Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

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    ORCID: 0000-0001-6703-7762

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    1. Published

      Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine

      Rasmussen, A. H., Olofsson, I., Chalmer, M. A., Olesen, Jes & Hansen, Thomas Folkmann, 2020, In: Journal of Medical Genetics. 57, p. 610-616

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

    2. Published

      Characterization of Familial and Sporadic Migraine

      Ravn, J., Chalmer, M. A., Oehrstroem, E. L., Kogelman, L. J. A. & Hansen, Thomas Folkmann, 2019, In: Headache. 59, 10, p. 1802-1807 6 p.

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

    3. Published

      The tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: a multi-centre case-control study and meta-analysis

      Saetre, P., Lundmark, P., Wang, August Gabriel, Hansen, Thomas Folkmann, Rasmussen, Henrik Berg, Djurovic, S., Melle, I., Andreassen, O. A., Werge, Thomas, Agartz, I., Hall, H., Terenius, L. & Jönsson, E. G., 5 Mar 2010, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 153B, 2, p. 387-96 10 p.

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

    4. Published

      Cerebral small vessel disease genomics and its implications across the lifespan

      Sargurupremraj, M., Suzuki, H., Jian, X., Sarnowski, C., Evans, T. E., Bis, J. C., Eiriksdottir, G., Sakaue, S., Terzikhan, N., Habes, M., Zhao, W., Armstrong, N. J., Hofer, E., Yanek, L. R., Hagenaars, S. P., Kumar, R. B., van den Akker, E. B., McWhirter, R. E., Trompet, S., Mishra, A. & 32 others, Saba, Y., Satizabal, C. L., Beaudet, G., Petit, L., Tsuchida, A., Zago, L., Schilling, S., Sigurdsson, S., Gottesman, R. F., Lewis, C. E., Aggarwal, N. T., Lopez, O. L., Smith, J. A., Valdés Hernández, M. C., van der Grond, J., Wright, M. J., Knol, M. J., Dörr, M., Thomson, R. J., Bordes, C., Le Grand, Q., Duperron, M. G., Smith, A. V., Niessen, W. J., Pers, Tune H, Ingason, A., Francke Christensen, A., Hansen, Thomas Folkmann, Werge, Thomas, Olesen, Jes, International Network against Thrombosis (INVENT) Consortium, I. N. A. T. (. C. & International Headache Genomics Consortium (IHGC), I. H. G. C. (., 2020, In: Nature Communications. 11, 1, 18 p., 6285.

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

    5. Published

      A genome-wide association study of social trust in 33,882 Danish blood donors

      Sequeros, C. B., Hansen, T. F., Westergaard, D., Louloudis, I., Kalamajski, S., Röder, T., Rohde, P. D., Schwinn, M., Clemmensen, L. H., Didriksen, M., Nyegaard, M., Hjalgrim, H., Nielsen, K. R., Bruun, M. T., Ostrowski, S. R., Erikstrup, C., Mikkelsen, S., Sørensen, E., Pedersen, O. B. V., Brunak, S. & 3 others, Banasik, Karina, Giordano, G. N. & DBDS Genomic Consortium, D. G. C., 2024, In: Scientific Reports. 14, 12 p., 1402.

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

    6. Published

      Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes

      Skotte, L., Fadista, J., Bybjerg-Grauholm, J., Appadurai, V., Hildebrand, M. S., Hansen, T. F., Banasik, K., Grove, J., Albiñana, C., Geller, F., Bjurström, C. F., Vilhjálmsson, B. J., Coleman, M., Damiano, J. A., Burgess, R., Scheffer, I. E., Pedersen, O. B. V., Erikstrup, C., Westergaard, D., Nielsen, K. R. & 19 others, Sørensen, E., Bruun, M. T., Liu, X., Hjalgrim, Henrik, Pers, Tune H, Mortensen, P. B., Mors, O., Nordentoft, Merete, Dreier, J. W., Børglum, A. D., Christensen, J., Hougaard, D. M., Buil, A., Hviid, Anders Peter, Melbye, M., Ullum, H., Berkovic, S. F., Werge, Thomas & Feenstra, B., 2022, In: Brain. 145, 2, p. 555–568

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

    7. Published

      A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

      Skuladottir, A. T., Bjornsdottir, G., Thorleifsson, G., Walters, G. B., Nawaz, M. S., Moore, K. H. S., Olason, P. I., Thorgeirsson, T. E., Sigurpalsdottir, B., Sveinbjornsson, G., Eggertsson, H. P., Magnusson, S. H., Oddsson, A., Bjornsdottir, A., Vikingsson, A., Sveinsson, O. A., Hrafnsdottir, M. G., Sigurdardottir, G. R., Halldorsson, B. V., Hansen, T. F. & 13 others, Paarup, H., Erikstrup, C., Nielsen, K., Klokker, Mads, Bruun, M. T., Sørensen, E., Banasik, Karina, Burgdorf, Kristoffer Sølvsten, Pedersen, Ole Birger Vesterager, Ullum, H., Jonsdottir, I., Stefansson, H. & Stefansson, K., 2021, In: Scientific Reports. 11, 1, 4188.

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

    8. Published

      A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

      Skuladottir, A. T., Bjornsdottir, G., Ferkingstad, E., Einarsson, G., Stefansdottir, L., Nawaz, M. S., Oddsson, A., Olafsdottir, T. A., Saevarsdottir, S., Walters, G. B., Magnusson, S. H., Bjornsdottir, A., Sveinsson, O. A., Vikingsson, A., Hansen, T. F., Jacobsen, R. L., Erikstrup, C., Schwinn, M., Brunak, S., Banasik, K. & 11 others, Ostrowski, Sisse Rye, Troelsen, Anders, Henkel, C., Pedersen, Ole Birger Vesterager, Jonsdottir, I., Gudbjartsson, D. F., Sulem, P., Thorgeirsson, T. E., Stefansson, H., Stefansson, K. & DBDS Genetic Consortium, D. G. C., 2022, In: Nature Communications. 13, 1, 9 p., 1598.

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

    9. Published

      GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

      Estonian Biobank, E. B. & DBDS Genomic Consortium, D. G. C., 2024, In: Communications Biology . 7, 1, 10 p., 504.

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

    10. 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

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    ID: 21418907