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Genomics Inform. 2017;15(2):65-68. Published online June 15, 2017 DOI: https://doi.org/10.5808/GI.2017.15.2.65 |
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A Variant in RUNX3 Is Associated with the Risk of Ankylosing Spondylitis in Koreans Genomics & Informatics. 2017;15(2):65  <italic>ADIPOQ</italic> Gene Variants Associated with Susceptibility to Obesity and Low Serum Adiponectin Levels in Healthy Koreans Epidemiology and Health. 2011;33:e2011003 Is RUNX3 a new player in the pathogenesis of ankylosing spondylitis? Rheumatology International. 2012;33(9):2449-2450 A CCR6 variant strongly associated with rheumatoid arthritis in two populations is not associated with ankylosing spondylitis Rheumatology International. 2012;33(9):2443-2444 Measures of symptoms and disease status in ankylosing spondylitis: Ankylosing Spondylitis Disease Activity Score (ASDAS), Ankylosing Spondylitis Quality of Life Scale (ASQoL), Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Bath Ankylosing Sp Arthritis Care & Research. 2011;63(S11):S47-S58 Ankylosing spondylitis measures: The Ankylosing Spondylitis Quality of Life (ASQOL) Scale, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Bath Ankylosing Spondylitis Functional Index (BASFI), Bath Ankylosing Spondylitis Global Score (BAS-G), Bath Ankylosing Spondylitis Metrology Index (BASMI), Dougados Functional Index (DFI), Health Assessment Questionnaire for the Spondyloarthropathies (HAQ-S), and Revised Leeds Disability Questionnaire (RLDQ) Arthritis & Rheumatism. 2003;49(S5):S197-S209 Ankylosing Spondylitis Surgical Treatment of Ankylosing Spondylitis Deformity. 2019;3-13 Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci Nature Genetics. 2013;45(7):730-738 RUNX3 and T-Bet in Immunopathogenesis of Ankylosing Spondylitis—Novel Targets for Therapy? Frontiers in Immunology. 2019;9: Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter Frontiers in Genetics. 2022;12: |
