Mike Gerards (M.)

Hemel, I. M. G. M., Steen, C., Denil, S. L. I. J., Ertaylan, G., Kutmon, M., Adriaens, M., & Gerards, M. (2025). The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphology. Mitochondrion, 81, Article 102008. https://doi.org/10.1016/j.mito.2025.102008

Hemel, I. M. G. M., Knoops, K., Lopez-Iglesias, C., & Gerards, M. (2025). The Curse of the Red Pearl: A Fibroblast-Specific Pearl-Necklace Mitochondrial Phenotype Caused by Phototoxicity. Biomolecules, 15(2), Article 304. https://doi.org/10.3390/biom15020304

Hemel, I. M. G. M., Arts, I. C. W., Moerel, M., & Gerards, M. (2025). The Matrix of Mitochondrial Imaging: Exploring Spatial Dimensions. Biomolecules, 15(2), Article 229. https://doi.org/10.3390/biom15020229

Pieterman, C., Jiang, J., Gerards, M., Ertaylan, G., Peeters, R., & de Kok, T. (2022). Finding the roadmap of a liver cell developing non-alcoholic fatty liver disease. Toxicology Letters, 368, S194-S194. https://doi.org/10.1016/j.toxlet.2022.07.528

Hemel, I. M. G. M., Sarantidou, R., & Gerards, M. (2021). It takes two to tango: The essential role of ER-mitochondrial contact sites in mitochondrial dynamics. International Journal of Biochemistry & Cell Biology, 141, Article 106101. https://doi.org/10.1016/j.biocel.2021.106101

Guo, L., Engelen, B. P. H., Hemel, I. M. G. M., de Coo, I. F. M., Vreeburg, M., Sallevelt, S. C. E. H., Hellebrekers, D. M. E. I., Jacobs, E. H., Sadeghi-Niaraki, F., van Tienen, F. H. J., Smeets, H. J. M., & Gerards, M. (2021). Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency. European Journal of Human Genetics, 29(12), 1789-1795. https://doi.org/10.1038/s41431-021-00947-1

Guo, L., Govindaraj, P., Kievit, M., de Coo, I. F. M., Gerards, M., Hellebrekers, D. M. E. I., Stassen, A. P. M., Gayathri, N., Taly, A. B., Sankaran, B. P., & Smeets, H. J. M. (2021). Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions. Neuromuscular Disorders, 31(9), 859-864. https://doi.org/10.1016/j.nmd.2021.06.014

Hemel, I. M. G. M., Engelen, B. P. H., Luber, N., & Gerards, M. (2021). A hitchhiker's guide to mitochondrial quantification. Mitochondrion, 59, 216-224. https://doi.org/10.1016/j.mito.2021.06.005

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

Bahhir, D., Yalgin, C., Ots, L., Jarvinen, S., George, J., Naudi, A., Krama, T., Krams, I., Tamm, M., Andjelkovic, A., Dufour, E., Gonzalez de Cozar, J. M., Gerards, M., Parhiala, M., Pamplona, R., Jacobs, H. T., & Joers, P. (2019). Manipulating mtDNA in vivo reprograms metabolism via novel response mechanisms. Plos Genetics, 15(10), Article 1008410. https://doi.org/10.1371/journal.pgen.1008410