Manuel Mattheisen

  1. 2013
  2. Published

    No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. / Degenhardt, Franziska; Priebe, Lutz; Strohmaier, Jana; Herms, Stefan; Hoffmann, Per; Mattheisen, Manuel; Mössner, Rainald; Nenadic, Igor; Sauer, Heinrich; Rujescu, Dan; Maier, Wolfgang; Schulze, Thomas G; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: Psychiatric Genetics, Vol. 23, No. 1, 02.2013, p. 45-6.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  3. Published

    A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. / Fernandes, Carla P D; Christoforou, Andrea; Giddaluru, Sudheer; Ersland, Kari M; Djurovic, Srdjan; Mattheisen, Manuel; Lundervold, Astri J; Reinvang, Ivar; Nöthen, Markus M; Rietschel, Marcella; Ophoff, Roel A; Hofman, Albert; Uitterlinden, André G; Werge, Thomas; Cichon, Sven; Espeseth, Thomas; Andreassen, Ole A; Steen, Vidar M; Le Hellard, Stephanie; Genetic Risk and Outcome of Psychosis (GROUP).

    In: PLOS ONE, Vol. 8, No. 12, 2013, p. e81052.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  4. Published

    Copy number variants in german patients with schizophrenia. / Priebe, Lutz; Degenhardt, Franziska; Strohmaier, Jana; Breuer, René; Herms, Stefan; Witt, Stephanie H; Hoffmann, Per; Kulbida, Rebecca; Mattheisen, Manuel; Moebus, Susanne; Meyer-Lindenberg, Andreas; Walter, Henrik; Mössner, Rainald; Nenadic, Igor; Sauer, Heinrich; Rujescu, Dan; Maier, Wolfgang; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: P L o S One, Vol. 8, No. 7, 2013, p. e64035.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  5. Published

    Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support. / Erk, S; Meyer-Lindenberg, A; Schmierer, P; Grimm, O; Tost, H; Mühleisen, T; Mattheisen, Manuel; Seiferth, N; Cichon, S; Rietschel, M; Nöthen, M M; Heinz, A; Walter, H.

    In: Translational Psychiatry, Vol. 3, 2013, p. e287.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  6. Published

    How isolated is the Faroese population & what are the prospects of mapping complex psychiatric disorders? / Als, Thomas Damm; Lescai, Francesco; Grove, Jakob; Mattheisen, Manuel; Demontis, Ditte; Wang, August G.; Andorsdottir, Gudrid; Biskopstø, Marjun; Nyegaard, Mette; Bolund, Lars; Mors, Ole; Wang, Jun; Børglum, Anders.

    2013. Poster session presented at XXIst World Congress of Psychiatric Genetics , Boston, Massachusetts, United States.

    Research output: Contribution to conferencePosterResearchpeer-review

  7. 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.; Ripke, S.; Sanders, A.R.; Kendler, K.S.; Levinson, D.F.; Sklar, P.; Holmans, P.A.; Lin, D.-Y.; Duan, J.; Ophoff, R.A.; Andreassen, O.A.; Scolnick, E.; Cichon, S.; St Clair, D.; Corvin, A.; Gurling, H.; Werge, Thomas; Rujescu, D.; Blackwood, D.H.R.; Pato, C.N.; Malhotra, A.K.; Purcell, S.; Dudbridge, F.; Neale, B.M.; Rossin, L.; Visscher, P.M.; Posthuma, D.; Ruderfer, D.M.; Fanous, A.; Stefansson, H.; Steinberg, S.; Mowry, B.J.; Golimbet, V.; De Hert, M.; Jönsson, E.G.; Bitter, I.; Pietiläinen, O.P.H.; Collier, D.A.; Tosato, S.; Agartz, I.; Albus, M.; Alexander, M.; Amdur, R.L.; Amin, Farooq; Bass, N.; Bergen, S.E.; Black, D.W.; Børglum, A.D.; Brown, M.A.; Bruggeman, R.; Buccola, N.G.; Byerley, W.F.; Cahn, W.; Cantor, Rita M.; Carr, V.J.; Catts, S.V.; Choudhury, K.; Cloninger, C.R.; Cormican, P.; Craddock, N.; Danoy, P.A.; Datta, Suvra; De Haan, L.; Demontis, Ditte; Dikeos, D.; Djurovic, S.; Donnelly, P.; Donohoe, G.; Duong, Linh Thi Thuy; Dwyer, S.; Fink-Jensen, Anders; Freedman, R.; Freimer, N.B.; Friedl, M.; Georgieva, L.; Giegling, I.; Gill, M.; Glenthøj, Birte Yding; Godard, S.; Hamshere, M.; Hansen, M.; Hansen, T.; Hartmann, A.M.; Henskens, F.A.; Hougaard, D.M.; Hultman, C.M.; Ingason, Andrés; Jablensky, A.V.; Jakobsen, K.D.; Jay, M.; Jürgens, G.; Kahn, R.S.; Keller, M.C.; Kenis, G.; Kenny, E.; Kim, Y.; Kirov, G.K.; Konnerth, H.; Konte, B.; Krabbendam, L.; Krasucki, R.; Lasseter, V.K.; Laurent, C.; Lawrence, J.; Lencz, T.; Lerer, F.B.; Liang, K.-Y.; Lichtenstein, P.; Lieberman, J.A.; Linszen, D.H.; Lönnqvist, J.; Loughland, C.M.; Maclean, A.W.; Maher, B.S.; Maier, W.; Mallet, J.; Malloy, P.; Mattheisen, Manuel; Mattingsdal, M.; McGhee, K.A.; McGrath, J.J.; McIntosh, A.; McLean, D.E.; McQuillin, A.; Melle, I.; Michie, P.T.; Milanova, V.; Morris, D.W.; Mors, Ole; Mortensen, Preben Bo; Moskvina, V.; Muglia, P.; Myin-Germeys, I.; Nertney, D.A.; Nestadt, G.; Nielsen, J.; Nikolov, I.; Nordentoft, Merete; Norton, N.; Nöthen, M.M.; O'Dushlaine, C.T.; Olincy, A.; Olsen, L.; O'Neill, F.A.; Ørntoft, T.F.; Owen, M.J.; Pantelis, C.; Papadimitriou, G.; Pato, M.T.; Peltonen, L.; Petursson, H.; Pickard, B.; Pimm, J.; Pulver, A.E.; Puri, V.; Quested, D.; Quinn, E.M.; Rasmussen, Henrik Berg; Réthelyi, J.M.; Ribble, R.; Rietschel, M.; Riley, B.P.; Ruggeri, M.; Schall, U.; Schulze, T.G.; Schwab, S.G.; Scott, R.J.; Shi, J.; Sigurdsson, Engilbert; Silverman, J.M.; Spencer, C.C.A.; Stefansson, K.; Strange, A.; Strengman, E.; Stroup, T.S.; Suvisaari, J.; Terenius, Lars T.; Thirumalai, S.; Thygesen, J.H.; Timm, S.; Toncheva, D.; Van Den Oord, E.; Van Os, J.; Van Winkel, R.; Veldink, J.; Walsh, D.; Wang, A.G.; Wiersma, D.; Wildenauer, D.B.; Williams, H.J.; Williams, Nigel M.A.; Wormley, B.; Zammit, S.; Sullivan, Patrick F.; O'Donovan, M.C.; Daly, Mark J.; Gejman, P.V.

    In: Psychological Medicine, Vol. 43, No. 12, 2013, p. 2563-2570.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  8. 2012
  9. Published

    Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. / Li, Ming; Wang, Yi; Zheng, Xue-bin; Ikeda, Masashi; Iwata, Nakao; Luo, Xiong-jian; Chong, Siow-Ann; Lee, Jimmy; Rietschel, Marcella; Zhang, Fengyu; Müller-Myhsok, Bertram; Cichon, Sven; Weinberger, Daniel R; Mattheisen, Manuel; Schulze, Thomas G; Martin, Nicholas G; Mitchell, Philip B; Schofield, Peter R; Liu, Jian-jun; Su, Bing; MooDS Consortium.

    In: Schizophrenia research, Vol. 142, No. 1-3, 12.2012, p. 200-5.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  10. Published

    Response to Zhu et al. / Christoforou, A.; Giddaluru, S.; Steen, V.M.; Le Hellard, S.; Mattheisen, Manuel.

    In: American Journal of Human Genetics, Vol. 91, No. 5, 02.11.2012, p. 969-970.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleCommunication

  11. Published

    Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. / Mattheisen, Manuel; Mühleisen, Thomas W; Strohmaier, Jana; Treutlein, Jens; Nenadic, Igor; Alblas, Margrieta; Meier, Sandra; Degenhardt, Franziska; Herms, Stefan; Hoffmann, Per; Witt, Stephanie H; Giegling, Ina; Sauer, Heinrich; Schulze, Thomas G; Rujescu, Dan; Nöthen, Markus M; Rietschel, Marcella; Cichon, Sven.

    In: Schizophrenia research, Vol. 141, No. 2-3, 11.2012, p. 262-5.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  12. Published

    VATER/VACTERL association : identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. / Bartels, Enrika; Schulz, Anna C; Mora, Nicole W; Pineda-Alvarez, Daniel E; Wijers, Charlotte H W; Marcelis, Carlo M; Stressig, Rüdiger; Ritgen, Jochen; Schmiedeke, Eberhard; Mattheisen, Manuel; Draaken, Markus; Hoffmann, Per; Hilger, Alina C; Dworschak, Gabriel C; Baudisch, Friederike; Ludwig, Michael; Bagci, Soyhan; Müller, Andreas; Gembruch, Ulrich; Geipel, Annegret; Berg, Christoph; Bartmann, Peter; Nöthen, Markus M; van Rooij, Iris A L M; Solomon, Benjamin D; Reutter, Heiko M.

    In: Clinical Dysmorphology, Vol. 21, No. 4, 10.2012, p. 191-5.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  13. Published

    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. / Rietschel, M.; Mattheisen, Manuel; Strohmaier, J.; Breuer, R.; Schmael, C.; Meier, S.; Nikitopoulos, J.; Schulze, T.G.; Degenhardt, F.; Mühleisen, T.W.; Herms, S.; Haenisch, B.; Priebe, L.; Basmanav, F.B.; Forstner, A.J.; Hoffmann, P.; Alexander, M.; Schumacher, Johannes; Nöthen, M.M.; Steffens, M.; Wienker, T.F.; Kirsch, P.; Esslinger, C.; Meyer-Lindenberg, A.; Demontis, D.; Børglum, A.D.; Czerski, P.M.; Kapelski, P.; Cichon, S.; Hauser, J.; Giegling, I.; Rujescu, D.; Strengman, E.; Ophoff, R.A.; Mors, O.; Mortensen, P.B.; Hougaard, D.M.; Orntoft, T.; Moebus, S.; Mössner, R.; Maier, W.; Wichmann, H.-E.; Schreiber, S.; Rivandeneira, F.; Uitterlinden, A.G.; Hofman, A.; Cantor, Robert; Erk, S.; Walter, H.; Craddock, N.; Owen, M.J.; O'Donovan, M.C.

    In: Molecular Psychiatry, Vol. 17, No. 9, 01.09.2012, p. 906-917.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  14. Published

    Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. / Ludwig, Kerstin U; Mangold, Elisabeth; Herms, Stefan; Nowak, Stefanie; Reutter, Heiko; Paul, Anna; Becker, Jessica; Herberz, Ruth; AlChawa, Taofik; Nasser, Entessar; Böhmer, Anne C; Mattheisen, Manuel; Alblas, Margrieta A; Barth, Sandra; Kluck, Nadine; Lauster, Carola; Braumann, Bert; Reich, Rudolf H; Hemprich, Alexander; Pötzsch, Simone; Blaumeiser, Bettina; Daratsianos, Nikolaos; Kreusch, Thomas; Murray, Jeffrey C; Marazita, Mary L; Ruczinski, Ingo; Scott, Alan F; Beaty, Terri H; Kramer, Franz-Josef; Wienker, Thomas F; Steegers-Theunissen, Regine P; Rubini, Michele; Mossey, Peter A; Hoffmann, Per; Lange, Christoph; Cichon, Sven; Propping, Peter; Knapp, Kolja Michael; Nöthen, Markus M.

    In: Nature Genetics, Vol. 44, No. 9, 09.2012, p. 968-71.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  15. Published

    Studies in humans and mice implicate neurocan in the etiology of mania. / Miró, Xavier; Meier, Sandra; Dreisow, Marie Luise; Frank, Josef; Strohmaier, Jana; Breuer, René; Schmäl, Christine; Albayram, Önder; Pardo-Olmedilla, María Teresa; Mühleisen, Thomas W; Degenhardt, Franziska A; Mattheisen, Manuel; Reinhard, Iris; Bilkei-Gorzo, Andras; Cichon, Sven; Seidenbecher, Constanze; Rietschel, Marcella; Nöthen, Markus M; Zimmer, Andreas.

    In: The American Journal of Psychiatry (Spanish Edition), Vol. 169, No. 9, 09.2012, p. 982-90.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  16. Published

    Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. / Mühleisen, Thomas W; Mattheisen, Manuel; Strohmaier, Jana; Degenhardt, Franziska; Priebe, Lutz; Schultz, C Christoph; Breuer, René; Meier, Sandra; Hoffmann, Per; Rivandeneira, Fernando; Hofman, Albert; Uitterlinden, André G; Moebus, Susanne; Gieger, Christian; Emeny, Rebecca; Ladwig, Karl-Heinz; Wichmann, H-Erich; Schwarz, Markus; Kammerer-Ciernioch, Jutta; Schlösser, Ralf G M; Nenadic, Igor; Sauer, Heinrich; Mössner, Rainald; Maier, Wolfgang; Rujescu, Dan; Lange, Christoph; Ophoff, Roel A; Schulze, Thomas G; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven; GROUP Investigators.

    In: Schizophrenia research, Vol. 138, No. 1, 06.2012, p. 69-73.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  17. Published

    Common variants at 12q14 and 12q24 are associated with hippocampal volume. / Bis, Joshua C; DeCarli, Charles; Smith, Albert Vernon; van der Lijn, Fedde; Crivello, Fabrice; Fornage, Myriam; Debette, Stephanie; Shulman, Joshua M; Schmidt, Helena; Srikanth, Velandai; Schuur, Maaike; Yu, Lei; Choi, Seung-Hoan; Sigurdsson, Sigurdur; Verhaaren, Benjamin F J; DeStefano, Anita L; Lambert, Jean-Charles; Jack, Clifford R; Struchalin, Maksim; Stankovich, Jim; Ibrahim-Verbaas, Carla A; Fleischman, Debra; Zijdenbos, Alex; den Heijer, Tom; Mazoyer, Bernard; Coker, Laura H; Enzinger, Christian; Danoy, Patrick; Amin, Najaf; Arfanakis, Konstantinos; van Buchem, Mark A; de Bruijn, Renée F A G; Beiser, Alexa; Dufouil, Carole; Huang, Juebin; Cavalieri, Margherita; Thomson, Russell; Niessen, Wiro; Chibnik, Lori B; Gislason, Gauti K; Hofman, Albert; Pikula, Aleksandra; Amouyel, Philippe; Freeman, Kevin B; Phan, Thanh G; Oostra, Ben A; Stein, Jason L; Medland, Sarah E; Vasquez, Alejandro Arias; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium ; Mattheisen, Manuel.

    In: Nature Genetics, Vol. 44, No. 5, 05.2012, p. 545-51.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  18. Published

    FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia. / Naz, G; Pasternack, S M; Perrin, C; Mattheisen, Manuel; Refke, M; Khan, S; Gul, A; Simons, M; Ahmad, W; Betz, R C.

    In: British Journal of Dermatology, Vol. 166, No. 5, 05.2012, p. 1088-94.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  19. Published

    Identification of common variants associated with human hippocampal and intracranial volumes. / Stein, Jason L; Medland, Sarah E; Vasquez, Alejandro Arias; Hibar, Derrek P; Senstad, Rudy E; Winkler, Anderson M; Toro, Roberto; Appel, Katja; Bartecek, Richard; Bergmann, Ørjan; Bernard, Manon; Brown, Andrew A; Cannon, Dara M; Chakravarty, M Mallar; Christoforou, Andrea; Domin, Martin; Grimm, Oliver; Hollinshead, Marisa; Holmes, Avram J; Homuth, Georg; Hottenga, Jouke-Jan; Langan, Camilla; Lopez, Lorna M; Hansell, Narelle K; Hwang, Kristy S; Kim, Sungeun; Laje, Gonzalo; Lee, Phil H; Liu, Xinmin; Loth, Eva; Lourdusamy, Anbarasu; Mattingsdal, Morten; Mohnke, Sebastian; Maniega, Susana Muñoz; Nho, Kwangsik; Nugent, Allison C; O'Brien, Carol; Papmeyer, Martina; Pütz, Benno; Ramasamy, Adaikalavan; Rasmussen, Jerod; Rijpkema, Mark; Risacher, Shannon L; Roddey, J Cooper; Rose, Emma J; Ryten, Mina; Shen, Li; Sprooten, Emma; Strengman, Eric; Mattheisen, Manuel; Alzheimer's Disease Neuroimaging Initiative.

    In: Nature Genetics, Vol. 44, No. 5, 05.2012, p. 552-61.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  20. Published

    Role of common and rare APP DNA sequence variants in Alzheimer disease. / Hooli, B V; Mohapatra, G; Mattheisen, Manuel; Parrado, A R; Roehr, J T; Shen, Y; Gusella, J F; Moir, R; Saunders, A J; Lange, C; Tanzi, R E; Bertram, L.

    In: Neurology Alert, Vol. 78, No. 16, 17.04.2012, p. 1250-7.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  21. Published

    Linkage-disequilibrium-based binning affects the interpretation of GWASs. / Christoforou, Andrea; Dondrup, Michael; Mattingsdal, Morten; Mattheisen, Manuel; Giddaluru, Sudheer; Nöthen, Markus M; Rietschel, Marcella; Cichon, Sven; Djurovic, Srdjan; Andreassen, Ole A; Jonassen, Inge; Steen, Vidar M; Puntervoll, Pål; Le Hellard, Stéphanie.

    In: American Journal of Human Genetics, Vol. 90, No. 4, 06.04.2012, p. 727-33.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  22. Published

    Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. / Degenhardt, Franziska; Priebe, Lutz; Herms, Stefan; Mattheisen, Manuel; Mühleisen, Thomas W; Meier, Sandra; Moebus, Susanne; Strohmaier, Jana; Groß, Magdalena; Breuer, René; Lange, Christoph; Hoffmann, Per; Meyer-Lindenberg, Andreas; Heinz, Andreas; Walter, Henrik; Lucae, Susanne; Wolf, Christiane; Müller-Myhsok, Bertram; Holsboer, Florian; Maier, Wolfgang; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 159B, No. 3, 04.2012, p. 263-73.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  23. Published

    Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder. / Priebe, L; Degenhardt, F A; Herms, S; Haenisch, B; Mattheisen, Manuel; Nieratschker, V; Weingarten, M; Witt, S; Breuer, R; Paul, T; Alblas, M; Moebus, S; Lathrop, M; Leboyer, M; Schreiber, S; Grigoroiu-Serbanescu, M; Maier, W; Propping, P; Rietschel, M; Nöthen, M M; Cichon, S; Mühleisen, T W.

    In: Molecular Psychiatry, Vol. 17, No. 4, 04.2012, p. 421-32.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  24. Published

    Nine new twin pairs with esophageal atresia : a review of the literature and performance of a twin study of the disorder. / Schulz, Anna Carina; Bartels, Enrika; Stressig, Rüdiger; Ritgen, Jochen; Schmiedeke, Eberhard; Mattheisen, Manuel; Draaken, Markus; Ludwig, Michael; Bagci, Soyhan; Müller, Andreas; Gembruch, Ulrich; Geipel, Annegret; Berg, Christoph; Heydweiller, Andreas; Bachour, Haitham; Schumacher, Johannes; Bartmann, Peter; Nöthen, Markus M; Reutter, Heiko.

    In: Birth Defects Research. Part A: Clinical and Molecular Teratology, Vol. 94, No. 3, 03.2012, p. 182-6.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  25. Published

    Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. / Frank, Josef; Cichon, Sven; Treutlein, Jens; Ridinger, Monika; Mattheisen, Manuel; Hoffmann, Per; Herms, Stefan; Wodarz, Norbert; Soyka, Michael; Zill, Peter; Maier, Wolfgang; Mössner, Rainald; Gaebel, Wolfgang; Dahmen, Norbert; Scherbaum, Norbert; Schmäl, Christine; Steffens, Michael; Lucae, Susanne; Ising, Marcus; Müller-Myhsok, Bertram; Nöthen, Markus M; Mann, Karl; Kiefer, Falk; Rietschel, Marcella.

    In: Addiction Biology (Online), Vol. 17, No. 1, 01.2012, p. 171-80.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  26. Published

    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. / Håvik, Bjarte; Degenhardt, Franziska A; Johansson, Stefan; Fernandes, Carla P D; Hinney, Anke; Scherag, André; Lybæk, Helle; Djurovic, Srdjan; Christoforou, Andrea; Ersland, Kari M; Giddaluru, Sudheer; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Mühleisen, Thomas W; Mattheisen, Manuel; Schimmelmann, Benno G; Renner, Tobias; Warnke, Andreas; Herpertz-Dahlmann, Beate; Sinzig, Judith; Albayrak, Özgür; Rietschel, Marcella; Nöthen, Markus M; Bramham, Clive R; Werge, Thomas; Hebebrand, Johannes; Haavik, Jan; Andreassen, Ole A; Cichon, Sven; Steen, Vidar M; Le Hellard, Stéphanie.

    In: P L o S One, Vol. 7, No. 4, 2012, p. e35424.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  27. Published

    Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. / Ersland, Kari M; Christoforou, Andrea; Stansberg, Christine; Espeseth, Thomas; Mattheisen, Manuel; Mattingsdal, Morten; Hardarson, Gudmundur A; Hansen, Thomas; Fernandes, Carla P D; Giddaluru, Sudheer; Breuer, René; Strohmaier, Jana; Djurovic, Srdjan; Nöthen, Markus M; Rietschel, Marcella; Lundervold, Astri J; Werge, Thomas; Cichon, Sven; Andreassen, Ole A; Reinvang, Ivar; Steen, Vidar M; Le Hellard, Stephanie.

    In: P L o S One, Vol. 7, No. 2, 2012, p. e31687.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

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