Thomas Werge

Thomas Werge

Clinical Professor

Member of:

  • Psychiatry


  1. Published

    Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study

    Sánchez, X. C., Montalbano, S., Vaez, M., Krebs, M. D., Byberg-Grauholm, J., Mortensen, P. B., Børglum, A. D., Hougaard, D. M., Nordentoft, Merete, Geschwind, D. H., Buil Demur, Alfonso Alberto, Schork, A. J., Thompson, W. K., Raznahan, A., Helenius, D., Werge, Thomas & Ingason, A., 2023, In: The Lancet Psychiatry. 10, 2, p. 129-138 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    Structural basis of organic cation transporter-3 inhibition

    Khanppnavar, B., Maier, J., Herborg, Freja, Gradisch, R., Lazzarin, E., Luethi, D., Yang, J. W., Qi, C., Holy, M., Jäntsch, K., Kudlacek, O., Schicker, K., Werge, Thomas, Gether, Ulrik, Stockner, T., Korkhov, V. M. & Sitte, H. H., 2022, In: Nature Communications. 13, 1, 13 p., 6714.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Accurate and Effective Detection of Recurrent Copy Number Variants in Large SNP Genotype Datasets

    Montalbano, S., Sánchez, X. C., Vaez, M., Helenius, D., Werge, Thomas & Ingason, A., 2022, In: Current Protocols. 2, 12, 21 p., e621.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

    Liu, X., Helenius, D., Skotte, L., Beaumont, R. N., Wielscher, M., Geller, F., Juodakis, J., Mahajan, A., Bradfield, J. P., Lin, F. T. J., Vogelezang, S., Bustamante, M., Ahluwalia, T. S., Pitkänen, N., Wang, C. A., Bacelis, J., Borges, M. C., Zhang, G., Bedell, B. A., Rossi, R. M. & 54 others, Skogstrand, K., Peng, S., Thompson, W. K., Appadurai, V., Lawlor, D. A., Kalliala, I., Power, C., McCarthy, M. I., Boyd, H. A., Marazita, M. L., Hakonarson, H., Hayes, M. G., Scholtens, D. M., Rivadeneira, F., Jaddoe, V. W. V., Vinding, R. K., Bisgaard, H., Knight, B. A., Pahkala, K., Raitakari, O., Helgeland, Ø., Johansson, S., Njølstad, P. R., Fadista, J., Schork, A. J., Nudel, R., Miller, D. E., Chen, X., Weirauch, M. T., Mortensen, P. B., Børglum, A. D., Nordentoft, Merete, Mors, O., Hao, K., Ryckman, K. K., Hougaard, D. M., Kottyan, L. C., Pennell, C. E., Lyytikainen, L., Bønnelykke, Klaus, Vrijheid, M., Felix, J. F., Lowe, W. L., Grant, S. F. A., Hyppönen, E., Jacobsson, B., Jarvelin, M., Muglia, L. J., Murray, J. C., Freathy, R. M., Werge, Thomas, Melbye, M., Buil, A. & Feenstra, B., 2 Sep 2019, In: Nature Communications. 10, 1, 13 p., 3927.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    A polygenic resilience score moderates the genetic risk for schizophrenia

    Hess, J. L., Tylee, D. S., Mattheisen, M., The Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Børglum, A. D., Als, T. D., Grove, J., Werge, T., Mortensen, P. B., Mors, O., Nordentoft, M., Hougaard, D. M., Byberg-grauholm, J., Bækvad-hansen, M., Greenwood, T. A., Tsuang, M. T., Curtis, D., Steinberg, S., Sigurdsson, E. & 6 others, Stefánsson, H., Stefánsson, K., Edenberg, H. J., Holmans, P., Faraone, S. V. & Glatt, S. J., 2021, In: Molecular Psychiatry. 26, p. 800–815

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    ADHD Working Group of the Psychiatric Genomics Consortium (PGC), A. W. G. O. T. P. G. C. (., Jan 2019, In: Nature Genetics. 51, 1, p. 63-75 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Large recurrent microdeletions associated with schizophrenia

    Stefansson, H., Rujescu, D., Cichon, S., Pietilainen, O. P., Ingason, A., Steinberg, S., Fossdal, R., Sigurdsson, E., Sigmundsson, T., Buizer-Voskamp, J. E., Hansen, T., Jakobsen, K. D., Muglia, P., Francks, C., Matthews, P. M., Gylfason, A., Halldorsson, B. V., Gudbjartsson, D., Thorgeirsson, T. E., Sigurdsson, A. & 31 others, Jonasdottir, A., Jonasdottir, A., Bjornsson, A., Mattiasdottir, S., Blondal, T., Haraldsson, M., Magnusdottir, B. B., Giegling, I., Moller, H. J., Hartmann, A., Shianna, K. V., Ge, D., Need, A. C., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Paunio, T., Toulopoulou, T., Bramon, E., Di, F. M., Wang, August Gabriel, Ullum, H., Olesen, Jes, Werge, Thomas, Wang, August Gabriel, Ullum, H., Olesen, Jes & GROUP, G., 2008, In: Nature Study. 455, 7210, p. 232-6 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Association of a dopamine beta-hydroxylase gene variant with depression in elderly women possibly reflecting noradrenergic dysfunction

    Togsverd, M., Tanko, L. B., Bagger, Y. Z., Hansen, T., Qin, G., Christiansen, C., Rasmussen, H. B. & Werge, Thomas, 2008, In: Journal of Affective Disorders. 106, 1-2, p. 169-172 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia

    Andreou, D., Saetre, P., Lundmark, P., Hansen, T., Timm, S., Melle, I., Djurovic, S., Andreassen, O. A., Werge, T., Hall, H., Agartz, I., Terenius, L., Jönsson, E. G., Andreou, D., Saetre, P., Lundmark, P., Hansen, T., Timm, S., Melle, I., Djurovic, S. & 6 others, Andreassen, O. A., Werge, Thomas, Hall, H., Agartz, I., Terenius, L. & Jönsson, E. G., 2009, In: Psychiatric Genetics. 19, 5, p. 273-4 1 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Disruption of the neurexin 1 gene is associated with schizophrenia

    Rujescu, D., Ingason, A., Cichon, S., Pietiläinen, O. P. H., Barnes, M. R., Toulopoulou, T., Picchioni, M., Vassos, E., Ettinger, U., Bramon, E., Murray, R., Ruggeri, M., Tosato, S., Bonetto, C., Steinberg, S., Sigurdsson, E., Sigmundsson, T., Petursson, H., Gylfason, A., Olason, P. I. & 31 others, Hardarsson, G., Jonsdottir, G. A., Gustafsson, O., Fossdal, R., Giegling, I., Möller, H., Hartmann, A. M., Hoffmann, P., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Djurovic, S., Melle, I., Andreassen, O. A., Hansen, T., Werge, Thomas, Kiemeney, L. A., Franke, B., Veltman, J., Buizer-Voskamp, J. E., GROUP Investigators, G. I., Sabatti, C., Ophoff, R. A., Rietschel, M., Nöthen, M. M., Stefansson, K., Peltonen, L. & Werge, Thomas, 2009, In: Human Molecular Genetics. 18, 5, p. 988-96 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE)

    Djurovic, S., Le Hellard, S., Kähler, A. K., Jönsson, E. G., Agartz, I., Steen, V. M., Hall, H., Wang, A. G., Rasmussen, H. B., Melle, I., Werge, T., Andreassen, O. A., Djurovic, S., Le Hellard, S., Kähler, A. K., Jönsson, E. G., Agartz, I., Steen, V. M., Hall, H., Wang, A. G. & 4 others, Rasmussen, H. B., Melle, I., Werge, Thomas & Andreassen, O. A., 2009, In: Psychiatry Research. 168, 3, p. 256-8 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Lack of association of the serotonin transporter gene promoter region polymorphism, 5-HTTLPR, including rs25531 with cigarette smoking and alcohol consumption

    Rasmussen, H., Bagger, Y., Tanko, L. B., Christiansen, C., Werge, Thomas, Rasmussen, H., Bagger, Y., Tanko, L. B., Christiansen, C. & Werge, Thomas, 2009, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 150B, 4, p. 575-80 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Suicidal Behavior and the Serotonin Transporter Gene Polymorphism (5-HTTLPR) with Novel Subtypes, in Danish Schizophrenic Patients

    Wang, August Gabriel, Rasmussen, Henrik Berg, Sørensen, H. J., Hvid, M., Breddam, C. H., Hansen, B., Bille, V. H., Garsdal, O., Jacoby, A., Søbye, K., Dam, O. H., Krogsbøl, H., Timm, S. & Werge, Thomas, 2009, In: Open Psychiatry Journal.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

    Anttila, V., Stefansson, H., Kallela, M., Todt, U., Terwindt, G. M., Calafato, M. S., Nyholt, D. R., Dimas, A. S., Freilinger, T., Müller-Myhsok, B., Artto, V., Inouye, M., Alakurtti, K., Kaunisto, M. A., Hämäläinen, E., de Vries, B., Stam, A. H., Weller, C. M., Heinze, A., Heinze-Kuhn, K. & 31 others, Goebel, I., Borck, G., Göbel, H., Steinberg, S., Wolf, C., Björnsson, A., Gudmundsson, G., Kirchmann, M., Hauge, A., Werge, Thomas, Schoenen, J., Eriksson, J. G., Hagen, K., Stovner, L., Wichmann, H., Meitinger, T., Alexander, M., Moebus, S., Schreiber, S., Aulchenko, Y. S., Breteler, M. M. B., Uitterlinden, A. G., Hofman, A., van Duijn, C. M., Tikka-Kleemola, P., Vepsäläinen, S., Lucae, S., Tozzi, F., Muglia, P., Olesen, Jes & International Headache Genetics Consortium, I. H. G. C., 1 Oct 2010, In: Nature Genetics. 42, 10, p. 869-73 5 p.

    Research output: Contribution to journalLetterResearchpeer-review

  15. Published

    An exploratory model for G x E interaction on hippocampal volume in schizophrenia; obstetric complications and hypoxia-related genes

    Haukvik, U. K., Saetre, P., McNeil, T., Bjerkan, P. S., Andreassen, O. A., Werge, Thomas, Jönsson, E. G. & Agartz, I., 1 Oct 2010, In: Progress in Neuro-Psychopharmacology & Biological Psychiatry. 34, 7, p. 1259-65 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders

    Duong, L., Klitten, L. L., Møller, R. S., Ingason, A., Jakobsen, K. D., Skjødt, C., Didriksen, M., Hjalgrim, H., Werge, Thomas & Tommerup, Niels, Apr 2012, In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 159B, 3, p. 354-8 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Lack of association between two dopamine D2 receptor gene polymorphisms and schizophrenia

    Caprini, S., Saetre, P., Melle, I., Djurovic, S., Andreassen, O. A., Skjødt, C., Doung, L., Werge, Thomas, Hall, H., Agartz, I., Terenius, L. & Jönsson, E. G., 1 Aug 2011, In: Psychiatric Genetics. 21, 4, p. 214-5 2 p.

    Research output: Contribution to journalLetterResearchpeer-review

  18. Published

    Kynurenine 3-monooxygenase polymorphisms: relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controls

    Holtze, M., Saetre, P., Engberg, G., Schwieler, L., Werge, Thomas, Andreassen, O. A., Hall, H., Terenius, L., Agartz, I., Jönsson, E. G., Schalling, M. & Erhardt, S., 2012, In: Journal of Psychiatry and Neuroscience. 37, 1, p. 53-7 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Reliability of clinical ICD-10 diagnoses among electroconvulsive therapy patients with chronic affective disorders

    Jakobsen, K. D., Hansen, T. F., Dam, H., Larsen, E. B., Gether, Ulrik & Werge, Thomas, 2008, In: European Journal of Psychiatry. 22, 3, p. 161-172 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

    Vassos, E., Steinberg, S., Cichon, S., Breen, G., Sigurdsson, E., Andreassen, O. A., Djurovic, S., Morken, G., Grigoroiu-Serbanescu, M., Diaconu, C. C., Czerski, P. M., Hauser, J., Babadjanova, G., Abramova, L. I., Mühleisen, T. W., Nöthen, M. M., Rietschel, M., McGuffin, P., St Clair, D., Gustafsson, O. & 28 others, Melle, I., Pietiläinen, O. P. H., Ruggeri, M., Tosato, S., Werge, Thomas, Ophoff, R. A., Rujescu, D., Børglum, A., Mors, O., Mortensen, P. B., Demontis, D., Hollegaard, M. V., van Winkel, R., Kenis, G., De Hert, M., Réthelyi, J. M., Bitter, I., Rubino, I. A., Golimbet, V., Kiemeney, L. A., van den Berg, L. H., Franke, B., Jönsson, E. G., Farmer, A., Stefansson, H., Stefansson, K., Collier, D. A. & GROUP Consortium, G. C., 2012, In: Biological Psychiatry. 72, 8, p. 645-50 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published

    Effects of postnatal anoxia on striatal dopamine metabolism and prepulse inhibition in rats

    Sandager-Nielsen, K., Andersen, M. B., Sager, T. N., Werge, Thomas & Scheel-Krüger, J., 2004, In: Pharmacology, Biochemistry and Behavior. 77, 4, p. 767-74 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    Submikroskopiske kromosomanomalier som årsag til skizofreni

    Hansen, T., Ingason, A. & Werge, Thomas, 2008, In: Ugeskrift for Laeger. 170, 46, p. 3773-6 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms

    Fanous, A. H., Zhou, B., Aggen, S. H., Bergen, S. E., Amdur, R. L., Duan, J., Sanders, A. R., Shi, J., Mowry, B. J., Olincy, A., Amin, F., Cloninger, C. R., Silverman, J. M., Buccola, N. G., Byerley, W. F., Black, D. W., Freedman, R., Dudbridge, F., Holmans, P. A., Ripke, S. & 8 others, Gejman, P. V., Kendler, K. S., Levinson, D. F., Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, S. P. G. A. S. (. C., Hansen, T. F., Werge, Thomas, Olsen, L. & Rasmussen, H. B., 2012, In: American Journal of Psychiatry. 169, 12, p. 1309-17 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Individualization of treatments with drugs metabolized by CES1: combining genetics and metabolomics

    Rasmussen, Henrik Berg, Bjerre, D., Linnet, Kristian, Jürgens, G., Dalhoff, Kim, Stefansson, H., Hankemeier, T., Kaddurah-Daouk, R., Taboureau, O., Brunak, Søren, Houmann, T., Jeppesen, Pia, Pagsberg, Anne Katrine, Plessen, K., Dyrborg, J., Hansen, Peter Riis, Hansen, P. E., Hughes, T., Werge, Thomas & INDICES Consortium, I. C., Apr 2015, In: Pharmacogenomics. 16, 6, p. 649-65

    Research output: Contribution to journalReviewResearchpeer-review

  25. Published

    Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

    Duong, L. T. T., Hoeffding, L. K., Petersen, K. B., Knudsen, C. D., Thygesen, J. H., Klitten, L. L., Tommerup, Niels, Ingason, A. & Werge, Thomas, Dec 2015, In: European Journal of Medical Genetics. 58, 12, p. 650-653 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

Previous 1 2 3 4 5 6 7 8 ...18 Next

ID: 34394780