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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
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
Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress
Additional Evidence Supports Association of Common Variants in COL11A1 with Increased Risk of Hip Osteoarthritis Susceptibility
Improved progression-free survival in irinotecan-treated metastatic colorectal cancer patients carrying the HNF1A coding variant p. I27L