Bertram Müller-Myhsok

	Bertram Müller-Myhsok, Prof. Dr. med. Research group leader RG Müller-Myhsok: Statistical Genetics
	Phone:	089/30622-246
	Fax:	089/30622-610
	Email:	bmm[a]mpipsykl.mpg.de
	Interests:	Statistical genetics, multivariate analysis, genome-wide analysis, pharmacogenetics
CV: Born 1962 in Ebern/Germany. Studie of medicine at the University of Würzburg. 1989-1990 Research fellow (Poste vert) INSERM, Paris. 1996 Habilitation Human Genetics (LMU Munich). Since 2002 Head of the research group "Statistical Genetics" at the MPI of Psychiatry. Since 2007 Adjunct Professor of Human Gentics at the Technical University of Munich. CV (pdf)
Selected publications: Kohli MA, Lucae S, Saemann PG, Schmidt MV, Demirkan A, Hek K, Czamara D, Alexander M, Salyakina D, Ripke S, Hoehn D, Specht M, Menke A, Hennings J, Heck A, Wolf C, Ising M, Schreiber S, Czisch M, Müller MB, Uhr M, Bettecken T, Becker A, Schramm J, Rietschel M, Maier W, Bradley B, Ressler KJ, Nöthen MM, Cichon S, Craig IW, Breen G, Lewis CM, Hofman A, Tiemeier H, van Duijn CM, Holsboer F, Müller-Myhsok B*, Binder EB* (2011) The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression. Neuron 70:252-65 (*joint senior authors) Kam-Thong T, Czamara D, Tsuda K, Borgwardt K, Lewis CM, Erhardt-Lehmann A, Hemmer B, Rieckmann P, Daake M, Weber F, Wolf C, Ziegler A, Pütz B, Holsboer F, Schölkopf B, Müller-Myhsok B (2011) EPIBLASTER - fast exhaustive two-locus epistasis detection strategy using graphical processing units. Eur J Hum Genet. 19:465-71 Uhr, M., Tontsch, A., Namendorf, C., Ripke, S., Lucae, S., Ising, M., Dose, T., Ebinger, M., Rosenhagen, M., Kohli, M., Kloiber, S., Salyakina, D., Bettecken, T., Specht, M., Putz, B., Binder, E. B., Müller-Myhsok, B., and Holsboer, F. (2008) Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression. Neuron 57: 203-209 Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T (2007) Genome-wide association study in restless legs syndrome identifies common variants in three genomic regions. Nat Genet 39:1000-1006 Seaman SR, Müller-Myhsok B (2005) Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies. Am J Hum Genet 76:399-408 Binder EB, Salyakina D, Lichtner P, Wochnik GM, Ising M, Pütz B, Papiol S, Seaman S, Lucae S, Kohli MA, Nickel T, Künzel HE, 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 JC, Lõhmussaar E, Strom TM, Bettecken T, Meitinger T, Uhr M, Rein T, Holsboer F, Müller-Myhsok B (2004) Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nat Genet 36:1319-1325

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