Publications

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Kaiser, K., Gyllborg, D., Procházka, J., Salašová, A., Kompaníková, P., Molina, F. L., Laguna-Goya, R., Radaszkiewicz, T., Harnoš, J., Procházková, M., Potěšil, D., Barker, R. A., Casado, Á. G., Zdráhal, Z., Sedláček, R., Arenas, E., Villaescusa, J. C. & Bryja, V. (2019). WNT5A is transported via lipoprotein particles in the cerebrospinal fluid to regulate hindbrain morphogenesis. Nature Communications, 10(1), Article 1498. https://doi.org/10.1038/s41467-019-09298-4
Kaleviste, E., Saare, M., Leahy, T. R., Bondet, V., Duffy, D., Mogensen, T. H., Jørgensen, S. E., Nurm, H., Ip, W., Davies, E. G., Sauer, S., Syvänen, A. C., Milani, L., Peterson, P. & Kisand, K. (2019). Interferon signature in patients with STAT1 gain-of-function mutation is epigenetically determined. European Journal of Immunology, 49(5), 790-800. https://doi.org/10.1002/eji.201847955
Karoglan, A., Pätzold, B., Pereira de Lima, J., Brüggemann, H., Tüting, T., Schanze, D., Guell, M. & Gollnick, H. (2019). Safety and Efficacy of Topically Applied Selected Cutibacterium acnes Strains over Five Weeks in Patients with Acne Vulgaris: An Open-label, Pilot Study. Acta Dermato-Venereologica, 99(13), 1253-1257. https://doi.org/10.2340/00015555-3323
Keppner, A., Maric, D., Sergi, C., Ansermet, C., De Bellis, D., Kratschmar, D. V., Canonica, J., Klusonova, P., Fenton, R. A., Odermatt, A., Crambert, G., Hoogewijs, D. & Hummler, E. (2019). Deletion of the serine protease CAP2/Tmprss4 leads to dysregulated renal water handling upon dietary potassium depletion. Scientific Reports, 9(1), Article 19540. https://doi.org/10.1038/s41598-019-55995-x
King, D., Glynn, M. D., Cindric, S., Kernan, D., O’Connell, T., Hakimjavadi, R., Kearney, S., Ackermann, T., Berbel, X. M., Llobera, A., Simonsen, U., Laursen, B. E., Redmond, E. M., Cahill, P. A. & Ducrée, J. (2019). Label-Free Multi Parameter Optical Interrogation of Endothelial Activation in Single Cells using a Lab on a Disc Platform. Scientific Reports, 9, Article 4157. https://doi.org/10.1038/s41598-019-40612-8
Kjaer, L., Skov, V., Andersen, M. T., Aggerholm, A., Clair, P., Gniot, M., Soeby, K., Udby, L., Dorff, M. H., Hasselbalch, H. & Pallisgaard, N. (2019). Variant-specific discrepancy when quantitating BCR-ABL1 e13a2 and e14a2 transcripts using the Europe Against Cancer qPCR assay. European Journal of Haematology, 103(1), 26-34. https://doi.org/10.1111/ejh.13238
Klein, M., Walters, R. K., Demontis, D., Stein, J. L., Hibar, D. P., Adams, H. H., Bralten, J., Mota, N. R., Schachar, R., Sonuga-Barke, E., Mattheisen, M., Neale, B. M., Thompson, P. M., Medland, S. E., Børglum, A. D., Faraone, S. V., Arias-Vasquez, A. & Franke, B. (2019). Genetic markers of ADHD-related variations in intracranial volume. American Journal of Psychiatry, 176(3), 228-238. https://doi.org/10.1176/appi.ajp.2018.18020149
Kogelman, L. J. A., Esserlind, A.-L., Francke Christensen, A., Awasthi, S., Ripke, S., Ingason, A., Davidsson, O. B., Erikstrup, C., Hjalgrim, H., Ullum, H., Olesen, J., Folkmann Hansen, T. & DBDS Genomic Consortium, The International Headache Genetics Consortium (2019). Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Neurology: Genetics, 5(6), Article e364. https://doi.org/10.1212/NXG.0000000000000364
Korsholm, L. M., Gál, Z., Lin, L., Quevedo, O., Ahmad, D. A., Dulina, E., Luo, Y., Bartek, J. & Larsen, D. H. (2019). Double-strand breaks in ribosomal RNA genes activate a distinct signaling and chromatin response to facilitate nucleolar restructuring and repair. Nucleic Acids Research, 47(15), 8019-8035. https://doi.org/10.1093/nar/gkz518