Thomas Werge

Thomas Werge

Clinical Professor

Member of:

  • Psychiatry


  1. Published

    Association between GLP-1 receptor gene polymorphisms with reward Learning, anhedonia, and depression diagnosis

    Eser, H. Y., Appadurai, V., Eren, C. Y., Yazici, D., Chen, C. Y., Ongur, D., Pizzagalli, D. A., Werge, Thomas & Hall, M. H., 2020, In: Acta Neuropsychiatrica. 32, 4, p. 218-225

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine

    Esserlind, A., Christensen, A. F., Le, H., Kirchmann, M., Hauge, A. W., Toyserkani, N. M., Hansen, Torben, Grarup, Niels, Werge, Thomas, Steinberg, S., Bettella, F., Stefansson, H. & Olesen, Jes, May 2013, In: European Journal of Neurology. 20, 5, p. 765-772 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample

    Esserlind, A., Christensen, A. F., Steinberg, S., Grarup, Niels, Pedersen, Oluf Borbye, Hansen, Torben, Werge, Thomas, Hansen, T. F., Husemoen, L. L. N., Linneberg, Allan René, Budtz-Joergensen, Esben, Westergaard, M. L., Stefansson, H. & Olesen, Jes, 2016, In: Cephalalgia : an international journal of headache. 36, 7, p. 1-9 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

    Fadista, J., Skotte, L., Karjalainen, J., Abner, E., Sørensen, E., Ullum, H., Werge, Thomas, Esko, T., Milani, L., Palotie, A., Daly, M., Melbye, M., Feenstra, B., Geller, F., IPSYCH Grp, I. G. & FinnGen Consortium, F. C., 2022, In: Nature Communications. 13, 11 p., 3200.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study

    Fadista, J., Yakimov, V., Võsa, U., Hansen, C. S., Kasela, S., Skotte, L., Geller, F., Courraud, J., Esko, T., Kukuškina, V., Buil, A., Melbye, M., Werge, Thomas, Hougaard, D. M., Milani, L., Bybjerg-Grauholm, J., Cohen, A. S. & Feenstra, B., 2021, In: Scientific Reports. 11, 17463.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

    Fan, C. C., McGrath, J. J., Appadurai, V., Buil, A., Gandal, M. J., Schork, A. J., Mortensen, P. B., Agerbo, E., Geschwind, S. A., Geschwind, D., Werge, Thomas, Thompson, W. K. & Pedersen, C. B., 2018, In: Nature Communications. 9, 7 p., 5296.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms

    Fanous, A. H., Zhou, B., Aggen, S. H., Bergen, S. E., Amdur, R. L., Duan, J., Sanders, A. R., Shi, J., Mowry, B. J., Olincy, A., Amin, F., Cloninger, C. R., Silverman, J. M., Buccola, N. G., Byerley, W. F., Black, D. W., Freedman, R., Dudbridge, F., Holmans, P. A., Ripke, S. & 8 others, Gejman, P. V., Kendler, K. S., Levinson, D. F., Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, S. P. G. A. S. (. C., Hansen, T. F., Werge, Thomas, Olsen, L. & Rasmussen, H. B., 2012, In: American Journal of Psychiatry. 169, 12, p. 1309-17 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Evaluating historical candidate genes for schizophrenia

    Farrell, M. S., Werge, Thomas, Sklar, P., Owen, M. J., Ophoff, R. A., O'Donovan, M. C., Corvin, A., Cichon, S. & Sullivan, P. F., 2015, In: Molecular Psychiatry. 20, p. 555-62 8 p.

    Research output: Contribution to journalReviewResearchpeer-review

  9. Published

    Genomisk medicin som forbrugervare

    Folkersen, L. & Werge, Thomas, 2019, In: Ugeskrift for Laeger. 181, 5 p., V11180789.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores

    Folkersen, L., Pain, O., Ingason, A., Werge, Thomas, Lewis, C. M. & Austin, J., 2020, In: Frontiers in Genetics. 11, 578.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes

    Forsingdal, A., Fejgin, K., Nielsen, V., Werge, Thomas & Nielsen, J., 2016, In: Translational Psychiatry. 6, 7, p. 1-9 9 p., e860.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?

    Forsingdal, A., Jørgensen, T. N., Olsen, L., Werge, Thomas, Didriksen, M. & Nielsen, J., 2019, In: Biological Psychiatry. 85, 1, p. 13-24 12 p.

    Research output: Contribution to journalReviewResearchpeer-review

  13. 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

  14. Published

    Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci

    Foss-Skiftesvik, J., Hagen, C. M., Mathiasen, R., Adamsen, D., Bækvad-Hansen, M., Børglum, A. D., Nordentoft, Merete, Werge, Thomas, Christiansen, M., Schmiegelow, Kjeld, Juhler, Marianne, Mortensen, P. B., Hougaard, D. M. & Bybjerg-Grauholm, J., 2021, In: Child's Nervous System. 37, p. 819–830

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

    Haney, J. R., CommonMind Consortium, C. C., PsychENCODE Consortium, P. C. & iPSYCH-BROAD Working Group, I. W. G., 9 Feb 2018, In: Science. 359, 6376, p. 693-697 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

    Ganna, A., Satterstrom, F. K., Zekavat, S. M., Das, I., Kurki, M. I., Churchhouse, C., Alfoldi, J., Martin, A. R., Havulinna, A. S., Byrnes, A., Thompson, W. K., Nielsen, P. R., Karczewski, K. J., Saarentaus, E., Rivas, M. A., Gupta, N., Pietiläinen, O., Emdin, C. A., Lescai, F., Bybjerg-Grauholm, J. & 28 others, Flannick, J., GoT2D/T2D-GENES Consortium, G. C., Mercader, J. M., Udler, M., SIGMA Consortium Helmsley IBD Exome Sequencing Project, S. C. H. I. E. S. P., FinMetSeq Consortium, F. C., iPSYCH-Broad Consortium, I. C., Laakso, M., Salomaa, V., Hultman, C., Ripatti, S., Hämäläinen, E., Moilanen, J. S., Körkkö, J., Kuismin, O., Nordentoft, Merete, Hougaard, D. M., Mors, O., Werge, Thomas, Mortensen, P. B., MacArthur, D., Daly, M. J., Sullivan, P. F., Locke, A. E., Palotie, A., Børglum, A. D., Kathiresan, S. & Neale, B. M., 2018, In: American Journal of Human Genetics. 102, 6, p. 1204-1211

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophrenia

    Gasse, C., Wimberley, T., Wang, Y., Mors, O., Børglum, A., Als, T. D., Werge, Thomas, Nordentoft, Merete, Hougaard, D. M. & Horsdal, H. T., 2019, In: Schizophrenia Research. 212, p. 79-85 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Genome-wide association study identifies four loci associated with eruption of permanent teeth

    Geller, F., Feenstra, B., Zhang, H., Shaffer, J. R., Hansen, T., Esserlind, A-L., Boyd, H. A., Nohr, E. A., Timpson, N. J., Fatemifar, G., Paternoster, L., Evans, D. M., Weyant, R. J., Levy, S. M., Lathrop, M., Smith, G. D., Murray, J. C., Olesen, J., Werge, T. M., Marazita, M. L. & 2 others, Sørensen, Thorkild I.A. & Melbye, M., 1 Sep 2011, In: P L o S Genetics. 7, 9, p. e1002275

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions

    Giovanoli, S., Werge, Thomas, Mortensen, P. B., Didriksen, M. & Meyer, U., 2019, In: Neuropsychopharmacology. 44, 4, p. 703-710 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. 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

  21. Published

    The population genomic legacy of the second plague pandemic

    Gopalakrishnan, S., Ebenesersdóttir, S. S., Lundstrøm, I. K. C., Turner-Walker, G., Moore, K. H. S., Luisi, P., Margaryan, A., Martin, M. D., Ellegaard, M. R., Magnússon, Ó., Sigurðsson, Á., Snorradóttir, S., Magnúsdóttir, D. N., Laffoon, J. E., van Dorp, L., Liu, X., Moltke, I., Ávila-Arcos, M. C., Schraiber, J. G., Rasmussen, S. & 40 others, Juan, D., Gelabert, P., de-Dios, T., Fotaki, Anna Katerina, Iraeta Orbegozo, Miren, Vågene, Åshild Joanne, Denham, S. D., Christophersen, A., Stenøien, H. K., Vieira, Filipe Garrett, Liu, Shanlin, Günther, T., Kivisild, T., Moseng, O. G., Skar, B., Cheung, C., Sandoval-Velasco, Marcela, Wales, N., Schroeder, Hannes, Campos, P. F., Guðmundsdóttir, V. B., Sicheritz-Pontén, Thomas, Petersen, Bent, Halgunset, J., Gilbert, E., Cavalleri, G. L., Hovig, E., Kockum, I., Olsson, T., Alfredsson, L., Hansen, Thomas Folkmann, Werge, Thomas, Willerslev, Eske, Balloux, F., Marques-Bonet, T., Lalueza-Fox, C., Nielsen, Rasmus, Stefánsson, K., Helgason, A. & Gilbert, M Thomas P, 2022, In: Current Biology. 32, 21, p. 4743-4751.e6

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations

    Gordon, A., Forsingdal, A., Klewe, I. V., Nielsen, J., Didriksen, M., Werge, Thomas & Geschwind, D. H., 2021, In: Molecular Psychiatry. 26, p. 1520–1534

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. 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

  24. Published

    Identification of common genetic risk variants for autism spectrum disorder

    Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, A. S. D. W. G. O. T. P. G. C., Mar 2019, In: Nature Genetics. 51, 3, p. 431-444

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M. & 126 others, Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, Celeste Michala, Hansen, J. W., Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U., Stefansson, K., Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M., Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, C. M., Hansen, J. W., Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U. & Stefansson, K., 2009, In: Nature Genetics. 41, 3, p. 342-7 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M., Thorleifsson, G., Helgadottir, H., Steinthorsdottir, V., Stefansson, H., Williams, C., Hui, J., Beilby, J., Warrington, N. M., James, A., Palmer, L. J., Koppelman, G. H., Heinzmann, A., Krueger, M., Boezen, H. M. & 53 others, Wheatley, A., Altmuller, J., Shin, H. D., Uh, S., Cheong, H. S., Jonsdottir, B., Gislason, D., Park, C., Rasmussen, L. M., Porsbjerg, Celeste Michala, Hansen, Jakob Werner, Backer, Vibeke, Werge, Thomas, Janson, C., Jönsson, U., Ng, M. C. Y., Chan, J., So, W. Y., Ma, R., Shah, S. H., Granger, C. B., Quyyumi, A. A., Levey, A. I., Vaccarino, V., Reilly, M. P., Rader, D. J., Williams, M. J. A., van Rij, A. M., Jones, G. T., Trabetti, E., Malerba, G., Pignatti, P. F., Boner, A., Pescollderungg, L., Girelli, D., Olivieri, O., Martinelli, N., Ludviksson, B. R., Ludviksdottir, D., Eyjolfsson, G. I., Arnar, D., Thorgeirsson, G., Deichmann, K., Thompson, P. J., Wjst, M., Hall, I. P., Postma, D. S., Gislason, T., Gulcher, J., Kong, A., Jonsdottir, I., Thorsteinsdottir, U. & Stefansson, K., Mar 2009, In: Nature Genetics. 41, 3, p. 342-7 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published

    Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression

    Guintivano, J., Byrne, E. M., Kiewa, J., Yao, S., Bauer, A. E., Aberg, K. A., Adams, M. J., Campbell, A., Campbell, M. L., Choi, K. W., Corfield, E. C., Havdahl, A., Hucks, D., Koen, N., Lu, Y., Mægbæk, M. L., Mullaert, J., Peterson, R. E., Raffield, L. M., Sallis, H. M. & 59 others, Sealock, J. M., Walker, A., Watson, H. J., Xiong, Y., Yang, J. M. K., Anney, R. J. L., Gordon-Smith, K., Hubbard, L., Jones, L. A., Mihaescu, R., Nyegaard, M., Pardiñas, A. F., Perry, A., Saquib, N., Shadyab, A. H., Viktorin, A., Andreassen, O. A., Bigdeli, T. B., Davis, L. K., Dennis, C., Di Florio, A., Dubertret, C., Feng, Y. A., Frey, B. N., Grigoriadis, S., Gloaguen, E., Jones, I., Kennedy, J. L., Krohn, H., Kallak, T. K., Li, Y., Martin, N. G., McIntosh, A. M., Milgrom, J., Munk-Olsen, T., Oberlander, T., Olsen, C. M., Ramoz, N., Reichborn-Kjennerud, T., Blackmore, E. R., Rubinow, D., Skalkidou, A., Smoller, J. W., Stein, D. J., Stowe, Z. N., Taylor, V., Tebeka, S., Tesli, M., Van Lieshout, R. J., van den Oord, E. J. C. G., Vigod, S. N., Werge, Thomas, Westlye, L. T., Whiteman, D. C., Zar, H. J., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, M. D. D. W. G. O. T. P. G. C., Wray, N., Meltzer-Brody, S. & Sullivan, P., 2023, In: The American Journal of Psychiatry. 180, 12, p. 884-895 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. 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

  29. Published

    Promoter variants in IL18 are associated with onset of depression in patients previously exposed to stressful-life events

    Haastrup, E., Bukh, Jens Otto Drachmann, Bock, C., Vinberg, Maj, Thørner, L. W., Hansen, T., Werge, Thomas, Kessing, Lars Vedel & Ullum, H., 2012, In: Journal of Affective Disorders. 136, 1-2, p. 134-138 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. Published

    Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

    Hagen, C. M., Gonçalves, V. F., Hedley, P. L., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hansen, C. S., Kanters, Jørgen K., Nielsen, J., Mors, O., Demur, A. B., Als, T. D., Nordentoft, Merete, Børglum, A., Mortensen, P. B., Kennedy, J., Werge, Thomas, Hougaard, D. M. & Christiansen, M., 1 Dec 2018, In: PLoS ONE. 13, 12, 14 p., e0208828.

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. Published

    The sequences of 150,119 genomes in the UK Biobank

    Halldorsson, B. V., Eggertsson, H. P., Moore, K. H. S., Hauswedell, H., Eiriksson, O., Ulfarsson, M. O., Palsson, G., Hardarson, M. T., Oddsson, A., Jensson, B. O., Kristmundsdottir, S., Sigurpalsdottir, B. D., Stefansson, O. A., Beyter, D., Holley, G., Tragante, V., Gylfason, A., Olason, P. I., Zink, F., Asgeirsdottir, M. & 27 others, Sverrisson, S. T., Sigurdsson, B., Gudjonsson, S. A., Sigurdsson, G. T., Halldorsson, G. H., Sveinbjornsson, G., Norland, K., Styrkarsdottir, U., Magnusdottir, D. N., Snorradottir, S., Kristinsson, K., Sobech, E., Pedersen, Ole Birger Vesterager, Brunak, Søren, Ostrowski, Sisse Rye, Banasik, Karina, Burgdorf, Kristoffer Sølvsten, Didriksen, Maria, Hansen, Thomas Folkmann, Hjalgrim, Henrik, Jemec, Gregor, Jennum, Poul, Jo­hans­son, Pär In­ge­mar , Ostrowski, Sisse Rye, Ullum, H., Werge, Thomas & DBDS Genetic Consortium, D. G. C., 2022, In: Nature. 607

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. Published

    Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

    Hamshere, M. L., Walters, J. T. R., Smith, R., Richards, A., Green, E., Grozeva, D., Jones, I., Forty, L., Jones, L. R., Gordon-Smith, K., Riley, B., O'Neill, T., Kendler, K. S., Sklar, P., Purcell, S., Kranz, J., Morris, D. J., Gill, M., Holmans, P., Craddock, N. & 13 others, Corvin, A., Owen, M. J., O'Donovan, M. C., The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC), Wellcome Trust Case Control Consortium+ (WTCCC+), Wellcome Trust Case Control Consortium 2 (WTCCC2), T. S. P. G. A. S. C. (. W. T. C. C. C. (. W. T. C. C. C. 2. (., Hansen, T., Olsen, L., Ingason, A., Schmock, H., Skjødt, C., Rosengren, A., Høffding, L. K. E., Thygesen, J. H. & Werge, Thomas, 2013, In: Molecular Psychiatry.

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. Published

    Elevated polygenic burden for autism is associated with differential DNA methylation at birth

    Hannon, E., Schendel, D., Ladd-Acosta, C., Grove, J., Hansen, C. S., Andrews, S. V., Hougaard, D. M., Bresnahan, M., Mors, O., Hollegaard, M. V., Bækvad-Hansen, M., Hornig, M., Mortensen, P. B., Børglum, A. D., Werge, T., Pedersen, M. G., Nordentoft, M., Buxbaum, J., Fallin, M. D., Bybjerg-Grauholm, J. & 2 others, Reichenberg, A. & Mill, J., 28 Mar 2018, In: Genome Medicine. 10, 13 p., 19.

    Research output: Contribution to journalJournal articleResearchpeer-review

  34. Published

    Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

    iPSYCH-Broad ASD Group, I. A. G., 15 Apr 2019, In: Philosophical Transactions of the Royal Society B: Biological Sciences. 374, 1770, 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  35. Published

    Submikroskopiske kromosomanomalier som arsag til skizofreni

    Hansen, T., Ingason, A. & Werge, Thomas, 2008, In: Ugeskrift for læger. 170, 46, p. 3773-3776 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. 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

  37. Published

    Submikroskopiske kromosomanomalier som årsag til skizofreni

    Hansen, T., Ingason, A. & Werge, Thomas, 2008, In: Ugeskrift for Laeger. 170, 46, p. 3773-6 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  38. Published

    Brain expressed microRNAs implicated in schizophrenia etiology

    Hansen, T., Olsen, L., Lindow, M., Jakobsen, K. D., Ullum, H., Jonsson, E., Andreassen, O. A., Djurovic, S., Melle, I., Agartz, I., Hall, H., Timm, S., Wang, August Gabriel & Werge, Thomas, 2007, In: P L o S One. 2, 9, p. e873

    Research output: Contribution to journalJournal articleResearchpeer-review

  39. Published

    Variation in the purinergic P2RX(7) receptor gene and schizophrenia

    Hansen, T., Jakobsen, K. D., Fenger, M., Nielsen, J., Krane, K., Fink-Jensen, Anders, Lublin, H., Ullum, H., Timm, S., Wang, August Gabriel, Jørgensen, Niklas Rye & Werge, Thomas, 2008, In: Schizophrenia Research. 104, 1-3, p. 146-52 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  40. 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

  41. 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

  42. 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

  43. Published

    An exploratory model for G x E interaction on hippocampal volume in schizophrenia; obstetric complications and hypoxia-related genes

    Haukvik, U. K., Saetre, P., McNeil, T., Bjerkan, P. S., Andreassen, O. A., Werge, Thomas, Jönsson, E. G. & Agartz, I., 1 Oct 2010, In: Progress in Neuro-Psychopharmacology & Biological Psychiatry. 34, 7, p. 1259-65 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  44. Published

    Does Pharmacogenetic Testing for CYP450 2D6 and 2C19 among Patients with Diagnoses within the Schizophrenic Spectrum Reduce Treatment Costs?

    Herbild, L., Andersen, S. E., Werge, Thomas, Rasmussen, H. B. & Jürgens, G., 4 Jun 2013, In: Basic & Clinical Pharmacology & Toxicology. 113, 4, p. 266–272 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  45. Published

    Do guidelines recommending pharmacogenetic testing of psychiatric patients affect treatment costs and the use of healthcare services?

    Herbild, L., Bech, M., Gyrd-Hansen, D., Christensen, M., Werge, Thomas & Nielsen, K. A., Mar 2011, In: Scandinavian Journal of Public Health. 39, 2, p. 147-55 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  46. Published

    Identifying dominant-negative actions of a dopamine transporter variant in patients with parkinsonism and neuropsychiatric disease

    Herborg, F., Jensen, K. L., Tolstoy, S., Arends, N., Posselt, L. P., Shekar, A., Aguilar, J., Lund, V. K., Erreger, K., Rickhag, M., Lycas, M. D., Lonsdale, M. N., Rahbek-Clemmensen, T., Sorensen, A. T., Newman, A. H., Lokkegaard, A., Kjaerulff, O., Werge, T., Moller, L. B., Matthies, H. J. G. & 4 others, Galli, A., Hjermind, L. E., Gether, Ulrik & IPSYCH Researchers, I. R., 2021, In: JCI insight. 6, 18, 21 p., 151496.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. Published

    A polygenic resilience score moderates the genetic risk for schizophrenia

    Hess, J. L., Tylee, D. S., Mattheisen, M., The Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Børglum, A. D., Als, T. D., Grove, J., Werge, T., Mortensen, P. B., Mors, O., Nordentoft, M., Hougaard, D. M., Byberg-grauholm, J., Bækvad-hansen, M., Greenwood, T. A., Tsuang, M. T., Curtis, D., Steinberg, S., Sigurdsson, E. & 6 others, Stefánsson, H., Stefánsson, K., Edenberg, H. J., Holmans, P., Faraone, S. V. & Glatt, S. J., 2021, In: Molecular Psychiatry. 26, p. 800–815

    Research output: Contribution to journalJournal articleResearchpeer-review

  48. Published

    Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register

    Hilker, Rikke Warming, Helenius, D., Fagerlund, Birgitte, Skytthe, A., Christensen, K., Werge, Thomas, Nordentoft, Merete & Glenthøj, Birte Yding, 15 Mar 2018, In: Biological Psychiatry. 83, 6, p. 492-498

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. Published

    Is an Early Age at Illness Onset in Schizophrenia Associated With Increased Genetic Susceptibility? Analysis of Data From the Nationwide Danish Twin Register

    Hilker, Rikke Warming, Helenius, D., Fagerlund, Birgitte, Skytthe, A., Christensen, K., Werge, Thomas, Nordentoft, Merete & Glenthøj, Birte Yding, Apr 2017, In: EBioMedicine. 18, p. 320-326

    Research output: Contribution to journalJournal articleResearchpeer-review

  50. Published

    Is an Early Age at Illness Onset in Schizophrenia Associated With Increased Genetic Susceptibility?

    Hilker, R., Helenius, D., Fagerlund, B., Skytthe, A., Christensen, K., Werge, Thomas, Nordentoft, Merete & Glenthøj, Birte Yding, 2017, In: EBioMedicine. 18, p. 320-326

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 34394780