Thomas Werge

Thomas Werge

Clinical Professor

Member of:

  • Psychiatry


  1. 2009
  2. 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

  3. Published

    Interaction between genetic polymorphisms and stressful life events in first episode depression

    Bukh, Jens Otto Drachmann, Bock, C., Vinberg, Maj, Werge, Thomas, Gether, Ulrik, Kessing, Lars Vedel, Bukh, J. D., Bock, C., Vinberg, Maj, Werge, Thomas, Gether, U. & Kessing, Lars Vedel, 2009, In: Journal of Affective Disorders. 119, 1-3, p. 107-15 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    No interactions between genetic polymorphisms and stressful life events on outcome of antidepressant treatment

    Bukh, Jens Otto Drachmann, Bock, C., Vinberg, Maj, Werge, Thomas, Gether, Ulrik, Kessing, Lars Vedel, Bukh, J. D., Bock, C., Vinberg, Maj, Werge, Thomas, Gether, U. & Kessing, Lars Vedel, 2009, In: European Neuropsychopharmacology.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Mutation screening of the glutamate cysteine ligase modifier (GCLM) gene in patients with schizophrenia

    Butticaz, C., Werge, Thomas, Beckmann, J. S., Cuénod, M., Do, K. Q., Rivolta, C., Butticaz, C., Werge, Thomas, Beckmann, J. S., Cuénod, M., Do, K. Q. & Rivolta, C., 2009, In: Psychiatric Genetics. 19, 4, p. 201-8 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE)

    Djurovic, S., Kähler, A. K., Kulle, B., Jönsson, E. G., Agartz, I., Le Hellard, S., Hall, H., Jakobsen, K. D., Hansen, T., Melle, I., Werge, T., Steen, V. M., Andreassen, O. A., Djurovic, S., Kähler, A. K., Kulle, B., Jönsson, E. G., Agartz, I., Le Hellard, S., Hall, H. & 6 others, Jakobsen, K. D., Hansen, T. F., Melle, I., Werge, Thomas, Steen, V. M. & Andreassen, O. A., 2009, In: Schizophrenia Research. 107, 2-3, p. 242-8 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. 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

  8. Published

    Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M. & 126 others, Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, Celeste Michala, Hansen, J. W., Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U., Stefansson, K., Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M., Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, C. M., Hansen, J. W., Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U. & Stefansson, K., 2009, In: Nature Genetics. 41, 3, p. 342-7 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M. & 53 others, Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, Celeste Michala, Hansen, Jakob Werner, Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U. & Stefansson, K., Mar 2009, In: Nature Genetics. 41, 3, p. 342-7 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published
  11. Published

    DTNBP1, NRG1, DAOA, DAO and GRM3 polymorphisms and schizophrenia: an association study

    Jönsson, E. G., Saetre, P., Vares, M., Andreou, D., Larsson, K., Timm, S., Rasmussen, H. B., Djurovic, S., Melle, I., Andreassen, O. A., Agartz, I., Werge, T., Hall, H., Terenius, L., Jönsson, E. G., Saetre, P., Vares, M., Andreou, D., Larsson, K., Timm, S. & 8 others, Rasmussen, H. B., Djurovic, S., Melle, I., Andreassen, O. A., Agartz, I., Werge, Thomas, Hall, H. & Terenius, L., 2009, In: Neuropsychobiology. 59, 3, p. 142-50 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 34394780