Hennings, J., M. Kohli, A. Heck, D. Roeske, T. Brückl, T. Klengel, A. Menke, B. Müller-Myhsok, M. Ising, F. Holsboer and S. Lucae: Polymorphisms in the BDNF gene are associated with antidepressant treatment response. In: European Neuropsychopharmacology 20, Suppl. 3, S427-S428 (2010).
Sullivan, P. F., E. J. C. de Geus, G. Willemsen, M. R. James, J. H. Smit, T. Zandbelt, V. Arolt, B. T. Baune, D. Blackwood, S. Cichon, W. L. Coventry, K. Domschke, A. Farmer, M. Fava, S. D. Gordon, Q. He, A. C. Heath, P. Heutink, F. Holsboer, W. J. Hoogendijk, J. J. Hottenga, Y. Hu, M. Kohli, D. Lin, S. Lucae, D. J. MacIntyre, W. Maier, K. A. McGhee, P. McGuffin, G. W. Montgomery, W. J. Muir, W. A. Nolen, M. M. Nöthen, R. H. Perlis, K. Pirlo, D. Posthuma, M. Rietschel, P. Rizzu, A. Schosser, A. B. Smit, J. W. Smoller, J. Y. Tzeng, R. van Dyck, M. Verhage, F. G. Zitman, N. G. Martin, N. R. Wray, D. I. Boomsma and B. W. J. H. Penninx: Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. In: Molecular Psychiatry 14, 4, 359-375 (2009).
Horstmann, S., S. Lucae, A. Menke, M. Kohli, T. Bettecken, M. Uhr, S. Ripke, M. Ising, B. Müller-Myhsok, F. Holsboer and E. B. Binder: Association of GRIK4 and 5-HTR2A with antidepressant treatment in the MARS cohort of depressed impatients. In: International Journal of Neuropsychopharmacology 11, Suppl. 1, 112-113 (2008).
Weber, F., B. Fontaine, I. Cournu-Rebeix, A. Kroner, M. Knop, S. Lutz, F. Müller-Sarnowski, M. Uhr, T. Bettecken, M. Kohli, S. Ripke, M. Ising, P. Rieckmann, D. Brassat, G. Semana, M. C. Babron, S. Mrejen, C. Gout, O. Lyon-Caen, J. Yaouanq, G. Edan, M. Clanet, F. Holsboer, F. Clerget-Darpoux and B. Müller-Myhsok: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. In: Journal of Neurology 255, Suppl. 2, 52-53 (2008).
Weber, F., B. Fontaine, I. Cournu-Rebeix, A. Kroner, M. Knop, S. Lutz, F. Müller-Sarnowski, M. Uhr, T. Bettecken, M. Kohli, S. Ripke, M. Ising, P. Rieckmann, D. Brassat, G. Semana, M. C. Babron, S. Mrejen, C. Gout, O. Lyon-Caen, J. Yaouanq, G. Edan, M. Clanet, F. Holsboer, F. Clerget-Darpoux and B. Müller-Myhsok: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. In: Genes and Immunity 9, 3, 259-263 (2008).
Kloiber, S., S. Ripke, M. Kohli, S. Reppermund, D. Salyakina, T. Bettecken, M. Ising, M. Uhr, S. Horstmann, T. Dose, P. G. Unschuld, J. Zihl, B. Müller-Myhsok, F. Holsboer and S. Lucae: Polymorphisms in the leptin gene are associated with resistance to antidepressant treatment and lower cognitive performance in depression. In: Pharmacopsychiatry 40, 5, 210-211 (2007).
Lucae, S., I. Marcus, P. Saemann, T. Bettecken, M. Uhr, S. Ripke, M. Kohli, S. Kloiber, B. Bondy, R. Rupprecht, K. Domschke, V. Arolt, P. Lichtner, F. Holsboer and B. Müller-Myhsok: Whole genome analysis reveals new potential drug targets as predictors of antidepressant treatment response. In: Pharmacopsychiatry 40, 5, 213-213 (2007).
Unschuld, P. G., M. Ising, A. Erhardt, S. Lucae, M. Kohli, S. Kloiber, D. Salyakina, C. K. Thoeringer, R. Lieb, M. Uhr, E. B. Binder, B. Müller-Myhsok, F. Holsboer and M. E. Keck: Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. In: Pharmacopsychiatry 40, 5, 217-217 (2007).
Unschuld, P. G., M. Ising, A. Erhardt, S. Lucae, S. Kloiber, M. Kohli, D. Salyakina, T. Welt, N. Kern, R. Lieb, M. Uhr, E. B. Binder, B. Müller-Myhsok, F. Holsboer and M. E. Keck: Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 144B, 4, 424-429 (2007).
Unschuld, P. G., A. Erhardt, M. Ising, S. Lucae, S. Kloiber, M. Kohli, E. B. Binder, B. Müller-Myhsok, M. E. Keck and F. Holsboer: An association candidate-gene study on genetic variations within HTR2A in patients suffering from panic disorder. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 141B, 7, 739-740 (2006).
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