Publications Bertram Müller-Myhsok

Journal Article (25)

1.
Journal Article
Glas, J.; Seiderer, J.; Tillack, C.; Pfennig, S.; Beigel, F.; Jürgens, M.; Olszak, T.; Laubender, R. P.; Weidinger, M.; Müller-Myhsok, B. et al.; Göke, B.; Ochsenkühn, T.; Lohse, P.; Diegelmann, J.; Czamara, D.; Brand, S.: The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. PLoS ONE 5 (12), e14466 (2010)
2.
Journal Article
Nischwitz, S.; Cepok, S.; Kroner, A.; Wolf, C.; Knop, M.; Müller-Sarnowski, F.; Pfister, H.; Roeske, D.; Rieckmann, P.; Hemmer, B. et al.; Ising, M.; Uhr, M.; Bettecken, T.; Holsboer, F.; Müller-Myhsok, B.; Weber, F.: Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. Journal of Neuroimmunology 227 (1-2), pp. 162 - 166 (2010)
3.
Journal Article
Anttila, V.; Stefansson, H.; Kallela, M.; Todt, U.; Terwindt, G. M.; Calafato, M. S.; Nyholt, D. R.; Dimas, A. S.; Freilinger, T.; Müller-Myhsok, B. et al.; Artto, V.; Inouye, M.; Alakurtti, K.; Kaunisto, M. A.; Hamalainen, E.; de Vries, B.; Stam, A. H.; Weller, C. M.; Heinze, A.; Heinze-Kuhn, K.; Goebel, I.; Borck, G.; Göbel, H.; Steinberg, S.; Wolf, C.; Bjornsson, A.; Gudmundsson, G.; Kirchmann, M.; Hauge, A.; Werge, T.; Schoenen, J.; Eriksson, J. G.; Hagen, K.; Stovner, L.; Wichmann, E.; Meitinger, T.; Alexander, M.; Moebus, S.; Schreiber, S.; Aulchenko, Y. S.; Breteler, M. M. B.; Uitterlinden, A. G.; Hofman, A.; van Duijn, C. M.; Tikka-Kleemola, P.; Vepsalainen, S.; Lucae, S.; Tozzi, F.; Muglia, P.; Barrett, J.; Kaprio, J.; Farkkila, M.; Peltonen, L.; Stefansson, K.; Zwart, J. A.; Ferrari, M. D.; Olesen, J.; Daly, M.; Wessman, M.; van den Maagdenberg, A. M. J. M.; Dichgans, M.; Kubisch, C.; Dermitzakis, E. T.; Frants, R. R.; Palotie, A.: Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nature Genetics 42 (10), pp. 869 - 873 (2010)
4.
Journal Article
Rietschel, M.; Mattheisen, M.; Frank, J.; Treutlein, J.; Degenhardt, F.; Breuer, R.; Steffens, M.; Mier, D.; Esslinger, C.; Walter, H. et al.; Kirsch, P.; Erk, S.; Schnell, K.; Herms, S.; Wichmann, H. E.; Schreiber, S.; Jockel, K. H.; Strohmaier, J.; Roeske, D.; Haenisch, B.; Gross, M.; Hoefels, S.; Lucae, S.; Binder, E. B.; Wienker, T. F.; Schulze, T. G.; Schmal, C.; Zimmer, A.; Juraeva, D.; Brors, B.; Bettecken, T.; Meyer-Lindenberg, A.; Müller-Myhsok, B.; Maier, W.; Nöthen, M. M.; Cichon, S.: Genome-Wide Association-, Replication-, and Neuroimaging Study Implicates HOMER1 in the Etiology of Major Depression. Biological Psychiatry 68 (6), pp. 578 - 585 (2010)
5.
Journal Article
Schulte-Körne, G.; Bruder, J.; Neuhoff, N.; Roeske, D.; Hoffmann, P.; Ludwig, K.; Nöthen, M. M.; Müller-Myhsok, B.: Brain gene interactions in dyslexia. International Journal of Psychophysiology 77 (3), pp. 229 - 230 (2010)
6.
Journal Article
Hennings, J.; Kohli, M.; Heck, A.; Roeske, D.; Brückl, T.; Klengel, T.; Menke, A.; Müller-Myhsok, B.; Ising, M.; Holsboer, F. et al.; Lucae, S.: Polymorphisms in the BDNF gene are associated with antidepressant treatment response. European Neuropsychopharmacology 20 (Suppl. 3), pp. S427 - S428 (2010)
7.
Journal Article
Ditzen, C.; Varadarajulu, J.; Czibere, L.; Gonik, M.; Targosz, B. S.; Hambsch, B.; Bettecken, T.; Kessler, M. S.; Frank, E.; Bunck, M. et al.; Teplytska, L.; Erhardt, A.; Holsboer, F.; Mueller-Myhsok, B.; Landgraf, R.; Turck, C. W.: Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways. Molecular Psychiatry 15 (7), pp. 702 - 711 (2010)
8.
Journal Article
Kloiber, S.; Kohli, M. A.; Brueckl, T.; Ripke, S.; Ising, M.; Uhr, M.; Menke, A.; Unschuld, P. G.; Horstmann, S.; Salyakina, D. et al.; Müller-Myhsok, B.; Binder, E. B.; Holsboer, F.; Lucae, S.: Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression. Molecular Psychiatry 15 (7), pp. 736 - 747 (2010)
9.
Journal Article
Hemminki, K.; Müller-Myhsok, B.; Lichtner, P.; Engel, C.; Chen, B. W.; Burwinkel, B.; Försti, A.; Sutter, C.; Wappenschmidt, B.; Hellebrand, H. et al.; Illig, T.; Arnold, N.; Niederacher, D.; Dworniczak, B.; Deissler, H.; Kast, K.; Gadzicki, D.; Meitinger, T.; Wichmann, H. E.; Kiechle, M.; Bartram, C. R.; Schmutzler, R. K.; Meindl, A.: Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients. International Journal of Cancer 126 (12), pp. 2858 - 2862 (2010)
10.
Journal Article
Allebrandt, K. V.; Teder-Laving, M.; Akyol, M.; Pichler, I.; Müller-Myhsok, B.; Pramstaller, P.; Merrow, M.; Meitinger, T.; Metspalu, A.; Roenneberg, T.: CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations. Biological Psychiatry 67 (11), pp. 1040 - 1047 (2010)
11.
Journal Article
Muglia, P.; Tozzi, F.; Galwey, N. W.; Francks, C.; Upmanyu, R.; Kong, X. Q.; Antoniades, A.; Domenici, E.; Perry, J.; Rothen, S. et al.; Vandeleur, C. L.; Mooser, V.; Waeber, G.; Vollenweider, P.; Preisig, M.; Lucae, S.; Müller-Myhsok, B.; Holsboer, F.; Middleton, L. T.; Roses, A. D.: Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. Molecular Psychiatry 15 (6), pp. 589 - 601 (2010)
12.
Journal Article
Unschuld, P. G.; Ising, M.; Roeske, D.; Erhardt, A.; Specht, M.; Kloiber, S.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.; Binder, E. B.: Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response. Neuropsychopharmacology 35 (7), pp. 1583 - 1592 (2010)
13.
Journal Article
Hennings, J. M.; Kohli, M. A.; Heck, A.; Roeske, D.; Horstmann, S.; Brückl, T.; Klengel, T.; Menke, A.; Müller-Myhsok, B.; Ising, M. et al.; Holsboer, F.; Lucae, S.: Polymorphisms in the BDNF Gene are Associated with Antidepressant Treatment Response. Biological Psychiatry 67 (9 Suppl.1), pp. 127S - 128S (2010)
14.
Journal Article
Kloiber, S.; Roeske, D.; Müller-Myhsok, B.; Hennings, J.; Holsboer, F.; Lucae, S.: Genome-Wide Association Study of Body Weight in Patients with Major Depression. Biological Psychiatry 67 (9 Suppl.1), p. 128S - 128S (2010)
15.
Journal Article
Meindl, A.; Hellebrand, H.; Wiek, C.; Erven, V.; Wappenschmidt, B.; Niederacher, D.; Freund, M.; Lichtner, P.; Hartmann, L.; Schaal, H. et al.; Ramser, J.; Honisch, E.; Kubisch, C.; Wichmann, H. E.; Kast, K.; Deissler, H.; Engel, C.; Müller-Myhsok, B.; Neveling, K.; Kiechle, M.; Mathew, C. G.; Schindler, D.; Schmutzler, R. K.; Hanenberg, H.: Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nature Genetics 42 (5), pp. 410 - 414 (2010)
16.
Journal Article
Menke, A.; Puetz, B.; Weber, P.; Eichelkraut, A.; Rex-Haffner, M.; Klengel, T.; Gonik, M.; Uhr, M.; Deussing, J.; Holsboer, F. et al.; Müller-Myhsok, B.; Binder, E. B.: Genome-Wide Gene-Expression Profiles Following Glucocorticoid Stimulation Associated with Major Depression. Biological Psychiatry 67 (9 Suppl.1), p. 129S - 129S (2010)
17.
Journal Article
Glas, J.; Seiderer, J.; Nagy, M.; Fries, C.; Beigel, F.; Weidinger, M.; Pfennig, S.; Klein, W.; Epplen, J. T.; Lohse, P. et al.; Folwaczny, M.; Göke, B.; Ochsenkühn, T.; Diegelmann, J.; Müller-Myhsok, B.; Roeske, D.; Brand, S.: Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset. PLoS ONE 5 (4), doi:10.1371/journal.pone.0010373 (2010)
18.
Journal Article
Kohli, M. A.; Salyakina, D.; Pfennig, A.; Lucae, S.; Horstmann, S.; Menke, A.; Kloiber, S.; Hennings, J.; Bradley, B. B.; Ressler, K. J. et al.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.; Binder, E. B.: Association of Genetic Variants in the Neurotrophic Receptor-Encoding Gene NTRK2 and a Lifetime History of Suicide Attempts in Depressed Patients. Archives of General Psychiatry 67 (4), pp. 348 - 359 (2010)
19.
Journal Article
Ludwig, K. U.; Roeske, D.; Herms, S.; Schumacher, J.; Warnke, A.; Plume, E.; Neuhoff, N.; Bruder, J.; Remschmidt, H.; Schulte-Korne, G. et al.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P.: Variation in GRIN2B Contributes to Weak Performance in Verbal Short-Term Memory in Children With Dyslexia. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 153B (2), pp. 503 - 511 (2010)
20.
Journal Article
Horstmann, S.; Lucae, S.; Menke, A.; Hennings, J. M.; Ising, M.; Roeske, D.; Müller-Myhsok, B.; Holsboer, F.; Binder, E. B.: Polymorphisms in GRIK4, HTR2A, and FKBP5 Show Interactive Effects in Predicting Remission to Antidepressant Treatment. Neuropsychopharmacology 35 (3), pp. 727 - 740 (2010)
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