Emeli Lundstrom
Solna, AB, Sweden
Last Updated: 09/26/2026
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Found 8 publications
Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies.
Journal: Annals of the rheumatic diseases
Published: June 15, 2022
Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome.
Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: March 17, 2022
Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases.
Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: September 21, 2021
Four Systemic Lupus Erythematosus Subgroups, Defined by Autoantibodies Status, Differ Regarding HLA-DRB1 Genotype Associations and Immunological and Clinical Manifestations.
Journal: ACR open rheumatology
Published: July 10, 2021
Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
Journal: Annals of the rheumatic diseases
Published: April 10, 2015
HLA-DRB1*04/*13 alleles are associated with vascular disease and antiphospholipid antibodies in systemic lupus erythematosus.
Journal: Annals of the rheumatic diseases
Published: August 16, 2012
Genetic evidence for involvement of adaptive immunity in the development of IgA nephropathy: MHC class II alleles are protective in a Caucasian population.
Journal: Human immunology
Published: June 10, 2012
Very high levels of anti-citrullinated protein antibodies are associated with HLA-DRB1*15 non-shared epitope allele in patients with rheumatoid arthritis.
Journal: Arthritis and rheumatism
Published: February 07, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026