Ghent University Academic Bibliography

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Genetic architecture of idiopathic inflammatory myopathies from meta‐analyses

Catherine Zhu, Younghun Han, Jinyoung Byun, Xiangjun Xiao, Simon Rothwell, Frederick W. Miller, Ingrid E. Lundberg, Peter K. Gregersen, Jiri Vencovsky, Vikram R. Shaw, et al.

(2025) ARTHRITIS & RHEUMATOLOGY. 77(6). p.750-764
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Autoantibodies against a subunit of mitochondrial respiratory chain complex I in inclusion body myositis

Antonella Notarnicola, Ceke Hellstrom, Begum Horuluoglu, Elisa Pin, Charlotta Preger, Francesco Bonomi, Boel De Paepe (UGent) , Jan De Bleecker (UGent) , Anneke J. Van der Kooi, Marianne De Visser, et al.

(2024) JOURNAL OF AUTOIMMUNITY. 149.
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- A2
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Discovery of new myositis genetic associations through leveraging other immune-mediated diseases

Guillermo Reales, Christopher I. Amos, Olivier Benveniste, Hector Chinoy, Jan De Bleecker (UGent) , Boel De Paepe (UGent) , Andrea Doria, Peter K. Gregersen, Janine A. Lamb, Vidya Limaye, et al.

(2024) HUMAN GENETICS AND GENOMICS ADVANCES. 5(4).
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Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry

Ryan Malcolm Hum, James B Lilleker, Janine A Lamb, Alexander G S Oldroyd, Guochun Wang, Lucy R Wedderburn, Louise P Diederichsen, Jens Schmidt, Maria Giovanna Danieli, Paula Oakley, et al.

(2024) RHEUMATOLOGY. 63(8). p.2093-2100
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Identification of novel associations and localization of signals in idiopathic inflammatory myopathies using genome‐wide imputation

Simon Rothwell, Christopher I. Amos, Frederick W. Miller, Lisa G. Rider, Ingrid E. Lundberg, Peter K. Gregersen, Jiri Vencovsky, Neil McHugh, Vidya Limaye, Albert Selva‐O'Callaghan, et al.

(2023) ARTHRITIS & RHEUMATOLOGY. 75(6). p.1021-1027
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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

Daniel Zhou, Emily King, Simon Rothwell, Olga Krystufkova, Antonella Notarnicola, Rabheh Aziz, Emeli Lundstrom, Blanka Stiburkova, Lauren Pachman, Gulnara Mamyrova, et al.

(2023) CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. In Clinical and Experimental Rheumatology 41(2). p.416-416
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Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies

Danlei Zhou, Emily H. King, Simon Rothwell, Olga Krystufkova, Antonella Notarnicola, Samantha Coss, Rabheh Abdul-Aziz, Katherine E. Miller, Amanda Dang, G. Richard Yu, et al.

(2023) ANNALS OF THE RHEUMATIC DISEASES. 82(2). p.235-245
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Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups

Simon Rothwell, Hector Chinoy, Janine A Lamb, Frederick W Miller, Lisa G Rider, Lucy R Wedderburn, Neil J McHugh, Andrew L Mammen, Zoe E Betteridge, Sarah L Tansley, et al.

(2019) ANNALS OF THE RHEUMATIC DISEASES. 78(7). p.996-1002
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Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis

Joanna E Parkes, Simon Rothwell, Alexander Oldroyd, Hector Chinoy, Janine A Lamb, the Myositis Genetics Consortium (MYOGEN), Jan De Bleecker (UGent) and Boel De Paepe (UGent)

(2018) ARTHRITIS RESEARCH & THERAPY. 20.
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Immune-array analysis in sporadic inclusion body myositis reveals HLA-DRB1 amino acid heterogeneity across the myositis spectrum

Simon Rothwell, Robert G Cooper, Ingrid E Lundberg, Peter K Gregersen, Michael G Hanna, Pedro M Machado, Megan K Herbert, Ger JM Pruijn, James B Lilleker, Mark Roberts, et al.

(2017) ARTHRITIS & RHEUMATOLOGY. 69(5). p.1090-1099

Academic Bibliography

Genetic architecture of idiopathic inflammatory myopathies from meta‐analyses

Autoantibodies against a subunit of mitochondrial respiratory chain complex I in inclusion body myositis

Discovery of new myositis genetic associations through leveraging other immune-mediated diseases

Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry

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

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies

Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups

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

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