Publications of T. Bettecken

Horstmann, S.; Lucae, S.; Menke, A.; Kohli, M.; Bettecken, T.; Uhr, M.; Ripke, S.; Ising, M.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Association of GRIK4 and 5-HTR2A with antidepressant treatment in the MARS cohort of depressed impatients. International Journal of Neuropsychopharmacology 11 (Suppl. 1), pp. 112 - 113 (2008)

Weber, F.; Fontaine, B.; Cournu-Rebeix, I.; Kroner, A.; Knop, M.; Lutz, S.; Müller-Sarnowski, F.; Uhr, M.; Bettecken, T.; Kohli, M. et al.; Ripke, S.; Ising, M.; Rieckmann, P.; Brassat, D.; Semana, G.; Babron, M. C.; Mrejen, S.; Gout, C.; Lyon-Caen, O.; Yaouanq, J.; Edan, G.; Clanet, M.; Holsboer, F.; Clerget-Darpoux, F.; Müller-Myhsok, B.: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Journal of Neurology 255 (Suppl. 2), pp. 52 - 53 (2008)

Menke, A.; Lucae, S.; Kloiber, S.; Horstmann, S.; Bettecken, T.; Uhr, M.; Ripke, S.; Ising, M.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Polymorphisms in metabotropic glutamate receptor 1 are associated with major depressive disorder. Biological Psychiatry 63 (7 Suppl. S), pp. 83S - 84S (2008)

Weber, F.; Fontaine, B.; Cournu-Rebeix, I.; Kroner, A.; Knop, M.; Lutz, S.; Müller-Sarnowski, F.; Uhr, M.; Bettecken, T.; Kohli, M. et al.; Ripke, S.; Ising, M.; Rieckmann, P.; Brassat, D.; Semana, G.; Babron, M. C.; Mrejen, S.; Gout, C.; Lyon-Caen, O.; Yaouanq, J.; Edan, G.; Clanet, M.; Holsboer, F.; Clerget-Darpoux, F.; Müller-Myhsok, B.: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Genes and Immunity 9 (3), pp. 259 - 263 (2008)

Benussi, L.; Binetti, G.; Sina, E.; Gigola, L.; Bettecken, T.; Meitinger, T.; Ghidoni, R.: A novel deletion in progranulin gene is associated with FTDP-17 and CBS. Neurobiology of Aging 29 (3), pp. 427 - 435 (2008)

Winkelmann, J.; Lichtner, P.; Schormair, B.; Uhr, M.; Hauk, S.; Stiasny-Kolster, K.; Trenkwalder, C.; Paulus, W.; Peclau, I.; Eisensehr, I. et al.; Illig, T.; Wichmann, H. E.; Pfister, H.; Golic, J.; Bettecken, T.; Pütz, B.; Holsboer, F.; Meitinger, T.; Müller-Myhsok, B.: Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Movement Disorders 23 (3), pp. 350 - 358 (2008)

Uhr, M.; Tontsch, A.; Namendorf, C.; Ripke, S.; Lucae, S.; Ising, M.; Dose, T.; Ebinger, M.; Rosenhagen, M.; Kohli, M. et al.; Kloiber, S.; Salyakina, D.; Bettecken, T.; Specht, M.; Pütz, B.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.: Polymorphisms in the drug transporter Gene ABCB1 predict antidepressant treatment response in depression. Neuron 57, pp. 203 - 209 (2008)

Heck, A.; Lieb, R.; Ellgas, A.; Pfister, H.; Lucae, S.; Erhardt, A.; Himmerich, H.; Horstmann, S.; Kloiber, S.; Ripke, S. et al.; Mueller-Myhsok, B.; Bettecken, T.; Uhr, M.; Holsboer, F.; Ising, M.: Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. Pharmacopsychiatry 40 (5), p. 209 - 209 (2007)

Kloiber, S.; Ripke, S.; Kohli, M.; Reppermund, S.; Salyakina, D.; Bettecken, T.; Ising, M.; Uhr, M.; Horstmann, S.; Dose, T. et al.; Unschuld, P. G.; Zihl, J.; Müller-Myhsok, B.; Holsboer, F.; Lucae, S.: Polymorphisms in the leptin gene are associated with resistance to antidepressant treatment and lower cognitive performance in depression. Pharmacopsychiatry 40 (5), pp. 210 - 211 (2007)

Kohli, M. A.; Salyakina, D.; Lucae, S.; Ising, M.; Bettecken, T.; Ripke, S.; Uhr, M.; Kloiber, S.; Horstmann, S.; Pütz, B. et al.; Reppermund, S.; Heck, A.; Pfister, H.; Holsboer, F.; Müller-Myhsok, B.: Susceptibility gene hunting for recurrent unipolar depression using 400k genome-wide genotype data. Pharmacopsychiatry 40 (5), p. 212 - 212 (2007)

Lucae, S.; Marcus, I.; Saemann, P.; Bettecken, T.; Uhr, M.; Ripke, S.; Kohli, M.; Kloiber, S.; Bondy, B.; Rupprecht, R. et al.; Domschke, K.; Arolt, V.; Lichtner, P.; Holsboer, F.; Müller-Myhsok, B.: Whole genome analysis reveals new potential drug targets as predictors of antidepressant treatment response. Pharmacopsychiatry 40 (5), p. 213 - 213 (2007)

Rujescu, D.; Giegling, I.; Hartmann, A. M.; Genius, J.; Grunze, H.; Bender, A.; Mulert, C.; Hegerl, U.; Muglia, P.; Birell, C. et al.; Ruppert, A.; Schon, S.; Meitinger, T.; Bettecken, T.; Keck, M.; Ohl, F.; Möller, H. J.: A complementary strategy to approach the genetics of schizophrenia. Schizophrenia Research 81 (Suppl. S), pp. 63 - 64 (2006)

Stöber, G.; Kohlmann, B.; Siekiera, M.; Rubie, C.; Gawlik, M.; Möller-Ehrlich, K.; Meitinger, T.; Bettecken, T.: Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia. BMC Psychiatry 5, doi:10.1186/1471-244X-5-36 (2005)

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

Binder, E. B.; Lichtner, P.; Bettecken, T.; Strom, T.; Uhr, M.; Meitinger, T.; Modell, S.; Holsboer, F.: Mutation analysis of genes regulating the hypothalamo-pituitary adrenal (HPA) axis in patients with depressive syndrome. American Journal of Medical Genetics 114 (7), pp. 752 - 753 (2002)

Binder, E. B.; Lichtner, P.; Uhr, M.; Bettecken, T.; Strom, T. M.; Meitinger, T.; Modell, S.; Holsboer, F.: Mutation analysis of genes regulating the hypothalamo-pituitary adrenal (HPA) axis in patients with depressive syndrome. American Journal of Human Genetics 71 (4 Suppl. Suppl. S), p. 468 - 468 (2002)

Dankowski, T.; Buck, D.; Andlauer, T. F.; Antony, G.; Bayas, A.; Bechmann, L.; Berthele, A.; Bettecken, T.; Chan, A.; Franke, A. et al.; Gold, R.; Graetz, C.; Haas, J.; Hecker, M.; Herms, S.; Hohlfeld, R.; Infante-Duarte, C.; Joeckel, K. -.; Kieseier, B. C.; Knier, B.; Knop, M.; Lichtner, P.; Lieb, W.; Lill, C. M.; Limmroth, V.; Linker, R. A.; Loleit, V.; Meuth, S.; Moebus, S.; Müller-Myhsok, B.; Nischwitz, S.; Noethen, M. M.; Friedemann, P.; Pütz, B.; Ruck, T.; Salmen, A.; Stangel, M.; Stellmann, J. -.; Strauch, K.; Stuerner, K. H.; Tackenberg, B.; Bergh, F. T.; Tumani, H.; Waldenberger, M.; Weber, F.; Wiend, H.; Wildemann, B.; Zettl, U. K.; Ziemann, U.; Zipp, F.; Hemmer, B.; Ziegler, A.: Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis. In HUMAN HEREDITY, 79 (1), pp. 32 - 33. 43rd European Mathematical Genetics Meeting (EMGM), Brest, France, April 16, 2015 - April 17, 2015. Karger, Basel, CH (2015)