The GEnetic Syntax Score: a genetic risk assessment implementation tool grading the complexity of coronary artery disease-rationale and design of the GESS study.

doi:10.1186/s12872-021-02092-5

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

The GEnetic Syntax Score: a genetic risk assessment implementation tool grading the complexity of coronary artery disease-rationale and design of the GESS study.

BMC cardiovascular disorders - 8 Jun 2021

Vizirianakis Ioannis S, Chatzopoulou Fani, Papazoglou Andreas S, Karagiannidis Efstratios, Sofidis Georgios, Stalikas Nikolaos, Stefopoulos Christos, Kyritsis Konstantinos A, Mittas Nikolaos, Theodoroula Nikoleta F, Lampri Aggeliki, Mezarli Eleni, Kartas Anastasios, Chatzidimitriou Dimitrios, Papa-Konidari Anna, Angelis Eleftherios, Karvounis Ηaralambos, Sianos Georgios

Abstract excerpt

BACKGROUND: Coronary artery disease (CAD) remains one of the leading causes of mortality worldwide and is associated with multiple inherited and environmental risk factors. This study is designed to identify, design, and develop a panel of genetic markers that combined with clinical and angiographic information, will facilitate the creation of a personalized risk prediction algorithm (GEnetic Syntax Score-GESS)....

Read the complete abstract on PubMed

Topics

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

Share to Clinical Decision-Making

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Angiography

Share to Coronary Artery Disease

Share to Decision Support Techniques

Share to Gene Regulatory Networks

Share to Greece

Share to Predictive Value of Tests

Share to Research Design

Source

Open in PubMed Open full text

Identifiers

PMID: 34103005
DOI: 10.1186/s12872-021-02092-5
PMCID: PMC8186185

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

The GEnetic Syntax Score: a genetic risk assessment implementation tool grading the complexity of coronary artery disease-rationale and design of the GESS study.PMID 34103005Read ↗

Predicting coronary artery disease severity through genomic profiling and machine learning modelling: The GEnetic SYNTAX Score (GESS) trialSemantic proximity Read ↗

Genetic Risk StratificationSemantic proximity Read ↗

Novel Polygenic Risk Score and Established Clinical Risk Factors for Risk Estimation of Aortic Stenosis.Semantic proximity Read ↗

Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden.Semantic proximity Read ↗

An AI-Integrated Framework for Precision Genomics in Coronary Artery Disease Using Whole Exome and Phenotypic DataSemantic proximity Read ↗

Effect of disclosing a polygenic risk score for coronary heart disease on adverse cardiovascular events: 10-year follow-up of the MI-GENES randomized clinical trialSemantic proximity Read ↗

Polygenic Risk and Coronary Artery Disease Severity.Semantic proximity Read ↗

A Machine Learning Model Utilizing a Novel SNP Shows Enhanced Prediction of Coronary Artery Disease Severity.Semantic proximity Read ↗

Genetic risk score and cardiovascular mortality in a southern european population with coronary artery disease.Semantic proximity Read ↗

Genetics of coronary artery disease: should they impact the choice of revascularization?Semantic proximity Read ↗

Polygenic risk in early-onset coronary artery disease with low prevalence of traditional cardiovascular risk factors.Semantic proximity Read ↗

Common sequence variants associated with coronary artery disease correlate with the extent of coronary atherosclerosis.Semantic proximity Read ↗

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