Items where Author is "Degenhardt, Franziska"

2021

Koutsouleris, Nikolaos and Dwyer, Dominic B. and Degenhardt, Franziska and Maj, Carlo and Urquijo-Castro, Maria Fernanda and Sanfelici, Rachele and Popovic, David and Oeztuerk, Oemer and Haas, Shalaila S. and Weiske, Johanna and Ruef, Anne and Kambeitz-Ilankovic, Lana and Antonucci, Linda A. and Neufang, Susanne and Schmidt-Kraepelin, Christian and Ruhrmann, Stephan and Penzel, Nora and Kambeitz, Joseph and Haidl, Theresa K. and Rosen, Marlene and Chisholm, Katharine and Riecher-Rössler, Anita and Egloff, Laura and Schmidt, André and Andreou, Christina and Hietala, Jarmo and Schirmer, Timo and Romer, Georg and Walger, Petra and Franscini, Maurizia and Traber-Walker, Nina and Schimmelmann, Benno G. and Flückiger, Rahel and Michel, Chantal and Rössler, Wulf and Borisov, Oleg and Krawitz, Peter M. and Heekeren, Karsten and Buechler, Roman and Pantelis, Christos and Falkai, Peter and Salokangas, Raimo K. R. and Lencer, Rebekka and Bertolino, Alessandro and Borgwardt, Stefan and Noethen, Markus and Brambilla, Paolo and Wood, Stephen J. and Upthegrove, Rachel and Schultze-Lutter, Frauke and Theodoridou, Anastasia and Meisenzahl, Eva. (2021) Multimodal Machine Learning Workflows for Prediction of Psychosis in Patients With Clinical High-Risk Syndromes and Recent-Onset Depression. JAMA Psychiatry, 78 (2). pp. 195-209.

2016

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.

2015

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.

Luo, Xiong-Jian and Mattheisen, Manuel and Li, Ming and Huang, Liang and Rietschel, Marcella and Børglum, Anders D. and Als, Thomas D. and van den Oord, Edwin J. and Aberg, Karolina A. and Mors, Ole and Mortensen, Preben Bo and Luo, Zhenwu and Degenhardt, Franziska and Cichon, Sven and Schulze, Thomas G. and Nöthen, Markus M. and iPSYCH-GEMS, SCZ working group and MooDS, SCZ Consortium and Su, Bing and Zhao, Zhongming and Gan, Lin and Yao, Yong-Gang. (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. Schizophrenia Bulletin, 41 (6). pp. 1294-1308.

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.

2014

Hammer, Christian and Degenhardt, Franziska and Priebe, Lutz and Stutz, Adrian M. and Heilmann, Stefanie and Waszak, Sebastian M. and Schlattl, Andreas and Mangold, Elisabeth and Hoffmann, Per and MooDS Consortium, and Nöthen, Markus M. and Rietschel, Marcella and Rappold, Gudrun and Korbel, Jan O. and Cichon, Sven and Niesler, Beate. (2014) A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar disorders, 16 (7). pp. 764-768.

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.

Jamain, Stéphane and Cichon, Sven and Etain, Bruno and Muhleisen, Thomas W. and Georgi, Alexander and Zidane, Nora and Chevallier, Lucie and Deshommes, Jasmine and Nicolas, Aude and Henrion, Annabelle and Degenhardt, Franziska and Mattheisen, Manuel and Priebe, Lutz and Mathieu, Flavie and Kahn, Jean-Pierre and Henry, Chantal and Boland, Anne and Zelenika, Diana and Gut, Ivo and Heath, Simon and Lathrop, Mark and Maier, Wolfgang and Albus, Margot and Rietschel, Marcella and Schulze, Thomas G. and McMahon, Francis J. and Kelsoe, John R. and Hamshere, Marian and Craddock, Nicholas and Nothen, Markus M. and Bellivier, Frank and Leboyer, Marion. (2014) Common and rare variant analysis in early-onset bipolar disorder vulnerability. PLoS ONE, 9 (8). e104326.

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.

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.

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.