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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
Improved progression-free survival in irinotecan-treated metastatic colorectal cancer patients carrying the HNF1A coding variant p. I27L
High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in south eastern Australia
Exome array analysis identifies variants in SPOCD1 and BTN3A2 that affect risk for gastric cancer
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