Thomas Werge

Thomas Werge

Clinical Professor

Member of:

  • Psychiatry


Publication year:
All
401 - 427 out of 427Page size: 50
Sort by: 1st author
  1. 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 journal › Journal article › Research › peer-review

  2. Published

    Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

    Vassos, E., Steinberg, S., Cichon, S., Breen, G., Sigurdsson, E., Andreassen, O. A., Djurovic, S., Morken, G., Grigoroiu-Serbanescu, M., Diaconu, C. C., Czerski, P. M., Hauser, J., Babadjanova, G., Abramova, L. I., Mühleisen, T. W., Nöthen, M. M., Rietschel, M., McGuffin, P., St Clair, D., Gustafsson, O. & 28 others, Melle, I., Pietiläinen, O. P. H., Ruggeri, M., Tosato, S., Werge, Thomas, Ophoff, R. A., Rujescu, D., Børglum, A., Mors, O., Mortensen, P. B., Demontis, D., Hollegaard, M. V., van Winkel, R., Kenis, G., De Hert, M., Réthelyi, J. M., Bitter, I., Rubino, I. A., Golimbet, V., Kiemeney, L. A., van den Berg, L. H., Franke, B., Jönsson, E. G., Farmer, A., Stefansson, H., Stefansson, K., Collier, D. A. & GROUP Consortium, G. C., 2012, In: Biological Psychiatry. 72, 8, p. 645-50 6 p.

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

  3. Published

    A study of the genetic architecture of social responsiveness in families with parental schizophrenia or bipolar disorder and population-based controls

    Veddum, L., Greve, A. N., Gregersen, M., Andreassen, A. K., Knudsen, C. B., Brandt, J. M., Krantz, M. F., Søndergaard, A., Burton, B. K., Jepsen, J. R. M., Hemager, N., Werge, Thomas, Thorup, Anne, Nordentoft, Merete, Mors, O. & Nudel, R., 2023, In: Psychiatry Research. 326, 115280.

    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

    Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language

    iPSYCH-Broad-PGC ADHD Consortium, I. A. C., 2019, In: Translational Psychiatry. 9, 1, 12 p., 35.

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

  6. Published

    Neuropeptide Y genes and suicidal behaviour among schizophrenic patients

    Wang, August Gabriel, Koefoed, P., Jacoby, A. S., Woldbye, David Paul Drucker, Rasmussen, Henrik Berg, Timm, S., Dam, H., Jakobsen, K. D., Nordentoft, Merete, Jürgens, Gesche, Sorensen, H. J., Garsdal, O., Hvid, M. & Werge, Thomas, Jun 2013, In: Psychiatric Genetics. 23, 3, p. 139-40 2 p.

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

  7. Published

    Suicidal Behavior and the Serotonin Transporter Gene Polymorphism (5-HTTLPR) with Novel Subtypes, in Danish Schizophrenic Patients

    Wang, August Gabriel, Rasmussen, Henrik Berg, Sørensen, H. J., Hvid, M., Breddam, C. H., Hansen, B., Bille, V. H., Garsdal, O., Jacoby, A., Søbye, K., Dam, O. H., Krogsbøl, H., Timm, S. & Werge, Thomas, 2009, In: Open Psychiatry Journal.

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

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

  9. Published

    Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS

    Wang, Y., Thompson, W. K., Schork, A. J., Holland, D., Chen, C-H., Bettella, F., Desikan, R. S., Li, W., Witoelar, A., Zuber, V., Devor, A., Nöthen, M. M., Rietschel, M., Chen, Q., Werge, T., Cichon, S., Weinberger, D. R., Djurovic, S., O'Donovan, M. C., Visscher, P. M. & 2 others, Andreassen, O. A. & Dale, A. M., 2016, In: P L o S Genetics. 12, 1, 22 p., e1005803.

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

  10. Published

    Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations

    Wang, Y., Karstoft, Karen-Inge, Nievergelt, C. M., Maihofer, A. X., Stein, M. B., Ursano, R. J., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hougaard, D. M., Andreassen, O. A., Werge, Thomas, Thompson, W. K. & Andersen, S. B., 2019, In: Journal of Affective Disorders. 252, p. 350-357 8 p.

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

  11. Published

    Genetic correlates of phenotypic heterogeneity in autism

    Warrier, V., Zhang, X., Reed, P., Havdahl, A., Moore, T. M., Cliquet, F., Leblond, C. S., Rolland, T., Rosengren, A., Caceres, A. S. J., Hayward, H., Crawley, D., Faulkner, J., Sabet, J., Ellis, C., Oakley, B., Loth, E., Charman, T., Murphy, D., Holt, R. & 33 others, Waldman, J., Upadhyay, J., Gunby, N., Lai, M. C., Renouf, G., Ruigrok, A., Taylor, E., Ziauddeen, H., Deakin, J., di Bruttopilo, S. A., van Dijk, S., Rijks, Y., Koops, T., Douma, M., Spaan, A., Selten, I., Steffers, M., van Themaat, A. V. L., Bast, N., Baumeister, S., O’Dwyer, L., Bours, C., Rausch, A., von Rhein, D., Cornelissen, I., de Bruin, Y., Graauwmans, M., Kostrzewa, E., Werge, Thomas, Nordentoft, Merete, EU-AIMS LEAP, E. L., iPSYCH-Autism Working Group, I. W. G. & Spectrum 10K and APEX Consortia, S. 1. A. A. C., 2022, In: Nature Genetics. 54, 9, p. 1293-1304 12 p.

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

  12. Published

    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

    Anorexia Nervosa Genetics Initiative, A. N. G. I., Aug 2019, In: Nature Genetics. 51, 8, p. 1207-1214

    Research output: Contribution to journal › Letter › Research › peer-review

  13. Published

    Common Genetic Variation and Age of Onset of Anorexia Nervosa

    Watson, H. J., Thornton, L. M., Yilmaz, Z., Baker, J. H., Coleman, J. R. I., Adan, R. A. H., Alfredsson, L., Andreassen, O. A., Ask, H., Berrettini, W. H., Boehnke, M., Boehm, I., Boni, C., Buehren, K., Bulant, J., Burghardt, R., Chang, X., Cichon, S., Cone, R. D., Courtet, P. & 157 others, Crow, S., Crowley, J. J., Danner, U. N., de Zwaan, M., Dedoussis, G., DeSocio, J. E., Dick, D. M., Dikeos, D., Dina, C., Djurovic, S., Dmitrzak-Weglarz, M., Docampo-Martinez, E., Duriez, P., Egberts, K., Ehrlich, S., Eriksson, J. G., Escaramís, G., Esko, T., Estivill, X., Farmer, A., Fernández-Aranda, F., Fichter, M. M., Föcker, M., Foretova, L., Forstner, A. J., Frei, O., Gallinger, S., Giegling, I., Giuranna, J., Gonidakis, F., Gorwood, P., Gratacòs, M., Guillaume, S., Guo, Y., Hakonarson, H., Hauser, J., Havdahl, A., Hebebrand, J., Helder, S. G., Herms, S., Herpertz-Dahlmann, B., Herzog, W., Hinney, A., Hübel, C., Hudson, J. I., Imgart, H., Jamain, S., Janout, V., Jiménez-Murcia, S., Jones, I. R., Julià, A., Kalsi, G., Kaminská, D., Kaprio, J., Karhunen, L., Kas, M. J. H., Keel, P. K., Kennedy, J. L., Keski-Rahkonen, A., Kiezebrink, K., Klareskog, L., Klump, K. L., Knudsen, G. P. S., La Via, M. C., Le Hellard, S., Leboyer, M., Li, D., Lilenfeld, L., Lin, B., Lissowska, J., Luykx, J., Magistretti, P., Maj, M., Marsal, S., Marshall, C. R., Mattingsdal, M., Meulenbelt, I., Micali, Nadia, Mitchell, K. S., Monteleone, A. M., Monteleone, P., Myers, R., Navratilova, M., Ntalla, I., O'Toole, J. K., Ophoff, R. A., Padyukov, L., Pantel, J., Papežová, H., Pinto, D., Raevuori, A., Ramoz, N., Reichborn-Kjennerud, T., Ricca, V., Ripatti, S., Ripke, S., Ritschel, F., Roberts, M., Rotondo, A., Rujescu, D., Rybakowski, F., Scherag, A., Scherer, S. W., Schmidt, U., Scott, L. J., Seitz, J., Silén, Y., Šlachtová, L., Slagboom, P. E., Slof-Op ‘t Landt, M. C. T., Slopien, A., Sorbi, S., Świątkowska, B., Tortorella, A., Tozzi, F., Treasure, J., Tsitsika, A., Tyszkiewicz-Nwafor, M., Tziouvas, K., van Elburg, A. A., van Furth, E. F., Walton, E., Widen, E., Zerwas, S., Zipfel, S., Bergen, A. W., Boden, J. M., Brandt, H., Crawford, S., Halmi, K. A., Horwood, L. J., Johnson, C., Kaplan, A. S., Kaye, W. H., Mitchell, J. E., Olsen, C. M., Pearson, J. F., Pedersen, N. L., Strober, M., Werge, Thomas, Whiteman, D. C., Woodside, D. B., Gordon, S., Maguire, S., Larsen, J. T., Parker, R., Petersen, L. V., Jordan, J., Kennedy, M., Wade, T. D., Birgegård, A., Lichtenstein, P., Landén, M., Martin, N. G., Mortensen, P. B., Breen, G. & Bulik, C. M., 2022, In: Biological Psychiatry Global Open Science. 2, 4, p. 368-378 11 p.

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

  14. Published

    Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

    Weiner, D. J., Ling, E., Erdin, S., Tai, D. J. C., Yadav, R., Grove, J., Fu, J. M., Nadig, A., Carey, C., Baya, N., Bybjerg-Grauholm, J., Mortensen, P. B., Werge, T., Demontis, D., Mors, O., Nordentoft, M., Als, T. D., Baekvad-Hansen, M., Rosengren, A., Havdahl, A. & 33 others, Hedemand, A., Palotie, A., Chakravarti, A., Arking, D., Sulovari, A., Starnawska, A., Thiruvahindrapuram, B., de Leeuw, C., Carey, C., Ladd-Acosta, C., van der Merwe, C., Devlin, B., Cook, E. H., Eichler, E., Corfield, E., Dieleman, G., Schellenberg, G., Hakonarson, H., Coon, H., Dziobek, I., Vorstman, J., Girault, J., Sutcliffe, J. S., Duan, J., Nurnberger, J., Hallmayer, J., Buxbaum, J., Hinney, A., Larsson, H., Dalsgaard, Søren, iPSYCH Consortium, I. C., ASD Working Group of the Psychiatric Genomics Consortium, A. W. G. O. T. P. G. C. & ADHD Working Group of the Psychiatric Genomics Consortium, A. W. G. O. T. P. G. C., 2022, In: Nature Genetics. 54, p. 1630-1639

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

  15. Published

    Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

    Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B., Børglum, A. D. & 32 others, Smith, G. D., Daly, M. J., Robinson, E. B., Bækvad-Hansen, M., Dumont, A., Hansen, C., Hansen, T. F., Howrigan, D., Mattheisen, M., Moran, J., Mors, O., Nordentoft, Merete, Nørgaard-Pedersen, B., Poterba, T., Poulsen, J., Stevens, C., Anttila, V., Holmans, P., Huang, H., Klei, L., Lee, P. H., Medland, S. E., Neale, B., Weiss, L. A., Zwaigenbaum, L., Yu, T. W., Wittemeyer, K., Willsey, A. J., Wijsman, E. M., Wassink, T. H., Psychiatric Genomics Consortium Autism Group, P. G. C. A. G. & iPSYCH-Broad Autism Group, I. A. G., Jul 2017, In: Nature Genetics. 49, 7, p. 978-985 8 p.

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

  16. Published

    Det genetiske grundlag for psykiske lidelser

    Werge, Thomas & Fink-Jensen, Anders, 22 Mar 2010, In: Ugeskrift for Laeger. 172, 12, p. 962 1 p.

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

  17. Published

    Response to Boot et al. Letter

    Werge, Thomas, Ingason, A., Kirov, G., Rujescu, D. & Sigurdsson, E., 2012, In: American Journal of Psychiatry. 169, 1, p. 97 1 p.

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

  18. Published

    Genetic liability to ADHD and substance use disorders in individuals with ADHD

    Wimberley, T., Agerbo, E., Horsdal, H. T., Ottosen, C., Brikell, I., Als, T. D., Demontis, D., Børglum, A. D., Nordentoft, Merete, Mors, O., Werge, Thomas, Hougaard, D., Bybjerg-Grauholm, J., Hansen, M. B., Mortensen, P. B., Thapar, A., Riglin, L., Langley, K. & Dalsgaard, S., 2020, In: Addiction. 115, 7, p. 1368-1377

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

  19. Published

    Dysbindin and d-amino-acid-oxidase gene polymorphisms associated with positive and negative symptoms in schizophrenia

    Wirgenes, K. V., Djurovic, S., Agartz, I., Jonsson, E. G., Werge, Thomas, Melle, I., Andreassen, O. A., Wirgenes, K. V., Djurovic, S., Agartz, I., Jonsson, E. G., Werge, Thomas, Melle, I. & Andreassen, O. A., 2009, In: Neuropsychobiology. 60, 1, p. 31-6 5 p.

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

  20. 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

  21. 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

  22. Published

    A saturated map of common genetic variants associated with human height

    Yengo, L., Vedantam, S., Marouli, E., Sidorenko, J., Bartell, E., Sakaue, S., Graff, M., Eliasen, A. U., Jiang, Y., Raghavan, S., Miao, J., Arias, J. D., Graham, S. E., Mukamel, R. E., Spracklen, C. N., Yin, X., Chen, S-H., Ferreira, T., Highland, H. H., Ji, Y. & 37 others, Karaderi, Tugce, Lin, K., Lull, K., Malden, D. E., Lepola, Mette Andersen, Appadurai, V., Bork-Jensen, J., Burgdorf, Kristoffer Sølvsten, Hansen, Thomas Folkmann, Jonsson, Anna Elisabet, Jorgensen, T., Liu, J., Møllehave, Line Tang, Smit, Roelof Adriaan Johan, Zhao, J., Bisgaard, H., Bønnelykke, Klaus, Dantoft, T. M., Grarup, Niels, Hansen, Torben, Jackson, R. D., Karpe, F., Kovacs, P., Lind, L., Linneberg, Allan René, Pedersen, Oluf Borbye, Werge, Thomas, Sun, Y., Loos, Ruth, Winkler, T. W., 23andMe Res Team, 2. R. T., VA Million Vet Program, V. M. V. P., DiscovEHR DiscovEHR MyCode Communi, D. D. M. C., eEMERGE Elect Med Records Genomics, E. E. M. R. G., LifeLines Cohort Study, L. C. S., PRACTICAL consortium, P. C. & Understanding Soc Sci Grp, U. S. S. G., 2022, In: Nature. 610, p. 704–712

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

  23. Published

    Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes

    de Jong, S., van Eijk, K. R., Zeegers, D. W. L. H., Strengman, E., Janson, E., Veldink, J. H., van den Berg, L. H., Cahn, W., Kahn, R. S., Boks, M. P. M., Ophoff, R. A., PGC Schizophrenia (GWAS) Consortium, P. S. (. C., Werge, Thomas, Hansen, T., Ingason, A., Olsen, L. & Thygesen, J. H., 2012, In: European Journal of Human Genetics. 20, 9, p. 1004-8 5 p.

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

  24. Published

    Schizophrenia genetic variants are not associated with intelligence

    van Scheltinga, A. F. T., Bakker, S. C., van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S., Psychiatric Genome-Wide Association Study (GWAS) Consortium, P. G. A. S. (. C., Werge, Thomas, Hansen, T. & Ingason, A., 2013, In: Psychological Medicine. p. 1-8 8 p.

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

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

  26. Published

    Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder

    Østergaard, S. D., Trabjerg, B. B., Als, T. D., Climent, C. A., Privé, F., Vilhjálmsson, B. J., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hougaard, D. M., Nordentoft, Merete, Werge, Thomas, Demontis, D., Mortensen, P. B., Børglum, A. D., Mors, O. & Agerbo, E., 2020, In: Translational Psychiatry. 10, 1, 335.

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

  27. 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

Previous 1...5 6 7 8 9 Next

ID: 34394780