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Harrisberger, F. Smieskova, R. Vogler, C. Egli, T. Schmidt, A. Lenz, C. Simon, A E. Riecher-Rössler, A. Papassotiropoulos, A. & Borgwardt, S. (2016). Impact of polygenic schizophrenia-related risk and hippocampal volumes on the onset of psychosis. Translational psychiatry6, S. e868.
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Heck, A., Fastenrath, M., Coynel, D., Auschra, B., Bickel, H. Freytag, V., Gschwind, L., Hartmann, F., Jessen, F. Kaduszkiewicz, H. Maier, W. Milnik, A., Pentzek, M. Riedel-Heller, S G. Spalek, K. Vogler, C., Wagner, M. Weyerer, S. Wolfsgruber, S. de Quervain, D J-F. & Papassotiropoulos, A. (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 Psychiatry72, S. 1029-36. edoc
Luksys, G., Fastenrath, M., Coynel, D., Freytag, V., Gschwind, L., Heck, A., Jessen, F. Maier, W. Milnik, A., Riedel-Heller, S G. Scherer, M. Spalek, K., Vogler, C., Wagner, M. Wolfsgruber, S. Papassotiropoulos, A., & de Quervain, D 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 America112, S. E4939-48.
Papassotiropoulos, A., & de Quervain, D J F. (2015). Failed drug discovery in psychiatry: time for human genome-guided solutions. Trends in cognitive sciences19, S. 183-7. edoc
Schicktanz, N., Fastenrath, M., Milnik, A., Spalek, K. Auschra, B., Nyffeler, T. Papassotiropoulos, A., de Quervain, D J-F. & Schwegler, K. (2015). Continuous theta burst stimulation over the left dorsolateral prefrontal cortex decreases medium load working memory performance in healthy humans. PLoS one10, S. e0120640. edoc
Spalek, K., Fastenrath, M., Ackermann, S. Auschra, B., Coynel, D., Frey, J. Gschwind, L., Hartmann, F., van der Maarel, N. Papassotiropoulos, A., de Quervain, D., & Milnik, A.(2015). Sex-dependent dissociation between emotional appraisal and memory: a large-scale behavioral and fMRI study. The Journal of neuroscience : the official journal of the Society for Neuroscience35, S. 920-35.
Walter, M. Bentz, D. Schicktanz, N. Milnik, A. Aerni, A. Gerhards, C. Schwegler, K. Vogel, M. Blum, J. Schmid, O. Roozendaal, B. Lang, U E. Borgwardt, S. & de Quervain, D. (2015). Effects of cortisol administration on craving in heroin addicts.Translational psychiatry5, S. e610.
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Gyurko, D M. Soti, C. Stetak, A. & Csermely, P. (2014). System level mechanisms of adaptation, learning, memory formation and evolvability: the role of chaperone and other networks. Current protein & peptide science15, S. 171-88.
Harrisberger, F. Spalek, K. Smieskova, R. Schmidt, A. Coynel, D. Milnik, A. Fastenrath, M., Freytag, V., Gschwind, L. Walter, A. Vogel, T. Bendfeldt, K. de Quervain, D J -F. Papassotiropoulos, A., & Borgwardt, S. (2014). The association of the BDNF Val66Met polymorphism and the hippocampal volumes in healthy humans : a joint meta-analysis of published and new data. Neuroscience and biobehavioral reviews42, S. 267-278.edoc
Heck, A., Fastenrath, M., Ackermann, S. Auschra, B., Bickel, H. Coynel, D., Gschwind, L., Jessen, F. Kaduszkiewicz, H. Maier, W. Milnik, A., Pentzek, M. Riedel-Heller, S G. Ripke, S. Spalek, K. Sullivan, P. Vogler, C., Wagner, M. Weyerer, S. Wolfsgruber, S. de Quervain, D J-F. & Papassotiropoulos, A. (2014). Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity. Neuron81, S. 1203-13. edoc
Ising, M. Mather, K A. Zimmermann, P. Brueckl, T. Hoehne, N. Heck, A., Schenk, L A. Rujescu, D. Armstrong, N J. Sachdev, P S. & Reppermund, S. (2014). Genetic effects on information processing speed are moderated by age - converging results from three samples. Genes, brain and behavior13, S. 501-507. edoc
Luksys, G., Ackermann, S. Coynel, D. Fastenrath, M., Gschwind, L. Heck, A., Rasch, B. Spalek, K. Vogler, C., Papassotiropoulos, A., & de Quervain, D. (2014). BAIAP2 is related to emotional modulation of human memory strength. PLoS one9, S. e83707.edoc (Open Access)
Scheibehenne, B., Todd, P M. van den Berg, S M. Hatemi, P K. Eaves, L J. & Vogler, C.(2014). Genetic influences on dietary variety - results from a twin study. Appetite : eating and drinking77, S. 131-8. edoc
Schicktanz, N., Schwegler, K., Fastenrath, M., Spalek, K. Milnik, A., Papassotiropoulos, A., Nyffeler, T. & de Quervain, D J-F. (2014). Motor threshold predicts working memory performance in healthy humans. Annals of clinical and translational neurology1, S. 69-73. edoc
Stetak, A. (2014). Forgetting is regulated via Musashi-mediated translational control of the Arp2/3 complex. Cell156, S. 1153-66. edoc
Vogler, C. Gschwind, L. Coynel, D. Freytag, V. Milnik, A. Egli, T. Heck, A. de Quervain, D J-F. & Papassotiropoulos, A. (2014). Substantial SNP-based heritability estimates for working memory performance. Translational psychiatry4, S. e438. edoc
Vukojevic, V., Kolassa, I-T. Fastenrath, M., Gschwind, L., Spalek, K., Milnik, A., Heck, A., Vogler, C., Wilker, S. Demougin, P. Peter, F. Atucha, E. Stetak, A. Roozendaal, B. Elbert, T. Papassotiropoulos, A., & de Quervain, D 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 : the official journal of the Society for Neuroscience34, S. 10274-84. edoc
Wilker, S. Pfeiffer, A. Kolassa, S. Elbert, T. Lingenfelder, B. Ovuga, E. Papassotiropoulos, A., de Quervain, D., & Kolassa, I-T. (2014). The role of FKBP5 genotype in moderating long-term effectiveness of exposure-based psychotherapy for posttraumatic stress disorder. Translational psychiatry4, S. e403. edoc
Ackermann, S. Hartmann, F., Papassotiropoulos, A., de Quervain, D., & Rasch, B. (2013). Associations between Basal Cortisol Levels and Memory Retrieval in Healthy Young Individuals. Journal of Cognitive Neuroscience25, S. 1896-907.
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Ackermann, S. Heck, A., Rasch, B. Papassotiropoulos, A., & de Quervain, D J-F. (2013). The BclI polymorphism of the glucocorticoid receptor gene is associated with emotional memory performance in healthy individuals. Psychoneuroendocrinology38, S. 1203-7.edoc
Bentz, D. Michael, T. Wilhelm, F H. Hartmann, F., Kunz, S. Rudolf von Rohr, I R. & de Quervain, D. (2013). Influence of stress on fear memory processes in an aversive differential conditioning paradigm in humans. PsychoneuroendocrinologyURL
Bentz, D. Michael, T. Wilhelm, F H. Hartmann, F R. Kunz, S. von Rohr, I R R. & de Quervain, D J-F. (2013). Influence of stress on fear memory processes in an aversive differential conditioning paradigm in humans. Psychoneuroendocrinology38, S. 1186-97. edoc
Easton, A C. Lourdusamy, A. Loth, E. Toro, R. Torro, R. Giese, K P. Kornhuber, J. de Quervain, D J-F. Papassotiropoulos, A. Fernandes, C. Müller, C P. & Schumann, G. (2013). CAMK2A polymorphisms predict working memory performance in humans.Molecular psychiatry18, S. 850-2. edoc
Hennings, J M. Kohli, M A. Czamara, D. Giese, M. Eckert, A. Wolf, C. Heck, A., Domschke, K. Arolt, V. Baune, B T. Horstmann, S. Brückl, T. Klengel, T. Menke, A. Müller-Myhsok, B. Ising, M. Uhr, M. & Lucae, S. (2013). Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach. PloS one8, S. e64947.
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Papassotiropoulos, A., Gerhards, C., Heck, A., Ackermann, S. Aerni, A., Schicktanz, N., Auschra, B., Demougin, P. Mumme, E. Elbert, T. Ertl, V. Gschwind, L., Hanser, E. Huynh, K-D. Jessen, F. Kolassa, I-T. Milnik, A., Paganetti, P. Spalek, K., Vogler, C., Muhs, A. Pfeifer, A. & de Quervain, D J-F. (2013). Human genome-guided identification of memory-modulating drugs. Proceedings of the National Academy of Sciences of the United States of America110, S. E4369-74. edoc
Wilker, S. Kolassa, S. Vogler, C., Lingenfelder, B. Elbert, T. Papassotiropoulos, A., de Quervain, D J-F. & Kolassa, I-T. (2013). The role of memory-related gene WWC1 (KIBRA) in lifetime posttraumatic stress disorder : evidence from two independent samples from African conflict regions. Biological psychiatry74, S. 664-71. edoc
Ackermann, S. Spalek, K., Rasch, B. Gschwind, L., Coynel, D., Fastenrath, M., Papassotiropoulos, A., & de Quervain, D J-F. (2012). Testosterone levels in healthy men are related to amygdala reactivity and memory performance.Psychoneuroendocrinology37, S. 1417-24. edoc
de Quervain, D J-F. Kolassa, I-T. Ackermann, S. Aerni, A., Boesiger, P. Demougin, P. Elbert, T. Ertl, V. Gschwind, L., Hadziselimovic, N. Hanser, E. Heck, A., Hieber, P. Huynh, K-D. Klarhöfer, M. Luechinger, R. Rasch, B. Scheffler, K. Spalek, K., Stippich, C. Vogler, C., Vukojevic, V., Stetak, A. & Papassotiropoulos, A. (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 America109, S. 8746-51. edoc
Mata, R. Hau, R. Papassotiropoulos, A., & Hertwig, R. (2012). DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART). PLoS one7, S. e39135. edoc
Milnik, A., Heck, A., Vogler, C., Heinze, H-J. de Quervain, D J-F. & Papassotiropoulos, A.(2012). Association of KIBRA with episodic and working memory: a meta-analysis.American journal of medical genetics. Part B, Neuropsychiatric genetics159B, S. 958-69. edoc
Quast, C. Altmann, A. Weber, P. Arloth, J. Bader, D. Heck, A., Pfister, H. Müller-Myhsok, B. Erhardt, A. & Binder, E B. (2012). Rare variants in TMEM132D in a case-control sample for panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics159B, S. 896-907.
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Erhardt, A. Czibere, L. Roeske, D. Lucae, S. Unschuld, P G. Ripke, S. Specht, M. Kohli, M A. Kloiber, S. Ising, M. Heck, A. Pfister, H. Zimmermann, P. Lieb, R. Pütz, B. Uhr, M. Weber, P. Deussing, J M. Gonik, M. Bunck, M. Kebler, M S. Frank, E. Hohoff, C. Domschke, K. Krakowitzky, P. Maier, W. Bandelow, B. Jacob, C. Deckert, J. Schreiber, S. Strohmaier, J. Nöthen, M. Cichon, S. Rietschel, M. Bettecken, T. Keck, M E. Landgraf, R. Müller-Myhsok, B. Holsboer, F. & Binder, E B. (2011). TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular psychiatry16, S. 647-63.
Fulda, S. Szesny, N. Ising, M. Heck, A., Grübl, A. Lieb, R. & Reppermund, S. (2011). Further evidence for executive dysfunction in subjects with RLS from a non-clinical sample. Sleep medicine12, S. 1003-7.
Hauer, D. Weis, F. Papassotiropoulos, A., Schmoeckel, M. Beiras-Fernandez, A. Lieke, J. Kaufmann, I. Kirchhoff, F. Vogeser, M. Roozendaal, B. Briegel, J. de Quervain, D., & Schelling, G. (2011). Relationship of a common polymorphism of the glucocorticoid receptor gene to traumatic memories and posttraumatic stress disorder in patients after intensive care therapy. Critical care medicine39, S. 643-50.
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Luksys, G., & Sandi, C. (2011). Neural mechanisms and computations underlying stress effects on learning and memory. Current opinion in neurobiology21, S. 502-8.
Menke, A. Sämann, P. Kloiber, S. Czamara, D. Lucae, S. Hennings, J. Heck, A., Kohli, M A. Czisch, M. Müller-Myhsok, B. Holsboer, F. & Binder, E B. (2011). Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology, S. Epub ahead of print.
Papassotiropoulos, A. Henke, K. Stefanova, E. Aerni, A. Müller, A. Demougin, P. Vogler, C. Sigmund, J C. Gschwind, L. Huynh, K-D. Coluccia, D. Mondadori, C R. Hänggi, J. Buchmann, A. Kostic, V. Novakovic, I. van den Bussche, H. Kaduszkiewicz, H. Weyerer, S. Bickel, H. Riedel-Heller, S. Pentzek, M. Wiese, B. Dichgans, M. Wagner, M. Jessen, F. Maier, W. & de Quervain, D J-F. (2011). A genome-wide survey of human short-term memory. Molecular psychiatry16, S. 184-92. edoc
Papassotiropoulos, A., & de Quervain, D J-F. (2011). Genetics of human episodic memory : dealing with complexity. Trends in cognitive sciences15, S. 381-7. edoc
Cathomas, F. Vogler, C., Euler-Sigmund, J C. de Quervain, D J-F. & Papassotiropoulos, A. (2010). Fine-mapping of the brain-derived neurotrophic factor (BDNF) gene supports an association of the Val66Met polymorphism with episodic memory. International journal of neuropsychopharmacology : official scientific journal of the Collegium Internationale Neuro-psychopharmacologicum13, S. 975-80. edoc
Freitag, C M. (2010). Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. Journal of neural transmission : journal of the International Society for Neurovegetative Research117, S. 259-67. edoc
Kolassa, I-T. Ertl, V. Eckart, C. Glöckner, F. Kolassa, S. Papassotiropoulos, A., de Quervain, D J-F. & Elbert, T. (2010). Association study of trauma load and SLC6A4 promoter polymorphism in posttraumatic stress disorder : evidence from survivors of the Rwandan genocide. The Journal of clinical psychiatry71, S. 543-7. edoc
Rasch, B. Papassotiropoulos, A. & de Quervain, D-F. (2010). Imaging genetics of cognitive functions : Focus on episodic memory. NeuroImage53, S. 870-7. edoc
Rasch, B. Spalek, K. Buholzer, S. Luechinger, R. Boesiger, P. de Quervain, D J-F. & Papassotiropoulos, A. (2010). Aversive stimuli lead to differential amygdala activation and connectivity patterns depending on catechol-O-methyltransferase Val158Met genotype. NeuroImage52, S. 1712-9. edoc
Thal, D R. Papassotiropoulos, A., Saido, T C. Griffin, W S T. Mrak, R E. Kölsch, H. Del Tredici, K. Attems, J. & Ghebremedhin, E. (2010). Capillary cerebral amyloid angiopathy identifies a distinct APOE epsilon4-associated subtype of sporadic Alzheimer's disease.Acta neuropathologica120, S. 169-83. edoc
Vogler, C., Gschwind, L., Röthlisberger, B. Huber, A. Filges, I. Miny, P. Auschra, B., Stetak, A. Demougin, P. Vukojevic, V. Kolassa, I-T. Elbert, T. de Quervain, D J-F. & Papassotiropoulos, A. (2010). Microarray-based maps of copy-number variant regions in European and sub-saharan populations. PLoS one5, S. e15246. edoc
Webster, J. Reiman, E M. Zismann, V L. Joshipura, K D. Pearson, J V. Hu-Lince, D. Huentelman, M J. Craig, D W. Coon, K D. Beach, T. Rohrer, K C. Zhao, A S. Leung, D. Bryden, L. Marlowe, L. Kaleem, M. Mastroeni, D. Grover, A. Rogers, J. Heun, R. Jessen, F. Kölsch, H. Heward, C B. Ravid, R. Hutton, M L. Melquist, S. Petersen, R C. Caselli, R J. Papassotiropoulos, A., Stephan, D A. Hardy, J. & Myers, A. (2010). Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis. International journal of molecular epidemiology and genetics1, S. 19-30. edoc
Brein, G. (2009). Root Incompatibilities in the Pyramid Texts. Lingua Aegyptia 17 (Proceedings of the Fourth International Conference on Egyptian Grammar (Crossroads IV) Basel, March 19-22, 2009), S. 1-8.
Heck, A. Lieb, R. Ellgas, A. Pfister, H. Lucae, S. Roeske, D. Pütz, B. Müller-Myhsok, B. Uhr, M. Holsboer, F. & Ising, M. (2009). Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. Genes, brain, and behavior8, S. 464-72.
Heck, A., Lieb, R. Ellgas, A. Pfister, H. Lucae, S. Erhardt, A. Himmerich, H. Horstmann, S. Kloiber, S. Ripke, S. Müller-Myhsok, B. Bettecken, T. Uhr, M. Holsboer, F. & 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. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics150B, S. 104-14.
Hoerndli, F J. Walser, M. Fröhli Hoier, E. de Quervain, D., Papassotiropoulos, A., & Hajnal, A. (2009). A conserved function of C. elegans CASY-1 calsyntenin in associative learning. PLoS one4, S. e4880. edoc
Kolassa, I-T. Kolassa, S. Ertl, V. Papassotiropoulos, A., & De Quervain, D J-F. (2009). The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val(158)Met Polymorphism. Biological Psychiatry67, S. 304-8. edoc
Luksys, G., Gerstner, W. & Sandi, C. (2009). Stress, genotype and norepinephrine in the prediction of mouse behavior using reinforcement learning. Nature neuroscience12, S. 1180-6.
Rasch, B. Spalek, K. Buholzer, S. Luechinger, R. Boesiger, P. Papassotiropoulos, A. & de Quervain, D J-F. (2009). A genetic variation of the noradrenergic system is related to differential amygdala activation during encoding of emotional memories. Proceedings of the National Academy of Sciences of the United States of America106, S. 19191-6.edoc
Unschuld, P G. Ising, M. Specht, M. Erhardt, A. Ripke, S. Heck, A., Kloiber, S. Straub, V. Brueckl, T. Müller-Myhsok, B. Holsboer, F. & Binder, E 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. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics150B, S. 1100-9.
Vogler, C., Spalek, K., Aerni, A., Demougin, P. Müller, A. Huynh, K-D. Papassotiropoulos, A., & de Quervain, D J-F. (2009). CPEB3 is associated with human episodic memory. Frontiers in behavioral neuroscience3, S. 4. edoc
Corneveaux, J J. Liang, W S. Reiman, E M. Webster, J A. Myers, A J. Zismann, V L. Joshipura, K D. Pearson, J V. Hu-Lince, D. Craig, D W. Coon, K D. Dunckley, T. Bandy, D. Lee, W. Chen, K. Beach, T G. Mastroeni, D. Grover, A. Ravid, R. Sando, S B. Aasly, J O. Heun, R. Jessen, F. Kölsch, H. Rogers, J. Hutton, M L. Melquist, S. Petersen, R C. Alexander, G E. Caselli, R J. Papassotiropoulos, A., Stephan, D A. & Huentelman, M J. (2008). Evidence for an association between KIBRA and late-onset Alzheimer's disease. Neurobiology of aging31, S. 901-9. edoc
Hermens, F. Luksys, G., Gerstner, W. Herzog, M H. & Ernst, U. (2008). Modeling spatial and temporal aspects of visual backward masking. Psychological review115, S. 83-100.
Reiman, E M. Chen, K. Caselli, R J. Alexander, G E. Bandy, D. Adamson, J L. Lee, W. Cannon, A. Stephan, E A. Stephan, D A. & Papassotiropoulos, A. (2008). Cholesterol-related genetic risk scores are associated with hypometabolism in Alzheimer's-affected brain regions. NeuroImage40, S. 1214-21.
Romanos, M. Freitag, C. Jacob, C. Craig, D W. Dempfle, A. Nguyen, T T. Halperin, R. Walitza, S. Renner, T J. Seitz, C. Romanos, J. Palmason, H. Reif, A. Heine, M. Windemuth-Kieselbach, C. Vogler, C. Sigmund, J. Warnke, A. Schäfer, H. Meyer, J. Stephan, D A. & Lesch, K P. (2008). Genome-wide linkage analysis of ADHD using high-density SNP arrays : novel loci at 5q13.1 and 14q12. Molecular psychiatry13, S. 522-30. edoc
Sigmund, J C. Vogler, C., Huynh, K-D. de Quervain, D J-F. & Papassotiropoulos, A. (2008). Fine-mapping at the HTR2A locus reveals multiple episodic memory-related variants. Biological psychology79, S. 239-42. edoc
Coon, K D. Myers, A J. Craig, D W. Webster, J A. Pearson, J V. Lince, D H. Zismann, V L. Beach, T G. Leung, D. Bryden, L. Halperin, R F. Marlowe, L. Kaleem, M. Walker, D G. Ravid, R. Heward, C B. Rogers, J. Papassotiropoulos, A., Reiman, E M. Hardy, J. & Stephan, D A. (2007). A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. The Journal of clinical psychiatry68, S. 613-8. edoc
De Ferrari, G V. Papassotiropoulos, A., Biechele, T. Wavrant De-Vrieze, F. Avila, M E. Major, M B. Myers, A. Sáez, K. Henríquez, J P. Zhao, A. Wollmer, M A. Nitsch, R M. Hock, C. Morris, C M. Hardy, J. & Moon, R T. (2007). Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America104, S. 9434-9. edoc
de Quervain, D J-F. Kolassa, I-T. Ertl, V. Onyut, P L. Neuner, F. Elbert, T. & Papassotiropoulos, A. (2007). A deletion variant of the alpha2b-adrenoceptor is related to emotional memory in Europeans and Africans. Nature neuroscience10, S. 1137-9. edoc
Hoerndli, F J. Pelech, S. Papassotiropoulos, A., & Götz, J. (2007). Aβ treatment and P301L tau expression in an Alzheimer's disease tissue culture model act synergistically to promote aberrant cell cycle re-entry. The European journal of neuroscience26, S. 60-72. edoc
Huentelman, M J. Papassotiropoulos, A., Craig, D W. Hoerndli, F J. Pearson, J V. Huynh, K-D. Corneveaux, J. Hänggi, J. Mondadori, C R A. Buchmann, A. Reiman, E M. Henke, K. de Quervain, D J-F. & Stephan, D A. (2007). Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Human molecular genetics16, S. 1469-77. edoc
Mondadori, C R A. de Quervain, D J-F. Buchmann, A. Mustovic, H. Wollmer, M A. Schmidt, C F. Boesiger, P. Hock, C. Nitsch, R M. Papassotiropoulos, A., & Henke, K. (2007). Better memory and neural efficiency in young apolipoprotein E epsilon4 carriers. Cerebral cortex17, S. 1934-47. edoc
Pearson, J V. Huentelman, M J. Halperin, R F. Tembe, W D. Melquist, S. Homer, N. Brun, M. Szelinger, S. Coon, K D. Zismann, V L. Webster, J A. Beach, T. Sando, S B. Aasly, J O. Heun, R. Jessen, F. Kolsch, H. Tsolaki, M. Daniilidou, M. Reiman, E M. Papassotiropoulos, A., Hutton, M L. Stephan, D A. & Craig, D W. (2007). Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. American journal of human genetics80, S. 126-39. edoc
Reiman, E M. Webster, J A. Myers, A J. Hardy, J. Dunckley, T. Zismann, V L. Joshipura, K D. Pearson, J V. Hu-Lince, D. Huentelman, M J. Craig, D W. Coon, K D. Liang, W S. Herbert, R H. Beach, T. Rohrer, K C. Zhao, A S. Leung, D. Bryden, L. Marlowe, L. Kaleem, M. Mastroeni, D. Grover, A. Heward, C B. Ravid, R. Rogers, J. Hutton, M L. Melquist, S. Petersen, R C. Alexander, G E. Caselli, R J. Kukull, W. Papassotiropoulos, A., & Stephan, D A. (2007). GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Neuron54, S. 713-20. edoc
Tagarakis, G I. Tsolaki-Tagaraki, F. Tsolaki, M. Diegeler, A. Kazis, D. Rouska, E. & Papassotiropoulos, A. (2007). The role of SOAT-1 polymorphisms in cognitive decline and delirium after bypass heart surgery. Clinical research in cardiology96, S. 600-3. edoc
Tagarakis, G I. Tsolaki-Tagaraki, F. Tsolaki, M. Diegeler, A. Tsilimingas, N B. & Papassotiropoulos, A. (2007). The role of apolipoprotein E in cognitive decline and delirium after bypass heart operations. American journal of Alzheimer's disease and other dementias22, S. 223-8. edoc
Wollmer, M A. Sleegers, K. Ingelsson, M. Zekanowski, C. Brouwers, N. Maruszak, A. Brunner, F. Huynh, K-D. Kilander, L. Brundin, R-M. Hedlund, M. Giedraitis, V. Glaser, A. Engelborghs, S. De Deyn, P P. Kapaki, E. Tsolaki, M. Daniilidou, M. Molyva, D. Paraskevas, G P. Thal, D R. Barcikowska, M. Kuznicki, J. Lannfelt, L. Van Broeckhoven, C. Nitsch, R M. Hock, C. & Papassotiropoulos, A. (2007). Association study of cholesterol-related genes in Alzheimer's disease. Neurogenetics8, S. 179-88.edoc
Coon, K D. Siegel, A M. Yee, S J. Dunckley, T L. Mueller, C. Nagra, R M. Tourtellotte, W W. Reiman, E M. Papassotiropoulos, A., Petersen, F F. Stephan, D A. & Kirsch, W M. (2006). Preliminary demonstration of an allelic association of the IREB2 gene with Alzheimer's disease. Journal of Alzheimer's disease9, S. 225-33. edoc
Coon, K D. Valla, J. Szelinger, S. Schneider, L E. Niedzielko, T L. Brown, K M. Pearson, J V. Halperin, R. Dunckley, T. Papassotiropoulos, A., Caselli, R J. Reiman, E M. & Stephan, D A. (2006). Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencing. Mitochondrion6, S. 194-210. edoc
de Quervain, D J-F. & Papassotiropoulos, A. (2006). Identification of a genetic cluster influencing memory performance and hippocampal activity in humans. Proceedings of the National Academy of Sciences of the United States of America103, S. 4270-4. edoc
Papassotiropoulos, A., Fountoulakis, M. Dunckley, T. Stephan, D A. & Reiman, E M. (2006). Genetics, transcriptomics, and proteomics of Alzheimer's disease. The Journal of clinical psychiatry67, S. 652-70. edoc
Papassotiropoulos, A., Stephan, D A. Huentelman, M J. Hoerndli, F J. Craig, D W. Pearson, J V. Huynh, K-D. Brunner, F. Corneveaux, J. Osborne, D. Wollmer, M A. Aerni, A. Coluccia, D. Hänggi, J. Mondadori, C R A. Buchmann, A. Reiman, E M. Caselli, R J. Henke, K. & de Quervain, D J-F. (2006). Common Kibra alleles are associated with human memory performance. Science314, S. 475-8. edoc
Wollmer, M A. Kapaki, E. Hersberger, M. Muntwyler, J. Brunner, F. Tsolaki, M. Akatsu, H. Kosaka, K. Michikawa, M. Molyva, D. Paraskevas, G P. Lütjohann, D. von Eckardstein, A. Hock, C. Nitsch, R M. & Papassotiropoulos, A. (2006). Ethnicity-dependent genetic association of ABCA2 with sporadic Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics141B, S. 534-6. edoc
Wollmer, M A. Nitsch, R M. Hock, C. & Papassotiropoulos, A. (2006). Genetic association study on colony-stimulating factor 1 in Alzheimer's disease. Neuro-degenerative diseases3, S. 334-7. edoc
Kornblum, C. Schröder, R. Müller, K. Vorgerd, M. Eggers, J. Bogdanow, M. Papassotiropoulos, A. Fabian, K. Klockgether, T. & Zange, J. (2005). Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions : a placebo-controlled, double-blind 31P-MRS crossover study. European journal of neurology12, S. 300-9. edoc
Papassotiropoulos, A., Henke, K. Aerni, A. Coluccia, D. Garcia, E. Wollmer, M A. Huynh, K-D. Monsch, A U. Stähelin, H B. Hock, C. Nitsch, R M. & de Quervain, D J-F. (2005). Age-dependent effects of the 5-hydroxytryptamine-2a-receptor polymorphism (His452Tyr) on human memory. NeuroReport16, S. 839-42. edoc
Papassotiropoulos, A., Lambert, J-C. Wavrant-De Vrièze, F. Wollmer, M A. von der Kammer, H. Streffer, J R. Maddalena, A. Huynh, K-D. Wolleb, S. Lutjohann, D. Schneider, B. Thal, D R. Grimaldi, L M E. Tsolaki, M. Kapaki, E. Ravid, R. Konietzko, U. Hegi, T. Pasch, T. Jung, H. Braak, H. Amouyel, P. Rogaev, E I. Hardy, J. Hock, C. & Nitsch, R M. (2005). Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease. Neuro-degenerative diseases2, S. 233-41. edoc
Papassotiropoulos, A., Tsolaki, M. Wollmer, M A. Molyva, D. Thal, D R. Huynh, K-D. Tracy, J. Staehelin, H B. Monsch, A U. Nitsch, R M. & Hock, C. (2005). No association of a non-synonymous PLAU polymorphism with Alzheimer's disease and disease-related traits. American journal of medical genetics. Part B, Neuropsychiatric genetics132B, S. 21-3. edoc
Papassotiropoulos, A., Wollmer, M A. Aguzzi, A. Hock, C. Nitsch, R M. & de Quervain, D J-F. (2005). The prion gene is associated with human long-term memory. Human molecular genetics14, S. 2241-6. edoc
Papassotiropoulos, A., Wollmer, M A. Tsolaki, M. Brunner, F. Molyva, D. Lütjohann, D. Nitsch, R M. & Hock, C. (2005). A cluster of cholesterol-related genes confers susceptibility for Alzheimer's disease. The Journal of clinical psychiatry66, S. 940-7.edoc
Alberici, A. Gobbo, C. Panzacchi, A. Nicosia, F. Ghidoni, R. Benussi, L. Hock, C. Papassotiropoulos, A. Liberini, P. Growdon, J H. Frisoni, G B. Villa, A. Zanetti, O. Cappa, S. Fazio, F. & Binetti, G. (2004). Frontotemporal dementia : impact of P301L tau mutation on a healthy carrier. Journal of neurology, neurosurgery, and psychiatry75, S. 1607-10. edoc
Chen, F. Wollmer, M A. Hoerndli, F. Münch, G. Kuhla, B. Rogaev, E I. Tsolaki, M. Papassotiropoulos, A., & Götz, J. (2004). Role for glyoxalase I in Alzheimer's disease.Proceedings of the National Academy of Sciences of the United States of America101, S. 7687-92. edoc
de Quervain, D J-F. Poirier, R. Wollmer, M A. Grimaldi, L M E. Tsolaki, M. Streffer, J R. Hock, C. Nitsch, R M. Mohajeri, M H. & Papassotiropoulos, A. (2004). Glucocorticoid-related genetic susceptibility for Alzheimer's disease. Human molecular genetics13, S. 47-52. edoc
Maddalena, A S. Papassotiropoulos, A., Gonzalez-Agosti, C. Signorell, A. Hegi, T. Pasch, T. Nitsch, R M. & Hock, C. (2004). Cerebrospinal fluid profile of amyloid beta peptides in patients with Alzheimer's disease determined by protein biochip technology. Neuro-degenerative diseases1, S. 231-5. edoc
Bagli, M. Papassotiropoulos, A., Hampel, H. Becker, K. Jessen, F. Bürger, K. Ptok, U. Rao, M L. Möller, H-J. Maier, W. & Heun, R. (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 neuroscience253, S. 44-8.edoc
de Quervain, D J-F. Henke, K. Aerni, A. Coluccia, D. Wollmer, M A. Hock, C. Nitsch, R M. & Papassotiropoulos, A. (2003). A functional genetic variation of the 5-HT2a receptor affects human memory. Nature neuroscience6, S. 1141-2. edoc
Hock, C. Konietzko, U. Streffer, J R. Tracy, J. Signorell, A. Müller-Tillmanns, B. Lemke, U. Henke, K. Moritz, E. Garcia, E. Wollmer, M A. Umbricht, D. de Quervain, D J F. Hofmann, M. Maddalena, A. Papassotiropoulos, A., & Nitsch, R M. (2003). Antibodies against beta-amyloid slow cognitive decline in Alzheimer's disease. Neuron38, S. 547-54. edoc
Maddalena, A. Papassotiropoulos, A., Müller-Tillmanns, B. Jung, H H. Hegi, T. Nitsch, R M. & Hock, C. (2003). Biochemical diagnosis of Alzheimer disease by measuring the cerebrospinal fluid ratio of phosphorylated tau protein to beta-amyloid peptide42.Archives of neurology60, S. 1202-6. edoc
Papassotiropoulos, A., Streffer, J R. Tsolaki, M. Schmid, S. Thal, D. Nicosia, F. Iakovidou, V. Maddalena, A. Lütjohann, D. Ghebremedhin, E. Hegi, T. Pasch, T. Träxler, M. Brühl, A. Benussi, L. Binetti, G. Braak, H. Nitsch, R M. & Hock, C. (2003). Increased brain beta-amyloid load, phosphorylated tau, and risk of Alzheimer disease associated with an intronic CYP46 polymorphism. Archives of neurology60, S. 29-35.edoc
Schmidt, S. Marrosu, G M. Kölsch, H. Haase, C G. Ferenczik, S. Sokolowski, P. Köhler, W. Schmidt, M. Papassotiropoulos, A., Heun, R. Grosse-Wilde, H. & Klockgether, T. (2003). Genetic variations and humoral immune responses to myelin oligodendroglia glycoprotein in adult phenotypes of X-linked adrenoleukodystrophy. Journal of neuroimmunology135, S. 148-53. edoc
Schmidt, S. Papassotiropoulos, A., Sotgiu, S. Kölsch, H. Arru, G. Fois, M L. Haase, C G. Schmitz, S. König, N. Harzheim, M. Heun, R. & Klockgether, T. (2003). Investigation of a genetic variation of a variable number tandem repeat polymorphism of interleukin-6 gene in patients with multiple sclerosis. Journal of neurology250, S. 607-11. edoc
Streffer, J R. Papassotiropoulos, A. Kurosinski, P. Signorell, A. Wollmer, M A. Tsolaki, M. Iakovidou, V. Hörndli, F. Bosset, J. Götz, J. Nitsch, R M. & Hock, C. (2003). Saitohin gene is not associated with Alzheimer's disease. Journal of neurology, neurosurgery, and psychiatry74, S. 362-3. edoc
Wollmer, M A. Streffer, J R. Tsolaki, M. Grimaldi, L M E. Lütjohann, D. Thal, D. von Bergmann, K. Nitsch, R M. Hock, C. & Papassotiropoulos, A. (2003). Genetic association of acyl-coenzyme A : cholesterol acyltransferase with cerebrospinal fluid cholesterol levels, brain amyloid load, and risk for Alzheimer's disease. Molecular psychiatry8, S. 635-8. edoc
Wollmer, M A. Streffer, J R. Lütjohann, D. Tsolaki, M. Iakovidou, V. Hegi, T. Pasch, T. Jung, H H. Bergmann, K v. Nitsch, R M. Hock, C. & Papassotiropoulos, A. (2003). ABCA1 modulates CSF cholesterol levels and influences the age at onset of Alzheimer's disease. Neurobiology of aging24, S. 421-6. edoc
Hock, C. Konietzko, U. Papassotiropoulos, A., Wollmer, A. Streffer, J. von Rotz, R C. Davey, G. Moritz, E. & Nitsch, R M. (2002). Generation of antibodies specific for beta-amyloid by vaccination of patients with Alzheimer disease. Nature medicine8, S. 1270-5. edoc
Kockler, M. Nitardy, A. Papassotiropoulos, A. Ptok, U. Maier, W. & Heun, R. (2002). Physical disorders and causes of death in relatives of Alzheimer's disease patients.International journal of geriatric psychiatry17, S. 335-42. edoc
Majores, M. Kolsch, H. Bagli, M. Papassotiropoulos, A., Lohmann, P L. Schmitz, S. Rao, M L. Maier, W. & Heun, R. (2002). Cathepsin D : screening for new polymorphisms using single-strand conformation polymorphism analysis. International journal of molecular medicine9, S. 185-7. edoc
Papassotiropoulos, A. Lütjohann, D. Bagli, M. Locatelli, S. Jessen, F. Buschfort, R. Ptok, U. Björkhem, I. von Bergmann, K. & Heun, R. (2002). 24S-hydroxycholesterol in cerebrospinal fluid is elevated in early stages of dementia. Journal of psychiatric research36, S. 27-32. edoc
Papassotiropoulos, A., Lewis, H D. Bagli, M. Jessen, F. Ptok, U. Schulte, A. Shearman, M S. & Heun, R. (2002). Cerebrospinal fluid levels of beta-amyloid(42) in patients with Alzheimer's disease are related to the exon 2 polymorphism of the cathepsin D gene.NeuroReport13, S. 1291-4. edoc
Wollmer, M A. Papassotiropoulos, A., Streffer, J R. Grimaldi, L M E. Kapaki, E. Salani, G. Paraskevas, G P. Maddalena, A. de Quervain, D. Bieber, C. Umbricht, D. Lemke, U. Bosshardt, S. Degonda, N. Henke, K. Hegi, T. Jung, H H. Pasch, T. Hock, C. & Nitsch, R M. (2002). Genetic polymorphisms and cerebrospinal fluid levels of tissue inhibitor of metalloproteinases 1 in sporadic Alzheimer's disease. Psychiatric genetics : an international journal devoted to studies on inherited factors in disorders of the brain and behaviour12, S. 155-60. edoc
Heun, R. Papassotiropoulos, A. Jessen, F. Maier, W. & Breitner, J C. (2001). A family study of Alzheimer disease and early- and late-onset depression in elderly patients.Archives of general psychiatry58, S. 190-6. edoc
Jessen, F. Flacke, S. Granath, D O. Manka, C. Scheef, L. Papassotiropoulos, A. Schild, H H. & Heun, R. (2001). Encoding and retrieval related cerebral activation in continuous verbal recognition. Cognitive brain research12, S. 199-206. edoc
Jessen, F. Kucharski, C. Fries, T. Papassotiropoulos, A. Hoenig, K. Maier, W. & Heun, R. (2001). Sensory gating deficit expressed by a disturbed suppression of the P50 event-related potential in patients with Alzheimer's disease. American journal of psychiatry158, S. 1319-21. edoc
Kölsch, H. Ptok, U. Bagli, M. Papassotiropoulos, A. Schmitz, S. Barkow, K. Kockler, M. Rao, M L. Maier, W. & Heun, R. (2001). Gene polymorphisms of interleukin-1alpha influence the course of Alzheimer's disease. Annals of neurology49, S. 818-9. edoc
Papassotiropoulos, A. Hock, C. & Nitsch, R M. (2001). Genetics of interleukin 6 : implications for Alzheimer's disease. Neurobiology of aging22, S. 863-71. edoc
Ptok, U. Papassotiropoulos, A. & Heun, R. (2001). Mental health in spouses of patients with gerontopsychiatric disorders. International journal of geriatric psychiatry16, S. 1014-6. edoc
Ptok, U. Papassotiropoulos, A. Maier, W. & Heun, R. (2001). Seasonal distribution of births in patients with Alzheimer's disease and elderly depressive patients. European psychiatry16, S. 157-61. edoc
Ptok, U. Seeher, C. Jessen, F. Papassotiropoulos, A. & Heun, R. (2001). Inter-rater reliability of family history information on psychiatric disorders in relatives. European archives of psychiatry and clinical neuroscience251, S. 279-83. edoc
Bagli, M. Papassotiropoulos, A. Jessen, F. Rao, M L. Maier, W. & Heun, R. (2000). Gene-gene interaction between interleukin-6 and alpha2-macroglobulin influences the risk for Alzheimer's disease. Annals of neurology47, S. 138-9. edoc
Bagli, M. Papassotiropoulos, A. Jessen, F. Schmitz, S. Rao, M L. Maier, W. & Heun, R. (2000). Identical distribution of the alpha 2-macroglobulin pentanucleotide deletion in subjects with Alzheimer disease and controls in a German population. American journal of medical genetics96, S. 775-7. edoc
Bagli, M. Papassotiropoulos, A. Knapp, M. Jessen, F. Luise Rao, M. Maier, W. & Heun, R. (2000). Association between an interleukin-6 promoter and 3' flanking region haplotype and reduced Alzheimer's disease risk in a German population. Neuroscience letters283, S. 109-12. edoc
Finckh, U. von der Kammer, H. Velden, J. Michel, T. Andresen, B. Deng, A. Zhang, J. Müller-Thomsen, T. Zuchowski, K. Menzer, G. Mann, U. Papassotiropoulos, A. Heun, R. Zurdel, J. Holst, F. Benussi, L. Stoppe, G. Reiss, J. Miserez, A R. Staehelin, H B. Rebeck, G W. Hyman, B T. Binetti, G. Hock, C. Growdon, J H. & Nitsch, R M. (2000). Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. Archives of neurology57, S. 1579-83. edoc
Heun, R. Kockler, M. & Papassotiropoulos, A. (2000). Distinction of early- and late-onset depression in the elderly by their lifetime symptomatology. International journal of geriatric psychiatry15, S. 1138-42. edoc
Heun, R. Papassotiropoulos, A. & Ptok, U. (2000). Subthreshold depressive and anxiety disorders in the elderly. European psychiatry15, S. 173-82. edoc
Jessen, F. Block, W. Träber, F. Keller, E. Flacke, S. Papassotiropoulos, A. Lamerichs, R. Heun, R. & Schild, H H. (2000). Proton MR spectroscopy detects a relative decrease of N-acetylaspartate in the medial temporal lobe of patients with AD. Neurology55, S. 684-8. edoc
Jessen, F. Heun, R. Erb, M. Granath, D O. Klose, U. Papassotiropoulos, A. & Grodd, W. (2000). The concreteness effect : evidence for dual coding and context availability.Brain and Language74, S. 103-12. edoc
Lütjohann, D. Papassotiropoulos, A. Björkhem, I. Locatelli, S. Bagli, M. Oehring, R D. Schlegel, U. Jessen, F. Rao, M L. von Bergmann, K. & Heun, R. (2000). Plasma 24S-hydroxycholesterol (cerebrosterol) is increased in Alzheimer and vascular demented patients. Journal of lipid research41, S. 195-8. edoc
Majores, M. Bagli, M. Papassotiropoulos, A. Schwab, S G. Jessen, F. Rao, M L. Maier, W. & Heun, R. (2000). Allelic association between the D10S1423 marker and Alzheimer's disease in a German population. Neuroscience letters289, S. 224-6. edoc
Papassotiropoulos, A. Bagli, M. Becker, K. Jessen, F. Maier, W. Rao, M L. Ludwig, M. & Heun, R. (2000). No association between an intronic biallelic polymorphism of the FE65 gene and Alzheimer's disease. International journal of molecular medicine6, S. 587-9. edoc
Papassotiropoulos, A. Bagli, M. Jessen, F. Frahnert, C. Rao, M L. Maier, W. & Heun, R. (2000). Confirmation of the association between bleomycin hydrolase genotype and Alzheimer's disease. Molecular psychiatry5, S. 213-5. edoc
Papassotiropoulos, A. Bagli, M. Jessen, F. Maier, W. Förstl, H. Kurz, A. & Heun, R. (2000). Interaction of two genes possibly involved in the regulation of the amyloid precursor protein (APP) processing. Molecular psychiatry5, S. 240-1. edoc
Papassotiropoulos, A. Bagli, M. Kurz, A. Kornhuber, J. Förstl, H. Maier, W. Pauls, J. Lautenschlager, N. & Heun, R. (2000). A genetic variation of cathepsin D is a major risk factor for Alzheimer's disease. Annals of neurology47, S. 399-403. edoc
Papassotiropoulos, A. Lütjohann, D. Bagli, M. Locatelli, S. Jessen, F. Rao, M L. Maier, W. Björkhem, I. von Bergmann, K. & Heun, R. (2000). Plasma 24S-hydroxycholesterol : a peripheral indicator of neuronal degeneration and potential state marker for Alzheimer's disease. NeuroReport11, S. 1959-62. edoc
Ptok, U. Papassotiropoulos, A. Maier, W. & Heun, R. (2000). Advanced parental age : a risk factor for Alzheimer's disease or depression in the elderly?. International psychogeriatrics12, S. 445-51. edoc
Schmidt, S. Papassotiropoulos, A. Bagli, M. Harzheim, M. Heun, R. & Klockgether, T. (2000). No association of serum levels of interleukin-6 and its soluble receptor components with a genetic variation in the 3'flanking region of the interleukin-6 gene in patients with multiple sclerosis. Neuroscience letters294, S. 139-42. edoc
Schröder, R. Vielhaber, S. Wiedemann, F R. Kornblum, C. Papassotiropoulos, A. Broich, P. Zierz, S. Elger, C E. Reichmann, H. Seibel, P. Klockgether, T. & Kunz, W S. (2000). New insights into the metabolic consequences of large-scale mtDNA deletions : a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. Journal of neuropathology and experimental neurology59, S. 353-60.edoc
Schulze, T G. Müller, D J. Krauss, H. Scherk, H. Ohlraun, S. Syagailo, Y V. Windemuth, C. Neidt, H. Grässle, M. Papassotiropoulos, A. Heun, R. Nöthen, M M. Maier, W. Lesch, K P. & Rietschel, M. (2000). Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder. American journal of medical genetics96, S. 801-3. edoc
Bagli, M. Papassotiropoulos, A. Schwab, S G. Jessen, F. Rao, M L. Maier, W. & Heun, R. (1999). No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a German population. Journal of the neurological sciences167, S. 34-6. edoc
Heun, R. Klose, U. Jessen, F. Erb, M. Papassotiropoulos, A. Lotze, M. & Grodd, W. (1999). Functional MRI of cerebral activation during encoding and retrieval of words.Human brain mapping8, S. 157-69. edoc
Kühn, K U. Meyer, K. Nöthen, M M. Gänsicke, M. Papassotiropoulos, A. & Maier, W. (1999). Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors : replication tests. American journal of medical genetics88, S. 168-72. edoc
Papassotiropoulos, A. Bagli, M. Feder, O. Jessen, F. Maier, W. Rao, M L. Ludwig, M. Schwab, S G. & Heun, R. (1999). Genetic polymorphism of cathepsin D is strongly associated with the risk for developing sporadic Alzheimer's disease. Neuroscience letters262, S. 171-4. edoc
Papassotiropoulos, A. Bagli, M. Jessen, F. Bayer, T A. Maier, W. Rao, M L. & Heun, R. (1999). A genetic variation of the inflammatory cytokine interleukin-6 delays the initial onset and reduces the risk for sporadic Alzheimer's disease. Annals of neurology45, S. 666-8. edoc
Papassotiropoulos, A. Bagli, M. Jessen, F. Rao, M L. Schwab, S G. & Heun, R. (1999). Early-onset and late-onset depression are independent of the genetic polymorphism of apolipoprotein E. Dementia and geriatric cognitive disorders10, S. 258-61. edoc
Papassotiropoulos, A. Hawellek, B. Frahnert, C. Rao, G S. & Rao, M L. (1999). The risk of acute suicidality in psychiatric inpatients increases with low plasma cholesterol.Pharmacopsychiatry32, S. 1-4. edoc
Papassotiropoulos, A. & Heun, R. (1999). Screening for depression in the elderly : a study on misclassification by screening instruments and improvement of scale performance. Progress in neuro-psychopharmacology & biological psychiatry23, S. 431-46. edoc
Papassotiropoulos, A. & Heun, R. (1999). Detection of subthreshold depression and subthreshold anxiety in the elderly. International journal of geriatric psychiatry14, S. 643-50. edoc
Papassotiropoulos, A. Heun, R. & Maier, W. (1999). The impact of dementia on the detection of depression in elderly subjects from the general population. Psychological medicine29, S. 113-20. edoc
Schwab, S G. Bagli, M. Papassotiropoulos, A. Jessen, F. Maier, W. Rao, M L. & Heun, R. (1999). Alpha-1-antichymotrypsin gene polymorphism and risk for sporadic Alzheimer's disease in a German population. Dementia and geriatric cognitive disorders10, S. 469-72. edoc
Heun, R. Müller, H. & Papassotiropoulos, A. (1998). Differential validity of informant-based diagnoses of dementia and depression in index subjects and in their first-degree relatives. Social psychiatry and psychiatric epidemiology33, S. 510-3. edoc
Heun, R. Papassotiropoulos, A. & Jennssen, F. (1998). The validity of psychometric instruments for detection of dementia in the elderly general population. International journal of geriatric psychiatry13, S. 368-80. edoc
Rao, M L. Hawellek, B. Papassotiropoulos, A. Deister, A. & Frahnert, C. (1998). Upregulation of the platelet Serotonin2A receptor and low blood serotonin in suicidal psychiatric patients. Neuropsychobiology38, S. 84-9. edoc
Papassotiropoulos, A. Heun, R. & Maier, W. (1997). Age and cognitive impairment influence the performance of the General Health Questionnaire. Comprehensive psychiatry38, S. 335-40. edoc
Papassotiropoulos, A. Ludwig, M. Naib-Majani, W. & Rao, G S. (1996). Induction of apoptosis and secondary necrosis in rat dorsal root ganglion cell cultures by oxidized low density lipoprotein. Neuroscience letters209, S. 33-6. edoc
Rao, M L. Pelzer, E. Papassotiropoulos, A. Tiemeier, H. Jönck, L. & Möller, H J. (1996). Selective slow-wave sleep deprivation influences blood serotonin profiles and serum melatonin concentrations in healthy subjects. Biological Psychiatry40, S. 664-7. edoc
Rao, M L. Bräunig, P. & Papassotiropoulos, A. (1994). Autoaggressive behavior is closely related to serotonin availability in schizoaffective disorder. Pharmacopsychiatry27, S. 202-6. edoc

Aufsätze in Sammelbänden

Wasmuth, M. & Brein, G. (2013). Das Alabastergefäß VA Ass. 2258 aus Assur. In Budka, J. Gundacker, R. & Pieke, G. (Eds.), Florilegium Aegyptiacum - Eine wissenschaftliche Blütenlese von Schülern und Freunden für Helmut Satzinger zum 75. Geburtstag am 21. Jänner 2013 (pp. S. 343-367). (= Göttinger Miszellen Beihefte Nr. 14). Göttingen.


Wilker, S. Elbert, T. Papassotiropoulos, A., de Quervain, D J -F. & Kolassa, I-T. (2014). Responce to: Further Support for an Association between the Memory-Related Gene WWC1 and Posttraumatic Stress Disorder: Results from the Detroit Neighborhood Health Study. Biological psychiatry76, S. E27-E28. edoc
Easton, A C. Lourdusamy, A. Loth, E. Toro, R. Torro, R. Giese, K P. Kornhuber, J. de Quervain, D J-F. Papassotiropoulos, A. Fernandes, C. Müller, C P. & Schumann, G. (2013). CAMK2A polymorphisms predict working memory performance in humans.Molecular psychiatry18, S. 850-2. edoc
Schneider, A. Falkai, P. & Papassotiropoulos, A. (2010). [Molecular principles of tau-induced toxicity: new experimental therapy strategies for treatment of Alzheimer's disease]. Der Nervenarzt81, S. 1289-90, 1292, 1294, passim.
Heck, A. Lieb, R. Unschuld, P G. Ellgas, A. Pfister, H. Lucae, S. Erhardt, A. Himmerich, H. Horstmann, S. Kloiber, S. Ripke, S. Müller-Myhsok, B. Bettecken, T. Uhr, M. Holsboer, F. & Ising, M. (2008). Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism. Molecular psychiatry13, S. 831-2.
Tagarakis, G I. Tsolaki-Tagaraki, F. Tsolaki, M. Diegeler, A. Stylianakis, G E. Kazis, D. Tsilimingas, N B. & Papassotiropoulos, A. (2008). Are genetic components related to cognitive decline after coronary artery surgery? : Genetics and brain function after bypass heart surgery. Journal of cardiac surgery23, S. 280-1. edoc
Koller, M F. Papassotiropoulos, A., Henke, K. Behrends, B. Noda, S. Kratzer, A. Hock, C. & Hofmann, M. (2005). Evidence of a genetic basis of Morgagni-Stewart-Morel syndrome : a case report of identical twins. Neuro-degenerative diseases2, S. 56-60.edoc
Aerni, A. Traber, R. Hock, C. Roozendaal, B. Schelling, G. Papassotiropoulos, A., Nitsch, R M. Schnyder, U. & de Quervain, D J-F. (2004). Low-dose cortisol for symptoms of posttraumatic stress disorder. American Journal of Psychiatry161, S. 1488-90. edoc
Papassotiropoulos, A., & Hock, C. (2002). Biochemical markers of Alzheimer's disease : wish and reality. Neurobiology of aging23, S. 513-4. edoc