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2023

Amare, A. T., A. Thalamuthu, K. O. Schubert, J. M. Fullerton, M. Ahmed, S. Hartmann, S. Papiol, U. Heilbronner, F. Degenhardt, F. Tekola-Ayele, L. Hou, Y.-H. Hsu, T. Shekhtman, M. Adli, N. Akula, K. Akiyama, R. Ardau, B. Arias, J.-M. Aubry, R. Hasler, H. Richard-Lepouriel, N. Perroud, L. Backlund, A. K. Bhattacharjee, F. Bellivier, A. Benabarre, S. Bengesser, J. M. Biernacka, A. Birner, C. Marie-Claire, P. Cervantes, H.-C. Chen, C. Chillotti, S. Cichon, C. Cruceanu, P. M. Czerski, N. Dalkner, M. Del Zompo, J. R. DePaulo, B. Étain, S. Jamain, P. Falkai, A. J. Forstner, L. Frisen, M. A. Frye, S. Gard, J. S. Garnham, F. S. Goes, M. Grigoroiu-Serbanescu, A. J. Fallgatter, S. Stegmaier, T. Ethofer, S. Biere, K. Petrova, C. Schuster, K. Adorjan, M. Budde, M. Heilbronner, J. L. Kalman, M. O. Kohshour, D. Reich-Erkelenz, S. K. Schaupp, E. C. Schulte, F. Senner, T. Vogl, I.-G. Anghelescu, V. Arolt, U. Dannlowski, D. Dietrich, C. Figge, M. Jäger, F. U. Lang, G. Juckel, C. Konrad, J. Reimer, M. Schmauß, A. Schmitt, C. Spitzer, M. von Hagen, J. Wiltfang, J. Zimmermann, T. F. M. Andlauer, A. Fischer, F. Bermpohl, P. Ritter, S. Matura, A. Gryaznova, I. Falkenberg, C. Yildiz, T. Kircher, J. Schmidt, M. Koch, K. Gade, S. Trost, I. S. Haussleiter, M. Lambert, A. C. Rohenkohl, V. Kraft, P. Grof, R. Hashimoto, J. Hauser, S. Herms, P. Hoffmann, E. Jiménez, J.-P. Kahn, L. Kassem, P.-H. Kuo, T. Kato, J. Kelsoe, S. Kittel-Schneider, E. Ferensztajn-Rochowiak, B. König, I. Kusumi, G. Laje, M. Landén, C. Lavebratt, M. Leboyer, S. G. Leckband, A. Tortorella, M. Manchia, L. Martinsson, M. J. McCarthy, S. McElroy, F. Colom, V. Millischer, M. Mitjans, F. M. Mondimore, P. Monteleone, C. M. Nievergelt, M. M. Nöthen, T. Novák, C. O’Donovan, N. Ozaki, A. Pfennig, C. Pisanu, J. B. Potash, A. Reif, E. Reininghaus, G. A. Rouleau, J. K. Rybakowski, M. Schalling, P. R. Schofield, B. W. Schweizer, G. Severino, P. D. Shilling, K. Shimoda, C. Simhandl, C. M. Slaney, A. Squassina, T. Stamm, P. Stopkova, M. Maj, G. Turecki, E. Vieta, J. Veeh, S. H. Witt, A. Wright, P. P. Zandi, P. B. Mitchell, M. Bauer, M. Alda, M. Rietschel, F. J. McMahon, T. G. Schulze, S. R. Clark, and B. T. Baune (2023). "Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder." Mol. Psychiatry 28: 5251–5261. doi.org/10.1038/s41380-023-02149-1.

David, F. S., F. Stein, T. F. M. Andlauer, F. Streit, S. H. Witt, S. Herms, P. Hoffmann, S. Heilmann-Heimbach, N. Opel, J. Repple, A. Jansen, I. Nenadić, S. Papiol, U. Heilbronner, J. L. Kalman, S. K. Schaupp, F. Senner, E. C. Schulte, P. G. Falkai, T. G. Schulze, U. Dannlowski, T. Kircher, M. Rietschel, M. M. Nöthen, A. Krug, and A. J. Forstner (2023). "Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders." Schizophrenia Research 252: 161–171. doi.org/10.1016/j.schres.2023.01.002.

Foo, J. C., S. Redler, A. J. Forstner, F. B. Basmanav, L. Pethukova, J. Guo, F. Streit, S. H. Witt, L. Sirignano, L. Zillich, S. Awasthi, S. Ripke, A. M. Christiano, F. Tesch, J. Schmitt, M. M. Nöthen, R. C. Betz, M. Rietschel, and J. Frank (2023). "Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives." J. Eur. Acad. Dermatol. Venereol. 37(8): 1547–1555. doi.org/10.1111/jdv.18921.

Tantchik, W., M. J. Green, Y. Quidé, S. Erk, S. Mohnke, C. Wackerhagen, N. Romanczuk-Seiferth, H. Tost, K. Schwarz, C. Moessnang, D. Bzdok, A. Meyer-Lindenberg, A. Heinz, and H. Walter (2023). "Investigating the neural correlates of affective mentalizing and their association with general intelligence in patients with schizophrenia." Schizophrenia Research 254: 190–198. doi.org/10.1016/j.schres.2023.02.004.

Wen, J., A. Zellner, N. C. Braun, T. Bajaj, N. C. Gassen, M. Peitz, and O. Brüstle (2023). "Loss of function of FIP200 in human pluripotent stem cell-derived neurons leads to axonal pathology and hyperactivity - Translational Psychiatry." Transl Psychiatry 13(143): 1–11. doi.org/10.1038/s41398-023-02432-3.

2022

Caramaschi, D., A. Neumann, A. Cardenas, G. Tindula, S. Alemany, L. Zillich, G. Pesce, J. M. T. Lahti, A. Havdahl, R. Mulder, J. F. Felix, H. Tiemeier, L. Sirignano, J. Frank, S. H. Witt, M. Rietschel, M. Deuschle, K. Huen, B. Eskenazi, T. S. Send, M. Ferrer, M. Gilles, M. de Agostini, N. Baïz, S. L. Rifas-Shiman, T. Kvist, D. Czamara, S. T. Tuominen, C. L. Relton, D. Rai, S. J. London, K. Räikkönen, N. Holland, I. Annesi-Maesano, F. Streit, M.-F. Hivert, E. Oken, J. Sunyer, C. A. M. Cecil, and G. Sharp (2022). "Meta-analysis of epigenome-wide associations between DNA methylation at birth and childhood cognitive skills." Molecular Psychiatry 27(4): 2126-2135. doi.org/10.1038/s41380-022-01441-w.

Cearns, M., A. T. Amare, K. O. Schubert, A. Thalamuthu, J. Frank, F. Streit, M. Adli, N. Akula, K. Akiyama, R. Ardau, B. Arias, J.-M. Aubry, L. Backlund, A. K. Bhattacharjee, F. Bellivier, A. Benabarre, S. Bengesser, J. M. Biernacka, A. Birner, C. Brichant-Petitjean, P. Cervantes, H.-C. Chen, C. Chillotti, S. Cichon, C. Cruceanu, P. M. Czerski, N. Dalkner, A. Dayer, F. Degenhardt, M. Del Zompo, J. R. DePaulo, B. Étain, P. Falkai, A. J. Forstner, L. Frisen, M. A. Frye, J. M. Fullerton, S. Gard, J. S. Garnham, F. S. Goes, M. Grigoroiu-Serbanescu, P. Grof, R. Hashimoto, J. Hauser, U. Heilbronner, S. Herms, P. Hoffmann, A. Hofmann, L. Hou, Y.-H. Hsu, S. Jamain, E. Jiménez, J.-P. Kahn, L. Kassem, P.-H. Kuo, T. Kato, J. Kelsoe, S. Kittel-Schneider, S. Kliwicki, B. König, I. Kusumi, G. Laje, M. Landén, C. Lavebratt, M. Leboyer, S. G. Leckband, M. Maj, t. M. D. D. W. G. o. t. P. G. Consortium, M. Manchia, L. Martinsson, M. J. McCarthy, S. McElroy, F. Colom, M. Mitjans, F. M. Mondimore, P. Monteleone, C. M. Nievergelt, M. M. Nöthen, T. Novák, C. O'Donovan, N. Ozaki, V. Millischer, S. Papiol, A. Pfennig, C. Pisanu, J. B. Potash, A. Reif, E. Reininghaus, G. A. Rouleau, J. K. Rybakowski, M. Schalling, P. R. Schofield, B. W. Schweizer, G. Severino, T. Shekhtman, P. D. Shilling, K. Shimoda, C. Simhandl, C. M. Slaney, A. Squassina, T. Stamm, P. Stopkova, F. Tekola-Ayele, A. Tortorella, G. Turecki, J. Veeh, E. Vieta, S. H. Witt, G. Roberts, P. P. Zandi, M. Alda, M. Bauer, F. J. McMahon, P. B. Mitchell, T. G. Schulze, M. Rietschel, S. R. Clark, and B. T. Baune (2022). "Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach." British Journal of Psychiatry 220(4): 219–228. doi.org/10.1192/bjp.2022.28.

Cortes Hidalgo, A. P., H. Tiemeier, S. A. Metcalf, M. Monninger, A. Meyer-Lindenberg, P.-M. Aggensteiner, M. J. Bakermans-Kranenburg, T. White, T. Banaschewski, M. H. van IJzendoorn, and N. E. Holz (2022). "No robust evidence for an interaction between early-life adversity and protective factors on global and regional brain volumes." Developmental Cognitive Neuroscience 58: 101166. doi.org/10.1016/j.dcn.2022.101166.

Effenberger, P. S., T. S. Send, M. Gilles, I. A. C. Wolf, J. Frank, S. Bongard, R. Kumsta, S. H. Witt, M. Rietschel, M. Deuschle, and F. Streit (2022). "Urbanicity, behavior problems and HPA axis regulation in preschoolers." Psychoneuroendocrinology 137: 105660. www.ncbi.nlm.nih.gov/pubmed/35033927.

Holz, N. E., D. L. Floris, A. Llera, P. M. Aggensteiner, S. M. Kia, T. Wolfers, S. Baumeister, B. Böttinger, J. C. Glennon, P. J. Hoekstra, A. Dietrich, M. C. Saam, U. M. E. Schulze, D. J. Lythgoe, S. C. R. Williams, P. Santosh, M. Rosa-Justicia, N. Bargallo, J. Castro-Fornieles, C. Arango, M. J. Penzol, S. Walitza, A. Meyer-Lindenberg, M. Zwiers, B. Franke, J. Buitelaar, J. Naaijen, D. Brandeis, C. Beckmann, T. Banaschewski, and A. F. Marquand (2022). "Age-related brain deviations and aggression." Psychological Medicine: 1-10. doi.org/10.1017/S003329172200068X.

Kalman, J. L., S. Papiol, M. Grigoroiu-Serbanescu, K. Adorjan, H. Anderson-Schmidt, K. Brosch, M. Budde, A. L. Comes, K. Gade, A. Forstner, D. Grotegerd, T. Hahn, M. Heilbronner, U. Heilbronner, S. Heilmann-Heimbach, F. Klohn-Saghatolislam, M. O. Kohshour, S. Meinert, T. Meller, N. Mullins, I. Nenadic, M. M. Nothen, J. K. Pfarr, D. Reich-Erkelenz, M. Rietschel, K. G. Ringwald, S. Schaupp, E. C. Schulte, F. Senner, F. Stein, F. Streit, T. Vogl, P. Falkai, U. Dannlowski, T. Kircher, T. G. Schulze, and T. F. M. Andlauer (2022). "Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients." J Affect Disord 296: 532-540. doi.org/10.1016/j.jad.2021.09.073.

Meyer-Lindenberg, A., and D. Hirjak (2022). "Schizophrenia as a categorical diagnosis: A view from the neural risk architecture." Schizophrenia Research 242: 87-90. doi.org/10.1016/j.schres.2022.01.021.

Meyer-Lindenberg, H., C. Moessnang, B. Oakley, J. Ahmad, L. Mason, E. J. H. Jones, H. L. Hayward, J. Cooke, D. Crawley, R. Holt, J. Tillmann, T. Charman, S. Baron-Cohen, T. Banaschewski, C. Beckmann, H. Tost, A. Meyer-Lindenberg, J. K. Buitelaar, D. G. Murphy, M. J. Brammer, and E. Loth (2022). "Facial expression recognition is linked to clinical and neurofunctional differences in autism." Molecular Autism 13(1): 1–18. doi.org/10.1186/s13229-022-00520-7.

Michurina, A., M. S. Sakib, C. Kerimoglu, D. M. Krüger, L. Kaurani, M. R. Islam, P. D. Joshi, S. Schröder, T. P. Centeno, J. Zhou, R. Pradhan, J. Cha, X. Xu, G. Eichele, E. M. Zeisberg, A. Kranz, A. F. Stewart, and A. Fischer (2022). "Postnatal expression of the lysine methyltransferase SETD1B is essential for learning and the regulation of neuron-enriched genes." EMBO J 41(1): e106459. doi.org/10.15252/embj.2020106459.

Schulte, E. C., I. Kondofersky, M. Budde, S. Papiol, F. Senner, S. K. Schaupp, D. Reich-Erkelenz, F. Klöhn-Saghatolislam, J. L. Kalman, K. Gade, M. Hake, A. L. Comes, H. Anderson-Schmidt, K. Adorjan, G. Juckel, M. Schmauß, J. Zimmermann, J. Reimer, J. Wiltfang, E. Z. Reininghaus, I.-G. Anghelescu, C. Konrad, C. Figge, M. von Hagen, M. Jäger, D. E. Dietrich, C. Spitzer, S. H. Witt, A. J. Forstner, M. Rietschel, M. M. Nöthen, P. Falkai, U. Heilbronner, N. S. Mueller, and T. G. Schulze (2022). "A novel longitudinal clustering approach to psychopathology across diagnostic entities in the hospital-based PsyCourse study." Schizophrenia Research 244: 29–38. doi.org/10.1016/j.schres.2022.05.001.

Tielke, A., H. Martins, M. A. Pelzl, A. Maaser-Hecker, F. S. David, C. S. Reinbold, F. Streit, L. Sirignano, M. Schwarz, H. Vedder, J. Kammerer-Ciernioch, M. Albus, M. Borrmann-Hassenbach, M. Hautzinger, K. Hünten, F. Degenhardt, S. B. Fischer, E. C. Beins, S. Herms, P. Hoffmann, T. G. Schulze, S. H. Witt, M. Rietschel, S. Cichon, M. M. Nöthen, G. Schratt, and A. J. Forstner (2022). "Genetic and functional analyses implicate microRNA 499A in bipolar disorder development." Transl Psychiatry 12(437): 1–10. doi.org/10.1038/s41398-022-02176-6.

Wendel, B., M. Heidenreich, M. Budde, M. Heilbronner, M. Oraki Kohshour, S. Papiol, P. Falkai, T. G. Schulze, U. Heilbronner, and H. Bickeböller (2022). "Kalpra: A kernel approach for longitudinal pathway regression analysis integrating network information with an application to the longitudinal PsyCourse Study." Front Genet 13. doi.org/10.3389/fgene.2022.1015885.

2021

Andlauer, T. F. M., T. W. Mühleisen, F. Hoffstaedter, A. Teumer, K. Wittfeld, A. Teuber, C. S. Reinbold, D. Grotegerd, R. Bülow, S. Caspers, U. Dannlowski, S. Herms, P. Hoffmann, T. Kircher, H. Minnerup, S. Moebus, I. Nenadić, H. Teismann, U. Völker, A. Etkin, K. Berger, H. J. Grabe, M. M. Nöthen, K. Amunts, S. B. Eickhoff, P. G. Sämann, B. Müller-Myhsok, and S. Cichon (2021). "Genetic factors influencing a neurobiological substrate for psychiatric disorders." Translational Psychiatry 11(1): 192. doi.org/10.1038/s41398-021-01317-7.

Bopp, S. K., U. Heilbronner, P. Schlattmann, P. J. Buspavanich, U. E. Lang, A. Heinz, T. G. Schulze, M. Adli, T. W. Muhleisen, and R. Ricken (2021). "A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression." Eur Neuropsychopharmacol 53: 114-119. www.ncbi.nlm.nih.gov/pubmed/34653833.

Durstewitz, D., Q. J. M. Huys, and G. Koppe (2021). "Psychiatric Illnesses as Disorders of Network Dynamics." Biol Psychiatry Cogn Neurosci Neuroimaging 6(9): 865-876. www.ncbi.nlm.nih.gov/pubmed/32249208.

Effenberger, P. S., F. Streit, S. Bardtke, M. Gilles, I. A.-C. Wolf, A. Schröder, M. W. Sütterlin, S. H. Witt, M. Rietschel, M. Deuschle, and T. S. Send (2021). "Relationship Between Parental Big Five And Children’s Ability To Delay Gratification." J Child Fam Stud: 1–10. doi.org/10.1007/s10826-021-02196-8.

Garvert, L., B. T. Baune, K. Berger, D. I. Boomsma, G. Breen, A. Greinacher, S. P. Hamilton, D. F. Levinson, C. M. Lewis, S. Lucae, P. K. E. Magnusson, N. G. Martin, A. M. McIntosh, O. Mors, B. Muller-Myhsok, B. W. J. H. Penninx, R. H. Perlis, G. Pistis, J. B. Potash, M. Preisig, M. Rietschel, J. Shi, J. W. Smoller, H. Tiemeier, R. Uher, U. Völker, H. Völzke, M. Weissman, H. J. Grabe, and S. Van der Auwera (2021). "The Association between genetically determined ABO Blood Types and Major Depressive Disorder." Psychiatry Research: 113837. doi.org/10.1016/j.psychres.2021.113837.

Guzman-Parra, J., F. Streit, A. J. Forstner, J. Strohmaier, M. J. González, S. Gil Flores, F. J. Cabaleiro Fabeiro, F. del Río Noriega, F. Perez Perez, J. Haro González, G. Orozco Diaz, Y. de Diego-Otero, B. Moreno-Kustner, G. Auburger, F. Degenhardt, S. Heilmann-Heimbach, S. Herms, P. Hoffmann, J. Frank, J. C. Foo, L. Sirignano, S. H. Witt, S. Cichon, F. Rivas, F. Mayoral, M. M. Nöthen, T. F. M. Andlauer, and M. Rietschel (2021). "Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families." Transl Psychiatry 11(31): 1–10. doi.org/10.1038/s41398-020-01146-0.

Heilbronner, U., S. Papiol, M. Budde, T. F. M. Andlauer, J. Strohmaier, F. Streit, J. Frank, F. Degenhardt, S. Heilmann-Heimbach, S. H. Witt, A. J. Forstner, A. Loerbroks, M. Amelang, T. Sturmer, B. Mueller-Myhsok, M. M. Noethen, M. Rietschel, and T. G. Schulze (2021). ""The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment." American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 186(2): 77-89. onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajmg.b.32837.

Heilbronner, U., F. Streit, T. Vogl, F. Senner, S. K. Schaupp, D. Reich-Erkelenz, S. Papiol, M. O. Kohshour, F. Klöhn-Saghatolislam, J. L. Kalman, M. Heilbronner, K. Gade, A. L. Comes, M. Budde, T. F. M. Andlauer, H. Anderson-Schmidt, K. Adorjan, T. Stürmer, A. Loerbroks, M. Amelang, E. Poisel, J. Foo, S. Heilmann-Heimbach, A. J. Forstner, F. Degenhardt, J. Zimmermann, J. Wiltfang, M. von Hagen, C. Spitzer, M. Schmauss, E. Reininghaus, J. Reimer, C. Konrad, G. Juckel, F. U. Lang, M. Jäger, C. Figge, A. J. Fallgatter, D. E. Dietrich, U. Dannlowski, B. T. Baune, V. Arolt, I.-G. Anghelescu, M. M. Nöthen, S. H. Witt, O. A. Andreassen, C.-H. Chen, P. Falkai, M. Rietschel, T. G. Schulze, and E. C. Schulte (2021). "Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection." BJPsych Open 7(6). doi.org/10.1192/bjo.2021.1030.

Islam, M. R., L. Kaurani, T. Berulava, U. Heilbronner, M. Budde, T. P. Centeno, V. Elerdashvili, M. P. Zafieriou, E. Benito, S. M. Sertel, M. Goldberg, F. Senner, J. L. Kalman, S. Burkhardt, A. S. Oepen, M. S. Sakib, C. Kerimolgu, O. Wirths, H. Bickeboller, C. Bartels, F. Brosseron, K. Buerger, N. C. Cosma, K. Fliessbach, M. T. Heneka, D. Janowitz, I. Kilimann, L. Kleinedam, C. Laske, C. D. Metzger, M. H. Munk, R. Perneczky, O. Peters, J. Priller, B. S. Rauchmann, N. Roy, A. Schneider, A. Spottke, E. J. Spruth, S. Teipel, M. Tscheuschler, M. Wagner, J. Wiltfang, E. Duzel, F. Jessen, G. Delcode Study, S. O. Rizzoli, W. H. Zimmermann, T. G. Schulze, P. Falkai, F. Sananbenesi, and A. Fischer (2021). "A microRNA signature that correlates with cognition and is a target against cognitive decline." EMBO Mol Med: e13659. www.ncbi.nlm.nih.gov/pubmed/34633146.

Klockmeier, K., E. Silva Ramos, T. Rasko, A. Marti Pastor, and E. E. Wanker (2021). "Schizophrenia risk candidate protein ZNF804A interacts with STAT2 and influences interferon-mediated gene transcription in mammalian cells." J Mol Biol 433(19): 167184. www.ncbi.nlm.nih.gov/pubmed/34364876.

Le Clerc, S., L. Lombardi, B. T. Baune, A. T. Amare, K. O. Schubert, L. Hou, S. R. Clark, S. Papiol, M. Cearns, U. Heilbronner, F. Degenhardt, F. Tekola-Ayele, Y. H. Hsu, T. Shekhtman, M. Adli, N. Akula, K. Akiyama, R. Ardau, B. Arias, J. M. Aubry, L. Backlund, A. K. Bhattacharjee, F. Bellivier, A. Benabarre, S. Bengesser, J. M. Biernacka, A. Birner, C. Brichant-Petitjean, P. Cervantes, H. C. Chen, C. Chillotti, S. Cichon, C. Cruceanu, P. M. Czerski, N. Dalkner, A. Dayer, M. Del Zompo, J. R. DePaulo, B. Etain, S. Jamain, P. Falkai, A. J. Forstner, L. Frisen, M. A. Frye, J. M. Fullerton, S. Gard, J. S. Garnham, F. S. Goes, M. Grigoroiu-Serbanescu, P. Grof, R. Hashimoto, J. Hauser, S. Herms, P. Hoffmann, E. Jimenez, J. P. Kahn, L. Kassem, P. H. Kuo, T. Kato, J. R. Kelsoe, S. Kittel-Schneider, E. Ferensztajn-Rochowiak, B. Konig, I. Kusumi, G. Laje, M. Landen, C. Lavebratt, S. G. Leckband, A. Tortorella, M. Manchia, L. Martinsson, M. J. McCarthy, S. L. McElroy, F. Colom, V. Millischer, M. Mitjans, F. M. Mondimore, P. Monteleone, C. M. Nievergelt, M. M. Nothen, T. Novak, C. O'Donovan, N. Ozaki, U. Osby, A. Pfennig, J. B. Potash, A. Reif, E. Reininghaus, G. A. Rouleau, J. K. Rybakowski, M. Schalling, P. R. Schofield, B. W. Schweizer, G. Severino, P. D. Shilling, K. Shimoda, C. Simhandl, C. M. Slaney, C. Pisanu, A. Squassina, T. Stamm, P. Stopkova, M. Maj, G. Turecki, E. Vieta, J. Veeh, S. H. Witt, A. Wright, P. P. Zandi, P. B. Mitchell, M. Bauer, M. Alda, M. Rietschel, F. J. McMahon, T. G. Schulze, J. L. Spadoni, W. Boukouaci, J. R. Richard, P. Le Corvoisier, C. Barrau, J. F. Zagury, M. Leboyer, and R. Tamouza (2021). "HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders." Sci Rep 11(1): 17823. www.ncbi.nlm.nih.gov/pubmed/34497278.

Polushina, T., N. Banerjee, S. Giddaluru, F. Bettella, T. Espeseth, A. J. Lundervold, S. Djurovic, S. Cichon, P. Hoffmann, M. M. Nothen, V. M. Steen, O. A. Andreassen, and S. Le Hellard (2021). "Identification of pleiotropy at the gene level between psychiatric disorders and related traits." Transl Psychiatry 11(1): 410. www.ncbi.nlm.nih.gov/pubmed/34326310.

Reichert, M., G. Gan, M. Renz, U. Braun, S. Brüßler, I. Timm, R. Ma, O. Berhe, A. Benedyk, A. Moldavski, J. I. Schweiger, O. Hennig, F. Zidda, C. Heim, T. Banaschewski, H. Tost, U. W. Ebner-Priemer, and A. Meyer-Lindenberg (2021). "Ambulatory assessment for precision psychiatry: Foundations, current developments and future avenues." Experimental Neurology 345: 113807. doi.org/10.1016/j.expneurol.2021.113807.

Schmitt, S., T. Meller, F. Stein, K. Brosch, K. Ringwald, J.-K. Pfarr, C. Bordin, N. Peusch, O. Steinsträter, D. Grotegerd, K. Dohm, S. Meinert, K. Förster, R. Redlich, N. Opel, T. Hahn, A. Jansen, A. J. Forstner, F. Streit, S. H. Witt, M. Rietschel, B. Müller-Myhsok, M. M. Nöthen, U. Dannlowski, A. Krug, T. Kircher, and I. Nenadić (2021). "Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity." Psychol. Med.: 1–12. doi.org/10.1017/S0033291721001082.

Schweiger, J. I., N. Capraz, C. Akdeniz, U. Braun, T. Ebalu, C. Moessnang, O. Berhe, Z. Zang, E. Schwarz, E. Bilek, A. Meyer-Lindenberg, and H. Tost (2021). "Brain structural correlates of upward social mobility in ethnic minority individuals." Soc Psychiatry Psychiatr Epidemiol: 1–11. www.ncbi.nlm.nih.gov/pubmed/34383084.

Secker, C., S. Kostova, H. Niederlechner, S. Beetz, I. Wendland, M. J. Liebich, O. Polzer, M. Groh, S. Schnoegl, P. Trepte, and E. E. Wanker (2021). "CellFIE: CRISPR- and Cell Fusion-based Two-hybrid Interaction Mapping of Endogenous Proteins." J Mol Biol 433(24): 167305. doi.org/10.1016/j.jmb.2021.167305.

Sirignano, L., J. Frank, L. Kranaster, S. H. Witt, F. Streit, L. Zillich, A. Sartorius, M. Rietschel, and J. C. Foo (2021). "Methylome-wide change associated with response to electroconvulsive therapy in depressed patients - Translational Psychiatry." Transl Psychiatry 11(347): 1–9. doi.org/10.1038/s41398-021-01474-9.

Smigielski, L., S. Papiol, A. Theodoridou, K. Heekeren, M. Gerstenberg, D. Wotruba, R. Buechler, P. Hoffmann, S. Herms, K. Adorjan, H. Anderson-Schmidt, M. Budde, A. L. Comes, K. Gade, M. Heilbronner, U. Heilbronner, J. L. Kalman, F. Klöhn-Saghatolislam, D. Reich-Erkelenz, S. K. Schaupp, E. C. Schulte, F. Senner, I.-G. Anghelescu, V. Arolt, B. T. Baune, U. Dannlowski, D. E. Dietrich, A. J. Fallgatter, C. Figge, M. Jäger, G. Juckel, C. Konrad, V. Nieratschker, J. Reimer, E. Reininghaus, M. Schmauß, C. Spitzer, M. von Hagen, J. Wiltfang, J. Zimmermann, A. Gryaznova, L. Flatau-Nagel, M. Reitt, M. Meyers, B. Emons, I. S. Haußleiter, F. U. Lang, T. Becker, M. E. Wigand, S. H. Witt, F. Degenhardt, A. J. Forstner, M. Rietschel, M. M. Nöthen, T. F. M. Andlauer, W. Rössler, S. Walitza, P. Falkai, T. G. Schulze, and E. Grünblatt (2021). "Polygenic risk scores across the extended psychosis spectrum." Transl Psychiatry 11(600): 1–11. doi.org/10.1038/s41398-021-01720-0.

Tüngler, A., S. Van der Auwera, K. Wittfeld, S. Frenzel, J. Terock, N. Röder, G. Homuth, H. Völzke, R. Bülow, H. J. Grabe, and D. Janowitz (2021). "Body mass index but not genetic risk is longitudinally associated with altered structural brain parameters." Sci Rep 11(24246): 1–11. doi.org/10.1038/s41598-021-03343-3.

Van der Auwera, S., S. Ameling, M. Nauck, H. Völzke, U. Völker, and H. J. Grabe (2021). "Association between different dimensions of childhood traumatization and plasma micro-RNA levels in a clinical psychiatric sample." Journal of Psychiatric Research 139: 113–119. doi.org/10.1016/j.jpsychires.2021.05.023.

Van der Auwera, S., L. Garvert, G. Fuellen, M. Nauck, H. Völzke, U. Völker, and H. J. Grabe (2021). "The genetic predisposition to longevity acts through behavioral phenotypes in females." Eur. Neuropsychopharmacol. 45: 1–14. doi.org/10.1016/j.euroneuro.2021.02.014.

Wendel, B., S. Papiol, T. F. M. Andlauer, J. Zimmermann, J. Wiltfang, C. Spitzer, F. Senner, E. C. Schulte, M. Schmauss, S. K. Schaupp, J. Repple, E. Reininghaus, J. Reimer, D. Reich-Erkelenz, N. Opel, I. Nenadic, S. Meinert, C. Konrad, F. Klohn-Saghatolislam, T. Kircher, J. L. Kalman, G. Juckel, A. Jansen, M. Jager, M. Heilbronner, M. von Hagen, K. Gade, C. Figge, A. J. Fallgatter, D. E. Dietrich, U. Dannlowski, A. L. Comes, M. Budde, B. T. Baune, V. Arolt, I. G. Anghelescu, H. Anderson-Schmidt, K. Adorjan, P. Falkai, T. G. Schulze, H. Bickeboller, and U. Heilbronner (2021). "A genome-wide association study of the longitudinal course of executive functions." Transl Psychiatry 11(1): 386. www.ncbi.nlm.nih.gov/pubmed/34247186.

Zhang, X., U. Braun, A. Harneit, Z. Zang, L. S. Geiger, R. F. Betzel, J. Chen, J. I. Schweiger, K. Schwarz, J. R. Reinwald, S. Fritze, S. Witt, M. Rietschel, M. M. Nöthen, F. Degenhardt, E. Schwarz, D. Hirjak, A. Meyer-Lindenberg, D. S. Bassett, and H. Tost (2021). "Generative network models of altered structural brain connectivity in schizophrenia." NeuroImage 225: 117510. doi.org/10.1016/j.neuroimage.2020.117510.

2020

Amare, A. T., Schubert, K.O., Hou, L. et al. (2020). "Association of polygenic score for major depression with response to lithium in patients with bipolar disorder." Mol Psychiatry 20. doi.org/10.1038/s41380-020-0689-5.

Andlauer, T. F. M., J. Link, D. Martin, M. Ryner, C. Hermanrud, V. Grummel, M. Auer, H. Hegen, L. Aly, C. Gasperi, B. Knier, B. Müller-Myhsok, P. E. H. Jensen, F. Sellebjerg, I. Kockum, T. Olsson, M. Pallardy, S. Spindeldreher, F. Deisenhammer, A. Fogdell-Hahn, and B. Hemmer (2020). "Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS." BMC Med 18(1): 1–23. doi.org/10.1186/s12916-020-01769-6.

Arloth, J., G. Eraslan, T. F. M. Andlauer, J. Martins, S. Iurato, B. Kühnel, M. Waldenberger, J. Frank, R. Gold, B. Hemmer, F. Luessi, S. Nischwitz, F. Paul, H. Wiendl, C. Gieger, S. Heilmann-Heimbach, T. Kacprowski, M. Laudes, T. Meitinger, A. Peters, R. Rawal, K. Strauch, S. Lucae, B. Müller-Myhsok, M. Rietschel, F. J. Theis, E. B. Binder, and N. S. Mueller (2020). "DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning." PLoS Comput Biol 16(2): e1007616. doi.org/10.1371/journal.pcbi.1007616.

Berulava, T., E. Buchholz, V. Elerdashvili, T. Pena, M. R. Islam, D. Lbik, B. A. Mohamed, A. Renner, D. von Lewinski, M. Sacherer, K. E. Bohnsack, M. T. Bohnsack, G. Jain, V. Capece, N. Cleve, S. Burkhardt, G. Hasenfuss, A. Fischer, and K. Toischer (2020). "Changes in m6A RNA methylation contribute to heart failure progression by modulating translation." Eur J Heart Fail 22(1): 54-56. doi.org/10.1002/ejhf.1672.

Bonk, S., J. Hertel, H. U. Zacharias, J. Terock, D. Janowitz, G. Homuth, M. Nauck, H. Völzke, H. Meyer zu Schwabedissen, S. Van der Auwera, and H. J. Grabe (2020). "Vitamin D moderates the interaction between 5-HTTLPR and childhood abuse in depressive disorders." Sci Rep 10(22394): 1–9. doi.org/10.1038/s41598-020-79388-7.

Bousman, C. A., S. A. Bengesser, K. J. Aitchison, A. T. Amare, H. Aschauer, B. T. Baune, B. B. Asl, J. R. Bishop, M. Burmeister, B. Chaumette, L.-S. Chen, Z. A. Cordner, J. Deckert, F. Degenhardt, L. E. DeLisi, L. Folkersen, J. L. Kennedy, T. E. Klein, J. L. McClay, F. J. McMahon, R. Musil, N. L. Saccone, K. Sangkuhl, R. M. Stowe, E.-C. Tan, A. K. Tiwari, C. C. Zai, G. Zai, J. Zhang, A. Gaedigk, and D. J. Müller (2020). "Review and Consensus on Pharmacogenomic Testing in Psychiatry." Pharmacopsychiatry. doi.org/10.1055/a-1288-1061.

Ching, C. R. K., D. P. Hibar, T. P. Gurholt, A. Nunes, S. I. Thomopoulos, C. Abe, I. Agartz, R. M. Brouwer, D. M. Cannon, S. M. C. de Zwarte, L. T. Eyler, P. Favre, T. Hajek, U. K. Haukvik, J. Houenou, M. Landen, T. A. Lett, C. McDonald, L. Nabulsi, Y. Patel, M. E. Pauling, T. Paus, J. Radua, M. G. Soeiro-de-Souza, G. Tronchin, N. E. M. van Haren, E. Vieta, H. Walter, L. L. Zeng, M. Alda, J. Almeida, D. Alnaes, S. Alonso-Lana, C. Altimus, M. Bauer, B. T. Baune, C. E. Bearden, M. Bellani, F. Benedetti, M. Berk, A. C. Bilderbeck, H. P. Blumberg, E. Boen, I. Bollettini, C. Del Mar Bonnin, P. Brambilla, E. J. Canales-Rodriguez, X. Caseras, O. Dandash, U. Dannlowski, G. Delvecchio, A. M. Diaz-Zuluaga, D. Dima, E. Duchesnay, T. Elvsashagen, S. C. Fears, S. Frangou, J. M. Fullerton, D. C. Glahn, J. M. Goikolea, M. J. Green, D. Grotegerd, O. Gruber, B. C. M. Haarman, C. Henry, F. M. Howells, V. Ives-Deliperi, A. Jansen, T. T. J. Kircher, C. Knochel, B. Kramer, B. Lafer, C. Lopez-Jaramillo, R. Machado-Vieira, B. J. MacIntosh, E. M. T. Melloni, P. B. Mitchell, I. Nenadic, F. Nery, A. C. Nugent, V. Oertel, R. A. Ophoff, M. Ota, B. J. Overs, D. L. Pham, M. L. Phillips, J. A. Pineda-Zapata, S. Poletti, M. Polosan, E. Pomarol-Clotet, A. Pouchon, Y. Quide, M. M. Rive, G. Roberts, H. G. Ruhe, R. Salvador, S. Sarro, T. D. Satterthwaite, A. H. Schene, K. Sim, J. C. Soares, M. Stablein, D. J. Stein, C. K. Tamnes, G. V. Thomaidis, C. V. Upegui, D. J. Veltman, M. Wessa, L. T. Westlye, H. C. Whalley, D. H. Wolf, M. J. Wu, L. N. Yatham, C. A. Zarate, P. M. Thompson, O. A. Andreassen, and E. B. D. W. Group (2020). "What we learn about bipolar disorder from large-scale neuroimaging: Findings and future directions from the ENIGMA Bipolar Disorder Working Group." Hum Brain Mapp. doi.org/10.1371/journal.pcbi.1007616.

Coleman, J. R. I., H. A. Gaspar, J. Bryois, E. M. Byrne, A. J. Forstner, P. A. Holmans, C. A. de Leeuw, M. Mattheisen, A. McQuillin, J. M. Whitehead Pavlides, T. H. Pers, S. Ripke, E. A. Stahl, S. Steinberg, V. Trubetskoy, M. Trzaskowski, Y. Wang, P. G. Consortium, and G. Breen (2020). "The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls." Biol Psychiatry 88(2): 169–184. doi.org/10.1016/j.biopsych.2019.10.015.

Comes, A. L., D. Czamara, K. Adorjan, H. Anderson-Schmidt, T. F. M. Andlauer, M. Budde, K. Gade, M. Hake, J. L. Kalman, S. Papiol, D. Reich-Erkelenz, F. Klöhn-Saghatolislam, S. K. Schaupp, E. C. Schulte, F. Senner, G. Juckel, M. Schmauß, J. Zimmermann, J. Reimer, E. Reininghaus, I.-G. Anghelescu, C. Konrad, A. Thiel, C. Figge, M. von Hagen, M. Koller, D. E. Dietrich, S. Stierl, H. Scherk, S. H. Witt, S. Sivalingam, F. Degenhardt, A. J. Forstner, M. Rietschel, M. M. Nöthen, J. Wiltfang, P. Falkai, T. G. Schulze, and U. Heilbronner (2020). "The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorder." Int J Bipolar Disord 8(1): 1--12. doi.org/10.1186/s40345-019-0176-6.

de Zwarte, S. M. C., R. M. Brouwer, I. Agartz, M. Alda, S. Alonso-Lana, C. E. Bearden, A. Bertolino, A. Bonvino, E. Bramon, E. E. L. Buimer, W. Cahn, E. J. Canales-Rodríguez, D. M. Cannon, T. D. Cannon, X. Caseras, J. Castro-Fornieles, Q. Chen, Y. Chung, E. De la Serna, C. del Mar Bonnin, C. Demro, A. Di Giorgio, G. E. Doucet, M. C. Eker, S. Erk, M. Fatjó-Vilas, S. C. Fears, S. F. Foley, S. Frangou, J. M. Fullerton, D. C. Glahn, V. M. Goghari, J. M. Goikolea, A. L. Goldman, A. S. Gonul, O. Gruber, T. Hajek, E. L. Hawkins, A. Heinz, C. H. Ongun, M. H. J. Hillegers, J. Houenou, H. E. H. Pol, C. M. Hultman, M. Ingvar, V. Johansson, E. G. Jönsson, F. Kane, M. J. Kempton, M. M. G. Koenis, M. Kopecek, B. Krämer, S. M. Lawrie, R. K. Lenroot, M. Marcelis, V. S. Mattay, C. McDonald, A. Meyer-Lindenberg, S. Michielse, P. B. Mitchell, D. Moreno, R. M. Murray, B. Mwangi, L. Nabulsi, J. Newport, C. A. Olman, J. van Os, B. J. Overs, A. Ozerdem, G. Pergola, M. M. Picchioni, C. Piguet, E. Pomarol-Clotet, J. Radua, I. S. Ramsay, A. Richter, G. Roberts, R. Salvador, A. S. Aydogan, S. Sarró, P. R. Schofield, E. M. Simsek, F. Simsek, J. C. Soares, S. R. Sponheim, G. Sugranyes, T. Toulopoulou, G. Tronchin, E. Vieta, H. Walter, D. R. Weinberger, H. C. Whalley, M.-J. Wu, N. Yalin, O. A. Andreassen, C. R. K. Ching, S. I. Thomopoulos, T. G. M. van Erp, N. Jahanshad, P. M. Thompson, R. S. Kahn, and N. E. M. van Haren (2020). "Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder." Hum Brain Mapp n/a(n/a). doi.org/10.1002/hbm.25206.

Dwyer, D. B., J. L. Kalman, M. Budde, J. Kambeitz, A. Ruef, L. A. Antonucci, L. Kambeitz-Ilankovic, A. Hasan, I. Kondofersky, H. Anderson-Schmidt, K. Gade, D. Reich-Erkelenz, K. Adorjan, F. Senner, S. Schaupp, T. F. M. Andlauer, A. L. Comes, E. C. Schulte, F. Klöhn-Saghatolislam, A. Gryaznova, M. Hake, K. Bartholdi, L. Flatau-Nagel, M. Reitt, S. Quast, S. Stegmaier, M. Meyers, B. Emons, I. S. Haußleiter, G. Juckel, V. Nieratschker, U. Dannlowski, T. Yoshida, M. Schmauß, J. Zimmermann, J. Reimer, J. Wiltfang, E. Reininghaus, I.-G. Anghelescu, V. Arolt, B. T. Baune, C. Konrad, A. Thiel, A. J. Fallgatter, C. Figge, M. von Hagen, M. Koller, F. U. Lang, M. E. Wigand, T. Becker, M. Jäger, D. E. Dietrich, H. Scherk, C. Spitzer, H. Folkerts, S. H. Witt, F. Degenhardt, A. J. Forstner, M. Rietschel, M. M. Nöthen, N. Mueller, S. Papiol, U. Heilbronner, P. Falkai, T. G. Schulze, and N. Koutsouleris (2020). "An Investigation of Psychosis Subgroups With Prognostic Validation and Exploration of Genetic Underpinnings The PsyCourse Study." JAMA PSYCHIATRY 77(5): 523–533. doi.org/10.1001/jamapsychiatry.2019.4910.

Faber, H., D. Kurtoic, G. Krishnamoorthy, P. Weber, B. Pütz, B. Müller-Myhsok, F. Weber, and T. F. M. Andlauer (2020). "Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes." Front Immunol 11. doi.org/10.3389/fimmu.2020.02165.

Foo, J. C., L. Sirignano, N. Trautmann, J. Kim, S. H. Witt, F. Streit, J. Frank, L. Zillich, A. Meyer-Lindenberg, U. Ebner-Priemer, C. Schilling, M. Schredl, Y. Yamamoto, M. Gilles, M. Deuschle, and M. Rietschel (2020). "Association of Locomotor Activity During Sleep Deprivation Treatment With Response." Front Psychiatry 11(688). doi.org/10.3389/fpsyt.2020.00688.

Forstner, A. J., S. B. Fischer, L. M. Schenk, J. Strohmaier, A. Maaser-Hecker, C. S. Reinbold, S. Sivalingam, J. Hecker, F. Streit, F. Degenhardt, S. H. Witt, J. Schumacher, H. Thiele, P. Nürnberg, J. Guzman-Parra, G. O. Diaz, G. Auburger, M. Albus, M. Borrmann-Hassenbach, M. J. González, S. G. Flores, F. J. C. Fabeiro, F. del Río Noriega, F. P. Perez, J. H. González, F. Rivas, F. Mayoral, M. Bauer, A. Pfennig, A. Reif, S. Herms, P. Hoffmann, M. Pirooznia, F. S. Goes, M. Rietschel, M. M. Nöthen, and S. Cichon (2020). "Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families." Transl Psychiatry 10(1): 1--10. doi.org/10.1038/s41398-020-0732-y.

Grasby, K. L., N. Jahanshad, J. N. Painter, L. Colodro-Conde, J. Bralten, D. P. Hibar, P. A. Lind, F. Pizzagalli, C. R. K. Ching, M. A. B. McMahon, N. Shatokhina, L. C. P. Zsembik, S. I. Thomopoulos, A. H. Zhu, L. T. Strike, I. Agartz, S. Alhusaini, M. A. A. Almeida, D. Alnæs, I. K. Amlien, M. Andersson, T. Ard, N. J. Armstrong, A. Ashley-Koch, J. R. Atkins, M. Bernard, R. M. Brouwer, E. E. L. Buimer, R. Bülow, C. Bürger, D. M. Cannon, M. Chakravarty, Q. Chen, J. W. Cheung, B. Couvy-Duchesne, A. M. Dale, S. Dalvie, T. K. de Araujo, G. I. de Zubicaray, S. M. C. de Zwarte, A. Den Braber, N. T. Doan, K. Dohm, S. Ehrlich, H.-R. Engelbrecht, S. Erk, C. C. Fan, I. O. Fedko, S. F. Foley, J. M. Ford, M. Fukunaga, M. E. Garrett, T. Ge, S. Giddaluru, A. L. Goldman, M. J. Green, N. A. Groenewold, D. Grotegerd, T. P. Gurholt, B. A. Gutman, N. K. Hansell, M. A. Harris, M. B. Harrison, C. C. Haswell, M. Hauser, S. Herms, D. J. Heslenfeld, N. F. Ho, D. Hoehn, P. Hoffmann, L. Holleran, M. 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Haenig, C., N. Atias, A. K. Taylor, A. Mazza, M. H. Schaefer, J. Russ, S.-P. Riechers, S. Jain, M. Coughlin, J.-F. Fontaine, B. D. Freibaum, L. Brusendorf, M. Zenkner, P. Porras, M. Stroedicke, S. Schnoegl, K. Arnsburg, A. Boeddrich, L. Pigazzini, P. Heutink, J. P. Taylor, J. Kirstein, M. A. Andrade-Navarro, R. Sharan, and E. E. Wanker (2020). "Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains." Cell Reports 32(7): 108050. doi.org/10.1016/j.celrep.2020.108050.

Hagenaars, S. P., J. R. I. Coleman, S. W. Choi, H. Gaspar, M. J. Adams, D. M. Howard, K. Hodgson, M. Traylor, T. M. Air, T. F. M. Andlauer, V. Arolt, B. T. Baune, E. B. Binder, D. H. R. Blackwood, D. I. Boomsma, A. Campbell, M. Cearns, D. Czamara, U. Dannlowski, K. Domschke, E. J. C. de Geus, S. P. Hamilton, C. Hayward, I. B. Hickie, J. J. Hottenga, M. Ising, I. Jones, L. Jones, Z. Kutalik, S. Lucae, N. G. Martin, Y. Milaneschi, B. Mueller-Myhsok, M. J. Owen, S. Padmanabhan, B. W. J. H. Penninx, G. Pistis, D. J. Porteous, M. Preisig, S. Ripke, S. I. Shyn, P. F. Sullivan, J. B. Whitfield, N. R. Wray, A. M. McIntosh, I. J. Deary, G. Breen, and C. M. Lewis (2020). "Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression." Am J Med Genet n/a(n/a). doi.org/10.1002/ajmg.b.32807.

Holz, N. E., H. Tost, and A. Meyer-Lindenberg (2020). "Resilience and the brain: a key role for regulatory circuits linked to social stress and support." Molecular Psychiatry 25(2): 379-396. www.ncbi.nlm.nih.gov/pubmed/31628419.

Moessnang, C., S. Baumeister, J. Tillmann, D. Goyard, T. Charman, S. Ambrosino, S. Baron-Cohen, C. Beckmann, S. Bölte, C. Bours, D. Crawley, F. Dell’Acqua, S. Durston, C. Ecker, V. Frouin, H. Hayward, R. Holt, M. Johnson, E. Jones, M.-C. Lai, M. V. Lombardo, L. Mason, M. Oldenhinkel, A. Persico, A. S. J. Cáceres, W. Spooren, E. Loth, D. G. M. Murphy, J. K. Buitelaar, T. Banaschewski, D. Brandeis, H. Tost, and A. Meyer-Lindenberg (2020). "Social brain activation during mentalizing in a large autism cohort: the Longitudinal European Autism Project." Molecular Autism 11(1): 1--17. link.springer.com/article/10.1186/s13229-020-0317-x.

Reichert, M., U. Braun, G. Gan, I. Reinhard, M. Giurgiu, R. Ma, Z. X. Zang, O. Hennig, E. D. Koch, L. Wieland, J. Schweiger, D. Inta, A. Hoell, C. Akdeniz, A. Zipf, U. W. Ebner-Priemer, H. Tost, and A. Meyer-Lindenberg (2020). "A neural mechanism for affective well-being: Subgenual cingulate cortex mediates real-life effects of nonexercise activity on energy." Science Advances 6(45): 10. doi.org/10.1126/sciadv.aaz8934.

Schulze, L. N., J. Klinger-König, S. Stolzenburg, J. Wiese, S. Speerforck, S. Van der Auwera-Palitschka, H. Völzke, H. J. Grabe, and G. Schomerus (2020). "Shame, self-identification with having a mental illness, and willingness to seek help in northeast Germany." Psychiatry Research 285: 112819. www.sciencedirect.com/science/article/pii/S0165178119320888.

Schwarz, K., C. Moessnang, J. Schweiger, S. Baumeister, M. M. Plichta, D. Brandeis, T. Banaschewski, C. Wackerhagen, S. Erk, H. Walter, H. Tost, and A. Meyer-Lindenberg (2020). "Transdiagnostic Prediction of Affective, Cognitive, and Social Function Through Brain Reward Anticipation in Schizophrenia, Bipolar Disorder, Major Depression, and Autism Spectrum Diagnoses." SCHIZOPHRENIA BULLETIN 46(3): 592–602. doi.org/10.1093/schbul/sbz075.

Terock, J., A. Hannemann, S. Van der Auwera, D. Janowitz, C. Spitzer, S. Bonk, H. Völzke, and H. J. Grabe (2020). "Posttraumatic stress disorder is associated with reduced vitamin D levels and functional polymorphisms of the vitamin D binding-protein in a population-based sample." Prog. Neuro-Psychopharmacol. Biol. Psychiatry 96: 109760. doi.org/10.1016/j.pnpbp.2019.109760.

Terock, J., S. Van der Auwera, D. Janowitz, K. Wittfeld, A. Teumer, and H. J. Grabe (2020). "Functional polymorphisms of the mineralocorticoid receptor gene NR3C2 are associated with diminished memory decline: Results from a longitudinal general-population study." Mol Genet Genomic Med n/a(n/a): e1345. doi.org/10.1002/mgg3.1345.

Wei, Y. B., M. McCarthy, H. Ren, T. Carrillo-Roa, T. Shekhtman, A. DeModena, J. J. Liu, S. G. Leckband, O. Mors, M. Rietschel, N. Henigsberg, A. Cattaneo, E. B. Binder, K. J. Aitchison, and J. R. Kelsoe (2020). "A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression." Mol Psychiatry 25(6): 1312–1322. doi.org/10.1038/s41380-019-0397-1.

Witt, S. H., J. Frank, U. Frischknecht, J. Treutlein, F. Streit, J. C. Foo, L. Sirignano, H. Dukal, F. Degenhardt, A. Koopmann, S. Hoffmann, G. Koller, O. Pogarell, U. W. Preuss, P. Zill, K. Adorjan, T. G. Schulze, M. Nöthen, R. Spanagel, F. Kiefer, and M. Rietschel (2020). "Acute alcohol withdrawal and recovery in men lead to profound changes in DNA methylation profiles – a longitudinal clinical study." Addiction 115(11): 2034-2044. doi.org/10.1111/add.15020.

2019

Andlauer, T. F. M., Guzman-Parra, J., Streit, F., Strohmaier, J., González, M. J., Gil Flores, S., Cabaleiro Fabeiro, F. J., Del Río Noriega, F., Perez, F. P., Haro González, J., Orozco Diaz, G., de Diego-Otero, Y., Moreno-Küstner, B., Auburger, G., Degenhardt, F., Heilmann-Heimbach, S., Herms, S., Hoffmann, P., Frank, J., Foo, J. C., Treutlein, J., Witt, S. H., Cichon, S., Kogevinas, M., Rivas, F., Mayoral, F., Müller-Myhsok, B., Forstner, A. J., Nöthen, M. M. and Rietschel, M. (2019). "Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders." J Mol. Psychiatry. www.ncbi.nlm.nih.gov/pubmed/31712721.

Awasthi, A., Ramachandran, B., Ahmed, S., Benito, E., Shinoda, Y., Nitzan, N., Heukamp, A., Rannio, S., Martens, H., Barth, J., Burk, K., Wang, Y. T., Fischer, A. and Dean, C. (2019). "Synaptotagmin-3 drives AMPA receptor endocytosis, depression of synapse strength, and forgetting." Science 363(6422). www.ncbi.nlm.nih.gov/pubmed/30545844.

Bilek, E., Itz, M. L., Stossel, G., Ma, R., Berhe, O., Clement, L., Zang, Z., Robnik, L., Plichta, M. M., Neukel, C., Schmahl, C., Kirsch, P., Meyer-Lindenberg, A. and Tost, H. (2019). "Deficient Amygdala Habituation to Threatening Stimuli in Borderline Personality Disorder Relates to Adverse Childhood Experiences." Biol Psychiatry 86(12): 930-938. www.ncbi.nlm.nih.gov/pubmed/31366446.

Bilek, E., Zang, Z., Wolf, I., Henrich, F., Moessnang, C., Braun, U., Treede, R. D., Magerl, W., Meyer-Lindenberg, A. and Tost, H. (2019). "Neural network-based alterations during repetitive heat pain stimulation in major depression." Eur Neuropsychopharmacol 29(9): 1033-1040. www.ncbi.nlm.nih.gov/pubmed/31320209.

Bin Wei, Y., McCarthy, M., Ren, H., Carrillo-Roa, T., Shekhtman, T., DeModena, A., Liu, J. J., Leckband, S. G., Mors, O., Rietschel, M., Henigsberg, N., Cattaneo, A., Binder, E. B., Aitchison, K. J. and Kelsoe, J. R. (2019). "A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression." Mol Psychiatry. www.ncbi.nlm.nih.gov/pubmed/30874608.

Bittner, N., Jockwitz, C., Muhleisen, T. W., Hoffstaedter, F., Eickhoff, S. B., Moebus, S., Bayen, U. J., Cichon, S., Zilles, K., Amunts, K. and Caspers, S. (2019). "Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults." Nat Commun 10(1): 621. www.ncbi.nlm.nih.gov/pubmed/30728360.

Budde, M., Anderson-Schmidt, H., Gade, K., Reich-Erkelenz, D., Adorjan, K., Kalman, J. L., Senner, F., Papiol, S., Andlauer, T. F. M., Comes, A. L., Schulte, E. C., Klohn-Saghatolislam, F., Gryaznova, A., Hake, M., Bartholdi, K., Flatau, L., Reitt, M., Quast, S., Stegmaier, S., Meyers, M., Emons, B., Haussleiter, I. S., Juckel, G., Nieratschker, V., Dannlowski, U., Schaupp, S. K., Schmauss, M., Zimmermann, J., Reimer, J., Schulz, S., Wiltfang, J., Reininghaus, E., Anghelescu, I. G., Arolt, V., Baune, B. T., Konrad, C., Thiel, A., Fallgatter, A. J., Figge, C., von Hagen, M., Koller, M., Lang, F. U., Wigand, M. E., Becker, T., Jager, M., Dietrich, D. E., Stierl, S., Scherk, H., Spitzer, C., Folkerts, H., Witt, S. H., Degenhardt, F., Forstner, A. J., Rietschel, M., Nothen, M. M., Falkai, P., Schulze, T. G. and Heilbronner, U. (2019). "A longitudinal approach to biological psychiatric research: The PsyCourse study." Am J Med Genet B Neuropsychiatr Genet 180(2): 89-102. www.ncbi.nlm.nih.gov/pubmed/30070057.

Budde, M., Friedrichs, S., Alliey-Rodriguez, N., Ament, S., Badner, J. A., Berrettini, W. H., Bloss, C. S., Byerley, W., Cichon, S., Comes, A. L., Coryell, W., Craig, D. W., Degenhardt, F., Edenberg, H. J., Foroud, T., Forstner, A. J., Frank, J., Gershon, E. S., Goes, F. S., Greenwood, T. A., Guo, Y., Hipolito, M., Hood, L., Keating, B. J., Koller, D. L., Lawson, W. B., Liu, C., Mahon, P. B., McInnis, M. G., McMahon, F. J., Meier, S. M., Mühleisen, T. W., Murray, S. S., Nievergelt, C. M., Nurnberger, J. I., Nwulia, E. A., Potash, J. B., Quarless, D., Rice, J., Roach, J. C., Scheftner, W. A., Schork, N. J., Shekhtman, T., Shilling, P. D., Smith, E. N., Streit, F., Strohmaier, J., Szelinger, S., Treutlein, J., Witt, S. H., Zandi, P. P., Zhang, P., Zöllner, S., Bickeböller, H., Falkai, P. G., Kelsoe, J. R., Nöthen, M. M., Rietschel, M., Schulze, T. G. and Malzahn, D. (2019). "Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder." European Neuropsychopharmacology: The Journal of the European College of Neuropsychopharmacology 29(1): 156-170. www.ncbi.nlm.nih.gov/pubmed/30503783.

Comes, A. L., Senner, F., Budde, M., Adorjan, K., Anderson-Schmidt, H., Andlauer, T. F. M., Gade, K., Hake, M., Heilbronner, U., Kalman, J. L., Reich-Erkelenz, D., Klohn-Saghatolislam, F., Schaupp, S. K., Schulte, E. C., Juckel, G., Dannlowski, U., Schmauss, M., Zimmermann, J., Reimer, J., Reininghaus, E., Anghelescu, I. G., Arolt, V., Baune, B. T., Konrad, C., Thiel, A., Fallgatter, A. J., Nieratschker, V., Figge, C., von Hagen, M., Koller, M., Becker, T., Wigand, M. E., Jager, M., Dietrich, D. E., Stierl, S., Scherk, H., Spitzer, C., Folkerts, H., Witt, S. H., Degenhardt, F., Forstner, A. J., Rietschel, M., Nothen, M. M., Wiltfang, J., Falkai, P., Schulze, T. G. and Papiol, S. (2019). "The genetic relationship between educational attainment and cognitive performance in major psychiatric disorders." Transl Psychiatry 9(1): 210. www.ncbi.nlm.nih.gov/pubmed/31462630.

Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hamalainen, E., Kajantie, E., Laivuori, H., Villa, P. M., Reynolds, R. M., Nystad, W., Haberg, S. E., London, S. J., O'Donnell, K. J., Garg, E., Meaney, M. J., Entringer, S., Wadhwa, P. D., Buss, C., Jones, M. J., Lin, D. T. S., MacIsaac, J. L., Kobor, M. S., Koen, N., Zar, H. J., Koenen, K. C., Dalvie, S., Stein, D. J., Kondofersky, I., Muller, N. S., Theis, F. J., Major Depressive Disorder Working Group of the Psychiatric Genomics, C., Raikkonen, K. and Binder, E. B. (2019). "Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns." Nat Commun 10(1): 2548. www.ncbi.nlm.nih.gov/pubmed/31186427.

Dedic, N., Kuhne, C., Gomes, K. S., Hartmann, J., Ressler, K. J., Schmidt, M. V. and Deussing, J. M. (2019). "Deletion of CRH From GABAergic Forebrain Neurons Promotes Stress Resilience and Dampens Stress-Induced Changes in Neuronal Activity." Front Neurosci 13: 986. www.ncbi.nlm.nih.gov/pubmed/31619956.

Durstewitz, D., Koppe, G. and Meyer-Lindenberg, A. (2019). "Deep neural networks in psychiatry." Mol Psychiatry 24(11): 1583-1598. www.ncbi.nlm.nih.gov/pubmed/30770893.

Foo, J. C., Streit, F., Frank, J., Witt, S. H., Treutlein, J., Major Depressive Disorder Working Group of the Psychiatric Genomics, C., Baune, B. T., Moebus, S., Jöckel, K.-H., Forstner, A. J., Nöthen, M. M., Rietschel, M., Sartorius, A. and Kranaster, L. (2019). "Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy." American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics 180(1): 35-45. www.ncbi.nlm.nih.gov/pubmed/30507021.

Goelman, G., Dan, R., Stossel, G., Tost, H., Meyer-Lindenberg, A. and Bilek, E. (2019). "Bidirectional signal exchanges and their mechanisms during joint attention interaction - A hyperscanning fMRI study." Neuroimage 198: 242-254. www.ncbi.nlm.nih.gov/pubmed/31112784.

Harneit, A., Braun, U., Geiger, L. S., Zang, Z., Hakobjan, M., van Donkelaar, M. M. J., Schweiger, J. I., Schwarz, K., Gan, G., Erk, S., Heinz, A., Romanczuk-Seiferth, N., Witt, S., Rietschel, M., Walter, H., Franke, B., Meyer-Lindenberg, A. and Tost, H. (2019). "MAOA-VNTR genotype affects structural and functional connectivity in distributed brain networks." Hum Brain Mapp 40(18): 5202-5212. www.ncbi.nlm.nih.gov/pubmed/31441562.

Ing, A., Samann, P. G., Chu, C., Tay, N., Biondo, F., Robert, G., Jia, T., Wolfers, T., Desrivieres, S., Banaschewski, T., Bokde, A. L. W., Bromberg, U., Buchel, C., Conrod, P., Fadai, T., Flor, H., Frouin, V., Garavan, H., Spechler, P. A., Gowland, P., Grimmer, Y., Heinz, A., Ittermann, B., Kappel, V., Martinot, J. L., Meyer-Lindenberg, A., Millenet, S., Nees, F., van Noort, B., Orfanos, D. P., Martinot, M. P., Penttila, J., Poustka, L., Quinlan, E. B., Smolka, M. N., Stringaris, A., Struve, M., Veer, I. M., Walter, H., Whelan, R., Andreassen, O. A., Agartz, I., Lemaitre, H., Barker, E. D., Ashburner, J., Binder, E., Buitelaar, J., Marquand, A., Robbins, T. W., Schumann, G. and Consortium, I. (2019). "Identification of neurobehavioural symptom groups based on shared brain mechanisms." Nat Hum Behav 3(12): 1306-1318. www.ncbi.nlm.nih.gov/pubmed/31591521.

Jain, G., Stuendl, A., Rao, P., Berulava, T., Pena Centeno, T., Kaurani, L., Burkhardt, S., Delalle, I., Kornhuber, J., Hull, M., Maier, W., Peters, O., Esselmann, H., Schulte, C., Deuschle, C., Synofzik, M., Wiltfang, J., Mollenhauer, B., Maetzler, W., Schneider, A. and Fischer, A. (2019). "A combined miRNA-piRNA signature to detect Alzheimer's disease." Transl Psychiatry 9(1): 250. www.ncbi.nlm.nih.gov/pubmed/31591382.

Jensen, L. R., Garrett, L., Hölter, S. M., Rathkolb, B., Rácz, I., Adler, T., Prehn, C., Hans, W., Rozman, J., Becker, L., Aguilar-Pimentel, J. A., Puk, O., Moreth, K., Dopatka, M., Walther, D. J., von Bohlen Und Halbach, V., Rath, M., Delatycki, M., Bert, B., Fink, H., Blümlein, K., Ralser, M., Van Dijck, A., Kooy, F., Stark, Z., Müller, S., Scherthan, H., Gecz, J., Wurst, W., Wolf, E., Zimmer, A., Klingenspor, M., Graw, J., Klopstock, T., Busch, D., Adamski, J., Fuchs, H., Gailus-Durner, V., de Angelis, M. H., von Bohlen Und Halbach, O., Ropers, H.-H. and Kuss, A. W. (2019). "A mouse model for intellectual disability caused by mutations in the X-linked 2'Omethyltransferase Ftsj1 gene." Biochimica Et Biophysica Acta. Molecular Basis of Disease 1865(9): 2083-2093. www.ncbi.nlm.nih.gov/pubmed/30557699.

Kalman, J. L., Bresnahan, M., Schulze, T. G. and Susser, E. (2019). "Predictors of persisting psychotic like experiences in children and adolescents: A scoping review." Schizophr Res 209: 32-39. www.ncbi.nlm.nih.gov/pubmed/31109737.

Kalman, J. L., Papiol, S., Forstner, A. J., Heilbronner, U., Degenhardt, F., Strohmaier, J., Adli, M., Adorjan, K., Akula, N., Alda, M., Anderson-Schmidt, H., Andlauer, T. F., Anghelescu, I.-G., Ardau, R., Arias, B., Arolt, V., Aubry, J.-M., Backlund, L., Bartholdi, K., Bauer, M., Baune, B. T., Becker, T., Bellivier, F., Benabarre, A., Bengesser, S., Bhattacharjee, A. K., Biernacka, J. M., Birner, A., Brichant-Petitjean, C., Budde, M., Cervantes, P., Chillotti, C., Cichon, S., Clark, S. R., Colom, F., Comes, A. L., Cruceanu, C., Czerski, P. M., Dannlowski, U., Dayer, A., Del Zompo, M., DePaulo, J. R., Dietrich, D. E., Étain, B., Ethofer, T., Falkai, P., Fallgatter, A., Figge, C., Flatau, L., Folkerts, H., Frisen, L., Frye, M. A., Fullerton, J. M., Gade, K., Gard, S., Garnham, J. S., Goes, F. S., Grigoroiu-Serbanescu, M., Gryaznova, A., Hake, M., Hauser, J., Herms, S., Hoffmann, P., Hou, L., Jäger, M., Jamain, S., Jiménez, E., Juckel, G., Kahn, J.-P., Kassem, L., Kelsoe, J., Kittel-Schneider, S., Kliwicki, S., Klohn-Sagatholislam, F., Koller, M., König, B., Konrad, C., Lackner, N., Laje, G., Landén, M., Lang, F. U., Lavebratt, C., Leboyer, M., Leckband, S. G., Maj, M., Manchia, M., Martinsson, L., McCarthy, M. J., McElroy, S. L., McMahon, F. J., Mitchell, P. B., Mitjans, M., Mondimore, F. M., Monteleone, P., Nieratschker, V., Nievergelt, C. M., Novák, T., Ösby, U., Pfennig, A., Potash, J. B., Reich-Erkelenz, D., Reif, A., Reimer, J., Reininghaus, E., Reitt, M., Ripke, S., Rouleau, G. A., Rybakowski, J. K., Schalling, M., Scherk, H., Schmauß, M., Schofield, P. R., Schubert, K. O., Schulte, E. C., Schulz, S., Senner, F., Severino, G., Shekhtman, T., Shilling, P. D., Simhandl, C., Slaney, C. M., Spitzer, C., Squassina, A., Stamm, T., Stegmaier, S., Stierl, S., Stopkova, P., Thiel, A., Tighe, S. K., Tortorella, A., Turecki, G., Vieta, E., Veeh, J., von Hagen, M., Wigand, M. E., Wiltfang, J., Witt, S., Wright, A., Zandi, P. P., Zimmermann, J., Nöthen, M., Rietschel, M. and Schulze, T. G. (2019). "Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study." Bipolar Disorders 21(1): 68-75. www.ncbi.nlm.nih.gov/pubmed/29956436.

Klinger-Konig, J., Hertel, J., Van der Auwera, S., Frenzel, S., Pfeiffer, L., Waldenberger, M., Golchert, J., Teumer, A., Nauck, M., Homuth, G., Volzke, H. and Grabe, H. J. (2019). "Methylation of the FKBP5 gene in association with FKBP5 genotypes, childhood maltreatment and depression." Neuropsychopharmacology 44(5): 930-938. www.ncbi.nlm.nih.gov/pubmed/30700816.

Koppe, G., Guloksuz, S., Reininghaus, U. and Durstewitz, D. (2019). "Recurrent Neural Networks in Mobile Sampling and Intervention." Schizophrenia Bulletin 45(2): 272-276. www.ncbi.nlm.nih.gov/pubmed/30496527.

Korecki, A. J., Hickmott, J. W., Lam, S. L., Dreolini, L., Mathelier, A., Baker, O., Kuehne, C., Bonaguro, R. J., Smith, J., Tan, C. V., Zhou, M., Goldowitz, D., Deussing, J. M., Stewart, A. F., Wasserman, W. W., Holt, R. A. and Simpson, E. M. (2019). "Twenty-Seven Tamoxifen-Inducible iCre-Driver Mouse Strains for Eye and Brain; Including Seventeen Carrying a New Inducible-First Constitutive-Ready Allele." Genetics. www.ncbi.nlm.nih.gov/pubmed/30765420.

Leuchs, L., Schneider, M. and Spoormaker, V. I. (2019). "Measuring the conditioned response: A comparison of pupillometry, skin conductance, and startle electromyography." Psychophysiology 56(1): e13283. www.ncbi.nlm.nih.gov/pubmed/30259985.

Meijer, M., Rehbach, K., Brunner, J. W., Classen, J. A., Lammertse, H. C. A., van Linge, L. A., Schut, D., Krutenko, T., Hebisch, M., Cornelisse, L. N., Sullivan, P. F., Peitz, M., Toonen, R. F., Brustle, O. and Verhage, M. (2019). "A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons." Cell Rep 27(7): 2199-2211 e2196. www.ncbi.nlm.nih.gov/pubmed/31091456.

Meller, T., Schmitt, S., Stein, F., Brosch, K., Mosebach, J., Yuksel, D., Zaremba, D., Grotegerd, D., Dohm, K., Meinert, S., Forster, K., Redlich, R., Opel, N., Repple, J., Hahn, T., Jansen, A., Andlauer, T. F. M., Forstner, A. J., Heilmann-Heimbach, S., Streit, F., Witt, S. H., Rietschel, M., Muller-Myhsok, B., Nothen, M. M., Dannlowski, U., Krug, A., Kircher, T. and Nenadic, I. (2019). "Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects." Schizophr Res. www.ncbi.nlm.nih.gov/pubmed/31076262.

Paul, R., Andlauer, T. F. M., Czamara, D., Hoehn, D., Lucae, S., Putz, B., Lewis, C. M., Uher, R., Muller-Myhsok, B., Ising, M. and Samann, P. G. (2019). "Treatment response classes in major depressive disorder identified by model-based clustering and validated by clinical prediction models." Transl Psychiatry 9(1): 187. www.ncbi.nlm.nih.gov/pubmed/31383853.

Rhee, H. J., Shaib, A. H., Rehbach, K., Lee, C., Seif, P., Thomas, C., Gideons, E., Guenther, A., Krutenko, T., Hebisch, M., Peitz, M., Brose, N., Brustle, O. and Rhee, J. S. (2019). "An Autaptic Culture System for Standardized Analyses of iPSC-Derived Human Neurons." Cell Rep 27(7): 2212-2228 e2217. www.ncbi.nlm.nih.gov/pubmed/31091457.

Schwarz, E., Doan, N. T., Pergola, G., Westlye, L. T., Kaufmann, T., Wolfers, T., Brecheisen, R., Quarto, T., Ing, A. J., Carlo, P. D., Gurholt, T. P., Harms, R. L., Noirhomme, Q., Moberget, T., Agartz, I., Andreassen, O. A., Bellani, M., Bertolino, A., Blasi, G., Brambilla, P., Buitelaar, J. K., Cervenka, S., Flyckt, L., Frangou, S., Franke, B., Hall, J., Heslenfeld, D. J., Kirsch, P., McIntosh, A. M., Nothen, M. M., Papassotiropoulos, A., de Quervain, D. J., Rietschel, M., Schumann, G., Tost, H., Witt, S. H., Zink, M., Meyer-Lindenberg, A. and Imagemend Consortium, K. S. P. C. (2019). "Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder." Transl Psychiatry 9(1): 12. www.ncbi.nlm.nih.gov/pubmed/30664633.

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. and Tost, H. (2019). "Effects of BDNF Val66Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans." Neuropsychopharmacology 44(3): 590-597. www.ncbi.nlm.nih.gov/pubmed/30375508.

Send, T. S., Bardtke, S., Gilles, M., Wolf, I. A. C., Sütterlin, M. W., Kirschbaum, C., Laucht, M., Witt, S. H., Rietschel, M., Streit, F. and Deuschle, M. (2019). "Stress reactivity in preschool-aged children: Evaluation of a social stress paradigm and investigation of the impact of prenatal maternal stress." Psychoneuroendocrinology 101: 223-231. www.ncbi.nlm.nih.gov/pubmed/30471571.

Send, T. S., Bardtke, S., Gilles, M., Wolf, I. A. C., Sutterlin, M. W., Wudy, S. A., Wang, R., Laucht, M., Witt, S. H., Rietschel, M., Streit, F. and Deuschle, M. (2019). "Prenatal maternal stress is associated with lower cortisol and cortisone levels in the first morning urine of 45-month-old children." Psychoneuroendocrinology 103: 219-224. www.ncbi.nlm.nih.gov/pubmed/30711899.

Spalthoff, R., Degenhardt, F., Awasthi, S., Heilmann-Heimbach, S., Besteher, B., Gaser, C., Ripke, S., Nothen, M. M. and Nenadic, I. (2019). "Effects of a neurodevelopmental genes based polygenic risk score for schizophrenia and single gene variants on brain structure in non-clinical subjects: A preliminary report." Schizophr Res. www.ncbi.nlm.nih.gov/pubmed/31395486.

Strohmaier, J., Witt, S. H., Frank, J., Lemme, N., Flatau, L., Streit, F., Foo, J. C., Reitt, M., Rujescu, D., Schulze, T. G., Lanzerath, D., Illes, F., Degenhardt, F. and Rietschel, M. (2019). "Attitudes toward the right to autonomous decision-making in psychiatric genetic testing: Controversial and context-dependent." Am J Med Genet B Neuropsychiatr Genet 180(8): 555-565. www.ncbi.nlm.nih.gov/pubmed/30912305.

Terock, J., Hannemann, A., Janowitz, D., Van der Auwera, S., Bahls, M., Volzke, H. and Grabe, H. J. (2019). "Differential activation of the renin-angiotensin-aldosterone-system in response to childhood and adulthood trauma." Psychoneuroendocrinology 107: 232-240. www.ncbi.nlm.nih.gov/pubmed/31174161.

Terock, J., Van der Auwera, S., Hannemann, A., Janowitz, D., Homuth, G., Teumer, A. and Grabe, H. J. (2019). "Interaction of childhood trauma with rs1360780 of the FKBP5 gene on trait resilience in a general population sample." J Psychiatr Res 116: 104-111. www.ncbi.nlm.nih.gov/pubmed/31226578.

Terock, J., Van der Auwera, S., Janowitz, D., Klinger-Konig, J., Schmidt, C. O., Freyberger, H. J. and Grabe, H. J. (2019). "The relation of alexithymia, chronic perceived stress and declarative memory performance: Results from the general population." Psychiatry Res 271: 405-411. www.ncbi.nlm.nih.gov/pubmed/30530059.

Tost, H., Reichert, M., Braun, U., Reinhard, I., Peters, R., Lautenbach, S., Hoell, A., Schwarz, E., Ebner-Priemer, U., Zipf, A. and Meyer-Lindenberg, A. (2019). "Neural correlates of individual differences in affective benefit of real-life urban green space exposure." Nat Neurosci 22(9): 1389-1393. www.ncbi.nlm.nih.gov/pubmed/31358990.

Van der Auwera, S., Ameling, S., Wittfeld, K., d'Harcourt Rowold, E., Nauck, M., Volzke, H., Suhre, K., Najafi-Shoushtari, H., Methew, J., Ramachandran, V., Bulow, R., Volker, U. and Grabe, H. J. (2019). "Association of childhood traumatization and neuropsychiatric outcomes with altered plasma micro RNA-levels." Neuropsychopharmacology 44(12): 2030-2037. www.ncbi.nlm.nih.gov/pubmed/31284290.

van der Lee, S. J., Conway, O. J., Jansen, I., Carrasquillo, M. M., Kleineidam, L., van den Akker, E., Hernandez, I., van Eijk, K. R., Stringa, N., Chen, J. A., Zettergren, A., Andlauer, T. F. M., Diez-Fairen, M., Simon-Sanchez, J., Lleo, A., Zetterberg, H., Nygaard, M., Blauwendraat, C., Savage, J. E., Mengel-From, J., Moreno-Grau, S., Wagner, M., Fortea, J., Keogh, M. J., Blennow, K., Skoog, I., Friese, M. A., Pletnikova, O., Zulaica, M., Lage, C., de Rojas, I., Riedel-Heller, S., Illan-Gala, I., Wei, W., Jeune, B., Orellana, A., Then Bergh, F., Wang, X., Hulsman, M., Beker, N., Tesi, N., Morris, C. M., Indakoetxea, B., Collij, L. E., Scherer, M., Morenas-Rodriguez, E., Ironside, J. W., van Berckel, B. N. M., Alcolea, D., Wiendl, H., Strickland, S. L., Pastor, P., Rodriguez Rodriguez, E., Desgesco, E., Eadb, Ifgc, I., Ipdgc, RiMod, F. T. D., Netherlands Brain, B., Boeve, B. F., Petersen, R. C., Ferman, T. J., van Gerpen, J. A., Reinders, M. J. T., Uitti, R. J., Tarraga, L., Maier, W., Dols-Icardo, O., Kawalia, A., Dalmasso, M. C., Boada, M., Zettl, U. K., van Schoor, N. M., Beekman, M., Allen, M., Masliah, E., de Munain, A. L., Pantelyat, A., Wszolek, Z. K., Ross, O. A., Dickson, D. W., Graff-Radford, N. R., Knopman, D., Rademakers, R., Lemstra, A. W., Pijnenburg, Y. A. L., Scheltens, P., Gasser, T., Chinnery, P. F., Hemmer, B., Huisman, M. A., Troncoso, J., Moreno, F., Nohr, E. A., Sorensen, T. I. A., Heutink, P., Sanchez-Juan, P., Posthuma, D., Group, G. S., Clarimon, J., Christensen, K., Ertekin-Taner, N., Scholz, S. W., Ramirez, A., Ruiz, A., Slagboom, E., van der Flier, W. M. and Holstege, H. (2019). "A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity." Acta Neuropathol 138(2): 237-250. www.ncbi.nlm.nih.gov/pubmed/31131421.

Wackerhagen, C., Veer, I. M., Erk, S., Mohnke, S., Lett, T. A., Wustenberg, T., Romanczuk-Seiferth, N. Y., Schwarz, K., Schweiger, J. I., Tost, H., Meyer-Lindenberg, A., Heinz, A. and Walter, H. (2019). "Amygdala functional connectivity in major depression - disentangling markers of pathology, risk and resilience." Psychol Med: 1-11. www.ncbi.nlm.nih.gov/pubmed/31637983.

Zannas, A. S., Jia, M., Hafner, K., Baumert, J., Wiechmann, T., Pape, J. C., Arloth, J., Kodel, M., Martinelli, S., Roitman, M., Roh, S., Haehle, A., Emeny, R. T., Iurato, S., Carrillo-Roa, T., Lahti, J., Raikkonen, K., Eriksson, J. G., Drake, A. J., Waldenberger, M., Wahl, S., Kunze, S., Lucae, S., Bradley, B., Gieger, C., Hausch, F., Smith, A. K., Ressler, K. J., Muller-Myhsok, B., Ladwig, K. H., Rein, T., Gassen, N. C. and Binder, E. B. (2019). "Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-kappaB-driven inflammation and cardiovascular risk." Proc Natl Acad Sci U S A 116(23): 11370-11379. www.ncbi.nlm.nih.gov/pubmed/31113877.

2018

Bedenk, B. T., Almeida-Corrêa, S., Jurik, A., Dedic, N., Grünecker, B., Genewsky, A. J., Kaltwasser, S. F., Riebe, C. J., Deussing, J. M., Czisch, M. and Wotjak, C. T. (2018). "Mn2+dynamics in manganese-enhanced MRI (MEMRI): Cav1.2 channel-mediated uptake and preferential accumulation in projection terminals." NeuroImage 169: 374-382. www.ncbi.nlm.nih.gov/pubmed/29277401.

Benito, E., Kerimoglu, C., Ramachandran, B., Pena-Centeno, T., Jain, G., Stilling, R. M., Islam, M. R., Capece, V., Zhou, Q., Edbauer, D., Dean, C. and Fischer, A. (2018). "RNA-Dependent Intergenerational Inheritance of Enhanced Synaptic Plasticity after Environmental Enrichment." Cell Reports 23(2): 546-554. www.ncbi.nlm.nih.gov/pubmed/29642011.

Binz, T. M., Rietschel, L., Streit, F., Hofmann, M., Gehrke, J., Herdener, M., Quednow, B. B., Martin, N. G., Rietschel, M., Kraemer, T. and Baumgartner, M. R. (2018). "Endogenous cortisol in keratinized matrices: Systematic determination of baseline cortisol levels in hair and the influence of sex, age and hair color." Forensic Science International 284: 33-38. www.ncbi.nlm.nih.gov/pubmed/29331681.

Brainstorm, C., Anttila, V., …., Curtis, D., Gejman, P. V., Henskens, F., Mattingsdal, M., Oh, S.-Y., Scott, R., Webb, B., Breen, G., Churchhouse, C., Bulik, C. M., Daly, M., Dichgans, M., Faraone, S. V., Guerreiro, R., Holmans, P., Kendler, K. S., Koeleman, B., Mathews, C. A., Price, A., Scharf, J., Sklar, P., Williams, J., Wood, N. W., Cotsapas, C., Palotie, A., Smoller, J. W., Sullivan, P., Rosand, J., Corvin, A. and Neale, B. M. (2018). "Analysis of shared heritability in common disorders of the brain." Science (New York, N.Y.) 360(6395). www.ncbi.nlm.nih.gov/pubmed/29930110.

Braun, U., Schaefer, A., Betzel, R. F., Tost, H., Meyer-Lindenberg, A. and Bassett, D. S. (2018). "From Maps to Multi-dimensional Network Mechanisms of Mental Disorders." Neuron 97(1): 14-31. www.ncbi.nlm.nih.gov/pubmed/29301099.

Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Swedish Bipolar Study, G., Moo, D. S. B. C., Walter, H., Erk, S., Heinz, A., Amin, N., van Duijn, C. M., Meyer-Lindenberg, A., Tost, H., Xiao, X., Yamamoto, T., Rietschel, M. and Li, M. (2018). "The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders." Molecular Psychiatry 23(2): 400-412. www.ncbi.nlm.nih.gov/pubmed/28070120.

Chen, J., Cao, H., Meyer-Lindenberg, A. and Schwarz, E. (2018). "Male increase in brain gene expression variability is linked to genetic risk for schizophrenia." Translational Psychiatry 8(1): 140. www.ncbi.nlm.nih.gov/pubmed/30068996.

Clemm von Hohenberg, C., Weber-Fahr, W., Lebhardt, P., Ravi, N., Braun, U., Gass, N., Becker, R., Sack, M., Cosa Linan, A., Gerchen, M. F., Reinwald, J. R., Oettl, L.-L., Meyer-Lindenberg, A., Vollmayr, B., Kelsch, W. and Sartorius, A. (2018). "Lateral habenula perturbation reduces default-mode network connectivity in a rat model of depression." Translational Psychiatry 8(1): 68. www.ncbi.nlm.nih.gov/pubmed/29581421.

Comes, A. L., Papiol, S., Mueller, T., Geyer, P. E., Mann, M. and Schulze, T. G. (2018). "Proteomics for blood biomarker exploration of severe mental illness: pitfalls of the past and potential for the future." Translational Psychiatry 8(1): 160. www.ncbi.nlm.nih.gov/pubmed/30115926.

Corominas, J., Klein, M., Zayats, T., Rivero, O., Ziegler, G. C., Pauper, M., Neveling, K., Poelmans, G., Jansch, C., Svirin, E., Geissler, J., Weber, H., Reif, A., Arias Vasquez, A., Galesloot, T. E., Kiemeney, L. A. L. M., Buitelaar, J. K., Ramos-Quiroga, J.-A., Cormand, B., Ribasés, M., Hveem, K., Gabrielsen, M. E., Hoffmann, P., Cichon, S., Haavik, J., Johansson, S., Jacob, C. P., Romanos, M., Franke, B. and Lesch, K.-P. (2018). "Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing." Molecular Psychiatry. www.ncbi.nlm.nih.gov/pubmed/30116028.

Culverhouse, R. C., Saccone, N. L., Horton, A. C., Ma, Y., Anstey, K. J., Banaschewski, T., Burmeister, M., Cohen-Woods, S., Etain, B., Fisher, H. L., Goldman, N., Guillaume, S., Horwood, J., Juhasz, G., Lester, K. J., Mandelli, L., Middeldorp, C. M., Olié, E., Villafuerte, S., Air, T. M., Araya, R., Bowes, L., Burns, R., Byrne, E. M., Coffey, C., Coventry, W. L., Gawronski, K. a. B., Glei, D., Hatzimanolis, A., Hottenga, J. J., Jaussent, I., Jawahar, C., Jennen-Steinmetz, C., Kramer, J. R., Lajnef, M., Little, K., Zu Schwabedissen, H. M., Nauck, M., Nederhof, E., Petschner, P., Peyrot, W. J., Schwahn, C., Sinnamon, G., Stacey, D., Tian, Y., Toben, C., Van der Auwera, S., Wainwright, N., Wang, J. C., Willemsen, G., Anderson, I. M., Arolt, V., Åslund, C., Bagdy, G., Baune, B. T., Bellivier, F., Boomsma, D. I., Courtet, P., Dannlowski, U., de Geus, E. J. C., Deakin, J. F. W., Easteal, S., Eley, T., Fergusson, D. M., Goate, A. M., Gonda, X., Grabe, H. J., Holzman, C., Johnson, E. O., Kennedy, M., Laucht, M., Martin, N. G., Munafò, M. R., Nilsson, K. W., Oldehinkel, A. J., Olsson, C. A., Ormel, J., Otte, C., Patton, G. C., Penninx, B. W. J. H., Ritchie, K., Sarchiapone, M., Scheid, J. M., Serretti, A., Smit, J. H., Stefanis, N. C., Surtees, P. G., Völzke, H., Weinstein, M., Whooley, M., Nurnberger, J. I., Breslau, N. and Bierut, L. J. (2018). "Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression." Molecular Psychiatry 23(1): 133-142. www.ncbi.nlm.nih.gov/pubmed/28373689.

de Boni, L., Gasparoni, G., Haubenreich, C., Tierling, S., Schmitt, I., Peitz, M., Koch, P., Walter, J., Wüllner, U. and Brüstle, O. (2018). "DNA methylation alterations in iPSC- and hESC-derived neurons: potential implications for neurological disease modeling." Clinical Epigenetics 10: 13. www.ncbi.nlm.nih.gov/pubmed/29422978.

Dedic, N., Chen, A. and Deussing, J. M. (2018). "The CRF Family of Neuropeptides and their Receptors - Mediators of the Central Stress Response." Current Molecular Pharmacology 11(1): 4-31. www.ncbi.nlm.nih.gov/pubmed/28260504.

Dedic, N., Kühne, C., Jakovcevski, M., Hartmann, J., Genewsky, A. J., Gomes, K. S., Anderzhanova, E., Pöhlmann, M. L., Chang, S., Kolarz, A., Vogl, A. M., Dine, J., Metzger, M. W., Schmid, B., Almada, R. C., Ressler, K. J., Wotjak, C. T., Grinevich, V., Chen, A., Schmidt, M. V., Wurst, W., Refojo, D. and Deussing, J. M. (2018). "Chronic CRH depletion from GABAergic, long-range projection neurons in the extended amygdala reduces dopamine release and increases anxiety." Nature Neuroscience 21(6): 803-807. www.ncbi.nlm.nih.gov/pubmed/29786085.

Dedic, N., Pöhlmann, M. L., Richter, J. S., Mehta, D., Czamara, D., Metzger, M. W., Dine, J., Bedenk, B. T., Hartmann, J., Wagner, K. V., Jurik, A., Almli, L. M., Lori, A., Moosmang, S., Hofmann, F., Wotjak, C. T., Rammes, G., Eder, M., Chen, A., Ressler, K. J., Wurst, W., Schmidt, M. V., Binder, E. B. and Deussing, J. M. (2018). "Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood." Molecular Psychiatry 23(3): 533-543. www.ncbi.nlm.nih.gov/pubmed/28696432.

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Toutounji, H. and Durstewitz, D. (2018). "Detecting Multiple Change Points Using Adaptive Regression Splines With Application to Neural Recordings." Frontiers in Neuroinformatics 12. www.ncbi.nlm.nih.gov/pubmed/30349472.

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2017

Agís-Balboa, R. C., Pinheiro, P. S., Rebola, N., Kerimoglu, C., Benito, E., Gertig, M., Bahari-Javan, S., Jain, G., Burkhardt, S., Delalle, I., Jatzko, A., Dettenhofer, M., Zunszain, P. A., Schmitt, A., Falkai, P., Pape, J. C., Binder, E. B., Mulle, C., Fischer, A. and Sananbenesi, F. (2017). "Formin 2 links neuropsychiatric phenotypes at young age to an increased risk for dementia." The EMBO journal 36(19): 2815-2828. www.ncbi.nlm.nih.gov/pubmed/28768717.

Badenes, S. M., Fernandes, T. G., Miranda, C. C., Pusch‐Klein, A., Haupt, S., Rodrigues, C. A. V., Diogo, M. M., Brüstle, O. and Cabral, J. M. S. (2017). "Long‐term expansion of human induced pluripotent stem cells in a microcarrier‐based dynamic system." Journal of Chemical Technology and Biotechnology 92(3): 492-503. onlinelibrary.wiley.com/wol1/doi/10.1002/jctb.5074/full.

Bernardi, R. E., Broccoli, L., Hirth, N., Justice, N. J., Deussing, J. M., Hansson, A. C. and Spanagel, R. (2017). "Dissociable Role of Corticotropin Releasing Hormone Receptor Subtype 1 on Dopaminergic and D1 Dopaminoceptive Neurons in Cocaine Seeking Behavior." Frontiers in Behavioral Neuroscience 11: 221. www.ncbi.nlm.nih.gov/pubmed/29180955.

Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S. A., Abdellaoui, A., Andlauer, T. F. M., Beekman, A. T. F., Berger, K., Blackwood, D. H. R., Boomsma, D. I., Breen, G., Buttenschøn, H. N., Byrne, E. M., Cichon, S., Clarke, T. K., Couvy-Duchesne, B., Craddock, N., de Geus, E. J. C., Degenhardt, F., Dunn, E. C., Edwards, A. C., Fanous, A. H., Forstner, A. J., Frank, J., Gill, M., Gordon, S. D., Grabe, H. J., Hamilton, S. P., Hardiman, O., Hayward, C., Heath, A. C., Henders, A. K., Herms, S., Hickie, I. B., Hoffmann, P., Homuth, G., Hottenga, J. J., Ising, M., Jansen, R., Kloiber, S., Knowles, J. A., Lang, M., Li, Q. S., Lucae, S., MacIntyre, D. J., Madden, P. a. F., Martin, N. G., McGrath, P. J., McGuffin, P., McIntosh, A. M., Medland, S. E., Mehta, D., Middeldorp, C. M., Milaneschi, Y., Montgomery, G. W., Mors, O., Müller-Myhsok, B., Nauck, M., Nyholt, D. R., Nöthen, M. M., Owen, M. J., Penninx, B. W. J. H., Pergadia, M. L., Perlis, R. H., Peyrot, W. J., Porteous, D. J., Potash, J. B., Rice, J. P., Rietschel, M., Riley, B. P., Rivera, M., Schoevers, R., Schulze, T. G., Shi, J., Shyn, S. I., Smit, J. H., Smoller, J. W., Streit, F., Strohmaier, J., Teumer, A., Treutlein, J., Van der Auwera, S., van Grootheest, G., van Hemert, A. M., Völzke, H., Webb, B. T., Weissman, M. M., Wellmann, J., Willemsen, G., Witt, S. H., Levinson, D. F., Lewis, C. M., Wray, N. R., Flint, J., Sullivan, P. F. and Kendler, K. S. (2017). "Genetic effects influencing risk for major depressive disorder in China and Europe." Translational Psychiatry 7(3): e1074. www.ncbi.nlm.nih.gov/pubmed/28350396.

Bilek, E., Stößel, G., Schäfer, A., Clement, L., Ruf, M., Robnik, L., Neukel, C., Tost, H., Kirsch, P. and Meyer-Lindenberg, A. (2017). "State-Dependent Cross-Brain Information Flow in Borderline Personality Disorder." JAMA psychiatry 74(9): 949-957. www.ncbi.nlm.nih.gov/pubmed/28768322.

Café-Mendes, C. C., Ferro, E. S., Torrão, A. S., Crunfli, F., Rioli, V., Schmitt, A., Falkai, P., Britto, L. R., Turck, C. W. and Martins-de-Souza, D. (2017). "Peptidomic analysis of the anterior temporal lobe and corpus callosum from schizophrenia patients." Journal of Proteomics 151: 97-105. www.ncbi.nlm.nih.gov/pubmed/27321914.

Cao, H., Chen, J., Meyer-Lindenberg, A. and Schwarz, E. (2017). "A polygenic score for schizophrenia predicts glycemic control." Translational Psychiatry 7(12): 1295. www.ncbi.nlm.nih.gov/pubmed/29249829.

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2016

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Becker, R., Braun, U., Schwarz, A.J., Gass, N., Schweiger, J.I., Weber-Fahr, W., Schenker, E., Spedding, M., Clemm von Hohenberg, C., Risterucci, C., Zang, Z., Grimm, O., Tost, H., Sartorius, A., Meyer-Lindenberg, A., 2016. Species-conserved reconfigurations of brain network topology induced by ketamine. Transl Psychiatry 6, e786. doi.org/10.1038/tp.2016.53

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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., MooDS SCZ Consortium, Werge, T., Mors, O., Hougaard, D.M., Børglum, A.D., Wray, N.R., Rietschel, M., Nordentoft, M., Mortensen, P.B., Mattheisen, M., 2016. High loading of polygenic risk in cases with chronic schizophrenia. Mol. Psychiatry 21, 969–974. doi.org/10.1038/mp.2015.130

Mohnke, S., Erk, S., Schnell, K., Romanczuk-Seiferth, N., Schmierer, P., Romund, L., Garbusow, M., Wackerhagen, C., Ripke, S., Grimm, O., Haller, L., Witt, S.H., Degenhardt, F., Tost, H., Heinz, A., Meyer-Lindenberg, A., Walter, H., 2016. Theory of mind network activity is altered in subjects with familial liability for schizophrenia. Soc Cogn Affect Neurosci 11, 299–307. doi.org/10.1093/scan/nsv111

Rietschel, L., Streit, F., Zhu, G., McAloney, K., Kirschbaum, C., Frank, J., Hansell, N.K., Wright, M.J., McGrath, J.J., Witt, S.H., Rietschel, M., Martin, N.G., 2016. Hair Cortisol and Its Association With Psychological Risk Factors for Psychiatric Disorders: A Pilot Study in Adolescent Twins. Twin Res Hum Genet 19, 438–446. doi.org/10.1017/thg.2016.50

Streit, F., Memic, A., Hasandedić, L., Rietschel, L., Frank, J., Lang, M., Witt, S.H., Forstner, A.J., Degenhardt, F., Wüst, S., Nöthen, M.M., Kirschbaum, C., Strohmaier, J., Oruc, L., Rietschel, M., 2016. Perceived stress and hair cortisol: Differences in bipolar disorder and schizophrenia. Psychoneuroendocrinology 69, 26–34. doi.org/10.1016/j.psyneuen.2016.03.010

Uhrig, S., Hirth, N., Broccoli, L., von Wilmsdorff, M., Bauer, M., Sommer, C., Zink, M., Steiner, J., Frodl, T., Malchow, B., Falkai, P., Spanagel, R., Hansson, A.C., Schmitt, A., 2016. Reduced oxytocin receptor gene expression and binding sites in different brain regions in schizophrenia: A post-mortem study. Schizophr. Res. 177, 59–66. doi.org/10.1016/j.schres.2016.04.019

Uribe-Mariño, A., Gassen, N.C., Wiesbeck, M.F., Balsevich, G., Santarelli, S., Solfrank, B., Dournes, C., Fries, G.R., Masana, M., Labermeier, C., Wang, X.-D., Hafner, K., Schmid, B., Rein, T., Chen, A., Deussing, J.M., Schmidt, M.V., 2016. Prefrontal Cortex Corticotropin-Releasing Factor Receptor 1 Conveys Acute Stress-Induced Executive Dysfunction. Biol. Psychiatry 80, 743–753. doi.org/10.1016/j.biopsych.2016.03.2106

Van der Auwera, S., Teumer, A., Hertel, J., Homuth, G., Völker, U., Lucht, M.J., Degenhardt, F., Schulze, T., Rietschel, M., Nöthen, M.M., John, U., Nauck, M., Grabe, H.J., 2016. The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine. Eur Neuropsychopharmacol 26, 1507–1515. doi.org/10.1016/j.euroneuro.2016.03.019

Wallwiener, S., Strohmaier, J., Wallwiener, L.-M., Schönfisch, B., Zipfel, S., Brucker, S.Y., Rietschel, M., Wallwiener, C.W., 2016. Sexual Function Is Correlated With Body Image and Partnership Quality in Female University Students. J Sex Med 13, 1530–1538. doi.org/10.1016/j.jsxm.2016.07.020

2015

Arloth, J., Bogdan, R., Weber, P., Frishman, G., Menke, A., Wagner, K.V., Balsevich, G., Schmidt, M.V., Karbalai, N., Czamara, D., Altmann, A., Trümbach, D., Wurst, W., Mehta, D., Uhr, M., Klengel, T., Erhardt, A., Carey, C.E., Conley, E.D., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC), Ruepp, A., Müller-Myhsok, B., Hariri, A.R., Binder, E.B., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium PGC, 2015. Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. Neuron 86, 1189–1202. doi.org/10.1016/j.neuron.2015.05.034

Basmanav, F.B., Forstner, A.J., Fier, H., Herms, S., Meier, S., Degenhardt, F., Hoffmann, P., Barth, S., Fricker, N., Strohmaier, J., Witt, S.H., Ludwig, M., Schmael, C., Moebus, S., Maier, W., Mössner, R., Rujescu, D., Rietschel, M., Lange, C., Nöthen, M.M., Cichon, S., 2015. Investigation of the role of TCF4 rare sequence variants in schizophrenia. Am. J. Med. Genet. B Neuropsychiatr. Genet. 168B, 354–362. doi.org/10.1002/ajmg.b.32318

Bender, J., Engeholm, M., Ederer, M.S., Breu, J., Møller, T.C., Michalakis, S., Rasko, T., Wanker, E.E., Biel, M., Martinez, K.L., Wurst, W., Deussing, J.M., 2015. Corticotropin-Releasing Hormone Receptor Type 1 (CRHR1) Clustering with MAGUKs Is Mediated via Its C-Terminal PDZ Binding Motif. PLoS ONE 10, e0136768. doi.org/10.1371/journal.pone.0136768

Brennand, K.J., Marchetto, M.C., Benvenisty, N., Brüstle, O., Ebert, A., Izpisua Belmonte, J.C., Kaykas, A., Lancaster, M.A., Livesey, F.J., McConnell, M.J., McKay, R.D., Morrow, E.M., Muotri, A.R., Panchision, D.M., Rubin, L.L., Sawa, A., Soldner, F., Song, H., Studer, L., Temple, S., Vaccarino, F.M., Wu, J., Vanderhaeghen, P., Gage, F.H., Jaenisch, R., 2015. Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders. Stem Cell Reports 5, 933–945. doi.org/10.1016/j.stemcr.2015.10.011

Buch, S., Stickel, F., Trépo, E., Way, M., Herrmann, A., Nischalke, H.D., Brosch, M., Rosendahl, J., Berg, T., Ridinger, M., Rietschel, M., McQuillin, A., Frank, J., Kiefer, F., Schreiber, S., Lieb, W., Soyka, M., Semmo, N., Aigner, E., Datz, C., Schmelz, R., Brückner, S., Zeissig, S., Stephan, A.-M., Wodarz, N., Devière, J., Clumeck, N., Sarrazin, C., Lammert, F., Gustot, T., Deltenre, P., Völzke, H., Lerch, M.M., Mayerle, J., Eyer, F., Schafmayer, C., Cichon, S., Nöthen, M.M., Nothnagel, M., Ellinghaus, D., Huse, K., Franke, A., Zopf, S., Hellerbrand, C., Moreno, C., Franchimont, D., Morgan, M.Y., Hampe, J., 2015. A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nat. Genet. 47, 1443–1448. doi.org/10.1038/ng.3417

Dannlowski, U., Kugel, H., Grotegerd, D., Redlich, R., Suchy, J., Opel, N., Suslow, T., Konrad, C., Ohrmann, P., Bauer, J., Kircher, T., Krug, A., Jansen, A., Baune, B.T., Heindel, W., Domschke, K., Forstner, A.J., Nöthen, M.M., Treutlein, J., Arolt, V., Hohoff, C., Rietschel, M., Witt, S.H., 2015. NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression. Neuropsychopharmacology 40, 2510–2516. doi.org/10.1038/npp.2015.86

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., 2015. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Transl Psychiatry 5, e678. doi.org/10.1038/tp.2015.159

Frank, J., Lang, M., Witt, S.H., Strohmaier, J., Rujescu, D., Cichon, S., Degenhardt, F., Nöthen, M.M., Collier, D.A., Ripke, S., Naber, D., Rietschel, M., 2015. Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients. Mol. Psychiatry 20, 150–151. doi.org/10.1038/mp.2014.56

Gade, K., Malzahn, D., Anderson-Schmidt, H., Strohmaier, J., Meier, S., Frank, J., Falkai, P.G., Rietschel, M., Schulze, T.G., 2015. Functional outcome in major psychiatric disorders and associated clinical and psychosocial variables: A potential cross-diagnostic phenotype for further genetic investigations? World J. Biol. Psychiatry 16, 237–248. doi.org/10.3109/15622975.2014.995221

Gorris, R., Fischer, J., Erwes, K.L., Kesavan, J., Peterson, D.A., Alexander, M., Nöthen, M.M., Peitz, M., Quandel, T., Karus, M., Brüstle, O., 2015. Pluripotent stem cell-derived radial glia-like cells as stable intermediate for efficient generation of human oligodendrocytes. Glia 63, 2152–2167. doi.org/10.1002/glia.22882

Heilbronner, U., Malzahn, D., Strohmaier, J., Maier, S., Frank, J., Treutlein, J., Mühleisen, T.W., Forstner, A.J., Witt, S.H., Cichon, S., Falkai, P., Nöthen, M.M., Rietschel, M., Schulze, T.G., 2015. A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder. Eur Neuropsychopharmacol 25, 2262–2270. doi.org/10.1016/j.euroneuro.2015.09.012

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Kumar, D., Dedic, N., Flachskamm, C., Voulé, S., Deussing, J.M., Kimura, M., 2015. Cacna1c (Cav1.2) Modulates Electroencephalographic Rhythm and Rapid Eye Movement Sleep Recovery. Sleep 38, 1371–1380. doi.org/10.5665/sleep.4972

Luo, X.-J., Mattheisen, M., Li, M., Huang, L., Rietschel, M., Børglum, A.D., Als, T.D., van den Oord, E.J., Aberg, K.A., Mors, O., Mortensen, P.B., Luo, Z., Degenhardt, F., Cichon, S., Schulze, T.G., Nöthen, M.M., iPSYCH-GEMS SCZ working group, MooDS SCZ Consortium, Su, B., Zhao, Z., Gan, L., Yao, Y.-G., 2015. 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. Schizophr Bull 41, 1294–1308. doi.org/10.1093/schbul/sbv017

Peykov, S., Berkel, S., Schoen, M., Weiss, K., Degenhardt, F., Strohmaier, J., Weiss, B., Proepper, C., Schratt, G., Nöthen, M.M., Boeckers, T.M., Rietschel, M., Rappold, G.A., 2015. Identification and functional characterization of rare SHANK2 variants in schizophrenia. Mol. Psychiatry 20, 1489–1498. doi.org/10.1038/mp.2014.172

Spyroglou, A., Riester, A., Mueller-Peltzer, K., Lu, A., Rohde, J., Hantel, C., Kuehne, C., Kulle, A., Riepe, F., Deussing, J.M., Beuschlein, F., 2015. Adrenal and Ovarian Phenotype of a Tissue-Specific Urocortin 2-Overexpressing Mouse Model. Endocrinology 156, 2646–2656. doi.org/10.1210/en.2014-1971

Stappert, L., Roese-Koerner, B., Brüstle, O., 2015. The role of microRNAs in human neural stem cells, neuronal differentiation and subtype specification. Cell Tissue Res. 359, 47–64. doi.org/10.1007/s00441-014-1981-y

Stepniak, B., Kästner, A., Poggi, G., Mitjans, M., Begemann, M., Hartmann, A., Van der Auwera, S., Sananbenesi, F., Krueger-Burg, D., Matuszko, G., Brosi, C., Homuth, G., Völzke, H., Benseler, F., Bagni, C., Fischer, U., Dityatev, A., Grabe, H.-J., Rujescu, D., Fischer, A., Ehrenreich, H., 2015. Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. EMBO Mol Med 7, 1565–1579. doi.org/10.15252/emmm.201505696

Van der Auwera, S., Wittfeld, K., Homuth, G., Teumer, A., Hegenscheid, K., Grabe, H.J., 2015. No association between polygenic risk for schizophrenia and brain volume in the general population. Biol. Psychiatry 78, e41-42. doi.org/10.1016/j.biopsych.2015.02.038

Willert, A., Mohnke, S., Erk, S., Schnell, K., Romanczuk-Seiferth, N., Quinlivan, E., Schreiter, S., Spengler, S., Herold, D., Wackerhagen, C., Romund, L., Garbusow, M., Lett, T., Stamm, T., Adli, M., Heinz, A., Bermpohl, F., Walter, H., 2015. Alterations in neural Theory of Mind processing in euthymic patients with bipolar disorder and unaffected relatives. Bipolar Disord 17, 880–891. doi.org/10.1111/bdi.12352

2014

Giusti, S.A., Vercelli, C.A., Vogl, A.M., Kolarz, A.W., Pino, N.S., Deussing, J.M., Refojo, D., 2014. Behavioral phenotyping of Nestin-Cre mice: implications for genetic mouse models of psychiatric disorders. J Psychiatr Res 55, 87–95. doi.org/10.1016/j.jpsychires.2014.04.002

Karus, M., Blaess, S., Brüstle, O., 2014. Self-organization of neural tissue architectures from pluripotent stem cells. J. Comp. Neurol. 522, 2831–2844. doi.org/10.1002/cne.23608

Mühleisen, T.W., Leber, M., Schulze, T.G., Strohmaier, J., Degenhardt, F., Treutlein, J., Mattheisen, M., Forstner, A.J., 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., 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., Krasnow, V., Chuchalin, A., Babadjanova, G., Pantelejeva, G., Abramova, L.I., Tiganov, A.S., Polonikov, A., Khusnutdinova, E., Alda, M., Grof, P., Rouleau, G.A., Turecki, G., Laprise, C., Rivas, F., Mayoral, F., Kogevinas, M., Grigoroiu-Serbanescu, M., Propping, P., Becker, T., Rietschel, M., Nöthen, M.M., Cichon, S., 2014. Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun 5, 3339. doi.org/10.1038/ncomms4339

Schizophrenia Working Group of the Psychiatric Genomics Consortium, 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511, 421–427. doi.org/10.1038/nature13595

Treutlein, J., Strohmaier, J., Frank, J., Mühleisen, T.W., Degenhardt, F., Witt, S.H., Schulze, T.G., Cichon, S., Nöthen, M.M., Rietschel, M., 2014. Smoking behaviour: investigation of the coaction of environmental and genetic risk factors. Psychiatr. Genet. 24, 279–280. doi.org/10.1097/YPG.0000000000000051