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Dive into the research topics where Petra Zwijnenburg is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Response to Letter to the Editor on “Standardized multidisciplinary care for children and adolescents with differences of sex development: a health intelligence approach”
Willemsen, L. A., Stoter, M., van den Boogaard, E., Both, S., Groen, L. A., Kreukels, B. P. C., Kuiper, K. C., Nieuwersteeg, J. N., Roussel, N. A., van der Sluijs Veer, L., de Vries, A. L. C., Zwijnenburg, P. J. G., den Heijer, M., Oosterlaan, J. & Hannema, S. E., Apr 2026, In: journal of sexual medicine. 23, 4Research output: Contribution to journal › Comment/Letter to the editor › Academic
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Standardized multidisciplinary care for children and adolescents with differences of sex development: a health intelligence approach
Willemsen, L. A., Stoter, M., van den Boogaard, E., Both, S., Groen, L. A., Kreukels, B. P. C., Kuiper, K. C., Nieuwersteeg, J. N., Roussel, N. A., van der Sluijs Veer, L., de Vries, A. L. C., Zwijnenburg, P. J. G., den Heijer, M., Oosterlaan, J. & Follow Me DSD study group, 1 Feb 2026, In: journal of sexual medicine. 23, 2, qdaf382.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile18 Downloads (Pure) -
A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter release
van Boven, M. A., Mestroni, M., Zwijnenburg, P. J. G., Verhage, M. & Cornelisse, L. N., Jun 2024, In: Molecular psychiatry. 29, 6, p. 1798-1809 12 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile72 Downloads (Pure) -
DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7
van der Laan, L., Karimi, K., Rooney, K., Lauffer, P., McConkey, H., Caro, P., Relator, R., Levy, M. A., Bhai, P., Mignot, C., Keren, B., Briuglia, S., Sobering, A. K., Li, D., Vissers, L. E. L. M., Dingemans, A. J. M., Valenzuela, I., Verberne, E. A., Misra-Isrie, M. & Zwijnenburg, P. J. G. & 8 others, , 1 Mar 2024, In: Genetics in medicine. 26, 3, p. 101050 101050.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile27 Downloads (Pure) -
Refining the 9q34.3 microduplication syndrome reveals mild neurodevelopmental features associated with a distinct global DNA methylation profile
Rots, D., Rooney, K., Relator, R., Kerkhof, J., McConkey, H., Pfundt, R., Marcelis, C., Willemsen, M. H., van Hagen, J. M., Zwijnenburg, P., Alders, M., Õunap, K., Reimand, T., Fjodorova, O., Berland, S., Liahjell, E. B., Bojovic, O., Kriek, M., Ruivenkamp, C. & Bonati, M. T. & 4 others, , Jun 2024, In: Clinical genetics. 105, 6, p. 655-660 6 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile29 Downloads (Pure)