Andrei Alexsson

Uppsala, C, Sweden

Last Updated: 09/26/2026

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Found 15 publications

Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome.

Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome.

Journal: RMD open

Published: July 19, 2021

Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort.

Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: May 14, 2021

Variants in BANK1 are associated with lupus nephritis of European ancestry.

Variants in BANK1 are associated with lupus nephritis of European ancestry.

Journal: Genes and immunity

Published: February 26, 2021

PD-L1 and IDO1 are potential targets for treatment in patients with primary diffuse large B-cell lymphoma of the CNS.

PD-L1 and IDO1 are potential targets for treatment in patients with primary diffuse large B-cell lymphoma of the CNS.

Journal: Acta oncologica (Stockholm, Sweden)

Published: February 13, 2021

Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus.

Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus.

Journal: Annals of the rheumatic diseases

Published: December 15, 2020

Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing.

Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing.

Journal: Annals of the rheumatic diseases

Published: July 20, 2020

High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus.

High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus.

Journal: Annals of the rheumatic diseases

Published: August 27, 2019

Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus.

Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus.

Journal: Annals of the rheumatic diseases

Published: March 26, 2019

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts.

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts.

Journal: European journal of human genetics : EJHG

Published: April 28, 2018

Novel gene variants associated with cardiovascular disease in systemic lupus erythematosus and rheumatoid arthritis.

Novel gene variants associated with cardiovascular disease in systemic lupus erythematosus and rheumatoid arthritis.

Journal: Annals of the rheumatic diseases

Published: October 30, 2017

DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus.

DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus.

Journal: Annals of the rheumatic diseases

Published: September 12, 2017

Plasmacytoid dendritic cells and RNA-containing immune complexes drive expansion of peripheral B cell subsets with an SLE-like phenotype.

Plasmacytoid dendritic cells and RNA-containing immune complexes drive expansion of peripheral B cell subsets with an SLE-like phenotype.

Journal: PloS one

Published: May 04, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026