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

Thrombotic antiphospholipid syndrome shows strong haplotypic association with SH2B3-ATXN2 locus.

PloS one - 1 Jan 2013

Ochoa Eguzkine, Iriondo Mikel, Bielsa Ana, Ruiz-Irastorza Guillermo, Estonba Andone, Zubiaga Ana M

Abstract excerpt

BACKGROUND: Thrombotic antiphospholipid syndrome is defined as a complex form of thrombophilia that is developed by a fraction of antiphospholipid antibody (aPLA) carriers. Little is known about the genetic risk factors involved in thrombosis development among aPLA carriers. METHODS: To identify...

Read the complete abstract on PubMed

Topics

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

Share to Adaptor Proteins, Signal Transducing
Share to Antiphospholipid Syndrome
Share to Ataxins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to DNA Copy Number Variations

Share to Gene Order

Share to Genetic Loci

Share to Intracellular Signaling Peptides and Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 23844121
DOI: 10.1371/journal.pone.0067897
PMCID: PMC3701057

Genes

ATXN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23844121-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Thrombotic antiphospholipid syndrome shows strong haplotypic association with SH2B3-ATXN2 locus.PMID 23844121Read ↗

Genetic determinants of arterial thrombosis in primary antiphospholipid syndrome: a systematic review.Semantic proximity Read ↗

Identification of phenotypes in thrombotic primary antiphospholipid syndrome using cluster analysis: a step toward personalized medicine.Semantic proximity Read ↗

Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura.Semantic proximity Read ↗

Genetic analysis of patients with triple positive primary antiphospholipid syndromeSemantic proximity Read ↗

The association of STAT4 single nucleotide polymorphisms with thrombotic manifestations in a cohort of patients with autoimmune diseases and antiphospholipid antibodiesSemantic proximity Read ↗

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.Semantic proximity Read ↗

DNMT3A/TET2/ASXL1 mutations are an age-independent thrombotic risk factor in polycythemia vera patients: an observational studySemantic proximity Read ↗

A genome-wide association study suggests new susceptibility loci for primary antiphospholipid syndromeSemantic proximity Read ↗

Genetic Factors in Antiphospholipid Syndrome: Preliminary Experience with Whole Exome Sequencing.Semantic proximity Read ↗

A genome-wide association study in chronic thromboembolic pulmonary hypertension and the ADAMTS13-VWF axisSemantic proximity Read ↗

A Genome-Wide Association Study Suggests New Susceptibility Loci for Primary Antiphospholipid Syndrome.Semantic proximity Read ↗

A large-scale exome array analysis of venous thromboembolism.Semantic proximity Read ↗

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