The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (148)

Journal Article
Schick, A.; Wessa, M.; Vollmayr, B.; Kuehner, C.; Kanske, P.: Indirect assessment of an interpretation bias in humans: Neurophysiological and behavioral correlates. Frontiers in Human Neuroscience 7, 272 (2013)
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Götschel, F.; Berg, D.; Gruber, W.; Bender, C.; Eberl, M.; Friedel, M.; Sonntag, J.; Rungeler, E.; Hache, H.; Wierling, C. K. et al.; Nietfeld, W.; Lehrach, H.; Frischauf, A.; Schwartz-Albiez, R.; Aberger, F.; Korf, U.: Synergism between Hedgehog-GLI and EGFR Signaling in Hedgehog-Responsive Human Medulloblastoma Cells Induces Downregulation of Canonical Hedgehog-Target Genes and Stabilized Expression of GLI1. PLoS One 8 (6), p. e65403 - e65403 (2013)
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Kessler, T.; Hache, H.; Wierling, C.: Integrative analysis of cancer-related signaling pathways. Frontiers in Physiology 4, p. 4:124 - 4:124 (2013)
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Pichler, I.; Del Greco, F.; Gögele, M.; Lill, C. M.; Bertram, L.; Do, C. B.; Eriksson, N.; Foroud, T.; Myers, R. H.; Nalls, M. et al.; Keller, M. F.; Benyamin, B.; Whitfield, J. B.; Pramstaller, P. P.; Hicks, A. A.; Thompson, J. R.; Minelli, C.; Consortium, P. G.; Consor, I. P. D. G.; Consor, W. T. C. C.; Consortium, G. I. S.: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study. PLoS Medicine 10 (6), p. e1001462 - e1001462 (2013)
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Viswanathan, J.; Haapasalo, A.; Kurkinen, K. M. A.; Natunen, T.; Makinen, P.; Bertram, L.; Soininen, H.; Tanzi, R. E.; Hiltunen, M.: Ubiquilin-1 Modulates gamma-Secretase-Mediated epsilon-Site Cleavage in Neuronal Cells. Biochemistry 52 (22), pp. 3899 - 3912 (2013)
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Salih, M. A.; Tzschach, A.; Oystreck, D. T.; Hassan, H. H.; AlDrees, A.; Elmalik, S. A.; El Khashab, H. Y.; Wienker, T. F.; Abu-Amero, K. K.; Bosley, T. M.: A newly recognized autosomal recessive syndrome affecting neurologic function and vision. American Journal of Medical Genetics Part A 161A (6), pp. 1207 - 1213 (2013)
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Tavernier, G.; Mlody, B.; Demeester, J.; Adjaye, J.; De Smedt, S. C.: Current methods for inducing pluripotency in somatic cells. Advanced Materials 25 (20), pp. 2765 - 71 (2013)
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Zazzu, V.; Regierer, B.; Kühn, A.; Sudbrak, R.; Lehrach, H.: IT Future of Medicine: from molecular analysis to clinical diagnosis and improved treatment. New Biotechnology 30 (4), pp. 362 - 365 (2013)
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Holzhauser, S.; Freiwald, A.; Weise, C.; Multhaup, G.; Han, C.-T.; Sauer, S.: Discovery and Characterization of Protein-Modifying Natural Products by MALDI Mass Spectrometry Reveal Potent SIRT1 and p300 Inhibitors. Angewandte Chemie International Edition 52 (19), pp. 5171 - 5174 (2013)
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Hirata, H.; Nanda, I.; van Riesen, A.; McMichael, G.; Hu, H.; Hambrock, M.; Papon, M. A.; Fischer, U.; Marouillat, S.; Ding, C. et al.; Alirol, S.; Bienek, M.; Preisler-Adams, S.; Grimme, A.; Seelow, D.; Webster, R.; Haan, E.; MacLennan, A.; Stenzel, W.; Yap, T. Y.; Gardner, A.; Nguyen, L. S.; Shaw, M.; Lebrun, N.; Haas, S. A.; Kress, W.; Haaf, T.; Schellenberger, E.; Chelly, J.; Viot, G.; Shaffer, L. G.; Rosenfeld, J. A.; Kramer, N.; Falk, R.; El-Khechen, D.; Escobar, L. F.; Hennekam, R.; Wieacker, P.; Hubner, C.; Ropers, H. H.; Gecz, J.; Schuelke, M.; Laumonnier, F.; Kalscheuer, V. M.: ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity. The American Journal of Human Genetics 92 (5), pp. 681 - 695 (2013)
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Montgomery, S. B.; Goode, D. L.; Kvikstad, E.; Albers, C. H.; Zhang, Z. D.; Mu, X. J.; Ananda, G.; Howie, B.; Karczewski, K. J.; Smith, K. S. et al.; Anaya, V.; Richardson, R.; Davis, J.; 1000 Genome Project, C.; Timmermann, B.; MacArthur, D. G.; Sidow, A.; Duret, L.; Gerstein, M.; Makova, K. D.; Marchini, J.; McVean, G.; Lunter, G.: The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome Research 23 (5), pp. 749 - 761 (2013)
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Onkes, W.; Fredrik, R.; Micci, F.; Schonbeck, B. J.; Martin-Subero, J. I.; Ullmann, R.; Hilpert, F.; Brautigam, K.; Janssen, O.; Maass, N. et al.; Siebert, R.; Heim, S.; Arnold, N.; Weimer, J.: Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV-3. Genes, Chromosomes and Cancer 52 (5), pp. 512 - 522 (2013)
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Papari, E.; Bastami, M.; Farhadi, A.; Abedini, S.; Hosseini, M.; Bahman, I.; Mohseni, M.; Garshasbi, M.; Moheb, L. A.; Behjati, F. et al.; Kahrizi, K.; Ropers, H.-H.; Najmabadi, H.: Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations. Clinical Genetics: an international journal of genetics in medicine 83 (5), pp. 488 - 490 (2013)
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Smallwood, J.: Distinguishing how from why the mind wanders: A process-occurrence framework for self-generated mental activity. Psychological Bulletin 139 (3), pp. 519 - 535 (2013)
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Smallwood, J.: Searching for the elements of thought: Reply to Franklin, Mrazek, Broadway, and Schooler. Psychological Bulletin 139 (3), pp. 542 - 547 (2013)
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Starokadomskyy, P.; Gluck, N.; Li, H.; Chen, B.; Wallis, M.; Maine, G. N.; Mao, X.; Zaidi, I. W.; Hein, M. Y.; McDonald, F. J. et al.; Lenzner, S.; Zecha, A.; Ropers, H. H.; Kuss, A. W.; McGaughran, J.; Gecz, J.; Burstein, E.: CCDC22 deficiency in humans blunts activation of proinflammatory NF-kappaB signaling. The Journal of Clinical Investigation 123 (5), pp. 2244 - 2256 (2013)
Journal Article
Steinbeis, N.; Singer, T.: The effects of social comparison on social emotions and behavior during childhood: The ontogeny of envy and Schadenfreude predicts developmental changes in equity-related decisions. Journal of Experimental Child Psychology 115 (1), pp. 198 - 209 (2013)
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Gilling, M.; Rasmussen, H. B.; Calloe, K.; Sequeira, A. F.; Baretto, M.; Oliveira, G.; Almeida, J.; Lauritsen, M. B.; Ullmann, R.; Boonen, S. E. et al.; Brondum-Nielsen, K.; Kalscheuer, V. M.; Tumer, Z.; Vicente, A. M.; Schmitt, N.; Tommerup, N.: Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders. Frontiers in Genetics 4, p. 4:54 - 4:54 (2013)
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Aydin, A.; Desai, N.; Bernhardt, A. M.; Treede, H.; Detter, C.; Sheikhzadeh, S.; Rybczynski, M.; Hillebrand, M.; Lorenzen, V.; Mortensen, K. et al.; Robinson, P. N.; Berger, J.; Reichenspurner, H.; Meinertz, T.; Willems, S.; von Kodolitsch, Y.: Ascending aortic aneurysm and aortic valve dysfunction in bicuspid aortic valve disease. International Journal of Cardiology (164(3)), pp. 301 - 305 (2013)
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Vogl, M. R.; Reiprich, S.; Küspert, M.; Kosian, T.; Schrewe, H.; Nave, K.-A.; Wegner, M.: Sox10 cooperates with the mediator subunit 12 during terminal differentiation of myelinating glia. The Journal of Neuroscience: the Official Journal of the Society for Neuroscience 33 (15), pp. 6679 - 6690 (2013)
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