Onderzoeksoutput per jaar
Onderzoeksoutput per jaar
Samenwerkingen en hoofdonderzoeksgebieden uit de afgelopen vijf jaar
Recente externe samenwerking op landen-/regioniveau. Duik in de details door op de stippen te klikken of
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Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients with Cerebellar Ataxia
Ghorbani, F., De Boer, E. N., Benjamins-Stok, M., Verschuuren-Bemelmans, C. C., Knapper, J., De Boer-Bergsma, J., De Vries, J. J., Sikkema-Raddatz, B., Verbeek, D. S., Westers, H. & Van Diemen, C. C., 2-feb.-2023, In: Neurology: Genetics. 9, 1, e200050.Onderzoeksoutput: Article › Academic › peer review
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Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia
Ghorbani, F., de Boer, E. N., Benjamins-Stok, M., Verschuuren-Bemelmans, C. C., Knapper, J., de Boer-Bergsma, J., de Vries, J. J., Sikkema-Raddatz, B., Verbeek, D. S., Westers, H. & van Diemen, C. C., 2-feb.-2023, In: Neurology. Genetics. 9, 1, 8 blz., e200050.Onderzoeksoutput: Article › Academic › peer review
Open AccessBestand -
Early onset ataxia with comorbid myoclonus and epilepsy: A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement
van Noort, S. A. M., van der Veen, S., de Koning, T. J., de Koning-Tijssen, M. A. J., Verbeek, D. S. & Sival, D. A., jul.-2023, In: European Journal of Paediatric Neurology. 45, blz. 47-54 8 blz.Onderzoeksoutput: Article › Academic › peer review
Open AccessBestand1 Citaat (Scopus)7 Downloads (Pure) -
The pathogenetic basis for a disease continuum in early- and late-onset ataxia-dystonia supports a unified genetic diagnostic approach
Garofalo, M., Vansenne, F., Verbeek, D. S. & Sival, D. A., mrt.-2023, In: European Journal of Paediatric Neurology. 43, blz. 44-51 8 blz.Onderzoeksoutput: Article › Academic › peer review
Open AccessBestand12 Downloads (Pure) -
Developmental neurobiology of cerebellar and Basal Ganglia connections
Sival, D. A., Noort, S. A. M. V., Tijssen, M. A. J., de Koning, T. J. & Verbeek, D. S., jan.-2022, In: European Journal of Paediatric Neurology. 36, blz. 123-129 7 blz.Onderzoeksoutput: Article › Academic › peer review
Open AccessBestand7 Citaten (Scopus)57 Downloads (Pure)
Datasets
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WDR45, one gene associated with multiple neurodevelopmental disorders
Cong, Y. (Contributor), So, V. (Contributor), de Koning-Tijssen, M. (Contributor), Verbeek, D. (Contributor), Reggiori, F. (Contributor) & Mauthe, M. (Contributor), University of Groningen, 12-apr.-2021
DOI: 10.6084/m9.figshare.14401601.v1
Dataset
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WDR45, one gene associated with multiple neurodevelopmental disorders
Cong, Y. (Contributor), So, V. (Contributor), de Koning-Tijssen, M. (Contributor), Verbeek, D. (Contributor), Reggiori, F. (Contributor) & Mauthe, M. (Contributor), figshare Academic Research System, 12-apr.-2021
DOI: 10.6084/m9.figshare.14401601, https://tandf.figshare.com/articles/dataset/_i_WDR45_i_one_gene_associated_with_multiple_neurodevelopmental_disorders/14401601
Dataset
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Additional file 2 of Parkinson’s disease–associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy
Ma, K. Y. (Contributor), Fokkens, M. (Contributor), Reggiori, F. (Contributor), Mari, M. (Contributor) & Verbeek, D. (Contributor), figshare Academic Research System, 15-jun.-2021
DOI: 10.6084/m9.figshare.14782512.v1
Dataset