Luis Lopes

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Associate Professor

University College London

United Kingdom

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About

Dr. Luis Lopes is an Associate Professor at University College London, specializing in cardiomyopathy and its genetic implications. His recent research includes the reassessment of genetic variants in cardiomyopathy and the electrophysiological characteristics of various cardiac conditions. He has also contributed to studies on hypertrophic cardiomyopathy and personalized treatment approaches, focusing on mechanical, demographic, and genetic factors. His work aims to enhance the understanding and clinical management of cardiac diseases, particularly in the context of arrhythmias and heart structure.

Recent Grants

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Discovering the causes of mutation-negative hypertrophic cardiomyopathy

Open Date: 2019-10-14

Close Date: 2022-10-13

Grant: Close

Discovering the causes of mutation-negative hypertrophic cardiomyopathy

Open Date: 2019-10-01

Close Date: 2022-10-01

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2022

Collaborators (18)

William Weintraub

UNITED STATES

Luis Lopes

Research Interests

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About

Recent Grants

Articles (20)

Reassessment and reclassification of variants of unknown significance in patients with cardiomyopathy in a specialist department

The Mechanical and Perfusion Basis of Exercise Limitation in Apical Hypertrophic Cardiomyopathy

Electrophysiological Characterization of Subclinical and Overt Hypertrophic Cardiomyopathy by Magnetic Resonance Imaging-Guided Electrocardiography

Demographic-Based Personalized Left Ventricular Hypertrophy Thresholds for Hypertrophic Cardiomyopathy Diagnosis.

Electrophysiological Phenotype-Genotype Study of Sustained Monomorphic Ventricular Tachycardia in Inherited, High Arrhythmic Risk, Left Ventricular Cardiomyopathy.

Genetic basis of right and left ventricular heart shape

Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice

Mitral Annulus Disjunction: A Comprehensive Cardiovascular Magnetic Resonance Phenotype and Clinical Outcomes Study

Distal Ventricular Pacing for Drug-Refractory Mid-Cavity Obstructive Hypertrophic Cardiomyopathy: A Randomized, Placebo-Controlled Trial of Personalized Pacing.

Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy.

Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy

Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank Participants

Natural History of MYH7-Related Dilated Cardiomyopathy

Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

Integrin a7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice.

Focando no Ventrículo Direito na Síndrome PRKAG2

Early Childhood-Onset Hypertrophic Cardiomyopathy in a Family With an In-Frame MYH7 Deletion

Blunted coronary flow velocity reserve is associated with impairment in systolic function and functional capacity in hypertrophic cardiomyopathy

Precision measurement of cardiac structure and function in cardiovascular magnetic resonance using machine learning

Collaborators (18)

William Weintraub

Alan Pittman

Andreia Nunes

james moon

Juan Pablo Kaski

Eduardo Villacorta

Javier Limeres Freire

Christopher M Kramer

Andrew Landstrom

Javier Bermejo

George Joy

Róbert Sepp

Michele Orini

Jens Mogensen

Emma Matthews

Alessandra Esposito

Perry Elliott

Anuj Goel

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