Publications of B. Müller-Myhsok

Salyakina, D.; Binder, E. B.; Ising, M.; Uhr, M.; Lucae, S.; Müller-Myhsok, B.: Within- and Inter-gene interactions in FKBP5 and GR genes and its association with early response. Pharmacopsychiatry 38 (5), p. 274 - 274 (2005)

Seaman, S. R.; Müller-Myhsok, B.: On rapid simulation of P values in association studies - Reply to Lin. American Journal of Human Genetics 77 (3), pp. 514 - 515 (2005)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Welt, T.; Kloiber, S.; Kern, N.; Salyakina, D.; Binder, E. B.; Brückl, T. et al.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the serotonin receptor gene HTR2A modulate disease severity and susceptibility for anxiety disorders but not depression and are associated with specific personality traits. Pharmacopsychiatry 38 (5), p. 282 - 282 (2005)

Müller-Myhsok, B.: The usefulness of single nucleotide polymorphisms (SNPs) for genetic epidemiological investigation of complex psychiatric diseases. Progress in Neuro-Psychopharmacology & Biological Psychiatry 29 (6), pp. 1017 - 1020 (2005)

Klopstock, T.; Elstner, M.; Lücking, C. B.; Müller-Myhsok, B.; Gasser, T.; Botz, E.; Lichtner, P.; Hörtnagel, K.: Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease. Neuroscience Letters 379 (3), pp. 195 - 198 (2005)

Seaman, S. R.; Müller-Myhsok, B.: Rapid simulation of P values for product methods and multiple-testing adjustment in association studies. American Journal of Human Genetics 76 (3), pp. 399 - 408 (2005)

Asmus, F.; Schoenian, S.; Lichtner, P.; Munz, M.; Mayer, P.; Müller-Myhsok, B.; Zimprich, A.; Remschmidt, H.; Hebebrand, J.; Bandmann, O. et al.; Gasser, T.: Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome. Neurogenetics 6 (1), pp. 55 - 56 (2005)

Prestel, J.; Sharma, M.; Leitner, P.; Zimprich, A.; Vaughan, J. R.; Dürr, A.; Bonifati, V.; De Michele, G.; Hanagasi, H. A.; Farrer, M. et al.; Hofer, A.; Asmus, F.; Volpe, G.; Meco, G.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.: PARK11 is not linked with Parkinson's disease in European families. European Journal of Human Genetics 13 (2), pp. 193 - 197 (2005)

Leal, S. M.; Yan, K.; Müller-Myhsok, B.: SimPed: A simulation program to generate haplotype and genotype data for pedigree structures. Human Heredity 60 (2), pp. 119 - 122 (2005)

Salyakina, D.; Seaman, S. R.; Browning, B. L.; Dudbridge, F.; Müller-Myhsok, B.: Evaluation of Nyholt`s Procedure for Multiple Testing Correction. Human Heredity 60, pp. 19 - 25 (2005)

Ziegler, A.; König, I. R.; Deimel, W.; Plume, E.; Nöthen, M. M.; Propping, P.; Kleensang, A.; Müller-Myhsok, B.; Warnke, A.; Remschmidt, H. et al.; Schulte-Körne, G.: Developmental dyslexia - Recurrence risk estimates from a German bi-center study using the single proband sib pair design. Human Heredity 59 (3), pp. 136 - 143 (2005)

Zimprich, A.; Biskup, S.; Leitner, P.; Lichtner, P.; Farrer, M.; Lincoln, S.; Kachergus, J.; Hulihan, M.; Uitti, R. J.; Calne, D. B. et al.; Stoessl, A. J.; Pfeiffer, R. F.; Patenge, N.; Carbajal, I. C.; Vieregge, P.; Asmus, F.; Müller-Myhsok, B.; Dickson, D. W.; Meitinger, T.; Strom, T. M.; Wszolek, Z. K.; Gasser, T.: Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology. Neuron 44 (4), pp. 601 - 607 (2004)

Barden, N.; Harvey, M.; Shink, E.; Tremblay, M.; Gagne, B.; Raymond, C.; Labbe, M.; St Onge, L.; Stadler, H.; Sillaber, I. et al.; Paez-Pereda, M.; Müller-Myhsok, B.; Binder, E.; Holsboer, F.: Identification and characterisation of a gene predisposing to both bipolar and unipolar afective disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), p. 122 - 122 (2004)

Binder, E. B.; Salyakina, D.; Wochnik, G.; Ising, M.; Pütz, B.; Kern, N.; Lucae, S.; Mueller, J. C.; Lohmussaar, E.; Meitinger, T. et al.; Baghai, T.; Bondy, B.; Rupprecht, R.; Uhr, M.; Rein, T.; Holsboer, F.; Müller-Myhsok, B.: Polymorphisms in FKBP5, a co-chaperone of the glucocorticoid receptor are associated with response to antidepressant drugs. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), p. 13 - 13 (2004)

Erhardt, A.; Kern, N.; Knorr, C. C.; Poluda, L.; Thoeringer, C. K.; Unschuld, G.; Salyakina, D.; Pütz, B.; Holsboer, F.; Binder, E. B. et al.; Müller-Myhsok, B.; Keck, M. E.: Possible association of oxytocin and prolactin polymorphisms with panic and anxiety disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), p. 66 - 66 (2004)

Keck, M. E.; Kern, N.; Erhardt, A.; Ising, M.; Unschuld, P. G.; Knorr, C. C.; Poluda, L.; Thoeringer, C. K.; Salyakina, D.; Pütz, B. et al.; Holsboer, F.; Müller-Myhsok, B.; Binder, E.: Interactions of polymorphisms in corticotropin releasing hormone receptor 1 (CRHR1) and vasopressin receptor 1B (V1B) genes predispose for panic disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), pp. 64 - 65 (2004)

Kern, N.; Binder, E. B.; Pfennig, A.; Erhardt, A.; Ising, M.; Lucae, S.; Salyakina, D.; Pütz, B.; Holsboer, F.; Müller-Myhsok, B. et al.; Keck, M. E.: Possible association of angiotensin 1 converting enzyme polymorphisms with syndromal panic attacks. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), pp. 66 - 67 (2004)

Lucae, S.; Binder, E. B.; Pütz, B.; Salyakina, D.; Mueller-Myhsok, B.; Ising, M.; Horstmann, S.; Unschuld, P.; Holsboer, F.: Association of SNP within the serotonin transporter gene with depressive disorder and associated functional parameters. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), pp. 38 - 39 (2004)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Kern, N.; Lucae, S.; Horstmann, S.; Salyakina, D.; Pütz, B.; Binder, E. B.; Müller-Myhsok, B. et al.; Holsboer, F.; Keck, M. E.: Polymorphisms in serotonin receptor genes HTR1B, HTR2A, HTR2C and HTR4 are possibly associated with specific personality traits in patients suffering from anxiety disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 130B (1), pp. 67 - 68 (2004)

Wszolek, Z. K.; Pfeiffer, R. F.; Tsuboi, Y.; Uitti, R. J.; McComb, R. D.; Stoessl, A. J.; Strongosky, A. J.; Zimprich, A.; Müller-Myhsok, B.; Farrer, M. J. et al.; Gasser, T.; Calne, D. B.; Dickson, D. W.: Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 62 (9), pp. 1619 - 1622 (2004)