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Publications

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), Circulation: Genomic and Precision Medicine

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

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

Kanoni S. et al, (2022), Genome biology, 23

A saturated map of common genetic variants associated with human height.

Yengo L. et al, (2022), Nature

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Ramdas S. et al, (2022), American journal of human genetics, 109, 1366 - 1387

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

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