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The association analysis between CYP24A1 genetic polymorphisms and the risk of ischemic stroke in Chinese Han population
Contribution of IL-7/7R genetic polymorphisms in coronary heart disease in Chinese Han population.
CBS gene polymorphism and promoter methylation-mediating effects on the efficacy of folate therapy in patients with hyperhomocysteinemia
Association of LAG3 genetic variation with an increased risk of PD in Chinese female population.
Combining newborn metabolic and genetic screening for neonatal intrahepatic cholestasis caused by citrin deficiency
Angiotensin-Ⅱ and angiotensin-(1-7) imbalance affects comorbidity of depression and coronary heart disease
LRCH1 polymorphisms linked to delayed encephalopathy after acute carbon monoxide poisoning identified by GWAS analysis followed by Sequenom MassARRAY® validation
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population
PPARG Pro12Ala Polymorphism with CKD in Asians: A Meta-Analysis Combined with a Case-Control Study—A Key for Reaching Null Association
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy