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Marika Kvarnström

Researcher at Karolinska Institutet

Publications -  58
Citations -  1825

Marika Kvarnström is an academic researcher from Karolinska Institutet. The author has contributed to research in topics: Population & Autoantibody. The author has an hindex of 19, co-authored 50 publications receiving 1304 citations. Previous affiliations of Marika Kvarnström include Karolinska University Hospital.

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Journal ArticleDOI

Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjogren's syndrome.

Christopher J. Lessard, +67 more
- 01 Nov 2013 - 
TL;DR: The results highlight the importance of genes that are involved in both innate and adaptive immunity in Sjögren's syndrome, including TNFAIP3, PTTG1, PRDM1, DGKQ, FCGR2A, IRAK1BP1, ITSN2 and PHIP, among others.
Journal ArticleDOI

Influence of geolocation and ethnicity on the phenotypic expression of primary Sjögren's syndrome at diagnosis in 8310 patients: a cross-sectional study from the Big Data Sjögren Project Consortium.

Pilar Brito-Zerón, +49 more
TL;DR: This study provides the first evidence of a strong influence of geolocation and ethnicity on the phenotype of primary Sjögren's syndrome at diagnosis.
Journal Article

How immunological profile drives clinical phenotype of primary Sjögren's syndrome at diagnosis: analysis of 10,500 patients (Sjögren Big Data Project).

Pilar Brito-Zerón, +51 more
TL;DR: The strong influence of immunological markers on the phenotype of primary SjS at diagnosis is confirmed in the largest multi-ethnic international cohort ever analysed, with a greater influence for cryoglobulinaemic-related markers in comparison with Ro/La autoantibodies and ANA.
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The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.

Leah C. Kottyan, +81 more
TL;DR: Both SLE elements of the statistical model appear to operate in Sjögren's syndrome and systemic sclerosis whereas only the IRF5-TNPO3 gene-spanning haplotype is associated with primary biliary cirrhosis, demonstrating the nuance of similarity and difference in autoimmune disease risk mechanisms at IRF 5- TNPO3.