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Publications

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

Graham SE. et al, (2021), Nature

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Lagou V. et al, (2021), Nature Communications, 12

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), Nature communications, 12

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Harper AR. et al, (2021), Nature Genetics, 53, 135 - 142

Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine, 13

Genetic variation in CADM2 as a link between psychological traits and obesity

Morris J. et al, (2019), Scientific Reports, 9

Associations of autozygosity with a broad range of human phenotypes.

Clark DW. et al, (2019), Nature communications, 10

A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction

Douglas G. et al, (2019), Cardiovascular Research

A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

Sung YJ. et al, (2019), Human Molecular Genetics, 28, 2615 - 2633

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease

Magosi LE. et al, (2019), Bioinformatics

Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

de Vries PS. et al, (2019), American Journal of Epidemiology, 188, 1033 - 1054

Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

Bentley AR. et al, (2019), Nature Genetics, 51, 636 - 648

Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease

Grace C. et al, (2018), Scientific Reports, 8

Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets

Lempiäinen H. et al, (2018), Scientific Reports, 8

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Evangelou E. et al, (2018), Nature Genetics, 50, 1755 - 1755

Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants

Chai JT. et al, (2018), Arteriosclerosis, Thrombosis, and Vascular Biology, 38, 2718 - 2730

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Evangelou E. et al, (2018), Nature Genetics, 50, 1412 - 1425

Neonatal MicroRNA Profile Determines Endothelial Function in Offspring of Hypertensive Pregnancies

Yu GZ. et al, (2018), Hypertension, 72, 937 - 945

Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion

Ehsan M. et al, (2018), Journal of Molecular and Cellular Cardiology, 121, 287 - 296

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