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

Journal article

Harper AR. 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

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

Plasma cytokines and risk of coronary heart disease in the PROCARDIS study.

Journal article

Clarke R. et al, (2018), Open Heart, 5

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