edoc

Items where Author is "Uhr, M."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2014 | 2011 | 2009 | 2008 | 2007 | 2006 | 2004
Number of items: 15.

2014

Menke, A. and Arloth, J. and Gerber, M. and Rex-Haffner, M. and Uhr, M. and Holsboer, F. and Binder, E. and Holsboer-Trachsler, E. and Beck, J.. (2014) Dexamethasone stiumulated gene expression in peripheral blood indicates glucocorticoid-receptor hypersensitivity in job-related exhaustion. Psychoneuroendocrinology, Vol. 44. pp. 35-46.

2011

Zimmermann, P. and Brückl, T. and Nocon, A. and Pfister, H. and Binder, E. and Uhr, M. and Lieb, R. and Moffitt, T. and Caspi, A. and Holsboer, F. and Ising, M.. (2011) Interaction of FKBP5 gene variants and adverse life events in predicting depression onset : results from a 10-year prospective community study. American journal of psychiatry, Vol. 168. pp. 1107-1116.

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.

2009

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.

Zimmermann, P. and Brueckl, T. and Pfister, H. and Lieb, R. and Wittchen, H. U. and Holsboer, F. and Ising, M. and Binder, E. B. and Uhr, M. and Nocon, A.. (2009) The interplay of variations in the FKBP5 gene and adverse life events in predicting the first onset of depression during a ten-year follow-up. Pharmacopsychiatry, Vol. 42, H. 5. p. 249.

2008

Erhardt, A. and Lucae, S. and Kern, N. and Unschuld, P. G. and Ising, M. and Lieb, R. and Uhr, M. and Hohoff, C. and Deckert, J. and Bandelow, B. and Maier, W. and Binder, E. B. and Müller-Myhsok, B. and Keck, M. E. and Holsboer, F.. (2008) Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks. Molecular Psychiatry, Vol. 13. pp. 242-243.

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.

Unschuld, P. G. and Ising, M. and Erhardt, A. and Lucae, S. and Kohli, M. and Kloiber, S. and Salyakina, D. and Thoeringer, C. K. and Kern, N. and Lieb, R. and Uhr, M. and Binder, E. and Müller-Myhsok, B. and Holsboer, F. and Keck, M. E.. (2008) Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. Journal of affective disorders, Vol. 105, H. 1-3. pp. 177-184.

2007

Thoeringer, C. K. and Binder, E. B. and Salyakina, D. and Erhardt, A. and Ising, M. and Unschuld, P. G. and Kern, N. and Lucae, S. and Brueckl, T. M. and Mueller, B. M. and Fuchs, B. and Puetz, B. and Lieb, R. and Uhr, M. and Holsboer, F. and Mulller-Myshok, B. and Keck, M. E.. (2007) Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks. Journal of psychiatric research, Vol. 41, H. 7. pp. 579-584.

Erhardt, A. and Lucae, S. and Unschuld, P. G. and Ising, M. and Kern, N. and Salyakina, D. and Lieb, R. and Uhr, M. and Binder, E. B. and Keck, M. E. and Müller-Myhsok, B. and Holsboer, F.. (2007) Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders. Journal of affective disorders, Vol. 101, H. 1-3. pp. 159-168.

Unschuld, P. G. and Ising, M. and Erhardt, A. and Lucae, S. and Kloiber, S. and Kohli, M. and Salyakina, D. and Welt, T. and Kern, N. and Lieb, R. and Uhr, M. and Binder, E. B. and Müller-Myhsok, B. and Holsboer, F. and Keck, M. E.. (2007) Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 144B, H. 4. pp. 424-429.

2006

Lucae, S. and Salyakina, D. and Barden, N. and Harvey, M. and Gagné, B. and Labbé, M. and Binder, E. B. and Uhr, M. and Paez-Pereda, M. and Sillaber, I. and Ising, M. and Brückl, T. and Lieb, R. and Holsboer, F. and Müller-Myhsok, B.. (2006) P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder. Human molecular genetics, Vol. 15, H. 16. pp. 2438-2445.

2004

Binder, E. B. and Salyakina, D. and Lichtner, P. and Wochnik, G. M. and Ising, M. and Pütz, B. and Papiol, S. and Seaman, S. and Lucae, S. and Kohli, M. A. and Nickel, T. and Künzel, H. E. and Fuchs, B. and Majer, M. and Pfennig, A. and Kern, N. and Brunner, J. and Modell, S. and Baghai, T. and Deiml, T. and Zill, P. and Bondy, B. and Rupprecht, R. and Messer, T. and Köhnlein, O. and Dabitz, H. and Brückl, T. and Müller, N. and Pfister, H. and Lieb, R. and Mueller, J. C. and Lohmussar, E. and Strom, T. and Bettecken, T. and Meitinger, T. and Uhr, M. and Rein, T. and Holsboer, F. and Müller-Myhsok, B.. (2004) Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nature genetics, Vol. 36, H. 12. pp. 1319-1325.

This list was generated on Tue Sep 25 06:15:04 2018 CEST.