Items where Author is "Hoffmann, Per"

2022

Rickenbacher, Marc and Reinbold, Céline S. and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Wueest, Alexandra S. and Monsch, Andreas U. and Steiner, Luzius A. and Goettel, Nicolai. (2022) Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. Journal of neurosurgical anesthesiology, 34 (2). pp. 248-250.

2020

Imahorn, Elias and Aushev, Magomet and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Reichelt, Julia and Itin, Peter H. and Burger, Bettina. (2020) Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific reports, 10 (1). p. 14952.

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.

Johnson, Michael R. and Behmoaras, Jacques and Bottolo, Leonardo and Krishnan, Michelle L. and Pernhorst, Katharina and Meza Santoscoy, Paola L. and Rossetti, Tiziana and Speed, Doug and Srivastava, Prashant K. and Chadeau-Hyam, Marc and Hajji, Nabil and Dabrowska, Dabrowska and Rotival, Maxime and Razzaghi, Banafsheh and Kovac, Stjepana and Wanisch, Klaus and Grillo, Federico W. and Slaviero, Anna and Langley, Sarah R. and Shkura, Kirill and Roncon, Paolo and De, Tisham and Mattheisen, Manuel and Niehusmann, Pitt and O'Brien, Terence J. and Petrovski, Slave and von Lehe, Marec and Hoffmann, Per and Eriksson, Johan and Coffey, Alison J. and Cichon, Sven and Walker, Matthew and Simonato, Michele and Danis, Bénédicte and Mazzuferi, Manuela and Foerch, Patrik and Schoch, Susanne and De Paola, Vincenzo and Kaminski, Rafal M. and Cunliffe, Vincent T. and Becker, Albert J. and Petretto, Enrico. (2015) Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nature Communications, 6. p. 6031.

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.

Christoforou, Andrea and Espeseth, Thomas and Davies, Gail and Fernandes, Carla P. D. and Giddaluru, Sudheer and Mattheisen, Manuel and Tenesa, Albert and Harris, Sarah E. and McLachlan Liewald, David Cherry and Payton, Antony and Ollier, William and Horan, Michael A. and Pendleton, Neil and Haggarty, Paul and Djurovic, Srdjan and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Starr, John M. and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Deary, Ian J. and Le Hellard, Stephanie. (2014) GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes, Brain and Behavior, 13 (7). pp. 663-674.

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.

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.