Items where Author is "Heck, A."

Yes

Spalek, K. and Coynel, D. and Freytag, V. and Hartmann, F. and Heck, A. and Milnik, A. and de Quervain, D. and Papassotiropoulos, A.. (2016) A common NTRK2 variant is associated with emotional arousal and brain white-matter integrity in healthy young subjects. Translational Psychiatry, 6. e758.

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.

Papassotiropoulos, 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.

Milnik, 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.

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.

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.

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Ellgas, A. and Pfister, H. and Lieb, R. and Puetz, B. and Uhr, M. and Hohoff, C. and Maier, W. and Bandelow, B. and Domschke, K. and Jacob, C. and Deckert, J. and Landgraf, R. and Bettecken, T. and Keck, M. E. 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, Vol. 16, H. 6. pp. 647-663.

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.

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.

Heck, 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 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.