Thomas Folkmann Hansen

Thomas Folkmann Hansen

Associate Professor

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    ORCID: 0000-0001-6703-7762

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    1. 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 journal › Journal article › Research › peer-review

    2. 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/Report › Ph.D. thesis › Research

    3. 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 journal › Journal article › Research › peer-review

    4. 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 journal › Journal article › Research › peer-review

    5. 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 journal › Journal article › Research › peer-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 journal › Journal article › Research › peer-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 journal › Journal article › Research › peer-review

    8. 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 journal › Journal article › Research › peer-review

    9. 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 journal › Journal article › Research › peer-review

    10. 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 journal › Journal article › Research › peer-review

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    ID: 21418907