SNP information rs13387042

Research and publications:

  17529974   Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.

  18612136   Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk.

  18772892   Can genes for mammographic density inform cancer aetiology?

  18785201   Novel breast cancer risk alleles and endometrial cancer risk.

  18973230   Breast cancer susceptibility alleles and ovarian cancer risk in 2 study populations.

  19088016   Genetic susceptibility loci for breast cancer by estrogen receptor status.

  19092773   Breast cancer susceptibility: current knowledge and implications for genetic counselling.

  19232126   Association between breast cancer susceptibility loci and mammographic density: the Multiethnic Cohort.

  19330030   A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

  19519208   Polygenic susceptibility to breast cancer: current state-of-the-art.

  19567422   Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.

  19656774   Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

  19789366   Evaluation of 11 breast cancer susceptibility loci in African-American women.

  19843326   Genetic variation in insulin-like growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriers.

  19931039   Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty.

  20056641   Multiple genetic variants in telomere pathway genes and breast cancer risk.

  20085711   Leveraging genetic variability across populations for the identification of causal variants.

  20146796   Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.

  20233625   Translational research in the Gynecologic Oncology Group: evaluation of ovarian cancer markers, profiles, and novel therapies.

  20237344   Performance of common genetic variants in breast-cancer risk models.

  20418484   Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

  20453838   Genome-wide association study identifies five new breast cancer susceptibility loci.

  20484103   Genetic and clinical predictors for breast cancer risk assessment and stratification among Chinese women.

  20505153   A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.

  20554749   FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women.

  20585100   Genome-wide association studies of cancer.

  20605201   Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study.

  20664043   Incidence of breast cancer and its subtypes in relation to individual and multiple low-penetrance genetic susceptibility loci.

  20699374   Evaluation of breast cancer susceptibility loci in Chinese women.

  20956782   Assessment of clinical validity of a breast cancer risk model combining genetic and clinical information.

  20957429   Discriminatory accuracy and potential clinical utility of genomic profiling for breast cancer risk in BRCA-negative women.

  21037853   Breast cancer in the personal genomics era.

  21049069   Identification of Novel Susceptibility Genes for Breast Cancer - Genome-Wide Association Studies or Evaluation of Candidate Genes?

  21102626   Caution in generalizing known genetic risk markers for breast cancer across all ethnic/racial populations.

  21118973   Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

  21132113   Direct-to-Consumer Genetic and Genomic Testing: Preparing Nurse Practitioners for Genomic Healthcare.

  21194473   Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study.

  21219822   [Recent progress in genetic variants associated with cancer and their implications in diagnostics development].

  21269472   Genetic variation of ESR1 and its co-activator PPARGC1B is synergistic in augmenting the risk of estrogen receptor-positive breast cancer.

  21445572   Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies.

  21468051   Polygenic susceptibility to prostate and breast cancer: implications for personalised screening.

  21475998   Replication of five GWAS-identified loci and breast cancer risk among Hispanic and non-Hispanic white women living in the Southwestern United States.

  21514219   Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence

  21596841   Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.

  21639959   Annual conference on hereditary cancers 2009 szczecin, poland. 10-11 december 2009. Abstracts.

  21655367   In search of breast cancer culprits: suspecting the suspected and the unsuspected.

  21791674   Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium.

  21795501   Replication of GWAS breast cancer susceptibility loci in the Women's Health Initiative African American SHARe Study.

  21844186   Common breast cancer susceptibility loci are associated with triple-negative breast cancer.

  21852243   Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans.

  21852249   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.

  21931568   Genome-wide association study identifies four loci associated with eruption of permanent teeth.

  21949660   Genetic variants at chromosomes 2q35, 5p12, 6q25.1, 10q26.13, and 16q12.1 influence the risk of breast cancer in men.

  21965274   Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study.

  22028405   Estimating causal effects of genetic risk variants for breast cancer using marker data from bilateral and familial cases.

  22045194   Combined effect of low-penetrant SNPs on breast cancer risk.

  22053997   Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

  22087758   Single nucleotide polymorphisms associated with risk of contralateral breast cancer in the Women's Environment, Cancer and Radiation Epidemiology (WECARE) study.

  22269215   Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women.

  22287734   Evaluation of breast cancer susceptibility loci on 2q35, 3p24, 17q23 and FGFR2 genes in Taiwanese women with breast cancer.

  22314178   Breast cancer risk prediction and individualised screening based on common genetic variation and breast density measurement.

  22357627   Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry.

  22433456   Reproductive aging-associated common genetic variants and the risk of breast cancer.

  22452962   A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.

  22454379   Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk.

  22532573   The role of genetic breast cancer susceptibility variants as prognostic factors.

  22747683   Genetic variants associated with breast size also influence breast cancer risk.

  22778704   The association between single-nucleotide polymorphisms of ORAI1 gene and breast cancer in a Taiwanese population.

  22806168   A multistage genetic association study identifies breast cancer risk loci at 10q25 and 16q24.

  22867275   Genetic predisposition, parity, age at first childbirth and risk for breast cancer.

  22910930   Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians.

  22972951   Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status.

  23136140   Genetic susceptibility loci for subtypes of breast cancer in an African American population.

  23221726   Gene-environment interactions for breast cancer risk among Chinese women: a report from the Shanghai Breast Cancer Genetics Study.

  23354978   Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.

  23474973   Incremental impact of breast cancer SNP panel on risk classification in a screening population of white and African American women.

  23486537   Comparison of genetic variation of breast cancer susceptibility genes in Chinese and German populations.

  23535825   Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls.

  23544014   Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors.

  23563089   Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women.

  23577780   Associations between single-nucleotide polymorphisms and epidural ropivacaine consumption in patients undergoing breast cancer surgery.

  23593120   Evaluating genome-wide association study-identified breast cancer risk variants in African-American women.

  23635555   The relationship between eight GWAS-identified single-nucleotide polymorphisms and primary breast cancer outcomes.

  23650637   Deconvoluting complex tissues for expression quantitative trait locus-based analyses.

  23776363   The genetics of breast cancer: risk factors for disease.

  23893088   The associations between a polygenic score, reproductive and menstrual risk factors and breast cancer risk.

  24025454   Hereditary breast cancer: ever more pieces to the polygenic puzzle.

  24086368   An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.

  24171766   Common low-penetrance risk variants associated with breast cancer in Polish women.

  24218030   Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.

  24242184   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.

  24266904   Breast cancer prediction using genome wide single nucleotide polymorphism data.

  24359602   Common breast cancer risk variants in the post-COGS era: a comprehensive review.

  24373701   Breast cancer susceptibility loci in association with age at menarche, age at natural menopause and the reproductive lifespan.

  24510657   Evaluating 17 breast cancer susceptibility loci in the Nashville breast health study.

  24532140   Association of genetic variants at TOX3, 2q35 and 8q24 with the risk of familial and early-onset breast cancer in a South-American population.

  24743323   Genetic predisposition to in situ and invasive lobular carcinoma of the breast.

  24771903   Breast Cancer Risk - From Genetics to Molecular Understanding of Pathogenesis.

  24792587   Reproductive windows, genetic loci, and breast cancer risk.

  24895409   Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women.