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A rare missense variant in TCF7L2 associates with colorectal cancer risk by interacting with a GWAS-identified regulatory variant in the MYC enhancer
Fabry disease: review and experience during newborn screening
Robust identification of mosaic variants in congenital heart disease
Functional Polymorphisms in BARD1 Association with Neuroblastoma in a regional Han Chinese Population
Relationship between a Weighted Multi-Gene Algorithm and Blood Pressure Controlin Hypertension
Comparison of Nutrigenomics Technology Interface Tools for Consumers and Health Professionals: A Sequential Explanatory Mixed Methods Investigation
Polymorphisms in IGF2/H19 gene locus are associated with platinum-based chemotherapeutic response in Chinese patients with epithelial ovarian cancer
Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese Children
Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients
Impact of ANXA5 polymorphisms on glioma risk and patient prognosis