Browse by Basel Contributors ID
2018Egli, Tobias and Coynel, David and Spalek, Klara and Fastenrath, Matthias and Freytag, Virginie and Heck, Angela and Loos, Eva and Auschra, Bianca and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F. and Milnik, Annette. (2018) Identification of Two Distinct Working Memory-Related Brain Networks in Healthy Young Adults. eNeuro, 5 (1). e0222-17.2018. 2017Petrovska, Jana and Coynel, David and Fastenrath, Matthias and Milnik, Annette and Auschra, Bianca and Egli, Tobias and Gschwind, Leo and Hartmann, Francina and Loos, Eva and Sifalakis, Klara and Vogler, Christian and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas and Heck, Angela. (2017) The NCAM1 gene set is linked to depressive symptoms and their brain structural correlates in healthy individuals. Journal of Psychiatric Research, 91. pp. 116-123. 2016Milnik, Annette and Vogler, Christian and Demougin, Philippe and Egli, Tobias and Freytag, Virginie and Hartmann, Francina and Heck, Angela and Peter, Fabian and Spalek, Klara and Stetak, Attila and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas and Vukojevic, Vanja. (2016) Common epigenetic variation in a European population of mentally healthy young adults. Journal of Psychiatric Research, 83. pp. 260-268. 2015Luksys, 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. 2014Heck, 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. Ising, M. and Mather, K. A. and Zimmermann, P. and Brückl, T. and Höhne, N. and Heck, A. and Schenk, L. A. and Rujescu, D. and Armstrong, N. J. and Sachdev, P. S. and Reppermund, S.. (2014) Genetic effects on information processing speed are moderated by age - converging results from three samples. Genes, brain and behavior, Vol. 13, H. 5. pp. 501-507. Vogler, C. and Gschwind, L. and Coynel, D. and Freytag, V. and Milnik, A. and Egli, T. and Heck, A. and de Quervain, D. J.-F. and Papassotiropoulos, A.. (2014) Substantial SNP-based heritability estimates for working memory performance. Translational psychiatry, 4 (9). e438. Vukojevic, Vanja and Kolassa, Iris-T. and Fastenrath, Matthias and Gschwind, Leo and Spalek, Klara and Milnik, Annette and Heck, Angela and Vogler, Christian and Wilker, Sarah and Demougin, Philippe and Peter, Fabian and Atucha, Erika and Stetak, Attila and Roozendaal, Benno and Elbert, Thomas and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F.. (2014) Epigenetic modification of the glucocorticoid receptor gene is linked to traumatic memory and post-traumatic stress disorder risk in genocide survivors. Journal of Neuroscience, 34 (31). pp. 10274-10284. 2013Papassotiropoulos, A. and Stefanova, E. and Vogler, C. and Gschwind, L. and Ackermann, S. and Spalek, K. and Rasch, B. and Heck, A. and Aerni, A. and Hanser, E. and Demougin, P. and Huynh, K.-D. and Luechinger, R. and Klarhöfer, M. and Novakovic, I. and Kostic, V. and Boesiger, P. and Scheffler, K. and de Quervain, D. J.-F.. (2013) A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Molecular psychiatry, 18 (2). pp. 255-263. Ackermann, Sandra and Heck, Angela and Rasch, Björn and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F.. (2013) The BclI polymorphism of the glucocorticoid receptor gene is associated with emotional memory performance in healthy individuals. Psychoneuroendocrinology, Vol. 38, H. 7. pp. 1203-1207. Papassotiropoulos, Andreas and Gerhards, Christiane and Heck, Angela and Ackermann, Sandra and Aerni, Amanda and Schicktanz, Nathalie and Auschra, Bianca and Demougin, Philippe and Mumme, Eva and Elbert, Thomas and Ertl, Verena and Gschwind, Leo and Hanser, Edveena and Huynh, Kim-Dung and Jessen, Frank and Kolassa, Iris-Tatjana and Milnik, Annette and Paganetti, Paolo and Spalek, Klara and Vogler, Christian and Muhs, Andreas and Pfeifer, Andrea and de Quervain, Dominique J.-F.. (2013) Human genome-guided identification of memory-modulating drugs. Proceedings of the National Academy of Sciences of the United States of America, 110 (46). E4369-E4374. Hennings, Johannes M. and Kohli, Martin A. and Czamara, Darina and Giese, Maria and Eckert, Anne and Wolf, Christiane and Heck, Angela and Domschke, Katharina and Arolt, Volker and Baune, Bernhard T. and Horstmann, Sonja and Brückl, Tanja and Klengel, Torsten and Menke, Andreas and Müller-Myhsok, Bertram and Ising, Marcus and Uhr, Manfred and Lucae, Susanne. (2013) Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach. PLoS ONE, 8 (6). e64947. 2012Milnik, A. and Heck, A. and Vogler, C. and Heinze, H. J. and de Quervain, D. J. and Papassotiropoulos, A.. (2012) Association of KIBRA with episodic and working memory: a meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics, 159B (8). pp. 958-969. de Quervain, Dominique J.-F. and Kolassa, Iris-Tatjana and Ackermann, Sandra and Aerni, Amanda and Boesiger, Peter and Demougin, Philippe and Elbert, Thomas and Ertl, Verena and Gschwind, Leo and Hadziselimovic, Nils and Hanser, Edveena and Heck, Angela and Hieber, Petra and Huynh, Kim-Dung and Klarhöfer, Markus and Luechinger, Roger and Rasch, Björn and Scheffler, Klaus and Spalek, Klara and Stippich, Christoph and Vogler, Christian and Vukojevic, Vanja and Stetak, Attila and Papassotiropoulos, Andreas. (2012) PKCα is genetically linked to memory capacity in healthy subjects and to risk for posttraumatic stress disorder in genocide survivors. Proceedings of the National Academy of Sciences of the United States of America, 109 (22). pp. 8746-8751. Quast, Carina and Altmann, Andre and Weber, Peter and Arloth, Janine and Bader, Daniel and Heck, Angela and Pfister, Hildegard and Müller-Myhsok, Bertram and Erhardt, Angelika and Binder, Elisabeth B.. (2012) Rare variants in TMEM132D in a case-control sample for panic disorder. American Journal of Medical Genetics, 159B (8). pp. 896-907. 2011Heck, Angela and Vogler, Christian and Gschwind, Leo and Ackermann, Sandra and Auschra, Bianca and Spalek, Klara and Rasch, Björn and de Quervain, Dominique and Papassotiropoulos, Andreas. (2011) Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. PLoS ONE, 6 (12). e29337. Fulda, S. and Szesny, N. and Ising, M. and Heck, A. and Grubl, A. and Lieb, R. and Reppermund, S.. (2011) Further evidence for executive dysfunction in subjects with RLS from a non-clinical sample. Sleep Medicine, Vol. 12, Iss. 10. pp. 1003-1007. Heck, Angela and Pfister, Hildegard and Czamara, Darina and Müller-Myhsok, Bertram and Pütz, Benno and Lucae, Susanne and Hennings, Johannes and Ising, Marcus.. (2011) Evidence for associations between MDGA2 polymorphisms and harm avoidance: replication and extension of a genome-wide association finding. Psychiatric Genetics, 21 (5). pp. 257-260. Menke, Andreas and Sämann, Philipp and Kloiber, Stefan and Czamara, Darina and Lucae, Susanne and Hennings, Johannes and Heck, Angela and Kohli, Martin A. and Czisch, Michael and Müller-Myhsok, Bertram and Holsboer, Florian and Binder, Elisabeth B.. (2011) Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology, 37 (4). pp. 565-575. Klengel, T. and Heck, A. and Pfister, H. and Brückl, T. and Hennings, J. M. and Menke, A. and Czamara, D. and Müller-Myhsok, B. and Ising, M.. (2011) Somatization in major depression--clinical features and genetic associations. Acta Psychiatrica Scandinavica, 124 (4). pp. 317-328. 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. Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Specht, M. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Pfister, H. and Zimmermann, P. and Lieb, R. and Pütz, B. and Uhr, M. and Weber, P. and Deussing, J. M. and Gonik, M. and Bunck, M. and Kebler, M. S. and Frank, E. and Hohoff, C. and Domschke, K. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Jacob, C. and Deckert, J. and Schreiber, S. and Strohmaier, J. and Nöthen, M. and Cichon, S. and Rietschel, M. and Bettecken, T. and Keck, M. E. and Landgraf, R. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry, 16 (6). pp. 647-663. 2009Heck, A. and Lieb, R. and Ellgas, A. and Pfister, H. and Lucae, L. and Erhardt, . and Himmerich, H. and Horstmann, S. and Kloiber, S. and Ripke, S. and Müller-Myhsok, B. and Bettecken, T. and Uhr, M. and Holsboer, F. and Ising, M.. (2009) Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. American Journal of Medical Genetics, 150B (1). pp. 104-114. Heck, A. and Lieb, R. and Ellgas, A. and Pfister, H. and Lucae, S. and Roeske, D. and Pütz, B. and Müller-Myhsok, B. and Uhr, M. and Holsboer, F. and Ising, M.. (2009) Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. Genes, Brain and Behavior, 8 (4). pp. 464-472. Unschuld, Paul G. and Ising, Marcus and Specht, Michael and Erhardt, Angelika and Ripke, Stephan and Heck, Angela and Kloiber, Stefan and Straub, Verica and Brueckl, Tanja and Müller-Myhsok, Bertram and Holsboer, Florian and Binder, Elisabeth B.. (2009) Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders. American Journal of Medical Genetics, 150B (8). pp. 1100-1109. 2008Heck, A. and Lieb, R. and Unschuld, P. G. and Ellgas, A. and Pfister, H. and Lucae, S. and Erhardt, A. and Himmerich, H. and Horstmann, S. and Kloiber, S. and Ripke, S. and Müller-Myhsok, B. and Bettecken, T. and Uhr, M. and Holsboer, F. and Ising, M.. (2008) Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism. Molecular Psychiatry, 13 (9). pp. 831-832. |
