Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings.
Zheng SL. et al, (2025), Nat Genet
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
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
Author Correction: The power of genetic diversity in genome-wide association studies of lipids.
Graham SE. et al, (2023), Nature
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.
Yu M. et al, (2023), Circ Genom Precis Med
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
Acknowledgment 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.
Kanoni S. et al, (2022), Genome Biol, 23
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
A saturated map of common genetic variants associated with human height.
Yengo L. et al, (2022), Nature, 610, 704 - 712
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Ramdas S. et al, (2022), Am J Hum Genet, 109, 1366 - 1387
The power of genetic diversity in genome-wide association studies of lipids.
Graham SE. et al, (2021), Nature, 600, 675 - 679
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
Grace C. et al, (2021), Genet Epidemiol
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Lagou V. et al, (2021), Nat Commun, 12
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Harper AR. et al, (2021), Nat Genet, 53, 135 - 142
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Harper AR. et al, (2021), Nat Genet, 53, 135 - 142