Items where Author is "Maier, Wolfgang"

2018

Freytag, Virginie and Vukojevic, Vanja and Wagner-Thelen, Holger and Milnik, Annette and Vogler, Christian and Leber, Markus and Weinhold, Leonie and Böhmer, Anne C. and Riedel-Heller, Steffi and Maier, Wolfgang and de Quervain, Dominique J.-F. and Ramirez, Alfredo and Papassotiropoulos, Andreas. (2018) Genetic estimators of DNA methylation provide insights into the molecular basis of polygenic traits. Translational Psychiatry, 8 (31). pp. 1-13.

2017

Freytag, Virginie and Carrillo-Roa, Tania and Milnik, Annette and Sämann, Philipp G. and Vukojevic, Vanja and Coynel, David and Demougin, Philippe and Egli, Tobias and Gschwind, Leo and Jessen, Frank and Loos, Eva and Maier, Wolfgang and Riedel-Heller, Steffi G. and Scherer, Martin and Vogler, Christian and Wagner, Michael and Binder, Elisabeth B. and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas. (2017) A peripheral epigenetic signature of immune system genes is linked to neocortical thickness and memory. Nature Communications, 8. p. 15193.

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

Luksys, Gediminas and Fastenrath, Matthias and Coynel, David and Freytag, Virginie and Gschwind, Leo and Heck, Angela and Jessen, Frank and Maier, Wolfgang and Milnik, Annette and Riedel-Heller, Steffi G. and Scherer, Martin and Spalek, Klara and Vogler, Christian and Wagner, Michael and Wolfsgruber, Steffen and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F.. (2015) Computational dissection of human episodic memory reveals mental process-specific genetic profiles. Proceedings of the National Academy of Sciences of the United States of America, 112 (35). E4939-E4948.

Heck, Angela and Fastenrath, Matthias and Coynel, David and Auschra, Bianca and Bickel, Horst and Freytag, Virginie and Gschwind, Leo and Hartmann, Francina and Jessen, Frank and Kaduszkiewicz, Hanna and Maier, Wolfgang and Milnik, Annette and Pentzek, Michael and Riedel-Heller, Steffi G. and Spalek, Klara and Vogler, Christian and Wagner, Michael and Weyerer, Siegfried and Wolfsgruber, Steffen and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas. (2015) Genetic Analysis of Association Between Calcium Signaling and Hippocampal Activation, Memory Performance in the Young and Old, and Risk for Sporadic Alzheimer Disease. JAMA Psychiatry, 72 (10). pp. 1029-1036.

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.

2014

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.

Heck, Angela and Fastenrath, Matthias and Ackermann, Sandra and Auschra, Bianca and Bickel, Horst and Coynel, David and Gschwind, Leo and Jessen, Frank and Kaduszkiewicz, Hanna and Maier, Wolfgang and Milnik, Annette and Pentzek, Michael and Riedel-Heller, Steffi G. and Ripke, Stephan and Spalek, Klara and Sullivan, Patrick and Vogler, Christian and Wagner, Michael and Weyerer, Siegfried and Wolfsgruber, Steffen and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas. (2014) Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity. Neuron, 81 (5). pp. 1203-1213.

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.

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.

2011

Kohli, Martin A. and Lucae, Susanne and Saemann, Philipp G. and Schmidt, Mathias V. and Demirkan, Ayse and Hek, Karin and Czamara, Darina and Alexander, Michael and Salyakina, Daria and Ripke, Stephan and Hoehn, David and Specht, Michael and Menke, Andreas and Hennings, Johannes and Heck, Angela and Wolf, Christiane and Ising, Marcus and Schreiber, Stefan and Czisch, Michael and Müller, Marianne B. and Uhr, Manfred and Bettecken, Thomas and Becker, Albert and Schramm, Johannes and Rietschel, Marcella and Maier, Wolfgang and Bradley, Bekh and Ressler, Kerry J. and Nöthen, Markus M. and Cichon, Sven and Craig, Ian W. and Breen, Gerome and Lewis, Cathryn M. and Hofman, Albert and Tiemeier, Henning and van Duijn, Cornelia M. and Holsboer, Florian and Müller-Myhsok, Bertram and Binder, Elisabeth B.. (2011) The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron, 70 (2). pp. 252-265.

2003

Bagli, Metin and Papassotiropoulos, Andreas and Hampel, Harald and Becker, Karin and Jessen, Frank and Bürger, Katharina and Ptok, U. and Rao, Marie Luise and Möller, Hans-Jürgen and Maier, Wolfgang and Heun, Reinhard. (2003) Polymorphisms of the gene encoding the inflammatory cytokine interleukin-6 determine the magnitude of the increase in soluble interleukin-6 receptor levels in Alzheimer's disease : Results of a pilot study. European archives of psychiatry and clinical neuroscience, Vol. 253, H. 1. pp. 44-48.

2002

Majores, Micael and Kolsch, Heike and Bagli, Metin and Papassotiropoulos, Andreas and Lohmann, Petra Louise and Schmitz, Sandra and Rao, Marie Luise and Maier, Wolfgang and Heun, Reinhard. (2002) Cathepsin D : screening for new polymorphisms using single-strand conformation polymorphism analysis. International journal of molecular medicine, Vol. 9, H. 2. pp. 185-187.