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

Is there still room for additional common susceptibility alleles for venous thromboembolism?

Journal of thrombosis and haemostasis : JTH - 1 Sept 2016

Trégouët D A, Delluc A, Roche A, Derbois C, Olaso R, Germain M, de Andrade M, Tang W, Chasman D I, van Hylckama Vlieg A, Reitsma P H, Kabrhel C, Smith N, Morange P E

Abstract excerpt

UNLABELLED: Essentials Genetic architecture of venous thromboembolism (VTE) remains to be fully disentangled. 11 newly discovered candidate polymorphisms were genotyped in 3019 VTE cases and 2605 controls. None of the 11 polymorphisms were significantly associated with VTE risk. Additional major efforts are needed to identify VTE-associated genetic variants. SUMMARY: Background Through a meta-analysis of 12...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to France

Share to Genome-Wide Association Study

Share to Regression Analysis

Share to Risk Factors

Share to Venous Thromboembolism

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 27326655
DOI: 10.1111/jth.13392
PMCID: PMC5152582

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

Is there still room for additional common susceptibility alleles for venous thromboembolism?PMID 27326655Read ↗

What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies.Semantic proximity Read ↗

Deciphering the molecular basis of venous thromboembolism: where are we and where should we go?Semantic proximity Read ↗

Venous thromboembolic disease genetics: from variants to function.Semantic proximity Read ↗

Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.Semantic proximity Read ↗

Genetic risk factors for venous thromboembolism.Semantic proximity Read ↗

Common genetic risk factors of venous thromboembolism in Western and Asian populations.Semantic proximity Read ↗

GENETIC DETERMINANTS OF THROMBOSIS.Semantic proximity Read ↗

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.Semantic proximity Read ↗

The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.Semantic proximity Read ↗

Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.Semantic proximity Read ↗

[Advances in the genetics of venous thromboembolic disease].Semantic proximity Read ↗

A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.Semantic proximity Read ↗

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