Chrysoula Dalageorgou
St George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype.
Journal: International journal of cardiology
Published: June 11, 2019
Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation database.
Journal: European journal of human genetics : EJHG
Published: November 16, 2017
Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy.
Journal: European journal of medical genetics
Published: June 06, 2015
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: May 03, 2015
Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.
Journal: Heart (British Cardiac Society)
Published: October 30, 2014
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.
Journal: Journal of medical genetics
Published: February 12, 2013
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.
Journal: Circulation. Cardiovascular genetics
Published: November 22, 2011
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.
Journal: Journal of the American College of Cardiology
Published: November 09, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026