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Items where Author is "Ising, M."

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Number of items: 24.

2016

Schwantes-An, T. H. and Zhang, J. and Chen, L. S. and Hartz, S. M. and Culverhouse, R. C. and Chen, X. and Coon, H. and Frank, J. and Kamens, H. M. and Konte, B. and Kovanen, L. and Latvala, A. and Legrand, L. N. and Maher, B. S. and Melroy, W. E. and Nelson, E. C. and Reid, M. W. and Robinson, J. D. and Shen, P. H. and Yang, B. Z. and Andrews, J. A. and Aveyard, P. and Beltcheva, O. and Brown, S. A. and Cannon, D. S. and Cichon, S. and Corley, R. P. and Dahmen, N. and Degenhardt, L. and Foroud, T. and Gaebel, W. and Giegling, I. and Glatt, S. J. and Grucza, R. A. and Hardin, J. and Hartmann, A. M. and Heath, A. C. and Herms, S. and Hodgkinson, C. A. and Hoffmann, P. and Hops, H. and Huizinga, D. and Ising, M. and Johnson, E. O. and Johnstone, E. and Kaneva, R. P. and Kendler, K. S. and Kiefer, F. and Kranzler, H. R. and Krauter, K. S. and Levran, O. and Lucae, S. and Lynskey, M. T. and Maier, W. and Mann, K. and Martin, N. G. and Mattheisen, M. and Montgomery, G. W. and Muller-Myhsok, B. and Murphy, M. F. and Neale, M. C. and Nikolov, M. A. and Nishita, D. and Nothen, M. M. and Nurnberger, J. and Partonen, T. and Pergadia, M. L. and Reynolds, M. and Ridinger, M. and Rose, R. J. and Rouvinen-Lagerstrom, N. and Scherbaum, N. and Schmal, C. and Soyka, M. and Stallings, M. C. and Steffens, M. and Treutlein, J. and Tsuang, M. and Wall, T. L. and Wodarz, N. and Yuferov, V. and Zill, P. and Bergen, A. W. and Chen, J. and Cinciripini, P. M. and Edenberg, H. J. and Ehringer, M. A. and Ferrell, R. E. and Gelernter, J. and Goldman, D. and Hewitt, J. K. and Hopfer, C. J. and Iacono, W. G. and Kaprio, J. and Kreek, M. J. and Kremensky, I. M. and Madden, P. A. and McGue, M. and Munafo, M. R. and Philibert, R. A. and Rietschel, M. and Roy, A. and Rujescu, D. and Saarikoski, S. T. and Swan, G. E. and Todorov, A. A. and Vanyukov, M. M. and Weiss, R. B. and Bierut, L. J. and Saccone, N. L.. (2016) Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2). pp. 151-169.

2014

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.

2011

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.

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.

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.

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.

Brueckl, T. and Lieb, R. and Pfister, H. and Wittchen, H. U. and Holsboer, F. and Ising, M. and Zimmermann, P.. (2009) Polymorphisms in the serotonin receptor 2A gene (HTR2A), parenting styles and the risk of depression in young adulthood: results from a family study. Pharmacopsychiatry, Vol. 42, H. 5. p. 213.

Sievers, C. and Dimopoulou, C. and Pfister, H. and Lieb, R. and Steffin, B. and Roemmler, J. and Schopohl, J. and Mueller, M. and Schneider, H. J. and Ising, M. and Wittchen, H.-U. and Stalla, G. K.. (2009) Prevalence of mental disorders in acromegaly : a cross-sectional study in 81 acromegalic patients. Clinical endocrinology, Vol. 71. pp. 691-701.

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.

Keck, M. E. and Kern, N. and Erhardt, A. and Unschuld, P. G. and Ising, M. and Salyakina, D. and Müller, M. B. and Knorr, C. C. and Lieb, R. and Hohoff, C. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Fritze, J. and Deckert, J. and Holsboer, F. and Müller-Myhsok, B. and Binder, E. B.. (2008) Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1196-1204.

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.

Ising, M. and Brand, S. and Hemmeter, U. and Hatzinger, M.. (2008) Vulnerabilitätsfaktoren für depressive Erkrankungen, Leading Opinions. Neurologie & Psychiatrie, Vol. 8. pp. 8-10.

2007

Sievers, C. and Dimopoulou, C. and Pfister, H. and Lieb, R. and Steffin, B. and Roemmler, J. and Schopohl, J. and Mueller, M. and Schneider, H. J. and Ising, M. and Wittchen, H. U. and Stalla, G. K.. (2007) A shifted psychopathological risk profile in acromegalic patients? : abstract. Experimental and clinical endocrinology & diabetes, Vol. 115, H. 8. p. 553.

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.

Zimmermann, P. and Brueckl, T. and Lieb, R. and Ising, M. and Wittchen, H. U.. (2007) The interplay of familial depression liability and adverse life events in predicting the first onset of depression during a ten-year follow-up. Pharmacopsychiatry, Vol. 40, H. 5. p. 219.

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 Wed Nov 25 10:14:18 2020 CET.