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R. Kamps

Recent publications
  • Kamps, R., & Robinson, E. L. (2024). LNC-ing Genetics in Mitochondrial Disease. Non-coding RNA, 10(6), Article 57. https://doi.org/10.3390/ncrna10060057
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  • Nazzari, M., Romitti, M., Kip, A. M., Kamps, R., Costagliola, S., van de Beucken, T., Moroni, L., & Caiment, F. (2024). Impact of benzo[a]pyrene, PCB153 and sex hormones on human ESC-Derived thyroid follicles using single cell transcriptomics. Environment International, 188, Article 108748. https://doi.org/10.1016/j.envint.2024.108748
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  • Vallbona-Garcia, A., Lindsey, P. J., Kamps, R., Stassen, A. P. M., Nguyen, N., van Tienen, F. H. J., Hamers, I. H. J., Hardij, R., van Gisbergen, M. W., Benedikter, B. J., de Coo, I. F. M., Webers, C. A. B., Gorgels, T. G. M. F., & Smeets, H. J. M. (2023). Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup. Frontiers in Ophthalmology, 3, Article 1309836. https://doi.org/10.3389/fopht.2023.1309836
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  • Otten, A. B. C., Kamps, R., Lindsey, P., Gerards, M., Pendeville-Samain, H., Muller, M., van Tienen, F. H. J., & Smeets, H. J. M. (2020). TfamKnockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos. Frontiers in Cell and Developmental Biology, 8, Article 381. https://doi.org/10.3389/fcell.2020.00381
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  • Azodi, M., Kamps, R., Heymans, S., & Robinson, E. L. (2020). The Missing "lnc" between Genetics and Cardiac Disease. Non-coding RNA, 6(1), Article 3. https://doi.org/10.3390/ncrna6010003
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  • Kamps, R. (2020). Resolving the role of genetic defects and mtDNA copy number in mitochondrial disease and development. [Doctoral Thesis, Maastricht University]. Maastricht University. https://doi.org/10.26481/dis.20201120rk
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  • Theunissen, T. E. J., Nguyen, M., Kamps, R., Hendrickx, A. T., Sallevelt, S. C. E. H., Gottschalk, R. W. H., Calis, C. M., Stassen, A. P. M., de Koning, B., Mulder-Den Hartog, E. N. M., Schoonderwoerd, K., Fuchs, S. A., Hilhorst-Hofstee, Y., de Visser, M., Vanoevelen, J., Szklarczyk, R., Gerards, M., de Coo, I. F. M., Hellebrekers, D. M. E., & Smeets, H. J. M. (2018). Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause. Frontiers in Genetics, 9(OCT), Article 400. https://doi.org/10.3389/fgene.2018.00400
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  • Geraets, I. M. E., Chanda, D., van Tienen, F. H. J., van den Wijngaard, A., Kamps, R., Neumann, D., Liu, Y., Glatz, J. F. C., Luiken, J. J. F. P., & Nabben, M. (2018). Human embryonic stem cell-derived cardiomyocytes as an in vitro model to study cardiac insulin resistance. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1864(5), 1960-1967. https://doi.org/10.1016/j.bbadis.2017.12.025
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  • Kamps, R., Szklarczyk, R., Theunissen, T. E., Hellebrekers, D. M. E. I., Sallevelt, S. C. E. H., Boesten, I. B., de Koning, B., van den Bosch, B. J., Salomons, G. S., Simas-Mendes, M., Verdijk, R., Schoonderwoerd, K., de Coo, I. F. M., Vanoevelen, J. M., & Smeets, H. J. M. (2018). Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease. European Journal of Human Genetics, 26(4), 537-551. https://doi.org/10.1038/s41431-017-0058-2
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  • Theunissen, T. E. J., Gerards, M., Hellebrekers, D. M. E. I., van Tienen, F. H., Kamps, R., Sallevelt, S. C. E. H., Hartog, E. N. M. M. .-D., Scholte, H. R., Verdijk, R. M., Schoonderwoerd, K., de Coo, I. F. M., Szklarczyk, R., & Smeets, H. J. M. (2017). Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect. Frontiers in molecular neuroscience, 10, Article 336. https://doi.org/10.3389/fnmol.2017.00336
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