Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

Member of:

    ORCID: 0000-0001-6703-7762

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    11 - 20 out of 116Page size: 10
    1. 2011
    2. Published

      At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia

      Hansen, T., Ingason, A., Djurovic, S., Melle, I., Fenger, M., Gustafsson, O., Jakobsen, K. D., Rasmussen, H. B., Tosato, S., Rietschel, M., Frank, J., Owen, M., Bonetto, C., Suvisaari, J., Thygesen, J. H., Pétursson, H., Lönnqvist, J., Sigurdsson, E., Giegling, I., Craddock, N. & 12 others, O'Donovan, M. C., Ruggeri, M., Cichon, S., Ophoff, R. A., Pietiläinen, O., Peltonen, L., Nöthen, M. M., Rujescu, D., St Clair, D., Collier, D. A., Andreassen, O. A. & Werge, Thomas, 1 Jul 2011, In: Biological Psychiatry. 70, 1, p. 59-63 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      Kynurenine 3-monooxygenase (KMO) polymorphisms in schizophrenia: An association study

      Holtze, M., Saetre, P., Erhardt, S., Schwieler, L., Werge, Thomas, Hansen, Thomas Folkmann, Nielsen, J., Djurovic, S., Melle, I., Andreassen, O. A., Hall, H., Terenius, L., Agartz, I., Engberg, G., Jönsson, E. G. & Schalling, M., Apr 2011, In: Schizophrenia Research. 127, 1-3, p. 270-2 3 p.

      Research output: Contribution to journal › Letter › Research › peer-review

    4. Published

      The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

      Håvik, B., Le Hellard, S., Rietschel, M., Lybæk, H., Djurovic, S., Mattheisen, M., Mühleisen, T. W., Degenhardt, F., Priebe, L., Maier, W., Breuer, R., Schulze, T. G., Agartz, I., Melle, I., Hansen, T., Bramham, C. R., Nöthen, M. M., Stevens, B., Werge, T., Andreassen, O. A. & 2 others, Cichon, S. & Steen, V. M., 2011, In: Biological Psychiatry. 70, 1, p. 35-42 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Copy number variations of chromosome 16p13.1 region associated with schizophrenia

      Ingason, A., Rujescu, D., Cichon, S., Sigurdsson, E., Sigmundsson, T., Pietiläinen, O. P. H., Buizer-Voskamp, J. E., Strengman, E., Francks, C., Muglia, P., Gylfason, A., Gustafsson, O., Olason, P. I., Steinberg, S., Hansen, T. F., Jakobsen, K. D., Rasmussen, H. B., Giegling, I., Möller, H-J., Hartmann, A. & 29 others, Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Bramon, E., Kiemeney, L. A., Franke, B., Murray, R., Vassos, E., Toulopoulou, T., Mühleisen, T. W., Tosato, S., Ruggeri, M., Djurovic, S., Andreassen, O. A., Zhang, Z., Werge, Thomas, Ophoff, R. A., Rietschel, M., Nöthen, M. M., Petursson, H., Stefansson, H., Peltonen, L., Collier, D., Stefansson, K., St Clair, D. M. & GROUP Investigators, G. I., 1 Jan 2011, In: Molecular Psychiatry. 16, 1, p. 17-25 9 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    6. Published

      Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

      Ingason, A., Kirov, G., Giegling, I., Hansen, T., Isles, A. R., Jakobsen, K. D., Kristinsson, K. T., le Roux, L., Gustafsson, O., Craddock, N., Möller, H-J., McQuillin, A., Muglia, P., Cichon, S., Rietschel, M., Ophoff, R. A., Djurovic, S., Andreassen, O. A., Pietiläinen, O. P. H., Peltonen, L. & 22 others, Dempster, E., Collier, D. A., St Clair, D., Rasmussen, Henrik Berg, Glenthøj, Birte Yding, Kiemeney, L. A., Franke, B., Tosato, S., Bonetto, C., Saemundsen, E., Hreidarsson, S. J., Nöthen, M. M., Gurling, H., O'Donovan, M. C., Owen, M. J., Sigurdsson, E., Petursson, H., Stefansson, H., Rujescu, D., Stefansson, K., Werge, Thomas & GROUP Investigators, G. I., 1 Apr 2011, In: American Journal of Psychiatry. 168, 4, p. 408-417 10 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

      Kähler, A. K., Djurovic, S., Rimol, L. M., Brown, A. A., Athanasiu, L., Jönsson, E. G., Hansen, T., Gústafsson, O., Hall, H., Giegling, I., Muglia, P., Cichon, S., Rietschel, M., Pietiläinen, O. P. H., Peltonen, L., Bramon, E., Collier, D., St Clair, D., Sigurdsson, E., Petursson, H. & 8 others, Rujescu, D., Melle, I., Werge, Thomas, Steen, V. M., Dale, A. M., Matthews, R. T., Agartz, I. & Andreassen, O. A., 1 Jan 2011, In: Biological Psychiatry. 69, 1, p. 90-6 7 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      Expanding the range of ZNF804A variants conferring risk of psychosis

      Steinberg, S., Mors, O., Børglum, A., Gustafsson, O., Werge, T., Mortensen, P. B., Andreassen, O. A., Sigurdsson, E., Thorgeirsson, T. E., Böttcher, Y., Olason, P., Ophoff, R. A., Cichon, S., Gudjonsdottir, I. H., Pietiläinen, O. P. H., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T. F., Athanasiu, L. & 31 others, Suvisaari, J., Lonnqvist, J., Paunio, T., Hartmann, A., Jürgens, G., Nordentoft, Merete, Hougaard, D., Norgaard-Pedersen, B., Breuer, R., Möller, H., Giegling, I., Glenthøj, Birte Yding, Rasmussen, Henrik Berg, Mattheisen, M., Bitter, I., Réthelyi, J. M., Sigmundsson, T., Fossdal, R., Thorsteinsdottir, U., Ruggeri, M., Tosato, S., Strengman, E., Genetic Risk and Outcome in Psychosis, G. R. A. O. I. P., Kiemeney, L. A., Melle, I., Djurovic, S., Abramova, L., Kaleda, V., Walshe, M., Bramon, E. & Vassos, E., Jan 2011, In: Molecular Psychiatry. 16, 1, p. 59-66 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      Dual association of a TRKA polymorphism with schizophrenia

      Van Schijndel, J. E., Van Zweeden, M., Van Loo, K. M. J., Djurovic, S., Andreassen, O. A., Hansen, T., Werge, T., Nyegaard, M., Sørensen, K. M., Nordentoft, M., Mortensen, P. B., Mors, O., Børglum, A., Del-Favero, J., Norrback, K-F., Adolfsson, R., Hert, M. D., Claes, S., Cichon, S., Rietschel, M. & 4 others, Nöthen, M. M., Kallunki, P., Pedersen, J. T. & Martens, G. J. M., 2011, In: Psychiatric Genetics. 21, 3, p. 125-31 7 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. 2015
    11. Published

      Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death

      Hoeffding, L. K., Kock, K. F., Johnsen, I. G., Hansen, Thomas Folkmann & Werge, Thomas, Jan 2015, In: Case Reports in Perinatal Medicine.

      Research output: Contribution to journal › Journal article › Research › peer-review

    12. 2016
    13. Published

      Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

      Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., Farh, K-H., Cuenca-Leon, E., Muona, M., Furlotte, N. A., Kurth, T., Ingason, A., McMahon, G., Ligthart, L., Terwindt, G. M., Kallela, M., Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H. & 31 others, Steinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimäki, T., Sarin, A., Wedenoja, J., Hinds, D. A., Buring, J. E., Schürks, M., Ridker, P. M., Hrafnsdottir, M. G., Stefansson, H., Ring, S. M., Hottenga, J., Penninx, B. W. J. H., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Malik, R., Heath, A. C., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Christensen, A. F., Hansen, Thomas Folkmann, Werge, Thomas, Olesen, Jes & International Headache Genetics Consortium, I. H. G. C., Aug 2016, In: Nature Genetics. 48, 8, p. 856-66 11 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

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    ID: 21418907