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Evaluation of the Relationship Between Common Variants in the TLR-9 Gene and Hip Osteoarthritis Susceptibility
Additional evidence supports association of common genetic variants in MMP3 and TIMP2 with increased risk of chronic Achilles tendinopathy susceptibility
Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke. The Tromsø Study
Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review
Characteristics of Slow Progression to Type 1 Diabetes in Children With Increased HLA-Conferred Disease Risk
Association of rs356219 and rs3822086 polymorphisms with the risk of Parkinson’s disease: a meta-analysis
Replication of previous genome-wide association studies of HKDC1, BACE2, SLC16A11 and TMEM163 SNPs in a gestational diabetes mellitus case–control sample from Han Chinese population
Glutamate ionotropic receptor NMDA type subunit 2A (GRIN 2A) gene polymorphism (rs4998386) and Parkinson’s disease susceptibility: A meta‐analysis
Genetic variants in GRHL3 and risk for neural tube defects: A case–control and case–parent triad/control study
Association of genetic polymorphisms with age at menarche in Russian women