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PPARG Pro12Ala Polymorphism with CKD in Asians: A Meta-Analysis Combined with a Case-Control Study—A Key for Reaching Null Association
LRCH1 polymorphisms linked to delayed encephalopathy after acute carbon monoxide poisoning identified by GWAS analysis followed by Sequenom MassARRAY® validation
Lower S-adenosylmethionine Levels and DNA Hypomethylation of Placental Growth Factor (PlGF) in Placental Tissue of Early-Onset Preeclampsia-Complicated Pregnancies
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy
The Effect of Haplotypes in the CETP and LIPC Genes on the Triglycerides to HDL-C Ratio and Its Components in the Roma and Hungarian General Populations
ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
ATP-sensitive potassium channels gene polymorphism rs1799858 affects the risk of macro-/micro-vascular arteriosclerotic event in patients with increased low-density lipoprotein cholesterol levels.
Epigenetic Marks at the Ribosomal DNA Promoter in Skeletal Muscle Are Negatively Associated With Degree of Impairment in Cerebral Palsy
Study on the Association Between CYP24A1 Genetic Polymorphisms and Risks Related to Postmenopausal Breast Cancer
Impact of NR5A2 and RYR2 3′ UTR polymorphisms on the risk of breast cancer in a Chinese Han population