dr. D.S. (Dineke) Verbeek

Associate professor (Tenure track) /adjunct hoogleraar

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E-mail:
d.s.verbeek umcg.nl

Research

  1. 2019
  2. 2018
  3. Bazov, I., Sarkisyan, D., Kononenko, O., Watanabe, H., Taqi, M. M., Stålhandske, L., ... Bakalkin, G. (2018). Neuronal Expression of Opioid Gene is Controlled by Dual Epigenetic and Transcriptional Mechanism in Human Brain. Cerebral Cortex, 28(9), 3129-3142. https://doi.org/10.1093/cercor/bhx181
  4. 2017
  5. Nibbeling, E. A. R., Duarri, A., Verschuuren-Bemelmans, C. C., Fokkens, M. R., Karjalainen, J. M., Smeets, C. J. L. M., ... Verbeek, D. S. (2017). Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. Brain, 140(11), 2860-2878. https://doi.org/10.1093/brain/awx251
  6. 2016
  7. 2015
  8. Nibbeling, E., Schaake, S., Tijssen, M. A., Weissbach, A., Groen, J. L., Altenmueller, E., ... Lohmann, K. (2015). Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia. Journal of Neurology, 262(5), 1340-1343. https://doi.org/10.1007/s00415-015-7718-3
  9. Duarri , A., Nibbeling, E. A. R., Fokkens, M. R., Meijer, M., Boerrigter, M., Verschuuren - Bemelmans, C. C., ... Verbeek, D. S. (2015). Functional Analysis Helps to Define KCNC3 Mutational Spectrum in Dutch Ataxia Cases. PLoS ONE, 10(3), [e0116599]. https://doi.org/10.1371/journal.pone.0116599
  10. Groen, J. L., Andrade, A., Ritz, K., Jalalzadeh, H., Haagmans, M., Bradley, T. E. J., ... Tijssen, M. A. J. (2015). CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. Human Molecular Genetics, 24(4), 987-993. https://doi.org/10.1093/hmg/ddu513
  11. 2014
  12. 2013
  13. 2012
  14. Taqi, M. M., Warmlander, S. K. T. S., Yamskova, O., Madani, F., Bazov, I., Luo, J., ... Bakalkin, G. (2012). Conformation Effects of CpG Methylation on Single-Stranded DNA Oligonucleotides: Analysis of the Opioid Peptide Dynorphin-Coding Sequences. PLoS ONE, 7(6), [e39605]. https://doi.org/10.1371/journal.pone.0039605
  15. 2011
  16. 2010
  17. Bakalkin, G., Watanabe, H., Jezierska, J., Depoorter, C., Verschuuren - Bemelmans, C., Bazov, I., ... Verbeek, D. S. (2010). Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23. American Journal of Human Genetics, 87(5), 593-603. https://doi.org/10.1016/j.ajhg.2010.10.001
  18. 2009
  19. Muller, P. A. J., van de Sluis, B., Groot, A. J., Verbeek, D., Vonk, W. I. M., Maine, G. N., ... Klomp, L. W. J. (2009). Nuclear-Cytosolic Transport of COMMD1 Regulates NF-kappa B and HIF-1 Activity. Traffic, 10(5), 514-527. https://doi.org/10.1111/j.1600-0854.2009.00892.x
  20. 2008
  21. 2005
  22. Verbeek, DS., van de Warrenburg, BPC., Hennekam, FAM., Dooijes, D., Ippel, PF., Verschuuren-Bemelmans, CC., ... Sinke, RJ. (2005). Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population. HUMAN GENETICS, 117(1), 88-91. https://doi.org/10.1007/s00439-005-1278-z
  23. 2004
  24. 2002

ID: 321781