Dr Friederike Ehrhart (F.)

van Beek, D., Iyer, A., Ehrhart, F., Evelo, C. T., de Kok, T. M., Arts, I. C. W., Adriaens, M. E., & Kutmon, M. (2026). Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease. Bioinformatics, 42, Article btag592. https://doi.org/10.1093/bioinformatics/btag592

Iyer, A., Doornbos, C., Evelo, C., Kutmon, M., & Ehrhart, F. (2026). GSEA and the coexpression network approach identify novel pathway connections of molecular processes affected in Porto-sinusoidal vascular disease. PLOS ONE, 21(5), Article e0347338. https://doi.org/10.1371/journal.pone.0347338

Valeanu, A., Duan, Y., Acosta, J. M., de Kok, T. M., van Amelsvoort, T., & Ehrhart, F. (2026). A dataset of rare copy number variants associated with neurodevelopmental and neuropsychiatric disorders. Scientific data, 13(1), Article 977. https://doi.org/10.1038/s41597-026-07345-6

Ehrhart, F., Martens, H., Rosenblum, N. D., Schedl, A., Schlesinger, T. A., Gjerstad, A. C., Haffner, D., Ho, J., Evelo, C. T., Woolf, A. S., Weber, R. G., & Schaefer, F. (2026). Molecular pathways of kidney development and their applications to clinical research. Kidney International, 109(2), 287-296. https://doi.org/10.1016/j.kint.2025.09.032

Ozisik, O., Kara, N. S., Abbassi-Daloii, T., Térézol, M., Kuijper, E. C., Queralt-Rosinach, N., Jacobsen, A., Sezerman, O. U., Roos, M., Evelo, C. T., Baudot, A., Ehrhart, F., & Mina, E. (2025). A collaborative network analysis for the interpretation of transcriptomics data in Huntington’s disease. Scientific Reports, 15(1), Article 1412. https://doi.org/10.1038/s41598-025-85580-4

Wijnbergen, D., Johari, M., Ozisik, O., 't Hoen, P. A. C., Ehrhart, F., Baudot, A., Evelo, C. T., Udd, B., Roos, M., & Mina, E. (2025). Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression. Orphanet Journal of Rare Diseases, 20(1), Article 27. https://doi.org/10.1186/s13023-024-03526-x

Fiaz, H., Khan, A. R., Ehrhart, F., Hussain, M., Evelo, C. T. A., Awan, F. R., & Coort, S. L. M. (2025). Investigating the role of Vitamin D and its targeted gene-pathway interactions involved in cardiometabolic health. International Journal of Health Sciences, 19(3), 29-42. https://doi.org/10.25259/OA04_8774

Bayjanov, J. R., Doornbos, C., Ozisik, O., Shin, W., Queralt-Rosinach, N., Wijnbergen, D., Saulnier-Blache, J. S., Schanstra, J. P., Buffin-Meyer, B., Klein, J., Fernández, J. M., Kaliyaperumal, R., Baudot, A., ’t Hoen, P. A. C., & Ehrhart, F. (2024). Integrative analysis of multi-omics data reveals importance of collagen and the PI3K AKT signalling pathway in CAKUT. Scientific Reports, 14(1), Article 20731. https://doi.org/10.1038/s41598-024-71721-8

Fuchs, C., 't Hoen, P. A. C., Mueller, A. R., Ehrhart, F., & Van Karnebeek, C. D. M. (2024). Drug repurposing in Rett and Rett-like syndromes: a promising yet underrated opportunity? Frontiers in medicine, 11, Article 1425038. https://doi.org/10.3389/fmed.2024.1425038

Bahram Sangani, N., Koetsier, J., Mélius, J., Kutmon, M., Ehrhart, F., Evelo, C. T., Curfs, L. M. G., Reutelingsperger, C. P., & Eijssen, L. M. T. (2024). A novel insight into neurological disorders through HDAC6 protein-protein interactions. Scientific Reports, 14(1), Article 14666. https://doi.org/10.1038/s41598-024-65094-1