Publications

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Misceo, D., Terkelsen, T., Bøen, S. M., Bjørnstad, P. M., Strand, M. E., Orszagh, V. C., Jensen, U. B. & Frengen, E. (2026). CRISPR Activation Reveals the Spliceogenicity of an Intronic NEB Variant in Fetuses With Arthrogryposis Multiplex Congenita 6. Clinical Genetics, 109(4), 772-777. https://doi.org/10.1111/cge.70097
Møhlenberg, M., Jørgensen, S. E., Marije van der Sluis, R., Zillinger, T., Hinke, D. M., Hollensen, A. K., Hansen, A. L., Hausfater, P., Gorochov, G., Tubach, F., Ghosn, J., Laouenan, C., Storgaard, M., Holm, C. K., Su, H., Pérez de Diego, R., Pujol, A., Zhang, S.-Y., Zhang, Q. ... COVID Human Genetic Effort (2026). Defective RNA Polymerase III sensing of mitochondrial DNA in pulmonary epithelial cells impairs type I IFN immunity to SARS-CoV-2. Proceedings of the National Academy of Sciences of the United States of America, 123(12), Article e2522111123. https://doi.org/10.1073/pnas.2522111123
Mushunuri, A., Adesoji, O., Krause, R., May, P., Lerche, H., Becker, A., Grimm, D., Nothnagel, M., Schulz, H. & International League Against Epilepsy Consortium on Complex Epilepsies (2026). Genetic risk factor identification for common epilepsies guided by integrative omics data analysis. Epilepsia, 67(3), 1406-1420. https://doi.org/10.1111/epi.70021
Nast, A., Al Wattar, B. H., Beylot Barry, M., Brüggemann, H., Bukvić Mokos, Z., Caruana, D. M., Degitz, K., Dessinioti, C., Dréno, B., Driessen, R. J. B., Gollnick, H., Hædersdal, M., Katoulis, A., Läuchli, S., Lambert, J., Layton, A. M., Micali, G., Ochsendorf, F. R., Sathyapalan, T. ... Pennitz, A. (2026). Update of the EuroGuiDerm evidence-based guideline for the treatment of acne—Short version. Journal of the European Academy of Dermatology and Venereology. Advance online publication. https://doi.org/10.1111/jdv.70331
Natividad Avila, M., Jung, S., Satterstrom, F. K., Fu, J. M., Levy, T., Sloofman, L. G., Klei, L., Pichardo, T., Marquez, D., Stevens, C. R., Cusick, C. M., Ames, J. L., Campos, G. S., Cerros, H., Chaskel, R., Costa, C. I. S., Cuccaro, M. L., Lopez, A. D. P., Fernandez, M. ... The Autism Sequencing Consortium (ASC) (2026). Deleterious coding variation associated with autism is shared across ancestries. Nature Medicine, 32(4), 1519-1529. https://doi.org/10.1038/s41591-026-04228-6
Noes-Holt, G., Jensen, K. L., Comaposada-Baró, R., Jager, S. E., Richner, M., Goddard, C. M., Kowenicki, M. B. K., Sivertsen, L., Jiménez-Fernández, L., Andersen, R. C., Lilja, J. H., Larsen, A. H., Boesgaard, S. P., Houser, G. A., Christensen, N. R., Marino, A., Tappe-Theodor, A., Wierer, M., Vægter, C. B. ... Sørensen, A. T. (2026). Recombinant dimeric PICK1 peptide inhibitors for long-term relief of chronic pain by AAV therapeutics. Cell reports. Medicine, 7(6), Article 102800. https://doi.org/10.1016/j.xcrm.2026.102800
Ogunjimi, B., Warren-Gash, C., Ouwendijk, W. J. D., Breuer, J., Mogensen, T. H. & Koelle, D. M. (2026). Varicella zoster virus and the central nervous system. Nature Reviews Microbiology, 24(6), 425-439. https://doi.org/10.1038/s41579-026-01289-9
Oliveira, J. P., Nielsen, P. K., Pereira, S., Dória, S., Freixo, J. P. & Nielsen, R. (2026). Nonprogressive Nephrotic Range Proteinuria Because of Indirect Cubilin Dysfunction. Kidney International Reports, 11(1), 241-245. https://doi.org/10.1016/j.ekir.2025.09.046