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

Journal article

McGurk KA. et al, (2021), Human molecular genetics

Heritability of haemodynamics in the ascending aorta.

Journal article

McGurk KA. et al, (2020), Scientific reports, 10, 14356 - 14356

A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy.

Journal article

Hayesmoore JBG. et al, (2020), Circ Genom Precis Med

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Journal article

Seselgyte R. et al, (2019), J Dent Res, 98, 659 - 665

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.

Journal article

de Vries PS. et al, (2019), American journal of epidemiology

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

Journal article

Giri A. et al, (2019), Nat Genet, 51, 51 - 62

Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield.

Journal article

Thomson KL. et al, (2018), Genetics in medicine : official journal of the American College of Medical Genetics

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

Journal article

Evangelou E. et al, (2018), Nat Genet, 50, 1412 - 1425

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