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)

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)

Zimprich, A.; Müller-Myhsok, B.; Farrer, M.; Leitner, P.; Sharma, M.; Hulihan, M.; Lockhart, P.; Strongosky, A.; Kachergus, J.; Calne, D. B. et al.; Stoessl, J.; Uitti, R. J.; Pfeiffer, R. F.; Trenkwalder, C.; Homann, N.; Ott, E.; Wenzel, K.; Asmus, F.; Hardy, J.; Wszolek, Z.; Gasser, T.: The PARK8 locus in autosomal dominant parkinsonism: Confirmation of linkage and further delineation of the disease-containing interval. American Journal of Human Genetics 74 (1), pp. 11 - 19 (2004)

Kern, N.; Binder, E. B.; Künzel, H. E.; Pfennig, A.; Fuchs, B.; Ising, M.; Erhardt, A.; Lucae, S.; Müller-Myhsok, B.; Modell, S. et al.; Keck, M. E.; Holsboer, F.: Is there a genetic continuum between anxiety and depression? Pharmacopsychiatry 36 (5), p. 239 - 239 (2003)

Pfennig, A.; Kuenzel, H. E.; Kern, N.; Fuchs, B.; Brunner, J.; Ising, M.; Modell, S.; Müller-Myhsok, B.; Binder, E. B.; Holsboer, F.: HPA axis dysregulation and suicidal behavior in depression - Differentiation of a genetically distinct subgroup? Pharmacopsychiatry 36 (5), pp. 252 - 253 (2003)

Winkelmann, J.; Lichtner, P.; Strom, T. M.; Trenkwalder, C.; Meitinger, T.; Müller-Myhsok, B.: Evidence for genetic heterogeneity in Restless Legs Syndrome. Pharmacopsychiatry 36 (5), p. 273 - 273 (2003)

Andlauer, T. F. M.; Müller-Myhsok, B.; Ripke, S.: Statistical genetics: genome-wide studies. In: Psychiatric genetics: a primer for clinical and basic scientists, pp. 57 - 69 (Eds. Schulze, T. G.; McMahon, F. J.). Oxford Univ. Press, New York (2018)

Renzi, C.; Provencal, N.; Bassil, K. C.; Evers, K.; Kihlbom, U.; Radford, E. J.; Koupil, I.; Mueller-Myhsok, B.; Hansson, M. G.; Rutten, B. P. F.: From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health. In: NEUROEPIGENETICS AND MENTAL ILLNESS, pp. 299 - 323 (Ed. Rutten, B. P. F.). ELSEVIER ACADEMIC PRESS, Cambridge (2018)

Müller-Myhsok, B.: Genetische Grundlagen der Wirksamkeit von Antidepressiva. Forschungsbericht 2006 - Max-Planck-Institut für Psychiatrie. In: Jahrbuch (Ed. Max-Planck-Gesellschaft). Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V., München (2006)

Gola, D.; Andlauer, T.; Mirza-Schreiber, N.; Zeng, L.; Müller-Myhsok, B.; Koenig, I. R.: How well can we classify coronary artery disease using all genetic data and choosing the best classification algorithm? 27th Annual Meeting of the International Genetic Epidemiology Society (IGES), San Diego, USA, October 14, 2018 - October 16, 2018. GENETIC EPIDEMIOLOGY 42 (7), 41, pp. 701 - 702 (2018)

Anderson-Schmidt, H.; Papiol, S.; Andlauer, T.; Heilbronner, U.; Budde, M.; Kalman, J.; Degenhardt, F.; Noethen, M.; Strohmaier, J.; Frank, J. et al.; Witt, S.; Müller-Myhsok, B.; Falkai, P.; Rietschel, M.; Schulze, T. G.: USING POLYGENIC SCORES BASED ON SCHNEIDERIAN FIRST RANK SYMPTOMS TO CHARACTERIZE DISEASE TRAJECTORIES IN SEVERE MENTAL ILLNESSES. 24th World Congress of Psychiatric Genetics (WCPG 2016), Jerusalem, ISRAEL, October 30, 2016 - November 04, 2016. EUROPEAN NEUROPSYCHOPHARMACOLOGY 27 (S3), pp. S395 - S396 (2017)