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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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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., Haessler, J., Lyytikäinen, L-P., Repetto, L., Concas, M. P., van den Berg, M. E., Weiss, S., Baldassari, A. R., Bartz, T. M., Cook, J. P., Evans, D. S., & 146 others , Dec 2022, In: Nature communications. 13, 1, p. 5144 1 p., 5144.Research output: Contribution to journal › Article › Academic › peer-review
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Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
KORA-Study Group, Tanck, M. W. T., Christoffels, V. M., Boogerd, C. J. & Postma, A. V., 21 Jan 2022, In: Circulation Research. 130, 2, p. 166-180 15 p.Research output: Contribution to journal › Article › Academic › peer-review
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