Publications

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Bentzen, N. & Christensen, K. S. (2018). PSOAP - korte og dækkende praksisnotater. Månedsskrift for Almen Praksis, 9(96), 664-670.
Scott, K. M., Saha, S., Lim, C. C. W., Aguilar-Gaxiola, S., Al-Hamzawi, A., Alonso, J., Benjet, C., Bromet, E. J., Bruffærts, R., Caldas-De-Almeida, J. M., De Girolamo, G., De Jonge, P., Degenhardt, L., Florescu, S., Gureje, O., Haro, J. M., Hu, C., Karam, E. G., Kovess-Masfety, V. ... McGrath, J. J. (2018). Psychotic experiences and general medical conditions: A cross-national analysis based on 28 002 respondents from 16 countries in the WHO World Mental Health Surveys. Psychological Medicine, 48(16), 2730-2739. https://doi.org/10.1017/S0033291718000363
Kovess-Masfety, V., Saha, S., Lim, C. C. W., Aguilar-Gaxiola, S., Al-Hamzawi, A., Alonso, J., Borges, G., de Girolamo, G., de Jonge, P., Demyttenaere, K., Florescu, S., Haro, J. M., Hu, C., Karam, E. G., Kawakami, N., Lee, S., Lepine, J. P., Navarro-Mateu, F., ten Have, M. ... the WHO World Mental Health Survey Collaborators (2018). Psychotic experiences and religiosity: data from the WHO World Mental Health Surveys. Acta Psychiatrica Scandinavica, 137(4), 306-315. https://doi.org/10.1111/acps.12859
Bonàs-Guarch, S., Guindo-Martínez, M., Miguel-Escalada, I., Grarup, N., Sebastian, D., Rodriguez-Fos, E., Sánchez, F., Planas-Fèlix, M., Cortes-Sánchez, P., González, S., Timshel, P., Pers, T. H., Morgan, C. C., Moran, I., Atla, G., González, J. R., Puiggros, M., Martí, J., Andersson, E. A. ... Torrents, D. (2018). Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Nature Communications, 9(1), 2162. https://doi.org/10.1038/s41467-018-04170-3
Grarup, N., Hansen, T., Jørgensen, M. E., Li, J., Lin, L.-A., Pedersen, O., Witte, D. R., CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, MAGIC Investigators & Understanding Society Scientific Group (2018). Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics, 50(5), 765-766. https://doi.org/10.1038/s41588-018-0082-3, https://doi.org/10.1038/s41588-018-0050-y
GoT2D/T2D-GENES Consortium (2018). Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. American Journal of Human Genetics, 102(6), 1204-1211. https://doi.org/10.1016/j.ajhg.2018.05.002
Pontoppidan, M., Keilow, M., Dietrichson, J., Solheim, O. J., Opheim, V., Gustafson, S. & Andersen, S. C. (2018). Randomised controlled trials in Scandinavian educational research. Educational Research, 60(3), 311-335. https://doi.org/10.1080/00131881.2018.1493351
Bonàs-Guarch, S., Guindo-Martínez, M., Miguel-Escalada, I., Grarup, N., Sebastian, D., Rodriguez-Fos, E., Sánchez, F., Planas-Fèlix, M., Cortes-Sánchez, P., González, S., Timshel, P., Pers, T. H., Morgan, C. C., Moran, I., Atla, G., González, J. R., Puiggros, M., Martí, J., Andersson, E. A. ... Torrents, D. (2018). Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Nature Communications, 9(1), 321. Article 321. https://doi.org/10.1038/s41467-017-02380-9
Sarink, D., Schock, H., Johnson, T., Chang-Claude, J., Overvad, K., Olsen, A., Tjønneland, A., Arveux, P., Fournier, A., Kvaskoff, M., Boeing, H., Karakatsani, A., Trichopoulou, A., La Vecchia, C., Masala, G., Agnoli, C., Panico, S., Tumino, R., Sacerdote, C. ... Fortner, R. T. (2018). Receptor activator of nuclear factor kB ligand, osteoprotegerin, and risk of death following a breast cancer diagnosis: results from the EPIC cohort. BMC Cancer, 18(1), 1010. Article 1010. https://doi.org/10.1186/s12885-018-4887-3