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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  • Site-wide: 2,474
  • In genetics: 98
• Year to date:
  • Site-wide: 39,604
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  • Site-wide: None

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

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  • Site-wide: 3,747
  • In genetics: 167
• Year to date:
  • Site-wide: 39,415
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  • Site-wide: 51,372

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

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  • Site-wide: 5,496
  • In genomics: 643
• Year to date:
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  • Site-wide: 33,299

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

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  • Site-wide: 29,807
  • In genomics: 2,731
• Year to date:
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  • Site-wide: 66,779

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • In genetics: 1,583
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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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  • Site-wide: 33,097
  • In genetics: 1,632
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Bi-allelic MCM10 mutations cause telomere shortening with immune dysfunction and cardiomyopathy

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  • Site-wide: 39,854
  • In molecular biology: 1,148
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Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

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  • In genetics: 2,351
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Metabolic Profiling of Aortic Stenosis and Hypertrophic Cardiomyopathy Identifies Mechanistic Contrasts in Substrate Utilisation

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  • Site-wide: 49,448
  • In systems biology: 1,174
• Year to date:
  • Site-wide: 53,307
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Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

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  • Site-wide: 62,591
  • In genetics: 2,955
• Year to date:
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Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome

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  • Site-wide: 78,176
  • In genetics: 3,622
• Year to date:
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  • Site-wide: 65,907