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Professor Pier Lambiase

Barts Heart Centre, London (United Kingdom of Great Britain & Northern Ireland)

Prof. Pier Lambiase is Professor of Cardiology at UCL & leads the Inherited arrhythmia service at Barts Heart Centre aswell as the clinical electrophysiology research group. He has published widely on arrhythmia mechanisms in specific inherited conditions and co-authored/advised national & international guidelines on genetic diagnosis aswell as sudden death prevention in inherited ion channel disorders (JACC 2015-2016, ESC 2021). He described the arrhythmogenic phenotypes in Brugada Syndrome (Circulation 2009) and ARVC (Eur Ht J, 2012). He has published over 200 peer review papers and raised >£5M in grants from BHF, Welcome Trust & MRC over the past 5 years & was awarded the BCS Michael Davies early career research award in 2015. He leads a biomedical engineering group to utilise high density electrical mapping data to enable deep phenotyping of specific gene mutation carriers aswell as UK Biobank population data combining genomic and physiological parameters (MRC project grant).

Weighty matters! Deciding the best care for atrial fibrillation patients with obesity

Event: ESC Congress 2024

Topic: Pathophysiology and Mechanisms

Session type: Symposium

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The dilemma of sudden cardiac death prediction in low-risk populations

Event: ESC Congress 2024

Topic: Epidemiology, Prognosis, Outcome

Session type: Advances in Science

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Atrial fibrillation: treatment 7 - ablation

Event: EHRA 2024

Topic: Atrial Fibrillation (AF)

Session type: Moderated ePosters

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Clinical - Genetics

Event: EHRA 2023

Topic: Basic Science

Session type: Abstract Sessions

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Ventricular arrhythmias and SCD Round 2

Event: EHRA 2023

Topic: Ventricular Arrhythmias and Sudden Cardiac Death (SCD)

Session type: Clinical Cases

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Inherited diseases and ventricular arrhythmias

Event: ESC Congress 2021 - The Digital Experience

Topic: Ventricular Arrhythmias and Sudden Cardiac Death (SCD)

Session type: Abstract Sessions

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Meet the Experts - Brugada Syndrome: all you need to know

Event: ESC Congress 2019

Topic: Ion Channel Disorders

Session type: Focus with the Experts

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Devices in inherited cardiac conditions

Event: EHRA 2018

Topic: Device Therapy

Session type: How To ...

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Inherited arrhythmogenic diseases: genetics, risk stratification and sudden cardiac death

Event: EHRA EUROPACE - CARDIOSTIM 2017

Topic: Molecular biology / genetics

Session type: New ESC Guidelines

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Prediction of sudden death: do we have a crystal ball?

Event: ESC Congress 2016

Topic: Sudden death / resuscitation

Session type: Advances in Science

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