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- Journal Article
- A1
- open access
Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry
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- Journal Article
- A2
- open access
Discovery of new myositis genetic associations through leveraging other immune-mediated diseases
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- Journal Article
- A1
- open access
Identification of novel associations and localization of signals in idiopathic inflammatory myopathies using genome‐wide imputation
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Low gene copy numbers of complement C4 and complement C4A deficiency are strong and highly significant genetic risk factors for idiopathic inflammatory myopathy and its major subgroups
(2023) CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. In Clinical and Experimental Rheumatology 41(2). p.416-416 -
Clinical features of extra-muscular disease in dermatomyositis and anti-synthetase syndrome patients with skin involvement classified by presence of disease-specific autoantibodies : results from the EuroMyositis registry
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- Journal Article
- A1
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Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups
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- Journal Article
- A1
- open access
The EuroMyositis registry : an international collaborative tool to facilitate myositis research
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Immune-array analysis in sporadic inclusion body myositis reveals HLA-DRB1 amino acid heterogeneity across the myositis spectrum
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Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
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International immunochip study in the idiopathic inflammatory myopathies identifies novel susceptability loci and confirms HLA as strongest genetic risk factor