Adrien Bloch

Life-threatening events in patients with LQT3 on and off beta-blockers: Insights from a case series.

Journal: Heart rhythm O2

Published: February 16, 2026

Distinct patterns of ventricular fibrillation onset in primary electrical diseases: insights from a retrospective multicentre registry.

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: July 26, 2025

Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathies.

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: July 04, 2025

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome.

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 30, 2025

Making Sense of Missense: Benchmarking MutScore for Variant Interpretation in Inherited Cardiac Diseases.

Journal: Molecular diagnosis & therapy

Published: April 27, 2025

Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathies.

Journal: International journal of cardiology

Published: June 25, 2024

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Journal: Heart rhythm

Published: June 06, 2024

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.

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: March 05, 2024

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Journal: Clinical genetics

Published: December 06, 2023

Molecular genetic screening after non-ischaemic sudden cardiac arrest and no overt cardiomyopathy in real life: A major tool for the aetiological diagnostic work-up.

Journal: Archives of cardiovascular diseases

Published: October 20, 2023

Life-threatening events in patients with LQT3 on and off beta-blockers: Insights from a case series.

Life-threatening events in patients with LQT3 on and off beta-blockers: Insights from a case series.

Distinct patterns of ventricular fibrillation onset in primary electrical diseases: insights from a retrospective multicentre registry.

Distinct patterns of ventricular fibrillation onset in primary electrical diseases: insights from a retrospective multicentre registry.

Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathies.

Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathies.

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome.

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome.

Making Sense of Missense: Benchmarking MutScore for Variant Interpretation in Inherited Cardiac Diseases.

Making Sense of Missense: Benchmarking MutScore for Variant Interpretation in Inherited Cardiac Diseases.

Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathies.

Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathies.

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Molecular genetic screening after non-ischaemic sudden cardiac arrest and no overt cardiomyopathy in real life: A major tool for the aetiological diagnostic work-up.

Molecular genetic screening after non-ischaemic sudden cardiac arrest and no overt cardiomyopathy in real life: A major tool for the aetiological diagnostic work-up.

Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?

Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?

Titin copy number variations associated with dominant inherited phenotypes.

Titin copy number variations associated with dominant inherited phenotypes.