Personal profile
Research interests
Peripheral neuropathies like Charcot-Marie-Tooth disease (CMT)
Specialisation
Neurogenetica
Education/Academic qualification
PhD, Development of Culture Systems for Human Keratinocytes: Application as a model for normal and disturbed epidermal differentiation, Radboud Universiteit Nijmegen
1 Mar 1993 → 26 May 1998
Award Date: 26 May 1998
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Dive into the research topics where Fred van Ruissen 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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Genetic testing of common and rare variants in dementia patients from a memory clinic: Dementia-related genetic testing in memory clinic
de Rojas, I., Hulsman, M., Tesi, N., van Spaendonk, R. M. L., van der Schaar, J., Dijkstra, J. I. R., van der Flier, W. M., van Ruissen, F., Jansen, P. R., Reinders, M. T., van Haelst, M. M., Pijnenburg, Y. A. L., Fernandez, M. V., Ruiz, A., Holstege, H. H. & van der Lee, S. J., Dec 2025, In: Alzheimer's Research & Therapy. 17, 1, p. 225 225.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile23 Downloads (Pure) -
Prevalence of Pathogenic Variants and Eligibility Criteria for Genetic Testing in Patients Who Visit a Memory Clinic
van der Lee, S. J., Hulsman, M., van Spaendonk, R., van der Schaar, J., Dijkstra, J., Tesi, N., van Ruissen, F., Elting, M., Reinders, M., de Rojas, I., Verschuuren-Bemelmans, C. C., van der Flier, W. M., van Haelst, M. M., de Geus, C., Pijnenburg, Y. & Holstege, H., 27 Jan 2025, In: Neurology. 104, 4, e210273.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Genetic Testing in patients with Dementia: A Data-Driven Clinical Decision Tree for Memory Clinics
van der Lee, S. J., Hulsman, M., van Spaendonk, R. M. L., van der Schaar, J. J., Dijkstra, J. I. R., Tesi, N., van der Flier, W. M., van Ruissen, F., Elting, M., Reinders, M. J. T., de Rojas, I., van Haelst, M. M., Verschuuren-Bemelmans, C. C., de Geus, C. M., Pijnenburg, Y. A. L., Holstege, H. & Lee, S. J. V. D., 2024.Research output: Working paper › Preprint
File21 Downloads (Pure) -
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia
de Boer, S. C. M., Woolley, L., Mol, M. O., Serpente, M., Reus, L. M., van Minkelen, R., van Vugt, J. F. A., Sorrentino, F., Veldink, J. H., Seelaar, H., Galimberti, D., van Ruissen, F., Mead, S., Rogaeva, E., Pijnenburg, Y. A. L. & van der Lee, S. J., Dec 2022, In: Acta neuropathologica communications. 10, 1, p. 141 1 p., 141.Research output: Contribution to journal › Comment/Letter to the editor › Academic
Open AccessFile20 Downloads (Pure) -
Pathogenic variants in three families with distal muscle involvement
Weterman, M. A. J., Bronk, M., Jongejan, A., Hoogendijk, J. E., Krudde, J., Karjosukarso, D., Goebel, H. H., Aronica, E., Jöbsis, G. J., van Ruissen, F., van Spaendonck-Zwarts, K. Y., de Visser, M. & Baas, F., 2022, (E-pub ahead of print) In: Neuromuscular disorders.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile3 Downloads (Pure)