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

The incidence of the thrombophilic SNPs rs6025, rs1799963, rs2066865, rs2289252, and rs8176719 in chronic thromboembolic pulmonary hypertension.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis - 1 Jan 2000

Kvasnička Jan, Jansa Pavel, Cífková Renata, Dušková Daniela, Bobčíková Petra, Ševčík Martin, Zenáhlíková Zuzana, Kvasnička Tomáš

Abstract excerpt

INTRODUCTION: Chronic thromboembolic pulmonary hypertension (CTEPH) and venous thromboembolism (VTE) are thought to share many common risk factors. Our study aimed to determine the frequencies of 5 thrombosis-related gene single nucleotide polymorphisms (SNPs) associated with VTE in patients with CTEPH (n 129) compared with a control group of healthy individuals without a history of VTE (n 2637). METHODS: The...

Read the complete abstract on PubMed

Topics

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

Share to ABO Blood-Group System
Share to Factor V

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibrinogen

Share to Hypertension, Pulmonary

Share to Prothrombin

Share to Pulmonary Embolism

Share to Thrombophilia

Share to Venous Thromboembolism

Source

Open in PubMed Open full text

Identifiers

PMID: 39150410
DOI: 10.1177/10760296241271369
PMCID: PMC11329958

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The incidence of the thrombophilic SNPs rs6025, rs1799963, rs2066865, rs2289252, and rs8176719 in chronic thromboembolic pulmonary hypertension.PMID 39150410Read ↗

Shared and Distinct Genomics of Chronic Thromboembolic Pulmonary Hypertension and Pulmonary Embolism.Semantic proximity Read ↗

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

Identification of the Novel Variants in Patients With Chronic Thromboembolic Pulmonary Hypertension.Semantic proximity Read ↗

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

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

The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls.Semantic proximity Read ↗

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

Genetic and Clinical Determinants of Chronic Thromboembolic Pulmonary Hypertension: The Role of PAI-1 Polymorphism.Semantic proximity Read ↗

CTEPH has shared and distinct genetic associations with pulmonary embolism in a genome-wide association studySemantic proximity Read ↗

Myeloproliferative Diseases as Possible Risk Factor for Development of Chronic Thromboembolic Pulmonary Hypertension-A Genetic Study.Semantic proximity Read ↗

Fibrinogen Aα Thr312Ala polymorphism specifically contributes to chronic thromboembolic pulmonary hypertension by increasing fibrin resistance.Semantic proximity Read ↗

Molecular Research in Chronic Thromboembolic Pulmonary HypertensionSemantic proximity Read ↗

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