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Publications

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Lagou V. et al, (2021), Nat Commun, 12

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

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

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

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

Feitosa MF. et al, (2018), PLOS ONE, 13, e0198166 - e0198166

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

Sung YJ. et al, (2018), The American Journal of Human Genetics, 102, 375 - 400

A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11

Bhutta MF. et al, (2017), Scientific Reports, 7

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