Alexa Vermeer

Medical Specialist, ACS - Heart Failure & Arrhythmias Affiliatie UvA Medical Specialist, Human genetics

Specialization

Focus of research

Latest publications

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 othersMonserrat, L., Miranda, A. M. A., Kanemaru, K., Cranley, J., van Zeggeren, I. E., Aronica, E. M. A., Ripolone, M., Zanotti, S., Sveinbjornsson, G., Ivarsdottir, E. V., Hólm, H., Guðbjartsson, D. F., Skúladóttir, Á. T., Stefánsson, K., Nadauld, L., Knowlton, K. U., Ostrowski, S. R., Sørensen, E., Vesterager Pedersen, O. B., Ghouse, J., Rand, S., Bundgaard, H., Ullum, H., Erikstrup, C., Aagaard, B., Bruun, M. T., Christiansen, M., Jensen, H. K., Carere, D. A., Cummings, C. T., Fishler, K., Tøring, P. M., Brusgaard, K., Juul, T. M., Saaby, L., Winkel, B. G., Mogensen, J., Fortunato, F., Comi, G. P., Ronchi, D., van Tintelen, J. P., Noseda, M., Airola, M. V., Christiaans, I., Wilde, A. A. M., Wilders, R., Clur, S-A., Verkerk, A. O., Bezzina, C. R. & Lahrouchi, N., 5 Jul 2024, In: medRxiv.
Research output: Contribution to journal › Article › Academic
Tropomyosin–troponin complex in inherited cardiomyopathies
Krijger, C., Sequeira, V., van den Boogaard, M., Veerman, C. C., Hoetjes, N. J., Poel, E., Tanck, M. W. T., Lekanne Deprez, R. H., Vermeer, A. M. C., van der Velden, J., Amin, A. S. & Juárez, C. K., Jul 2024, In: Heart Rhythm. 21, 7, p. 1173-1175 3 p.
Research output: Contribution to journal › Article › Academic › peer-review
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
Jansen, M., de Brouwer, R., Hassanzada, F., Schoemaker, A. E., Schmidt, A. F., Kooijman-Reumerman, M. D., Bracun, V., Slieker, M. G., Dooijes, D., Vermeer, A. M. C., Wilde, A. A. M., Amin, A. S., Lekanne Deprez, R. H., Herkert, J. C., Christiaans, I., de Boer, R. A., Jongbloed, J. D. H., van Tintelen, J. P., Asselbergs, F. W. & Baas, A. F., Jan 2024, In: JACC: Heart Failure. 12, 1, p. 134-147 14 p.
Research output: Contribution to journal › Article › Academic › peer-review
All publications

Alexa Vermeer

Specialization

Focus of research

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

Tropomyosin–troponin complex in inherited cardiomyopathies

Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

Amsterdam UMC makes use of cookies