Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

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    ORCID: 0000-0001-6703-7762

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    1. Published

      A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

      Ingason, A., Giegling, I., Cichon, S., Hansen, T., Rasmussen, H. B., Nielsen, J., Jürgens, G., Muglia, P., Hartmann, A. M., Strengman, E., Vasilescu, C., Mühleisen, T. W., Djurovic, S., Melle, I., Lerer, B., Möller, H-J., Francks, C., Pietiläinen, O. P. H., Lonnqvist, J., Suvisaari, J. & 21 others, Tuulio-Henriksson, A., Walshe, M., Vassos, E., Di Forti, M., Murray, R., Bonetto, C., Tosato, S., Cantor, R. M., Rietschel, M., Craddock, N., Owen, M. J., Peltonen, L., Andreassen, O. A., Nöthen, M. M., St Clair, D., Ophoff, R. A., O'Donovan, M. C., Collier, D. A., Werge, Thomas, Rujescu, D. & GROUP Investigators, G. I., 1 Apr 2010, In: Human Molecular Genetics. 19, 7, p. 1379-86 8 p.

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

    2. 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

    3. 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

    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

      Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

      Häppölä, P., Gormley, P., Nuottamo, M. E., Artto, V., Sumelahti, M. L., Nissilä, M., Keski-Säntti, P., Ilmavirta, M., Kaunisto, M. A., Hämäläinen, E. I., Ripatti, S., Pirinen, M., Wessman, M., Palotie, A., Kallela, M., International Headache Genetics Consortium (IHGC), I. H. G. C. (., Hansen, Thomas Folkmann & Olesen, Jes, 2022, In: Cephalalgia. 42, 4-5, p. 345-356 12 p.

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

    6. 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

    7. 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

    8. Published

      The differentiating effect of COVID-19-associated stress on the morbidity of blood donors with symptoms of hidradenitis suppurativa, hyperhidrosis, or psoriasis

      Henning, M. A. S., Didriksen, M., Ibler, Kristina Sophie, Ostrowski, Sisse Rye, Erikstrup, C., Nielsen, K., Sækmose, S. G., Hansen, Thomas Folkmann, Ullum, H., Thørner, L. W., Kaspersen, K. A., Mikkelsen, S., Jemec, Gregor & Pedersen, Ole Birger Vesterager, 2023, In: Quality of Life Research. 32, p. 2925–2937 13 p.

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

    9. Published

      Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement

      Henkel, C., Styrkársdóttir, U., Thorleifsson, G., Stefánsdóttir, L., Björnsdóttir, G., Banasik, K., Brunak, S., Erikstrup, C., Dinh, K. M., Hansen, T. F., Nielsen, K. R., Bruun, M. T., Dowsett, J., Brodersen, T., Thorgeirsson, T. E., Gromov, K., Boesen, M. P., Ullum, H., Ostrowski, S. R., Pedersen, O. B. & 3 others, Stefánsson, K., Troelsen, A. & DBDS Genomic Consortium, D. G. C., 2023, In: Annals of the Rheumatic Diseases. 82, p. 384-392

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

    10. Published

      Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

      Helgadottir, A., Thorleifsson, G., Alexandersson, K. F., Tragante, V., Thorsteinsdottir, M., Eiriksson, F. F., Gretarsdottir, S., Björnsson, E., Magnusson, O., Sveinbjornsson, G., Jonsdottir, I., Steinthorsdottir, V., Ferkingstad, E., Jensson, B. Ö., Stefansson, H., Olafsson, I., Christensen, A. H., Torp-Pedersen, C., Køber, L., Pedersen, O. B. & 23 others, Erikstrup, C., Sørensen, E., Brunak, Søren, Banasik, Karina, Hansen, Thomas Folkmann, Nyegaard, M., Eyjolfssson, G. I., Sigurdardottir, O., Thorarinsson, B. L., Matthiasson, S. E., Steingrimsdottir, T., Bjornsson, E. S., Danielsen, R., Asselbergs, F. W., Arnar, D. O., Ullum, H., Bundgård, Henning, Sulem, P., Thorsteinsdottir, U., Thorgeirsson, G., Holm, H., Gudbjartsson, D. F. & Stefansson, K., 2020, In: European Heart Journal. 41, 28, p. 2618-2628 11 p.

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

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    ID: 21418907