Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

Member of:


    1. 2004
    2. Published

      Cancer predisposition in mice deficient for the metastasis-associated Mts1(S100A4) gene

      Naaman, C. E. L., Grum-Schwensen, B., Mansouri, A., Grigorian, M., Santoni Rugiu, Eric, Hansen, Thomas Folkmann, Kriajevska, M., Schafer, B. W., Heizmann, C. W., Lukanidin, E. & Ambartsumian, N., 29 Apr 2004, In: Oncogene. 23, 20, p. 3670-3680 11 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    3. 2009
    4. 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

    5. Published

      Molecular genetics in schizophreniaMolecular genetics in schizophrenia

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

      Research output: Book/ReportPh.D. thesisResearch

    6. Published

      Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia

      van Schijndel, J. E., van Loo, K. M. J., van Zweeden, M., Djurovic, S., Andreassen, O. A., Hansen, Thomas Folkmann, Werge, Thomas, Kallunki, P., Pedersen, J. T. & Martens, G. J. M., 2009, In: Journal of Psychiatric Research. 43, 15, p. 1195-9 4 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    7. 2010
    8. Published

      Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia

      Vares, M., Saetre, P., Deng, H., Cai, G., Liu, X., Hansen, Thomas Folkmann, Rasmussen, Henrik Berg, Werge, Thomas, Melle, I., Djurovic, S., Andreassen, O. A., 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. 610-8 9 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    9. 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 journalJournal articleResearchpeer-review

    10. 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 journalJournal articleResearchpeer-review

    11. Published

      Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

      Le Hellard, S., Mühleisen, T. W., Djurovic, S., Fernø, J., Ouriaghi, Z., Mattheisen, M., Vasilescu, C., Raeder, M. B., Hansen, T. F., Strohmaier, J., Georgi, A., Brockschmidt, F. F., Melle, I., Nenadic, I., Sauer, H., Rietschel, M., Nöthen, M. M., Werge, T., Andreassen, O. A., Cichon, S. & 1 others, Steen, V. M., 1 May 2010, In: Molecular Psychiatry. 15, 5, p. 463-72 10 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    12. Published

      Diastolic dysfunction predicts new-onset atrial fibrillation and cardiovascular events in patients with acute myocardial infarction and depressed left ventricular systolic function: a CARISMA substudy

      Jons, C., Joergensen, R. M., Hassager, Christian, Gang, U. J. O., Dixen, Ulrik, Johannesen, A., Olsen, N. T., Hansen, Thomas Folkmann, Messier, M., Huikuri, H. V., Thomsen, P. E. B., Gang, U. J. O. & Olsen, N. T., 1 Aug 2010, In: European Journal of Echocardiography. 11, 7, p. 602-7 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    13. 2011
    14. Published

      Dual association of a TRKA polymorphism with schizophrenia

      Van Schijndel, J. E., Van Zweeden, M., Van Loo, K. M. J., Djurovic, S., Andreassen, O. A., Hansen, T., Werge, T., Nyegaard, M., Sørensen, K. M., Nordentoft, M., Mortensen, P. B., Mors, O., Børglum, A., Del-Favero, J., Norrback, K-F., Adolfsson, R., Hert, M. D., Claes, S., Cichon, S., Rietschel, M. & 4 others, Nöthen, M. M., Kallunki, P., Pedersen, J. T. & Martens, G. J. M., 2011, In: Psychiatric Genetics. 21, 3, p. 125-31 7 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    15. 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

    16. 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 journalJournal articleResearchpeer-review

    17. 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

    18. Published

      Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

      Kähler, A. K., Djurovic, S., Rimol, L. M., Brown, A. A., Athanasiu, L., Jönsson, E. G., Hansen, T., Gústafsson, O., Hall, H., Giegling, I., Muglia, P., Cichon, S., Rietschel, M., Pietiläinen, O. P. H., Peltonen, L., Bramon, E., Collier, D., St Clair, D., Sigurdsson, E., Petursson, H. & 8 others, Rujescu, D., Melle, I., Werge, Thomas, Steen, V. M., Dale, A. M., Matthews, R. T., Agartz, I. & Andreassen, O. A., 1 Jan 2011, In: Biological Psychiatry. 69, 1, p. 90-6 7 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    19. 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 journalJournal articleResearchpeer-review

    20. 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 journalLetterResearchpeer-review

    21. 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 journalJournal articleResearchpeer-review

    22. 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

    23. 2015
    24. 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

    25. 2016
    26. Published

      RNA sequencing of trigeminal ganglia in Rattus Norvegicus after glyceryl trinitrate infusion with relevance to migraine

      Pedersen, S. H., Sørensen, L. M., Ramachandran, R., Sibbesen, Jonas Andreas, Yakimov, V., Christensen, R. E., Hansen, Thomas Folkmann, Krogh, Anders, Olesen, Jes & Olesen, I. J., 2016, In: P L o S One. 11, 5, 13 p., e0155039.

      Research output: Contribution to journalJournal articleResearchpeer-review

    27. 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

    28. 2017
    29. Published

      Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

      Winsvold, B. S., Bettella, F., Witoelar, A., Anttila, V., Gormley, P., Kurth, T., Terwindt, G. M., Freilinger, T., Frei, O., Shadrin, A., Wang, Y., Dale, A. M., van den Maagdenberg, A. M. J. M., Nyholt, D. R., Palotie, A., Andreassen, O. A., Zwart, J. A., Artto, V., Belin, A. C., Boomsma, D. I. & 31 others, Børte, S., Chasman, D. I., Cherkas, L., Christensen, A. F., Cormand, B., Cuenca-Leon, E., Davey-Smith, G., Dichgans, M., van Duijn, C., Eising, E., Esko, T., Esserlind, A. L., Ferrari, M., Frants, R. R., Freilinger, T., Furlotte, N., Griffiths, L., Hamalainen, E., Hansen, Thomas Folkmann, Hiekkala, M., Arfan Ikram, M., Ingason, A., Järvelin, M. R., Kajanne, R., Kallela, M., Kaprio, J., Kaunisto, M., Kubisch, C., Kurki, M., Olesen, Jes & International Headache Genetics Consortium, I. H. G. C., 2017, In: PLoS ONE. 12, 9, 15 p., e0185663.

      Research output: Contribution to journalJournal articleResearchpeer-review

    30. 2018
    31. Published

      Age at first birth in women is genetically associated with increased risk of schizophrenia

      Ni, G., Gratten, J., Wray, N. R., Lee, S. H., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. H., Holmans, P. A., Lee, P., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F. & 281 others, Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chen, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Cloninger, C. R., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Degenhardt, F., Del Favero, J., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Frank, J., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Genovese, G., Georgieva, L., Giegling, I., Giusti-Rodríguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Haan, L. D., Hammer, C., Hamshere, M. L., Hansen, M., Hansen, Thomas Folkmann, Haroutunian, V., Hartmann, A. M., Henskens, F. A., Herms, S., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Juliá, A., Kahn, R. S., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Keller, M. C., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kähler, A. K., Laurent, C., Keong, J. L. C., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K. Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lönnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Maier, W., Mallet, J., Marsal, S., Mattheisen, M., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Müller-Myhsok, B., Nelis, M., Nenadic, I., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'callaghan, E., O'dushlaine, C., O'neill, F. A., Oh, S. Y., Olincy, A., Olsen, L., Os, J. V., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietiläinen, O., Pimm, J., Pocklington, A. J., Powell, J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Ruderfer, D. M., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schulze, T. G., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stahl, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Strohmaier, J., Stroup, T. S., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Witt, S. H., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Cichon, S., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gill, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jönsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarroll, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Nöthen, M. M., Ophoff, R. A., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Rietschel, M., Riley, B. P., Rujescu, D., Sham, P. C., Sklar, P., Clair, D. S., Weinberger, D. R., Wendland, J. R., Werge, Thomas, Daly, M. J., Sullivan, P. F. & O'donovan, M. C., 2018, In: Scientific Reports. 8, 1, p. 1-14 10168.

      Research output: Contribution to journalJournal articleResearchpeer-review

    32. 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

    33. 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

    34. Published

      Molecular genetic overlap between migraine and major depressive disorder

      Yang, Y., Zhao, H., Boomsma, D. I., Ligthart, L., Belin, A. C., Smith, G. D., Esko, T., Freilinger, T. M., Hansen, T. F., Ikram, M. A., Kallela, M., Kubisch, C., Paraskevi, C., Strachan, D. P., Wessman, M., Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T. & 30 others, Pers, Tune 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., 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., Christensen, A. F., Hansen, Thomas Folkmann, Werge, Thomas & Olesen, Jes, 2018, In: European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    35. Published

      Polygenic risk score: use in migraine research

      Chalmer, M. A., Esserlind, A., Olesen, Jes & Hansen, Thomas Folkmann, 2018, In: The Journal of Headache and Pain. 19, 1, p. 1-10 29.

      Research output: Contribution to journalReviewResearchpeer-review

    36. Published

      UGT polymorphisms and lamotrigine clearance during pregnancy

      Petrenaite, Vaiva, Öhman, I., Ekström, L., Sæbye, D., Hansen, Thomas Folkmann, Tomson, T. & Sabers, A., 2018, In: Epilepsy Research. 140, p. 199-208 10 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    37. Published

      Transcriptomic profiling of trigeminal nucleus caudalis and spinal cord dorsal horn

      Kogelman, L. J. A., Elgaard-Christensen, R., Olesen, Jes, Jansen-Olesen, I. & Hansen, Thomas Folkmann, 1 Aug 2018, In: Brain Research. 1692, p. 23-33

      Research output: Contribution to journalJournal articleResearchpeer-review

    38. 2019
    39. 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 journalJournal articleResearchpeer-review

    40. Published

      Comparing migraine with and without aura to healthy controls using RNA sequencing

      Kogelman, L. J. A., Falkenberg, K., Halldorsson, G. H., Poulsen, L. U., Worm, J., Ingason, A., Stefansson, H., Stefansson, K., Hansen, Thomas Folkmann & Olesen, Jes, 2019, In: Cephalalgia. 39, 11, p. 1435-1444 10 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    41. Published

      Migraine polygenic risk score associates with efficacy of migraine-specific drugs

      Kogelman, L. J. A., Esserlind, A-L., Christensen, A. F., Awasthi, S., Ripke, S., Ingason, A., Davidsson, O. B., Erikstrup, C., Hjalgrim, H., Ullum, H., Olesen, J., Hansen, T. F., Gudbjartsson, D., Gastafsson, O., Stefansson, K., Stefansson, H., Porsteinsdottir, U., Andersen, S., Banasik, K., Brunak, S. & 73 others, Buil, A., Burgdorf, K., Gregor, J., Jennum, Poul, Nielsen, K. R., Nyegaard, M., Paarup, H. M., Pedersen, O. B., Sørensen, E., Werge, Thomas, Anttila, V., Artto, V., Belin, A. C., de Boer, I., Boomsma, D. I., Borte, S., Chasman, D. I., Cherkas, L., Cormand, B., Cuenca-Leon, E., Davey-Smith, G., Dichgans, M., van Duijn, C., Esko, T., Ferrari, M., Frants, R. R., Freilinger, T., Furlotte, N., Gormley, P., Griffiths, L., Hamalainen, E., Hiekkala, M., Ikram, M. A., Jarvelin, M., Kajanne, R., Kallela, M., Kaprio, J., Kaunisto, M., Kubisch, C., Kurki, M., Kurth, T., Launer, L., Lehtimaki, T., Lessel, D., Ligthart, L., Litterman, N., van den Maagdenberg, A., Macaya, A., Malik, R., Mangino, M., McMahon, G., Muller-Myhsok, B., Neale, B. M., Northover, C., Nyholt, D. R., Palotie, A., Palta, P., Pedersen, L., Pedersen, N., Posthuma, D., Pozo-Rosich, P., Pressman, A., Raitakari, O., Schurks, M., Sintas, C., Steinberg, S., Strachan, D., Terwindt, G., Vila-Pueyo, M., Wessman, M., Winsvold, B. S., Zhao, H. & Zwart, J., 2019, In: Neurology: Genetics. 5, 6, 12 p., e364.

      Research output: Contribution to journalJournal articleResearchpeer-review

    42. Published

      Nosographic analysis of osmophobia and field testing of diagnostic criteria including osmophobia

      Chalmer, M. A., Hansen, Thomas Folkmann & Olesen, Jes, 2019, In: Cephalalgia. 39, 1, p. 38-43 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    43. Published

      Persons who have never had a headache. Socio-demographic characteristics

      Olofsson, I. A., Erikstrup, C., Sørensen, E., Paarup, H. M., Mathiasen, H. P., Hjalmgrim, H., Banasik, Karina, Nielsen, K. R., Burgdorf, K. S., Pedersen, Ole Birger Vesterager, Ullum, H., Olesen, Jes & Hansen, Thomas Folkmann, 2019, In: Cephalalgia. 39, 1, suppl., p. 88-89 1 p.

      Research output: Contribution to journalConference abstract in journalResearchpeer-review

    44. 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

    45. 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

    46. 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

    47. 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

    48. Published

      The preferences of potential stakeholders in psychiatric genomic research regarding consent procedures and information delivery

      Sundby, A., Boolsen, Merete Watt, Burgdorf, K. S., Ullum, H., Hansen, Thomas Folkmann, Middleton, A. & Mors, O., Jan 2019, In: European Psychiatry. 55, p. 29-35 7 p., 55.

      Research output: Contribution to journalJournal articleResearchpeer-review

    49. 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

    50. Published

      Herpes Simplex Virus Type 1 infection is associated with suicidal behavior and first registered psychiatric diagnosis in a healthy population

      Nissen, J., Trabjerg, B., Pedersen, M. G., Banasik, K., Pedersen, O. B., Sørensen, E., Nielsen, K. R., Erikstrup, C., Petersen, M. S., Paarup, H. M., Bruun-Rasmussen, P., Westergaard, D., Hansen, T. F., Pedersen, C. B., Werge, T., Torrey, F., Hjalgrim, H., Mortensen, P. B., Yolken, R., Brunak, S. & 2 others, Ullum, H. & Burgdorf, K. S., Oct 2019, In: Psychoneuroendocrinology. 108, p. 150-154

      Research output: Contribution to journalJournal articleResearchpeer-review

    51. 2020
    52. 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

    53. 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 journalJournal articleResearchpeer-review

    54. 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

    55. 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

    56. 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

    57. 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

    58. 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

    59. 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

    60. 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 journalJournal articleResearchpeer-review

    Previous 1 2 3 Next

    ID: 21418907