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Heritability of haemodynamics in the ascending aorta.

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

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

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

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

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

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

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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.

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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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