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Three variants in the nicotinamide adenine dinucleotide phosphate oxidase complex are associated with HCV‐related liver damage
Genetics association study and functional analysis on osteoporosis susceptibility gene BDNF
Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis
Risk alleles for IgA nephropathy-associated SNPs conferred completely opposite effects to idiopathic membranous nephropathy in Chinese Han
Significant association of CXCL12 rs501120 with coronary artery disease and atorvastatin therapy
Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population
Functional polymorphisms in PD-L1 gene are associated with the prognosis of patients with early stage non-small cell lung cancer
HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions
A prospective study of dietary and supplemental zinc intake and risk of type 2 diabetes depending on genetic variation in SLC30A8
TNF receptors 1 and 2 exert distinct region‐specific effects on striatal and hippocampal grey matter volumes (VBM) in healthy adults