Show
Sort by
-
Autoantibodies against a subunit of mitochondrial respiratory chain complex I in inclusion body myositis
-
- Journal Article
- A2
- open access
Discovery of new myositis genetic associations through leveraging other immune-mediated diseases
-
- Journal Article
- A1
- open access
Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry
-
- Journal Article
- A1
- open access
Identification of novel associations and localization of signals in idiopathic inflammatory myopathies using genome‐wide imputation
-
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 -
- Journal Article
- A1
- open access
Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups
-
- Journal Article
- A1
- open access
Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis
-
Immune-array analysis in sporadic inclusion body myositis reveals HLA-DRB1 amino acid heterogeneity across the myositis spectrum
-
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
-
Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies