Peer-reviewed publikationer

Peer-reviewed publications

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Krüger, M., Pietsch, J., Bauer, J., Kopp, S., Carvalho, D. T. O., Baatout, S., Moreels, M., Melnik, D., Wehland, M., Egli, M., Jayashree, S., Kobberø, S. D., Corydon, T. J., Nebuloni, S., Gass, S., Evert, M., Infanger, M. & Grimm, D. (2019). Growth of Endothelial Cells in Space and in Simulated Microgravity - a Comparison on the Secretory Level. Cellular Physiology and Biochemistry, 52(5), 1039-1060. https://doi.org/10.33594/000000071
Braun, E., Hotter, D., Koepke, L., Zech, F., Groß, R., Sparrer, K. M. J., Müller, J. A., Pfaller, C. K., Heusinger, E., Wombacher, R., Sutter, K., Dittmer, U., Winkler, M., Simmons, G., Jakobsen, M. R., Conzelmann, K.-K., Pöhlmann, S., Münch, J., Fackler, O. T. ... Sauter, D. (2019). Guanylate-Binding Proteins 2 and 5 Exert Broad Antiviral Activity by Inhibiting Furin-Mediated Processing of Viral Envelope Proteins. Cell Reports, 27(7), 2092-2104.e10. https://doi.org/10.1016/j.celrep.2019.04.063
Mullins, N., Bigdeli, T. B., Børglum, A. D., Coleman, J. R. I., Demontis, D., Mehta, D., Power, R. A., Ripke, S., Stahl, E. A., Starnawska, A., Anjorin, A., Corvin, A., Sanders, A. R., Forstner, A. J., Reif, A., Koller, A. C., Tkowska, B. S., Baune, B. T., Müller-Myhsok, B. ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium (2019). GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores. American Journal of Psychiatry, 176(8), 651-660. https://doi.org/10.1176/appi.ajp.2019.18080957
Martin, R. M., Ikeda, K., Cromer, M. K., Uchida, N., Nishimura, T., Romano, R., Tong, A. J., Lemgart, V. T., Camarena, J., Pavel-Dinu, M., Sindhu, C., Wiebking, V., Vaidyanathan, S., Dever, D. P., Bak, R. O., Laustsen, A., Lesch, B. J., Jakobsen, M. R., Sebastiano, V. ... Porteus, M. H. (2019). Highly Efficient and Marker-free Genome Editing of Human Pluripotent Stem Cells by CRISPR-Cas9 RNP and AAV6 Donor-Mediated Homologous Recombination. Cell Stem Cell, 24(5), 821-828.e5. https://doi.org/10.1016/j.stem.2019.04.001
Sari-Ak, D., Bahrami, S., Laska, M. J., Drncova, P., Fitzgerald, D. J., Schaffitzel, C., Garzoni, F. & Berger, I. (2019). High-Throughput Production of Influenza Virus-Like Particle (VLP) Array by Using VLP-factory™, a MultiBac Baculoviral Genome Customized for Enveloped VLP Expression. I R. Vincentelli (red.), Methods in Molecular Biology: Methods and Protocols (Bind 2025, s. 213-226). Humana Press. https://doi.org/10.1007/978-1-4939-9624-7_10
Li, A., Geyer, F. C., Blecua, P., Lee, J. Y., Selenica, P., Brown, D. N., Pareja, F., Lee, S. S. K., Kumar, R., Rivera, B., Bi, R., Piscuoglio, S., Wen, H. Y., Lozada, J. R., Gularte-Mérida, R., Cavallone, L., Rezoug, Z., Nguyen-Dumont, T., Peterlongo, P. ... KConFab Investigators (2019). Homologous recombination DNA repair defects in PALB2-associated breast cancers. npj Breast Cancer, 5(1), Artikel 23. https://doi.org/10.1038/s41523-019-0115-9
Hensel, N., Raker, V., Förthmann, B., Detering, N. T., Kubinski, S., Buch, A., Katzilieris-Petras, G., Spanier, J., Gudi, V., Wagenknecht, S., Kopfnagel, V., Werfel, T. A., Stangel, M., Beineke, A., Kalinke, U., Paludan, S. R., Sodeik, B. & Claus, P. (2019). HSV-1 triggers paracrine fibroblast growth factor response from cortical brain cells via immediate-early protein ICP0. Journal of Neuroinflammation, 16(1), Artikel 248. https://doi.org/10.1186/s12974-019-1647-5
Gomez-Ospina, N., Scharenberg, S. G., Mostrel, N., Bak, R. O., Mantri, S., Quadros, R. M., Gurumurthy, C. B., Lee, C., Bao, G., Suarez, C. J., Khan, S., Sawamoto, K., Tomatsu, S., Raj, N., Attardi, L. D., Aurelian, L. & Porteus, M. H. (2019). Human genome-edited hematopoietic stem cells phenotypically correct Mucopolysaccharidosis type I. Nature Communications, 10(1), 4045. Artikel 4045. https://doi.org/10.1038/s41467-019-11962-8
Lafaille, F. G., Harschnitz, O., Lee, Y. S., Zhang, P., Hasek, M. L., Kerner, G., Itan, Y., Ewaleifoh, O., Rapaport, F., Carlile, T. M., Carter-Timofte, M. E., Paquet, D., Dobbs, K., Zimmer, B., Gao, D., Rojas-Duran, M. F., Kwart, D., Rattina, V., Ciancanelli, M. J. ... Zhang, S. Y. (2019). Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis. Nature Medicine, 25(12), 1873-1884. https://doi.org/10.1038/s41591-019-0672-3
de Groot, T., Ebert, L. K., Christensen, B. M., Andralojc, K., Cheval, L., Doucet, A., Mao, C., Baumgarten, R., Low, B. E., Sandhoff, R., Wiles, M. V., Deen, P. M. T. & Korstanje, R. (2019). Identification of Acer2 as a First Susceptibility Gene for Lithium-Induced Nephrogenic Diabetes Insipidus in Mice. Journal of the American Society of Nephrology : JASN, 30(12), 2322-2336. https://doi.org/10.1681/ASN.2018050549
Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., Awashti, S., Belliveau, R., Bettella, F., Buxbaum, J. D., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Cerrato, F., Chambert, K., Christensen, J. H. ... Børglum, A. D. (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics, 51(3), 431-444. https://doi.org/10.1038/s41588-019-0344-8
Hotter, D., Bosso, M., Jønsson, K. L., Krapp, C., Stürzel, C. M., Das, A., Littwitz-Salomon, E., Berkhout, B., Russ, A., Wittmann, S., Gramberg, T., Zheng, Y., Martins, L. J., Planelles, V., Jakobsen, M. R., Hahn, B. H., Dittmer, U., Sauter, D. & Kirchhoff, F. (2019). IFI16 Targets the Transcription Factor Sp1 to Suppress HIV-1 Transcription and Latency Reactivation. Cell Host & Microbe, 25(6), 858-872.e13. https://doi.org/10.1016/j.chom.2019.05.002
Tansey, M. G. & Romero-Ramos, M. (2019). Immune system responses in Parkinson's Disease: early and dynamic. The European journal of neuroscience, 49(3), 364-383. https://doi.org/10.1111/ejn.14290
Nudel, R., Benros, M. E., Krebs, M. D., Allesøe, R. L., Lemvigh, C. K., Bybjerg-Grauholm, J., Børglum, A. D., Daly, M. J., Nordentoft, M., Mors, O., Hougaard, D. M., Mortensen, P. B., Buil, A., Werge, T., Rasmussen, S. & Thompson, W. K. (2019). Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders. European Journal of Human Genetics, 27(9), 1445-1455. https://doi.org/10.1038/s41431-019-0402-9
Su, J., Hughes, A. D., Simonsen, U., Nielsen-Kudsk, J. E., Parker, K. H., Howard, L. S. & Mellemkjaer, S. (2019). Impact of Pulmonary Endarterectomy on Pulmonary Arterial Wave Propagation and Reservoir Function. American Journal of Physiology: Heart and Circulatory Physiology, 317(3), H505-H516. https://doi.org/10.1152/ajpheart.00181.2019
Jensen, T. B., Bartels, D., Sædder, E. A., Poulsen, B. K., Andersen, S. E., Christensen, M. M. H., Nielsen, L. & Christensen, H. R. (2019). Implementation of TNF-biosimilars (Infliximab and Eternacept) in Danish departments of rheumatology. Annals of the Rheumatic Diseases, 78(Suppl. 2), 237-237. Artikel OP0310. https://doi.org/10.1136/annrheumdis-2019-eular.1383
Moosa, S., Gregersen, P. A., Hald, J. D. & Vogel, I. (2019). Implications of identifying a PLS3 deletion as an incidental finding on prenatal testing. Poster-session præsenteret på The 14th biannual International Skeletal Dysplasia Society Meeting , Oslo.
Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hämäläinen, E., Kajantie, E., Laivuori, H., Villa, P. M., Reynolds, R. M., Nystad, W., Håberg, S. E., London, S. J., O'Donnell, K. J., Garg, E., Meaney, M. J., Entringer, S., Wadhwa, P. D., Buss, C. ... Binder, E. B. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications, 10, Artikel 2548. https://doi.org/10.1038/s41467-019-10461-0
Zhang, W., Voloudakis, G., Rajagopal, V. M., Readhead, B., Dudley, J. T., Schadt, E. E., Björkegren, J. L. M., Kim, Y., Fullard, J. F., Hoffman, G. E. & Roussos, P. (2019). Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits. Nature Communications, 10(1), 1-13. Artikel 3834. https://doi.org/10.1038/s41467-019-11874-7
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
Nievergelt, C. M., Maihofer, A. X., Klengel, T., Atkinson, E. G., Chen, C. Y., Choi, K. W., Coleman, J. R. I., Dalvie, S., Duncan, L. E., Gelernter, J., Levey, D. F., Logue, M. W., Polimanti, R., Provost, A. C., Ratanatharathorn, A., Stein, M. B., Torres, K., Aiello, A. E., Almli, L. M. ... Koenen, K. C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10(1), Artikel 4558. https://doi.org/10.1038/s41467-019-12576-w