Ohli, M. A.; Salyakina, D.; Binder, E. B.; Lucae, S.; Ising, M.; Ripke, S.; Horstmann, S.; Kloiber, S.; Pütz, B.; Fey, K. et al.; Uhr, M.; Müller, M. B.; Holsboer, F.; Müller-Myhsok, B.: SNPs in the NTRK2 gene are associated with age-at-onset of depressive disorder and attempted suicide. Pharmacopsychiatry 40 (5), pp. 211 - 212 (2007)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Kohli, M.; Kloiber, S.; Salyakina, D.; Thoeringer, C. K.; Lieb, R.; Uhr, M. et al.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. Pharmacopsychiatry 40 (5), p. 217 - 217 (2007)

Erhardt, A.; Lucae, S.; Unschuld, P. G.; Ising, M.; Kern, N.; Salyakina, D.; Lieb, R.; Uhr, M.; Binder, E. B.; Keck, M. E. et al.; Müller-Myhsok, B.; Holsboer, F.: Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders. Journal of Affective Disorders 101 (1-3), pp. 159 - 168 (2007)

Winkelmann, J.; Schormair, B.; Lichtner, P.; Ripke, S.; Xiong, L.; Jalilzadeh, S.; Fulda, S.; Pütz, B.; Eckstein, G.; Hauk, S. et al.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Peglau, I.; Eisensehr, I.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, E.; Holsboer, F.; Müller-Myhsok, B.; Meitinger, T.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nature Genetics 39 (8), pp. 1000 - 1006 (2007)

Rosenberger, A.; Sharma, M.; Müller-Myhsok, B.; Gasser, T.; Bickeböller, H.: Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease. BMC Genetics 8, doi: 10.1186/1471-2156-8-44 (2007)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Kloiber, S.; Kohli, M.; Salyakina, D.; Welt, T.; Kern, N.; Lieb, R. et al.; Uhr, M.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 144B (4), pp. 424 - 429 (2007)

Anthoni, H.; Zucchelli, M.; Matsson, H.; Müller-Myhsok, B.; Fransson, I.; Schumacher, J.; Massinen, S.; Onkamo, P.; Warnke, A.; Griesemann, H. et al.; Hoffmann, P.; Nopola-Hemmi, J.; Lyytinen, H.; Schulte-Koerne, G.; Kere, J.; Nothen, M. M.; Peyrard-Janvid, M.: A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics 16 (6), pp. 667 - 677 (2007)

Opherk, C.; Peters, N.; O'Sullivan, M.; Holtmannspötter, M.; Gschwendtner, A.; Müller-Myhsok, B.; Dichgans, M.: Heritability of MRI lesion volume in CADASIL: Evidence for genetic modifiers. Stroke 38 (2), pp. 583 - 584 (2007)

Kemlink, D.; Polo, O.; Montagna, P.; Provini, F.; Stiasny-Kolster, K.; Oertel, W.; de Weerd, A.; Nevsimalova, S.; Sonka, K.; Högl, B. et al.; Frauscher, B.; Poewe, W.; Trenkwalder, C.; Pramstaller, P. P.; Ferini-Strambi, L.; Zucconi, M.; Konofal, E.; Arnulf, I.; Hadjigeorgiou, G. M.; Happe, S.; Klein, C.; Hiller, A.; Lichtner, P.; Meitinger, T.; Müller-Myhsok, B.; Winkelmann, J.: Family-based association study of the loci 2 and 3 in a European restless legs syndrome population. Movement Disorders 22 (2), pp. 207 - 212 (2007)

Thoeringer, C. K.; Binder, E. B.; Salyakina, D.; Erhardt, A.; Ising, M.; Unschuld, P. G.; Kern, N.; Lucae, S.; Brueckl, T. M.; Mueller, M. B. et al.; Fuchs, B.; Puetz, B.; Lieb, R.; Uhr, M.; Holsboer, F.; Mueller-Myhsok, B.; Keck, M.: Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks. Journal of Psychiatric Research 41, doi:10.1016/j.jpsychires.2006.06.001, pp. 579 - 584 (2007)

Opherk, C.; Peters, N.; Holtmannspötter, M.; Gschwendtner, A.; Müller-Myhsok, B.; Dichgans, M.: Heritability of MRI lesion volume in CADASIL - Evidence for genetic modifiers. Stroke 37 (11), pp. 2684 - 2689 (2006)

Bender, A.; Koch, W.; Elstner, M.; Schombacher, Y.; Bender, J.; Moeschl, M.; Gekeler, F.; Müller-Myhsok, B.; Gasser, T.; Tatsch, K. et al.; Klopstock, T.: Creatine supplementation in Parkinson disease: A placebo-controlled randomized pilot trial. Neurology 67 (7), pp. 1262 - 1264 (2006)

Unschuld, P. G.; Erhardt, A.; Ising, M.; Lucae, S.; Kloiber, S.; Kohli, M.; Binder, E. B.; Müller-Myhsok, B.; Keck, M. E.; Holsboer, F.: An association candidate-gene study on genetic variations within HTR2A in patients suffering from panic disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 141B (7), pp. 739 - 740 (2006)

Liebetanz, K. M.; Winkelmann, J.; Trenkwalder, C.; Pütz, B.; Dichgans, M.; Gasser, T.; Müller-Myhsok, B.: RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. Neurology 67 (2), pp. 320 - 321 (2006)

Glas, J.; Torok, H. P.; Tonenchi, L.; Müller-Myhsok, B.; Mussack, T.; Wetzke, M.; Klein, W.; Epplen, J. T.; Griga, T.; Schiemann, U. et al.; Lohse, P.; Seiderer, J.; Schnitzler, F.; Brand, S.; Ochsenkuhn, T.; Folwaczny, M.; Folwaczny, C.: Role of the NFKB1-94ins/delATTG promoter polymorphism in IBD and potential interactions with Polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes. Inflammatory Bowel Diseases 12 (7), pp. 606 - 611 (2006)

Sharma, M.; Müller, J. C.; Zimprich, A.; Lichtner, P.; Hofer, A.; Leitner, P.; Maass, S.; Berg, D.; Dürr, A.; Bonifati, V. et al.; De Michele, G.; Oostra, B.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.: The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. Journal of Medical Genetics 43 (7), pp. 557 - 562 (2006)

Barden, N.; Harvey, M.; Gagne, B.; Shink, E.; Tremblay, M.; Raymond, C.; Labbe, M.; Villeneuve, A.; Rochette, D.; Bordeleau, L. et al.; Stadler, H.; Holsboer, F.; Müller-Myhsok, B.: Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 141B (4), pp. 374 - 382 (2006)

Binder, E. B.; Lucae, S.; Salyakina, D.; Lichtner, P.; Meitinger, T.; Bondy, B.; Wochnik, G.; Rein, T.; Holsboer, F.; Müller-Myhsok, B.: SNPs in FKBP5 determine a novel subtype of depression characterized by rapid response to antidepressant treatment. European Neuropsychopharmacology 16 (Suppl. 1), p. S75 - S75 (2006)

Erhardt, A.; Unschuld, P. G.; Lucae, S.; Ising, M.; Salyakina, D.; Pütz, B.; Müller-Myhsok, B.; Binder, E. B.; Holsboer, F.; Keck, M. E.: Possible genetic implications of the endo-cannabinoid system in anxiety disorders versus depressive disorders. European Neuropsychopharmacology 16 (Suppl. 1), p. S88 - S88 (2006)

Baghai, T. C.; Binder, E. B.; Schule, C.; Salyakina, D.; Eser, D.; Lucae, S.; Zwanzger, P.; Haberger, C.; Zill, P.; Ising, M. et al.; Deiml, T.; Uhr, M.; Illig, T.; Wichmann, H.-E.; Modell, S.; Nothdurfter, C.; Holsboer, F.; Müller-Myhsok, B.; Möller, H.-J.; Rupprecht, R.; Bondy, B.: Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism. Molecular Psychiatry 11, pp. 1003 - 1015 (2006)