Manuel Mattheisen

  1. 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

  2. Published

    XRCC5 as a Risk Gene for Alcohol Dependence : Evidence from a Genome-Wide Gene-Set Based Analysis and Follow-up Studies in Drosophila and Humans. / Juraeva, Dilafruz; Treutlein, Jens; Scholz, Henrike; Frank, Josef; Degenhardt, Franziska; Cichon, Sven; Ridinger, Monika; Mattheisen, Manuel; Witt, Stephanie H; Lang, Maren; Sommer, Wolfgang H; Hoffmann, Per; Herms, Stefan; Wodarz, Norbert; Soyka, Michael; Zill, Peter; Maier, Wolfgang; Jünger, Elisabeth; Gaebel, Wolfgang; Dahmen, Norbert; Scherbaum, Norbert; Schmäl, Christine; Steffens, Michael; Lucae, Susanne; Ising, Marcus; Smolka, Michael N; Zimmermann, Ulrich S; Müller-Myhsok, Bertram; Nöthen, Markus M; Mann, Karl; Kiefer, Falk; Spanagel, Rainer; Brors, Benedikt; Rietschel, Marcella.

    In: Neuropsychopharmacology, Vol. 40, 2015, p. 361–371.

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

  3. Published

    Whole-genome association analysis of treatment response in obsessive-compulsive disorder. / Qin, H; Samuels, J F; Wang, Y; Zhu, Y; Grados, M A; Riddle, M A; Greenberg, B D; Knowles, J A; Fyer, A J; McCracken, J T; Murphy, D L; Rasmussen, S A; Cullen, B A; Piacentini, J; Geller, D; Stewart, S E; Pauls, D; Bienvenu, O J; Goes, F S; Maher, B; Pulver, A E; Valle, D; Mattheisen, M; McLaughlin, N C; Liang, K-Y; Nurmi, E L; Askland, K D; Nestadt, G; Shugart, Y Y.

    In: Molecular Psychiatry, 31.03.2015.

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

  4. Published

    Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. / Lescai, F; Als, T D; Li, Q; Nyegaard, M; Andorsdottir, Gudrid; Biskopstø, Marjun; Hedemand, A; Fiorentino, A; O'Brien, Niamh L; Jarram, Alex; Liang, T J; Grove, J; Pallesen, J; Eickhardt, E; Mattheisen, M; Bolund, L; Demontis, D; Wang, A G; McQuillin, A.; Mors, O; Wang, J; Børglum, A D.

    In: Translational Psychiatry, Vol. 7, No. 2, 14.02.2017, p. e1034.

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

  5. 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

  6. 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

  7. Published

    Using genetic drug-target networks to develop new drug hypotheses for major depressive disorder. / Gaspar, Héléna A; Gerring, Zachary; Hübel, Christopher; Middeldorp, Christel M; Derks, Eske M; Breen, Gerome; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Translational Psychiatry, Vol. 9, No. 1, 117, 2019.

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

  8. 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

  9. 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

  10. Published

    The association between neonatal vitamin D status and risk of schizophrenia. / Eyles, Darryl W.; Trzaskowski, Maciej; Vinkhuyzen, Anna A.E.; Mattheisen, Manuel; Meier, Sandra; Gooch, Helen; Anggono, Victor; Cui, Xiaoying; Tan, Men Chee; Burne, Thomas H.J.; Jang, Se Eun; Kvaskoff, David; Hougaard, David M.; Nørgaard-Pedersen, Bent; Cohen, Arieh; Agerbo, Esben; Pedersen, Carsten B.; Børglum, Anders D.; Mors, Ole; Sah, Pankaj; Wray, Naomi R.; Mortensen, Preben B.; McGrath, John J.

    In: Scientific Reports, Vol. 8, No. 1, 17692, 01.12.2018.

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

  11. Published

    The anorexia nervosa genetics initiative (ANGI) : Overview and methods. / Thornton, Laura M; Munn-Chernoff, Melissa A; Baker, Jessica H; Juréus, Anders; Parker, Richard; Henders, Anjali K; Larsen, Janne T; Petersen, Liselotte; Watson, Hunna J; Yilmaz, Zeynep; Kirk, Katherine M; Gordon, Scott; Leppä, Virpi M; Martin, Felicity C; Whiteman, David C; Olsen, Catherine M; Werge, Thomas M; Pedersen, Nancy L; Kaye, Walter; Bergen, Andrew W; Halmi, Katherine A; Strober, Michael; Kaplan, Allan S; Blake Woodside, D; Mitchell, James; Johnson, Craig L; Brandt, Harry; Crawford, Steven; John Horwood, L; Boden, Joseph M; Pearson, John F; Duncan, Laramie E; Grove, Jakob; Mattheisen, Manuel; Jordan, Jennifer; Kennedy, Martin A; Birgegård, Andreas; Lichtenstein, Paul; Norring, Claes; Wade, Tracey D; Montgomery, Grant W; Martin, Nicholas G; Landén, Mikael; Mortensen, Preben Bo; Sullivan, Patrick F; Bulik, Cynthia M.

    In: Contemporary Clinical Trials, Vol. 74, 2018, p. 61-69.

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

  12. 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

  13. 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

  14. 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

  15. Published

    The 5-HTTLPR polymorphism affects network-based functional connectivity in the visual-limbic system in healthy adults. / Cao, Hengyi; Harneit, Anais; Walter, Henrik; Erk, Susanne; Braun, Urs; Moessnang, Carolin; Geiger, Lena S.; Zang, Zhenxiang; Mohnke, Sebastian; Heinz, Andreas; Romanczuk-Seiferth, Nina; Mühleisen, Thomas; Mattheisen, Manuel; Witt, Stephanie H.; Cichon, Sven; Nöthen, Markus M.; Rietschel, Marcella; Meyer-Lindenberg, Andreas; Tost, Heike.

    In: Neuropsychopharmacology, Vol. 43, No. 2, 2018, p. 406-414.

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

  16. Published

    Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. / Johnson, Michael R; Behmoaras, Jacques; Bottolo, Leonardo; Krishnan, Michelle L; Pernhorst, Katharina; Santoscoy, Paola L Meza; Rossetti, Tiziana; Speed, Doug; Srivastava, Prashant K; Chadeau-Hyam, Marc; Hajji, Nabil; Dabrowska, Aleksandra; Rotival, Maxime; Razzaghi, Banafsheh; Kovac, Stjepana; Wanisch, Klaus; Grillo, Federico W; Slaviero, Anna; Langley, Sarah R; Shkura, Kirill; Roncon, Paolo; De, Tisham; Mattheisen, Manuel; Niehusmann, Pitt; O'Brien, Terence J; Petrovski, Slave; von Lehe, Marec; Hoffmann, Per; Eriksson, Johan; Coffey, Alison J; Cichon, Sven; Walker, Matthew; Simonato, Michele; Danis, Bénédicte; Mazzuferi, Manuela; Foerch, Patrik; Schoch, Susanne; De Paola, Vincenzo; Kaminski, Rafal M; Cunliffe, Vincent T; Becker, Albert J; Petretto, Enrico.

    In: Nature Communications, Vol. 6, 23.01.2015, p. 6031.

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

  17. Published

    Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function. / Luo, Xiong-Jian; Mattheisen, Manuel; Li, Ming; Huang, Liang; Rietschel, Marcella; Børglum, Anders D; Als, Thomas Damm; van den Oord, Edwin J; Aberg, Karolina A; Mors, Ole; Mortensen, Preben Bo; Luo, Zhenwu; Degenhardt, Franziska; Cichon, Sven; Schulze, Thomas G; Nöthen, Markus M; Su, Bing; Zhao, Zhongming; Gan, Lin; Yao, Yong-Gang; iPSYCH-GEMS SCZ working group (Jakob Grove, member).

    In: Schizophrenia Bulletin, 10.03.2015.

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

  18. 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

  19. 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

  20. 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

  21. Published

    Specific anxiety disorders and subsequent risk for bipolar disorder : a nationwide study. / Meier, Sandra M; Uher, Rudolf; Mors, Ole; Dalsgaard, Søren; Munk-Olsen, Trine; Laursen, Thomas M; Mattheisen, Manuel; Nordentoft, Merete; Mortensen, Preben B; Pavlova, Barbara.

    In: World Psychiatry, Vol. 15, No. 2, 06.2016, p. 187-188.

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

  22. 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

  23. Published

    Shared genetic risk between eating disorder- and substance-use-related phenotypes : Evidence from genome-wide association studies. / Munn-Chernoff, Melissa A.; Johnson, Emma C.; Chou, Yi Ling; Coleman, Jonathan R.I.; Thornton, Laura M.; Walters, Raymond K.; Yilmaz, Zeynep; Baker, Jessica H.; Hübel, Christopher; Gordon, Scott; Medland, Sarah E.; Watson, Hunna J.; Gaspar, Héléna A.; Bryois, Julien; Hinney, Anke; Leppä, Virpi M.; Mattheisen, Manuel; Ripke, Stephan; Yao, Shuyang; Giusti-Rodríguez, Paola; Hanscombe, Ken B.; Adan, Roger A.H.; Alfredsson, Lars; Ando, Tetsuya; Andreassen, Ole A.; Berrettini, Wade H.; Boehm, Ilka; Boni, Claudette; Boraska Perica, Vesna; Buehren, Katharina; Burghardt, Roland; Cassina, Matteo; Cichon, Sven; Clementi, Maurizio; Cone, Roger D.; Courtet, Philippe; Crow, Scott; Crowley, James J.; Danner, Unna N.; Davis, Oliver S.P.; de Zwaan, Martina; Dedoussis, George; Degortes, Daniela; DeSocio, Janiece E.; Dick, Danielle M.; Dikeos, Dimitris; Dina, Christian; Dmitrzak-Weglarz, Monika; Docampo, Elisa; Duncan, Laramie E.; Egberts, Karin; Ehrlich, Stefan; Escaramís, Geòrgia; Esko, Tõnu; Estivill, Xavier; Farmer, Anne; Favaro, Angela; Fernández-Aranda, Fernando; Fichter, Manfred M.; Fischer, Krista; Föcker, Manuel; Foretova, Lenka; Forstner, Andreas J.; Forzan, Monica; Franklin, Christopher S.; Gallinger, Steven; Giegling, Ina; Giuranna, Johanna; Gonidakis, Fragiskos; Gorwood, Philip; Gratacos Mayora, Monica; Guillaume, Sébastien; Guo, Yiran; Hakonarson, Hakon; Hatzikotoulas, Konstantinos; Hauser, Joanna; Hebebrand, Johannes; Helder, Sietske G.; Herms, Stefan; Herpertz-Dahlmann, Beate; Herzog, Wolfgang; Huckins, Laura M.; Hudson, James I.; Imgart, Hartmut; Inoko, Hidetoshi; Janout, Vladimir; Jiménez-Murcia, Susana; Julià, Antonio; Kalsi, Gursharan; Kaminská, Deborah; Karhunen, Leila; Karwautz, Andreas; Kas, Martien J.H.; Kennedy, James L.; Keski-Rahkonen, Anna; Kiezebrink, Kirsty; Kim, Youl Ri; Klump, Kelly L.; Knudsen, Gun Peggy S.; La Via, Maria C.; Le Hellard, Stephanie; Levitan, Robert D.; Li, Dong; Lilenfeld, Lisa; Lin, Bochao Danae; Lissowska, Jolanta; Luykx, Jurjen; Magistretti, Pierre J.; Maj, Mario; Mannik, Katrin; Marsal, Sara; Marshall, Christian R.; Mattingsdal, Morten; McDevitt, Sara; McGuffin, Peter; Metspalu, Andres; Meulenbelt, Ingrid; Micali, Nadia; Mitchell, Karen; Monteleone, Alessio Maria; Monteleone, Palmiero; Nacmias, Benedetta; Navratilova, Marie; Ntalla, Ioanna; O'Toole, Julie K.; Ophoff, Roel A.; Padyukov, Leonid; Palotie, Aarno; Pantel, Jacques; Papezova, Hana; Pinto, Dalila; Rabionet, Raquel; Raevuori, Anu; Ramoz, Nicolas; Reichborn-Kjennerud, Ted; Ricca, Valdo; Ripatti, Samuli; Ritschel, Franziska; Roberts, Marion; Rotondo, Alessandro; Rujescu, Dan; Rybakowski, Filip; Santonastaso, Paolo; Scherag, André; Scherer, Stephen W.; Schmidt, Ulrike; Schork, Nicholas J.; Schosser, Alexandra; Seitz, Jochen; Slachtova, Lenka; Slagboom, P. Eline; Slof-Op't Landt, Margarita C.T.; Slopien, Agnieszka; Sorbi, Sandro; Świątkowska, Beata; Szatkiewicz, Jin P.; Tachmazidou, Ioanna; Tenconi, Elena; Tortorella, Alfonso; Tozzi, Federica; Treasure, Janet; Tsitsika, Artemis; Tyszkiewicz-Nwafor, Marta; Tziouvas, Konstantinos; van Elburg, Annemarie A.; van Furth, Eric F.; Wagner, Gudrun; Walton, Esther; Widen, Elisabeth; Zeggini, Eleftheria; Zerwas, Stephanie; Zipfel, Stephan; Bergen, Andrew W.; Boden, Joseph M.; Brandt, Harry; Crawford, Steven; Halmi, Katherine A.; Horwood, L. John; Johnson, Craig; Kaplan, Allan S.; Kaye, Walter H.; Mitchell, James; Olsen, Catherine M.; Pearson, John F.; Pedersen, Nancy L.; Strober, Michael; Werge, Thomas; Whiteman, David C.; Woodside, D. Blake; Grove, Jakob; Henders, Anjali K.; Larsen, Janne T.; Parker, Richard; Petersen, Liselotte V.; Jordan, Jennifer; Kennedy, Martin A.; Birgegård, Andreas; Lichtenstein, Paul; Norring, Claes; Landén, Mikael; Mortensen, Preben Bo; Polimanti, Renato; McClintick, Jeanette N.; Adkins, Amy E.; Aliev, Fazil; Bacanu, Silviu Alin; Batzler, Anthony; Bertelsen, Sarah; Biernacka, Joanna M.; Bigdeli, Tim B.; Chen, Li Shiun; Clarke, Toni Kim; Degenhardt, Franziska; Docherty, Anna R.; Edwards, Alexis C.; Foo, Jerome C.; Fox, Louis; Frank, Josef; Hack, Laura M.; Hartmann, Annette M.; Hartz, Sarah M.; Heilmann-Heimbach, Stefanie; Hodgkinson, Colin; Hoffmann, Per; Hottenga, Jouke Jan; Konte, Bettina; Lahti, Jari; Lahti-Pulkkinen, Marius; Lai, Dongbing; Ligthart, Lannie; Loukola, Anu; Maher, Brion S.; Mbarek, Hamdi; McIntosh, Andrew M.; McQueen, Matthew B.; Meyers, Jacquelyn L.; Milaneschi, Yuri; Palviainen, Teemu; Peterson, Roseann E.; Ryu, Euijung; Saccone, Nancy L.; Salvatore, Jessica E.; Sanchez-Roige, Sandra; Schwandt, Melanie; Sherva, Richard; Streit, Fabian; Strohmaier, Jana; Thomas, Nathaniel; Wang, Jen Chyong; Webb, Bradley T.; Wedow, Robbee; Wetherill, Leah; Wills, Amanda G.; Zhou, Hang; Boardman, Jason D.; Chen, Danfeng; Choi, Doo Sup; Copeland, William E.; Culverhouse, Robert C.; Dahmen, Norbert; Degenhardt, Louisa; Domingue, Benjamin W.; Frye, Mark A.; Gäbel, Wolfgang; Hayward, Caroline; Ising, Marcus; Keyes, Margaret; Kiefer, Falk; Koller, Gabriele; Kramer, John; Kuperman, Samuel; Lucae, Susanne; Lynskey, Michael T.; Maier, Wolfgang; Mann, Karl; Männistö, Satu; Müller-Myhsok, Bertram; Murray, Alison D.; Nurnberger, John I.; Preuss, Ulrich; Räikkönen, Katri; Reynolds, Maureen D.; Ridinger, Monika; Scherbaum, Norbert; Schuckit, Marc A.; Soyka, Michael; Treutlein, Jens; Witt, Stephanie H.; Wodarz, Norbert; Zill, Peter; Adkins, Daniel E.; Boomsma, Dorret I.; Bierut, Laura J.; Brown, Sandra A.; Bucholz, Kathleen K.; Costello, E. Jane; de Wit, Harriet; Diazgranados, Nancy; Eriksson, Johan G.; Farrer, Lindsay A.; Foroud, Tatiana M.; Gillespie, Nathan A.; Goate, Alison M.; Goldman, David; Grucza, Richard A.; Hancock, Dana B.; Harris, Kathleen Mullan; Hesselbrock, Victor; Hewitt, John K.; Hopfer, Christian J.; Iacono, William G.; Johnson, Eric O.; Karpyak, Victor M.; Kendler, Kenneth S.; Kranzler, Henry R.; Krauter, Kenneth; Lind, Penelope A.; McGue, Matt; MacKillop, James; Madden, Pamela A.F.; Maes, Hermine H.; Magnusson, Patrik K.E.; Nelson, Elliot C.; Nöthen, Markus M.; Palmer, Abraham A.; Penninx, Brenda W.J.H.; Porjesz, Bernice; Rice, John P.; Rietschel, Marcella; Riley, Brien P.; Rose, Richard J.; Shen, Pei Hong; Silberg, Judy; Stallings, Michael C.; Tarter, Ralph E.; Vanyukov, Michael M.; Vrieze, Scott; Wall, Tamara L.; Whitfield, John B.; Zhao, Hongyu; Neale, Benjamin M.; Wade, Tracey D.; Heath, Andrew C.; Montgomery, Grant W.; Martin, Nicholas G.; Sullivan, Patrick F.; Kaprio, Jaakko; Breen, Gerome; Gelernter, Joel; Edenberg, Howard J.; Bulik, Cynthia M.; Agrawal, Arpana.

    In: Addiction Biology, Vol. 26, No. 1, e12880, 01.2021.

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

  24. 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

  25. Published

    Secondary depression in severe anxiety disorders : a population-based cohort study in Denmark. / Meier, Sandra M; Petersen, Liselotte; Mattheisen, Manuel; Mors, Ole; Mortensen, Preben B; Laursen, Thomas M.

    In: The Lancet, Vol. 2, No. 6, 06.2015, p. 515-23.

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

  26. Published

    Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206. / Hauberg, Mads Engel; Holm-Nielsen, Marie Hebsgaard; Mattheisen, Manuel; Askou, Anne Louise; Grove, Jakob; Børglum, Anders Dupont; Corydon, Thomas Juhl.

    In: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, Vol. 26, No. 9, 09.2016, p. 1522-6.

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

  27. 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

  28. 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

  29. 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

  30. 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

  31. Published

    Retraction for Dixson et al., 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, Vol. 111, No. 37, 16.09.2014, p. 13582.

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

  32. 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

  33. 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

  34. 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

  35. 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

  36. 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

  37. Published

    RICOPILI : Rapid Imputation for COnsortias PIpeLIne. / Lam, Max; Awasthi, Swapnil; Watson, Hunna J.; Goldstein, Jackie; Panagiotaropoulou, Georgia; Trubetskoy, Vassily; Karlsson, Robert; Frei, Oleksander; Fan, Chun Chieh; De Witte, Ward; Mota, Nina R.; Mullins, Niamh; Brügger, Kim; Lee, S. Hong; Wray, Naomi R.; Skarabis, Nora; Huang, Hailiang; Neale, Benjamin; Daly, Mark J.; Mattheisen, Manuel; Walters, Raymond; Ripke, Stephan.

    In: Bioinformatics (Oxford, England), Vol. 36, No. 3, 2020, p. 930-933.

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

  38. 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

  39. Published

    Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder. / Trzaskowski, Maciej; Mehta, Divya; Peyrot, Wouter J.; Hawkes, David; Davies, Daniel; Howard, David M.; Kemper, Kathryn E.; Sidorenko, Julia; Maier, Robert; Ripke, Stephan; Mattheisen, Manuel; Baune, Bernhard T.; Grabe, Hans J.; Heath, Andrew C.; Jones, Lisa; Jones, Ian; Madden, Pamela A. F.; McIntosh, Andrew M.; Breen, Gerome; Lewis, Cathryn M.; Borglum, Anders D.; Sullivan, Patrick F.; Martin, Nicholas G.; Kendler, Kenneth S.; Levinson, Douglas F.; Wray, Naomi R.; Major Depress Disorder Working G.

    In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 180, No. 6, 09.2019, p. 439-447.

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

  40. Published

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

    In: Nature Genetics, Vol. 51, No. 7, 07.2019, p. 1193-1193.

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

  41. Published

    Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. / O'Dushlaine, Colm; Rossin, Lizzy; Lee, Phil H.; Duncan, Laramie; Parikshak, Neelroop N.; Newhouse, Stephen; Ripke, Stephan; Neale, Benjamin M.; Purcell, Shaun M.; Posthuma, Danielle; Nurnberger, John I.; Lee, S. Hong; Faraone, Stephen V.; 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; Bayes, Monica; Bellivier, Frank; Bergen, Sarah E.; Berrettini, Wade; Betancur, Catalina; Bettecken, Thomas; Biederman, Joseph; Binder, Elisabeth B.; Black, Donald W.; Mattheisen, Manuel; Meier, Sandra; IIBDGC; Network & Pathway Anal Subgrp Psyc.

    In: Nature Neuroscience, Vol. 18, No. 2, 02.2015, p. 199-209.

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

  42. 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

  43. Published

    Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. / Guo, W.; Samuels, J. F.; Wang, Y.; Cao, H.; Ritter, M.; Nestadt, P. S.; Krasnow, J.; 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.; Culten, B. A.; Piacentini, J.; Pauls, D. L.; Bienvenu, O. J.; Stewart, S. E.; Goes, F. S.; Maher, B.; Pulver, A. E.; Valle, D.; Mattheisen, M.; Qian, J.; Nestad, G.; Shugart, Y. Y.

    In: European Neuropsychopharmacology, Vol. 27, No. 7, 07.2017, p. 657-666.

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

  44. Published

    Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia : A Danish Population-Based Study and Meta-analysis. / Agerbo, Esben; Sullivan, Patrick F; Vilhjálmsson, Bjarni J; Pedersen, Carsten B; Mors, Ole; Børglum, Anders D; Hougaard, David M; Hollegaard, Mads V; Meier, Sandra; Mattheisen, Manuel; Ripke, Stephan; Wray, Naomi R; Mortensen, Preben B.

    In: J A M A Psychiatry, 07.2015.

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

  45. Published

    Pneumothorax risk factors in smokers with and without chronic obstructive pulmonary disease. / Hobbs, Brian D; Foreman, Marilyn G; Bowler, Russell; Jacobson, Francine; Make, Barry J; Castaldi, Peter J; San José Estépar, Raúl; Silverman, Edwin K; Hersh, Craig P; COPDGene Investigators ; Mattheisen, Manuel.

    In: American Thoracic Society. Annals (Online), Vol. 11, No. 9, 11.2014, p. 1387-94.

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

  46. Published

    Phenotypic and genetic heterogeneity among subjects with mild airflow obstruction in COPDGene. / Lee, Jin Hwa; Cho, Michael H; McDonald, Merry-Lynn N; Hersh, Craig P; Castaldi, Peter J; Crapo, James D; Wan, Emily S; Dy, Jennifer G; Chang, Yale; Regan, Elizabeth A; Hardin, Megan; DeMeo, Dawn L; Silverman, Edwin K; COPDGene Investigators ; Mattheisen, Manuel.

    In: Kokyuukika, Vol. 108, No. 10, 10.2014, p. 1469-80.

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

  47. 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

  48. Published

    Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci. / 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. 26, No. 10, 15.05.2017, p. 1942-1951.

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

  49. 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

  50. 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

  51. Published

    Obsessive-Compulsive Disorder and Autism Spectrum Disorders : Longitudinal and Offspring Risk. / Meier, Sandra M; Petersen, Liselotte; Schendel, Diana; Mattheisen, Manuel; Mortensen, Preben B; Mors, Ole.

    In: PLOS ONE, Vol. 10, No. 11, 2015, p. e0141703.

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

  52. Published

    Novel genetic loci underlying human intracranial volume identified through genome-wide association. / Adams, Hieab H H; Hibar, Derrek P; Chouraki, Vincent; Stein, Jason L; Nyquist, Paul A; Rentería, Miguel E; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha; Desrivières, Sylvane; Beecham, Ashley H; Jahanshad, Neda; Wittfeld, Katharina; Van der Lee, Sven J; Abramovic, Lucija; Alhusaini, Saud; Amin, Najaf; Andersson, Micael; Arfanakis, Konstantinos; Aribisala, Benjamin S; Armstrong, Nicola J; Athanasiu, Lavinia; Axelsson, Tomas; Beiser, Alexa; Bernard, Manon; Bis, Joshua C; Blanken, Laura M E; Blanton, Susan H; Bohlken, Marc M; Boks, Marco P; Bralten, Janita; Brickman, Adam M; Carmichael, Owen; Chakravarty, M Mallar; Chauhan, Ganesh; Chen, Qiang; Ching, Christopher R K; Cuellar-Partida, Gabriel; Braber, Anouk Den; Doan, Nhat Trung; Ehrlich, Stefan; Filippi, Irina; Ge, Tian; Giddaluru, Sudheer; Goldman, Aaron L; Gottesman, Rebecca F; Greven, Corina U; Grimm, Oliver; Griswold, Michael E; Guadalupe, Tulio; Hass, Johanna; Haukvik, Unn K; Hilal, Saima; Hofer, Edith; Hoehn, David; Holmes, Avram J; Hoogman, Martine; Janowitz, Deborah; Jia, Tianye; Kasperaviciute, Dalia; Kim, Sungeun; Klein, Marieke; Kraemer, Bernd; Lee, Phil H; Liao, Jiemin; Liewald, David C M; Lopez, Lorna M; Luciano, Michelle; Macare, Christine; Marquand, Andre; Matarin, Mar; Mather, Karen A; Mattheisen, Manuel; Mazoyer, Bernard; McKay, David R; McWhirter, Rebekah; Milaneschi, Yuri; Mirza-Schreiber, Nazanin; Muetzel, Ryan L; Maniega, Susana Muñoz; Nho, Kwangsik; Nugent, Allison C; Loohuis, Loes M Olde; Oosterlaan, Jaap; Papmeyer, Martina; Pappa, Irene; Pirpamer, Lukas; Pudas, Sara; Pütz, Benno; Rajan, Kumar B; Ramasamy, Adaikalavan; Richards, Jennifer S; Risacher, Shannon L; Roiz-Santiañez, Roberto; Rommelse, Nanda; Rose, Emma J; Royle, Natalie A; Rundek, Tatjana; Sämann, Philipp G; Satizabal, Claudia L; Schmaal, Lianne; Schork, Andrew J; Shen, Li; Shin, Jean; Shumskaya, Elena; Smith, Albert V; Sprooten, Emma; Strike, Lachlan T; Teumer, Alexander; Thomson, Russell; Tordesillas-Gutierrez, Diana; Toro, Roberto; Trabzuni, Daniah; Vaidya, Dhananjay; Van der Grond, Jeroen; Van der Meer, Dennis; Van Donkelaar, Marjolein M J; Van Eijk, Kristel R; Van Erp, Theo G M; Van Rooij, Daan; Walton, Esther; Westlye, Lars T; Whelan, Christopher D; Windham, Beverly G; Winkler, Anderson M; Woldehawariat, Girma; Wolf, Christiane; Wolfers, Thomas; Xu, Bing; Yanek, Lisa R; Yang, Jingyun; Zijdenbos, Alex; Zwiers, Marcel P; Agartz, Ingrid; Aggarwal, Neelum T; Almasy, Laura; Ames, David; Amouyel, Philippe; Andreassen, Ole A; Arepalli, Sampath; Assareh, Amelia A; Barral, Sandra; Bastin, Mark E; Becker, Diane M; Becker, James T; Bennett, David A; Blangero, John; van Bokhoven, Hans; Boomsma, Dorret I; Brodaty, Henry; Brouwer, Rachel M; Brunner, Han G; Buckner, Randy L; Buitelaar, Jan K; Bulayeva, Kazima B; Cahn, Wiepke; Calhoun, Vince D; Cannon, Dara M; Cavalleri, Gianpiero L; Chen, Christopher; Cheng, Ching-Yu; Cichon, Sven; Cookson, Mark R; Corvin, Aiden; Crespo-Facorro, Benedicto; Curran, Joanne E; Czisch, Michael; Dale, Anders M; Davies, Gareth E; De Geus, Eco J C; De Jager, Philip L; de Zubicaray, Greig I; Delanty, Norman; Depondt, Chantal; DeStefano, Anita L; Dillman, Allissa; Djurovic, Srdjan; Donohoe, Gary; Drevets, Wayne C; Duggirala, Ravi; Dyer, Thomas D; Erk, Susanne; Espeseth, Thomas; Evans, Denis A; Fedko, Iryna O; Fernández, Guillén; Ferrucci, Luigi; Fisher, Simon E; Fleischman, Debra A; Ford, Ian; Foroud, Tatiana M; Fox, Peter T; Francks, Clyde; Fukunaga, Masaki; Gibbs, J Raphael; Glahn, David C; Gollub, Randy L; Göring, Harald H H; Grabe, Hans J; Green, Robert C; Gruber, Oliver; Gudnason, Vilmundur; Guelfi, Sebastian; Hansell, Narelle K; Hardy, John; Hartman, Catharina A; Hashimoto, Ryota; Hegenscheid, Katrin; Heinz, Andreas; Le Hellard, Stephanie; Hernandez, Dena G; Heslenfeld, Dirk J; Ho, Beng-Choon; Hoekstra, Pieter J; Hoffmann, Wolfgang; Hofman, Albert; Holsboer, Florian; Homuth, Georg; Hosten, Norbert; Hottenga, Jouke-Jan; Pol, Hilleke E Hulshoff; Ikeda, Masashi; Ikram, M Kamran; Jr, Clifford R Jack; Jenkinson, Mark; Johnson, Robert; Jönsson, Erik G; Jukema, J Wouter; Kahn, René S; Kanai, Ryota; Kloszewska, Iwona; Knopman, David S; Kochunov, Peter; Kwok, John B; Lawrie, Stephen M; Lemaître, Hervé; Liu, Xinmin; Longo, Dan L; Jr, W T Longstreth; Lopez, Oscar L; Lovestone, Simon; Martinez, Oliver; Martinot, Jean-Luc; Mattay, Venkata S; McDonald, Colm; McIntosh, Andrew M; McMahon, Katie L; McMahon, Francis J; Mecocci, Patrizia; Melle, Ingrid; Meyer-Lindenberg, Andreas; Mohnke, Sebastian; Montgomery, Grant W; Morris, Derek W; Mosley, Thomas H; Mühleisen, Thomas W; Müller-Myhsok, Bertram; Nalls, Michael A; Nauck, Matthias; Nichols, Thomas E; Niessen, Wiro J; Nöthen, Markus M; Nyberg, Lars; Ohi, Kazutaka; Olvera, Rene L; Ophoff, Roel A; Pandolfo, Massimo; Paus, Tomas; Pausova, Zdenka; Penninx, Brenda W J H; Pike, G Bruce; Potkin, Steven G; Psaty, Bruce M; Reppermund, Simone; Rietschel, Marcella; Roffman, Joshua L; Romanczuk-Seiferth, Nina; Rotter, Jerome I; Ryten, Mina; Sacco, Ralph L; Sachdev, Perminder S; Saykin, Andrew J; Schmidt, Reinhold; Schofield, Peter R; Sigurdsson, Sigurdur; Simmons, Andy; Singleton, Andrew; Sisodiya, Sanjay M; Smith, Colin; Smoller, Jordan W; Soininen, Hilkka; Srikanth, Velandai; Steen, Vidar M; Stott, David J; Sussmann, Jessika E; Thalamuthu, Anbupalam; Tiemeier, Henning; Toga, Arthur W; Traynor, Bryan J; Troncoso, Juan; Turner, Jessica A; Tzourio, Christophe; Uitterlinden, Andre G; Hernández, Maria C Valdés; Van der Brug, Marcel; Van der Lugt, Aad; Van der Wee, Nic J A; Van Duijn, Cornelia M; Van Haren, Neeltje E M; Van T Ent, Dennis; Van Tol, Marie-Jose; Vardarajan, Badri N; Veltman, Dick J; Vernooij, Meike W; Völzke, Henry; Walter, Henrik; Wardlaw, Joanna M; Wassink, Thomas H; Weale, Michael E; Weinberger, Daniel R; Weiner, Michael W; Wen, Wei; Westman, Eric; White, Tonya; Wong, Tien Y; Wright, Clinton B; Zielke, H Ronald; Zonderman, Alan B; Deary, Ian J; DeCarli, Charles; Schmidt, Helena; Martin, Nicholas G; De Craen, Anton J M; Wright, Margaret J; Launer, Lenore J; Schumann, Gunter; Fornage, Myriam; Franke, Barbara; Debette, Stéphanie; Medland, Sarah E; Ikram, M Arfan; Thompson, Paul M.

    In: Nature Neuroscience, Vol. 19, 03.10.2016, p. 1569-1582.

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

  53. Published

    Novel genetic loci associated with hippocampal volume. / Hibar, Derrek P.; Adams, Hieab H. H.; Jahanshad, Neda; Chauhan, Ganesh; Stein, Jason L.; Hofer, Edith; Renteria, Miguel E.; Bis, Joshua C.; Arias-Vasquez, Alejandro; Ikram, M. Kamran; Desrivieres, Sylvane; Vernooij, Meike W.; Abramovic, Lucija; Alhusaini, Saud; Amin, Najaf; Andersson, Micael; Arfanakis, Konstantinos; Aribisala, Benjamin S.; Armstrong, Nicola J.; Athanasiu, Lavinia; Axelsson, Tomas; Beecham, Ashley H.; Beiser, Alexa; Bernard, Manon; Blanton, Susan H.; Bohlken, Marc M.; Boks, Marco P.; Bralten, Janita; Brickman, Adam M.; Carmichael, Owen; Chakravarty, M. Mallar; Chen, Qiang; Ching, Christopher R. K.; Chouraki, Vincent; Cuellar-Partida, Gabriel; Crivello, Fabrice; Den Braber, Anouk; Nhat Trung Doan; Ehrlich, Stefan; Giddaluru, Sudheer; Goldman, Aaron L.; Gottesman, Rebecca F.; Grimm, Oliver; Griswold, Michael E.; Guadalupe, Tulio; Gutman, Boris A.; Hass, Johanna; Haukvik, Unn K.; Hoehn, David; Holmes, Avram J.; Hoogman, Martine; Janowitz, Deborah; Jia, Tianye; Jorgensen, Kjetil N.; Karbalai, Nazanin; Kasperaviciute, Dalia; Kim, Sungeun; Klein, Marieke; Kraemer, Bernd; Lee, Phil H.; Liewald, David C. M.; Lopez, Lorna M.; Luciano, Michelle; Macare, Christine; Marquand, Andre F.; Matarin, Mar; Mather, Karen A.; Mattheisen, Manuel; McKay, David R.; Milaneschi, Yuri; Maniega, Susana Munoz; Nho, Kwangsik; Nugent, Allison C.; Nyquist, Paul; Loohuis, Loes M. Olde; Oosterlaan, Jaap; Papmeyer, Martina; Pirpamer, Lukas; Puetz, Benno; Ramasamy, Adaikalavan; Richards, Jennifer S.; Risacher, Shannon L.; Roiz-Santianez, Roberto; Rommelse, Nanda; Ropele, Stefan; Rose, Emma J.; Royle, Natalie A.; Rundek, Tatjana; Saemann, Philipp G.; Saremi, Arvin; Satizabal, Claudia L.; Schmaal, Lianne; Schork, Andrew J.; Shen, Li; Shin, Jean; Shumskaya, Elena; Smith, Albert V.; Sprooten, Emma; Strike, Lachlan T.; Teumer, Alexander; Tordesillas-Gutierrez, Diana; Toro, Roberto; Trabzuni, Daniah; Trompet, Stella; Vaidya, Dhananjay; Van der Grond, Jeroen; Van der Lee, Sven J.; Van der Meer, Dennis; Van Donkelaar, Marjolein M. J.; Van Eijk, Kristel R.; Van Erp, Theo G. M.; Van Rooij, Daan; Walton, Esther; Westlye, Lars T.; Whelan, Christopher D.; Windham, Beverly G.; Winkler, Anderson M.; Wittfeld, Katharina; Woldehawariat, Girma; Wolf, Christiane; Wolfers, Thomas; Yanek, Lisa R.; Yang, Jingyun; Zijdenbos, Alex; Zwiers, Marcel P.; Agartz, Ingrid; Almasy, Laura; Ames, David; Amouyel, Philippe; Andreassen, Ole A.; Arepalli, Sampath; Assareh, Amelia A.; Barral, Sandra; Bastin, Mark E.; Becker, Diane M.; Becker, James T.; Bennett, David A.; Blangero, John; van Bokhoven, Hans; Boomsma, Dorret I.; Brodaty, Henry; Brouwer, Rachel M.; Brunner, Han G.; Buckner, Randy L.; Buitelaar, Jan K.; Bulayeva, Kazima B.; Cahn, Wiepke; Calhoun, Vince D.; Cannon, Dara M.; Cavalleri, Gianpiero L.; Cheng, Ching-Yu; Cichon, Sven; Cookson, Mark R.; Corvin, Aiden; Crespo-Facorro, Benedicto; Curran, Joanne E.; Czisch, Michael; Dale, Anders M.; Davies, Gareth E.; De Craen, Anton J. M.; De Geus, Eco J. C.; De Jager, Philip L.; De Zubicaray, Greig I.; Deary, Ian J.; Debette, Stephanie; DeCarli, Charles; Delanty, Norman; Depondt, Chantal; DeStefano, Anita; Dillman, Allissa; Djurovic, Srdjan; Donohoe, Gary; Drevets, Wayne C.; Duggirala, Ravi; Dyer, Thomas D.; Enzinger, Christian; Erk, Susanne; Espeseth, Thomas; Fedko, Iryna O.; Fernandez, Guillen; Ferrucci, Luigi; Fisher, Simon E.; Fleischman, Debra A.; Ford, Ian; Fornage, Myriam; Foroud, Tatiana M.; Fox, Peter T.; Francks, Clyde; Fukunaga, Masaki; Gibbs, J. Raphael; Glahn, David C.; Gollub, Randy L.; Goring, Harald H. H.; Green, Robert C.; Gruber, Oliver; Gudnason, Vilmundur; Guelfi, Sebastian; Haberg, Asta K.; Hansell, Narelle K.; Hardy, John; Hartman, Catharina A.; Hashimoto, Ryota; Hegenscheid, Katrin; Heinz, Andreas; Le Hellard, Stephanie; Hernandez, Dena G.; Heslenfeld, Dirk J.; Ho, Beng-Choon; Hoekstra, Pieter J.; Hoffmann, Wolfgang; Hofman, Albert; Holsboer, Florian; Homuth, Georg; Hosten, Norbert; Hottenga, Jouke-Jan; Huentelman, Matthew; Pol, Hilleke E. Hulshoff; Ikeda, Masashi; Jack, Clifford R.; Jenkinson, Mark; Johnson, Robert; Joensson, Erik G.; Jukema, J. Wouter; Kahn, Rene S.; Kanai, Ryota; Kloszewska, Iwona; Knopman, David S.; Kochunov, Peter; Kwok, John B.; Lawrie, Stephen M.; Lemaitre, Herve; Liu, Xinmin; Longo, Dan L.; Lopez, Oscar L.; Lovestone, Simon; Martinez, Oliver; Martinot, Jean-Luc; Mattay, Venkata S.; McDonald, Colm; McIntosh, Andrew M.; McMahon, Francis J.; McMahon, Katie L.; Mecocci, Patrizia; Melle, Ingrid; Meyer-Lindenberg, Andreas; Mohnke, Sebastian; Montgomery, Grant W.; Morris, Derek W.; Mosley, Thomas H.; Muhleisen, Thomas W.; Mueller-Myhsok, Bertram; Nalls, Michael A.; Nauck, Matthias; Nichols, Thomas E.; Niessen, Wiro J.; Nothen, Markus M.; Nyberg, Lars; Ohi, Kazutaka; Olvera, Rene L.; Ophoff, Roel A.; Pandolfo, Massimo; Paus, Tomas; Pausova, Zdenka; Penninx, Brenda W. J. H.; Pike, G. Bruce; Potkin, Steven G.; Psaty, Bruce M.; Reppermund, Simone; Rietschel, Marcella; Roffman, Joshua L.; Romanczuk-Seiferth, Nina; Rotter, Jerome I.; Ryten, Mina; Sacco, Ralph L.; Sachdev, Perminder S.; Saykin, Andrew J.; Schmidt, Reinhold; Schmidt, Helena; Schofield, Peter R.; Sigursson, Sigurdur; Simmons, Andrew; Singleton, Andrew; Sisodiya, Sanjay M.; Smith, Colin; Smoller, Jordan W.; Soininen, Hilkka; Steen, Vidar M.; Stott, David J.; Sussmann, Jessika E.; Thalamuthu, Anbupalam; Toga, Arthur W.; Traynor, Bryan J.; Troncoso, Juan; Tsolaki, Magda; Tzourio, Christophe; Uitterlinden, Andre G.; Hernandez, Maria C. Valdes; Van der Brug, Marcel; van der Lugt, Aad; van der Wee, Nic J. A.; Van Haren, Neeltje E. M.; van't Ent, Dennis; Van Tol, Marie-Jose; Vardarajan, Badri N.; Vellas, Bruno; Veltman, Dick J.; Voelzke, Henry; Walter, Henrik; Wardlaw, Joanna M.; Wassink, Thomas H.; Weale, Michael E.; Weinberger, Daniel R.; Weiner, Michael W.; Wen, Wei; Westman, Eric; White, Tonya; Wong, Tien Y.; Wright, Clinton B.; Zielke, Ronald H.; Zonderman, Alan B.; Martin, Nicholas G.; Van Duijn, Cornelia M.; Wright, Margaret J.; Longstreth, W. T.; Schumann, Gunter; Grabe, Hans J.; Franke, Barbara; Launer, Lenore J.; Medland, Sarah E.; Seshadri, Sudha; Thompson, Paul M.; Ikram, M. Arfan.

    In: Nature Communications, Vol. 8, 13624, 18.01.2017.

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

  54. Published

    Nordic OCD & Related Disorders Consortium : Rationale, design, and methods. / Mataix-Cols, David; Hansen, Bjarne; Mattheisen, Manuel; Karlsson, Elinor K.; Addington, Anjené M.; Boberg, Julia; Djurfeldt, Diana R.; Halvorsen, Matthew; Lichtenstein, Paul; Solem, Stian; Lindblad-Toh, Kerstin; Haavik, Jan; Kvale, Gerd; Rück, Christian; Crowley, James J.; Nordic OCD and Related Disorders Consortium (NORDiC).

    In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 183, No. 1, 01.2020, p. 38-50.

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

  55. Published

    Nonsyndromic cleft lip with or without cleft palate and cancer : Evaluation of a possible common genetic background through the analysis of GWAS data. / Dunkhase, Eva; Ludwig, Kerstin U; Knapp, Michael; Skibola, Christine F; Figueiredo, Jane C; Hosking, Fay Julie; Ellinghaus, Eva; Landi, Maria Teresa; Ma, Hongxia; Nakagawa, Hidewaki; Kim, Jong-Won; Han, Jiali; Yang, Ping; Böhmer, Anne C; Mattheisen, Manuel; Nöthen, Markus M; Mangold, Elisabeth.

    In: Genomics data, Vol. 10, 12.2016, p. 22-29.

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

  56. 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

  57. 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

  58. Published

    No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. / Johnson, Emma C; Bjelland, Douglas W; Howrigan, Daniel P; Abdellaoui, Abdel; Breen, Gerome; Borglum, Anders; Cichon, Sven; Degenhardt, Franziska; Forstner, Andreas J; Frank, Josef; Genovese, Giulio; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hoffman, Per; Maier, Wolfgang; Mattheisen, Manuel; Morris, Derek; Mowry, Bryan; Müller-Mhysok, Betram; Neale, Benjamin; Nenadic, Igor; Nöthen, Markus M; O'Dushlaine, Colm; Rietschel, Marcella; Ruderfer, Douglas M; Rujescu, Dan; Schulze, Thomas G; Simonson, Matthew A; Stahl, Eli; Strohmaier, Jana; Witt, Stephanie H; Sullivan, Patrick F; Keller, Matthew C; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

    In: P L o S Genetics, Vol. 12, No. 10, 10.2016, p. e1006343.

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

  59. 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

  60. Published

    New data and an old puzzle : the negative association between schizophrenia and rheumatoid arthritis. / Lee, S Hong; Byrne, Enda M; Hultman, Christina M; Kähler, Anna; Vinkhuyzen, Anna Ae; Ripke, Stephan; Andreassen, Ole A; Frisell, Thomas; Gusev, Alexander; Hu, Xinli; Karlsson, Robert; Mantzioris, Vasilis X; McGrath, John J; Mehta, Divya; Stahl, Eli A; Zhao, Qiongyi; Kendler, Kenneth S; Sullivan, Patrick F; Price, Alkes L; O'Donovan, Michael; Okada, Yukinori; Mowry, Bryan J; Raychaudhuri, Soumya; Wray, Naomi R; Byerley, William; Cahn, Wiepke; Cantor, Rita M; Cichon, Sven; Cormican, Paul; Curtis, David; Djurovic, Srdjan; Escott-Price, Valentina; Gejman, Pablo V; Georgieva, Lyudmila; Giegling, Ina; Hansen, Thomas F; Ingason, Andrés; Kim, Yunjung; Konte, Bettina; Lee, Phil H; McIntosh, Andrew; McQuillin, Andrew; Morris, Derek W; Nöthen, Markus M; O'Dushlaine, Colm; Olincy, Ann; Olsen, Line; Pato, Carlos N; Pato, Michele T; Mattheisen, Manuel; Schizophrenia Working Group of the Psychiatric Genomics Consortium and Rheumatoid Arthritis Consortium International.

    In: International Journal of Epidemiology, 18.08.2015.

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

  61. 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

  62. Published

    Mortality Among Persons With Obsessive-Compulsive Disorder in Denmark. / Meier, Sandra M; Mattheisen, Manuel; Mors, Ole; Schendel, Diana; Mortensen, Preben B; Plessen, Kerstin J.

    In: JAMA Psychiatry, Vol. 73, No. 3, 27.01.2016, p. 268-274.

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

  63. Published

    MicroRNA hsa-miR-4717-5p regulates RGS2 and may be a risk factor for anxiety-related traits. / Hommers, Leif; Raab, Annette; Bohl, Alexandra; Weber, Heike; Scholz, Claus-Jürgen; Erhardt, Angelika; Binder, Elisabeth; Arolt, Volker; Gerlach, Alexander; Gloster, Andrew; Kalisch, Raffael; Kircher, Tilo; Lonsdorf, Tina; Ströhle, Andreas; Zwanzger, Peter; Mattheisen, Manuel; Cichon, Sven; Lesch, Klaus-Peter; Domschke, Katharina; Reif, Andreas; Lohse, Martin J; Deckert, Jürgen.

    In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 02.04.2015.

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

  64. 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

  65. 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

  66. 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

  67. Published

    Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE. / Dietter, Johannes; Mattheisen, Manuel; Fürst, Robert; Rüschendorf, Franz; Wienker, Thomas F; Strauch, Konstantin.

    In: Bioinformatics (Online), Vol. 23, No. 1, 01.01.2007, p. 64-70.

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

  68. 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

  69. Published

    Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. / Satterstrom, F. Kyle; Kosmicki, Jack A.; Wang, Jiebiao; Breen, Michael S.; De Rubeis, Silvia; An, Joon Yong; Peng, Minshi; Collins, Ryan; Grove, Jakob; Klei, Lambertus; Stevens, Christine; Reichert, Jennifer; Mulhern, Maureen S.; Artomov, Mykyta; Gerges, Sherif; Sheppard, Brooke; Xu, Xinyi; Bhaduri, Aparna; Norman, Utku; Brand, Harrison; Schwartz, Grace; Nguyen, Rachel; Guerrero, Elizabeth E.; Dias, Caroline; Autism Sequencing Consortium; iPSYCH-Broad Consortium ; Børglum, Anders D.

    In: Cell, Vol. 180, No. 3, 02.2020, p. 568-584.e23.

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

  70. Published

    Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. / Maier, Robert; Moser, Gerhard; Chen, Guo-Bo; Ripke, Stephan; Coryell, William; Potash, James B; Scheftner, William A; Shi, Jianxin; Weissman, Myrna M; Hultman, Christina M; Landén, Mikael; Levinson, Douglas F; Kendler, Kenneth S; Smoller, Jordan W; Wray, Naomi R; Lee, S Hong; Cross-Disorder Working Group of the Psychiatric Genomics Consortium ; Mattheisen, Manuel.

    In: American Journal of Human Genetics, Vol. 96, No. 2, 05.02.2015, p. 283-94.

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

  71. 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

  72. 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

  73. 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

  74. E-pub ahead of print

    Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. / Yang, Zhiyu; Wu, Hanrui; Lee, Phil H; Tsetsos, Fotis; Davis, Lea K; Yu, Dongmei; Lee, Sang Hong; Dalsgaard, Søren; Haavik, Jan; Barta, Csaba; Zayats, Tetyana; Eapen, Valsamma; Wray, Naomi R; Devlin, Bernie; Daly, Mark; Neale, Benjamin; Børglum, Anders D; Crowley, James J; Scharf, Jeremiah; Mathews, Carol A; Faraone, Stephen V; Franke, Barbara; Mattheisen, Manuel; Smoller, Jordan W; Paschou, Peristera.

    In: Biological Psychiatry, 08.01.2021.

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

  75. 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

  76. Published

    Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. / Czamara, Darina; Eraslan, Gökçen; Page, Christian M; Lahti, Jari; Lahti-Pulkkinen, Marius; Hämäläinen, Esa; Kajantie, Eero; Laivuori, Hannele; Villa, Pia M; Reynolds, Rebecca M; Nystad, Wenche; Håberg, Siri E; London, Stephanie J; O'Donnell, Kieran J; Garg, Elika; Meaney, Michael J; Entringer, Sonja; Wadhwa, Pathik D; Buss, Claudia; Jones, Meaghan J; Lin, David T S; MacIsaac, Julie L; Kobor, Michael S; Koen, Nastassja; Zar, Heather J; Koenen, Karestan C; Dalvie, Shareefa; Stein, Dan J; Kondofersky, Ivan; Müller, Nikola S; Theis, Fabian J; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Räikkönen, Katri; Binder, Elisabeth B.

    In: Nature Communications, Vol. 10, 2548, 06.2019.

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

  77. 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

  78. Published

    Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia. / Benros, Michael E; Trabjerg, Betina B; Meier, Sandra; Mattheisen, Manuel; Mortensen, Preben B; Mors, Ole; Børglum, Anders D; Hougaard, David M; Nørgaard-Pedersen, Bent; Nordentoft, Merete; Agerbo, Esben.

    In: Biological Psychiatry, Vol. 80, No. 8, 19.04.2016, p. 609–616.

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

  79. Published

    Inferential testing for linkage with GENEHUNTER-MODSCORE : the impact of the pedigree structure on the null distribution of multipoint MOD scores. / Mattheisen, Manuel; Dietter, Johannes; Knapp, Michael; Baur, Max P; Strauch, Konstantin.

    In: Genetic Epidemiology, Vol. 32, No. 1, 01.2008, p. 73-83.

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

  80. 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

  81. Published

    Increased mortality among people with anxiety disorders : total population study. / Meier, Sandra M; Mattheisen, Manuel; Mors, Ole; Mortensen, Preben B; Laursen, Thomas M; Penninx, Brenda W.

    In: British Journal of Psychiatry, Vol. 209, No. 3, 2016, p. 216-221.

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

  82. Published

    Improving genetic prediction by leveraging genetic correlations among human diseases and traits. / Maier, Robert M.; Zhu, Zhihong; Lee, Sang Hong; Trzaskowski, Maciej; Ruderfer, Douglas M.; Stahl, Eli A.; Ripke, Stephan; Wray, Naomi R.; Yang, Jian; Visscher, Peter M.; Robinson, Matthew R.; Forstner, Andreas J.; Mcquillin, Andrew; Trubetskoy, Vassily; Wang, Weiqing; Wang, Yunpeng; Coleman, Jonathan R.I.; Gaspar, Héléna A.; De Leeuw, Christiaan A.; Whitehead Pavlides, Jennifer M.; Olde Loohuis, Loes M.; Pers, Tune H.; Lee, Phil H.; Charney, Alexander W.; Dobbyn, Amanda L.; Huckins, Laura; Boocock, James; Giambartolomei, Claudia; Roussos, Panos; Mullins, Niamh; Awasthi, Swapnil; Agerbo, Esben; Als, Thomas D.; Pedersen, Carsten Bøcker; Grove, Jakob; Kupka, Ralph; Regeer, Eline J.; Anjorin, Adebayo; Casas, Miquel; Mahon, Pamela B.; Allardyce, Judith; Escott-Price, Valentina; Forty, Liz; Fraser, Christine; Kogevinas, Manolis; Frank, Josef; Streit, Fabian; Strohmaier, Jana; Treutlein, Jens; Witt, Stephanie H.; Kennedy, James L.; Strauss, John S.; Garnham, Julie; O'donovan, Claire; Slaney, Claire; Steinberg, Stacy; Thorgeirsson, Thorgeir E.; Hautzinger, Martin; Steffens, Michael; Perlis, Roy H.; Sánchez-Mora, Cristina; Hipolito, Maria; Lawson, William B.; Nwulia, Evaristus A.; Levy, Shawn E.; Foroud, Tatiana M.; Jamain, Stéphane; Young, Allan H.; Mckay, James D.; Albani, Diego; Zandi, Peter; Potash, James B.; Zhang, Peng; Raymond Depaulo, J.; Bergen, Sarah E.; Juréus, Anders; Karlsson, Robert; Kandaswamy, Radhika; Mcguffin, Peter; Rivera, Margarita; Lissowska, Jolanta; Cruceanu, Cristiana; Lucae, Susanne; Cervantes, Pablo; Budde, Monika; Gade, Katrin; Heilbronner, Urs; Pedersen, Marianne Giørtz; Morris, Derek W.; Weickert, Cynthia Shannon; Weickert, Thomas W.; Macintyre, Donald J.; Lawrence, Jacob; Elvsåshagen, Torbjørn; Smeland, Olav B.; Djurovic, Srdjan; Xi, Simon; Green, Elaine K.; Czerski, Piotr M.; Hauser, Joanna; Xu, Wei; Vedder, Helmut; Oruc, Lilijana; Spijker, Anne T.; Gordon, Scott D.; Medland, Sarah E.; Curtis, David; Mühleisen, Thomas W.; Badner, Judith; Scheftner, William A.; Sigurdsson, Engilbert; Schork, Nicholas J.; Schatzberg, Alan F.; Bækvad-Hansen, Marie; Bybjerg-Grauholm, Jonas; Hansen, Christine Søholm; Knowles, James A.; Szelinger, Szabolcs; Montgomery, Grant W.; Boks, Marco; Adolfsson, Annelie Nordin; Hoffmann, Per; Bauer, Michael; Pfennig, Andrea; Leber, Markus; Kittel-Schneider, Sarah; Reif, Andreas; Del-Favero, Jurgen; Fischer, Sascha B.; Herms, Stefan; Reinbold, Céline S.; Degenhardt, Franziska; Koller, Anna C.; Maaser, Anna; Ori, Anil; Dale, Anders M.; Fan, Chun Chieh; Greenwood, Tiffany A.; Nievergelt, Caroline M.; Shehktman, Tatyana; Shilling, Paul D.; Byerley, William; Bunney, William; Alliey-Rodriguez, Ney; Clarke, Toni Kim; Liu, Chunyu; Coryell, William; Akil, Huda; Burmeister, Margit; Flickinger, Matthew; Li, Jun Z.; Mcinnis, Melvin G.; Meng, Fan; Thompson, Robert C.; Watson, Stanley J.; Zollner, Sebastian; Guan, Weihua; Green, Melissa J.; Craig, David; Sobell, Janet L.; Milani, Lili; Gordon-Smith, Katherine; Knott, Sarah V.; Perry, Amy; Parra, José Guzman; Mayoral, Fermin; Rivas, Fabio; Rice, John P.; Barchas, Jack D.; Børglum, Anders D.; Mortensen, Preben Bo; Mors, Ole; Grigoroiu-Serbanescu, Maria; Bellivier, Frank; Etain, Bruno; Leboyer, Marion; Ramos-Quiroga, Josep Antoni; Agartz, Ingrid; Amin, Farooq; Azevedo, Maria H.; Bass, Nicholas; Black, Donald W.; Blackwood, Douglas H.R.; Bruggeman, Richard; Buccola, Nancy G.; Choudhury, Khalid; Cloninger, C. Robert; Corvin, Aiden; Craddock, Nicholas; Daly, Mark J.; Datta, Susmita; Donohoe, Gary J.; Duan, Jubao; Dudbridge, Frank; Fanous, Ayman; Freedman, Robert; Freimer, Nelson B.; Friedl, Marion; Gill, Michael; Gurling, Hugh; De Haan, Lieuwe; Hamshere, Marian L.; Hartmann, Annette M.; Holmans, Peter A.; Kahn, René S.; Keller, Matthew C.; Kenny, Elaine; Kirov, George K.; Krabbendam, Lydia; Krasucki, Robert; Lencz, Todd; Levinson, Douglas F.; Lieberman, Jeffrey A.; Lin, Dan Yu; Linszen, Don H.; Magnusson, Patrik K.E.; Maier, Wolfgang; Malhotra, Anil K.; Mattheisen, Manuel; Mattingsdal, Morten; Mccarroll, Steven A.; Medeiros, Helena; Melle, Ingrid; Milanova, Vihra; Myin-Germeys, Inez; Neale, Benjamin M.; Ophoff, Roel A.; Owen, Michael J.; Pimm, Jonathan; Purcell, Shaun M.; Puri, Vinay; Quested, Digby J.; Rossin, Lizzy; Sanders, Alan R.; Shi, Jianxin; Sklar, Pamela; St Clair, David; Stroup, T. Scott; Van Os, Jim; Wiersma, Durk; Zammit, Stanley.

    In: Nature Communications, Vol. 9, No. 1, 02769-6, 01.12.2018.

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

  83. 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

  84. Published

    Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. / Li, Ming; Luo, Xiong-Jian; Landén, Mikael; Bergen, Sarah E; Hultman, Christina M; Li, Xiao; Zhang, Wen; Yao, Yong-Gang; Zhang, Chen; Liu, Jiewei; Mattheisen, Manuel; Cichon, Sven; Mühleisen, Thomas W; Degenhardt, Franziska A; Nöthen, Markus M; Schulze, Thomas G; Grigoroiu-Serbanescu, Maria; Li, Hao; Fuller, Chris K; Chen, Chunhui; Dong, Qi; Chen, Chuansheng; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean-Pierre; Henry, Chantal; Preisig, Martin; Kutalik, Zoltán; Castelao, Enrique; Wright, Adam; Mitchell, Philip B; Fullerton, Janice M; Schofield, Peter R; Montgomery, Grant W; Medland, Sarah E; Gordon, Scott D; Martin, Nicholas G; Rietschel, Marcella; Liu, Chunyu; Kleinman, Joel E; Hyde, Thomas M; Weinberger, Daniel R; Su, Bing; MooDS Consortium.

    In: British Journal of Psychiatry, 03.09.2015.

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

  85. Published

    Identification of the BRD1 interaction network and its impact on mental disorder risk. / Fryland, Tue; Christensen, Jane H; Pallesen, Jonatan; Mattheisen, Manuel; Palmfeldt, Johan; Bak, Mads; Grove, Jakob; Demontis, Ditte; Blechingberg, Jenny; Ooi, Hong Sain; Nyegaard, Mette; Hauberg, Mads E; Tommerup, Niels; Gregersen, Niels; Mors, Ole; Corydon, Thomas J; Nielsen, Anders L; Børglum, Anders D.

    In: Genome Medicine, Vol. 8, No. 1, 03.05.2016, p. 53.

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

  86. Published

    Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. / Forstner, Andreas J; Hecker, Julian; Hofmann, Andrea; Maaser, Anna; Reinbold, Céline S; Mühleisen, Thomas W; Leber, Markus; Strohmaier, Jana; Degenhardt, Franziska; Treutlein, Jens; Mattheisen, Manuel; Schumacher, Johannes; Streit, Fabian; 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; Schenk, Lorena M; Fischer, Sascha B; Sivalingam, Sugirthan; 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; Krasnov, Valery; Chuchalin, Alexander; Babadjanova, Gulja; Pantelejeva, Galina; Abramova, Lilia I; Tiganov, Alexander S; Polonikov, Alexey; Khusnutdinova, Elza; Alda, Martin; Cruceanu, Cristiana; Rouleau, Guy A; Turecki, Gustavo; Laprise, Catherine; Rivas, Fabio; Mayoral, Fermin; Kogevinas, Manolis; Grigoroiu-Serbanescu, Maria; Becker, Tim; Schulze, Thomas G; Rietschel, Marcella; Cichon, Sven; Fier, Heide; Nöthen, Markus M.

    In: PLOS ONE, Vol. 12, No. 2, 2017, p. e0171595.

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

  87. 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

  88. 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

  89. 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

  90. 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

  91. Published

    Identification of common genetic risk variants for autism spectrum disorder. / Grove, Jakob; Ripke, Stephan; Als, Thomas D; Mattheisen, Manuel; Walters, Raymond K; Won, Hyejung; Pallesen, Jonatan; Agerbo, Esben; Andreassen, Ole A; Anney, Richard; Awashti, Swapnil; Belliveau, Rich; Bettella, Francesco; Buxbaum, Joseph D; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Christensen, Jane H; Churchhouse, Claire; Dellenvall, Karin; Demontis, Ditte; De Rubeis, Silvia; Devlin, Bernie; Djurovic, Srdjan; Dumont, Ashley L; Goldstein, Jacqueline I; Hansen, Christine S; Hauberg, Mads Engel; Hollegaard, Mads V; Hope, Sigrun; Howrigan, Daniel P; Huang, Hailiang; Hultman, Christina M; Klei, Lambertus; Maller, Julian; Martin, Joanna; Martin, Alicia R; Moran, Jennifer L; Nyegaard, Mette; Nærland, Terje; Palmer, Duncan S; Palotie, Aarno; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; dPoterba, Timothy; Poulsen, Jesper Buchhave; Pourcain, Beate St; Qvist, Per; Rehnström, Karola ; Reichenberg, Abraham; Reichert, Jennifer ; Robinson, Elise B.; Roeder, Kathryn; Roussos, Panos; Saemundsen, Evald; Sandin, Sven; Satterstrom, F. Kyle; Smith, George Davey; Stefansson, Hreinn; Steinberg, Stacy; Stevens, Christine; Sullivan, Patrick F; Turley, Patrick; Walters, G. Bragi; Xu, Xinyi ; Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium; BUPGEN; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; 23andMe Research Team; Stefansson, Kari; Geschwind, Daniel H; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Neale, Benjamin M; Daly, Mark J; Børglum, Anders D.

    In: Nature Genetics, Vol. 51, No. 3, 02.2019, p. 431-444.

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

  92. Published

    Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1. / Chang, Hong; Li, Lingyi; Peng, Tao; Grigoroiu-Serbanescu, Maria; Bergen, Sarah E.; Landén, Mikael; Hultman, Christina M.; Forstner, Andreas J.; Strohmaier, Jana; Hecker, Julian; Schulze, Thomas G.; Müller-Myhsok, Bertram; Reif, Andreas; Mitchell, Philip B.; Martin, Nicholas G.; Cichon, Sven; Nöthen, Markus M.; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean Pierre; Henry, Chantal; Rietschel, Marcella; Backlund, Lena; Frisén, Louise; Lavebratt, Catharina; Schalling, Martin; Ösby, Urban; Mühleisen, Thomas W.; Leber, Markus; Degenhardt, Franziska; Treutlein, Jens; Mattheisen, Manuel; Hofmann, Andrea; Breuer, René; Meier, Sandra; Herms, Stefan; Hoffmann, Per; Lacour, André; Witt, Stephanie H.; Streit, Fabian; Lucae, Susanne; Maier, Wolfgang; Schwarz, Markus; Vedder, Helmut; Kammerer-Ciernioch, Jutta; Pfennig, Andrea; Bauer, Michael; Hautzinger, Martin; Wright, Adam; Fullerton, Janice M.; Schofield, Peter R.; Montgomery, Grant W.; Medland, Sarah E.; Gordon, Scott D.; Becker, Tim; Schumacher, Johannes; Propping, Peter; Xiao, Xiao; Li, Ming.

    In: Molecular Neurobiology, Vol. 54, No. 7, 09.2017, p. 5166-5176.

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

  93. Published

    INCREASED MORTALITY AMONG PERSONS WITH ANXIETY DISORDERS AND DEPRESSION : A TOTAL POPULATION STUDY. / Meier, Sandra; Mattheisen, Manuel; Mors, Ole; Mortensen, Preben Bo; Munk, Thomas; Penninx, Brenda.

    In: European Neuropsychopharmacology, Vol. 27, 10.2017, p. S267-S267.

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

  94. 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

  95. 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

  96. 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

  97. Published

    High loading of polygenic risk in cases with chronic schizophrenia. / Meier, S M; Agerbo, E; Maier, R; Pedersen, C B; Lang, M; Grove, J; Hollegaard, M V; Demontis, D; Trabjerg, B B; Hjorthøj, C; Ripke, S; Degenhardt, F; Nöthen, M M; Rujescu, D; Maier, W; Werge, T; Mors, O; Hougaard, D M; Børglum, A D; Wray, N R; Rietschel, M; Nordentoft, M; Mortensen, P B; Mattheisen, M; MooDS SCZ Consortium.

    In: Molecular Psychiatry, 01.09.2015, p. 1-6.

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

  98. Published

    High factor VIII levels in venous thromboembolism show linkage to imprinted loci on chromosomes 5 and 11. / Berger, Mario; Mattheisen, Manuel; Kulle, Bettina; Schmidt, Henriette; Oldenburg, Johannes; Bickeböller, Heike; Walter, Ulrich; Lindner, Tom H; Strauch, Konstantin; Schambeck, Christian M.

    In: Blood, Vol. 105, No. 2, 15.01.2005, p. 638-44.

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

  99. Published

    Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. / Hübel, Christopher; Gaspar, Héléna A.; Coleman, Jonathan R.I.; Finucane, Hilary; Purves, Kirstin L.; Hanscombe, Ken B.; Prokopenko, Inga; Graff, Mariaelisa; Ngwa, Julius S.; Workalemahu, Tsegaselassie; O'Reilly, Paul F.; Bulik, Cynthia M.; Breen, Gerome; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Tourette Syndrome/Obsessive-Compulsive Disorder Working Group of the Psychiatric Genomics Consortium; MAGIC Investigators; Eating Disorders Working Group of the Psychiatric Genomics Consortium.

    In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 180, No. 6, 09.2019, p. 428-438.

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

  100. 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

  101. 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

  102. 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

  103. Published

    Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. / Zhou, Hang; Sealock, Julia M; Sanchez-Roige, Sandra; Clarke, Toni-Kim; Levey, Daniel F; Cheng, Zhongshan; Li, Boyang; Polimanti, Renato; Kember, Rachel L; Smith, Rachel Vickers; Thygesen, Johan H; Morgan, Marsha Y; Atkinson, Stephen R; Thursz, Mark R; Nyegaard, Mette; Mattheisen, Manuel; Børglum, Anders D; Johnson, Emma C; Justice, Amy C; Palmer, Abraham A; McQuillin, Andrew; Davis, Lea K; Edenberg, Howard J; Agrawal, Arpana; Kranzler, Henry R; Gelernter, Joel.

    In: Nature Neuroscience, Vol. 23, No. 7, 07.2020, p. 809-818.

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

  104. Published

    Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. / Howard, David M; Adams, Mark J; Clarke, Toni-Kim; Hafferty, Jonathan D; Gibson, Jude; Shirali, Masoud; Coleman, Jonathan R I; Hagenaars, Saskia P; Ward, Joey; Wigmore, Eleanor M; Alloza, Clara; Shen, Xueyi; Barbu, Miruna C; Xu, Eileen Y; Whalley, Heather C; Marioni, Riccardo E; Porteous, David J; Davies, Gail; Deary, Ian J; Hemani, Gibran; Berger, Klaus; Teismann, Henning; Rawal, Rajesh; Arolt, Volker; Baune, Bernhard T; Dannlowski, Udo; Domschke, Katharina; Tian, Chao; Hinds, David A; Trzaskowski, Maciej; Byrne, Enda M.; Ripke, Stephan; Smith, Daniel J; Sullivan, Patrick F; Wray, Naomi R; Breen, Gerome; Lewis, Cathryn M; McIntosh, Andrew M; 23andMe Research Team.

    In: Nature Neuroscience, Vol. 22, No. 3, 03.2019, p. 343-352.

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

  105. 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

  106. 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

  107. Published

    Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. / Generation Scotland; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: PLOS ONE, Vol. 13, No. 12, e0209160, 20.12.2018.

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

  108. Published

    Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. / Coleman, Jonathan R. I.; Peyrot, Wouter J.; Purves, Kirstin L.; Davis, Katrina A. S.; Rayner, Christopher; Choi, Shing Wan; Hubel, Christopher; Gaspar, Helena A.; Kan, Carol; Van der Auwera, Sandra; Adams, Mark James; Lyall, Donald M.; Choi, Karmel W.; Psychiat Genomics Consortium; Dunn, Erin C.; Vassos, Evangelos; Danese, Andrea; Maughan, Barbara; Grabe, Hans J.; Lewis, Cathryn M.; O'Reilly, Paul F.; McIntosh, Andrew M.; Smith, Daniel J.; Wray, Naomi R.; Hotopf, Matthew; Eley, Thalia C.; Breen, Gerome.

    In: Molecular Psychiatry, Vol. 25, No. 7, 2020, p. 1430-1446.

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

  109. 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

  110. 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

  111. 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

  112. 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

  113. 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

  114. 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

  115. 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

  116. 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

  117. 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

  118. 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

  119. 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

  120. 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

  121. 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

  122. 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

  123. 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

  124. 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

  125. 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

  126. 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

  127. 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

  128. 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

  129. 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

  130. 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

  131. 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

  132. 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

  133. 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

  134. 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

  135. 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

  136. 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

  137. 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

  138. 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

  139. 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

  140. 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

  141. 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

  142. 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

  143. 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

  144. 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

  145. 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

  146. 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

  147. 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

  148. 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

  149. 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

  150. 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

  151. 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

  152. 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

  153. 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

  154. 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

  155. 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

  156. 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

  157. 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

  158. 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

  159. 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

  160. 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

  161. 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

  162. 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

  163. 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

  164. 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

  165. 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

  166. 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

  167. 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

  168. 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

  169. 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

  170. 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

  171. 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

  172. 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

  173. 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

  174. 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

  175. 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

  176. 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

  177. 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

  178. 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

  179. 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

  180. 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

  181. 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

  182. 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

  183. 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

  184. 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

  185. 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

  186. 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

  187. 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

  188. 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

  189. 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

  190. 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

  191. 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

  192. 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

  193. 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

  194. 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

  195. 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

  196. 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

  197. 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

  198. 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

  199. 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

  200. 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

  201. 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

  202. 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

  203. 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

  204. 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

  205. 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

  206. 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

  207. 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

  208. 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