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Items where Author is "Witt, Stephanie H."

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Number of items: 17.

Article

Schwarz, Emanuel and Doan, Nhat Trung and Pergola, Giulio and Westlye, Lars T. and Kaufmann, Tobias and Wolfers, Thomas and Brecheisen, Ralph and Quarto, Tiziana and Ing, Alex J. and Di Carlo, Pasquale and Gurholt, Tiril P. and Harms, Robbert L. and Noirhomme, Quentin and Moberget, Torgeir and Agartz, Ingrid and Andreassen, Ole A. and Bellani, Marcella and Bertolino, Alessandro and Blasi, Giuseppe and Brambilla, Paolo and Buitelaar, Jan K. and Cervenka, Simon and Flyckt, Lena and Frangou, Sophia and Franke, Barbara and Hall, Jeremy and Heslenfeld, Dirk J. and Kirsch, Peter and McIntosh, Andrew M. and Nöthen, Markus M. and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F. and Rietschel, Marcella and Schumann, Gunter and Tost, Heike and Witt, Stephanie H. and Zink, Mathias and Meyer-Lindenberg, Andreas and Imagemend Consortium, Karolinska Schizophrenia Project Consortium. (2019) Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder. Translational Psychiatry, 9 (1). p. 12.

Degenhardt, Franziska and Heinemann, Barbara and Strohmaier, Jana and Pfohl, Marvin A. and Giegling, Ina and Hofmann, Andrea and Ludwig, Kerstin U. and Witt, Stephanie H. and Ludwig, Michael and Forstner, Andreas J. and Albus, Margot and Schwab, Sibylle G. and Borrmann-Hassenbach, Margitta and Lennertz, Leonard and Wagner, Michael and Hoffmann, Per and Rujescu, Dan and Maier, Wolfgang and Cichon, Sven and Rietschel, Marcella and Nothen, Markus M.. (2016) Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatric Genetics, 26 (6). pp. 293-296.

Heilbronner, Urs and Malzahn, Dörthe and Strohmaier, Jana and Maier, Sandra and Frank, Josef and Treutlein, Jens and Muhleisen, Thomas W. and Forstner, Andreas J. and Witt, Stephanie H. and Cichon, Sven and Falkai, Peter and Nothen, Markus M. and Rietschel, Marcella and Schulze, Thomas 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. European Neuropsychopharmacology, 25 (12). pp. 2262-2270.

Basmanav, F. Buket and Forstner, Andreas J. and Fier, Heide and Herms, Stefan and Meier, Sandra and Degenhardt, Franziska and Hoffmann, Per and Barth, Sandra and Fricker, Nadine and Strohmaier, Jana and Witt, Stephanie H. and Ludwig, Michael and Schmael, Christine and Moebus, Susanne and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Rietschel, Marcella and Lange, Christoph and Nöthen, Markus M. and Cichon, Sven. (2015) Investigation of the Role of TCF4 Rare Sequence Variants in Schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168B (5). pp. 354-362.

Juraeva, Dilafruz and Treutlein, Jens and Scholz, Henrike and Frank, Josef and Degenhardt, Franziska and Cichon, Sven and Ridinger, Monika and Mattheisen, Manuel and Witt, Stephanie H. and Lang, Maren and Sommer, Wolfgang H. and Hoffmann, Per and Herms, Stefan and Wodarz, Norbert and Soyka, Michael and Zill, Peter and Maier, Wolfgang and Jünger, Elisabeth and Gaebel, Wolfgang and Dahmen, Norbert and Scherbaum, Norbert and Schmäl, Christine and Steffens, Michael and Lucae, Susanne and Ising, Marcus and Smolka, Michael N. and Zimmermann, Ulrich S. and Müller-Myhsok, Bertram and Nöthen, Markus M. and Mann, Karl and Kiefer, Falk and Spanagel, Rainer and Brors, Benedikt and Rietschel, Marcella. (2015) XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans. Neuropsychopharmacology, 40 (2). pp. 361-371.

Witt, Stephanie H. and Kleindienst, Nikolaus and Frank, Josef and Treutlein, Jens and Muhleisen, Thomas W. and Degenhardt, Franziska and Jungkunz, Martin and Krumm, Bertram and Cichon, Sven and Tadic, André and Dahmen, Norbert and Schwarze, Cornelia E. and Schott, Björn H. and Dietl, Lydia and Nöthen, Markus M. and Mobascher, Arian and Lieb, Klaus and Roepke, Stefan and Rujescu, Dan and Rietschel, Marcella and Schmahl, Christian and Bohus, Martin. (2014) Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Psychiatric Genetics, 24 (6). pp. 262-265.

Nieratschker, Vanessa and Grosshans, Martin and Frank, Josef and Strohmaier, Jana and von der Goltz, Christoph and El-Maarri, Osman and Witt, Stephanie H. and Cichon, Sven and Nöthen, Markus M. and Kiefer, Falk and Rietschel, Marcella. (2014) Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age. Addiction Biology, 19 (2). pp. 305-311.

Schott, Björn H. and Assmann, Anne and Schmierer, Phöbe and Soch, Joram and Erk, Susanne and Garbusow, Maria and Mohnke, Sebastian and Pohland, Lydia and Romanczuk-Seiferth, Nina and Barman, Adrian and Wustenberg, Torsten and Haddad, Linda and Grimm, Oliver and Witt, Stephanie H. and Richter, Sylvia and Klein, Marieke and Schutze, Hartmut and Muhleisen, Thomas W. and Cichon, Sven and Rietschel, Marcella and Noethen, Markus M. and Tost, H. and Gundelfinger, Eckart D. and Duzel, Emrah and Heinz, Andreas and Meyer-Lindenberg, Andreas and Seidenbecher, Constanze I. and Walter, Henrik . (2014) Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding. Translational Psychiatry, 4. e372.

Mohnke, Sebastian and Erk, Susanne and Schnell, Knut and Schütz, Claudia and Romanczuk-Seiferth, Nina and Grimm, Oliver and Haddad, Leila and Pohland, Lydia and Garbusow, Maria and Schmitgen, Mike M. and Kirsch, Peter and Esslinger, Christine and Rietschel, Marcella and Witt, Stephanie H. and Nöthen, Markus M. and Cichon, Sven and Mattheisen, Manuel and Mühleisen, Thomas and Jensen, Jimmy and Schott, Björn H. and Maier, Wolfgang and Heinz, Andreas and Meyer-Lindenberg, Andreas and Walter, Henrik . (2014) Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network. Neuropsychopharmacology, 39 (5). pp. 1196-1205.

Muhleisen, Thomas W. and Leber, Markus and Schulze, Thomas G. and Strohmaier, Jana and Degenhardt, Franziska and Treutlein, Jens and Mattheisen, Manuel and Forstner, Andreas J. and Schumacher, Johannes and Breuer, René and Meier, Sandra and Herms, Stefan and Hoffmann, Per and Lacour, André and Witt, Stephanie H. and Reif, Andreas and Müller-Myhsok, Bertram and Lucae, Susanne and Maier, Wolfgang and Schwarz, Markus and Vedder, Helmut and Kammerer-Ciernioch, Jutta and Pfennig, Andrea and Bauer, Michael and Hautzinger, Martin and Moebus, Susanne and Priebe, Lutz and Czerski, Piotr M. and Hauser, Joanna and Lissowska, Jolanta and Szeszenia-Dabrowska, Neonila and Brennan, Paul and McKay, James and Wright, Adam and Mitchell, Philip B and Fullerton, Janice M. and Schofield, Peter R. and Montgomery, Grant W. and Medland, Sarah E. and Gordon, Scott D. and Martin, Nicolas G. and Krasnow, Valery and Chuchalin, Alexander and Babadjanova, Gulja and Pantelejeva, Galina and Abramova, Lilia I. and Tiganov, Alexander S. and Polonikov, Alexey and Khusnutdinova, Elza and Alda, Martin and Grof, Paul and Rouleau, Guy A. and Turecki, Gustavo and Laprise, Catherine and Rivas, Fabio and Mayoral, Fermin and Kogevinas, Manolis and Grigoroiu-Serbanescu, Maria and Propping, Peter and Becker, Tim and Rietschel, Marcella and Nöthen, Markus M. and Cichon, Sven. (2014) Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun, 5. p. 3339.

Erk, Susanne and Meyer-Lindenberg, Andreas and Schmierer, Phöbe and Mohnke, Sebastian and Grimm, Oliver and Garbusow, Maria and Haddad, Leila and Poehland, Lydia and Muhleisen, Thomas W. and Witt, Stephanie H. and Tost, Heike and Kirsch, Peter and Romanczuk-Seiferth, Nina and Schott, Björn H. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. Biological Psychiatry, 76 (6). pp. 466-475.

Juraeva, Dilafruz and Haenisch, Britta and Zapatka, Marc and Frank, Josef and Group Investigators, and Psych-Gems Scz Working Group, and Witt, Stephanie H. and Muhleisen, Thomas W. and Treutlein, Jens and Strohmaier, Jana and Meier, Sandra and Degenhardt, Franziska and Giegling, Ina and Ripke, Stephan and Leber, Markus and Lange, Christoph and Schulze, Thomas G. and Mössner, Rainald and Nenadic, Igor and Sauer, Heinrich and Rujescu, Dan and Maier, Wolfgang and Borglum, Anders and Ophoff, Roel A. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Mattheisen, Manuel and Brors, Benedikt. (2014) Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS Genetics, 10 (6). e1004345.

Witt, Stephanie H. and Juraeva, Dilafruz and Sticht, Carsten and Strohmaier, Jana and Meier, S. and Treutlein, J. and Dukal, Helene and Frank, Josef and Lang, Maren and Deuschle, Michael and Schulze, T. G. and Degenhardt, F. and Mattheisen, Manuel and Brors, B. and Cichon, Sven and Nothen, M. M. and Witt, Christian C. and Rietschel, Marcella. (2014) Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder. Translational Psychiatry, 4. e426.

Forstner, Andreas J. and Basmanav, F. Buket and Mattheisen, Manuel and Böhmer, Anne Christin and Hollegaard, Mads V. and Janson, Esther and Strengman, Eric and Priebe, Lutz and Degenhardt, Franziska and Hoffmann, Per and Herms, Stefan and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Ophoff, Roel A. and Moebus, Susanne and Mortensen, Preben Bo and Borglum, A. D. and Hougaard, David M. and Frank, Josef and Witt, Stephanie H. and Rietschel, Marcella and Zimmermann, Andrea and Nöthen, Markus M. and Miro, Xavier and Cichon, Sven. (2014) Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. Journal of psychiatry & neuroscience, 39 (6). pp. 386-396.

Erk, Susanne and Meyer-Lindenberg, Andreas and Linden, David E. and Lancaster, Thomas and Mohnke, Sebastian and Grimm, Oliver and Degenhardt, Franziska and Holmans, Peter and Pocklington, Andrew and Schmierer, Phöbe and Haddad, Leila and Muhleisen, Thomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Romanczuk-Seiferth, Nina and Tost, Heike and Schott, Björn H. and Cichon, Sven and Nothen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects. NeuroImage, 94. pp. 147-154.

Treutlein, Jens and Strohmaier, Jana and Frank, Josef and Muhleisen, Thomas W. and Degenhardt, Franziska and Witt, Stephanie H. and Schulze, Thomas G. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella. (2014) Smoking behaviour: investigation of the coaction of environmental and genetic risk factors. Psychiatric Genetics, 24 (6). pp. 279-280.

Grimm, Oliver and Heinz, Andreas and Walter, Henrik and Kirsch, Peter and Erk, Susanne and Haddad, Leila and Plichta, Michael M. and Romanczuk-Seiferth, Nina and Pohland, Lydia and Mohnke, Sebastian and Muhleisen, Thoomas W. and Mattheisen, Manuel and Witt, Stephanie H. and Schafer, Axel and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Tost, Heike and Meyer-Lindenberg, Andreas. (2014) Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia. JAMA Psychiatry, 71 (5). pp. 531-539.

This list was generated on Sun Nov 27 02:12:22 2022 CET.