Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.

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

Community

Back to search

Article

Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.

Thrombosis and haemostasis - 1 Oct 2008

Arnold Marie-Luise, Lichy Christoph, Werner Inge, Radbruch Alexander, Wagner Simone, Grond-Ginsbach Caspar

Abstract excerpt

Variation in the gene that encodes the vitamin K epoxide reductase subunit 1 (VKORC1) was recently proposed as a genetic risk factor for stroke in a Chinese population. In this ethnic group, only two common haplotypes were observed, with the C-allele of the polymorphism rs2359612 (VKORC1: c.283+837C>T) associated with stroke and other cardiovascular diseases. Recently, the influence of VKORC1 haplotypes on venous...

Read the complete abstract on PubMed

Topics

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

Share to Age Distribution

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Brain Ischemia

Share to Germany

Share to Haplotypes

Share to Mixed Function Oxygenases

Share to Risk Factors

Share to Stroke

Share to Vitamin K Epoxide Reductases

Source

Open in PubMed

Identifiers

PMID: 18841283

Genes

VKORC1

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

Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.PMID 18841283Read ↗

Association between VKORC1 gene polymorphisms and ischemic cerebrovascular disease in Chinese Han population.Semantic proximity Read ↗

Association of functional VKORC1 promoter polymorphism with occurrence and clinical aspects of ischemic stroke in a Greek population.Semantic proximity Read ↗

Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans.Semantic proximity Read ↗

G-1639A but Not C1173T VKORC1 Gene Polymorphism Is Related to Ischemic Stroke and Its Various Risk Factors in Ukrainian Population.Semantic proximity Read ↗

VKORC1 haplotypes are associated with arterial vascular diseases (stroke, coronary heart disease, and aortic dissection).Semantic proximity Read ↗

VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation.Semantic proximity Read ↗

First study of C2491T FV mutation with ischaemic stroke risk in Morocco.Semantic proximity Read ↗

Genetic polymorphism of vitamin K epoxide reductase (VKORC1) 1173C>T in a Chinese and a Caucasian population.Semantic proximity Read ↗

A genetic study of Factor V Leiden (G1691A) mutation in young ischemic strokes with large vessel disease in a South Indian population.Semantic proximity Read ↗

Main haplotypes and mutational analysis of vitamin K epoxide reductase (VKORC1) in a Swedish population: a retrospective analysis of case records.Semantic proximity Read ↗

Thrombophilia screening in young patients with cryptogenic stroke. Prevalence of gene polymorphisms compared to healthy blood donors and impact on secondary stroke prevention.Semantic proximity Read ↗

The rs2108622 polymorphism is related to the early risk of ischemic stroke in non-valvular atrial fibrillation subjects under oral anticoagulation.Semantic proximity Read ↗

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