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Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease‐causing variants
CCR6, IL7R, FAS and Madcam-1 Single Nucleotide Polymorphisms Are Associated with Higher Incidence of Infections in Allogeneic Stem-Cell Transplant from a …
DNA of erythroid origin is present in human plasma and informs the types of anemia
Functional miR-146a, miR-149, miR-196a2 and miR-499 polymorphisms and the susceptibility to hepatocellular carcinoma: An updated meta-analysis
The Drosophila foraging gene human orthologue PRKG1 predicts individual differences in the effects of early adversity on maternal sensitivity
A pathway‐based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility
Analysis of DNA methylation in mammalian cells
A preliminary study of new single polymorphisms in the T helper type 17 pathway for psoriasis in the Korean population
The first international workshop on the epigenetics of osteoarthritis
Interaction of CYP2C19, P2Y12, and GPIIIa Variants Associates With Efficacy of Clopidogrel and Adverse Events on Patients With Ischemic Stroke