Publications of Michael Specht

Oexle, K.; Schormair, B.; Ried, J. S.; Czamara, D.; Heim, K.; Frauscher, B.; Hoegl, B.; Trenkwalder, C.; Fiedler, G. M.; Thiery, J. et al.; Lichtner, P.; Prokisch, H.; Specht, M.; Mueller-Myhsok, B.; Doering, A.; Gieger, C.; Peters, A.; Wichmann, H.-E.; Meitinger, T.; Winkelmann, J.: Dilution of candidates: the case of iron-related genes in restless legs syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 21 (4), pp. 410 - 414 (2013)

Erhardt, A.; Czibere, L.; Roeske, D.; Lucae, S.; Unschuld, P. G.; Ripke, S.; Specht, M.; Kohli, M. A.; Kloiber, S.; Ising, M. et al.; Heck, A.; Pfister, H.; Zimmermann, P.; Lieb, R.; Pütz, B.; Uhr, M.; Weber, P.; Deussing, J. M.; Gonik, M.; Bunck, M.; Kessler, M. S.; Frank, E.; Hohoff, C.; Domschke, K.; Krakowitzky, P.; Maier, W.; Bandelow, B.; Jacob, C.; Deckert, J.; Schreiber, S.; Strohmaier, J.; Nöthen, M.; Cichon, S.; Rietschel, M.; Bettecken, T.; Keck, M. E.; Landgraf, R.; Müller-Myhsok, B.; Holsboer, F.; Binder, E. B.: TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry 16 (6), pp. 647 - 663 (2011)

Kohli, M. A.; Lucae, S.; Sämann, P. G.; Schmidt, M. V.; Demirkan, A.; Hek, K.; Roeske, D.; Alexander, M.; Salyakina, D.; Ripke, S. et al.; Hoehn, D.; Specht, M.; Menke, A.; Hennings, J.; Heck, A.; Ising, M.; Schreiber, S.; Czisch, M.; Müller, M. B.; Uhr, M.; Bettecken, T.; Becker, A.; Schramm, J.; Bradley, B.; Ressler, K. J.; Nöthen, M. M.; Cichon, S.; Hofmann, A.; Tiemeier, H.; van Duijn, C. M.; Holsboer, F.; Müller-Myhsok, B.; Binder, E. B.: The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron 70, pp. 252 - 265 (2011)

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)

Unschuld, P. G.; Ising, M.; Specht, M.; Erhardt, A.; Ripke, S.; Heck, A.; Kloiber, S.; Straub, V.; Brueckl, T.; Müller-Myhsok, B. et al.; Holsboer, F.; Binder, E. B.: Polymorphisms in the GAD2 Gene-Region Are Associated With Susceptibility for Unipolar Depression and With a Risk Factor for Anxiety Disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 150B (8), pp. 1100 - 1109 (2009)

Unschuld, P. G.; Ising, M.; Roeske, D.; Erhardt, A.; Specht, M.; Ripke, S.; Uhr, M.; Kloiber, S.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Polymorphisms in the gene encoding the neuropeptide galanin are associated with HPA-axis dysregulation and symptome severity in major-depressive- and anxiety-disorder patients. Pharmacopsychiatry 42 (5), p. 244 - 244 (2009)

Uhr, M.; Tontsch, A.; Namendorf, C.; Ripke, S.; Lucae, S.; Ising, M.; Dose, T.; Ebinger, M.; Rosenhagen, M.; Kohli, M. et al.; Kloiber, S.; Salyakina, D.; Bettecken, T.; Specht, M.; Pütz, B.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.: Polymorphisms in the drug transporter Gene ABCB1 predict antidepressant treatment response in depression. Neuron 57, pp. 203 - 209 (2008)

Köhler, J.; Philippi, S.; Specht, M.; Rüegg, A.: Ontology based text indexing and querying for the semantic web. Knowledge-Based Systems 19 (8), pp. 744 - 754 (2006)