SNP information rs11249433

Research and publications:

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

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

  20095854   Novel breast cancer risk alleles and interaction with ionizing radiation among U.S. radiologic technologists.

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

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

  20482849   NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations.

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

  20585100   Genome-wide association studies of cancer.

  20699374   Evaluation of breast cancer susceptibility loci in Chinese women.

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

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

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

  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.

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

  21593217   Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

  21738711   Genetic variants at 1p11.2 and breast cancer risk: a two-stage study in Chinese women.

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

  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.

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

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

  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.

  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.

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

  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.

  23193118   Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the Breast and Prostate Cancer Cohort Consortium

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

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

  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.

  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.

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

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

  24292867   Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression.

  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.

  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.

  24941967   Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population.

  25027274   Testing calibration of risk models at extremes of disease risk.

  25057183   A robust association test for detecting genetic variants with heterogeneous effects.

  25139936   Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study.

  25253900   Breast Cancer Risk - Genes, Environment and Clinics.

  25255808   Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.

  25567532   The use of the Gail model, body mass index and SNPs to predict breast cancer among women with abnormal (BI-RADS 4) mammograms.

  25611573   Association of breast cancer risk loci with breast cancer survival.

  25881232   Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography.

  26070784   Genetic risk variants associated with in situ breast cancer.

  26175953   FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population.

  26472073   Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors.

  26510858   Patients with a High Polygenic Risk of Breast Cancer do not have An Increased Risk of Radiotherapy Toxicity.

  26559640   Automated amplicon design suitable for analysis of DNA variants by melting techniques.

  26757262   Gene-environment interaction and risk of breast cancer.

  26884359   Genetic predisposition to ductal carcinoma in situ of the breast.

  27079684   Genome-wide association studies and epigenome-wide association studies go together in cancer control.

  27392074   The Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case-Control Study.

  27556229   Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.

  28098224   Association of Genome-Wide Association Study (GWAS) Identified SNPs and Risk of Breast Cancer in an Indian Population.

  29382703   Common Genetic Variation and Breast Cancer Risk-Past, Present, and Future.

  31125336   Evaluation of significant genome-wide association studies risk - SNPs in young breast cancer patients.

  34257585   NOTCH Single Nucleotide Polymorphisms in the Predisposition of Breast and Colorectal Cancers in Saudi Patients.

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