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  • Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia breast cancer consortium
  • 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
  • Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer
  • Large Effects on Body Mass Index and Insulin Resistance of Fat Mass and Obesity Associated Gene (FTO) Variants in Patients with Polycystic Ovary Syndrome (PCOS)
  • Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies
  • Kalirin: a novel genetic risk factor for ischemic stroke
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