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Replication of results of a genome-wide association study on lung cancer survival in a Korean population
Replication Study of ESCC Susceptibility Genetic Polymorphisms Locating in the ADH1B-ADH1C-ADH7 Cluster Identified by GWAS
Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Risk stratification of organ-specific GVHD can be improved by single-nucleotide polymorphism-based risk models
RNASEL and MIR146A SNP-SNP Interaction as a Susceptibility Factor for Non-Melanoma Skin Cance
Role of IFN-ks, IFN-ks related genes and the DEPDC5 gene in Hepatitis B virus-related liver disease
Role of Nicotine Dependence in the Association between the Dopamine Receptor Gene DRD3 and Major Depressive Disorder
Sequence Variants in SLC6A3, DRD2, and BDNF Genes and Time to Levodopa-Induced Dyskinesias in Parkinson’s Disease
Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications
Single Nucleotide Polymorphisms in Proximity to K-Channel Genes Are Associated with Decreased Longitudinal QTc Variance