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Publications

Melorheostosis and Osteopoikilosis: A Review of Clinical Features and Pathogenesis.

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.

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

Anti-TNF modulation reduces myocardial inflammation and improves cardiovascular function in systemic rheumatic diseases.

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?

Wordsworth BP. et al, (2018), Curr opin rheumatol, 30, 319 - 323

Cardiovascular magnetic resonance characterization of myocardial and vascular function in rheumatoid arthritis patients.

Ntusi NAB. et al, (2018), Hellenic j cardiol

Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism.

Vecellio M. et al, (2018), Rmd open, 4

NOVEL INSIGHTS INTO THE CHARACTERISTICS AND IMPACT OF BONE PAIN IN ADULTS WITH FIBROUS DYSPLASIA

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.

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.

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.

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.

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.

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.

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.

Vecellio M. et al, (2016), Ann rheum dis, 75, 1534 - 1540

OP0231?Differential transcription factor binding could explain the genetic association of ankylosing spondylitis with polymorphisms in the IL23R-IL12RB2 intergenic region

(2016), Annals of the rheumatic diseases

OP0299?Susceptibility to ankylosing spondylitis is influenced independently by two closely adjacent Runx3 Snps, that show strong functional effect in different cell types

(2016), Annals of the rheumatic diseases

THU0364?Rare ERAP1 allotype combinations do not explain the ERAP1 association with ankylosing spondylitis

(2016), Annals of the rheumatic diseases

Susceptibility to ankylosing spondylitis is influenced independently by two closely adjacent RUNX3 single nucleotide polymorphisms that show strong functional effect in different cell types

(2016), Rheumatology

The association of a common functional polymorphism in the tumour necrosis factor receptor 1 gene (TNFRSF1A) and disease severity in ankylosing spondylitis

(2016), Rheumatology

Genetics of ankylosing spondylitis--insights into pathogenesis.

Brown MA. et al, (2016), Nat rev rheumatol, 12, 81 - 91

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