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Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: A large-scale genetic association study
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
Association of Renalase Genetic Variants With Longitudinal Blood Pressure Changes and Incidence of Hypertension
UMOD Polymorphisms Associated with Kidney Function, Serum Uromodulin and Risk of Mortality among Patients with Chronic Kidney Disease, Results from the C-STRIDE Study
Exploring the relation between high-activity COMT Val158Met genotype and psychopathy in male offenders
Harsh parenting and non-suicidal self-injury in adolescence: the mediating effect of depressive symptoms and the moderating effect of the COMT Val158Met polymorphism
Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study
Genetic Variant of PP2A Subunit Gene Confers an Increased Risk of Primary Liver Cancer in Chinese