Kluge, M.; Schüssler, P.; Bleninger, P.; Kleyer, S.; Uhr, M.; Weikel, J. C.; Yassouridis, A.; Zuber, V.; Steiger, A.: Ghrelin alone or co-administered with GHRH or CRH increases non-REM sleep and decreases REM sleep in young males. Psychoneuroendocrinology 33 (4), pp. 497 - 506 (2008)

Roosterman, D.; Kempkes, C.; Cottrell, G. S.; Padilla, B. E.; Bunnett, N. W.; Turck, C. W.; Steinhoff, M.: Endothelin-converting enzyme-1 degrades internalized somatostatin-14. Endocrinology 149 (5), pp. 2200 - 2207 (2008)

Schmidt, M. V.; Liebl, C.; Sterlemann, V.; Ganea, K.; Hartmann, J.; Harbich, D.; Alam, S.; Müller, M. B.: Neuropeptide Y mediates the initial hypothalamic-pituitary-adrenal response to maternal separation in the neonatal mouse. Journal of Endocrinology 197 (2), pp. 421 - 427 (2008)

Tozzi, F.; Prokopenko, I.; Perry, J. D.; Kennedy, J. L.; McCarthy, A. D.; Holsboer, F.; Berrettini, W.; Middleton, L. T.; Chilcoat, H. D.; Muglia, P.: Family history of depression is associated with younger age of onset in patients with recurrent depression. Psychological Medicine 38 (5), pp. 641 - 649 (2008)

Webb, S. M.; Badia, X.; Barahona, M. J.; Colao, A.; Strasburge, C. J.; Tabarin, A.; van Aken, M. O.; Pivonello, R.; Stalla, G.; Lamberts, S. W. J. et al.; Glusman, J. E.: Evaluation of health-related quality of life in patients with Cushing's syndrome with a new questionnaire. European Journal of Endocrinology 158 (5), pp. 623 - 630 (2008)

Ilg, R.; Wohlschläger, A. M.; Gaser, C.; Liebau, Y.; Dauner, R.; Woller, A.; Zimmer, C.; Zihl, J.; Mühlau, M.: Gray matter increase induced by practice correlates with task-specific activation: A combined functional and morphometric magnetic resonance Imaging study. Journal of Neuroscience 28 (16), pp. 4210 - 4215 (2008)

Freilinger, T.; Bohe, M.; Wegener, B.; Müller-Myhsok, B.; Dichgans, M.; Knoblauch, H.: Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. Cephalalgia 28 (4), pp. 403 - 407 (2008)

Göncz, E.; Strowski, M. Z.; Grötzinger, C.; Nowak, K. W.; Kaczmarek, P.; Sassek, M.; Mergler, S.; El-Zayat, B. F.; Theodoropoulou, M.; Stalla, G. K. et al.; Wiedenmann, B.; Plöckinger, U.: Orexin-A inhibits glucagon secretion and gene expression through a Foxo1-dependent pathway. Endocrinology 149 (4), pp. 1618 - 1626 (2008)

Ising, M.; Adena, S.; Binder, E.; Pfennig, A.; Schalling, M.; Mueller-Myhsok, B.; Modell, S.; Holsboer, F.: Genetic determinants of neurobiological vulnerability markers in depression. European Psychiatry 23 (Suppl. 2), p. S9 - S9 (2008)

Menke, A.; Lucae, S.; Kloiber, S.; Horstmann, S.; Bettecken, T.; Uhr, M.; Ripke, S.; Ising, M.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Polymorphisms in metabotropic glutamate receptor 1 are associated with major depressive disorder. Biological Psychiatry 63 (7 Suppl. S), pp. 83S - 84S (2008)

Owashi, T.; Otsubo, T.; Oshima, A.; Nakagome, K.; Higuchi, T.; Kamijima, K.: Relationships of DEX/CRH and GHRH test results to the outcome of depression - Preliminary results suggest the GHRH test may predict relapse after discharge. Journal of Psychiatric Research 42 (5), pp. 356 - 364 (2008)

Schreier, A.; Wittchen, H. U.; Hoefler, M.; Lieb, R.: Anxiety disorders in mothers and their children: prospective longitudinal community study. British Journal of Psychiatry 192 (4), pp. 308 - 309 (2008)

Seiderer, J.; Dambacher, J.; Leistner, D.; Tillack, C.; Glas, J.; Niess, J. H.; Pfennig, S.; Jürgens, M.; Müller-Myhsok, B.; Göke, B. et al.; Ochsenkühn, T.; Lohse, P.; Reinecker, H. C.; Brand, S.: Genotype-phenotype analysis of the CXCL 16 p.Ala181Val polymorphism in inflammatory bowel disease. Clinical Immunology 127 (1), pp. 49 - 55 (2008)

Seiderer, J.; Elben, I.; Diegelmann, J.; Glas, J.; Stallhofer, J.; Tillack, C.; Pfennig, S.; Jürgens, M.; Schmechel, S.; Konrad, A. et al.; Göke, B.; Ochsenkühn, T.; Müller-Myhsok, B.; Lohse, P.; Brand, S.: Role of the novel th17 cytokine IL-17F in inflammatory bowel disease (IBD): Upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.Hisl6lArg polymorphism in IBD. Inflammatory Bowel Diseases 14 (4), pp. 437 - 445 (2008)

Weber, F.; Fontaine, B.; Cournu-Rebeix, I.; Kroner, A.; Knop, M.; Lutz, S.; Müller-Sarnowski, F.; Uhr, M.; Bettecken, T.; Kohli, M. et al.; Ripke, S.; Ising, M.; Rieckmann, P.; Brassat, D.; Semana, G.; Babron, M. C.; Mrejen, S.; Gout, C.; Lyon-Caen, O.; Yaouanq, J.; Edan, G.; Clanet, M.; Holsboer, F.; Clerget-Darpoux, F.; Müller-Myhsok, B.: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Genes and Immunity 9 (3), pp. 259 - 263 (2008)

Gurel, Z.; Ronni, T.; Ho, S.; Kuchar, J.; Payne, K. J.; Turck, C. W.; Dovat, S.: Recruitment of Ikaros to pericentromeric heterochromatin is regulated by phosphorylation. Journal of Biological Chemistry 283 (13), pp. 8291 - 8300 (2008)

Silva, R.; Mesquita, A. R.; Bessa, J.; Sousa, J. C.; Sotiropoulos, I.; Leao, P.; Almeida, O. F. X.; Sousa, N.: Lithium blocks stress-induced changes in depressive-like behavior and hippocampal cell fate: The role of glycogen-synthase-kinase-3 beta. Neuroscience 152 (3), pp. 656 - 669 (2008)

Benussi, L.; Binetti, G.; Sina, E.; Gigola, L.; Bettecken, T.; Meitinger, T.; Ghidoni, R.: A novel deletion in progranulin gene is associated with FTDP-17 and CBS. Neurobiology of Aging 29 (3), pp. 427 - 435 (2008)

Erhardt, A.; Lucae, S.; Kern, N.; Unschuld, P. G.; Ising, M.; Lieb, R.; Uhr, M.; Hohoff, C.; Deckert, J.; Bandelow, B. et al.; Maier, W.; Binder, E. B.; Müller-Myhsok, B.; Keck, M. E.; Holsboer, F.: Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks. Molecular Psychiatry 13 (3), pp. 242 - 243 (2008)

Glas, J.; Konrad, A.; Schmechel, S.; Dambacher, J.; Seiderer, J.; Schroff, F.; Wetzke, M.; Roeske, D.; Torok, H. P.; Tonenchi, L. et al.; Pfennig, S.; Haller, D.; Griga, T.; Klein, W.; Epplen, J. T.; Folwaczny, C.; Lohse, P.; Göke, B.; Ochsenkühn, T.; Mussack, T.; Folwaczny, M.; Müller-Myhsok, B.; Brand, S.: The ATG16L1 Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population. American Journal of Gastroenterology 103 (3), pp. 682 - 691 (2008)