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| 35653516 | PHACTR1 modulates vascular compliance but not endothelial function: a translational study. | Cardiovascular Research | 2023 |
| 36441173 | Left ventricular anatomy in obstructive hypertrophic cardiomyopathy: beyond basal septal hypertrophy. | Eur Heart J Cardiovasc Imaging | 2023 |
| 38032573 | Exercise Capacity in Patients With Obstructive Hypertrophic Cardiomyopathy: SEQUOIA-HCM Baseline Characteristics and Study Design. | | 2023 |
| 38014537 | Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy. | | 2023 |
| 36778260 | Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy. | medRxiv | 2023 |
| 36899856 | Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in . | | 2023 |
| 37398003 | Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. | medRxiv | 2023 |
| 37017090 | Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2023 |
| 36702559 | Proteomic profiling identifies novel independent relationships between inflammatory proteins and myocardial infarction. | | 2023 |
| 37127261 | Comparing the effects of chemical Ca dyes and R-GECO on contractility and Ca transients in adult and human iPSC cardiomyocytes. | | 2023 |
| 36693378 | Loci for insulin processing and secretion provide insight into type 2 diabetes risk. | Am J Hum Genet | 2023 |
| 36691918 | Apolipoprotein Proteomics for Residual Lipid-Related Risk in Coronary Heart Disease. | | 2023 |
| 36918541 | Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. | Nat Commun | 2023 |
| 36599608 | Phase 2 Study of Aficamten in Patients With Obstructive Hypertrophic Cardiomyopathy. | J Am Coll Cardiol | 2023 |
| 34949103 | Provocation Testing and Therapeutic Response in a Newly Described Channelopathy: RyR2 Calcium Release Deficiency Syndrome. | Circ Genom Precis Med | 2022 |
| 36049495 | Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials. | Lancet | 2022 |
| 35692049 | Right ventricular function declines prior to left ventricular ejection fraction in hypertrophic cardiomyopathy. | Journal of Cardiovascular Magnetic Resonance | 2022 |
| 35803063 | Oxidized phospholipids on apolipoprotein B-100 versus plasminogen and risk of coronary heart disease in the PROCARDIS study. | Atherosclerosis | 2022 |
| 36267857 | Massively Parallel Sequencing of 43 Arrhythmia Genes in a Selected SUDI Cohort from Cape Town. | Journal of Pediatric Genetics | 2022 |
| 34672391 | Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes. | Genetic Epidemiology | 2022 |
| 34635131 | Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance study. | Journal of Cardiovascular Magnetic Resonance | 2021 |
| 34018815 | CalTrack: High-Throughput Automated Calcium Transient Analysis in Cardiomyocytes. | Circ Res | 2021 |
| 33637999 | Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant. | Basic Research in Cardiology | 2021 |
| 34229451 | Toward Replacing Late Gadolinium Enhancement With Artificial Intelligence Virtual Native Enhancement for Gadolinium-Free Cardiovascular Magnetic Resonance Tissue Characterization in Hypertrophic Cardiomyopathy. | Circulation | 2021 |
| 33891679 | A titan of Cardiovascular Research: Professor Peter Sleight (1929-2020). | Cardiovascular Research | 2021 |
| 34152793 | Time to Think Differently About Sarcomere-Negative Hypertrophic Cardiomyopathy. | Circulation | 2021 |
| 34147459 | Maximal Wall Thickness Measurement in Hypertrophic Cardiomyopathy: Biomarker Variability and its Impact on Clinical Care. | JACC Cardiovasc Imaging | 2021 |
| 33876560 | FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer. | J Thromb Haemost | 2021 |
| 33607192 | Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study. | Int J Cardiol | 2021 |
| 33558525 | Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33822779 | Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. | PLoS Genet | 2021 |
| 33712616 | Bi-allelic MCM10 variants associated with immune dysfunction and cardiomyopathy cause telomere shortening. | Nat Commun | 2021 |
| 33437986 | Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. | Hum Mol Genet | 2021 |
| 33495596 | Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. | Nat Genet | 2021 |
| 33356370 | Lp(a) (Lipoprotein[a]), an Exemplar for Precision Medicine: Insights From UK Biobank. | Arteriosclerosis, Thrombosis, and Vascular Biology | 2021 |
| 32732227 | Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy. | Journal of Medical Genetics | 2021 |
| 33402679 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 34780254 | Association Between Sarcomeric Variants in Hypertrophic Cardiomyopathy and Myocardial Oxygenation: Insights From a Novel Oxygen-Sensitive Cardiovascular Magnetic Resonance Approach. | Circulation | 2021 |
| 32618513 | Dilated cardiomyopathy mutations in thin-filament regulatory proteins reduce contractility, suppress systolic Ca, and activate NFAT and Akt signaling. | American Journal of Physiology - Heart and Circulatory Physiology | 2020 |
| 32083971 | Mavacamten rescues increased myofilament calcium sensitivity and dysregulation of Ca flux caused by thin filament hypertrophic cardiomyopathy mutations. | American Journal of Physiology - Heart and Circulatory Physiology | 2020 |
| 31584065 | A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction. | Cardiovascular Research | 2020 |
| 32414935 | Why does Russia have such high cardiovascular mortality rates? Comparisons of blood-based biomarkers with Norway implicate non-ischaemic cardiac damage. | Journal of Epidemiology and Community Health | 2020 |
| 31983222 | Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy. | Circulation | 2020 |
| 31983221 | Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy. | Circulation | 2020 |
| 32873833 | Heritability of haemodynamics in the ascending aorta. | Sci Rep | 2020 |
| 32695637 | Obesity-related ventricular remodelling is exacerbated in dilated and hypertrophic cardiomyopathy. | Cardiovascular Diagnosis and Therapy | 2020 |
| 32862661 | Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery Disease. | Circ Genom Precis Med | 2020 |
| 32686758 | Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes. | Eur J Hum Genet | 2020 |
| 31196449 | Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases. | J Am Coll Cardiol | 2019 |