Tervi A, Ramste M, Ollila HM. Response to Dr. Nicholas A. Flavahan’s and Dr. Ali H. Eid’s letters regarding our recent publication in Cell Genomics. Cell genomics. 2025;5(5):100885. doi:10.1016/j.xgen.2025.100885
Publications
Sept CE, Tak E, Goel V, et al. High-resolution CTCF footprinting reveals impact of chromatin state on cohesin extrusion. Nature communications. 2025;16(1):4506. doi:10.1038/s41467-025-57775-w
Eweje F, Ibrahim V, Shajii A, et al. Self-assembling protein nanoparticles for cytosolic delivery of nucleic acids and proteins. Nature biotechnology. 2025. doi:10.1038/s41587-025-02664-2
Hill N, Matulina LM, MacIntyre C, et al. Heterologous Surface Display Reveals Conserved Complement Inhibition and Functional Diversification of Borrelia burgdorferi Elp Proteins. Molecular microbiology. 2025;124(1):77-90. doi:10.1111/mmi.15369
Priedigkeit N, Harrison B, Shue R, et al. Clinicogenomic Characterization of Inflammatory Breast Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research. 2025;31(14):3072-3083. doi:10.1158/1078-0432.CCR-24-2081
Choksi D, Gutiérrez-MartÃnez L, Rist PM, et al. Use of the Brain Care Score to Estimate the Risk of Incident Cerebrovascular Events in Middle-Aged Women. Neurology. 2025;104(11):e213674. doi:10.1212/WNL.0000000000213674
Peuranheimo P, Kreivi HR, Ollgren J, et al. Increasing incidence and burden of obstructive sleep apnoea in the Finnish population: A cohort study from 2005 to 2019. Respiratory medicine. 2025;244:108155. doi:10.1016/j.rmed.2025.108155
Blum SM, Ouyang B, Zubiri L, et al. Tumor location as a risk factor for severe immune-related adverse events. Journal for immunotherapy of cancer. 2025;13(5). doi:10.1136/jitc-2024-011312
Horsdal HT, Albiñana C, Zhu Z, et al. Convergent evidence linking neonatal vitamin D status and risk of neurodevelopmental disorders: a Danish case-cohort study. The lancet. Psychiatry. 2025;12(6):410-420. doi:10.1016/S2215-0366(25)00099-9
Nava C, Cogne B, Santini A, et al. Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption. Nature genetics. 2025;57(6):1374-1388. doi:10.1038/s41588-025-02184-4