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Search results (160)

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

Kramarenko D. et al, (2026)

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

Zheng SL. et al, (2025), Nat Genet, 57, 563 - 571

Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project.

Ormondroyd E. et al, (2024), Eur J Hum Genet, 32, 1045 - 1052

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.

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.

Keaton JM. et al, (2024), Nat Genet, 56, 778 - 791

n autosomal dominant cardiac arrhythmia syndrome, ST Depression Syndrome, is caused by thede novocreation of a cardiomyocyte enhancer

de Villiers C. et al, (2024)

GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification.

Lagou V. et al, (2023), Nat Genet, 55, 1448 - 1461

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.

Yu M. et al, (2023), Circ Genom Precis Med, 16, 207 - 215

Correction: The power of genetic diversity in genome-wide association studies of lipids.

Graham SE. et al, (2023), Nature, 618, E19 - E20

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

Young WJ. et al, (2023), Nat Commun, 14

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

Aung N. et al, (2023), Circ Genom Precis Med, 16

cknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Wang N. et al, (2023), Journal of Translational Genetics and Genomics, 7, 1 - 2

Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

WALTERS R. et al, (2022), Genome Biology

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

Aragam KG. et al, (2022), Nat Genet, 54, 1803 - 1815

Saturated Map of Common Genetic Variants Associated with Human Height

WALTERS R. et al, (2022), Nature

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