Manuel Mattheisen

  1. Published

    1,25-Dihydroxyvitamin D modulates L-type voltage-gated calcium channels in a subset of neurons in the developing mouse prefrontal cortex. / Gooch, Helen; Cui, Xiaoying; Anggono, Victor; Trzaskowski, Maciej; Tan, Men Chee; Eyles, Darryl W; Burne, Thomas H J; Jang, Se Eun; Mattheisen, Manuel; Hougaard, David M; Pedersen, Bent Nørgaard; Cohen, Arieh; Mortensen, Preben B; Sah, Pankaj; McGrath, John J.

    In: Translational Psychiatry, Vol. 9, No. 1, 281, 2019.

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

  2. Published

    A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. / 23andMe Research Team; Psychiatric Genomics Consortium: ADHD Subgroup; iPSYCH–Broad ADHD Workgroup.

    In: Biological Psychiatry, Vol. 83, No. 12, 2018, p. 1044-1053.

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

  3. Published

    A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. / Hoffmann, K; Mattheisen, Manuel; Dahm, S; Nürnberg, P; Roe, C; Johnson, J; Cox, N J; Wichmann, H E; Wienker, T F; Schulze, J; Schwarz, P E; Lindner, T H.

    In: Diabetologia, Vol. 50, No. 7, 07.2007, p. 1418-22.

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

  4. Published

    A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31. / Habib, Rabia; Ansar, Muhammad; Mattheisen, Manuel; Shahid, Muhammad; Ali, Ghazanfar; Ahmad, Wasim; Betz, Regina C.

    In: P L o S One, Vol. 10, No. 6, 0129811, 26.06.2015.

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

  5. 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

  6. Published

    A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. / Lutz, Sharon M; Cho, Michael H; Young, Kendra; Hersh, Craig P; Castaldi, Peter J; McDonald, Merry-Lynn; Regan, Elizabeth; Mattheisen, Manuel; DeMeo, Dawn L; Parker, Margaret; Foreman, Marilyn; Make, Barry J; Jensen, Robert L; Casaburi, Richard; Lomas, David A; Bhatt, Surya P; Bakke, Per; Gulsvik, Amund; Crapo, James D; Beaty, Terri H; Laird, Nan M; Lange, Christoph; Hokanson, John E; Silverman, Edwin K; ECLIPSE Investigators.

    In: BMC Genetics, Vol. 16, 2015, p. 138.

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

  7. Published

    A major role for common genetic variation in anxiety disorders. / Purves, Kirstin L; Coleman, Jonathan R I; Meier, Sandra M; Rayner, Christopher; Davis, Katrina A S; Cheesman, Rosa; Bækvad-Hansen, Marie; Børglum, Anders D; Wan Cho, Shing; Jürgen Deckert, J; Gaspar, Héléna A; Bybjerg-Grauholm, Jonas; Hettema, John M; Hotopf, Matthew; Hougaard, David; Hübel, Christopher; Kan, Carol; McIntosh, Andrew M; Mors, Ole; Bo Mortensen, Preben; Nordentoft, Merete; Werge, Thomas; Nicodemus, Kristin K; Mattheisen, Manuel; Breen, Gerome; Eley, Thalia C.

    In: Molecular Psychiatry, Vol. 25, 12.2020, p. 3292-3303.

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

  8. 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

  9. 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

  10. Published

    A polygenic resilience score moderates the genetic risk for schizophrenia. / Hess, Jonathan L; Tylee, Daniel S; Mattheisen, Manuel; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH) ; Børglum, Anders D; Als, Thomas D; Grove, Jakob; Werge, Thomas; Mortensen, Preben Bo; Mors, Ole; Nordentoft, Merete; Hougaard, David M; Byberg-Grauholm, Jonas; Bækvad-Hansen, Marie; Greenwood, Tiffany A; Tsuang, Ming T; Curtis, David; Steinberg, Stacy; Sigurdsson, Engilbert; Stefánsson, Hreinn; Stefánsson, Kári; Edenberg, Howard J; Holmans, Peter; Faraone, Stephen V; Glatt, Stephen J.

    In: Molecular Psychiatry, Vol. 26, No. 3, 03.2021, p. 800–815.

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

  11. 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

  12. 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

  13. 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

  14. 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

  15. Published

    Altered Functional Subnetwork During Emotional Face Processing : A Potential Intermediate Phenotype for Schizophrenia. / Cao, Hengyi; Bertolino, Alessandro; Walter, Henrik; Schneider, Michael; Schäfer, Axel; Taurisano, Paolo; Blasi, Giuseppe; Haddad, Leila; Grimm, Oliver; Otto, Kristina; Dixson, Luanna; Erk, Susanne; Mohnke, Sebastian; Heinz, Andreas; Romanczuk-Seiferth, Nina; Mühleisen, Thomas W; Mattheisen, Manuel; Witt, Stephanie H; Cichon, Sven; Noethen, Markus; Rietschel, Marcella; Tost, Heike; Meyer-Lindenberg, Andreas.

    In: JAMA Psychiatry, Vol. 73, No. 6, 01.06.2016, p. 598-605.

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

  16. Published

    Analysis of shared heritability in common disorders of the brain. / Brainstorm Consortium.

    In: Science, Vol. 360, No. 6395, 8757, 22.06.2018, p. eaap8757.

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

  17. Published

    Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. / Rajkumar, A.P.; Christensen, Jane H.; Mattheisen, Manuel; Jacobsen, Iben; Bache, Iben; Pallesen, Jonatan; Grove, Jakob; Qvist, Per; Mcquillin, Andrew; Gurling, Hugh M.; Tümer, Zeynep; Mors, Ole; Børglum, Anders D.

    In: Bipolar Disorders (English Edition, Online), Vol. 17, No. 2, 01.01.2015, p. 205-211.

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

  18. Published

    Analysis of the influence of microRNAs in lithium response in bipolar disorder. / Reinbold, Céline S.; Forstner, Andreas J.; Hecker, Julian; Fullerton, Janice M.; Hoffmann, Per; Hou, Liping; Heilbronner, Urs; Degenhardt, Franziska; Adli, Mazda; Akiyama, Kazufumi; Akula, Nirmala; Ardau, Raffaella; Arias, Bárbara; Backlund, Lena; Benabarre, Antonio; Bengesser, Susanne; Bhattacharjee, Abesh K.; Biernacka, Joanna M.; Birner, Armin; Marie-Claire, Cynthia; Cervantes, Pablo; Chen, Guo Bo; Chen, Hsi Chung; Chillotti, Caterina; Clark, Scott R.; Colom, Francesc; Cousins, David A.; Cruceanu, Cristiana; Czerski, Piotr M.; Dayer, Alexandre; Étain, Bruno; Falkai, Peter; Frisén, Louise; Gard, Sébastien; Garnham, Julie S.; Goes, Fernando S.; Grof, Paul; Gruber, Oliver; Hashimoto, Ryota; Hauser, Joanna; Herms, Stefan; Jamain, Stéphane; Jiménez, Esther; Kahn, Jean Pierre; Kassem, Layla; Kittel-Schneider, Sarah; Kliwicki, Sebastian; König, Barbara; Kusumi, Ichiro; Lackner, Nina; Laje, Gonzalo; Landén, Mikael; Lavebratt, Catharina; Leboyer, Marion; Leckband, Susan G.; Jaramillo, Carlos A.López; MacQueen, Glenda; Manchia, Mirko; Martinsson, Lina; Mattheisen, Manuel; McCarthy, Michael J.; McElroy, Susan L.; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Nievergelt, Caroline M.; Ösby, Urban; Ozaki, Norio; Perlis, Roy H.; Pfennig, Andrea; Reich-Erkelenz, Daniela; Rouleau, Guy A.; Schofield, Peter R.; Schubert, K. Oliver; Schweizer, Barbara W.; Seemüller, Florian; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D.; Shimoda, Kazutaka; Simhandl, Christian; Slaney, Claire M.; Smoller, Jordan W.; Squassina, Alessio; Stamm, Thomas J.; Stopkova, Pavla; Tighe, Sarah K.; Tortorella, Alfonso; Turecki, Gustavo; Volkert, Julia; Witt, Stephanie H.; Wright, Adam J.; Trevor Young, L.; Zandi, Peter P.; Potash, James B.; DePaulo, J. Raymond; Bauer, Michael; Reininghaus, Eva; Novák, Tomáš; Aubry, Jean Michel; Maj, Mario; Baune, Bernhard T.; Mitchell, Philip B.; Vieta, Eduard; Frye, Mark A.; Rybakowski, Janusz K.; Kuo, Po Hsiu; Kato, Tadafumi; Grigoroiu-Serbanescu, Maria; Reif, Andreas; Zompo, Maria Del; Bellivier, Frank; Schalling, Martin; Wray, Naomi R.; Kelsoe, John R.; Alda, Martin; McMahon, Francis J.; Schulze, Thomas G.; Rietschel, Marcella; Nöthen, Markus M.; Cichon, Sven.

    In: Frontiers in Psychiatry, Vol. 9, No. MAY, 207, 31.05.2018.

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

  19. Published

    Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants. / Hauberg, Mads Engel; Roussos, Panos; Grove, Jakob; Børglum, Anders Dupont; Mattheisen, Manuel; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: JAMA Psychiatry, 09.03.2016.

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

  20. 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

  21. 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

  22. 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

  23. 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

  24. Published

    Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. / Schwantes-An, Tae-Hwi; Zhang, Juan; Chen, Li-Shiun; Hartz, Sarah M; Culverhouse, Robert C; Chen, Xiangning; Coon, Hilary; Frank, Josef; Kamens, Helen M; Konte, Bettina; Kovanen, Leena; Latvala, Antti; Legrand, Lisa N; Maher, Brion S; Melroy, Whitney E; Nelson, Elliot C; Reid, Mark W; Robinson, Jason D; Shen, Pei-Hong; Yang, Bao-Zhu; Andrews, Judy A; Aveyard, Paul; Beltcheva, Olga; Brown, Sandra A; Cannon, Dale S; Cichon, Sven; Corley, Robin P; Dahmen, Norbert; Degenhardt, Louisa; Foroud, Tatiana; Gaebel, Wolfgang; Giegling, Ina; Glatt, Stephen J; Grucza, Richard A; Hardin, Jill; Hartmann, Annette M; Heath, Andrew C; Herms, Stefan; Hodgkinson, Colin A; Hoffmann, Per; Hops, Hyman; Huizinga, David; Ising, Marcus; Johnson, Eric O; Johnstone, Elaine; Kaneva, Radka P; Kendler, Kenneth S; Kiefer, Falk; Kranzler, Henry R; Krauter, Ken S; Levran, Orna; Lucae, Susanne; Lynskey, Michael T; Maier, Wolfgang; Mann, Karl; Martin, Nicholas G; Mattheisen, Manuel; Montgomery, Grant W; Müller-Myhsok, Bertram; Murphy, Michael F; Neale, Michael C; Nikolov, Momchil A; Nishita, Denise; Nöthen, Markus M; Nurnberger, John; Partonen, Timo; Pergadia, Michele L; Reynolds, Maureen; Ridinger, Monika; Rose, Richard J; Rouvinen-Lagerström, Noora; Scherbaum, Norbert; Schmäl, Christine; Soyka, Michael; Stallings, Michael C; Steffens, Michael; Treutlein, Jens; Tsuang, Ming; Wall, Tamara L; Wodarz, Norbert; Yuferov, Vadim; Zill, Peter; Bergen, Andrew W; Chen, Jingchun; Cinciripini, Paul M; Edenberg, Howard J; Ehringer, Marissa A; Ferrell, Robert E; Gelernter, Joel; Goldman, David; Hewitt, John K; Hopfer, Christian J; Iacono, William G; Kaprio, Jaakko; Kreek, Mary Jeanne; Kremensky, Ivo M; Madden, Pamela A F; McGue, Matt; Munafò, Marcus R; Philibert, Robert A; Rietschel, Marcella; Roy, Alec; Rujescu, Dan; Saarikoski, Sirkku T; Swan, Gary E; Todorov, Alexandre A; Vanyukov, Michael M; Weiss, Robert B; Bierut, Laura J; Saccone, Nancy L.

    In: Behavior Genetics, Vol. 46, No. 2, 2016, p. 151–169.

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

  25. Published

    Association of the polygenic risk score for schizophrenia with mortality and suicidal behavior - A Danish population-based study. / Laursen, Thomas M; Trabjerg, Betina B; Mors, Ole; Børglum, Anders D; Hougaard, David M; Mattheisen, Manuel; Meier, Sandra M; Byrne, Enda M; Mortensen, Preben B; Munk-Olsen, Trine; Agerbo, Esben.

    In: Schizophrenia Research, Vol. 184, 2017, p. 122-127.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperConference abstract in journalResearchpeer-review

  26. 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

  27. 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

  28. Published

    Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. / Andlauer, Till F M; Guzman-Parra, Jose; Streit, Fabian; Strohmaier, Jana; González, Maria José; Gil Flores, Susana; Cabaleiro Fabeiro, Francisco J; Del Río Noriega, Francisco; Perez, Fermin Perez; Haro González, Jesus; Orozco Diaz, Guillermo; de Diego-Otero, Yolanda; Moreno-Küstner, Berta; Auburger, Georg; Degenhardt, Franziska; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hoffmann, Per; Frank, Josef; Foo, Jerome C; Treutlein, Jens; Witt, Stephanie H; Cichon, Sven; Kogevinas, Manolis; Rivas, Fabio; Mayoral, Fermín; Müller-Myhsok, Bertram; Forstner, Andreas J; Nöthen, Markus M; Rietschel, Marcella; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Molecular Psychiatry, Vol. 26, No. 4, 04.2021, p. 1286-1298.

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

  29. Published

    Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. / McDonald, Merry-Lynn Noelle; Won, Sungho; Mattheisen, Manuel; Castaldi, Peter J.; Cho, Michael H.; Rutten, Erica; Hardin, Megan; Yip, Wai-Ki; Rennard, Stephen I.; Lomas, David A.; Wouters, Emiel F. M.; Agusti, Alvar; Casaburi, Richard; Lange, Christoph P.; O'Connor, George; Hersh, Craig P.; Silverman, Edwin K.

    In: Journal of Cachexia, Sarcopenia and Muscle, Vol. 8, No. 3, 06.2017, p. 428-436.

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

  30. Published

    Brain-specific tryptophan hydroxylase 2 (TPH2) : a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder. / Cichon, Sven; Winge, Ingeborg; Mattheisen, Manuel; Georgi, Alexander; Karpushova, Anna; Freudenberg, Jan; Freudenberg-Hua, Yun; Babadjanova, Gulia; Van Den Bogaert, Ann; Abramova, Lilia I; Kapiletti, Sofia; Knappskog, Per M; McKinney, Jeffrey; Maier, Wolfgang; Jamra, Rami Abou; Schulze, Thomas G; Schumacher, Johannes; Propping, Peter; Rietschel, Marcella; Haavik, Jan; Nöthen, Markus M.

    In: Human Molecular Genetics, Vol. 17, No. 1, 01.01.2008, p. 87-97.

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

  31. 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

  32. Published

    Cannabis use, depression and self-harm : phenotypic and genetic relationships. / Hodgson, Karen; Coleman, Jonathan R.I.; Hagenaars, Saskia P.; Purves, Kirstin L.; Glanville, Kylie; Choi, Shing Wan; O'Reilly, Paul; Breen, Gerome; Lewis, Cathryn M.; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Addiction, Vol. 115, No. 3, 2020, p. 482-492.

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

  33. Published

    Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia. / Meier, Sandra M.; Kähler, Anna K.; Bergen, Sarah E.; Sullivan, Patrick F.; Hultman, Christina M.; Mattheisen, Manuel.

    In: Frontiers in Psychiatry, Vol. 11, 313, 06.2020.

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

  34. 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

  35. Published

    Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. / McDonald, Merry-Lynn N; Cho, Michael H; Sørheim, Inga-Cecilie; Lutz, Sharon M; Castaldi, Peter J; Lomas, David A; Coxson, Harvey O; Edwards, Lisa D; MacNee, William; Vestbo, Jørgen; Yates, Julie C; Agusti, Alvar; Calverley, Peter M A; Celli, Bartolome; Crim, Courtney; Rennard, Stephen I; Wouters, Emiel F M; Bakke, Per; Tal-Singer, Ruth; Miller, Bruce E; Gulsvik, Amund; Casaburi, Richard; Wells, J Michael; Regan, Elizabeth A; Make, Barry J; Hokanson, John E; Lange, Christoph; Crapo, James D; Beaty, Terri H; Silverman, Edwin K; Hersh, Craig P; Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators ; Mattheisen, Manuel.

    In: American Journal of Respiratory Cell and Molecular Biology (Online), Vol. 51, No. 5, 11.2014, p. 678-87.

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

  36. Published

    Common genetic variants influence human subcortical brain structures. / Hibar, Derrek P; Stein, Jason L; Renteria, Miguel E; Arias-Vasquez, Alejandro; Desrivières, Sylvane; Jahanshad, Neda; Toro, Roberto; Wittfeld, Katharina; Abramovic, Lucija; Andersson, Micael; Aribisala, Benjamin S; Armstrong, Nicola J; Bernard, Manon; Bohlken, Marc M; Boks, Marco P; Bralten, Janita; Brown, Andrew A; Mallar Chakravarty, M; Chen, Qiang; Ching, Christopher R K; Cuellar-Partida, Gabriel; den Braber, Anouk; Giddaluru, Sudheer; Goldman, Aaron L; Grimm, Oliver; Guadalupe, Tulio; Hass, Johanna; Woldehawariat, Girma; Holmes, Avram J; Hoogman, Martine; Janowitz, Deborah; Jia, Tianye; Kim, Sungeun; Klein, Marieke; Kraemer, Bernd; Lee, Phil H; Olde Loohuis, Loes M; Luciano, Michelle; Macare, Christine; Mather, Karen A; Mattheisen, Manuel; Milaneschi, Yuri; Nho, Kwangsik; Papmeyer, Martina; Ramasamy, Adaikalavan; Risacher, Shannon L; Roiz-Santiañez, Roberto; Rose, Emma J; Salami, Alireza; Sämann, Philipp G; The Alzheimer’s Disease Neuroimaging Initiative.

    In: Nature, 21.01.2015.

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

  37. Published

    Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. / GERAD1 Consortium:.

    In: Nature Genetics, Vol. 50, No. 3, 03.2018, p. 381-389.

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

  38. 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

  39. 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

  40. 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

  41. 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

  42. 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

  43. 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

  44. Published

    DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD. / Nissen, Judith Becker; Søholm Hansen, Christine; Starnawska, Anna; Mattheisen, Manuel; Børglum, Anders; Buttenschøn, Henriette Nørmølle; Hollegård, Mads.

    In: Frontiers in Psychiatry, Vol. 7, No. 35, 2016.

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

  45. 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

  46. Published

    Detecting significant genotype–phenotype association rules in bipolar disorder : market research meets complex genetics. / Breuer, René; Mattheisen, Manuel; Frank, Josef; Krumm, Bertram; Treutlein, Jens; Kassem, Layla; Strohmaier, Jana; Herms, Stefan; Mühleisen, Thomas W.; Degenhardt, Franziska; Cichon, Sven; Nöthen, Markus M.; Karypis, George; Kelsoe, John; Greenwood, Tiffany; Nievergelt, Caroline; Shilling, Paul; Shekhtman, Tatyana; Edenberg, Howard; Craig, David; Szelinger, Szabolcs; Nurnberger, John; Gershon, Elliot; Alliey-Rodriguez, Ney; Zandi, Peter; Goes, Fernando; Schork, Nicholas; Smith, Erin; Koller, Daniel; Zhang, Peng; Badner, Judith; Berrettini, Wade; Bloss, Cinnamon; Byerley, William; Coryell, William; Foroud, Tatiana; Guo, Yirin; Hipolito, Maria; Keating, Brendan; Lawson, William; Liu, Chunyu; Mahon, Pamela; McInnis, Melvin; Murray, Sarah; Nwulia, Evaristus; Potash, James; Rice, John; Scheftner, William; Zöllner, Sebastian; McMahon, Francis J.; Rietschel, Marcella; Schulze, Thomas G.

    In: International Journal of Bipolar Disorders, Vol. 6, No. 1, 24, 01.12.2018.

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

  47. Published

    Diagnosed Anxiety Disorders and the Risk of Subsequent Anorexia Nervosa : A Danish Population Register Study. / Meier, Sandra M; Bulik, Cynthia M; Thornton, Laura M; Mattheisen, Manuel; Mortensen, Preben B; Petersen, Liselotte.

    In: European Eating Disorders Review, Vol. 23, No. 6, 08.09.2015, p. 524-530.

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

  48. Published

    Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. / Hauberg, Mads E.; Fullard, John F.; Zhu, Lingxue; Cohain, Ariella T.; Giambartolomei, Claudia; Misir, Ruth; Reach, Sarah; Johnson, Jessica S.; Wang, Minghui; Mattheisen, Manuel; Børglum, Anders Dupont; Zhang, Bin; Sieberts, Solveig K.; Peters, Mette A.; Domenici, Enrico; Schadt, Eric E.; Devlin, Bernie; Sklar, Pamela; Roeder, Kathryn; Roussos, Panos; the CommonMind Consortium.

    In: Molecular Psychiatry, Vol. 24, No. 11, 11.2019, p. 1685-1695.

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

  49. Published

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. / Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gísli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Olafur O.; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads V.; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian B.; Martin, Alicia R.; Martin, Nicholas G.; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team ; Dalsgaard, Søren; Mors, Ole; Mortensen, Preben Bo; Børglum, Anders D.

    In: Nature Genetics, Vol. 51, 2019, p. 63–75.

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

  50. 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

  51. Published

    Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells. / Topol, Aaron; Zhu, Shijia; Hartley, Brigham J; English, Jane; Hauberg, Mads E; Tran, Ngoc; Rittenhouse, Chelsea Ann; Simone, Anthony; Ruderfer, Douglas M; Johnson, Jessica; Readhead, Ben; Hadas, Yoav; Gochman, Peter A; Wang, Ying-Chih; Shah, Hardik; Cagney, Gerard; Rapoport, Judith; Gage, Fred H; Dudley, Joel T; Sklar, Pamela; Mattheisen, Manuel; Cotter, David; Fang, Gang; Brennand, Kristen J.

    In: Cell Reports, Vol. 15, No. 5, 03.05.2016, p. 1024-36.

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

  52. Published

    Effects of BDNF Val 66 Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans. / Schweiger, J. I.; Bilek, E.; Schäfer, A.; Braun, U.; Moessnang, C.; Harneit, A.; Post, P.; Otto, K.; Romanczuk-Seiferth, N.; Erk, S.; Wackerhagen, C.; Mattheisen, M.; Mühleisen, T. W.; Cichon, S.; Nöthen, M. M.; Frank, J.; Witt, S. H.; Rietschel, M.; Heinz, A.; Walter, H.; Meyer-Lindenberg, A.; Tost, H.

    In: Neuropsychopharmacology, Vol. 44, No. 3, 02.2019, p. 590-597.

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

  53. 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

  54. 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

  55. 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

  56. Published

    Erratum : Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci (Human Molecular Genetics (2017) 26:10 (1942-1951) DOI: 10.1093/hmg/ddx103). / Fullard, John F.; Giambartolomei, Claudia; Hauberg, Mads E.; Xu, Ke; Voloudakis, Georgios; Shao, Zhiping; Bare, Christopher; Dudley, Joel T.; Mattheisen, Manuel; Robakis, Nikolaos K.; Haroutunian, Vahram; Roussos, Panos.

    In: Human Molecular Genetics, Vol. 29, No. 16, 08.2020, p. 2812.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperComment/debateResearchpeer-review

  57. Published

    Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. / Foo, Jerome C.; Streit, Fabian; Frank, Josef; Treutlein, Jens; Baune, Bernhard T.; Moebus, Susanne; Joeckel, Karl-Heinz; Forstner, Andreas J.; Noethen, Markus M.; Rietschel, Marcella; Sartorius, Alexander; Kranaster, Laura; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (Jakob Grove, member of -).

    In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 180, No. 1, 01.2019, p. 35-45.

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

  58. 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

  59. Published

    Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder. / Yilmaz, Zeynep; Halvorsen, Matthew; Bryois, Julien; Yu, Dongmei; Thornton, Laura M.; Zerwas, Stephanie; Micali, Nadia; Moessner, Rainald; Burton, Christie L.; Zai, Gwyneth; Erdman, Lauren; Kas, Martien J.; Arnold, Paul D.; Davis, Lea K.; Knowles, James A.; Breen, Gerome; Scharf, Jeremiah M.; Nestadt, Gerald; Mathews, Carol A.; Bulik, Cynthia M.; Mattheisen, Manuel; Crowley, James J.; Eating Disorders Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive–Compulsive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Molecular Psychiatry, Vol. 25, No. 9, 09.2020, p. 2036-2046.

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

  60. Published

    Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci. / Pinto, Dalila; Kasteleijn-Nolst Trenité, Dorothée G A; Cordell, Heather J; Mattheisen, Manuel; Strauch, Konstantin; Lindhout, Dick; Koeleman, Bobby P C.

    In: Genetic Epidemiology, Vol. 31, No. 1, 01.2007, p. 42-50.

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

  61. 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

  62. Published

    Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. / Herold, C; Hooli, B V; Mullin, K; Liu, T; Roehr, J T; Mattheisen, M; Parrado, A R; Bertram, L; Lange, C; Tanzi, R E.

    In: Molecular Psychiatry, 02.02.2016.

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

  63. 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

  64. 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

  65. Published

    Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains. / Erk, S.; Mohnke, S.; Ripke, S.; Lett, T. A.; Veer, I. M.; Wackerhagen, C.; Grimm, O.; Romanczuk-Seiferth, N.; Degenhardt, F.; Tost, H.; Mattheisen, M.; Muehleisen, T. W.; Charlet, K.; Skarabis, N.; Kiefer, F.; Cichon, S.; Witt, S. H.; Noethen, M. M.; Rietschel, M.; Heinz, A.; Meyer-Lindenberg, A.; Walter, H.

    In: Translational Psychiatry, Vol. 7, 997, 10.01.2017.

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

  66. 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

  67. 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

  68. 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

  69. Published

    Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. / Mühleisen, Thomas W.; Reinbold, Céline S.; Forstner, Andreas J.; Abramova, Lilia I.; Alda, Martin; Babadjanova, Gulja; Bauer, Michael; Brennan, Paul; Chuchalin, Alexander; Cruceanu, Cristiana; Czerski, Piotr M.; Degenhardt, Franziska; Fischer, Sascha B.; Fullerton, Janice M.; Gordon, Scott D.; Grigoroiu-Serbanescu, Maria; Grof, Paul; Hauser, Joanna; Hautzinger, Martin; Herms, Stefan; Hoffmann, Per; Kammerer-Ciernioch, Jutta; Khusnutdinova, Elza; Kogevinas, Manolis; Krasnov, Valery; Lacour, André; Laprise, Catherine; Leber, Markus; Lissowska, Jolanta; Lucae, Susanne; Maaser, Anna; Maier, Wolfgang; Martin, Nicholas G.; Mattheisen, Manuel; Mayoral, Fermin; McKay, James D.; Medland, Sarah E.; Mitchell, Philip B.; Moebus, Susanne; Montgomery, Grant W.; Müller-Myhsok, Bertram; Oruc, Lilijana; Pantelejeva, Galina; Pfennig, Andrea; Pojskic, Lejla; Polonikov, Alexey; Reif, Andreas; Rivas, Fabio; Rouleau, Guy A.; Schenk, Lorena M.; Schofield, Peter R.; Schwarz, Markus; Streit, Fabian; Strohmaier, Jana; Szeszenia-Dabrowska, Neonila; Tiganov, Alexander S.; Treutlein, Jens; Turecki, Gustavo; Vedder, Helmut; Witt, Stephanie H.; Schulze, Thomas G.; Rietschel, Marcella; Nöthen, Markus M.; Cichon, Sven.

    In: Journal of Affective Disorders, Vol. 228, 01.03.2018, p. 20-25.

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

  70. 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

  71. Published

    Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42 998 Individuals : A Meta-analysis. / Akingbuwa, Wonuola A; Hammerschlag, Anke R; Jami, Eshim S; Allegrini, Andrea G; Karhunen, Ville; Sallis, Hannah; Ask, Helga; Askeland, Ragna B; Baselmans, Bart; Diemer, Elizabeth; Hagenbeek, Fiona A; Havdahl, Alexandra; Hottenga, Jouke-Jan; Mbarek, Hamdi; Rivadeneira, Fernando; Tesli, Martin; van Beijsterveldt, Catharina; Breen, Gerome; Lewis, Cathryn M; Thapar, Anita; Boomsma, Dorret I; Kuja-Halkola, Ralf; Reichborn-Kjennerud, Ted; Magnus, Per; Rimfeld, Kaili; Ystrom, Eivind; Jarvelin, Marjo-Riitta; Lichtenstein, Paul; Lundstrom, Sebastian; Munafò, Marcus R; Plomin, Robert; Tiemeier, Henning; Nivard, Michel G; Bartels, Meike; Middeldorp, Christel M; and the Bipolar Disorder and Major Depressive Disorder Working Groups of the Psychiatric Genomics Consortium.

    In: JAMA Psychiatry, Vol. 77, No. 7, 07.2020, p. 715-728.

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

  72. Published

    Genetic Variants Associated With Anxiety and Stress-Related Disorders : A Genome-Wide Association Study and Mouse-Model Study. / Meier, Sandra M; Trontti, Kalevi; Purves, Kirstin L; Als, Thomas Damm; Grove, Jakob; Laine, Mikaela; Pedersen, Marianne Giørtz; Bybjerg-Grauholm, Jonas; Bækved-Hansen, Marie; Sokolowska, Ewa; Mortensen, Preben B; Hougaard, David M; Werge, Thomas; Nordentoft, Merete; Breen, Gerome; Børglum, Anders D; Eley, Thalia C; Hovatta, Iiris; Mattheisen, Manuel; Mors, Ole.

    In: J A M A Psychiatry, Vol. 76, No. 9, 09.2019, p. 924-932.

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

  73. Published

    Genetic architecture of subcortical brain structures in 38,851 individuals. / Satizabal, Claudia L.; Adams, Hieab H.H.; Hibar, Derrek P.; White, Charles C.; Knol, Maria J.; Stein, Jason L.; Scholz, Markus; Sargurupremraj, Muralidharan; Jahanshad, Neda; Roshchupkin, Gennady V.; Smith, Albert V.; Bis, Joshua C.; Jian, Xueqiu; Luciano, Michelle; Hofer, Edith; Teumer, Alexander; van der Lee, Sven J.; Yang, Jingyun; Yanek, Lisa R.; Lee, Tom V.; Li, Shuo; Hu, Yanhui; Koh, Jia Yu; Eicher, John D.; Desrivières, Sylvane; Arias-Vasquez, Alejandro; Chauhan, Ganesh; Athanasiu, Lavinia; Rentería, Miguel E.; Kim, Sungeun; Hoehn, David; Armstrong, Nicola J.; Chen, Qiang; Holmes, Avram J.; den Braber, Anouk; Kloszewska, Iwona; Andersson, Micael; Espeseth, Thomas; Grimm, Oliver; Abramovic, Lucija; Alhusaini, Saud; Milaneschi, Yuri; Papmeyer, Martina; Axelsson, Tomas; Ehrlich, Stefan; Roiz-Santiañez, Roberto; Kraemer, Bernd; Håberg, Asta K.; Jones, Hannah J.; Pike, G. Bruce; Stein, Dan J.; Stevens, Allison; Bralten, Janita; Vernooij, Meike W.; Harris, Tamara B.; Filippi, Irina; Witte, A. Veronica; Guadalupe, Tulio; Wittfeld, Katharina; Mosley, Thomas H.; Becker, James T.; Doan, Nhat Trung; Hagenaars, Saskia P.; Saba, Yasaman; Cuellar-Partida, Gabriel; Amin, Najaf; Hilal, Saima; Nho, Kwangsik; Mirza-Schreiber, Nazanin; Arfanakis, Konstantinos; Becker, Diane M.; Ames, David; Goldman, Aaron L.; Lee, Phil H.; Boomsma, Dorret I.; Lovestone, Simon; Giddaluru, Sudheer; Le Hellard, Stephanie; Mattheisen, Manuel; Bohlken, Marc M.; Kasperaviciute, Dalia; Schmaal, Lianne; Lawrie, Stephen M.; Agartz, Ingrid; Walton, Esther; Tordesillas-Gutierrez, Diana; Davies, Gareth E.; Shin, Jean; Ipser, Jonathan C.; Vinke, Louis N.; Hoogman, Martine; Jia, Tianye; Burkhardt, Ralph; Klein, Marieke; Crivello, Fabrice; Janowitz, Deborah; Carmichael, Owen; Haukvik, Unn K.; Aribisala, Benjamin S.; Schmidt, Helena; Strike, Lachlan T.; Cheng, Ching Yu; Risacher, Shannon L.; Pütz, Benno; Fleischman, Debra A.; Assareh, Amelia A.; Mattay, Venkata S.; Buckner, Randy L.; Mecocci, Patrizia; Dale, Anders M.; Cichon, Sven; Boks, Marco P.; Matarin, Mar; Penninx, Brenda W.J.H.; Calhoun, Vince D.; Chakravarty, M. Mallar; Marquand, Andre F.; Macare, Christine; Kharabian Masouleh, Shahrzad; Oosterlaan, Jaap; Amouyel, Philippe; Hegenscheid, Katrin; Rotter, Jerome I.; Schork, Andrew J.; Liewald, David C.M.; de Zubicaray, Greig I.; Wong, Tien Yin; Shen, Li; Sämann, Philipp G.; Brodaty, Henry; Roffman, Joshua L.; de Geus, Eco J.C.; Tsolaki, Magda; Erk, Susanne; van Eijk, Kristel R.; Cavalleri, Gianpiero L.; van der Wee, Nic J.A.; McIntosh, Andrew M.; Gollub, Randy L.; Bulayeva, Kazima B.; Bernard, Manon; Richards, Jennifer S.; Himali, Jayandra J.; Loeffler, Markus; Rommelse, Nanda; Hoffmann, Wolfgang; Westlye, Lars T.; Valdés Hernández, Maria C.; Hansell, Narelle K.; van Erp, Theo G.M.; Wolf, Christiane; Kwok, John B.J.; Vellas, Bruno; Heinz, Andreas; Olde Loohuis, Loes M.; Delanty, Norman; Ho, Beng Choon; Ching, Christopher R.K.; Shumskaya, Elena; Singh, Baljeet; Hofman, Albert; van der Meer, Dennis; Homuth, Georg; Psaty, Bruce M.; Bastin, Mark E.; Montgomery, Grant W.; Foroud, Tatiana M.; Reppermund, Simone; Hottenga, Jouke Jan; Simmons, Andrew; Meyer-Lindenberg, Andreas; Cahn, Wiepke; Whelan, Christopher D.; van Donkelaar, Marjolein M.J.; Yang, Qiong; Hosten, Norbert; Green, Robert C.; Thalamuthu, Anbupalam; Mohnke, Sebastian; Hulshoff Pol, Hilleke E.; Lin, Honghuang; Jack, Clifford R.; Schofield, Peter R.; Mühleisen, Thomas W.; Maillard, Pauline; Potkin, Steven G.; Wen, Wei; Fletcher, Evan; Toga, Arthur W.; Gruber, Oliver; Huentelman, Matthew; Davey Smith, George; Launer, Lenore J.; Nyberg, Lars; Jönsson, Erik G.; Crespo-Facorro, Benedicto; Koen, Nastassja; Greve, Douglas N.; Uitterlinden, André G.; Weinberger, Daniel R.; Steen, Vidar M.; Fedko, Iryna O.; Groenewold, Nynke A.; Niessen, Wiro J.; Toro, Roberto; Tzourio, Christophe; Longstreth, William T.; Ikram, M. Kamran; Smoller, Jordan W.; van Tol, Marie Jose; Sussmann, Jessika E.; Paus, Tomas; Lemaître, Hervé; Schroeter, Matthias L.; Mazoyer, Bernard; Andreassen, Ole A.; Holsboer, Florian; Depondt, Chantal; Veltman, Dick J.; Turner, Jessica A.; Pausova, Zdenka; Schumann, Gunter; van Rooij, Daan; Djurovic, Srdjan; Deary, Ian J.; McMahon, Katie L.; Müller-Myhsok, Bertram; Brouwer, Rachel M.; Soininen, Hilkka; Pandolfo, Massimo; Wassink, Thomas H.; Cheung, Joshua W.; Wolfers, Thomas; Martinot, Jean Luc; Zwiers, Marcel P.; Nauck, Matthias; Melle, Ingrid; Martin, Nicholas G.; Kanai, Ryota; Westman, Eric; Kahn, René S.; Sisodiya, Sanjay M.; White, Tonya; Saremi, Arvin; van Bokhoven, Hans; Brunner, Han G.; Völzke, Henry; Wright, Margaret J.; van ‘t Ent, Dennis; Nöthen, Markus M.; Ophoff, Roel A.; Buitelaar, Jan K.; Fernández, Guillén; Sachdev, Perminder S.; Rietschel, Marcella; van Haren, Neeltje E.M.; Fisher, Simon E.; Beiser, Alexa S.; Francks, Clyde; Saykin, Andrew J.; Mather, Karen A.; Romanczuk-Seiferth, Nina; Hartman, Catharina A.; DeStefano, Anita L.; Heslenfeld, Dirk J.; Weiner, Michael W.; Walter, Henrik; Hoekstra, Pieter J.; Nyquist, Paul A.; Franke, Barbara; Bennett, David A.; Grabe, Hans J.; Johnson, Andrew D.; Chen, Christopher; van Duijn, Cornelia M.; Lopez, Oscar L.; Fornage, Myriam; Wardlaw, Joanna M.; Schmidt, Reinhold; DeCarli, Charles; De Jager, Philip L.; Villringer, Arno; Debette, Stéphanie; Gudnason, Vilmundur; Medland, Sarah E.; Shulman, Joshua M.; Thompson, Paul M.; Seshadri, Sudha; Ikram, M. Arfan.

    In: Nature Genetics, Vol. 51, No. 11, 2019, p. 1624-1636.

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

  74. Published

    Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. / Project MinE GWAS Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: Nature Communications, Vol. 8, 21.03.2017, p. 14774.

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

  75. Published

    Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. / Tauer, Ulrike; Lorenz, Susanne; Lenzen, Kirsten P; Heils, Armin; Muhle, Hiltrud; Gresch, Meike; Neubauer, Bernd A; Waltz, Stephan; Rudolf, Gabrielle; Mattheisen, Manuel; Strauch, Konstantin; Nürnberg, Peter; Schmitz, Bettina; Stephani, Ulrich; Sander, Thomas.

    In: Annals of Neurology, Vol. 57, No. 6, 06.2005, p. 866-73.

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

  76. Published

    Genetic influences on schizophrenia and subcortical brain volumes : large-scale proof of concept. / Franke, Barbara; Stein, Jason L; Ripke, Stephan; Anttila, Verneri; Hibar, Derrek P; van Hulzen, Kimm J E; Arias-Vasquez, Alejandro; Smoller, Jordan W; Nichols, Thomas E; Neale, Michael C; McIntosh, Andrew M; Lee, Phil; McMahon, Francis J; Meyer-Lindenberg, Andreas; Mattheisen, Manuel; Andreassen, Ole A; Gruber, Oliver; Sachdev, Perminder S; Roiz-Santiañez, Roberto; Saykin, Andrew J; Ehrlich, Stefan; Mather, Karen A; Turner, Jessica A; Schwarz, Emanuel; Thalamuthu, Anbupalam; Yao, Yin; Ho, Yvonne Y W; Martin, Nicholas G; Wright, Margaret J; O'Donovan, Michael C; Thompson, Paul M; Neale, Benjamin M; Medland, Sarah E; Sullivan, Patrick F; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: Nature Neuroscience, Vol. 19, No. 3, 03.2016, p. 420-31.

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

  77. Published

    Genetic markers of ADHD-related variations in intracranial volume. / Klein, Marieke; Walters, Raymond K.; Demontis, Ditte; Stein, Jason L.; Hibar, Derrek P.; Adams, Hieab H.; Bralten, Janita; Mota, Nina Roth; Schachar, Russell; Sonuga-Barke, Edmund; Mattheisen, Manuel; Neale, Benjamin M.; Thompson, Paul M.; Medland, Sarah E.; Børglum, Anders D.; Faraone, Stephen V.; Arias-Vasquez, Alejandro; Franke, Barbara.

    In: American Journal of Psychiatry, Vol. 176, No. 3, 2019, p. 228-238.

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

  78. 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

  79. 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

  80. 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

  81. Published

    Genetic variants associated with response to lithium treatment in bipolar disorder : a genome-wide association study. / Hou, Liping; Heilbronner, Urs; Degenhardt, Franziska; Adli, Mazda; Akiyama, Kazufumi; Akula, Nirmala; Ardau, Raffaella; Arias, Bárbara; Backlund, Lena; Banzato, Claudio E M; Benabarre, Antoni; Bengesser, Susanne; Bhattacharjee, Abesh Kumar; Biernacka, Joanna M; Birner, Armin; Brichant-Petitjean, Clara; Bui, Elise T; Cervantes, Pablo; Chen, Guo-Bo; Chen, Hsi-Chung; Chillotti, Caterina; Cichon, Sven; Clark, Scott R; Colom, Francesc; Cousins, David A; Cruceanu, Cristiana; Czerski, Piotr M; Dantas, Clarissa R; Dayer, Alexandre; Étain, Bruno; Falkai, Peter; Forstner, Andreas J; Frisén, Louise; Fullerton, Janice M; Gard, Sébastien; Garnham, Julie S; Goes, Fernando S; Grof, Paul; Gruber, Oliver; Hashimoto, Ryota; Hauser, Joanna; Herms, Stefan; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jiménez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kittel-Schneider, Sarah; Kliwicki, Sebastian; König, Barbara; Kusumi, Ichiro; Lackner, Nina; Laje, Gonzalo; Landén, Mikael; Lavebratt, Catharina; Leboyer, Marion; Leckband, Susan G; Jaramillo, Carlos A López; MacQueen, Glenda; Manchia, Mirko; Martinsson, Lina; Mattheisen, Manuel; McCarthy, Michael J; McElroy, Susan L; Mitjans, Marina; Mondimore, Francis M; Monteleone, Palmiero; Nievergelt, Caroline M; Nöthen, Markus M; Ösby, Urban; Ozaki, Norio; Perlis, Roy H; Pfennig, Andrea; Reich-Erkelenz, Daniela; Rouleau, Guy A; Schofield, Peter R; Schubert, K Oliver; Schweizer, Barbara W; Seemüller, Florian; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D; Shimoda, Kazutaka; Simhandl, Christian; Slaney, Claire M; Smoller, Jordan W; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Tighe, Sarah K; Tortorella, Alfonso; Turecki, Gustavo; Volkert, Julia; Witt, Stephanie; Wright, Adam; Young, L Trevor; Zandi, Peter P; Potash, James B; DePaulo, J Raymond; Bauer, Michael; Reininghaus, Eva Z; Novák, Tomas; Aubry, Jean-Michel; Maj, Mario; Baune, Bernhard T; Mitchell, Philip B; Vieta, Eduard; Frye, Mark A; Rybakowski, Janusz K; Kuo, Po-Hsiu; Kato, Tadafumi; Grigoroiu-Serbanescu, Maria; Reif, Andreas; Del Zompo, Maria; Bellivier, Frank; Schalling, Martin; Wray, Naomi R; Kelsoe, John R; Alda, Martin; Rietschel, Marcella; McMahon, Francis J; Schulze, Thomas G.

    In: The Lancet, Vol. 387, No. 10023, 22.01.2016, p. 1085-93.

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

  82. 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

  83. 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

  84. Published

    Genetics of response to cognitive behavior therapy in adults with major depression : a preliminary report. / Andersson, Evelyn; Crowley, James J.; Lindefors, Nils; Ljótsson, Brjánn; Hedman-Lagerlöf, Erik; Boberg, Julia; El Alaoui, Samir; Karlsson, Robert; Lu, Yi; Mattheisen, Manuel; Kähler, Anna K.; Svanborg, Cecilia; Mataix-Cols, David; Mattsson, Simon; Forsell, Erik; Kaldo, Viktor; Schalling, Martin; Lavebratt, Catharina; Sullivan, Patrick F.; Rück, Christian.

    In: Molecular Psychiatry, Vol. 24, No. 4, 2019, p. 484-490.

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

  85. Published

    Genome-Wide Landscape of Genetic Variation with a Functional Impact on Predicted Binding Activity of Transcription Factor Binding Sites. / Eickhardt, Esben Ahlburg; Als, Thomas Damm; Mattheisen, Manuel; Hauberg, Mads Engel; Grove, Jakob; Børglum, Anders; Lescai, Francesco.

    2015. Poster session presented at ESHG 2015, Glasgow, United Kingdom.

    Research output: Contribution to conferencePosterResearchpeer-review

  86. Published

    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy. / Draaken, Markus; Knapp, Michael; Pennimpede, Tracie; Schmidt, Johanna M; Ebert, Anne-Karolin; Rösch, Wolfgang; Stein, Raimund; Utsch, Boris; Hirsch, Karin; Boemers, Thomas M; Mangold, Elisabeth; Heilmann, Stefanie; Ludwig, Kerstin U; Jenetzky, Ekkehart; Zwink, Nadine; Moebus, Susanne; Herrmann, Bernhard G; Mattheisen, Manuel; Nöthen, Markus M; Ludwig, Michael; Reutter, Heiko.

    In: P L o S Genetics, Vol. 11, No. 3, 03.2015, p. e1005024.

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

  87. Published

    Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. / Forstner, A J; Hofmann, A; Maaser, A; Sumer, S; Khudayberdiev, S; Mühleisen, T W; Leber, M; Schulze, T G; Strohmaier, J; Degenhardt, F; Treutlein, J; Mattheisen, M; Schumacher, J; Breuer, R; Meier, S; Herms, S; Hoffmann, P; Lacour, A; Witt, S H; Reif, A; Müller-Myhsok, B; Lucae, S; Maier, W; Schwarz, M; Vedder, H; Kammerer-Ciernioch, J; Pfennig, A; Bauer, M; Hautzinger, M; Moebus, S; Priebe, L; Sivalingam, S; Verhaert, A; Schulz, H; Czerski, P M; Hauser, J; Lissowska, J; Szeszenia-Dabrowska, N; Brennan, P; McKay, J D; Wright, A; Mitchell, P B; Fullerton, J M; Schofield, P R; Montgomery, G W; Medland, S E; Gordon, S D; Martin, N G; Krasnov, V; Chuchalin, A; Babadjanova, G; Pantelejeva, G; Abramova, L I; Tiganov, A S; Polonikov, A; Khusnutdinova, E; Alda, M; Cruceanu, C; Rouleau, G A; Turecki, G; Laprise, C; Rivas, F; Mayoral, F; Kogevinas, M; Grigoroiu-Serbanescu, M; Propping, P; Becker, T; Rietschel, M; Cichon, S; Schratt, G; Nöthen, M M.

    In: Translational Psychiatry, Vol. 5, 2015, p. e678.

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

  88. Published

    Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. / Wray, Naomi R; Ripke, Stephan; Mattheisen, Manuel; Trzaskowski, Maciej; Byrne, Enda M; Abdellaoui, Abdel; Adams, Mark J; Agerbo, Esben; Air, Tracy M; Andlauer, Till M F; Bacanu, Silviu-Alin; Bækvad-Hansen, Marie; Beekman, Aartjan F T; Bigdeli, Tim B; Binder, Elisabeth B; Blackwood, Douglas R H; Bryois, Julien; Buttenschøn, Henriette N; Bybjerg-Grauholm, Jonas; Cai, Na; Castelao, Enrique; Christensen, Jane Hvarregaard; Clarke, Toni-Kim; Coleman, Jonathan I R; Colodro-Conde, Lucía; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E; Crowley, Cheynna A; Dashti, Hassan S; Davies, Gail; Deary, Ian J; Degenhardt, Franziska; Derks, Eske M; Direk, Nese; Dolan, Conor V; Dunn, Erin C; Eley, Thalia C; Eriksson, Nicholas; Escott-Price, Valentina; Grove, Jakob; Hansen, Christine Søholm; Hansen, Thomas F; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Qvist, Per; Yang, Jian; Mors, Ole; Mortensen, Preben Bo; Nordentoft, Merete; Werge, Thomas; Børglum, Anders D; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Nature Genetics, Vol. 50, No. 5, 2018, p. 668-681.

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

  89. 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

  90. 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

  91. Published

    Genome-wide association study identifies 30 loci associated with bipolar disorder. / Stahl, Eli A; Breen, Gerome; Forstner, Andreas J; McQuillin, Andrew; Ripke, Stephan; Trubetskoy, Vassily; Mattheisen, Manuel; Wang, Yunpeng; Coleman, Jonathan R I; Gaspar, Héléna A; de Leeuw, Christiaan A; Steinberg, Stacy; Pavlides, Jennifer M Whitehead; Trzaskowski, Maciej; Byrne, Enda M; Pers, Tune H; Holmans, Peter A; Richards, Alexander L; Abbott, Liam; Agerbo, Esben; Akil, Huda; Albani, Diego; Alliey-Rodriguez, Ney; Als, Thomas D; Anjorin, Adebayo; Antilla, Verneri; Awasthi, Swapnil; Badner, Judith A; Bækvad-Hansen, Marie; Barchas, Jack D; Bass, Nicholas; Bauer, Michael; Belliveau, Richard; Bergen, Sarah E; Pedersen, Carsten Bøcker; Bøen, Erlend; Boks, Marco P; Boocock, James; Budde, Monika; Bunney, William; Burmeister, Margit; Bybjerg-Grauholm, Jonas; Byerley, William; Pedersen, Marianne Giørtz; Grove, Jakob; Xu, Wei; Zhang, Peng; Børglum, Anders D; Mors, Ole; Mortensen, Preben Bo; eQTLGen Consortium.

    In: Nature Genetics, Vol. 51, No. 5, 05.2019, p. 793-803.

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

  92. Published

    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. / Anorexia Nervosa Genetics Initiative.

    In: Nature Genetics, Vol. 51, No. 8, 08.2019, p. 1207-1214.

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

  93. 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

  94. 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

  95. 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

  96. Published

    Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP. / Wigmore, Eleanor M; Hafferty, Jonathan D; Hall, Lynsey S; Howard, David M; Clarke, Toni-Kim; Fabbri, Chiara; Lewis, Cathryn M; Uher, Rudolf; Navrady, Lauren B; Adams, Mark J; Zeng, Yanni; Campbell, Archie; Gibson, Jude; Thomson, Pippa A; Hayward, Caroline; Smith, Blair H; Hocking, Lynne J; Padmanabhan, Sandosh; Deary, Ian J; Porteous, David J; Mors, Ole; Mattheisen, Manuel; Nicodemus, Kristin K; McIntosh, Andrew M.

    In: The Pharmacogenomics Journal, Vol. 20, No. 2, 04.2020, p. 329-341.

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

  97. E-pub ahead of print

    Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. / HUNT All-In Psychiatry.

    In: Nature Genetics, 17.05.2021.

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

  98. E-pub ahead of print

    Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. / Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC).

    In: Molecular Psychiatry, 11.11.2019.

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

  99. 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

  100. 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

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