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  • Toll-like receptor and matrix metalloproteinase single nucleotide polymorphisms, haplotypes and polygenic risk score differentiated between tuberculosis disease and infection
  • Association between IL1RL1 gene polymorphisms and allergic rhinitis risk in the Chinese Han population
  • Pediatric spinal pilocytic astrocytomas form a distinct epigenetic subclass from pilocytic astrocytomas of other locations and diffuse leptomeningeal glioneuronal tumours
  • APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestry
  • Influence of UGT1A1 and SLC22A6 polymorphisms on the population pharmacokinetics and pharmacodynamics of raltegravir in HIV-infected adults: a NEAT001/ANRS143 sub-study
  • Association of polymorphism rs10841855 in the glycogen synthase 2 gene with hypercholesterolemia and type 2 diabetes mellitus
  • Statistic Value for Determination of Parents-child Relationship using Single Nucleotide Polymorphisms (SNPs) 44 Loci in Thai Individuals
  • Genetic Structure of Susceptibility to Cardiovascular Continuum Comorbidity
  • Genetic Variants within NOGGIN, COL1A1, COL5A1, and IGF2 are Associated with Musculoskeletal Injuries in Elite Male Australian Football League Players: A Preliminary Study
  • Protein network and pathway analysis in a pharmacogenetic study of cyclosporine treatment response in Greek patients with psoriasis
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