Rada, A., Hagemann, A., Aaberg Poulsen, C., Baumgartner, T., Berki, T., Blaabjerg, M., Brenner, J., Britton, J. W., Christiana, A., Ciano-Petersen, N. L., Crijnen, Y., Elišák, M., Farina, A., Friedman, A. R., Hayden, Z., Hébert, J., Holtkamp, M., Hong, Z., Honnorat, J., … Specht, U. (2024). Risk of Seizure Recurrence Due to Autoimmune Encephalitis With NMDAR, LGI1, CASPR2, and GABA B R Antibodies. Neurology Neuroimmunology & Neuroinflammation, 11(4). https://doi.org/10.1212/nxi.0000000000200225

Mani, N., Nygaard, R., & Mancia, F. (2022). Gone with the Wnt(less): a mechanistic perspective on the journey of Wnt. Biochemical Society Transactions, 50(6), 1763–1772. https://doi.org/10.1042/bst20220634

Yalcouyé, A., Traoré, O., Diarra, S., Schrauwen, I., Esoh, K., Kadlubowska, M. K., Bharadwaj, T., Adadey, S. M., Kéita, M., Guinto, C. O., Leal, S. M., Landouré, G., & Wonkam, A. (2022). A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family. Molecular Genetics & Genomic Medicine, 10(7). Portico. https://doi.org/10.1002/mgg3.1995

Chai, G., Szenker-Ravi, E., Chung, C., Li, Z., Wang, L., Khatoo, M., Marshall, T., Jiang, N., Yang, X., McEvoy-Venneri, J., Stanley, V., Anzenberg, P., Lang, N., Wazny, V., Yu, J., Virshup, D. M., Nygaard, R., Mancia, F., Merdzanic, R., … Gleeson, J. G. (2021). A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. New England Journal of Medicine, 385(14), 1292–1301. https://doi.org/10.1056/nejmoa2033911