SNP information rs13281615

Research and publications:

  17529967   Genome-wide association study identifies novel breast cancer susceptibility loci.

  17618282   A common genetic risk factor for colorectal and prostate cancer.

  17997823   Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases.

  18224312   Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment

  18349290   Association of genetic variants at 8q24 with breast cancer risk.

  18437204   Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.

  18535017   Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk.

  18577746   Multiple loci with different cancer specificities within the 8q24 gene desert.

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

  18625567   Association of chromosomal locus 8q24 and risk of prostate cancer: a hospital-based study of German patients treated with brachytherapy.

  18681954   Breast cancer susceptibility loci and mammographic density.

  18704501   Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers.

  18708391   Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. radiologic technologists.

  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.

  19005751   Low penetrance breast cancer predisposition SNPs are site specific.

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

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

  19094228   The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer.

  19304784   Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.

  19454617   Genetic variation in the chromosome 17q23 amplicon and breast cancer risk.

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

  19528667   Association of chromosome 8q variants with prostate cancer risk in Caucasian and Hispanic men.

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

  19607694   Low-risk susceptibility alleles in 40 human breast cancer cell lines.

  19639606   Correcting the “winner's curse” in odds ratios based on genome-wide association results for major complex human diseases.

  19648920   Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer.

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

  19767754   Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.

  19767755   Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

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

  19843670   Association of breast cancer susceptibility variants with risk of pancreatic cancer.

  19906782   Genome-wide association studies in cancer--current and future directions.

  20054709   Birth weight, breast cancer susceptibility loci, and breast cancer risk.

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

  20133699   Long-range enhancers on 8q24 regulate c-Myc.

  20145138   Common genetic variants associated with breast cancer and mammographic density measures that predict disease.

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

  20158306   Variation at 8q24 and 9p24 and risk of epithelial ovarian cancer.

  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.

  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.

  20530236   Genetic variation at chromosome 8q24 in osteosarcoma cases and controls.

  20530438   Unique SNP in CD44 intron 1 and its role in breast cancer development.

  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.

  20627891   An 8q24 gene desert variant associated with prostate cancer risk confers differential in vivo activity to a MYC enhancer.

  20699374   Evaluation of breast cancer susceptibility loci in Chinese women.

  20718042   Pooled versus individual genotyping in a breast cancer genome-wide association study.

  20885788   Germline variation controls the architecture of somatic alterations in tumors.

  20932292   Genome profiling of ERBB2-amplified breast cancers.

  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.

  21037568   A genome-wide association study of Hodgkin lymphoma identified novel susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).

  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?

  21051319   Risk of urinary bladder cancer is associated with 8q24 variant rs9642880[T] in multiple racial/ethnic groups: results from the Los Angeles-Shanghai case-control study.

  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.

  21197568   Risk of genome-wide association study newly identified genetic variants for breast cancer in Chinese women of Heilongjiang Province.

  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

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

  21637779   Characterizing genetic risk at known prostate cancer susceptibility loci in African Americans.

  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.

  21779458   Chromosome 8q24-Associated Cancers and MYC.

  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.

  21814516   A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.

  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.

  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.

  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.

  22160591   A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population.

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

  22303333   Replication of GWAS "Hits" by Race for Breast and Prostate Cancers in European Americans and African Americans.

  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.

  22558003   The 8q24 gene desert: an oasis of non-coding transcriptional activity.

  22726230   Interactive effect of genetic susceptibility with height, body mass index, and hormone replacement therapy on the risk of breast cancer.

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

  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.

  22965832   Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.

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