SNP information rs1219648

Research and publications:

  17529973   A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

  18285324   Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.

  18326623   Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.

  18478591   Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.

  18483326   FGFR2 is a breast cancer susceptibility gene in Jewish and Arab Israeli populations.

  18535005   The search for genes contributing to endometriosis risk

  18785201   Novel breast cancer risk alleles and endometrial cancer risk.

  18845558   Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese women.

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

  19028704   Hormone-dependent effects of FGFR2 and MAP3K1 in breast cancer susceptibility in a population-based sample of post-menopausal African-American and European-American women.

  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.

  19119171   AXIS inhibition protein 2, orofacial clefts and a family history of cancer.

  19219042   Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.

  19497954   Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer.

  19500394   Genetic variants of the FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study.

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

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

  19738052   A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.

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

  19861516   Variation in the FGFR2 gene and the effects of postmenopausal hormone therapy on invasive breast cancer.

  20056625   Variation in the FGFR2 gene and the effect of a low-fat dietary pattern on invasive breast cancer.

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

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

  20126254   Rare variants create synthetic genome-wide associations.

  20300826   Current evidence on the relationship between three polymorphisms in the FGFR2 gene and breast cancer risk: a meta-analysis.

  20364400   Quantitative assessment of the effect of FGFR2 gene polymorphism on the risk of breast cancer.

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

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

  20560208   Powerful SNP-set analysis for case-control genome-wide association studies.

  20585100   Genome-wide association studies of cancer.

  20640597   Risk of aggressive breast cancer in women of Han nationality carrying TGFB1 rs1982073 C allele and FGFR2 rs1219648 G allele in North China.

  20699374   Evaluation of breast cancer susceptibility loci in Chinese women.

  20853316   FGFR2 intronic SNPs and breast cancer risk: associations with tumor characteristics and interactions with exogenous exposures and other known breast cancer risk factors.

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

  21160077   Genetic correction of PSA values using sequence variants associated with PSA levels.

  21203894   Cancer susceptibility variants and the risk of adult glioma in a US case-control study.

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

  21382839   Relation of FGFR2 genetic polymorphisms to the association between oral contraceptive use and the risk of breast cancer in Chinese women.

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

  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

  21610108   A multistage association study identifies a breast cancer genetic locus at NCOA7.

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

  21695280   Pathways of distinction analysis: a new technique for multi-SNP analysis of GWAS data.

  21702935   Genetic variants in the MRPS30 region and postmenopausal breast cancer risk.

  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.

  21838531   Crosstalk between the FGFR2 and TP53 genes in breast cancer: data from an association study and epistatic interaction analysis.

  21853025   A bayesian method for evaluating and discovering disease loci associations.

  21869864   An integrative genomics approach to biomarker discovery in breast cancer.

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

  22144180   FGFR2 genotype and risk of radiation-associated breast cancer in Hodgkin lymphoma.

  22212363   A robust method for testing association in genome-wide association studies.

  22276117   The association between ATM IVS 22-77 T>C and cancer risk: a meta-analysis.

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

  22332084   Research advances at the Institute for Nutritional Sciences at Shanghai, China.

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

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

  22734045   Identifying genetic marker sets associated with phenotypes via an efficient adaptive score test.

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

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

  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.

  23107584   Identifying breast cancer risk loci by global differential allele-specific expression (DASE) analysis in mammary epithelial transcriptome.

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

  23169889   Tooth agenesis association with self-reported family history of cancer.

  23184080   Assessing interactions between the associations of fibroblast growth factor receptor 2 common genetic variants and hormone receptor status with breast cancer risk.

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

  23225170   Genetic variants in FGFR2 and MAP3K1 are associated with the risk of familial and early-onset breast cancer in a South-American population.

  23318652   Hereditary breast cancer in the Han Chinese population.

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

  23435034   Breast cancer susceptibility associated with rs1219648 (fibroblast growth factor receptor 2) and postmenopausal hormone therapy use in a population-based United States study.

  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.

  23519603   Variable selection and estimation in generalized linear models with the seamless L(0) penalty.

  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.

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

  23614025   A novel multiplex tetra-primer ARMS-PCR for the simultaneous genotyping of six single nucleotide polymorphisms associated with female cancers.

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

  23717390   Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm.

  23826324   The GSTP1 105Val allele increases breast cancer risk and aggressiveness but enhances response to cyclophosphamide chemotherapy in North China.

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

  24054997   Association between rs2981582 polymorphism in the FGFR2 gene and the risk of breast cancer in Mexican women.

  24080446   Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study.

  24143190   Genome-wide association study of breast cancer in the Japanese population.

  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.

  24265035   Risk of GWAS-identified genetic variants for breast cancer in a Chinese population: a multiple interaction analysis.

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

  24340245   Adiposity, inflammation, genetic variants and risk of post-menopausal breast cancer findings from a prospective-specimen-collection, retrospective-blinded-evaluation (PRoBE) design approach.

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

  24454457   Case-control study on the fibroblast growth factor receptor 2 gene polymorphisms associated with breast cancer in chinese han women.

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

  24832084   Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.

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

  24943593   Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumors.

  25285046   Graphical-model Based Multiple Testing under Dependence, with Applications to Genome-wide Association Studies.