Author: Hugh Watkins

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Preprints

Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary prevention

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: The case of hypertrophic cardiomyopathy

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Bi-allelic MCM10 mutations cause telomere shortening with immune dysfunction and cardiomyopathy

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Metabolic Profiling of Aortic Stenosis and Hypertrophic Cardiomyopathy Identifies Mechanistic Contrasts in Substrate Utilisation

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Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

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

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