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HLA-G+ 3196 polymorphism as a risk factor for cell mediated rejection following heart transplant
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis
Correlation of ATP Binding Cassette Transporter A1 Gene Polymorphisms and Lower Extremity Athero-sclerotic Disease
Associations of single nucleotide polymorphisms of UCP genes with diabetic retinopathy in Chinese Han population
Association study of SLC22A12 gene rs893006 and SLC2A9 gene rs11942223 with hyperuricemia
The study of Tibetan ancestry informative SNPs on high-altitude adaptive genes
Association study on interaction effects of CREB1 gene and BDNF gene polymorphisms and recurrent major depressive disorder
Genetic susceptibility of ABCC4, FCGR2A and BLK polymorphisms with Kawasaki disease in children from southern China
GATA3-IL-13 pathway gene polymorphisms are associated with serum IL-13 and asthma
Association between set shifting in attention deficit/hyperactivity disorder (ADHD) and NRXN1 gene