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

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A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1

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Genome-wide association study identifies novel breast cancer susceptibility loci

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New genetic variants improve personalized breast cancer diagnosis.

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Polymorphisms in ESR1 and FLJ43663 are associated with breast cancer risk in the Han population

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No association between a progesterone receptor gene promoter polymorphism (+331G>A) and breast cancer risk in Caucasian women: evidence from a literature-based meta-analysis

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Using gene-environment interaction analyses to clarify the role of well-done meat and heterocyclic amine exposure in the etiology of colorectal polyps

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Replication of GWAS “Hits” by Race for Breast and Prostate Cancers in European Americans and African Americans

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CHRNA9 polymorphisms and smoking exposure synergize to increase the risk of breast cancer in Taiwan

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An In Vivo Gain-of-Function Screen Identifies the Williams-Beuren Syndrome Gene GTF2IRD1 as a Mammary Tumor Promoter

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Association between genetic risk score for telomere length and risk of breast cancer

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Joint Effect of Genetic and Lifestyle Risk Factors on Type 2 Diabetes Risk among Chinese Men and Women

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Two-stage case–control study of DNMT-1 and DNMT-3B gene variants and breast cancer risk

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ESR1 single nucleotide polymorphisms predict breast cancer susceptibility in the central European Caucasian population.

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Genetic variants improve breast cancer risk prediction on mammograms.

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Genetic Variation in Transforming Growth Factor Beta 1 and Mammographic Density in Singapore Chinese Women

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Using Breast Cancer Risk Associated Polymorphisms to Identify Women for Breast Cancer Chemoprevention

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Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women

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Predictive polymorphisms for breast cancer in postmenopausal Mexican women

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Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population

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Genetic Variation in Peroxisome Proliferator–Activated Receptor Gamma, Soy, and Mammographic Density in Singapore Chinese Women

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Combination of a 15-SNP Polygenic Risk Score and Classical Risk Factors for the Prediction of Breast Cancer Risk in Cypriot Women

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A Common Variant in the SIAH2 Locus Is Associated with Estrogen Receptor-Positive Breast Cancer in the Chinese Han Population

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Discovery of rare coding variants in OGDHL and BRCA2 in relation to breast cancer risk in Chinese women

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Rs488087 single nucleotide polymorphism as predictive risk factor for pancreatic cancers

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Lipid peroxidation biomarkers associated with height and obesity measures in the opposite direction in women

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Comparisons of clinical characteristics, prognosis, epidemiological factors, and genetic susceptibility between HER2 ‐low and HER2 ‐zero breast cancer among Chinese females

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A common deletion in the haptoglobin gene associated with blood cholesterol levels among Chinese women

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Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

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Association of a single nucleotide polymorphism at 6q25.1,rs2046210, with endometrial cancer risk among Chinese women

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Polymorphisms of Insulin-Like Growth Factor 1 Pathway Genes and Breast Cancer Risk

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From BRCA1 to Polygenic Risk Scores: Mutation-Associated Risks in Breast Cancer-Related Genes

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Identification of a Breast Cancer Susceptibility Locus at 4q31.22 Using a Genome-Wide Association Study Paradigm

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Association of Type 2 Diabetes Genetic Variants with Breast Cancer Survival among Chinese Women

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Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa

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Identification of a novel susceptibility locus at 16q23.1 associated with childhood acute lymphoblastic leukemia in Han Chinese

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Breast Cancer Single-Nucleotide Polymorphisms: Statistical Significance and Clinical Utility

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Replication of genome-wide discovered breast cancer risk loci in the Cypriot population

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Update Breast Cancer 2018 (Part 3) – Genomics, Individualized Medicine and Immune Therapies – in the Middle of a New Era: Prevention and Treatment Strategies for Early Breast Cancer

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No association between genetic variants in angiogenesis and inflammation pathway genes and breast cancer survival among Chinese women

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A single nucleotide polymorphism of the TNRC9 gene associated with breast cancer risk in Chinese Han women

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Breast Cancer Susceptibility Variants and Mammographic Density Phenotypes in Norwegian Postmenopausal Women

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Variants in 6q25.1 Are Associated with Mammographic Density in Malaysian Chinese Women

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Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk

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Genetic contribution of GADD45A to susceptibility to sporadic and non-BRCA1/2 familial breast cancers: a systematic evaluation in Chinese populations

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Mcs5c: A Mammary Carcinoma Susceptibility Locus Located in a Gene Desert that Associates withTenascin CExpression

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Common Genetic Variants in the MicroRNA Biogenesis Pathway Are Not Associated with Breast Cancer Risk in Asian Women

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Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study

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Exogenous Hormones, Tumor Intrinsic Subtypes, and Breast Cancer

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Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

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Association between breast cancer genetic susceptibility variants and terminal duct lobular unit involution of the breast

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Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

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Genetic variants at chromosome 9p21, 10p15 and 10q22 and breast cancer susceptibility in a Chinese population

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Breast Cancer Association Studies in a Han Chinese Population using 10 European-ancestry-associated Breast Cancer Susceptibility SNPs

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Genetic variants of ESR1 and SGSM3 are associated with the susceptibility of breast cancer in the Chinese population

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ESR1 gene variants, haplotypes and diplotypes may influence the risk of breast cancer and mammographic density

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A Personal Breast Cancer Risk Stratification Model Using Common Variants and Environmental Risk Factors in Japanese Females

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Evaluating breast cancer predisposition genes in women of African ancestry

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A polymorphism in the nuclear receptor coactivator 7 gene and breast cancer susceptibility

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Search for Cancer Risk Factors with Microarray-Based Genome-Wide Association Studies

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Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

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Replication and Functional Genomic Analyses of the Breast Cancer Susceptibility Locus at 6q25.1 Generalize Its Importance in Women of Chinese, Japanese, and European Ancestry

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Association between a novel polymorphism (rs2046210) of the 6q25.1 locus and breast cancer risk

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Sequencing of Chromosomal Locus 6q25.1 Revealed Two Significant SNPs rs2046210 and rs2046211 Associated with Breast Cancer: A Case-Control Study in Egyptian Women

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