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 2nd Annual Danish Bioinformatics Conference, Odense, Denmark.
https://doi.org/10.1534/genetics.116.189498
Manikandan, V., Reinert, L., Paludan, S. R., Grove, J., Nielsen, P. F. R., Hougaard, D. M., Nordentoft, M., Werge, T., Børglum, A.
, Mortensen, P. B. & Demontis, D. (2016).
Gene-environmental interactions between genetic variants in antiviral response genes and prenatal maternal infections in schizophrenia. Poster session presented at American Society of Human Genetics 2016, Vancouver, Canada.
Starnawska, A., Demontis, D., McQuillin, A., O'Brien, N. L.
, Staunstrup, N. H., Mors, O., Nielsen, A. L., Børglum, A. D. & Nyegaard, M. (2016).
Hypomethylation of FAM63B in bipolar disorder patients.
Clinical Epigenetics (Print),
8(52), 1-6. Article 52.
https://doi.org/10.1186/s13148-016-0221-6
Fryland, T., Christensen, J. H., Pallesen, J., Mattheisen, M., Palmfeldt, J., Bak, M.
, Grove, J., Demontis, D., Blechingberg, J., Ooi, H. S., Nyegaard, M., Hauberg, M. E., Tommerup, N.
, Gregersen, N., Mors, O., Corydon, T. J., Nielsen, A. L. & Børglum, A. D. (2016).
Identification of the BRD1 interaction network and its impact on mental disorder risk.
Genome Medicine,
8(1), 53.
https://doi.org/10.1186/s13073-016-0308-x
Molgaard, S., Demontis, D., Nicholson, A. M., Finch, N. A., Petersen, R. C.
, Petersen, C. M., Rademakers, R.
, Nykjaer, A. & Glerup, S. (2016).
Soluble sortilin is present in excess and positively correlates with progranulin in CSF of aging individuals.
Experimental Gerontology,
84, 96-100.
https://doi.org/10.1016/j.exger.2016.09.002
Rohde, P. D., Madsen, L. S., Arvidson, S. M. N.
, Loeschcke, V., Demontis, D. & Kristensen, T. N. (2016).
Testing candidate genes for attention-deficit/hyperactivity disorder in fruit flies using a high throughput assay for complex behavior.
Fly,
10(1), 25-34. Article 1158365.
https://doi.org/10.1080/19336934.2016.1158365
Gregersen, N., Lescai, F., Liang, J., Li, Q.
, Als, T. D., Buttenschøn, H. N., Hedemand, A., Biskopstø, M., Wang, J., Wang, A.
, Børglum, A., Mors, O. & Demontis, D. (2016).
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
171(8), 1013-1022.
https://doi.org/10.1002/ajmg.b.32464
Demontis, D., Lescai, F., Børglum, A., Glerup, S., Østergaard, S. D., Mors, O., Li, Q., Liang, J., Jiang, H., Li, Y., Wang, J., Lesch, K.-P., Reif, A., Buitelaar, J. K. & Franke, B. (2016).
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder.
Journal of the American Academy of Child and Adolescent Psychiatry,
55(6), 521-523.
https://doi.org/10.1016/j.jaac.2016.03.009
Nyegaard, M., Rendtorff, N. D.
, Nielsen, M. S., Corydon, T. J., Demontis, D., Starnawska, A., Hedemand, A., Buniello, A., Niola, F., Overgaard, M. T., Leal, S. M., Ahmad, W.
, Wikman, F. P., Petersen, K. B., Crüger, D. G., Oostrik, J., Kremer, H., Tommerup, N., Frödin, M.
... Børglum, A. D. (2015).
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
PLoS Genetics,
11(7), e1005386.
https://doi.org/10.1371/journal.pgen.1005386
Starnawska, A., McQuillin, A.
, Demontis, D., Pen, A., Hedemand, A., Johannesen, M. D., Lescai, F., Als, T. D., Grove, J., Staunstrup, N. H., Nielsen, A. L., Jarram, A., O'Brian, N.
, Mors, O., Børglum, A. & Nyegaard, M. (2015).
DNA methylation of CACNA1C in bipolar disorder. Poster session presented at ESHG 2015, Glasgow, United Kingdom.