Montasser, May E.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Common variants associated with plasma triglycerides and risk for coronary artery disease

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes

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Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Young, W. J., Lahrouchi, N., Isaacs, A., Duong, T., Foco, L., Ahmed, F., Brody, J. A., Salman, R., Noordam, R., Benjamins, J.-W., et al. (2022) · Nature Communications

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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., Gharib, S. A., Gottlieb, D. J., Guo, X., Lane, J. M., et al. (2021) · Genome Medicine

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