Author: Bernard D Keavney

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Preprints

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

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Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot

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

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Large-scale examination of neuropsychiatric, cognitive and cardiovascular phenotypic associations with 15q11.2 BP1-BP2 deletion in ~500,000 UK Biobank individuals

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Genome-wide association study in European patients with congenital heart disease identifies risk loci for transposition of the great arteries and anomalies of the thoracic arteries and veins and expression of discovered candidate genes in the developing heart

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STX18-AS1 is a Long Noncoding RNA predisposing to Atrial Septal Defect via downregulation of NKX2-5 in differentiating cardiomyocytes

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