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Keavney BD

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney
Increased power for detection of parent-of-origin effects via the use of haplotype estimation
Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Common variation neighbouring micro-RNA 22 is sssociated with increased left ventricular mass
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of fallot

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