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Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases
Jordà, P., Lai, Y., Jeuken, A., Lemieux Perreault, L.-P., Goulet, E., Lahrouchi, N., Nozza, A., Tanck, M. W., Guerra, P., Cadrin-Tourigny, J., de Denus, S., Bezzina, C. R., Lettre, G., Busseuil, D., Dubé, M.-P., Tardif, J.-C. & Tadros, R., 1 Dec 2025, In: npj Genomic Medicine. 10, 1, 65.Research output: Contribution to journal › Article › Academic › peer-review
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Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
Nicastro, M., Vermeer, A. M. C., Postema, P. G., Tadros, R., Bowling, F. Z., Aegisdottir, H. M., Tragante, V., Mach, L., Postma, A. V., Lodder, E. M., van Duijvenboden, K., Zwart, R., Beekman, L., Wu, L., Jurgens, S. J., van der Zwaag, P. A., Alders, M., Allouba, M., Aguib, Y. & Santome, J. L. & 51 others, , 3 Jul 2025, In: American journal of human genetics. 112, 7, p. 1681-1698 18 p.Research output: Contribution to journal › Article › Academic › peer-review
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Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
Nicastro, M., Vermeer, A. M. C., Postema, P. G., Tadros, R., Bowling, F. Z., Aegisdottir, H. M., Tragante, V., Mach, L., Postma, A. V., Lodder, E. M., van Duijvenboden, K., Zwart, R., Beekman, L., Wu, L., van der Zwaag, P. A., Alders, M., Allouba, M., Aguib, Y., Santomel, J. L. & de Una, D. & 50 others, , 5 Jul 2024, In: medRxiv.Research output: Contribution to journal › Article › Academic
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