Research output per year
Research output per year
Personal profile
External positions
Board member - Cardio genetica - Stichting Cardiomyopathie-Onderzoek Nederland
1 Jan 2022 → 31 Dec 3999
"member supervisory board, Stichting LEEFH (landelijk expertisecentrum erf.h.onderzoek fam HVZ) - supervising/advising board of directors - LEEFH Foundation
1 Sept 2020 → 31 Dec 3999
lid managementteam Durrer Cardiovasculair Research Centrum - geen - Netherlands Heart Institute
1 Sept 2018 → 31 Dec 3999
lid medische adviesraad - geen duidelijke - Contactgroep Marfan Nederland
1 Sept 2018 → 31 Dec 3999
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant
van Drie, E., Jongbloed, J. D. H., Hoorntje, E., van der Zwaag, P. A., Cox, M. G. P. J., Deprez, R. H. L., Houweling, A. C., Proost, V. P., Wilde, A. A. M., Dooijes, D., Baas, A. F., Te Riele, A. S. J. M., van Spaendonck-Zwarts, K. Y., Lodder, E. M. & van Tintelen, J. P., 1 Aug 2025, In: International Journal of Cardiology. 432, 8 p., 133264.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile27 Downloads (Pure) -
A Plea for a Genetics-First Approach in Arrhythmogenic Cardiomyopathies
Te Riele, A. S. J. M., van Tintelen, J. P. & Hauer, R. N. W., 29 Apr 2025, In: Circulation. 151, 17, p. 1231-1234 4 p.Research output: Contribution to journal › Editorial › Academic › peer-review
-
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants
Filamin C Registry Consortium, 9 Apr 2025, In: JAMA Cardiology. 10, 4, p. 359-369 11 p.Research output: Contribution to journal › Article › Academic › peer-review
-
Arrhythmogenic Cardiomyopathy: Towards Genotype Based Diagnoses and Management
Muller, S. A., Bertoli, G., Wang, J., Gasperetti, A., Cox, M. G. P. J., Calkins, H., te Riele, A. S. J. M., Judge, D. P., Delmar, M., Hauer, R. N. W., Boink, G. J. J., Cerrone, M., van Tintelen, J. P. & James, C. A., Oct 2025, In: Journal of Cardiovascular Electrophysiology. 36, 10, p. 2662-2670 9 p.Research output: Contribution to journal › Review article › peer-review
Open AccessFile5 Downloads (Pure) -
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
Open AccessFile2 Downloads (Pure)