letzte Aktualisierung: 18.11.2022
Conrad, D., Wilker, S., Schneider, A., Karabatsiakis, A., Pfeiffer, A., Kolassa, S., Freytag, V., Vukojevic, V., Vogler, C., Milnik, A., Papassotiropoulos, A., de Quervain, D.- J.- F., Elbert, T. & Kolassa, I.-T. (2020). Integrated genetic, epigenetic, and gene set enrichment analyses identify NOTCH as a potential mediator for PTSD risk after trauma: Results from two independent African cohorts. Psychophysiology, 57(1), No. e13288.
Aeberhard, A., Gschwind, L., Kossowsky, J., Luksys, G., Papassotiropoulos, A., de Quervain, D. & Vogler, C. (2019). Introducing COSMOS: A web platform for multimodal game-based psychological assessment geared towards open science practice. Journal of Technology in Behavioral Sciences, 4, 234-244.
Wilker, S., Schneider, A., Conrad, D., Pfeiffer, A., Boeck, C., Lingenfelder, B., Freytag, V., Vukojevic, V., Vogler, C., Milnik, A., Papassotiropoulos, A., de Quervain, D.- J.- .- F., Elbert, T., Kolassa, S. & Kolassa, I.-T. (2018). Genetic variation is associated with PTSD risk and aversive memory: Evidence from two trauma - Exposed African samples and one healthy European sample. Translational Psychiatry, 8, No. 251.
Egli, T., Vukojevic, V., Sengstag, T., Jacquot, M., Cabezón, R., Coynel, D., Freytag, V., Heck, A., Vogler, C., de Quervain, D.- J.- F., Papassotiropoulos, A. & Milnik, A. (2017). Exhaustive search for epistatic effects on the human methylome. Scientific Reports, 7, No. 13669.
Freytag, V., Milnik, A., Vukojevic, V., Demougin, P., Egli, T., Vogler, C., Papassotiropoulos, A., Coynel, D., Gschwind, L., Loos, E., de Quervain, D.- J.- .- F., Carrillo-Roa, T., Mann, P. G. S., Binder, E. B., Jessen, F., Maier, W., Wagner, M., Riedel-Heller, S. G. & Scherer, M. (2017). A peripheral epigenetic signature of immune system genes is linked to neocortical thickness and memory. Nature Communications, 1-12.
Heck, A., Milnik, A., Vukojevic, V., Petrovska, J., Egli, T., Singer, J., Escobar, P., Sengstag, T., Coynel, D., Freytag, V., Fastenrath, M., Demougin, P., Loos, E., Hartmann, F., Schicktanz, N., Delarue Bizzini, B., Vogler, C., Kolassa, I.-T., Wilker, S., Elbert, T., Schwede, T., Beisel, C., Beerenwinkel, N., de Quervain, D.- J.- F. & Papassotiropoulos, A. (2017). Exome sequencing of healthy phenotypic extremes links TROVE2 to emotional memory and PtSD. Nature Human Behaviour, 1, No. 0081.
Petrovska, J., Milnik, A., Auschra, B., Egli, T., Gschwind, L., Hartmann, F., Vogler, C., Papassotiropoulos, A., Heck, A., Coynel, D., Fastenrath, M., Loos, E., Sifalakis, K. & de Quervain, D.- J.- .- F. (2017). The NCAM1 gene set is linked to depressive symptoms and their brain structural correlates in healthy individuals. Journal of Psychiatric Research, 116-123.
Milnik, A., Vogler, C., Demougin, P., Egli, T., Freytag, V., Hartmann, F., Heck, A., Peter, F., Spalek, K., Stetak, A., de Quervain, D.- J.- .- F., Papassotiropoulos, A. & Vukojevic, V. (2016). Common epigenetic variation in a European population of mentally healthy young adults. Journal of Psychiatric Research, 83, 260-268.
Heck, A., Fastenrath, M., Coynel, D., Auschra, B., Freytag, V., Gschwind, L., Hartmann, F., Milnik, A., Vogler, C., Papassotiropoulos, A., de Quervain, D.- J.- .- F., Spalek, K., Bickel, H., Jessen, F., Maier, W., Wagner, M., Wolfsgruber, S., Kaduszkiewicz, H., Pentzek, M., Riedel-Heller, S. G. & Weyerer, S. (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), 1029-1036.
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 America, 112(35), E4939-E4948.
Heck, A., Fastenrath, M., Ackermann, S., Auschra, B., Coynel, D., Gschwind, L., Milnik, A., Vogler, C., Weyerer, S., Papassotiropoulos, A., de Quervain, D.- J.- .- F., Spalek, K., Bickel, H., Jessen, F., Maier, W., Wagner, M., Wolfsgruber, S., Kaduszkiewicz, H., Pentzek, M., Riedel-Heller, S. G., Ripke, S. & Sullivan, P. (2014). Converging Genetic and Functional Brain Imaging Evidence Links Neuronal Excitability to Working Memory, Psychiatric Disease, and Brain Activity. Neuron, 81(5), 1203-1213.
Luksys, G., Ackermann, S., Coynel, D., Gschwind, L., Heck, A., Rasch, B., Vogler, C., Papassotiropoulos, A., Fastenrath, M., Spalek, K. & de Quervain, D. (2014). BAIAP2 Is Related to Emotional Modulation of Human Memory Strength. PLoS ONE, 9(1), No. e92933.
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, 131-138.
Vogler, C., Gschwind, L., Freytag, V., Milnik, A., Egli, T., Heck, A., Papassotiropoulos, A., de Quervain, D.- J.- F. & Coynel, D. (2014). Substantial SNP-based heritability estimates for working memory performance. Translational Psychiatry, 4, e438.
Vukojevic, V., Fastenrath, M., Gschwind, L., Spalek, K., Milnik, A., Heck, A., Vogler, C., Demougin, P., Peter, F., Stetak, A., Papassotiropoulos, A., Kolassa, I.-T., Wilker, S., de Quervain, D.- J.- .- F., Atucha, E., Roozendaal, B. & Elbert, T. (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), 10274-10284.
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. (2013). Human genome-guided identification of memory-modulating drugs. Proceedings of the National Academy of Sciences of the United States of America, 110, E4369-74.
Papassotiropoulos, A., Stefanova, E., Vogler, C., Gschwind, L., Ackermann, S., Spalek, K., Rasch, B., Heck, A., Aerni, A., Hanser, E., Demougin, P., Huynh, K.-D., Luechinger, R., Klarhöfer, M., Novakovic, I., Kostic, V., Boesiger, P., Scheffler, K. & de Quervain, D.-F. (2013). A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Molecular Psychiatry, 18(2), 255-263.
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 Psychiatry, 74(9), 664-671.
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. & Papassotiropolulos, A. (2012). PKC alpha 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), 8746-8751.
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 Genetics, 159(8), 958-969.
Vukojevic, V., Gschwind, L., Vogler, C., Demougin, P., de Quervain, D.- J.- F., Papassotiropoulos, A. & Stetak, A. (2012). A role for alpha-adducin (ADD-1) in nematode and human memory. The EMBO journal, 31, 1453 - 1466.
Heck, A., Vogler, C., Gschwind, L., Ackermann, S., Auschra, B., Spalek, K., Rasch, B., de Quervain, D. & Papassotiropoulos, A. (2011). Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. PLoS ONE, 6(12), No. e29337.
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 Psychiatry, 16(2), 184-192.
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, 13(8), 975-980.
Palmason, H., Moser, D., Sigmund, J., Vogler, C., Hänig, S., Schneider, A., Seitz, C., Marcus, A., Meyer, J. & Freitag, C. M. (2010). Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. Journal of Neural Transmission, 117(2), 259-267.
Vogler, C. (2010). Novel methods for the study of human cognition-related genetic variation. Dissertation, Universität, Fakultät für Psychologie, Basel.
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 ONE, 5(12), e15246.
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 Neuroscience (Online Journal), 3, No. 4.
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 Psychiatry, 13(5), 522-530.
Sigmund, J. C., Vogler, C., Huynh, K.-D., de Quervain, D.- J.- F. & Papassotirooulos, A. (2008). Fine-mapping at the HTR2A locus reveals multiple episodic memory-related variants. Biological Psychology, 79(2), 239-242.
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