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Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from medellÃn, Colombia
Physicians’ attitudes about multiplex tumor genomic testing
PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of BehÃ§et’s disease in a Chinese Han population
PI3K pathway activation in high-grade ductal carcinoma in situ-implications for progression to invasive breast carcinoma
Quantitative Methylation Level of the EPHX1 Promoter in Peripheral Blood DNA Is Associated with Polycystic Ovary Syndrome
PIK3CA mutations, phosphatase and tensin homolog, human epidermal growth factor receptor 2 and insulin-like growth factor 1 receptor and adjuvant tamoxifen resistance in postmenopausal breast cancer patients
Pilot study demonstrating potential association between breast cancer image-based risk phenotypes and genomic biomarkers
Placental leptin gene methylation and macrosomia during normal pregnancy
Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia
Novel candidate genes putatively involved in stress fracture predisposition detected by whole-exome sequencing