Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mannose-binding lectin variant alleles and the risk of arterial thrombosis in systemic lupus erythematosus.

The New England journal of medicine - 15 Jul 2004

Øhlenschlaeger Tommy, Garred Peter, Madsen Hans O, Jacobsen Søren

Abstract excerpt

BACKGROUND: Cardiovascular disease is an important complication in patients with systemic lupus erythematosus (SLE). Variant alleles of the mannose-binding lectin gene are associated with SLE as well as with severe atherosclerosis. We determined whether mannose-binding lectin variant alleles were associated with an increased risk of arterial thrombosis among patients with SLE. METHODS: Mannose-binding lectin...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Antibodies, Anticardiolipin
Share to Incidence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lupus Erythematosus, Systemic

Share to Mannose-Binding Lectin

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Share to Risk Factors

Share to Thrombosis

Source

Identifiers

PMID: 15254284
DOI: 10.1056/NEJMoa033122

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mannose-binding lectin variant alleles and the risk of arterial thrombosis in systemic lupus erythematosus.PMID 15254284Read ↗

Systemic lupus erythematosus in a multiethnic US cohort: XXXIV. Deficient mannose-binding lectin exon 1 polymorphisms are associated with cerebrovascular but not with other arterial thrombotic events.Semantic proximity Read ↗

Genetic risk factors for thrombosis in systemic lupus erythematosus.Semantic proximity Read ↗

Association of mannose-binding lectin gene polymorphisms with antiphospholipid syndrome, cardiovascular disease and chronic damage in patients with systemic lupus erythematosus.Semantic proximity Read ↗

Mannose-binding lectin polymorphisms and susceptibility to infection in systemic lupus erythematosus.Semantic proximity Read ↗

HLA-DRB1*04/*13 alleles are associated with vascular disease and antiphospholipid antibodies in systemic lupus erythematosus.Semantic proximity Read ↗

A polymorphism in TLR2 is associated with arterial thrombosis in a multiethnic population of patients with systemic lupus erythematosus.Semantic proximity Read ↗

Factor V Leiden, antiphospholipid antibodies and thrombosis in systemic lupus erythematosus.Semantic proximity Read ↗

A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus.Semantic proximity Read ↗

Thrombosis in systemic lupus erythematosus: congenital and acquired risk factors.Semantic proximity Read ↗

Factor V Leiden and prothrombin G20210A mutations and the risk of atherothrombotic events in systemic lupus erythematosus.Semantic proximity Read ↗

Novel gene variants associated with cardiovascular disease in systemic lupus erythematosus and rheumatoid arthritis.Semantic proximity Read ↗

Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.