Publications — Radcliffe Department of Medicine

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Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

Keaton JM. et al, (2024), Nat Genet

GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification.

Lagou V. et al, (2023), Nat Genet, 55, 1448 - 1461

Author Correction: The power of genetic diversity in genome-wide association studies of lipids.

Graham SE. et al, (2023), Nature

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.

Yu M. et al, (2023), Circ Genom Precis Med

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

Young WJ. et al, (2023), Nat Commun, 14

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), Circ Genom Precis Med, 16

Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Wang N. et al, (2023), Journal of Translational Genetics and Genomics, 7, 1 - 2

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

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

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

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

Yengo L. et al, (2022), Nature, 610, 704 - 712

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

Ramdas S. et al, (2022), Am J Hum Genet, 109, 1366 - 1387

The power of genetic diversity in genome-wide association studies of lipids.

Graham SE. et al, (2021), Nature, 600, 675 - 679

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), Nat Commun, 12

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

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

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

Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus.

van Zuydam NR. et al, (2020), Circ Genom Precis Med, 13

A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction.

Douglas G. et al, (2020), Cardiovasc Res, 116, 1863 - 1874

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

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

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