Search results (735)
« Back to PublicationsConcordance of genetic determinants of acute coronary artery disease between European and Chinese populations.
Journal article
Edris A. et al, (2026), Gigascience
Digital twin reconstruction of ventricular repolarisation identifies regional causes of T-wave abnormalities in hypertrophic cardiomyopathy
Preprint
Coleman JA. et al, (2026)
COVID-19 outcomes and persistent symptoms in patients with hypertrophic cardiomyopathy: association with pre-existing cardiovascular magnetic resonance phenotype.
Journal article
Singhal A. et al, (2026), Heart
Predictors of Long-Term Outcomes in Hypertrophic Cardiomyopathy: The NHLBI HCM Registry.
Journal article
HCMR Investigators . et al, (2026), JAMA
Biobank-Scale Plasma Proteomics Identifies Novel Biomarkers in Hypertrophic Cardiomyopathy.
Journal article
Chan JH. et al, (2026), Circ Genom Precis Med
Discovery of gene-alcohol interaction loci influencing blood pressure in 1.1 million individuals from multiple populations.
Preprint
Feitosa M. et al, (2026)
Rational discovery of therapeutic PAK1 allosteric activators.
Journal article
He Y. et al, (2026), Cell
Cardiomyopathy Gene Variants and Polygenic Risk Scores in Atrial Fibrillation: Evidence for an Atrial-First Phenotype.
Journal article
da Rocha GL. et al, (2026), J Am Coll Cardiol, 87, 1279 - 1299
Hypertrophic cardiomyopathy caused by filamin-C variants has restrictive and extracardiac features and a distinctive ECG.
Journal article
de Villiers C. et al, (2026), Heart Rhythm
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.
Preprint
Kramarenko DR. et al, (2026)
Left Atrial Reservoir Strain Predicts Atrial Fibrillation in Hypertrophic Cardiomyopathy: Insights from the NHLBI HCM Registry.
Journal article
Beyhoff N. et al, (2026), JACC Cardiovasc Imaging, 19, 133 - 135
Myocardial Entropy and Risk Predictors in Hypertrophic Cardiomyopathy: An Analysis From the NHLBI HCM Registry.
Journal article
Antiochos P. et al, (2025), Circ Cardiovasc Imaging, 18
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database.
Journal article
Gudmundsson S. et al, (2025), Nat Commun, 16