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- 2019
- Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus
-
NCF1-339 polymorphism is associated with altered formation of neutrophil extracellular traps, high serum interferon activity and antiphospholipid syndrome in systemic lupus erythematosus
Linge, Petrus LU ; Arve, Sabine LU
;
Olsson, Lina M.
;
Leonard, Dag
;
Sjöwall, Christopher
;
Frodlund, Martina
;
Gunnarsson, Iva
;
Svenungsson, Elisabet
;
Tydén, Helena
LU
and
Jönsen, Andreas
LU
, et al.
(2019)
In Annals of the Rheumatic Diseases
Mark
- A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
- Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus
- 2018
- DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus
- 2017
- Indelning av de reumatiska sjukdomarna
- Vad är reumatologi?
- A single nucleotide polymorphism in the NCF1 gene leading to reduced oxidative burst is associated with systemic lupus erythematosus
- Novel risk genes for systemic lupus erythematosus predicted by random forest classification
- Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients
- 2016
- Case definitions in Swedish register data to identify systemic lupus erythematosus.
- Direct and indirect costs for systemic lupus erythematosus in Sweden. A nationwide health economic study based on five defined cohorts.
- 2014
- Systemic Lupus Erythematosus Prevalence in Sweden in 2010: What Do National Registers Say?
- 2013
- Association of STAT4 Polymorphism with Severe Renal Insufficiency in Lupus Nephritis.
- HLA-DRB1*04/*13 alleles are associated with vascular disease and antiphospholipid antibodies in systemic lupus erythematosus
- Coronary Heart Disease in Systemic Lupus Erythematosus Is Associated With Interferon Regulatory Factor-8 Gene Variants
- Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations
- NCR3/NKp30 Contributes to Pathogenesis in Primary Sjogren's Syndrome
- 2012
-
IgG glycan hydrolysis by endoglycosidase S diminishes the proinflammatory properties of immune complexes from patients with systemic lupus erythematosus: A possible new treatment?
Lood, Christian LU ; Allhorn, Maria LU ; Lood, Rolf LU ; Gullstrand, Birgitta LU ; Olin, Anders LU ; Ronnblom, Lars ; Truedsson, Lennart LU ; Collin, Mattias LU
and
Bengtsson, Anders
LU
(2012)
In Arthritis and Rheumatism
64(8).
p.2698-2706
Mark
-
IgG glycan hydrolysis by EndoS diminishes the pro-inflammatory properties of immune complexes from patients with SLE - a possible new treatment?
Lood, Christian LU ; Allhorn, Maria LU ; Lood, Rolf LU ; Gullstrand, Birgitta LU ; Olin, Anders LU ; Rönnblom, Lars ; Truedsson, Lennart LU ; Collin, Mattias LU
and
Bengtsson, Anders
LU
(2012)
In Arthritis and Rheumatism
71.
Mark
- Pharmacokinetics, tolerability, and preliminary efficacy of paquinimod (ABR-215757), a new quinoline-3-carboxamide derivative: Studies in lupus-prone mice and a multicenter, randomized, double-blind, placebo-controlled, repeat-dose, dose-ranging study in patients with systemic lupus erythematosus
- Clinical manifestations and anti-phospholipid antibodies in 712 patients with systemic lupus erythematosus: evaluation of two diagnostic assays.
- Association between genetic variants in the tumour necrosis factor/lymphotoxin alpha/lymphotoxin beta locus and primary Sjogren's syndrome in Scandinavian samples
- 2011
- Potential association of muscarinic receptor 3 gene variants with primary Sjogren's syndrome
- Mutations in genes encoding complement inhibitors CD46 and CFH affect the age at nephritis onset in patients with systemic lupus erythematosus
- A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE
- 2010
- Gene Variants In Fam167A-Blk And Tnfsf4 Are Associated With Primary Sjogren'S Syndrome
- A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus
- 2009
- C1q inhibits immune complex induced IFN-alpha production in plasmacytoid dendritic cells-A novel link between C1q deficiency and SLE pathogenesis
- C1q Inhibits Immune Complex-Induced Interferon-alpha Production in Plasmacytoid Dendritic Cells A Novel Link Between C1q Deficiency and Systemic Lupus Erythematosus Pathogenesis
- A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
- 2008
- Effect on interferon-inducible gene expression signature by ABR215757, a new drug in development for SLE
- Role of C1q in regulation of IFN-alpha production
- A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5
- Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX