Specialization
Cardiac cellular electrophysiology
Focus of research
Cardiac impulse formation and propagation under normal and abnormal conditions
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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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SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias
Wang, J., Verkerk, A. O., Wilders, R., Zhang, Y., Zhang, K., Prakosa, A., Rivaud, M. R., Marsman, E. M. J., Boender, A. R., Klerk, M., Fokkert, L., de Jonge, B., Neef, K., Kirzner, O. F., Bezzina, C. R., Remme, C. A., Tan, H. L., Boukens, B. J., Devalla, H. D. & Trayanova, N. A. & 3 others, , 7 May 2025, In: European Heart journal. 46, 18, p. 1747-1762 16 p.Research output: Contribution to journal › Article* › Academic › peer-review
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Alleviating the Effects of Short QT Syndrome Type 3 by Allele-Specific Suppression of the KCNJ2 Mutant Allele
Wilders, R., 1 Dec 2024, In: International journal of molecular sciences. 25, 24, 13351.Research output: Contribution to journal › Article* › Academic › peer-review
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