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Thomas Werge

Thomas Werge

Clinical Professor


  1. 2017
  2. Published

    Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome : A study in male mice. / Didriksen, Michael; Fejgin, Kim; Nilsson, Simon R O; Birknow, Michelle Rosgaard; Grayton, Hannah M.; Larsen, Peter H.; Lauridsen, Jes B.; Nielsen, Vibeke; Celada, Pau; Santana, Noemi; Kallunki, Pekka; Christensen, Kenneth V; Werge, Thomas M.; Stensbøl, Tine B.; Egebjerg, Jan; Gastambide, Francois; Artigas, Francesc; Bastlund, Jesper F.; Nielsen, Jacob.

    In: Journal of Psychiatry and Neuroscience, Vol. 42, No. 1, 2017, p. 48-58.

    Publication: Research - peer-reviewJournal article

  3. Published

    Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies. / Hoeffding, Louise K E; Rosengren, Anders; Thygesen, Johan H; Schmock, Henriette; Werge, Thomas; Hansen, Thomas.

    In: Nordic Journal of Psychiatry, Vol. 71, No. 1, 01.2017, p. 20-25.

    Publication: Research - peer-reviewJournal article

  4. Published

    Quetiapine extended release versus aripiprazole in children and adolescents with first-episode psychosis: the multicentre, double-blind, randomised tolerability and efficacy of antipsychotics (TEA) trial. / Pagsberg, Anne Katrine; Jeppesen, Pia; Klauber, Dea Gowers; Jensen, Karsten Gjessing; Ruda, Ditte; Stentebjerg-Olesen, Marie; Jantzen, Peter; Rasmussen, Simone; Saldeen, Eva Ann-Sofie; Lauritsen, Maj-Britt Glenn; Bilenberg, Niels; Stenstrom, Anne Dorte; Nyvang, Louise; Madsen, Sarah; Werge, Thomas M.; Lange, Theis; Gluud, Christian; Skoog, Maria; Winkel, Per; Jepsen, Jens Richardt M.; Fagerlund, Birgitte; Correll, Christoph U; Fink-Jensen, Anders.

    In: The Lancet Psychiatry, Vol. 4, No. 8, 08.2017, p. 605-618.

    Publication: Research - peer-reviewJournal article

  5. 2016
  6. Published

    Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort. / Bertelsen, Birgitte; Stefánsson, Hreinn; Riff Jensen, Lars; Melchior, Linea; Debes, Nanette Mol; Groth, Camilla; Skov, Liselotte; Werge, Thomas; Karagiannidis, Iordanis; Tarnok, Zsanett; Barta, Csaba; Nagy, Peter; Farkas, Luca; Brøndum-Nielsen, Karen; Rizzo, Renata; Gulisano, Mariangela; Rujescu, Dan; Kiemeney, Lambertus A; Tosato, Sarah; Nawaz, Muhammad Sulaman; Ingason, Andrés; Unnsteinsdottir, Unnur; Steinberg, Stacy; Ludvigsson, Pétur; Stefansson, Kari; Kuss, Andreas Walter; Paschou, Peristera; Cath, Danielle; Hoekstra, Pieter J; Müller-Vahl, Kirsten; Stuhrmann, Manfred; Silahtaroglu, Asli; Pfundt, Rolph; Tümer, Zeynep.

    In: Biological Psychiatry, Vol. 79, No. 5, 01.03.2016, p. 383–391.

    Publication: Research - peer-reviewJournal article

  7. Published

    Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. / Bigdeli, Tim B.; Ripke, Stephan; Bacanu, Silviu-Alin; Lee, Sang Hong; Wray, Naomi R; Gejman, Pablo V; Rietschel, Marcella; Cichon, Sven; St Clair, David; Corvin, Aiden; Kirov, George; McQuillin, Andrew; Gurling, Hugh; Rujescu, Dan; Andreassen, Ole A.; Werge, Thomas; Blackwood, Douglas H R; Pato, Carlos N; Pato, Michele T; Malhotra, Anil K; O'Donovan, Michael C; Kendler, Kenneth S; Fanous, Ayman H; and Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 171, No. 2, 2016, p. 276-289.

    Publication: Research - peer-reviewJournal article

  8. Published

    Digital questionnaire platform in the Danish Blood Donor Study. / Burgdorf, Kristoffer Sølvsten; Felsted, N; Mikkelsen, Susan; Nielsen, M H; Thørner, Lise Wegner; Pedersen, Oluf Borbye; Sørensen, E; Nielsen, K R; Bruun, Mie Topholm; Werge, Thomas; Erikstrup, C; Hansen, T; Ullum, Henrik.

    In: Computer Methods and Programs in Biomedicine, Vol. 135, 12.07.2016, p. 101-104.

    Publication: Research - peer-reviewJournal article

  9. Published

    The influence of genetic constitution on migraine drug responses. / Christensen, Anne Francke; Esserlind, Ann-Louise; Werge, Thomas; Stefánsson, Hreinn; Stefánsson, Kári; Olesen, Jes.

    In: Cephalalgia : an international journal of headache, Vol. 36, No. 7, 06.2016, p. 624-39.

    Publication: Research - peer-reviewJournal article

  10. Published

    The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample. / Esserlind, Ann-Louise; Christensen, Anne Francke; Steinberg, Stacy; Grarup, Niels; Pedersen, Oluf; Hansen, Torben; Werge, Thomas; Hansen, Thomas Folkmann; Husemoen, Lise Lotte N; Linneberg, Allan René; Budtz-Jørgensen, Esben; Westergaard, Maria Lurenda; Stefansson, Hreinn; Olesen, Jes.

    In: Cephalalgia : an international journal of headache, Vol. 36, No. 7, 2016, p. 1-9.

    Publication: Research - peer-reviewJournal article

  11. Published

    15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes. / Forsingdal, A; Fejgin, Kim; Nielsen, Viggo; Werge, Thomas; Nielsen, J.

    In: Translational Psychiatry, Vol. 6, No. 7, e860, 2016, p. 1-9.

    Publication: Research - peer-reviewJournal article

  12. Published

    Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. / Gormley, Padhraig; Anttila, Verneri; Winsvold, Bendik S; Palta, Priit; Esko, Tonu; Pers, Tune H; Farh, Kai-How; Cuenca-Leon, Ester; Muona, Mikko; Furlotte, Nicholas A; Kurth, Tobias; Ingason, Andres; McMahon, George; Ligthart, Lannie; Terwindt, Gisela M; Kallela, Mikko; Freilinger, Tobias M; Ran, Caroline; Gordon, Scott G; Stam, Anine H; Steinberg, Stacy; Borck, Guntram; Koiranen, Markku; Quaye, Lydia; Adams, Hieab H H; Lehtimäki, Terho; Sarin, Antti-Pekka; Wedenoja, Juho; Hinds, David A; Buring, Julie E; Schürks, Markus; Ridker, Paul M; Hrafnsdottir, Maria Gudlaug; Stefansson, Hreinn; Ring, Susan M; Hottenga, Jouke-Jan; Penninx, Brenda W J H; Färkkilä, Markus; Artto, Ville; Kaunisto, Mari; Vepsäläinen, Salli; Malik, Rainer; Heath, Andrew C; Madden, Pamela A F; Martin, Nicholas G; Montgomery, Grant W; Kurki, Mitja I; Kals, Mart; Mägi, Reedik; Pärn, Kalle; Hämäläinen, Eija; Huang, Hailiang; Byrnes, Andrea E; Franke, Lude; Huang, Jie; Stergiakouli, Evie; Lee, Phil H; Sandor, Cynthia; Webber, Caleb; Cader, Zameel; Muller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Eriksson, Johan G; Salomaa, Veikko; Heikkilä, Kauko; Loehrer, Elizabeth; Uitterlinden, Andre G; Hofman, Albert; van Duijn, Cornelia M; Cherkas, Lynn; Pedersen, Linda M; Stubhaug, Audun; Nielsen, Christopher S; Männikkö, Minna; Mihailov, Evelin; Milani, Lili; Göbel, Hartmut; Esserlind, Ann-Louise; Christensen, Anne Francke; Hansen, Thomas Folkmann; Werge, Thomas; Kaprio, Jaakko; Aromaa, Arpo J; Raitakari, Olli; Ikram, M Arfan; Spector, Tim; Järvelin, Marjo-Riitta; Metspalu, Andres; Kubisch, Christian; Strachan, David P; Ferrari, Michel D; Belin, Andrea C; Dichgans, Martin; Wessman, Maija; van den Maagdenberg, Arn M J M; Zwart, John-Anker; Boomsma, Dorret I; Smith, George Davey; Stefansson, Kari; Eriksson, Nicholas; Daly, Mark J; Neale, Benjamin M; Olesen, Jes; Chasman, Daniel I; Nyholt, Dale R; Palotie, Aarno; International Headache Genetics Consortium.

    In: Nature Genetics, Vol. 48, No. 8, 08.2016, p. 856-66.

    Publication: Research - peer-reviewJournal article

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ID: 34394780