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

Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal.

Neuromuscular disorders : NMD - 1 Feb 2008

Needham Merrilee, Hooper Amanda, James Ian, van Bockxmeer Frank, Corbett Alastair, Day Timothy, Garlepp Michael J, Mastaglia Frank L

Abstract excerpt

Previous studies have differed as to whether APOE epsilon4 is a susceptibility factor for developing sporadic inclusion body myositis (sIBM), with a positive association being found only in an Australian cohort of cases. We have now re-examined this in a larger cohort of 57 sIBM cases and have also carried out a meta-analysis of all the published studies looking for evidence of a risk association or effect of...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Alleles

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Apolipoprotein E2

Share to Apolipoprotein E4

Share to APOE gene

Share to Genetic Predisposition to Disease

Share to Myositis, Inclusion Body

Share to Risk Factors

Source

Identifiers

PMID: 18060780
DOI: 10.1016/j.nmd.2007.09.005

Genes

APOE

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

Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal.PMID 18060780Read ↗

Genetics of inclusion-body myositis.Semantic proximity Read ↗

Association study reveals novel risk loci for sporadic inclusion body myositis.Semantic proximity Read ↗

Apolipoprotein E epsilon 4 in inclusion body myositis.Semantic proximity Read ↗

Sporadic inclusion body myositis: variability in prevalence and phenotype and influence of the MHC.Semantic proximity Read ↗

Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis.Semantic proximity Read ↗

Genetic advances in sporadic inclusion body myositis.Semantic proximity Read ↗

Apolipoprotein E allele frequencies in sporadic inclusion body myositis.Semantic proximity Read ↗

Apolipoprotein E and alpha-1-antichymotrypsin polymorphisms in sporadic inclusion body myositis.Semantic proximity Read ↗

The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis.Semantic proximity Read ↗

Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype.Semantic proximity Read ↗

Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases.Semantic proximity Read ↗

High-resolution HLA genotyping in inclusion body myositis refines 8.1 ancestral haplotype association to DRB1*03:01:01 and highlights pathogenic role of arginine-74 of DRβ1 chain.Semantic proximity Read ↗

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