Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Journal article
Lagou V. et al, (2021), Nat Commun, 12
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Journal article
Lagou V. et al, (2021), Nature communications, 12
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
Journal article
van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine, 13
Genetic variation in CADM2 as a link between psychological traits and obesity
Journal article
Morris J. et al, (2019), Scientific Reports, 9
Associations of autozygosity with a broad range of human phenotypes.
Journal article
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
Journal article
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
Journal article
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
Journal article
Magosi LE. et al, (2019), Bioinformatics
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
Journal article
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
Journal article
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
Journal article
Grace C. et al, (2018), Scientific Reports, 8
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets
Journal article
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
Journal article
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
Journal article
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
Journal article
Evangelou E. et al, (2018), Nature Genetics, 50, 1412 - 1425
Neonatal MicroRNA Profile Determines Endothelial Function in Offspring of Hypertensive Pregnancies
Journal article
Yu GZ. et al, (2018), Hypertension, 72, 937 - 945
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion
Journal article
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
Journal article
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
Journal article
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
Journal article
Bhutta MF. et al, (2017), Scientific Reports, 7