Amsterdam Cardiovascular Sciences
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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 Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias
Pham, C., Andrzejczyk, K., Jurgens, S. J., Lekanne Deprez, R., Palm, K. C. A., Vermeer, A. M. C., Nijman, J., Christiaans, I., Barge-Schaapveld, D. Q. C. M., van Dessel, P. F. H. M., Beekman, L., Choi, S. H., Lubitz, S. A., Skoric-Milosavljevic, D., van den Bersselaar, L., Jansen, P. R., Copier, J. S., Ellinor, P. T., Wilde, A. A. M., Bezzina, C. R., & 1 others, 1 Aug 2023, In: Circulation. Genomic and precision medicine. 16, 4, p. 328-336 9 p.Research output: Contribution to journal › Article › Academic › peer-review
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Chronically elevated branched chain amino acid levels are pro-arrhythmic
Portero, V., Nicol, T., Podliesna, S., Marchal, G. A., Baartscheer, A., Casini, S., Tadros, R., Treur, J. L., Tanck, M. W. T., Jane Cox, I. J., Probert, F., Hough, T. A., Falcone, S., Beekman, L., Müller-Nurasyid, M., Kastenmüller, G., Gieger, C., Peters, A., Kääb, S., Sinner, M. F., & 5 others, 1 May 2022, In: Cardiovascular research. 118, 7, p. 1742-1757 16 p.Research output: Contribution to journal › Article › Academic › peer-review
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