Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.
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Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.
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Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy.
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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
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Aragam KG. et al, (2022), Nat Genet
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
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Grace C. et al, (2021), Genet Epidemiol
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
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Harper AR. et al, (2021), Nat Genet, 53, 135 - 142
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
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Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers.
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Grace C. et al, (2019), BMC Bioinformatics, 20
Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease.
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Association analyses based on false discovery rate implicate new loci for coronary artery disease.
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A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
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