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List of works by Maria-Christina Kotta

Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk

scientific article published on 20 March 2020

Biventricular Arrhythmogenic Cardiomyopathy: a paradigmatic case

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

scientific article published on 01 September 2019

Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the Young

scientific article published on 06 December 2018

Calmodulinopathy: Functional Effects of CALM Mutations and Their Relationship With Clinical Phenotypes

scientific article published on 11 December 2018

Cardiac ion channel gene mutations in Greek long QT syndrome patients ⬇️

scientific article published on January 1, 2010

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

scientific article published on 10 May 2017

Effects of mutations and genetic overlap in inherited long-QT and Brugada arrhythmia syndromes.

scientific article

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

scientific article published on 7 September 2020

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

scientific article published on 19 October 2020

Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.

scientific article

Is Careful Assessment of Rare Variants in the RYR2 Gene Piercing the Guidelines' Strong Armor?

scientific article published on 01 February 2018

Phenotype reveals genotype in a Greek long QT syndrome family

scientific article published on 16 March 2006

Sudden Infant Death Syndrome and Genetics: Don't Throw Out the Infant With the Dirty Water

scientific article published on 01 March 2018

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

scientific article published on 5 October 2017

The role of genetics in primary ventricular fibrillation, inherited channelopathies and cardiomyopathies.

scientific article published on June 2017

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