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/debate/letter to the editorResearchpeer-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/debate/letter to the editorResearchpeer-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

    Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis. / Strom, Nora I.; Grove, Jakob; Meier, Sandra M.; Bækvad-Hansen, Marie; Becker Nissen, Judith; Damm Als, Thomas; Halvorsen, Matthew; Nordentoft, Merete; Mortensen, Preben B.; Hougaard, David M.; Werge, Thomas; Mors, Ole; Børglum, Anders D.; Crowley, James J.; Bybjerg-Grauholm, Jonas; Mattheisen, Manuel.

    In: Frontiers in Genetics, Vol. 12, 711624, 08.2021.

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

  46. 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

  47. 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

  48. 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

  49. 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

  50. 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

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