Melorheostosis and Osteopoikilosis: A Review of Clinical Features and Pathogenesis.
Journal article
Wordsworth P. and Chan M., (2019), Calcif tissue int, 104, 530 - 543
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.
Journal article
Watts L. et al, (2019), Genes immun, 20, 167 - 171
OP0231?Differential transcription factor binding could explain the genetic association of ankylosing spondylitis with polymorphisms in the IL23R-IL12RB2 intergenic region
Conference paper
(2018), Annals of the rheumatic diseases
THU0364?Rare ERAP1 allotype combinations do not explain the ERAP1 association with ankylosing spondylitis
Conference paper
(2018), Annals of the rheumatic diseases
Anti-TNF modulation reduces myocardial inflammation and improves cardiovascular function in systemic rheumatic diseases.
Journal article
Ntusi NAB. et al, (2018), Int j cardiol, 270, 253 - 259
Quantifying the genetic risk for the development of axial spondyloarthropathy: could this become a diagnostic tool?
Journal article
Wordsworth BP. et al, (2018), Curr opin rheumatol, 30, 319 - 323
Cardiovascular magnetic resonance characterization of myocardial and vascular function in rheumatoid arthritis patients.
Journal article
Ntusi NAB. et al, (2018), Hellenic j cardiol
Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism.
Journal article
Vecellio M. et al, (2018), Rmd open, 4
NOVEL INSIGHTS INTO THE CHARACTERISTICS AND IMPACT OF BONE PAIN IN ADULTS WITH FIBROUS DYSPLASIA
Conference paper
Watts L. et al, (2017), Osteoporosis international, 28, S244 - S244
Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis.
Journal article
Roberts AR. et al, (2017), Genes immun, 18, 105 - 108
Reply to Reeves et al.: No evidence for rare ERAP1 haplotypes and haplotype combinations in ankylosing spondylitis.
Journal article
Wordsworth BP. et al, (2017), Proc natl acad sci u s a, 114
ERAP1 association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations.
Journal article
Roberts AR. et al, (2017), Proc natl acad sci u s a, 114, 558 - 561
An ankylosing spondylitis-associated genetic variant in the IL23R-IL12RB2 intergenic region modulates enhancer activity and is associated with increased Th1-cell differentiation.
Journal article
Roberts AR. et al, (2016), Ann rheum dis, 75, 2150 - 2156
Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.
Journal article
Forestier-Zhang L. et al, (2016), Orphanet j rare dis, 11
The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.
Journal article
Javaid MK. et al, (2016), Orphanet j rare dis, 11
The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression.
Journal article
Vecellio M. et al, (2016), Ann rheum dis, 75, 1534 - 1540
OP0299?Susceptibility to ankylosing spondylitis is influenced independently by two closely adjacent Runx3 Snps, that show strong functional effect in different cell types
Conference paper
(2016), Annals of the rheumatic diseases
Genetics of ankylosing spondylitis--insights into pathogenesis.
Journal article
Brown MA. et al, (2016), Nat rev rheumatol, 12, 81 - 91