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Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy.

Journal article

Waring A. et al, (2021), J Med Genet, 58, 556 - 564

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

Journal article

McGurk KA. et al, (2021), Hum Mol Genet, 30, 500 - 513

Heritability of haemodynamics in the ascending aorta.

Journal article

McGurk KA. et al, (2020), Sci Rep, 10

Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy.

Journal article

Harper AR. et al, (2020), Circ Genom Precis Med, 13

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

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

Journal article

de Vries PS. et al, (2019), Am J Epidemiol, 188, 1033 - 1054

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

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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