IntegraMent

Publikationen

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., 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. doi.org/10.1016/j.neuroimage.2017.12.054

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., Fischer, A., 2018. RNA-Dependent Intergenerational Inheritance of Enhanced Synaptic Plasticity after Environmental Enrichment. Cell Rep 23, 546–554. doi.org/10.1016/j.celrep.2018.03.059

Binz, T.M., Rietschel, L., Streit, F., Hofmann, M., Gehrke, J., Herdener, M., Quednow, B.B., Martin, N.G., Rietschel, M., Kraemer, T., 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 Sci. Int. 284, 33–38. doi.org/10.1016/j.forsciint.2017.12.032

Braun, U., Schaefer, A., Betzel, R.F., Tost, H., Meyer-Lindenberg, A., Bassett, D.S., 2018. From Maps to Multi-dimensional Network Mechanisms of Mental Disorders. Neuron 97, 14–31. doi.org/10.1016/j.neuron.2017.11.007

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 Group, MooDS Bipolar Consortium, Walter, H., Erk, S., Heinz, A., Amin, N., van Duijn, C.M., Meyer-Lindenberg, A., Tost, H., Xiao, X., Yamamoto, T., Rietschel, M., Li, M., 2018. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Mol. Psychiatry 23, 400–412. doi.org/10.1038/mp.2016.231

Chen, J., Cao, H., Meyer-Lindenberg, A., Schwarz, E., 2018. Male increase in brain gene expression variability is linked to genetic risk for schizophrenia. Transl Psychiatry 8, 140. doi.org/10.1038/s41398-018-0200-0

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., Sartorius, A., 2018. Lateral habenula perturbation reduces default-mode network connectivity in a rat model of depression. Transl Psychiatry 8, 68. doi.org/10.1038/s41398-018-0121-y

Comes, A.L., Papiol, S., Mueller, T., Geyer, P.E., Mann, M., Schulze, T.G., 2018. Proteomics for blood biomarker exploration of severe mental illness: pitfalls of the past and potential for the future. Transl Psychiatry 8, 160. doi.org/10.1038/s41398-018-0219-2

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., Lesch, K.-P., 2018. Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Mol. Psychiatry. doi.org/10.1038/s41380-018-0210-6

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., 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. Mol. Psychiatry 23, 133–142. doi.org/10.1038/mp.2017.44

de Boni, L., Gasparoni, G., Haubenreich, C., Tierling, S., Schmitt, I., Peitz, M., Koch, P., Walter, J., Wüllner, U., Brüstle, O., 2018. DNA methylation alterations in iPSC- and hESC-derived neurons: potential implications for neurological disease modeling. Clin Epigenetics 10, 13. doi.org/10.1186/s13148-018-0440-0

Dedic, Nina, Chen, A., Deussing, J.M., 2018a. The CRF Family of Neuropeptides and their Receptors - Mediators of the Central Stress Response. Curr Mol Pharmacol 11, 4–31. doi.org/10.2174/1874467210666170302104053

Dedic, Nina, 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., Deussing, J.M., 2018b. Chronic CRH depletion from GABAergic, long-range projection neurons in the extended amygdala reduces dopamine release and increases anxiety. Nat. Neurosci. 21, 803–807. doi.org/10.1038/s41593-018-0151-z

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., Deussing, J.M., 2018. Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. Mol. Psychiatry 23, 533–543. doi.org/10.1038/mp.2017.133

Deussing, J.M., Arzt, E., 2018. P2X7 Receptor: A Potential Therapeutic Target for Depression? Trends Mol Med 24, 736–747. doi.org/10.1016/j.molmed.2018.07.005

Deussing, J.M., Chen, A., 2018. The Corticotropin-Releasing Factor Family: Physiology of the Stress Response. Physiol. Rev. 98, 2225–2286. doi.org/10.1152/physrev.00042.2017

Foo, J.C., Streit, F., Treutlein, J., Ripke, S., Witt, S.H., Strohmaier, J., Degenhardt, F., Forstner, A.J., Hoffmann, P., Soyka, M., Dahmen, N., Scherbaum, N., Wodarz, N., Heilmann-Heimbach, S., Herms, S., Cichon, S., Preuss, U., Gaebel, W., Ridinger, M., Hoffmann, S., Schulze, T.G., Maier, W., Zill, P., Müller-Myhsok, B., Ising, M., Lucae, S., Nöthen, M.M., Mann, K., Kiefer, F., Rietschel, M., Frank, J., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 2018. Shared genetic etiology between alcohol dependence and major depressive disorder. Psychiatr. Genet. 28, 66–70. doi.org/10.1097/YPG.0000000000000201

Fulterer, A., Andlauer, T.F.M., Ender, A., Maglione, M., Eyring, K., Woitkuhn, J., Lehmann, M., Matkovic-Rachid, T., Geiger, J.R.P., Walter, A.M., Nagel, K.I., Sigrist, S.J., 2018. Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses. Cell Rep 23, 1259–1274. doi.org/10.1016/j.celrep.2018.03.126

Geiger, L.S., Moessnang, C., Schäfer, A., Zang, Z., Zangl, M., Cao, H., van Raalten, T.R., Meyer-Lindenberg, A., Tost, H., 2018. Novelty modulates human striatal activation and prefrontal-striatal effective connectivity during working memory encoding. Brain Struct Funct. doi.org/10.1007/s00429-018-1679-0

Hughes, T., Sønderby, I.E., Polushina, T., Hansson, L., Holmgren, A., Athanasiu, L., Melbø-Jørgensen, C., Hassani, S., Hoeffding, L.K., Herms, S., Bergen, S.E., Karlsson, R., Song, J., Rietschel, M., Nöthen, M.M., Forstner, A.J., Hoffmann, P., Hultman, C.M., Landén, M., Cichon, S., Werge, T., Andreassen, O.A., Le Hellard, S., Djurovic, S., 2018. Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder. Transl Psychiatry 8, 210. doi.org/10.1038/s41398-018-0175-x

International Consortium on Lithium Genetics (ConLi+Gen), Amare, A.T., Schubert, K.O., Hou, L., Clark, S.R., Papiol, S., Heilbronner, U., Degenhardt, F., Tekola-Ayele, F., Hsu, Y.-H., Shekhtman, T., Adli, M., Akula, N., Akiyama, K., Ardau, R., Arias, B., Aubry, J.-M., Backlund, L., Bhattacharjee, A.K., Bellivier, F., Benabarre, A., Bengesser, S., Biernacka, J.M., Birner, A., Brichant-Petitjean, C., Cervantes, P., Chen, H.-C., Chillotti, C., Cichon, S., Cruceanu, C., Czerski, P.M., Dalkner, N., Dayer, A., Del Zompo, M., DePaulo, J.R., Étain, B., Falkai, P., Forstner, A.J., Frisen, L., Frye, M.A., Fullerton, J.M., Gard, S., Garnham, J.S., Goes, F.S., Grigoroiu-Serbanescu, M., Grof, P., Hashimoto, R., Hauser, J., Herms, S., Hoffmann, P., Hofmann, A., Jamain, S., Jiménez, E., Kahn, J.-P., Kassem, L., Kuo, P.-H., Kato, T., Kelsoe, J., Kittel-Schneider, S., Kliwicki, S., König, B., Kusumi, I., Laje, G., Landén, M., Lavebratt, C., Leboyer, M., Leckband, S.G., Tortorella, A., Manchia, M., Martinsson, L., McCarthy, M.J., McElroy, S., Colom, F., Mitjans, M., Mondimore, F.M., Monteleone, P., Nievergelt, C.M., Nöthen, M.M., Novák, T., O’Donovan, C., Ozaki, N., Ösby, U., Pfennig, A., Potash, J.B., Reif, A., Reininghaus, E., Rouleau, G.A., Rybakowski, J.K., Schalling, M., Schofield, P.R., Schweizer, B.W., Severino, G., Shilling, P.D., Shimoda, K., Simhandl, C., Slaney, C.M., Squassina, A., Stamm, T., Stopkova, P., Maj, M., Turecki, G., Vieta, E., Volkert, J., Witt, S., Wright, A., Zandi, P.P., Mitchell, P.B., Bauer, M., Alda, M., Rietschel, M., McMahon, F.J., Schulze, T.G., Baune, B.T., 2018. Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. JAMA Psychiatry 75, 65–74. doi.org/10.1001/jamapsychiatry.2017.3433

International Stem Cell Initiative, 2018. Assessment of established techniques to determine developmental and malignant potential of human pluripotent stem cells. Nat Commun 9, 1925. doi.org/10.1038/s41467-018-04011-3

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., Schulze, T.G., 2018. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. Bipolar Disord. doi.org/10.1111/bdi.12659

Krug, A., Dietsche, B., Zöllner, R., Yüksel, D., Nöthen, M.M., Forstner, A.J., Rietschel, M., Dannlowski, U., Baune, B.T., Maier, R., Witt, S.H., Kircher, T., 2018. Polygenic risk for schizophrenia affects working memory and its neural correlates in healthy subjects. Schizophr. Res. doi.org/10.1016/j.schres.2018.01.013

Leuchs, L., Schneider, M., Spoormaker, V.I., 2018. Measuring the conditioned response: A comparison of pupillometry, skin conductance, and startle electromyography. Psychophysiology e13283. doi.org/10.1111/psyp.13283

Mühleisen, T.W., Reinbold, C.S., Forstner, A.J., Abramova, L.I., Alda, M., Babadjanova, G., Bauer, M., Brennan, P., Chuchalin, A., Cruceanu, C., Czerski, P.M., Degenhardt, F., Fischer, S.B., Fullerton, J.M., Gordon, S.D., Grigoroiu-Serbanescu, M., Grof, P., Hauser, J., Hautzinger, M., Herms, S., Hoffmann, P., Kammerer-Ciernioch, J., Khusnutdinova, E., Kogevinas, M., Krasnov, V., Lacour, A., Laprise, C., Leber, M., Lissowska, J., Lucae, S., Maaser, A., Maier, W., Martin, N.G., Mattheisen, M., Mayoral, F., McKay, J.D., Medland, S.E., Mitchell, P.B., Moebus, S., Montgomery, G.W., Müller-Myhsok, B., Oruc, L., Pantelejeva, G., Pfennig, A., Pojskic, L., Polonikov, A., Reif, A., Rivas, F., Rouleau, G.A., Schenk, L.M., Schofield, P.R., Schwarz, M., Streit, F., Strohmaier, J., Szeszenia-Dabrowska, N., Tiganov, A.S., Treutlein, J., Turecki, G., Vedder, H., Witt, S.H., Schulze, T.G., Rietschel, M., Nöthen, M.M., Cichon, S., 2018. Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder 20–25.

Papanastasiou, E., Mouchlianitis, E., Joyce, D.W., McGuire, P., Banaschewski, T., Bokde, A.L.W., Bromberg, U., Büchel, C., Quinlan, E.B., Desrivières, S., Flor, H., Frouin, V., Garavan, H., Spechler, P., Gowland, P., Heinz, A., Ittermann, B., Martinot, J.-L., Paillère Martinot, M.-L., Artiges, E., Nees, F., Papadopoulos Orfanos, D., Poustka, L., Millenet, S., Fröhner, J.H., Smolka, M.N., Walter, H., Whelan, R., Schumann, G., Shergill, S., IMAGEN Consortium, 2018. Examination of the Neural Basis of Psychoticlike Experiences in Adolescence During Reward Processing. JAMA Psychiatry. doi.org/10.1001/jamapsychiatry.2018.1973

Papiol, S., Schulze, T.G., Alda, M., 2018. Genetics of Lithium Response in Bipolar Disorder. Pharmacopsychiatry 51, 206–211. doi.org/10.1055/a-0590-4992

Piel, J.H., Lett, T.A., Wackerhagen, C., Plichta, M.M., Mohnke, S., Grimm, O., Romanczuk-Seiferth, N., Degenhardt, F., Tost, H., Witt, S., Nöthen, M., Rietschel, M., Heinz, A., Meyer-Lindenberg, A., Walter, H., Erk, S., 2018. The effect of 5-HTTLPR and a serotonergic multi-marker score on amygdala, prefrontal and anterior cingulate cortex reactivity and habituation in a large, healthy fMRI cohort. Eur Neuropsychopharmacol. doi.org/10.1016/j.euroneuro.2017.12.014

Schäffner, I., Minakaki, G., Khan, M.A., Balta, E.-A., Schlötzer-Schrehardt, U., Schwarz, T.J., Beckervordersandforth, R., Winner, B., Webb, A.E., DePinho, R.A., Paik, J., Wurst, W., Klucken, J., Lie, D.C., 2018. FoxO Function Is Essential for Maintenance of Autophagic Flux and Neuronal Morphogenesis in Adult Neurogenesis. Neuron 99, 1188-1203.e6. doi.org/10.1016/j.neuron.2018.08.017

Schilling, C., Gappa, L., Schredl, M., Streit, F., Treutlein, J., Frank, J., Deuschle, M., Meyer-Lindenberg, A., Rietschel, M., Witt, S.H., 2018. Fast sleep spindle density is associated with rs4680 (Val108/158Met) genotype of catechol-O-methyltransferase (COMT). Sleep 41. doi.org/10.1093/sleep/zsy007

Streit, F., Treutlein, J., Frischknecht, U., Hermann, D., Mann, K., Kiefer, F., Sack, M., Hall, A.S.M., Frank, J., Witt, S.H., Foo, J.C., Degenhardt, F., Heilmann-Heimbach, S., Nöthen, M.M., Sommer, W.H., Spanagel, R., Rietschel, M., Ende, G., 2018. Glutamate concentration in the anterior cingulate cortex in alcohol dependence: association with alcohol withdrawal and exploration of contribution from glutamatergic candidate genes. Psychiatr. Genet. 28, 94–95. doi.org/10.1097/YPG.0000000000000202

Trepte, P., Kruse, S., Kostova, S., Hoffmann, S., Buntru, A., Tempelmeier, A., Secker, C., Diez, L., Schulz, A., Klockmeier, K., Zenkner, M., Golusik, S., Rau, K., Schnoegl, S., Garner, C.C., Wanker, E.E., 2018. LuTHy: a double-readout bioluminescence-based two-hybrid technology for quantitative mapping of protein-protein interactions in mammalian cells. Mol. Syst. Biol. 14, e8071.

Van der Auwera, S., Peyrot, W.J., Milaneschi, Y., Hertel, J., Baune, B., Breen, G., Byrne, E., Dunn, E.C., Fisher, H., Homuth, G., Levinson, D., Lewis, C., Mills, N., Mullins, N., Nauck, M., Pistis, G., Preisig, M., Rietschel, M., Ripke, S., Sullivan, P., Teumer, A., Völzke, H., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Boomsma, D.I., Wray, N.R., Penninx, B., Grabe, H., 2018. Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am. J. Med. Genet. B Neuropsychiatr. Genet. 177, 40–49. doi.org/10.1002/ajmg.b.32593

Vieta, E., Berk, M., Schulze, T.G., Carvalho, A.F., Suppes, T., Calabrese, J.R., Gao, K., Miskowiak, K.W., Grande, I., 2018. Bipolar disorders. Nat Rev Dis Primers 4, 18008. doi.org/10.1038/nrdp.2018.8

Vogel, B.O., Lett, T.A., Erk, S., Mohnke, S., Wackerhagen, C., Brandl, E.J., Romanczuk-Seiferth, N., Otto, K., Schweiger, J.I., Tost, H., Nöthen, M.M., Rietschel, M., Degenhardt, F., Witt, S.H., Meyer-Lindenberg, A., Heinz, A., Walter, H., 2018. The influence of MIR137 on white matter fractional anisotropy and cortical surface area in individuals with familial risk for psychosis. Schizophr. Res. 195, 190–196. doi.org/10.1016/j.schres.2017.09.030

Witt, S.H., Frank, J., Gilles, M., Lang, M., Treutlein, J., Streit, F., Wolf, I.A.C., Peus, V., Scharnholz, B., Send, T.S., Heilmann-Heimbach, S., Sivalingam, S., Dukal, H., Strohmaier, J., Sütterlin, M., Arloth, J., Laucht, M., Nöthen, M.M., Deuschle, M., Rietschel, M., 2018. Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation. BMC Genomics 19, 290. doi.org/10.1186/s12864-018-4652-7

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Schulz, H., Ruppert, A.-K., Herms, S., Wolf, C., Mirza-Schreiber, N., Stegle, O., Czamara, D., Forstner, A.J., Sivalingam, S., Schoch, S., Moebus, S., Pütz, B., Hillmer, A., Fricker, N., Vatter, H., Müller-Myhsok, B., Nöthen, M.M., Becker, A.J., Hoffmann, P., Sander, T., Cichon, S., 2017. Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. Nat Commun 8, 1511. doi.org/10.1038/s41467-017-01818-4

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Streit, F., Akdeniz, C., Haddad, L., Kumsta, R., Entringer, S., Frank, J., Yim, I.S., Zänkert, S., Witt, S.H., Kirsch, P., Rietschel, M., Wüst, S., 2017. Sex-specific association between functional neuropeptide S receptor gene (NPSR1) variants and cortisol and central stress responses. Psychoneuroendocrinology 76, 49–56. doi.org/10.1016/j.psyneuen.2016.10.027

Treutlein, J., Frank, J., Streit, F., Reinbold, C.S., Juraeva, D., Degenhardt, F., Rietschel, L., Witt, S.H., Forstner, A.J., Ridinger, M., Strohmaier, J., Wodarz, N., Dukal, H., Foo, J.C., Hoffmann, P., Herms, S., Heilmann-Heimbach, S., Soyka, M., Maier, W., Gaebel, W., Dahmen, N., Scherbaum, N., Müller-Myhsok, B., Lucae, S., Ising, M., Stickel, F., Berg, T., Roggenbuck, U., Jöckel, K.-H., Scholz, H., Zimmermann, U.S., Buch, S., Sommer, W.H., Spanagel, R., Brors, B., Cichon, S., Mann, K., Kiefer, F., Hampe, J., Rosendahl, J., Nöthen, M.M., Rietschel, M., 2017a. Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Genes (Basel) 8. doi.org/10.3390/genes8070183

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Uhrig, S., Vandael, D., Marcantoni, A., Dedic, N., Bilbao, A., Vogt, M.A., Hirth, N., Broccoli, L., Bernardi, R.E., Schönig, K., Gass, P., Bartsch, D., Spanagel, R., Deussing, J.M., Sommer, W.H., Carbone, E., Hansson, A.C., 2017. Differential Roles for L-Type Calcium Channel Subtypes in Alcohol Dependence. Neuropsychopharmacology 42, 1058–1069. doi.org/10.1038/npp.2016.266

Van der Auwera, S., Wittfeld, K., Shumskaya, E., Bralten, J., Zwiers, M.P., Onnink, A.M.H., Usberti, N., Hertel, J., Völzke, H., Völker, U., Hosten, N., Franke, B., Grabe, H.J., 2017. Predicting brain structure in population-based samples with biologically informed genetic scores for schizophrenia. Am. J. Med. Genet. B Neuropsychiatr. Genet. 174, 324–332. doi.org/10.1002/ajmg.b.32519

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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

Braun, U., Schäfer, A., Bassett, D.S., Rausch, F., Schweiger, J.I., Bilek, E., Erk, S., Romanczuk-Seiferth, N., Grimm, O., Geiger, L.S., Haddad, L., Otto, K., Mohnke, S., Heinz, A., Zink, M., Walter, H., Schwarz, E., Meyer-Lindenberg, A., Tost, H., 2016. Dynamic brain network reconfiguration as a potential schizophrenia genetic risk mechanism modulated by NMDA receptor function. Proc. Natl. Acad. Sci. U.S.A. 113, 12568–12573. doi.org/10.1073/pnas.1608819113

Cao, H., Bertolino, A., Walter, H., Schneider, M., Schäfer, A., Taurisano, P., Blasi, G., Haddad, L., Grimm, O., Otto, K., Dixson, L., Erk, S., Mohnke, S., Heinz, A., Romanczuk-Seiferth, N., Mühleisen, T.W., Mattheisen, M., Witt, S.H., Cichon, S., Noethen, M., Rietschel, M., Tost, H., Meyer-Lindenberg, A., 2016. Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia. JAMA Psychiatry 73, 598–605. doi.org/10.1001/jamapsychiatry.2016.0161

Chang, H., Li, L., Peng, T., Grigoroiu-Serbanescu, M., Bergen, S.E., Landén, M., Hultman, C.M., Forstner, A.J., Strohmaier, J., Hecker, J., Schulze, T.G., Müller-Myhsok, B., Reif, A., Mitchell, P.B., Martin, N.G., Cichon, S., Nöthen, M.M., Jamain, S., Leboyer, M., Bellivier, F., Etain, B., Kahn, J.-P., Henry, C., Rietschel, M., Swedish Bipolar Study Group, MooDS Consortium, Xiao, X., Li, M., 2016. Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1. Mol. Neurobiol. doi.org/10.1007/s12035-016-0041-x

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Degenhardt, F., Heinemann, B., Strohmaier, J., Pfohl, M.A., Giegling, I., Hofmann, A., Ludwig, K.U., Witt, S.H., Ludwig, M., Forstner, A.J., Albus, M., Schwab, S.G., Borrmann-Hassenbach, M., Lennertz, L., Wagner, M., Hoffmann, P., Rujescu, D., Maier, W., Cichon, S., Rietschel, M., Nöthen, M.M., 2016a. Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr. Genet. 26, 293–296. doi.org/10.1097/YPG.0000000000000145

Degenhardt, F., Krämer, L., Frank, J., Treutlein, J., Heilmann-Heimbach, S., Hecker, J., Fier, H.L., Lang, M., Witt, S.H., Koller, A.C., Mann, K., Hoffmann, S., Kiefer, F., Spanagel, R., Rietschel, M., Nöthen, M.M., 2016b. Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4. Alcohol. Clin. Exp. Res. 40, 1627–1632. doi.org/10.1111/acer.13125

Durstewitz, D., Koppe, G., Toutounji, H., 2016. Computational models as statistical tools. Current Opinion in Behavioral Sciences, Computational modelling 11, 93–99. doi.org/10.1016/j.cobeha.2016.07.004

Falk, A., Heine, V.M., Harwood, A.J., Sullivan, P.F., Peitz, M., Brüstle, O., Shen, S., Sun, Y.-M., Glover, J.C., Posthuma, D., Djurovic, S., 2016. Modeling psychiatric disorders: from genomic findings to cellular phenotypes. Mol. Psychiatry 21, 1167–1179. doi.org/10.1038/mp.2016.89

Falkai, P., Malchow, B., Wetzestein, K., Nowastowski, V., Bernstein, H.-G., Steiner, J., Schneider-Axmann, T., Kraus, T., Hasan, A., Bogerts, B., Schmitz, C., Schmitt, A., 2016a. Decreased Oligodendrocyte and Neuron Number in Anterior Hippocampal Areas and the Entire Hippocampus in Schizophrenia: A Stereological Postmortem Study. Schizophr Bull 42 Suppl 1, S4–S12. doi.org/10.1093/schbul/sbv157

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Franke, B., Stein, J.L., Ripke, S., Anttila, V., Hibar, D.P., van Hulzen, K.J.E., Arias-Vasquez, A., Smoller, J.W., Nichols, T.E., Neale, M.C., McIntosh, A.M., Lee, P., McMahon, F.J., Meyer-Lindenberg, A., Mattheisen, M., Andreassen, O.A., Gruber, O., Sachdev, P.S., Roiz-Santiañez, R., Saykin, A.J., Ehrlich, S., Mather, K.A., Turner, J.A., Schwarz, E., Thalamuthu, A., Yao, Y., Ho, Y.Y.W., Martin, N.G., Wright, M.J., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2, Enigma Consortium, O’Donovan, M.C., Thompson, P.M., Neale, B.M., Medland, S.E., Sullivan, P.F., 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nat. Neurosci. 19, 420–431. doi.org/10.1038/nn.4228

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Habes, M., Erus, G., Toledo, J.B., Zhang, T., Bryan, N., Launer, L.J., Rosseel, Y., Janowitz, D., Doshi, J., Van der Auwera, S., von Sarnowski, B., Hegenscheid, K., Hosten, N., Homuth, G., Völzke, H., Schminke, U., Hoffmann, W., Grabe, H.J., Davatzikos, C., 2016. White matter hyperintensities and imaging patterns of brain ageing in the general population. Brain 139, 1164–1179. doi.org/10.1093/brain/aww008

Hasan, A., Guse, B., Cordes, J., Wölwer, W., Winterer, G., Gaebel, W., Langguth, B., Landgrebe, M., Eichhammer, P., Frank, E., Hajak, G., Ohmann, C., Verde, P.E., Rietschel, M., Ahmed, R., Honer, W.G., Malchow, B., Karch, S., Schneider-Axmann, T., Falkai, P., Wobrock, T., 2016. Cognitive Effects of High-Frequency rTMS in Schizophrenia Patients With Predominant Negative Symptoms: Results From a Multicenter Randomized Sham-Controlled Trial. Schizophr Bull 42, 608–618. doi.org/10.1093/schbul/sbv142

Heilbronner, U., Gade, K., Herms, S., Strohmaier, J., Lang, M., Nöthen, M.M., Rietschel, M., Schulze, T.G., Degenhardt, F., 2016. Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia. Psychiatr. Genet. 26, 184–185. doi.org/10.1097/YPG.0000000000000135

Heinz, A., Schlagenhauf, F., Beck, A., Wackerhagen, C., 2016. Dimensional psychiatry: mental disorders as dysfunctions of basic learning mechanisms. J Neural Transm (Vienna) 123, 809–821. doi.org/10.1007/s00702-016-1561-2

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Isles, A.R., Ingason, A., Lowther, C., Walters, J., Gawlick, M., Stöber, G., Rees, E., Martin, J., Little, R.B., Potter, H., Georgieva, L., Pizzo, L., Ozaki, N., Aleksic, B., Kushima, I., Ikeda, M., Iwata, N., Levinson, D.F., Gejman, P.V., Shi, J., Sanders, A.R., Duan, J., Willis, J., Sisodiya, S., Costain, G., Werge, T.M., Degenhardt, F., Giegling, I., Rujescu, D., Hreidarsson, S.J., Saemundsen, E., Ahn, J.W., Ogilvie, C., Girirajan, S.D., Stefansson, H., Stefansson, K., O’Donovan, M.C., Owen, M.J., Bassett, A., Kirov, G., 2016. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. PLoS Genet. 12, e1005993. doi.org/10.1371/journal.pgen.1005993

Kirsten, H., Scholz, M., Kovacs, P., Grallert, H., Peters, A., Strauch, K., Frank, J., Rietschel, M., Nöthen, M.M., Witt, H., Rosendahl, J., 2016. Genetic variants of lipase activity in chronic pancreatitis. Gut 65, 184–185. doi.org/10.1136/gutjnl-2015-309521

Laimighofer, M., Krumsiek, J., Buettner, F., Theis, F.J., 2016. Unbiased Prediction and Feature Selection in High-Dimensional Survival Regression. J. Comput. Biol. 23, 279–290. doi.org/10.1089/cmb.2015.0192

Lang, M., Leménager, T., Streit, F., Fauth-Bühler, M., Frank, J., Juraeva, D., Witt, S.H., Degenhardt, F., Hofmann, A., Heilmann-Heimbach, S., Kiefer, F., Brors, B., Grabe, H.-J., John, U., Bischof, A., Bischof, G., Völker, U., Homuth, G., Beutel, M., Lind, P.A., Medland, S.E., Slutske, W.S., Martin, N.G., Völzke, H., Nöthen, M.M., Meyer, C., Rumpf, H.-J., Wurst, F.M., Rietschel, M., Mann, K.F., 2016. Genome-wide association study of pathological gambling. Eur. Psychiatry 36, 38–46. doi.org/10.1016/j.eurpsy.2016.04.001

Li, M., Huang, L., Grigoroiu-Serbanescu, M., Bergen, S.E., Landén, M., Hultman, C.M., Forstner, A.J., Strohmaier, J., Hecker, J., Schulze, T.G., Müller-Myhsok, B., Reif, A., Mitchell, P.B., Martin, N.G., Cichon, S., Nöthen, M.M., Alkelai, A., Lerer, B., Jamain, S., Leboyer, M., Bellivier, F., Etain, B., Kahn, J.-P., Henry, C., Rietschel, M., MooDS Consortium, Swedish Bipolar Study Group, 2016. Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. Mol. Neurobiol. 53, 6608–6619. doi.org/10.1007/s12035-015-9559-6

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

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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

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