Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Publications

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

Harper AR. et al, (2021), Nat Genet, 53, 135 - 142

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.

McGurk KA. et al, (2021), Human molecular genetics

Heritability of haemodynamics in the ascending aorta.

McGurk KA. et al, (2020), Scientific reports, 10, 14356 - 14356

Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy.

Waring A. et al, (2020), J Med Genet

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

WATKINS H., (2020), Nature Genetics

A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy.

Hayesmoore JBG. et al, (2020), Circ Genom Precis Med

Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease

Aragam KG. et al, (2019), CIRCULATION, 140

Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers

GOEL A., (2019), BMC Bioinformatics

Data-driven modelling of mutational hotspots and in-silico predictors in hypertrophic cardiomyopathy

Waring AJ. et al, (2019)

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.

Nethononda RM. et al, (2019), Sci Rep, 9

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

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Seselgyte R. et al, (2019), J Dent Res, 98, 659 - 665

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

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

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.

de Vries PS. et al, (2019), American journal of epidemiology

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

Giri A. et al, (2019), Nat Genet, 51, 51 - 62

Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield.

Thomson KL. et al, (2018), Genetics in medicine : official journal of the American College of Medical Genetics

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

Evangelou E. et al, (2018), Nat Genet, 50

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

Evangelou E. et al, (2018), Nat Genet, 50, 1412 - 1425

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

CHOUDHURY R., (2018), ATVB

Load More

1
2
3
4
5
6
7
...
»

Include forthcoming?