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List of works by Lia Crotti

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Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes

scientific article published on 30 June 2016
Does Pregnancy Increase Cardiac Risk for LQT1 Patients With the KCNQ1-A341V Mutation?

AKAP9 is a genetic modifier of congenital long-QT syndrome type 1

scientific article
Mutation-specific risk in two genetic forms of type 3 long QT syndrome

scientific article published in January 2010
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies

scientific article published on 26 February 2016
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

scientific article published on 10 May 2017
Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1.

scientific article
Ion channel diseases in children: manifestations and management

scientific article published on May 2008
Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: implications for the clinical management of LQT3 patients

scientific article published on 14 October 2013
Novel Perspectives in Redox Biology and Pathophysiology of Failing Myocytes: Modulation of the Intramyocardial Redox Milieu for Therapeutic Interventions-A Review Article from the Working Group of Cardiac Cell Biology, Italian Society of Cardiology

scientific article
A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

scientific article published on 08 April 2014
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
The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2.

scientific article published on 12 April 2017
Can a Message From the Dead Save Lives?⁎⁎Editorials published in the Journal of the American College of Cardiologyreflect the views of the authors and do not necessarily represent the views of JACCor the American College of Cardiology

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

scientific article published on 01 September 2019
Cardiac arrhythmias of genetic origin are important contributors to sudden infant death syndrome

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2

scientific article published on 01 June 2019
Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

scientific article published on 14 November 2017
Congenital short QT syndrome.

scientific article
Response by Crotti et al to Letter Regarding Article, "Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?"

scientific article
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1.

scientific article published on 6 April 2018
Modifier genes for sudden cardiac death

scientific article published on 01 November 2018
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
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability.

scientific article
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?

scientific article published on August 2016
Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patients.

scientific article published in January 2013
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene

scientific article published on 06 March 2019
Neuroimmune crosstalk in the pathophysiology of hypertension

scientific article published on 01 August 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene.

scientific article published on 7 April 2018
Pleiotropic mutations in ion channels: What lies behind them?

scientific article published on 07 October 2010
Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT Syndrome

scientific article published on 01 May 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation

scientific article published on 13 April 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation

scientific article published on 27 March 2019
Corrigendum: Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies

scientific article published on 18 May 2016
Drug-induced long QT syndrome and exome sequencing: Chinese shadows link past and future

scientific article published on 19 February 2014
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

scientific article published in August 2018
Physical Inactivity Is a Risk Factor for Primary Ventricular Fibrillation

scientific article published on 01 April 2019
Genetic predisposition to sudden cardiac death

scientific article published on January 1, 2011
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk

scientific article published on 20 March 2020
International Triadin Knockout Syndrome Registry

scientific article published on 01 February 2019
Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation".

scientific article published in January 2016
Gene symbol: KCNQ1

article
Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients

scientific article published in January 2015
From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

Cadherin 2-Related Arrhythmogenic Cardiomyopathy

Gene symbol: SCN5A. Disease: Brugada syndrome

scientific article
Worldwide Survey of COVID-19–Associated Arrhythmias

scientific article published in March 2021
Reply to the Editor— Propranolol Prevents Life-Threatening Arrhythmias in LQT3 Transgenic Mice: Implications for the Clinical Management of LQT3 Patients

scientific article published on January 1, 2014

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