Thomas Werge

Thomas Werge

Clinical Professor

Member of:

  • Psychiatry


Publication year:
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  1. Published

    Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium douglas.ruderfer@vanderbilt.edu, B. D. A. S. W. G. O. T. P. G. C. D. R. E., Psychosis Endophenotypes International Consortium, P. E. I. C. & Wellcome Trust Case-Control Consortium, W. T. C. C., 14 Jun 2018, In: Cell. 173, 7, p. 1705-1715.e16

    Research output: Contribution to journal › Journal article › Research › peer-review

  2. Published

    ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

    St Pourcain, B., Robinson, E. B., Anttila, V., Sullivan, B. B., Maller, J., Golding, J., Skuse, D., Ring, S., Evans, D. M., Zammit, S., Fisher, S. E., Neale, B. M., Anney, R. J. L., Ripke, S., Hollegaard, M. V., Werge, T., iPSYCH-SSI-Broad Autism Group, Ronald, A., Grove, J., Hougaard, D. M. & 4 others, Børglum, A. D., Mortensen, P. B., Daly, M. J. & Davey Smith, G., 2018, In: Molecular Psychiatry. 23, 2, p. 263-270

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods

    Thornton, L. M., Munn-Chernoff, M. A., Baker, J. H., Juréus, A., Parker, R., Henders, A. K., Larsen, J. T., Petersen, L., Watson, H. J., Yilmaz, Z., Kirk, K. M., Gordon, S., Leppä, V. M., Martin, F. C., Whiteman, D. C., Olsen, C. M., Werge, T. M., Pedersen, N. L., Kaye, W., Bergen, A. W. & 26 others, Halmi, K. A., Strober, M., Kaplan, A. S., Woodside, D. B., Mitchell, J., Johnson, C. L., Brandt, H., Crawford, S., Horwood, L. J., Boden, J. M., Pearson, J. F., Duncan, L. E., Grove, J., Mattheisen, M., Jordan, J., Kennedy, M. A., Birgegård, A., Lichtenstein, P., Norring, C., Wade, T. D., Montgomery, G. W., Martin, N. G., Landén, M., Mortensen, P. B., Sullivan, P. F. & Bulik, C. M., 2018, In: Contemporary Clinical Trials. 74, p. 61-69 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis

    Velthorst, E., Froudist-Walsh, S., Stahl, E., Ruderfer, D., Ivanov, I., Buxbaum, J., iPSYCH-Broad ASD Group, the IMAGEN consortium, Banaschewski, T., Bokde, A. L. W., Bromberg, U., Büchel, C., Burke Quinlan, E., Desrivières, S., Flor, H., Frouin, V., Garavan, H., Gowland, P., Heinz, A., Ittermann, B., Paillère Martinot, M. L. & 31 others, Artiges, E., Nees, F., Papadopoulos Orfanos, D., Paus, T., Poustka, L., Hohmann, S., Fröhner, J. H., Smolka, M. N., Walter, H., Whelan, R., Schumann, G., Reichenberg, A., Børglum, A. D., Grove, J., Mattheisen, M., Werge, Thomas, Mortensen, P. B., Pedersen, M. G., Pedersen, C. B., Mors, O., Nordentoft, Merete, Hougaard, D. M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hansen, C. S., Daly, M. J., Neale, B. M., Robinson, E. B., Cerrato, F., Dumont, A. & Goldstein, J., 2018, In: Translational Psychiatry. 8, 1, 204.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, T. M. D. D. W. G. O. T. P. G. C., 2018, In: Nature Genetics. 50, 5, p. 668-681 14 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

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

  7. Published

    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

    International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu, I. M. S. G. C. E. A. C. C. E., Sellebjerg, Finn Thorup, Ullum, H. & Werge, Thomas, 29 Nov 2018, In: Cell. 175, 6, p. 1679-1687.e7

    Research output: Contribution to journal › Journal article › Research › peer-review

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ID: 34394780