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

Whole-exome sequencing in evaluation of patients with venous thromboembolism

29 Jun 2017

Abstract excerpt

genes, and highly conserved areas of other genes with established or potential roles in coagulation or fibrinolysis. Ten patients (15.6%) had >1 variant. Sanger sequencing performed in family members of 4 study patients with and without VTE showed generally concordant results with thrombotic history. WES and extended thrombophilia testing are promising tools for improving our understanding of VTE pathogenesis and...

Read the complete abstract on PubMed

Topics

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

Share to Blood Coagulation and Thrombosis Mechanisms
Share to Hemophilia Treatment and Research
Share to Venous Thromboembolism Diagnosis and Management

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29296762
DOI: 10.1182/bloodadvances.2017005249

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole-exome sequencing in evaluation of patients with venous thromboembolismPMID 29296762Read ↗

Exploring genetic drivers of unexplained venous thromboembolism through whole-exome sequencing.Semantic proximity Read ↗

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

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

Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.Semantic proximity Read ↗

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

Multigene panel for thrombophilia testing in venous thromboembolism.Semantic proximity Read ↗

Assessment of a next generation sequencing gene panel strategy in 133 patients with negative thrombophilia screening.Semantic proximity Read ↗

Next-generation sequencing strategies in venous thromboembolism: in whom and for what purpose?Semantic proximity Read ↗

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.Semantic proximity Read ↗

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

Cross-Ancestry Investigation of Venous Thromboembolism Genomic PredictorsSemantic proximity Read ↗

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

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