Publications

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Moller, P., Sampson, J., Dominguez-Valentin, M., Burn, J., Sunde, L., Moeslein, G., Mecklin, J.-P. & Seppala, T. (2021). Recent advances in Lynch syndrome. Familial Cancer, 20(2), 117-118. https://doi.org/10.1007/s10689-020-00200-6
Møller, P., Sampson, J., Dominguez-Valentin, M., Burn, J., Sunde, L., Möslein, G., Mecklin, J. P. & Seppälä, T. (2021). Correction to: Letter to the Editor—Recent advances in Lynch syndrome (Familial Cancer, (2021), 20, 2, (117-118), 10.1007/s10689-020-00200-6). Familial Cancer, 20(2), 119. https://doi.org/10.1007/s10689-021-00246-0
Monici, M., Cialdai, F., Bani, D., Bacci, S., Morbidelli, L., Norfini, A., Balsamo, M., van Loon, J., Grimm, D., Riwaldt, S., Coppola, G., Surdo, L., Ferranti, F. & Pantalone, D. (2021). Suture in Space: Preparation of an Experiment on the Healing of Sutured Wounds on Board the ISS. Proceedings of the International Astronautical Congress, IAC, A1.
Mortensen, S. B., Hansen, A. B. E., Mogensen, T. H., Jakobsen, M. A., Beck, H. C., Harvald, E. B., Lambertsen, K. L., Johansen, I. S. & Andersen, D. C. (2021). Pyrin Inflammasome Activation Abrogates Interleukin-1 Receptor Antagonist, Suggesting a New Mechanism Underlying Familial Mediterranean Fever Pathogenesis. Arthritis and Rheumatology, 73(11), 2116-2126. https://doi.org/10.1002/art.41770
Moser, S., Sugano, Y., Wengi, A., Fisi, V., Lindtoft Rosenbaek, L., Mariniello, M., Loffing-Cueni, D., McCormick, J. A., Fenton, R. A. & Loffing, J. (2021). A five amino acids deletion in NKCC2 of C57BL/6 mice affects analysis of NKCC2 phosphorylation but does not impact kidney function. Acta Physiologica, 233(1), Article e13705. https://doi.org/10.1111/apha.13705
Mullins, N., Forstner, A. J., O'Connell, K. S., Coombes, B., Coleman, J. R. I., Qiao, Z., Als, T. D., Bigdeli, T. B., Børte, S., Bryois, J., Charney, A. W., Drange, O. K., Gandal, M. J., Hagenaars, S. P., Ikeda, M., Kamitaki, N., Kim, M., Krebs, K., Panagiotaropoulou, G. ... HUNT All-In Psychiatry (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics, 53(6), 817-829. https://doi.org/10.1038/s41588-021-00857-4
Munch, T. N., Hedley, P. L., Hagen, C. M., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Grove, J., Nordentoft, M., Børglum, A. D., Mortensen, P. B., Werge, T. M., Melbye, M., Hougaard, D. M. & Christiansen, M. (2021). Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study. Journal of Neurodevelopmental Disorders, 13(1), 19. Article 19. https://doi.org/10.1186/s11689-021-09367-0
Munn-Chernoff, M. A., Johnson, E. C., Chou, Y.-L., Coleman, J. R. I., Thornton, L. M., Walters, R. K., Yilmaz, Z., Baker, J. H., Hübel, C., Gordon, S., Medland, S. E., Watson, H. J., Gaspar, H. A., Bryois, J., Hinney, A., Leppä, V. M., Mattheisen, M., Ripke, S., Yao, S. ... Agrawal, A. (2021). Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology, 26(1), Article e12880. https://doi.org/10.1111/adb.12880
Nakamoto, C., Goto, Y., Tomizawa, Y., Fukata, Y., Fukata, M., Harpsøe, K., Gloriam, D. E., Aoki, K. & Takeuchi, T. (2021). A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro. Molecular Brain, 14(1), Article 173. https://doi.org/10.1186/s13041-021-00882-8