Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

Member of:


    1. Published

      Elucidating the relationship between migraine risk and brain structure using genetic data

      International Headache Genetics Consortium, I. H. G. C., 1 Sep 2022, In: Brain. 145, 9, p. 3214-3224 11 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    2. 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 journalJournal articleResearchpeer-review

    3. Published

      Experience of loneliness during the COVID-19 pandemic: a cross-sectional study of 50 968 adult Danes

      Christoffersen, L. A. N., Helenius, D., Schwinn, M., Erikstrup, C., Hjalgrim, Henrik, Nissen, J., Banasik, Karina, Nielsen, K., Kaspersen, K. A., Dinh, K. M., Bruun, M. T., Ostrowski, Sisse Rye, Sækmose, S., Hansen, Thomas Folkmann, Werge, Thomas, Didriksen, M. & Pedersen, Ole Birger Vesterager, 2023, In: BMJ Open. 13, 4, 9 p., e064033.

      Research output: Contribution to journalJournal articleResearchpeer-review

    4. Published

      Familial analysis reveals rare risk variants for migraine in regulatory regions

      Techlo, T. R., Rasmussen, A. H., Moller, P. L., Bottcher, M., Winther, S., Davidsson, O. B., Olofsson, I. A., Chalmer, M. A., Kogelman, L. J. A., Nyegaard, M., Olesen, Jes & Hansen, Thomas Folkmann, 2020, In: Neurogenetics. 21, 3, p. 149-157

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. Published

      Functional gene networks reveal distinct mechanisms segregating in migraine families

      Rasmussen, A. H., Kogelman, L. J. A., Kristensen, D. M., Chalmer, M. A., Olesen, Jes & Hansen, Thomas Folkmann, 2020, In: Brain. 143, p. 2945-2956 12 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    6. Published

      GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

      Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, M. J., Craddock, N. J., O'Donovan, M. C., Blackman, J., Lewis, D., Kirov, G. K. & 42 others, Qin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D., Bronstein, M., Darvasi, A., Lencz, T., Malhotra, A. K., Rujescu, D., Giegling, I., Werge, Thomas, Hansen, Thomas Folkmann, Ingason, A., Nöethen, M. M., Rietschel, M., Cichon, S., Djurovic, S., Andreassen, O. A., Cantor, R. M., Ophoff, R., Corvin, A., Morris, D. W., Gill, M., Pato, C. N., Pato, M. T., Macedo, A., Gurling, H. M. D., McQuillin, A., Pimm, J., Hultman, C., Lichtenstein, P., Sklar, P., Purcell, S. M., Scolnick, E., St Clair, D., Blackwood, D. H. R. & Kendler, K. S., 2011, In: Molecular Psychiatry. 16, 11, p. 1117-29 13 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    7. Published

      Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

      Bryois, J., Skene, N. G., Hansen, T. F., Kogelman, L. J. A., Watson, H. J., Liu, Z., Eating Disorders Working Group of the Psychiatric Genomics Consortium, Adan, R., Alfredsson, L., Ando, T., Andreassen, O., Baker, J., Bergen, A., Berrettini, W., Birgegård, A., Boden, J., Boehm, I., Boni, C., Boraska Perica, V., Brandt, H. & 44 others, Breen, G., Bryois, J., Buehren, K., Bulik, C., Burghardt, R., Cassina, M., Cichon, S., Clementi, M., Coleman, J., Cone, R., Courtet, P., Crawford, S., Crow, S., Crowley, J., Danner, U., Davis, O., de Zwaan, M., Dedoussis, G., Degortes, D., DeSocio, J., Dick, D., Hinney, A., Grove, J., Larsen, J., Mattheisen, M., Mortensen, P. B., Petersen, L., Werge, Thomas, Zeggini, E., Zerwas, S., Zipfel, S., International Headache Genetics Consortium, I. H. G. C., Anttila, V., Artto, V., Belin, A. C., Christensen, A. F., Esserlind, A., Kogelman, L. J. A., Olesen, Jes, Olesen, Jes, Winsvold, B. S., Zhao, H., Zwart, J. & 23andMe Research Team, 2. R. T., May 2020, In: Nature Genetics. 52, p. 482-493

      Research output: Contribution to journalJournal articleResearchpeer-review

    8. Published

      Genetic prediction of 33 blood group phenotypes using an existing genotype dataset

      Moslemi, C., Sækmose, S. G., Larsen, R., Bay, J. T., Brodersen, T., Didriksen, M., Hjalgrim, H., Banasik, K., Nielsen, K. R., Bruun, M. T., Dowsett, J., Dinh, K. M., Mikkelsen, S., Mikkelsen, C., Hansen, T. F., Ullum, H., Erikstrup, C., Brunak, S., Krogfelt, K. A., Storry, J. R. & 3 others, Ostrowski, Sisse Rye, Olsson, M. L. & Pedersen, Ole Birger Vesterager, 2023, In: Transfusion. 63, 12, p. 2297-2310 14 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    9. 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 journalJournal articleResearchpeer-review

    10. Published

      Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

      Hautakangas, H., Winsvold, B. S., Ruotsalainen, S. E., Bjornsdottir, G., Harder, A. V. E., Kogelman, L. J. A., Thomas, L. F., Noordam, R., Benner, C., Gormley, P., Artto, V., Banasik, K., Bjornsdottir, A., Boomsma, D. I., Brumpton, B. M., Burgdorf, K. S., Buring, J. E., Chalmer, M. A., de Boer, I., Dichgans, M. & 51 others, Erikstrup, C., Farkkila, M., Garbrielsen, M. E., Ghanbari, M., Hagen, K., Happola, P., Hottenga, J., Hrafnsdottir, M. G., Hveem, K., Johnsen, M. B., Kahonen, M., Kristoffersen, E. S., Kurth, T., Lehtimaki, T., Lighart, L., Magnusson, S. H., Malik, R., Pedersen, Ole Birger Vesterager, Pelzer, N., Penninx, B. W. J. H., Ran, C., Ridker, P. M., Rosendaal, F. R., Sigurdardottir, G. R., Skogholt, A. H., Sveinsson, O. A., Thorgeirsson, T. E., Ullum, H., Vijfhuizen, L. S., Widen, E., van Dijk, K. W., Aromaa, A., Belin, A. C., Freilinger, T., Ikram, M. A., Jarvelin, M., Raitakari, O. T., Terwindt, G. M., Kallela, M., Wessman, M., Olesen, Jes, Chasman, D. I., Nyholt, D. R., Stefansson, H., Stefansson, K., van den Maagdenberg, A. M. J. M., Hansen, Thomas Folkmann, Ripatti, S., Zwart, J., Palotie, A. & Pirinen, M., 2022, In: Nature Genetics. 54, p. 152-160 16 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

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    ID: 21418907