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  • New genetic associations detected in a host response study to hepatitis B vaccine
  • Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment
  • Association analysis of 3p21 with Crohns disease in a New Zealand population
  • Multiplex genotyping of CYP3A4, CYP3A5, CYP2C9 and CYP2C19 SNPs using MALDI-TOF mass spectrometry
  • Multiple Sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients
  • Association of Caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure
  • A population-based study of IGF axis polymorphisms and the esophageal inflammation, metaplasia, adenocarcinoma sequence
  • Assessment of DNA degradation and the genotyping success of highly degraded samples
  • Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment
  • HOXB13, a target of DNMT3B, is methylated at an upstream CpG island, and functions as a tumor suppressor in primary colorectal tumors
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