Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

Member of:


    1. Published

      Blood donation and migraine relief: A national population cohort study in Denmark

      Davidsson, O. B., Rostgaard, K., Chalmer, M. A., Kogelman, L. J. A., Aagaard, B., Brodersen, T., Bruun, M. T., Mikkelsen, Christina, Mikkelsen, S., Nyegaard, M., Pedersen, Ole Birger Vesterager, Ullum, H., Sørensen, E., Ostrowski, Sisse Rye, Erikstrup, C., Hansen, Thomas Folkmann & Hjalgrim, Henrik, 2024, In: Transfusion. 64, 4, p. 647–655 9 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    2. Published

      Self-reported restless legs syndrome and involuntary leg movements during sleep are associated with symptoms of attention deficit hyperactivity disorder

      Didriksen, M., Thørner, L. W., Erikstrup, C., Pedersen, Ole Birger Vesterager, Paarup, H. M., Petersen, M., Hansen, Thomas Folkmann, Banasik, Karina, Nielsen, K. R., Hjalgrim, Henrik, Jennum, Poul, Sørensen, E., Burgdorf, K. S. & Ullum, H., 2019, In: Sleep Medicine. 57, p. 115-121

      Research output: Contribution to journalJournal articleResearchpeer-review

    3. Published

      Cross-sectional study identifies lower risk of Staphylococcus aureus nasal colonization in Danish blood donors with hidradenitis suppurativa symptoms

      Dinh, K. M., Erikstrup, L. T., Andersen, Rune Kjærsgaard, Andersen, P. S., Mikkelsen, S., Kjerulff, B. D., Burgdorf, K. S., Hansen, Thomas Folkmann, Nielsen, K. R., Hjalgrim, H., Jemec, Gregor, Ullum, H., Erikstrup, C. & Pedersen, O. B., 2020, In: British Journal of Dermatology. 183, 2, p. 387-389

      Research output: Contribution to journalLetterResearchpeer-review

    4. Published

      Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor

      Dowsett, J., Ferkingstad, E., Rasmussen, L. J. H., Thørner, L. W., Magnússon, M. K., Sugden, K., Thorleifsson, G., Frigge, M., Burgdorf, K. S., Ostrowski, S. R., Sørensen, E., Erikstrup, C., Pedersen, O. B., Hansen, T. F., Banasik, K., Brunak, S., Tragante, V., Lund, S. H., Stefansdottir, L., Gunnarson, B. & 10 others, Poulton, R., Arseneault, L., Caspi, A., Moffitt, T. E., Gudbjartsson, D., Eugen-Olsen, J., Stefánsson, H., Stefánsson, K., Ullum, H. & DBDS Genomic Consortium, D. G. C., 2021, In: Communications Biology . 4, 1, p. 655

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. Published

      Cohort Profile: The Danish Blood Donor Study

      Erikstrup, C., Sørensen, E., Nielsen, K. R., Bruun, M. T., Petersen, M. S., Rostgaard, K., Thørner, L. W., Larsen, M., Mikkelsen, S., Dinh, K. M., Schwinn, M., Rigas, A. S., Didriksen, M., Dowsett, J., von Stemann, J. H., Brodersen, T., Paulsen, I. W., Hindhede, L., Sækmose, S. G., Kaspersen, K. A. & 10 others, Boldsen, J. K., Kjerulff, B., Werge, Thomas, Brunak, Søren, Banasik, Karina, Hansen, Thomas Folkmann, Ullum, H., Hjalgrim, Henrik, Ostrowski, Sisse Rye & Pedersen, Ole Birger Vesterager, 2023, In: International Journal of Epidemiology. 52, 3, p. e162-e171 10 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    6. Published

      Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

      Forstner, A. J., Awasthi, S., Wolf, C., Maron, E., Erhardt, A., Czamara, D., Eriksson, E., Lavebratt, C., Allgulander, C., Friedrich, N., Becker, J., Hecker, J., Rambau, S., Conrad, R., Geiser, F., Mcmahon, F. J., Moebus, S., Hess, T., Buerfent, B. C., Hoffmann, P. & 55 others, Herms, S., Heilmann-heimbach, S., Kockum, I., Olsson, T., Alfredsson, L., Weber, H., Alpers, G. W., Arolt, V., Fehm, L., Fydrich, T., Gerlach, A. L., Hamm, A., Kircher, T., Pané-farré, C. A., Pauli, P., Rief, W., Ströhle, A., Plag, J., Lang, T., Wittchen, H., Mattheisen, M., Meier, S., Metspalu, A., Domschke, K., Reif, A., Hovatta, I., Lindefors, N., Andersson, E., Schalling, M., Mbarek, H., Milaneschi, Y., De Geus, E. J. C., Boomsma, D. I., Penninx, B. W. J. H., Thorgeirsson, T. E., Steinberg, S., Stefansson, K., Stefansson, H., Müller-myhsok, B., Hansen, Thomas Folkmann, Børglum, A. D., Werge, Thomas, Mortensen, P. B., Nordentoft, Merete, Hougaard, D. M., Hultman, C. M., Sullivan, P. F., Nöthen, M. M., Woldbye, David Paul Drucker, Mors, O., Binder, E. B., Rück, C., Ripke, S., Deckert, J. & Schumacher, J., 2021, In: Molecular Psychiatry. 26, p. 4179–4190 12 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    7. Published

      Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

      Glanville, K. P., Coleman, J. R. I., Hanscombe, K. B., Euesden, J., Choi, S. W., Purves, K. L., Breen, G., Air, T. M., Andlauer, T. F. M., Baune, B. T., Binder, E. B., Blackwood, D. H. R., Boomsma, D. I., Buttenschøn, H. N., Colodro-Conde, L., Dannlowski, U., Direk, N., Dunn, E. C., Forstner, A. J., de Geus, E. J. C. & 31 others, Grabe, H. J., Hamilton, S. P., Jones, I., Jones, L. A., Knowles, J. A., Kutalik, Z., Levinson, D. F., Lewis, G., Lind, P. A., Lucae, S., Magnusson, P. K., McGuffin, P., McIntosh, A. M., Milaneschi, Y., Mors, O., Mostafavi, S., Müller-Myhsok, B., Pedersen, N. L., Penninx, B. W. J. H., Potash, J. B., Preisig, M., Ripke, S., Shi, J., Bækvad-Hansen, M., Hansen, C. S., Hansen, Thomas Folkmann, Pedersen, C. B., Pedersen, M. G., Nordentoft, Merete, Werge, Thomas & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, M. D. D. W. G. O. T. P. G. C., 2020, In: Biological Psychiatry. 87, 5, p. 419-430 12 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    8. Published

      The population genomic legacy of the second plague pandemic

      Gopalakrishnan, S., Ebenesersdóttir, S. S., Lundstrøm, I. K. C., Turner-Walker, G., Moore, K. H. S., Luisi, P., Margaryan, A., Martin, M. D., Ellegaard, M. R., Magnússon, Ó., Sigurðsson, Á., Snorradóttir, S., Magnúsdóttir, D. N., Laffoon, J. E., van Dorp, L., Liu, X., Moltke, I., Ávila-Arcos, M. C., Schraiber, J. G., Rasmussen, S. & 40 others, Juan, D., Gelabert, P., de-Dios, T., Fotaki, Anna Katerina, Iraeta Orbegozo, Miren, Vågene, Åshild Joanne, Denham, S. D., Christophersen, A., Stenøien, H. K., Vieira, Filipe Garrett, Liu, Shanlin, Günther, T., Kivisild, T., Moseng, O. G., Skar, B., Cheung, C., Sandoval-Velasco, Marcela, Wales, N., Schroeder, Hannes, Campos, P. F., Guðmundsdóttir, V. B., Sicheritz-Pontén, Thomas, Petersen, Bent, Halgunset, J., Gilbert, E., Cavalleri, G. L., Hovig, E., Kockum, I., Olsson, T., Alfredsson, L., Hansen, Thomas Folkmann, Werge, Thomas, Willerslev, Eske, Balloux, F., Marques-Bonet, T., Lalueza-Fox, C., Nielsen, Rasmus, Stefánsson, K., Helgason, A. & Gilbert, M Thomas P, 2022, In: Current Biology. 32, 21, p. 4743-4751.e6

      Research output: Contribution to journalJournal articleResearchpeer-review

    9. 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 journalJournal articleResearchpeer-review

    10. Published

      A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

      Guo, Y., Rist, P. M., Daghlas, I., Giulianini, F., 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. & 32 others, Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H., Steinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimäki, T., Sarin, A. P., Wedenoja, J., Hinds, D. A., Buring, J. E., Schürks, M., Ridker, P. M., Hrafnsdottir, M. G., Stefansson, H., Ring, S. M., Hottenga, J. J., Penninx, B. W. J. H., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Malik, R., Christensen, A. F., Hansen, Thomas Folkmann, Werge, Thomas, Olesen, Jes, The International Headache Genetics Consortium, T. I. H. G. C. & the 23andMe Research Team, T. 2. R. T., 2020, In: Nature Communications. 11, 1, 3368.

      Research output: Contribution to journalJournal articleResearchpeer-review

    11. Published

      The sequences of 150,119 genomes in the UK Biobank

      Halldorsson, B. V., Eggertsson, H. P., Moore, K. H. S., Hauswedell, H., Eiriksson, O., Ulfarsson, M. O., Palsson, G., Hardarson, M. T., Oddsson, A., Jensson, B. O., Kristmundsdottir, S., Sigurpalsdottir, B. D., Stefansson, O. A., Beyter, D., Holley, G., Tragante, V., Gylfason, A., Olason, P. I., Zink, F., Asgeirsdottir, M. & 27 others, Sverrisson, S. T., Sigurdsson, B., Gudjonsson, S. A., Sigurdsson, G. T., Halldorsson, G. H., Sveinbjornsson, G., Norland, K., Styrkarsdottir, U., Magnusdottir, D. N., Snorradottir, S., Kristinsson, K., Sobech, E., Pedersen, Ole Birger Vesterager, Brunak, Søren, Ostrowski, Sisse Rye, Banasik, Karina, Burgdorf, Kristoffer Sølvsten, Didriksen, Maria, Hansen, Thomas Folkmann, Hjalgrim, Henrik, Jemec, Gregor, Jennum, Poul, Jo­hans­son, Pär In­ge­mar , Ostrowski, Sisse Rye, Ullum, H., Werge, Thomas & DBDS Genetic Consortium, D. G. C., 2022, In: Nature. 607

      Research output: Contribution to journalJournal articleResearchpeer-review

    12. 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 journalJournal articleResearchpeer-review

    13. Published

      The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy

      Hansen, Thomas Folkmann & Møller, R. S., 2020, In: EBioMedicine. 58, 2 p., 102896.

      Research output: Contribution to journalComment/debateResearch

    14. Published

      The first step towards personalized risk prediction for common epilepsies

      Hansen, Thomas Folkmann & Møller, R. S., 2019, In: Brain. 142, p. 3316-3318 3 p.

      Research output: Contribution to journalComment/debateResearch

    15. Published

      Molecular genetics in schizophreniaMolecular genetics in schizophrenia

      Hansen, Thomas Folkmann, 2009, København: Museum Tusculanum.

      Research output: Book/ReportPh.D. thesisResearch

    16. Published

      DBDS Genomic Cohort, a prospective and comprehensive resource for integrative and temporal analysis of genetic, environmental and lifestyle factors affecting health of blood donors

      Hansen, T. F., Banasik, K., Erikstrup, C., Pedersen, O. B., Westergaard, D., Chmura, P. J., Nielsen, K., Thørner, L., Hjalgrim, H., Paarup, H., Larsen, M. A. H., Petersen, M., Jennum, P., Andersen, S., Nyegaard, M., Jemec, G. B. E., Olesen, J., Werge, T., Johansson, P. I., Sørensen, E. & 3 others, Brunak, Søren, Ullum, H. & Burgdorf, Kristoffer Sølvsten, 9 Jun 2019, In: BMJ Open. 9, 6, p. 1-7 7 p., e028401.

      Research output: Contribution to journalJournal articleResearchpeer-review

    17. Published

      Molecular genetics in schizophrenia: common and rare alleles

      Hansen, Thomas Folkmann, 2009, København: Faculty of Health Sciences, University of Copenhagen. 145 p.

      Research output: Book/ReportPh.D. thesisResearch

    18. Published

      Comorbidity of migraine with ADHD in adults

      Hansen, Thomas Folkmann, Hoeffding, L. K., Kogelman, L., Haspang, T. M., Ullum, H., Sørensen, E., Erikstrup, C., Pedersen, O. B., Nielsen, K. R., Hjalgrim, H., Paarup, H. M., Werge, Thomas & Burgdorf, K., 2018, In: BMC Neurology. 18, 1, p. 1-9 147.

      Research output: Contribution to journalJournal articleResearchpeer-review

    19. Published

      Predicting treatment response using pharmacy register in migraine

      Hansen, Thomas Folkmann, Chalmer, M. A., Haspang, T. M., Kogelman, L. & Olesen, Jes, 2019, In: Journal of Headache and Pain. 20, 8 p., 31.

      Research output: Contribution to journalJournal articleResearchpeer-review

    20. Published

      Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

      Harold, D., Connolly, S., Riley, B. P., Kendler, K. S., McCarthy, S. E., McCombie, W. R., Richards, A., Owen, M. J., O'Donovan, M. C., Walters, J., Donnelly, P., Bates, L., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A. & 32 others, Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Hopkins, L., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Pers, Tune H, Hansen, M., Hansen, Thomas Folkmann, Li, T., Olsen, L., Pantelis, C., Rasmussen, Henrik Berg, Werge, Thomas, Wellcome Trust Case Control Consortium 2, W. T. C. C. C. 2. & Schizophrenia Working Group of the Psychiatric Genomics Consortium, S. W. G. O. T. P. G. C., 2019, In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 180, 3, p. 223-231 9 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    21. 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

    22. 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

    23. 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 journalJournal articleResearchpeer-review

    24. 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 journalJournal articleResearchpeer-review

    25. 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 journalJournal articleResearchpeer-review

    ID: 21418907