Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

Member of:


    1. Published

      Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

      Arnau-Soler, A., Adams, M. J., Generation Scotland, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Hayward, C., Thomson, P. A., Porteous, D., Campbell, A., Smith, B. H., Black, C., Padmanabhan, S., McIntosh, A. M., Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Agerbo, E., Air, T. M. & 32 others, Andlauer, T. F. M., Bacanu, S. A., Bækvad-Hansen, M., Beekman, A. T. F., Bigdeli, T. B., Binder, E. B., Blackwood, D. H. R., Bryois, J., Buttenschøn, H. N., Bybjerg-Grauholm, J., Cai, N., Castelao, E., Christensen, J. H., Clarke, T. K., Coleman, J. R. I., Colodro-Conde, L., Couvy-Duchesne, B., Craddock, N., Crawford, G. E., Davies, G., Deary, I. J., Degenhardt, F., Derks, E. M., Direk, N., Dolan, C. V., Hansen, C. S., Hansen, Thomas Folkmann, Krogh, J., Pedersen, C. B., Pedersen, M. G., Nordentoft, Merete & Werge, Thomas, 2018, In: PLOS ONE. 13, 12, p. 1-29 e0209160.

      Research output: Contribution to journalJournal articleResearchpeer-review

    2. 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

    3. 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 journalJournal articleResearchpeer-review

    4. Published

      Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth

      Wang, Y., Nudel, R., Benros, Michael Eriksen, Skogstrand, K., Fishilevich, S., Lancet, D., Sun, J., Hougaard, D. M., Andreassen, O. A., Mortensen, P. B., Buil, A., Hansen, Thomas Folkmann, Thompson, W. K., Werge, Thomas & iPSYCH-BROAD, I., 2020, In: PLOS Genetics. 16, 11, e1009163.

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. 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

    6. 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

    7. 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

    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 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

    10. 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

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    ID: 21418907