Publications — Radcliffe Department of Medicine

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

Waring A. et al, (2021), J Med Genet, 58, 556 - 564

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

McGurk KA. et al, (2021), Hum Mol Genet, 30, 500 - 513

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

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

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

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

Heritability of haemodynamics in the ascending aorta.

McGurk KA. et al, (2020), Sci Rep, 10

Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy.

Harper AR. et al, (2020), Circ Genom Precis Med, 13

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

Grace C. et al, (2019), BMC Bioinformatics, 20

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

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

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), Hum Mol Genet, 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

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

Thomson KL. et al, (2019), Genet Med, 21, 1576 - 1584

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

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

de Vries PS. et al, (2019), Am J Epidemiol, 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), Nat Genet, 51, 636 - 648

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

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

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

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), Arterioscler Thromb Vasc Biol, 38, 2718 - 2730

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

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