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Department of Biomedicine

DemontisGroup

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Amidi , A., Agerbæk, M., Wu, L. M., Pedersen, A. D., Mehlsen, M. Y., Clausen, C. R., Demontis, D., Børglum, A., Harbøll, A. & Zachariae, R. (2017). Changes in cognitive functions and cerebral grey matter and their associations with inflammatory markers, endocrine markers, and APOE genotypes in testicular cancer patients undergoing treatment. Brain Imaging and Behavior, 11(3), 769-783. https://doi.org/10.1007/s11682-016-9552-3

Project MinE GWAS Consortium & Schizophrenia Working Group of the Psychiatric Genomics Consortium (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications, 8, 14774. Article 14774. https://doi.org/10.1038/ncomms14774

Rajagopal, V. M., Agerbo, E., Timmermann, A., Børglum, A. & Demontis, D. (2017). Genome-wide association study of dyslexia in the Danish population. Poster session presented at PhD Day 2017, Aarhus, Denmark.

Rohde, P. D., Demontis, D., Børglum, A., iPSYCH-Broad Consortium & Sørensen, P. (2017). Improved prediction of genetic predisposition to psychiatric disorders using genomic feature best linear unbiased prediction models. Poster session presented at ESHG 2017: European Society of Human Genetics Annual Meeting, Copenhagen, Denmark.

Scott, J. G., Giørtz Pedersen, M., Erskine, H. E., Bikic, A., Demontis, D., McGrath, J. J. & Dalsgaard, S. (2017). Mortality in individuals with disruptive behavior disorders diagnosed by specialist services: A nationwide cohort study. Psychiatry Research, 251, 255-260. https://doi.org/10.1016/j.psychres.2017.02.029

Rasmussen, M. K., Demontis, D. & Kasch, H. (2017). Sortilin gene SNP variant rs12037569 predicts chronic pain 12-14 years after whiplash injury. 669-669. Poster session presented at 3rd Congress of the European-Academy-of-Neurology, Amsterdam, Netherlands.

Lescai, F., Als, T. D., Li, Q., Nyegaard, M., Andorsdottir, G., Biskopstø, M., Hedemand, A., Fiorentino, A., O'Brien, N. L., Jarram, A., Liang, T. J., Grove, J., Pallesen, J., Eickhardt, E., Mattheisen, M., Bolund, L., Demontis, D., Wang, A. G., McQuillin, A. ... Børglum, A. D. (2017). Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. Translational Psychiatry, 7(2), e1034. Article 3. https://doi.org/10.1038/tp.2017.3

Starnawska, A., Demontis, D., Pen, A., Hedemand, A., Nielsen, A. L., Staunstrup, N. H., Grove, J., Als, T. D., Jarram, A., O'Brien, N. L., Mors, O., McQuillin, A., Børglum, A. D. & Nyegaard, M. (2016). CACNA1C hypermethylation is associated with bipolar disorder. Translational Psychiatry, 6(6), e831. Article e831. https://doi.org/10.1038/tp.2016.99

Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A. & Sørensen, P. (2016). Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes. Genetics (Print), 203(4), 1901-1913. https://doi.org/10.1534/genetics.116.189498

Rohde, P. D., Demontis, D., Castro Dias Cuyabano, B., Børglum, A. & Sørensen, P. (2016). Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes. 1901-1913. Poster session presented at 5th International Conference on Quantitative Genetics , Madison, United States.

Displaying results 61 to 70 out of 138

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Revised 06.12.2022

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Johanne Fangel Thygesen