Research output per year
Research output per year
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Dive into the research topics where Mariël Teunissen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Research output
- 6 Article
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Genetic variants for head size share genes and pathways with cancer
Knol, M. J., Poot, R. A., Evans, T. E., Satizabal, C. L., Mishra, A., Sargurupremraj, M., van der Auwera, S., Duperron, M.-G., Jian, X., Hostettler, I. C., van Dam-Nolen, D. H. K., Lamballais, S., Pawlak, M. A., Lewis, C. E., Carrion-Castillo, A., van Erp, T. G. M., Reinbold, C. S., Shin, J., Scholz, M. & Håberg, A. K. & 34 others, , 21 May 2024, In: Cell Reports Medicine. 5, 5, 101529.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks
Teunissen, M. W. A., Lewerissa, E., van Hugte, E. J. H., Wang, S., Ockeloen, C. W., Koolen, D. A., Pfundt, R., Marcelis, C. L. M., Brilstra, E., Howe, J. L., Scherer, S. W., Le Guillou, X., Bilan, F., Primiano, M., Roohi, J., Piton, A., de Saint Martin, A., Baer, S., Seiffert, S. & Platzer, K. & 11 others, , 4 Jul 2023, In: Human Molecular Genetics. 32, 14, p. 2373-2385 13 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Autism spectrum disorder and brain volume link through a set of mTOR-related genes
Arenella, M., Mota, N. R., Teunissen, M. W. A., Brunner, H. G. & Bralten, J., Jul 2023, In: Journal of Child Psychology and Psychiatry. 64, 7, p. 1007-1014 8 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Effectiveness and tolerability of lacosamide in children with drug resistant epilepsy
Driessen, J. T., Wammes-van der Heijden, E. A., Verschuure, P., Fasen, K. C. F. M., Teunissen, M. W. A. & Majoie, H. J. M., 2023, In: Epilepsy & Behavior Reports. 21, 1, 10 p., 100574.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case Report
Teunissen, M. W. A., Kamsteeg, E. J., Sallevelt, S. C. E. H., Pennings, M., Bauer, N. J. C., Vermeulen, R. J. & Nicolai, J., 9 Apr 2021, In: Neurology. Genetics. 7, 2, 5 p., 564.Research output: Contribution to journal › Article › Academic › peer-review
Open Access