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Literaturliste von Dr. Angela Heck

letzte Aktualisierung: 22.03.2018

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.

Spalek, K., Coynel, D., Freytag, V., Hartmann, F., de Quervain, D., Heck, A., Milnik, A. & Papassotiropoulos, A. (2016). A common NTRK2 variant is associated with emotional arousal and brain white-matter integrity in healthy young subjects. Translational Psychiatry.

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.

Ising, M., Mather, K. A., Zimmermann, P., Brückl, T., Höhne, 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 Behavior, 13(5), 501-507.

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.

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.

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. Psychoneuroendocrinology, 38(7), 1203-1207.

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., Bruckl, T., Klengel, T., Menke, A., Muller-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 one, 8, e64947.

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.

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.

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. (2012). Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology, 37(4), 565-575.

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.

Quast, C., Altmann, A., Weber, P., Arloth, J., Bader, D., Heck, A., Pfister, H., Müller-Myhsok, B., Ehrhardt, A. & Binder, E. B. B. (2012). Rare variants in TMEM132D in a case-control sample for panic disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159(8).

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., Keßler, 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 Psychiatry, 16, 647-663.

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 Medicine, 12(10), 1003-1007.

Heck, A., Pfister, H., Czamara, D., Muller-Myhsok, B., Pütz, B., Lucae, S., Hennings, J. & Ising, M. (2011). Evidence for associations between MDGA2 polymorphisms and harm avoidance: Replication and extension of a genome-wide association finding. Psychiatric genetics, 21(5), 257-260.

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.

Klengel, T., Heck, A., Pfister, H., Bruckl, T., Hennings, J. M., Menke, A., Czamara, D., Muller-Myhsok, B. & Ising, M. (2011). Somatization in major depression-clinical features and genetic associations. Acta psychiatrica Scandinavica, 124(4), 317-328.

Kohli, M. A., Lucae, S., Saemann, P. G., Schmidt, M. V., Demirkan, A., Hek, K., Czamara, D., Alexander, M., Salyakina, D., Ripke, S., Hoehn, D., Specht, M., Menke, A., Hennings, J., Heck, A., Wolf, C., Ising, M., Schreiber, S., Czisch, M., Müller, M. B., Uhr, M., Bettecken, T., Becker, A., Schramm, J., Rietschel, M., Maier, W., Bradley, B., Ressler, K. J., Nöthen, M. M., Cichon, S., Craig, I. W., Breen, G., Lewis, C. M., Hofman, A., Tiemeier, H., van Duijn, C. M., Holsboer, F., Muller-Myhsok, B. & Binder, E. B. (2011). The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron, 70(2), 252-265.

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 Behavior, 8(4), 464-472.

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, 150(1), 104 - 114.

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, 150(8), 1100-1109.

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 Psychiatry, 13(9), 831-832.

Ising, M., Heck, A. & Antov, M. I. (2008). Genetik der Stressreaktion. In W. Janke, M. Schmidt-Daffy & G. Debus (Hrsg.), Experimentelle Emotionspsychologie. Methodische Ansätze, Probleme, Ergebnisse (S. 481-500). Lengerich: Pabst.



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