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(1 - 24 of 25)
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Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Genome-wide association study of germline variants and breast cancer-specific mortality
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Exome-wide association study of plasma lipids in > 300,000 individuals
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Exome-wide association study of plasma lipids in > 300,000 individuals
Association analysis identifies 65 new breast cancer risk loci
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Rare and low-frequency coding variants alter human adult height
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
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