Search results (181)
« Back to PublicationsBiobank-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)
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.
Preprint
Kramarenko DR. et al, (2026)
Polygenic prediction of body mass index and obesity through the life course and across ancestries.
Journal article
Smit RAJ. et al, (2025), Nat Med, 31, 3151 - 3168
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
Journal article
Tadros R. et al, (2025), Nat Genet, 57, 530 - 538
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings.
Journal article
Zheng SL. et al, (2025), Nat Genet, 57, 563 - 571
Expanding Insights Into the Genetic Architecture of Coronary Artery Disease: A Multi-Ancestry and Multi-Trait Genome-Wide Meta-Analysis Among ∼2 Million Individuals
Conference paper
Murgia F. et al, (2025), GENETIC EPIDEMIOLOGY, 49
Right ventricular longitudinal strain but not right ventricular ejection fraction in hypertrophic cardiomyopathy associates with sarcomere positive status and adverse phenotypes
Conference paper
Agnel O. et al, (2025), EUROPEAN HEART JOURNAL, 46
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project.
Journal article
Ormondroyd E. et al, (2024), Eur J Hum Genet, 32, 1045 - 1052
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure.
Journal article
Ganji-Arjenaki M. et al, (2024), Kidney Int Rep, 9, 1849 - 1859
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
Journal article
Ojewunmi OO. et al, (2024), Hum Mol Genet, 33, 919 - 929
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.
Journal article
Keaton JM. et al, (2024), Nat Genet, 56, 778 - 791
An autosomal dominant cardiac arrhythmia syndrome, ST Depression Syndrome, is caused by thede novocreation of a cardiomyocyte enhancer
Preprint
de Villiers C. et al, (2024)
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project
Conference paper
Ormondroyd E. et al, (2024), EUROPEAN JOURNAL OF HUMAN GENETICS, 32, 1837 - 1838
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project
Conference paper
Ormondroyd E. et al, (2024), EUROPEAN JOURNAL OF HUMAN GENETICS, 32, 1837 - 1838