Manuel Mattheisen

  1. 2014
  2. Published

    Obsessive-compulsive disorder as a risk factor for schizophrenia : A nationwide study. / Meier, Sandra M; Petersen, Liselotte; Pedersen, Marianne G; Arendt, Mikkel C B; Nielsen, Philip R; Mattheisen, Manuel; Mors, Ole; Mortensen, Preben B.

    In: Archives of general psychiatry, Vol. 71, No. 11, 03.09.2014, p. 1215-1221.

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

  3. Published

    Beyond GWAS in COPD : Probing the Landscape between Gene-Set Associations, Genome-Wide Associations and Protein-Protein Interaction Networks. / McDonald, Merry-Lynn Noelle; Mattheisen, Manuel; Cho, Michael H; Liu, Yang-Yu; Harshfield, Benjamin; Hersh, Craig P; Bakke, Per; Gulsvik, Amund; Lange, Christoph; Beaty, Terri H; Silverman, Edwin K.

    In: Human Heredity, Vol. 78, No. 3, 27.08.2014, p. 131-139.

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

  4. Published

    Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder. / Witt, S H; Juraeva, D; Sticht, C; Strohmaier, J; Meier, S; Treutlein, J; Dukal, H; Frank, J; Lang, M; Deuschle, M; Schulze, T G; Degenhardt, F; Mattheisen, Manuel; Brors, B; Cichon, S; Nöthen, M M; Witt, C C; Rietschel, M.

    In: Translational Psychiatry, Vol. 4, e426, 19.08.2014.

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

  5. Published

    Biological insights from 108 schizophrenia-associated genetic loci. / Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: Nature, Vol. 511, No. 7510, 24.07.2014, p. 421-7.

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

  6. Published

    Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. / Gockel, Ines; Becker, Jessica; Wouters, Mira M; Niebisch, Stefan; Gockel, Henning R; Hess, Timo; Ramonet, David; Zimmermann, Julian; Vigo, Ana González; Trynka, Gosia; de León, Antonio Ruiz; de la Serna, Julio Pérez; Urcelay, Elena; Kumar, Vinod; Franke, Lude; Westra, Harm-Jan; Drescher, Daniel; Kneist, Werner; Marquardt, Jens U; Galle, Peter R; Mattheisen, Manuel; Annese, Vito; Latiano, Anna; Fumagalli, Uberto; Laghi, Luigi; Cuomo, Rosario; Sarnelli, Giovanni; Müller, Michaela; Eckardt, Alexander J; Tack, Jan; Hoffmann, Per; Herms, Stefan; Mangold, Elisabeth; Heilmann, Stefanie; Kiesslich, Ralf; von Rahden, Burkhard H A; Allescher, Hans-Dieter; Schulz, Henning G; Wijmenga, Cisca; Heneka, Michael T; Lang, Hauke; Hopfner, Karl-Peter; Nöthen, Markus M; Boeckxstaens, Guy E; de Bakker, Paul I W; Knapp, Michael; Schumacher, Johannes.

    In: Nature Genetics, 06.07.2014.

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

  7. Published

    GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. / Christoforou, Andrea; Espeseth, Thomas; Davies, Gail; Fernandes, Carla P D; Giddaluru, Sudheer; Mattheisen, Manuel; Tenesa, Albert; Harris, Sarah E; Liewald, David C; Payton, Antony; Ollier, William; Horan, Michael; Pendleton, Neil; Haggarty, Paul; Djurovic, Srdjan; Herms, Stefan; Hoffman, Per; Cichon, Sven; Starr, John M; Lundervold, Astri; Reinvang, Ivar; Steen, Vidar M; Deary, Ian J; Le Hellard, Stephanie.

    In: Genes, Brain and Behavior, 28.06.2014.

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

  8. Published

    Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. / Forstner, Andreas J; Basmanav, F B; Mattheisen, Manuel; Böhmer, Anne C; Hollegaard, Mads V; Janson, Esther; Strengman, Eric; Priebe, Lutz; Degenhardt, Franziska; Hoffmann, Per; Herms, Stefan; Maier, Wolfgang; Mössner, Rainald; Rujescu, Dan; Ophoff, Roel A; Moebus, Susanne; Mortensen, Preben B; Børglum, Anders D; Hougaard, David M; Frank, Josef; Witt, Stephanie H; Rietschel, Marcella; Zimmer, Andreas; Nöthen, Markus M; Miró, Xavier; Cichon, Sven; GROUP Investigators.

    In: Journal of Psychiatry and Neuroscience, Vol. 39, No. 6, 17.06.2014, p. 386-396.

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

  9. Published

    Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain. / Dixson, Luanna; Walter, Henrik; Schneider, Michael; Erk, Susanne; Schäfer, Axel; Haddad, Leila; Grimm, Oliver; Mattheisen, Manuel; Nöthen, Markus M; Cichon, Sven; Witt, Stephanie H; Rietschel, Marcella; Mohnke, Sebastian; Seiferth, Nina; Heinz, Andreas; Tost, Heike; Meyer-Lindenberg, Andreas.

    In: Proceedings of the National Academy of Sciences of the United States of America, 16.06.2014.

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

  10. Published

    Identification of pathways for bipolar disorder : a meta-analysis. / Nurnberger, John I; Koller, Daniel L; Jung, Jeesun; Edenberg, Howard J; Foroud, Tatiana; Guella, Ilaria; Vawter, Marquis P; Kelsoe, John R; Psychiatric Genomics Consortium Bipolar Group.

    In: J A M A Psychiatry, Vol. 71, No. 6, 06.2014, p. 657-64.

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

  11. Published

    Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia. / GROUP Investigators; iPSYCH-GEMS SCZ (Jakob Grove, member of -).

    In: P L o S Genetics, Vol. 10, No. 6, 06.2014, p. e1004345.

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

  12. Published

    Genome-wide association study and mouse expression data identify a highly conserved 32kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. / Reutter, Heiko; Draaken, Markus; Pennimpede, Tracie; Wittler, Lars; Brockschmidt, Felix F; Ebert, Anne-Karolin; Bartels, Enrika; Rösch, Wolfgang; Boemers, Thomas M; Hirsch, Karin; Schmiedeke, Eberhard; Meesters, Christian; Becker, Tim; Stein, Raimund; Utsch, Boris; Mangold, Elisabeth; Nordenskjöld, Agneta; Barker, Gillian; Kockum, Christina Clementsson; Zwink, Nadine; Holmdahl, Gundula; Läckgren, Göran; Jenetzky, Ekkehart; Feitz, Wouter Fj; Marcelis, Carlo; Wijers, Charlotte H W; van Rooij, Iris A L M; Gearhart, John P; Herrmann, Bernhard G; Ludwig, Michael; Boyadjiev, Simeon A; Nöthen, Markus M; Mattheisen, Manuel.

    In: Human Molecular Genetics, 22.05.2014.

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

  13. Published

    Genome-wide association study in obsessive-compulsive disorder : results from the OCGAS. / Mattheisen, Manuel; Samuels, J F; Wang, Y; Greenberg, B D; Fyer, A J; McCracken, J T; Geller, D A; Murphy, D L; Knowles, J A; Grados, M A; Riddle, M A; Rasmussen, S A; McLaughlin, N C; Nurmi, E L; Askland, K D; Qin, H-D; Cullen, B A; Piacentini, J; Pauls, D L; Bienvenu, O J; Stewart, S E; Liang, K-Y; Goes, F S; Maher, B; Pulver, A E; Shugart, Y Y; Valle, D; Lange, C; Nestadt, G.

    In: Molecular Psychiatry, 13.05.2014.

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

  14. Published

    Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. / Erk, Susanne; Meyer-Lindenberg, Andreas; Linden, David; Lancaster, Thomas; Mohnke, Sebastian; Grimm, Oliver; Degenhardt, Franziska; Holmans, Peter; Pocklington, Andrew; Schmierer, Phöbe; Haddad, Leila; Mühleisen, Thomas W; Mattheisen, Manuel; Witt, Stephanie H; Seiferth, Nina; Tost, Heike; Schott, Björn H; Cichon, Sven; Nöthen, Markus M; Rietschel, Marcella; Heinz, Andreas; Walter, Henrik.

    In: NeuroImage, 15.03.2014.

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

  15. Published

    Striatal Response to Reward Anticipation : Evidence for a Systems-Level Intermediate Phenotype for Schizophrenia. / Grimm, Oliver; Heinz, Andreas; Walter, Henrik; Kirsch, Peter; Erk, Susanne; Haddad, Leila; Plichta, Michael M; Romanczuk-Seiferth, Nina; Pöhland, Lydia; Mohnke, Sebastian; Mühleisen, Thomas W; Mattheisen, Manuel; Witt, Stephanie H; Schäfer, Axel; Cichon, Sven; Nöthen, Markus; Rietschel, Marcella; Tost, Heike; Meyer-Lindenberg, Andreas.

    In: J A M A Psychiatry, Vol. 71, No. 5, 12.03.2014, p. 531-539.

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

  16. Published

    Risk loci for chronic obstructive pulmonary disease : a genome-wide association study and meta-analysis. / Cho, Michael H; McDonald, Merry-Lynn N; Zhou, Xiaobo; Mattheisen, Manuel; Castaldi, Peter J; Hersh, Craig P; Demeo, Dawn L; Sylvia, Jody S; Ziniti, John; Laird, Nan M; Lange, Christoph; Litonjua, Augusto A; Sparrow, David; Casaburi, Richard; Barr, R Graham; Regan, Elizabeth A; Make, Barry J; Hokanson, John E; Lutz, Sharon; Dudenkov, Tanda Murray; Farzadegan, Homayoon; Hetmanski, Jacqueline B; Tal-Singer, Ruth; Lomas, David A; Bakke, Per; Gulsvik, Amund; Crapo, James D; Silverman, Edwin K; Beaty, Terri H; NETT Genetics, ICGN, ECLIPSE and COPDGene Investigators.

    In: The Lancet Respiratory Medicine, Vol. 2, No. 3, 03.2014, p. 214-25.

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

  17. Published

    The Hypercholesterolemia-Risk Gene SORT1 Facilitates PCSK9 Secretion. / Gustafsen, Camilla; Kjolby, Mads; Nyegaard, Mette; Mattheisen, Manuel; Lundhede, Jesper; Buttenschøn, Henriette; Mors, Ole; Bentzon, Jacob F; Madsen, Peder; Nykjaer, Anders; Glerup, Simon.

    In: Cell Metabolism, Vol. 19, No. 2, 10.02.2014, p. 310-8.

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

  18. Published

    Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder : differential involvement of immune-related gene loci. / Andreassen, O A; Harbo, H F; Wang, Y; Thompson, W K; Schork, A J; Mattingsdal, M; Zuber, V; Bettella, F; Ripke, S; Kelsoe, J R; Kendler, K S; O'Donovan, M C; Sklar, P; McEvoy, L K; Desikan, R S; Lie, B A; Djurovic, S; Dale, A M; The Psychiatric Genomics Consortium (PGC) Bipolar Disorder and Schizophrenia Work Groups ; Mattheisen, Manuel; Børglum, Anders.

    In: Molecular Psychiatry, 28.01.2014.

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

  19. Published

    The ENIGMA Consortium : large-scale collaborative analyses of neuroimaging and genetic data. / Thompson, Paul M; Stein, Jason L; Medland, Sarah E; Hibar, Derrek P; Vasquez, Alejandro Arias; Renteria, Miguel E; Toro, Roberto; Jahanshad, Neda; Schumann, Gunter; Franke, Barbara; Wright, Margaret J; Martin, Nicholas G; Agartz, Ingrid; Alda, Martin; Alhusaini, Saud; Almasy, Laura; Almeida, Jorge; Alpert, Kathryn; Andreasen, Nancy C; Andreassen, Ole A; Apostolova, Liana G; Appel, Katja; Armstrong, Nicola J; Aribisala, Benjamin; Bastin, Mark E; Bauer, Michael; Bearden, Carrie E; Bergmann, Orjan; Binder, Elisabeth B; Blangero, John; Bockholt, Henry J; Bøen, Erlend; Bois, Catherine; Boomsma, Dorret I; Booth, Tom; Bowman, Ian J; Bralten, Janita; Brouwer, Rachel M; Brunner, Han G; Brohawn, David G; Buckner, Randy L; Buitelaar, Jan; Bulayeva, Kazima; Bustillo, Juan R; Calhoun, Vince D; Cannon, Dara M; Cantor, Rita M; Carless, Melanie A; Caseras, Xavier; Mattheisen, Manuel; the Alzheimer’s Disease Neuroimaging Initiative, EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study (SYS) Group.

    In: Brain Imaging and Behavior, 08.01.2014.

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

  20. Published

    GENDER-SPECIFIC ASSOCIATION OF VARIANTS IN THE AKR1C1 GENE WITH DIMENSIONAL ANXIETY IN PATIENTS WITH PANIC DISORDER : ADDITIONAL EVIDENCE FOR THE IMPORTANCE OF NEUROSTEROIDS IN ANXIETY? / Quast, Carina; Reif, Andreas; Brückl, Tanja; Pfister, Hildegard; Weber, Heike; Mattheisen, Manuel; Cichon, Sven; Lang, Thomas; Hamm, Alfons; Fehm, Lydia; Ströhle, Andreas; Arolt, Volker; Domschke, Katharina; Kircher, Tilo; Wittchen, Hans-Ulrich; Pauli, Paul; Gerlach, Alexander L; Alpers, Georg W; Deckert, Jürgen; Rupprecht, Rainer; Binder, Elisabeth B; Erhardt, Angelika.

    In: Depression and Anxiety, 03.01.2014.

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

  21. Published

    Airway wall thickness is increased in COPD patients with bronchodilator responsiveness. / Kim, Victor; Desai, Parag; Newell, John D; Make, Barry J; Washko, George R; Silverman, Edwin K; Crapo, James D; Bhatt, Surya P; Criner, Gerard J; COPDGene Investigators ; Mattheisen, Manuel.

    In: Respiratory Research Review, Vol. 15, 2014, p. 84.

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

  22. Published

    Common and rare variant analysis in early-onset bipolar disorder vulnerability. / Jamain, Stéphane; Cichon, Sven; Etain, Bruno; Mühleisen, Thomas W; Georgi, Alexander; Zidane, Nora; Chevallier, Lucie; Deshommes, Jasmine; Nicolas, Aude; Henrion, Annabelle; Degenhardt, Franziska; Mattheisen, Manuel; Priebe, Lutz; Mathieu, Flavie; Kahn, Jean-Pierre; Henry, Chantal; Boland, Anne; Zelenika, Diana; Gut, Ivo; Heath, Simon; Lathrop, Mark; Maier, Wolfgang; Albus, Margot; Rietschel, Marcella; Schulze, Thomas G; McMahon, Francis J; Kelsoe, John R; Hamshere, Marian; Craddock, Nicholas; Nöthen, Markus M; Bellivier, Frank; Leboyer, Marion.

    In: PLOS ONE, Vol. 9, No. 8, 2014, p. e104326.

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

  23. Published

    DNAH5 is associated with total lung capacity in chronic obstructive pulmonary disease. / Lee, Jin Hwa; McDonald, Merry-Lynn N; Cho, Michael H; Wan, Emily S; Castaldi, Peter J; Hunninghake, Gary M; Marchetti, Nathaniel; Lynch, David A; Crapo, James D; Lomas, David A; Coxson, Harvey O; Bakke, Per S; Silverman, Edwin K; Hersh, Craig P; COPDGene and ECLIPSE Investigators ; Mattheisen, Manuel.

    In: Respiratory Research Review, Vol. 15, 2014, p. 97.

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

  24. Published

    Enrichment Analysis of Genomic features to Identify Genome-Wide Patterns of Insertions/Deletions in Cases of Psychiatric Disorders from the Faroe Islands. / Eickhardt, Esben Ahlburg; Als, Thomas Damm; Mattheisen, Manuel; Nyegaard, Mette; Demontis, Ditte; Grove, Jakob; Andorsdottir, Gudrid; Biskopstø, Marjun; Wang, August; Mors, Ole; Bolund, Lars; Wang, Jun; Børglum, Anders; Lescai, Francesco.

    2014. Poster session presented at XXII World Congress of Psychiatric Genetics, København, Danmark, Denmark.

    Research output: Contribution to conferencePosterResearchpeer-review

  25. Published

    Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene. / Wan, Emily S; Castaldi, Peter J; Cho, Michael H; Hokanson, John E; Regan, Elizabeth A; Make, Barry J; Beaty, Terri H; Han, MeiLan K; Curtis, Jeffrey L; Curran-Everett, Douglas; Lynch, David A; DeMeo, Dawn L; Crapo, James D; Silverman, Edwin K; COPDGene Investigators ; Mattheisen, Manuel.

    In: Respiratory Research Review, Vol. 15, 2014, p. 89.

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

  26. Published

    Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease. / Yildiz, Yildiz; Hoffmann, Per; Vom Dahl, Stefan; Breiden, Bernadette; Sandhoff, Roger; Niederau, Claus; Horwitz, Mia; Karlsson, Stefan; Filacamo, Mirella; Elstein, Deborah; Beck, Michael; Sandhoff, Konrad; Mengel, Eugen; Gonzalez, Maria C; Nöthen, Markus M; Sidransky, Ellen; Zimran, Ari; Mattheisen, Manuel.

    In: Orphanet Journal of Rare Diseases, Vol. 8, No. 1, 2014, p. 151.

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

  27. Published

    Genome-wide association study reveals two new risk loci for bipolar disorder. / Mühleisen, Thomas W; Leber, Markus; Schulze, Thomas G; Strohmaier, Jana; Degenhardt, Franziska; Treutlein, Jens; Mattheisen, Manuel; Forstner, Andreas J; Schumacher, Johannes; Breuer, René; Meier, Sandra; Herms, Stefan; Hoffmann, Per; Lacour, André; Witt, Stephanie H; Reif, Andreas; Müller-Myhsok, Bertram; Lucae, Susanne; Maier, Wolfgang; Schwarz, Markus; Vedder, Helmut; Kammerer-Ciernioch, Jutta; Pfennig, Andrea; Bauer, Michael; Hautzinger, Martin; Moebus, Susanne; Priebe, Lutz; Czerski, Piotr M; Hauser, Joanna; Lissowska, Jolanta; Szeszenia-Dabrowska, Neonila; Brennan, Paul; McKay, James D; Wright, Adam; Mitchell, Philip B; Fullerton, Janice M; Schofield, Peter R; Montgomery, Grant W; Medland, Sarah E; Gordon, Scott D; Martin, Nicholas G; Krasnow, Valery; Chuchalin, Alexander; Babadjanova, Gulja; Pantelejeva, Galina; Abramova, Lilia I; Tiganov, Alexander S; Polonikov, Alexey; Khusnutdinova, Elza; Alda, Martin; Grof, Paul; Rouleau, Guy A; Turecki, Gustavo; Laprise, Catherine; Rivas, Fabio; Mayoral, Fermin; Kogevinas, Manolis; Grigoroiu-Serbanescu, Maria; Propping, Peter; Becker, Tim; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: Nature Communications, Vol. 5, 2014, p. 3339.

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

  28. Published

    Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation. / Søes, Signe; Daugaard, Iben Lyster; Sørensen, Brita Singers; Carus, Andreas; Mattheisen, Manuel; Alsner, Jan; Overgaard, Jens; Hager, Henrik; Hansen, Lise Lotte; Kristensen, Lasse Sommer.

    In: Oncoscience, Vol. 1, No. 5, 2014, p. 367-74.

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

  29. Published

    Non-emphysematous chronic obstructive pulmonary disease is associated with diabetes mellitus. / Hersh, Craig P; Make, Barry J; Lynch, David A; Barr, R Graham; Bowler, Russell P; Calverley, Peter M A; Castaldi, Peter J; Cho, Michael H; Coxson, Harvey O; DeMeo, Dawn L; Foreman, Marilyn G; Han, MeiLan K; Harshfield, Benjamin J; Hokanson, John E; Lutz, Sharon; Ramsdell, Joe W; Regan, Elizabeth A; Rennard, Stephen I; Schroeder, Joyce D; Sciurba, Frank C; Steiner, Robert M; Tal-Singer, Ruth; van Beek, Edwin; Silverman, Edwin K; Crapo, James D; COPDGene and ECLIPSE Investigators ; Mattheisen, Manuel.

    In: B M C Pulmonary Medicine, Vol. 14, 2014, p. 164.

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

  30. Published

    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases. / Gusev, Alexander; Lee, S Hong; Trynka, Gosia; Finucane, Hilary; Vilhjálmsson, Bjarni Jóhann; Xu, Han; Zang, Chongzhi; Ripke, Stephan; Bulik-Sullivan, Brendan; Stahl, Eli; Kähler, Anna K; Hultman, Christina M; Purcell, Shaun M; McCarroll, Steven A; Daly, Mark; Pasaniuc, Bogdan; Sullivan, Patrick F; Neale, Benjamin M; Wray, Naomi R; Raychaudhuri, Soumya; Price, Alkes L; Schizophrenia Working Group of the Psychiatric Genomics Consortium (Manuel Mattheisen and Jakob Grove, members).

    In: American Journal of Human Genetics, Vol. 95, No. 5, 2014, p. 535-52.

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

  31. Published

    Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. / Nicodemus, Kristin K; Hargreaves, April; Morris, Derek; Anney, Richard; Gill, Michael; Corvin, Aiden; Donohoe, Gary; Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium.

    In: J A M A Psychiatry, Vol. 71, No. 7, 2014, p. 778-85.

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

  32. 2013
  33. Published

    Efficient Strategy for Detecting Gene × Gene Joint Action and Its Application in Schizophrenia. / Won, Sungho; Kwon, Min-Seok; Mattheisen, Manuel; Park, Suyeon; Park, Changsoon; Kihara, Daisuke; Cichon, Sven; Ophoff, Roel; Nöthen, Markus M; Rietschel, Marcella; Baur, Max; Uitterlinden, Andre G; Hofmann, A; Lange, Christoph; GROUP Investigators.

    In: Genetic Epidemiology, 23.11.2013.

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

  34. Published

    Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia. / Wouters, Mira M; Lambrechts, Diether; Becker, Jessica; Cleynen, Isabelle; Tack, Jan; Vigo, Ana G; Ruiz de León, Antonio; Urcelay, Elena; Pérez de la Serna, Julio; Rohof, Wout; Annese, Vito; Latiano, Anna; Palmieri, Orazio; Mattheisen, Manuel; Mueller, Michaela; Lang, Hauke; Fumagalli, Uberto; Laghi, Luigi; Zaninotto, Giovanni; Cuomo, Rosario; Sarnelli, Giovanni; Nöthen, Markus M; Vermeire, Séverine; Knapp, Kolja Michael; Gockel, Ines; Schumacher, Johannes; Boeckxstaens, Guy E.

    In: Gut, 20.11.2013.

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

  35. Published

    Further Evidence for the Impact of a Genome-Wide-Supported Psychosis Risk Variant in ZNF804A on the Theory of Mind Network. / Mohnke, Sebastian; Erk, Susanne; Schnell, Knut; Schütz, Claudia; Romanczuk-Seiferth, Nina; Grimm, Oliver; Haddad, Leila; Pöhland, Lydia; Garbusow, Maria; Schmitgen, Mike M; Kirsch, Peter; Esslinger, Christine; Rietschel, Marcella; Witt, Stephanie H; Nöthen, Markus M; Cichon, Sven; Mattheisen, Manuel; Mühleisen, Thomas; Jensen, Jimmy; Schott, Björn H; Maier, Wolfgang; Heinz, Andreas; Meyer-Lindenberg, Andreas; Walter, Henrik.

    In: Neuropsychopharmacology, 19.11.2013.

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

  36. Published

    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. / Luo, X-J; Li, Menxing; Huang, Liping; Steinberg, S; Mattheisen, Manuel; Liang, G; Donohoe, G; Shi, Y; Chen, Andrew C. N.; Yue, Wei; Alkelai, A; Lerer, B; Li, Z; Yi, Q; Rietschel, M; Cichon, S; Collier, D A; Tosato, S; Suvisaari, J; Rujescu, Dan; Golimbet, V; Silagadze, T; Durmishi, N; Milovancevic, M P; Stefansson, H; Schulze, T G; Nöthen, M M; Chen, Andrew C. N.; Lyne, R; Morris, D W; Gill, M; Corvin, A; Zhang, D; Dong, Q; Moyzis, R K; Stefansson, K; Sigurdsson, Eythor; Hu, F; Su, B; Gan, L; MooDS SCZ Consortium.

    In: Molecular Psychiatry, 20.08.2013.

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

  37. Published

    Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. / Lee, S Hong; Ripke, Stephan; Neale, Benjamin M; Faraone, Stephen V; Purcell, Shaun M; Perlis, Roy H; Mowry, Bryan J; Thapar, Anita; Goddard, Michael E; Witte, John S; Absher, Devin; Agartz, Ingrid; Akil, Huda; Amin, Farooq; Andreassen, Ole A; Anjorin, Adebayo; Anney, Richard; Anttila, Verneri; Arking, Dan E; Asherson, Philip; Azevedo, Maria H; Backlund, Lena; Badner, Judith A; Bailey, Anthony J; Banaschewski, Tobias; Barchas, Jack D; Barnes, Michael R; Barrett, Thomas B; Bass, Nicholas; Battaglia, Agatino; Bauer, Michael; Bayés, Mònica; Bellivier, Frank; Bergen, Sarah E; Berrettini, Wade; Betancur, Catalina; Bettecken, Thomas; Biederman, Joseph; Binder, Elisabeth B; Black, Donald W; Blackwood, Douglas H R; Bloss, Cinnamon S; Boehnke, Michael; Boomsma, Dorret I; Breen, Gerome; Breuer, René; Bruggeman, Richard; Cormican, Paul; Mattheisen, Manuel; Meier, Sandra; Cross-Disorder Group of the Psychiatric Genomics Consortium.

    In: Nature Genetics, 11.08.2013.

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

  38. Published

    Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex. / Qi, Lihong; Wang, Mei; Yagnik, Garima; Mattheisen, Manuel; Gearhart, John P; Lakshmanan, Yegappan; Ebert, Anne-Karolin; Rösch, Wolfgang; Ludwig, Michael; Draaken, Markus; Reutter, Heiko; Boyadjiev, Simeon A.

    In: Birth Defects Research. Part A: Clinical and Molecular Teratology, 02.08.2013.

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

  39. 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

  40. Published

    Rare autosomal copy number variations in early-onset familial Alzheimer's disease. / Hooli, B V; Kovacs-Vajna, Z M; Mullin, K; Blumenthal, M A; Mattheisen, Manuel; Zhang, C; Lange, C; Mohapatra, G; Bertram, L; Tanzi, R E.

    In: Molecular Psychiatry, 11.06.2013.

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

  41. Published

    On Association Analysis of Rare Variants Under Population Substructure : An Approach for the Detection of Subjects That Can Cause Bias in the Analysis-Topt : An Outlier Detection Method. / Qiao, Dandi; Mattheisen, Manuel; Lange, Christoph.

    In: Genetic Epidemiology, 14.05.2013.

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

  42. 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

  43. Published

    Identification of risk loci with shared effects on five major psychiatric disorders : a genome-wide analysis. / Smoller, Jordan W; Craddock, Nicholas; Kendler, Kenneth; Lee, Phil Hyoun; Neale, Benjamin M; Nurnberger, John I; Ripke, Stephan; Santangelo, Susan; Sullivan, Patrick F; Cross-Disorder Group of the Psychiatric Genomics Consortium ; Mattheisen, Manuel.

    In: Lancet, Vol. 381, No. 9875, 20.04.2013, p. 1371-9.

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

  44. Published

    Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. / Li, Menxing; Luo, X-J; Rietschel, M; Lewis, C M; Mattheisen, Manuel; Müller-Myhsok, B; Jamain, S; Leboyer, M; Landén, M; Thompson, P M; Cichon, S; Nöthen, M M; Schulze, T G; Sullivan, Neal P; Bergen, S E; Donohoe, G; Morris, D W; Hargreaves, A; Gill, M; Corvin, A; Hultman, C; Toga, A W; Shi, Lijuan; Lin, Q; Shi, H; Gan, L; Meyer-Lindenberg, A; Czamara, D; Henry, C; Etain, B; Bis, J C; Ikram, M A; Fornage, M; Debette, S; Launer, L J; Seshadri, S; Erk, S; Walter, H; Heinz, A; Bellivier, F; Stein, Jonathan; Medland, S E; Arias Vasquez, A; Hibar, D P; Franke, B; Martin, N G; Wright, M J; Su, B; MooDS Bipolar Consortium.

    In: Molecular Psychiatry, 09.04.2013.

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

  45. Published

    A mega-analysis of genome-wide association studies for major depressive disorder. / Ripke, Stephan; Wray, Naomi R; Lewis, Cathryn M; Hamilton, Steven P; Weissman, Myrna M; Breen, Gerome; Byrne, Enda M; Blackwood, Douglas H R; Boomsma, Dorret I; Cichon, Sven; Heath, Andrew C; Holsboer, Florian; Lucae, Susanne; Madden, Pamela A F; Martin, Nicholas G; McGuffin, Peter; Muglia, Pierandrea; Noethen, Markus M; Penninx, Brenda P; Pergadia, Michele L; Potash, James B; Rietschel, Marcella; Lin, Danyu; Müller-Myhsok, Bertram; Shi, Jianxin; Steinberg, Stacy; Grabe, Hans J; Lichtenstein, Paul; Magnusson, Patrik; Perlis, Roy H; Preisig, Martin; Smoller, Jordan W; Stefansson, Kari; Uher, Rudolf; Kutalik, Zoltan; Tansey, Katherine E; Teumer, Alexander; Viktorin, Alexander; Barnes, Michael R; Bettecken, Thomas; Binder, Elisabeth B; Breuer, René; Castro, Victor M; Churchill, Susanne E; Coryell, William H; Craddock, Nick; Craig, Ian W; Czamara, Darina; De Geus, Eco J; Mattheisen, Manuel; Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium.

    In: Molecular Psychiatry, Vol. 18, No. 4, 04.2013, p. 497-511.

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

  46. Published

    All SNPs are not created equal : genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. / Schork, Andrew J; Thompson, Wesley K; Pham, Phillip; Torkamani, Ali; Roddey, J Cooper; Sullivan, Patrick F; Kelsoe, John R; O'Donovan, Michael C; Furberg, Helena; Schork, Nicholas J; Andreassen, Ole A; Dale, Anders M; Tobacco and Genetics Consortium ; Mattheisen, Manuel.

    In: PLoS genetics, Vol. 9, No. 4, 04.2013, p. e1003449.

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

  47. Published

    Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder. / Meier, Sandra; Strohmaier, Jana; Breuer, Rene; Mattheisen, Manuel; Degenhardt, Franziska; Mühleisen, Thomas W; Schulze, Thomas G; Nöthen, Markus M; Cichon, Sven; Rietschel, Marcella; Wüst, Stefan.

    In: International Journal of Neuropsychopharmacology, Vol. 16, No. 3, 04.2013, p. 549-56.

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

  48. Published

    Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. / Terwisscha van Scheltinga, Afke F; Bakker, Steven C; van Haren, Neeltje E M; Derks, Eske M; Buizer-Voskamp, Jacobine E; Boos, Heleen B M; Cahn, Wiepke; Hulshoff Pol, Hilleke E; Ripke, Stephan; Ophoff, Roel A; Kahn, René S; Psychiatric Genome-wide Association Study Consortium ; Mattheisen, Manuel.

    In: Biological Psychiatry, Vol. 73, No. 6, 15.03.2013, p. 525-31.

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

  49. 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

  50. 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

  51. 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

  52. 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

  53. 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

  54. 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

  55. 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

  56. 2012
  57. 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

  58. 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

  59. 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

  60. 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

  61. 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

  62. 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

  63. 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

  64. 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

  65. 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

  66. 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

  67. 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

  68. 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

  69. 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

  70. 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

  71. 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

  72. 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

  73. 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

  74. 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

  75. 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

  76. 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

  77. 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

  78. Published

    Investigation of the genetic association between quantitative measures of psychosis and schizophrenia : a polygenic risk score analysis. / Derks, Eske M; Vorstman, Jacob A S; Ripke, Stephan; Kahn, Rene S; Ophoff, Roel A; Schizophrenia Psychiatric Genomic Consortium ; Mattheisen, Manuel.

    In: P L o S One, Vol. 7, No. 6, 2012, p. e37852.

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

  79. 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

  80. 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

  81. 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

  82. 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

  83. 2011
  84. Published

    Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant. / Erk, Susanne; Meyer-Lindenberg, Andreas; Opitz von Boberfeld, Carola; Esslinger, Christine; Schnell, Knut; Kirsch, Peter; Mattheisen, Manuel; Mühleisen, Thomas W; Cichon, Sven; Witt, Stephanie H; Rietschel, Marcella; Nöthen, Markus M; Walter, Henrik.

    In: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 31, No. 49, 07.12.2011, p. 18180-4.

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

  85. Published

    Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. / Mattheisen, Manuel; Psychiatric GWAS Consortium Bipolar Disorder Working Group.

    In: Nature Genetics, Vol. 43, No. 10, 10.2011, p. 977-83.

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

  86. Published

    The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. / Håvik, Bjarte; Le Hellard, Stephanie; Rietschel, Marcella; Lybæk, Helle; Djurovic, Srdjan; Mattheisen, Manuel; Mühleisen, Thomas W; Degenhardt, Franziska; Priebe, Lutz; Maier, Wolfgang; Breuer, Rene; Schulze, Thomas G; Agartz, Ingrid; Melle, Ingrid; Hansen, Thomas; Bramham, Clive R; Nöthen, Markus M; Stevens, Beth; Werge, Thomas; Andreassen, Ole A; Cichon, Sven; Steen, Vidar M.

    In: Advances in Biological Psychiatry, Vol. 70, No. 1, 01.07.2011, p. 35-42.

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

  87. Published

    Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype. / Breuer, R; Hamshere, M L; Strohmaier, J; Mattheisen, Manuel; Degenhardt, F; Meier, S; Paul, T; O'Donovan, M C; Mühleisen, T W; Schulze, T G; Nöthen, M M; Cichon, S; Craddock, N; Rietschel, M.

    In: Molecular Psychiatry, Vol. 16, No. 6, 06.2011, p. 587-9.

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

  88. Published

    Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. / Mühleisen, Thomas W; Basmanav, F Buket; Forstner, Andreas J; Mattheisen, Manuel; Priebe, Lutz; Herms, Stefan; Breuer, Rene; Moebus, Susanne; Nenadic, Igor; Sauer, Heinrich; Mössner, Rainald; Maier, Wolfgang; Rujescu, Dan; Ludwig, Michael; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: Schizophrenia research, Vol. 127, No. 1-3, 04.2011, p. 35-40.

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

  89. Published

    Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. / Cichon, Sven; Mühleisen, Thomas W; Degenhardt, Franziska A; Mattheisen, Manuel; Miró, Xavier; Strohmaier, Jana; Steffens, Michael; Meesters, Christian; Herms, Stefan; Weingarten, Moritz; Priebe, Lutz; Haenisch, Britta; Alexander, Michael; Vollmer, Jennifer; Breuer, René; Schmäl, Christine; Tessmann, Peter; Moebus, Susanne; Wichmann, H-Erich; Schreiber, Stefan; Müller-Myhsok, Bertram; Lucae, Susanne; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Henry, Chantal; Kahn, Jean-Pierre; Heath, Simon; Hamshere, Marian; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Schwarz, Markus; Vedder, Helmut; Kammerer-Ciernioch, Jutta; Reif, Andreas; Sasse, Johanna; Bauer, Michael; Hautzinger, Martin; Wright, Adam; Mitchell, Philip B; Schofield, Peter R; Montgomery, Grant W; Medland, Sarah E; Gordon, Scott D; Martin, Nicholas G; Gustafsson, Omar; Andreassen, Ole; Djurovic, Srdjan; Bipolar Disorder Genome Study (BiGS) Consortium.

    In: American Journal of Human Genetics, Vol. 88, No. 3, 11.03.2011, p. 372-81.

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

  90. Published

    Significance levels in genome-wide interaction analysis (GWIA). / Becker, Tim; Herold, Christine; Meesters, Christian; Mattheisen, Manuel; Baur, Max P.

    In: Annals of Human Genetics, Vol. 75, No. 1, 01.2011, p. 29-35.

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

  91. Published

    Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults. / Schreiner, Felix; El-Maarri, Osman; Gohlke, Bettina; Stutte, Sonja; Nuesgen, Nicole; Mattheisen, Manuel; Fimmers, Rolf; Bartmann, Peter; Oldenburg, Johannes; Woelfle, Joachim.

    In: B M C Medical Genetics, Vol. 12, 2011, p. 115.

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

  92. 2010
  93. Published

    Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. / Rietschel, Marcella; Mattheisen, Manuel; Frank, Josef; Treutlein, Jens; Degenhardt, Franziska; Breuer, René; Steffens, Michael; Mier, Daniela; Esslinger, Christine; Walter, Henrik; Kirsch, Peter; Erk, Susanne; Schnell, Knut; Herms, Stefan; Wichmann, H-Erich; Schreiber, Stefan; Jöckel, Karl-Heinz; Strohmaier, Jana; Roeske, Darina; Haenisch, Britta; Gross, Magdalena; Hoefels, Susanne; Lucae, Susanne; Binder, Elisabeth B; Wienker, Thomas F; Schulze, Thomas G; Schmäl, Christine; Zimmer, Andreas; Juraeva, Dilafruz; Brors, Benedikt; Bettecken, Thomas; Meyer-Lindenberg, Andreas; Müller-Myhsok, Bertram; Maier, Wolfgang; Nöthen, Markus M; Cichon, Sven.

    In: Biological Psychiatry, Vol. 68, No. 6, 15.09.2010, p. 578-85.

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

  94. Published

    Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. / Reutter, Heiko; Rüschendorf, Franz; Mattheisen, Manuel; Draaken, Markus; Bartels, Enrika; Hübner, Norbert; Hoffmann, Per; Payabvash, Seyedmedhi; Saar, Kathrin; Nöthen, Markus M; Kajbafzadeh, Abdol-Mohammad; Ludwig, Michael.

    In: Birth Defects Research. Part A: Clinical and Molecular Teratology, Vol. 88, No. 9, 09.2010, p. 757-61.

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

  95. Published

    The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia : findings from a large German case-control and family-based sample. / Nieratschker, Vanessa; Frank, Josef; Mühleisen, Thomas W; Strohmaier, Jana; Wendland, Jens R; Schumacher, Johannes; Treutlein, Jens; Breuer, René; Abou Jamra, Rami; Mattheisen, Manuel; Herms, Stefan; Schmäl, Christine; Maier, Wolfgang; Nöthen, Markus M; Cichon, Sven; Rietschel, Marcella; Schulze, Thomas G.

    In: Schizophrenia research, Vol. 122, No. 1-3, 09.2010, p. 24-30.

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

  96. Published

    A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry. / Strohmaier, Jana; Frank, Josef; Wendland, Jens R; Schumacher, Johannes; Jamra, Rami Abou; Treutlein, Jens; Nieratschker, Vanessa; Breuer, René; Mattheisen, Manuel; Herms, Stefan; Mühleisen, Thomas W; Maier, Wolfgang; Nöthen, Markus M; Cichon, Sven; Rietschel, Marcella; Schulze, Thomas G.

    In: Schizophrenia research, Vol. 118, No. 1-3, 05.2010, p. 98-105.

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

  97. Published

    Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples. / Le Hellard, S; Mühleisen, T W; Djurovic, S; Fernø, J; Ouriaghi, Z; Mattheisen, Manuel; Vasilescu, C; Raeder, M B; Hansen, T; Strohmaier, J; Georgi, A; Brockschmidt, F F; Melle, I; Nenadic, I; Sauer, H; Rietschel, M; Nöthen, M M; Werge, T; Andreassen, O A; Cichon, S; Steen, V M.

    In: Molecular Psychiatry, Vol. 15, No. 5, 05.2010, p. 463-72.

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

  98. Published

    Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. / McMahon, Francis J; Akula, Nirmala; Schulze, Thomas G; Muglia, Pierandrea; Tozzi, Federica; Detera-Wadleigh, Sevilla D; Steele, C J M; Breuer, René; Strohmaier, Jana; Wendland, Jens R; Mattheisen, Manuel; Mühleisen, Thomas W; Maier, Wolfgang; Nöthen, Markus M; Cichon, Sven; Farmer, Anne; Vincent, John B; Holsboer, Florian; Preisig, Martin; Rietschel, Marcella; Bipolar Disorder Genome Study (BiGS) Consortium.

    In: Nature Genetics, Vol. 42, No. 2, 02.2010, p. 128-31.

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

  99. Published

    Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. / Mangold, Elisabeth; Ludwig, Kerstin U; Birnbaum, Stefanie; Baluardo, Carlotta; Ferrian, Melissa; Herms, Stefan; Reutter, Heiko; de Assis, Nilma Almeida; Chawa, Taofik Al; Mattheisen, Manuel; Steffens, Michael; Barth, Sandra; Kluck, Nadine; Paul, Anna; Becker, Jessica; Lauster, Carola; Schmidt, Gül; Braumann, Bert; Scheer, Martin; Reich, Rudolf H; Hemprich, Alexander; Pötzsch, Simone; Blaumeiser, Bettina; Moebus, Susanne; Krawczak, Michael; Schreiber, Stefan; Meitinger, Thomas; Wichmann, Hans-Erich; Steegers-Theunissen, Regine P; Kramer, Franz-Josef; Cichon, Sven; Propping, Peter; Wienker, Thomas F; Knapp, Kolja Michael; Rubini, Michele; Mossey, Peter A; Hoffmann, Per; Nöthen, Markus M.

    In: Nature Genetics, Vol. 42, No. 1, 01.2010, p. 24-6.

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

  100. 2009
  101. Published

    Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin. / Mangold, Elisabeth; Reutter, Heiko; Birnbaum, Stefanie; Walier, Maja; Mattheisen, Manuel; Henschke, Henning; Lauster, Carola; Schmidt, Gül; Schiefke, Franziska; Reich, Rudolf H; Scheer, Martin; Hemprich, Alexander; Martini, Markus; Braumann, Bert; Krimmel, Michael; Opitz, Charlotte; Lenz, Jan-Hendrik; Kramer, Franz-Josef; Wienker, Thomas F; Nöthen, Markus M; Diaz Lacava, Amalia.

    In: American Journal of Medical Genetics. Part A, Vol. 149A, No. 12, 12.2009, p. 2680-94.

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

  102. Published

    Common variants conferring risk of schizophrenia. / Stefansson, Hreinn; Ophoff, Roel A.; Steinberg, Stacy; Andreassen, Ole A.; Cichon, Sven; Rujescu, Dan; Werge, Thomas; Pietiläinen, Olli P. H.; Mors, Ole; Mortensen, Preben B.; Sigurdsson, Engilbert; Gustafsson, Omar; Nyegaard, Mette; Tuulio-Henriksson, Annamari; Ingason, Andres; Hansen, Thomas; Suvisaari, Jaana; Lonnqvist, Jouko; Paunio, Tiina; Børglum, Anders D.; Hartmann, Annette; Fink-Jensen, Anders; Nordentoft, Merete; Hougaard, David; Norgaard-Pedersen, Bent; Böttcher, Yvonne; Olesen, Jes; Breuer, René; Möller, Hans-Jürgen; Giegling, Ina; Rasmussen, Henrik B.; Timm, Sally; Mattheisen, Manuel; Bitter, István; Réthelyi, János M.; Magnusdottir, Brynja B.; Sigmundsson, Thordur; Olason, Pall; Masson, Gisli; Gulcher, Jeffrey R.; Haraldsson, Magnus; Fossdal, Ragnheidur; Thorgeirsson, Thorgeir E.; Thorsteinsdottir, Unnur; Ruggeri, Mirella; Tosato, Sarah; Franke, Barbara; Strengman, Eric; Kiemeney, Lambertus A.; Kahn, René S.; Linszen, Don H.; van Os, Jim; Wiersma, Durk; Bruggeman, Richard; Cahn, Wiepke; de Haan, Lieuwe; Krabbendam, Lydia; Myin-Germeys, Inez; Melle, Ingrid; Djurovic, Srdjan; Abramova, Lilia; Kaleda, Vasily; Sanjuan, Julio; de Frutos, Rosa; Bramon, Elvira; Vassos, Evangelos; Fraser, Gillian; Ettinger, Ulrich; Picchioni, Marco; Walker, Nicholas; Toulopoulou, Timi; Need, Anna C.; Ge, Dongliang; Lim Yoon, Joeng; Shianna, Kevin V.; Freimer, Nelson B.; Cantor, Rita M.; Murray, Robin; Kong, Augustine; Golimbet, Vera; Carracedo, Angel; Arango, Celso; Costas, Javier; Jönsson, Erik G.; Terenius, Lars; Agartz, Ingrid; Petursson, Hannes; Nöthen, Markus M.; Rietschel, Marcella; Matthews, Paul M.; Muglia, Pierandrea; Peltonen, Leena; St Clair, David; Goldstein, David B.; Stefansson, Kari; Collier, David A.

    In: Nature, Volume 460, Issue 7256, pp. 744-747 (2009)., Vol. 460, 01.08.2009, p. 744-747.

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

  103. Published

    Supporting evidence for LRRTM1 imprinting effects in schizophrenia. / Ludwig, K U; Mattheisen, Manuel; Mühleisen, T W; Roeske, D; Schmäl, C; Breuer, R; Schulte-Körne, G; Müller-Myhsok, B; Nöthen, M M; Hoffmann, P; Rietschel, M; Cichon, S.

    In: Molecular Psychiatry, Vol. 14, No. 8, 08.2009, p. 743-5.

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

  104. Published

    The DISC locus and schizophrenia : evidence from an association study in a central European sample and from a meta-analysis across different European populations. / Schumacher, Johannes; Laje, Gonzalo; Abou Jamra, Rami; Becker, Tim; Mühleisen, Thomas W; Vasilescu, Catalina; Mattheisen, Manuel; Herms, Stefan; Hoffmann, Per; Hillmer, Axel M; Georgi, Alexander; Herold, Christine; Schulze, Thomas G; Propping, Peter; Rietschel, Marcella; McMahon, Francis J; Nöthen, Markus M; Cichon, Sven.

    In: Human Molecular Genetics, Vol. 18, No. 14, 15.07.2009, p. 2719-27.

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

  105. Published

    Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. / Treutlein, Jens; Mühleisen, Thomas W; Frank, Josef; Mattheisen, Manuel; Herms, Stefan; Ludwig, Kerstin U; Treutlein, Tsendsesmee; Schmael, Christine; Strohmaier, Jana; Bösshenz, Katja Veronika; Breuer, René; Paul, Torsten; Witt, Stephanie H; Schulze, Thomas G; Schlösser, Ralf G M; Nenadic, Igor; Sauer, Heinrich; Becker, Tim; Maier, Wolfgang; Cichon, Sven; Nöthen, Markus M; Rietschel, Marcella.

    In: Schizophrenia research, Vol. 111, No. 1-3, 06.2009, p. 123-30.

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

  106. Published

    A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. / Hoffmann, Katrin; Planitz, Christian; Rüschendorf, Franz; Müller-Myhsok, Bertram; Stassen, Hans H; Lucke, Barbara; Mattheisen, Manuel; Stumvoll, Michael; Bochmann, Rolf; Zschornack, Martin; Wienker, Thomas F; Nürnberg, Peter; Reis, André; Luft, Friedrich C; Lindner, Tom H.

    In: Journal of Hypertension, Vol. 27, No. 5, 05.2009, p. 983-90.

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