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Publications

Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter

Cohen CJ. et al, (2022), Frontiers in Genetics, 12

INVESTIGATING THE ANKYLOSING SPONDYLITIS-ASSOCIATED REGULATORY SNPS AT THE RUNX3 LOCUS WITH A FUNCTIONAL GENOMICS APPROACH

Vecellio M. et al, (2021), ANNALS OF THE RHEUMATIC DISEASES, 80, 411 - 411

Perspectives on the Genetic Associations of Ankylosing Spondylitis

Wordsworth BP. et al, (2021), Frontiers in Immunology, 12

COMPREHENSIVE EPIGENOMIC PROFILING REVEALS DISEASE-SPECIFIC CHROMATIN STATES IN ANKYLOSING SPONDYLITIS

Cohen CJ. et al, (2021), CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 39, 1155 - 1155

Functional Genomic Analysis of a RUNX3 Polymorphism Associated with Ankylosing Spondylitis

Vecellio M. et al, (2020), Arthritis & Rheumatology

A RUNX3 enhancer polymorphism associated with ankylosing spondylitis influences recruitment of Interferon Regulatory Factor 5 and factors of the Nucleosome Remodelling Deacetylase Complex in CD8+ T-cells

Vecellio M. et al, (2019)

The severity of ankylosing spondylitis and responses to anti-tumour necrosis factor biologics are not influenced by the tumour necrosis factor receptor polymorphism incriminated in multiple sclerosis

Watts L. et al, (2019), Genes & Immunity, 20, 167 - 171

Quantifying the genetic risk for the development of axial spondyloarthropathy

Wordsworth BP. et al, (2018), Current Opinion in Rheumatology, 30, 319 - 323

INVESTIGATING THE REGULATORY SNPS AT THE RUNX3 LOCUS ASSOCIATED WITH ANKYLOSING SPONDYLITIS

Vecellio ML. et al, (2018), ANNALS OF THE RHEUMATIC DISEASES, 77, 158 - 158

Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism

Vecellio M. et al, (2018), RMD Open, 4, e000628 - e000628

EXPLORING THE ANKYLOSING SPONDYLITIS-ASSOCIATED REGULATORY SNPs AT THE RUNX3 LOCUS

Vecellio M. et al, (2018), CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 36, 734 - 734

RUNX3 and T-Bet in Immunopathogenesis of Ankylosing Spondylitis-Novel Targets for Therapy?

Vecellio M. et al, (2018), Frontiers in immunology, 9

Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis

Roberts AR. et al, (2017), Genes & Immunity, 18, 105 - 108

An ankylosing spondylitis-associated genetic variant in theIL23R-IL12RB2intergenic region modulates enhancer activity and is associated with increased Th1-cell differentiation

Roberts AR. et al, (2016), Annals of the Rheumatic Diseases, 75, 2150 - 2156

The genetic association ofRUNX3with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression

Vecellio M. et al, (2016), Annals of the Rheumatic Diseases, 75, 1534 - 1540

THE ASSOCIATION OF A COMMON FUNCTIONAL POLYMORPHISM IN THE TUMOUR NECROSIS FACTOR RECEPTOR 1 GENE (TNFRSF1A) AND DISEASE SEVERITY IN ANKYLOSING SPONDYLITIS

Watts L. et al, (2016), RHEUMATOLOGY, 55, 150 - 150

A CCR6 variant strongly associated with rheumatoid arthritis in two populations is not associated with ankylosing spondylitis

Cohen CJ. et al, (2013), Rheumatology International, 33, 2443 - 2444

ANKYLOSING SPONDYLITIS IS STRONGLY ASSOCIATED WITH VARIANTS IN THE CMG2 GENE

Karaderi T. et al, (2013), RHEUMATOLOGY, 52, 47 - 48

Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians.

Karaderi T. et al, (2012), Clinical and experimental rheumatology, 30, 110 - 113

Human Th1 and Th17 Cells Exhibit Epigenetic Stability at Signature Cytokine and Transcription Factor Loci

Cohen CJ. et al, (2011), The Journal of Immunology, 187, 5615 - 5626

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