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Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Homocysteine promotes human endothelial cell dysfunction via site-specific epigenetic regulation of p66shc
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
Genetic Variants in the LEPR, CRY1, RNASEL, IL4, and ARVCF Genes Are Prognostic Markers of Prostate Cancer-Specific Mortality
Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF)
The association of the BLK gene with SLE was replicated in Chinese Han
Clinical Interest of pharmacogenetic polymorphisms in the immunosuppressive treatment after heart transplantation
DNA polymorphism and risk of esophageal squamous cell carcinoma in a population of North Xinjiang, China
VARS2 V552V variant as a prognostic marker in patients with early breast cancer