Pantazis I. Theotokis

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 25 publications

Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.

Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.

Journal: Research square

Published: February 06, 2026

Unsupervised feature extraction using deep learning empowers discovery of genetic determinants of the electrocardiogram.

Unsupervised feature extraction using deep learning empowers discovery of genetic determinants of the electrocardiogram.

Journal: Genome medicine

Published: February 08, 2025

Sex Differences in the Genetic Causes of Dilated Cardiomyopathy.

Sex Differences in the Genetic Causes of Dilated Cardiomyopathy.

Journal: Journal of the American College of Cardiology

Published: December 12, 2024

Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy.

Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy.

Journal: Circulation. Genomic and precision medicine

Published: November 28, 2023

Genetic constraint at single amino acid resolution in protein domains improves missense variant prioritisation and gene discovery.

Genetic constraint at single amino acid resolution in protein domains improves missense variant prioritisation and gene discovery.

Journal: Genome medicine

Published: September 18, 2023

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy.

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy.

Journal: Nature genetics

Published: September 13, 2023

Cardiomyopathies in 100,000 genomes project: interval evaluation improves diagnostic yield and informs strategies for ongoing gene discovery.

Cardiomyopathies in 100,000 genomes project: interval evaluation improves diagnostic yield and informs strategies for ongoing gene discovery.

Journal: Genome medicine

Published: July 30, 2023

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.

Journal: medRxiv : the preprint server for health sciences

Published: April 17, 2023

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.

Journal: Genome medicine

Published: April 04, 2023

Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings.

Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings.

Journal: Nature genetics

Published: March 30, 2023

The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.

The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.

Journal: American journal of human genetics

Published: March 15, 2023

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences

Published: February 13, 2023

Showing 1-12 of 25

Last Updated: 09/26/2026