Manuel Mattheisen

  1. 2013
  2. Published

    Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder. / Haenisch, Britta; Herms, Stefan; Mattheisen, Manuel; Steffens, Michael; Breuer, Rene; Strohmaier, Jana; Degenhardt, Franziska; Schmäl, Christine; Lucae, Susanne; Maier, Wolfgang; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: Journal of Affective Disorders, Vol. 146, No. 3, 25.04.2013, p. 438-40.

    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

    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

  5. Published

    αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior. / Easton, Alanna C; Lucchesi, Walter; Lourdusamy, Anbarasu; Lenz, Bernd; Solati, Jalal; Golub, Yulia; Lewczuk, Piotr; Fernandes, Cathy; Desrivieres, Sylvane; Dawirs, Ralph R; Moll, Gunther H; Kornhuber, Johannes; Frank, Josef; Hoffmann, Per; Soyka, Michael; Kiefer, Falk; Schumann, Gunter; Peter Giese, K; Müller, Christian P; Treutlein, Jens; Cichon, Sven; Ridinger, Monika; Mattheisen, Manuel; Herms, Stefan; Wodarz, Norbert; 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; Rietschel, Marcella; GESGA Consortium ; Mattheisen, Manuel.

    In: Neuropsychopharmacology, Vol. 38, No. 9, 08.2013, p. 1636-47.

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

  6. 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

  7. Published

    Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. / Andreassen, Ole A; Djurovic, Srdjan; Thompson, Wesley K; Schork, Andrew J; Kendler, Kenneth S; O'Donovan, Michael C; Rujescu, Dan; Werge, Thomas; van de Bunt, Martijn; Morris, Andrew P; McCarthy, Mark I; Roddey, J Cooper; McEvoy, Linda K; Desikan, Rahul S; Dale, Anders M; International Consortium for Blood Pressure GWAS ; Mattheisen, Manuel.

    In: American Journal of Human Genetics, Vol. 92, No. 2, 07.02.2013, p. 197-209.

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

  8. 2012
  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  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

    Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. / Meier, S; Mattheisen, Manuel; Vassos, E; Strohmaier, J; Treutlein, J; Josef, F; Breuer, R; Degenhardt, F; Mühleisen, T W; Müller-Myhsok, B; Steffens, M; Schmael, C; McMahon, F J; Nöthen, M M; Cichon, S; Schulze, T G; Rietschel, M; Kelsoe, John R; Greenwood, Tiffany A; Nievergelt, Caroline M; Barrett, Thomas B; McKinney, Rebecca; Shilling, Paul D; Schork, Nicholas J; Smith, Erin N; Bloss, Cinnamon S; Nurnberger, John; Edenberg, Howard J; Foroud, Tatiana; Koller, Daniel L; Gershon, Elliot S; Liu, Chun-Yu; Badner, Judith A; Scheftner, William; Lawson, William B; Nwulia, Evaristus A; Hipolito, Maria; Coryell, William; Rice, John; Byerley, William; McMahon, Francis; Chen, David T W; Schulze, Thomas G; Berrettini, Wade; Potash, James B; Zandi, Peter P; Mahon, Pamela B; McInnis, Melvin; Craig, David; Szelinger, Szabolcs; Bipolar Disorder Genome Study (BiGS) Consortium.

    In: Translational Psychiatry, Vol. 2, 2012, p. e165.

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

  17. Published

    Quick, "imputation-free" meta-analysis with proxy-SNPs. / Meesters, Christian; Leber, Markus; Herold, Christine; Angisch, Marina; Mattheisen, Manuel; Drichel, Dmitriy; Lacour, André; Becker, Tim.

    In: B M C Bioinformatics, Vol. 13, 2012, p. 231.

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

  18. 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

  19. 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

  20. 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

  21. Published

    Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. / Keller, Matthew C; Simonson, Matthew A; Ripke, Stephan; Neale, Ben M; Gejman, Pablo V; Howrigan, Daniel P; Lee, Sang Hong; Lencz, Todd; Levinson, Douglas F; Sullivan, Patrick F; Schizophrenia Psychiatric Genome-Wide Association Study Consortium ; Mattheisen, Manuel.

    In: PLoS genetics, Vol. 8, No. 4, 2012, p. e1002656.

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

  22. 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

  23. 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

  24. Published

    Integrated genome-wide pathway association analysis with INTERSNP. / Herold, Christine; Mattheisen, Manuel; Lacour, André; Vaitsiakhovich, Tatsiana; Angisch, Marina; Drichel, Dmitriy; Becker, Tim.

    In: Human Heredity, Vol. 73, No. 2, 2012, p. 63-72.

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

  25. Published

    Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder : a European multicenter study. / Hammer, C; Cichon, S; Mühleisen, T W; Haenisch, B; Degenhardt, F; Mattheisen, Manuel; Breuer, R; Witt, S H; Strohmaier, J; Oruc, L; Rivas, F; Babadjanova, G; Grigoroiu-Serbanescu, M; Hauser, J; Röth, R; Rappold, G; Rietschel, M; Nöthen, M M; Niesler, B.

    In: Translational Psychiatry, Vol. 2, 2012, p. e103.

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

  26. Published

    Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. / Gladwin, Thomas E; Derks, Eske M; Rietschel, Marcella; Mattheisen, Manuel; Breuer, René; Schulze, Thomas G; Nöthen, Markus M; Levinson, Douglas; Shi, Jianxin; Gejman, Pablo V; Cichon, Sven; Ophoff, Roel A; Genetic Risk and Outcome of Psychosis (GROUP).

    In: P L o S One, Vol. 7, No. 6, 2012, p. e38828.

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

  27. 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

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