomarkers in Breast Cancer - An Update |
Q52192129 | Birth and prematurity influence intestinal function in the newborn pig. |
Q50545166 | Bisection of bovine morulae and blastocysts from superovulated Danish dairy cows. |
Q56835471 | Blood Chemistry, Nutrient Metabolism, and Organ Weights in Fetal and Newborn Calves Derived from In Vitro-Produced Bovine Embryos1 |
Q41617470 | Body dimensions and birth and organ weights of calves derived from in vitro produced embryos cultured with or without serum and oviduct epithelium cells |
Q46115524 | Body mass index and breast cancer survival: a Mendelian randomization analysis |
Q100457582 | Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk |
Q61970254 | Breast Cancer Survival and Tumor Characteristics in Premenopausal Women Carrying theCHEK2*1100delCGermline Mutation |
Q40258706 | Breast Cancer Survival of BRCA1/BRCA2 Mutation Carriers in a Hospital-Based Cohort of Young Women. |
Q34327945 | Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 |
Q102073773 | Breast cancer risk factors and their effects on survival: a Mendelian randomisation study |
Q35940158 | Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. |
Q61970255 | Breast tumors induced by high-dose radiation display similar genetic profiles |
Q36449203 | CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer |
Q51392341 | CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. |
Q37524058 | CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populations |
Q35006280 | Calibration and discriminatory accuracy of prognosis calculation for breast cancer with the online Adjuvant! program: a hospital-based retrospective cohort study. |
Q34963894 | Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers |
Q30491311 | Cause-specific Mortality in a Population-based Cohort of 9799 Women Treated for Ductal Carcinoma In Situ |
Q37395510 | Chemotherapy for 70-Year-Old Women with Breast Cancer in Germany: A Survey by the German Breast Group |
Q55711192 | Clinical outcome for BRCA1 and BRCA2 mutation carriers after contralateral prophylactic mastectomy. |
Q42462630 | Clinical relevance of the putative stem cell marker p63 in breast cancer |
Q52672618 | Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. |
Q88446209 | Clinicopathological Risk Factors for an Invasive Breast Cancer Recurrence after Ductal Carcinoma In Situ-A Nested Case-Control Study |
Q52234383 | Coculture of bovine demiembryos prior to freezing |
Q34250074 | Combination of osteopontin and activated leukocyte cell adhesion molecule as potent prognostic discriminators in HER2- and ER-negative breast cancer |
Q44798882 | Combined ACTH and glucocorticoid treatment improves survival and organ maturation in premature newborn calves |
Q94486442 | Combined associations of a polygenic risk score and classical risk factors with breast cancer risk |
Q33627208 | Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients |
Q35891162 | Common breast cancer susceptibility loci are associated with triple-negative breast cancer |
Q35794653 | Common germline polymorphisms associated with breast cancer-specific survival |
Q34379032 | Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium |
Q31082788 | Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
Q103740231 | Comprehensive 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 |
Q34181322 | Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer |
Q92097678 | Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey |
Q57278898 | Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
Q30660858 | Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer |
Q37685729 | DNA mismatch repair gene MSH6 implicated in determining age at natural menopause |
Q30980437 | Data management and data analysis techniques in pharmacoepidemiological studies using a pre-planned multi-database approach: a systematic literature review. |
Q30861409 | Determinants of weight and length of Indonesian neonates. |
Q36246468 | Diabetes and Breast Cancer Subtypes. |
Q52245657 | Differential cleavage rates and sex determination in bovine embryos. |
Q27851413 | Do MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium |
Q55110745 | E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium. |
Q42493389 | Ease 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. |
Q46832322 | Elective cesarean delivery affects gut maturation and delays microbial colonization but does not increase necrotizing enterocolitis in preterm pigs |
Q61970226 | Erratum 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 |
Q57250672 | Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk |
Q51766497 | Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation. |
Q35477949 | Evaluation of the Dutch BRCA1/2 clinical genetic center referral criteria in an unselected early breast cancer population |
Q35653910 | Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk |
Q28246059 | Evidence of alternative promoters directing isoform-specific expression of human endothelin-converting enzyme-1 mRNA in cultured endothelial cells |
Q36720821 | Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors |
Q35064451 | Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation |
Q37342144 | Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation |
Q35916745 | Exceptions to the rule of informed consent for research with an intervention |
Q46247419 | Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer cases |
Q48222563 | Experimental endotoxemia induces leukocyte adherence and plasma extravasation within the rat pial microcirculation. |
Q37307305 | Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1,828 bilateral breast cancers and 7,030 controls |
Q37236216 | Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). |
Q36111237 | Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus |
Q35524465 | Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. |
Q61230414 | Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes |
Q92480972 | Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes |
Q39844032 | Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer |
Q36248936 | Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk |
Q34903062 | Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1. |
Q37367871 | Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. |
Q34979715 | Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium |
Q114182808 | Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element |
Q36124728 | Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus |
Q36742577 | Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers |
Q56835462 | GLP-2 stimulates intestinal growth in premature TPN-fed pigs by suppressing proteolysis and apoptosis |
Q40137431 | Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium |
Q61970256 | Genetic determinants of breast cancer characteristics and outcome in women under 50 years of age |
Q37739048 | Genetic modifiers of CHEK2*1100delC-associated breast cancer risk |
Q35925620 | Genetic predisposition to ductal carcinoma in situ of the breast |
Q35151684 | Genetic predisposition to in situ and invasive lobular carcinoma of the breast |
Q54338212 | Genetic variants in TGFβ-1 and PAI-1 as possible risk factors for cardiovascular disease after radiotherapy for breast cancer. |
Q35179897 | Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study |
Q34378972 | Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade |
Q36422109 | Genetic 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 |
Q30000080 | Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent |
Q28388497 | Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types |
Q36842233 | Genome-wide association analysis identifies three new breast cancer susceptibility loci |
Q35996692 | Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer |
Q63681757 | Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer |
Q24622610 | Genome-wide association studies identify four ER negative-specific breast cancer risk loci |
Q95329367 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses |
Q64040390 | Genome-wide association study of germline variants and breast cancer-specific mortality |
Q59566871 | Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility |
Q96432094 | Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk |
Q114182677 | Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis |
Q34158129 | Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome |
Q36276540 | Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization |
Q36547888 | Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers |
Q44386662 | High in vitro development after somatic cell nuclear transfer and trichostatin A treatment of reconstructed porcine embryos |
Q37121271 | High-throughput automated scoring of Ki67 in breast cancer tissue microarrays from the Breast Cancer Association Consortium |
Q35102646 | Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk |
Q36720814 | Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk |
Q36859142 | Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer |
Q36086247 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus |
Q34038964 | Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions |
Q36014067 | Identification of novel genetic markers of breast cancer survival |
Q46103372 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer |
Q57210017 | Imaging features and safety and efficacy of endovascular stroke treatment: a meta-analysis of individual patient-level data |
Q49259778 | Immunohistochemical localization of estrogen receptor-alpha in sex ducts and gonads of newborn piglets. |
Q38677974 | Impact of Age at Primary Breast Cancer on Contralateral Breast Cancer Risk in BRCA1/2 Mutation Carriers |
Q52875534 | Impact of trastuzumab treatment beyond disease progression for advanced/metastatic breast cancer on survival - results from a prospective, observational study in Germany. |
Q114184688 | Incorporating progesterone receptor expression into the PREDICT breast prognostic model |
Q51053686 | Independent prognostic value of screen detection in invasive breast cancer. |
Q45897710 | Inferior survival for young patients with contralateral compared to unilateral breast cancer: a nationwide population-based study in the Netherlands |
Q35104068 | Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer |
Q34898735 | Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors |
Q37699105 | Invited review: the preterm pig as a model in pediatric gastroenterology |
Q47190168 | Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium |
Q57191573 | Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair |
Q28267893 | Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair |
Q29416989 | Large-scale genotyping identifies 41 new loci associated with breast cancer risk |
Q37534934 | Long-term impact of the 70-gene signature on breast cancer outcome |
Q46340590 | Long-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 ( |
Q35119701 | Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium |
Q37692442 | Lower mitotic activity in BRCA1/2-associated primary breast cancers occurring after risk-reducing salpingo-oophorectomy |
Q43884136 | Macromolecule absorption and cortisol secretion in newborn calves derived from in vitro produced embryos |
Q37583102 | Mammographic screening detects low-risk tumor biology breast cancers |
Q46327439 | Maternal endometrial oedema may increase perinatal mortality of cloned and transgenic piglets |
Q114182490 | Mendelian randomisation study of smoking exposure in relation to breast cancer risk |
Q34497352 | MicroRNA related polymorphisms and breast cancer risk |
Q34123806 | Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls |
Q36897003 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer |
Q37356243 | Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. |
Q30374367 | No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. |
Q37079859 | No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing |
Q36388124 | No peri- and postnatal effects on calves born after transfer of in vitro produced embryos vitrified by the open pulled straw (OPS) method |
Q38422696 | Obtaining 'fresh' consent for genetic research with biological samples archived 10 years ago. |
Q38424053 | Opt-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 |
Q33651520 | Optimized outcome prediction in breast cancer by combining the 70-gene signature with clinical risk prediction algorithms |
Q50862667 | Outcome of BRCA1- compared with BRCA2-associated ovarian cancer: a nationwide study in the Netherlands. |
Q67995402 | Oviduct epithelial cell co-culture of early porcine embryos |
Q52171861 | Ovulation and embryonic developmental rate following hCG-stimulation in sows. |
Q28584533 | PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS |
Q47143943 | PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1. |
Q36184231 | PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2. |
Q52897434 | PREPARE 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 |
Q52897474 | PREPARE 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 |
Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
Q112572520 | Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes |
Q37307937 | Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium |
Q52867263 | Pazopanib (GW786034) and cyclophosphamide in patients with platinum-resistant, recurrent, pre-treated ovarian cancer - Results of the PACOVAR-trial. |
Q33382867 | Pegylated liposomal doxorubicin (CAELYX) in patients with advanced ovarian cancer: results of a German multicenter observational study |
Q36873786 | Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium |
Q96577047 | Personalized early detection and prevention of breast cancer: ENVISION consensus statement |
Q40077453 | Piglets born from handmade cloning, an innovative cloning method without micromanipulation |
Q62583133 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes |
Q36066735 | Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression |
Q47814471 | Postmortem findings in cloned and transgenic piglets dead before weaning |
Q92055460 | Prediction and clinical utility of a contralateral breast cancer risk model |
Q42551975 | Prediction of benefit from chemotherapy in ER-positive/HER2-negative breast cancer--a problem still to be solved |
Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
Q91832507 | Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts |
Q91521771 | Predictors of an Invasive Breast Cancer Recurrence after DCIS: A Systematic Review and Meta-analyses |
Q46233703 | Proceedings of the 7th Biannual International Symposium on Nasopharyngeal Carcinoma 2015: Yogyakarta, Indonesia. 4-6 June 2015. |
Q33519812 | Prognostic impact of thymidine phosphorylase expression in breast cancer--comparison of microarray and immunohistochemical data |
Q37350137 | Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups |
Q55508030 | Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation. |
Q96816951 | Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement |
Q90242034 | Publisher Correction: Shared heritability and functional enrichment across six solid cancers |
Q36009422 | RAD51B in Familial Breast Cancer |
Q31049054 | Randomised 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. |
Q29583867 | Rare and low-frequency coding variants alter human adult height |
Q114182625 | Rare germline copy number variants (CNVs) and breast cancer risk |
Q35155449 | Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia |
Q33429468 | Regulatory aspects of genetic research with residual human tissue: effective and efficient data coding |
Q45951126 | Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study. |
Q34201814 | Risk Factors for Endometriosis in a German Case-Control Study |
Q59567394 | Risk estimations and treatment decisions in early stage breast cancer: Agreement among oncologists and the impact of the 70-gene signature |
Q46789413 | Role of urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor type 1 (PAI-1) for prognosis in endometrial cancer |
Q36545934 | SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival |
Q69402030 | Sex determination of bovine embryos based on embryonic cleavage rates |
Q69402032 | Sex determination of bovine embryos using H-Y antibodies |
Q61118451 | Shared heritability and functional enrichment across six solid cancers |
Q64004349 | Shared heritability and functional enrichment across six solid cancers |
Q41612727 | Simplified cryopreservation of porcine cloned blastocysts |
Q34209206 | Skin-reducing Mastectomy with Primary Implant Reconstruction |
Q30423124 | Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types |
Q36131718 | 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 |
Q33593016 | Subtyping 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 |
Q33566957 | TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer |
Q46607547 | Ten-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 |
Q44255432 | Ten-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 |
Q59567583 | The 70-gene prognosis-signature predicts disease outcome in breast cancer patients with 1–3 positive lymph nodes in an independent validation study |
Q61970242 | The BIO-PIN paradigm: 'access to' or 'return of' results? |
Q49817640 | The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity. |
Q91178389 | The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer |
Q35974884 | The Impact of the Overall Radiotherapy Time on Clinical Outcome of Patients with Nasopharyngeal Carcinoma; A Retrospective Study |
Q35781316 | The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients |
Q52229674 | The freezability of biopsied bovine embryos. |
Q37690088 | The method of detection of ductal carcinoma in situ has no therapeutic implications: results of a population-based cohort study |
Q36142060 | The role of genetic breast cancer susceptibility variants as prognostic factors |
Q45222336 | The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li-Fraumeni syndrome and related phenotypes |
Q89961489 | Transcriptome-wide association study of breast cancer risk by estrogen-receptor status |
Q35937961 | Treatment with insulin (analogues) and breast cancer risk in diabetics; a systematic review and meta-analysis of in vitro, animal and human evidence |
Q38942058 | Trends in breast cancer incidence among women with type-2 diabetes in British general practice. |
Q54432641 | Tumour tissue: who is in control? |
Q92994868 | Two truncating variants in FANCC and breast cancer risk |
Q35038355 | Use of insulin and insulin analogs and risk of cancer - systematic review and meta-analysis of observational studies. |
Q33646542 | Use of metformin and survival of diabetic women with breast cancer |
Q90169993 | Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation |
Q43818515 | Vitamin A and iron supplementation of Indonesian pregnant women benefits vitamin A status of their infants |
Q35224593 | Worse 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] |
Q37414133 | rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk |
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