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 (160)

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Callard, F.; Smallwood, J.; Margulies, D. S.: Default positions: How neuroscience's historical legacy has hampered investigation of the resting mind. Frontiers in Psychology 3, 321 (2012)
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Zanni, G.; Cali, T.; Kalscheuer, V. M.; Ottolini, D.; Barresi, S.; Lebrun, N.; Montecchi-Palazzi, L.; Hu, H.; Chelly, J.; Bertini, E. et al.; Brini, M.; Carafoli, E.: Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Proceedings of the National Academy of Sciences of the United States of America 109 (36), pp. 14514 - 14519 (2012)
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Bucsenez, M.; Rüping, B.; Behrens, S.; Twyman, R. M.; Noll, G. A.; Prüfer, D.: Multiple cis-regulatory elements are involved in the complex regulation of the sieve element-specific MtSEO-F1 promoter from Medicago truncatula. Plant Biology 14 (5), pp. 714 - 724 (2012)
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Kanske, P.; Kotz, S. A.: Effortful control, depression, and anxiety correlate with the influence of emotion on executive attentional control. Biological Psychology 91 (1), pp. 88 - 95 (2012)
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Lill, C. M.; Bertram, L.: Developing the "next generation" of genetic association databases for complex diseases. Human Mutation 33 (9), pp. 1366 - 1372 (2012)
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Lill, C. M.; Liu, T.; Schjeide, B. M.; Roehr, J. T.; Akkad, D. A.; Damotte, V.; Alcina, A.; Ortiz, M. A.; Arroyo, R.; de Lapuente, A. L. et al.; Blaschke, P.; Winkelmann, A.; Gerdes, L. A.; Luessi, F.; Fernadez, O.; Izquierdo, G.; Antiguedad, A.; Hoffjan, S.; Cournu-Rebeix, I.; Gromöller, S.; Faber, H.; Liebsch, M.; Meissner, E.; Chanvillard, C.; Touze, E.; Pico, F.; Corcia, P.; Dörner, T.; Steinhagen-Thiessen, E.; Baeckman, L.; Heekeren, H. R.; Li, S. C.; Lindenberger, U.; Chan, A.; Hartung, H. P.; Aktas, O.; Lohse, P.; Kumpfel, T.; Kubisch, C.; Epplen, J. T.; Zettl, U. K.; Fontaine, B.; Vandenbroeck, K.; Matesanz, F.; Urcelay, E.; Bertram, L.; Zipp, F.: Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Journal of Medical Genetics (London) 49 (9), pp. 558 - 562 (2012)
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Ricciardi, S.; Ungaro, F.; Hambrock, M.; Rademacher, N.; Stefanelli, G.; Brambilla, D.; Sessa, A.; Magagnotti, C.; Bachi, A.; Giarda, E. et al.; Verpelli, C.; Kilstrup-Nielsen, C.; Sala, C.; Kalscheuer, V. M.; Broccoli, V.: CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons. Nature Cell Biology 14 (9), pp. 911 - 923 (2012)
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Sobrido, M. J.; Cacheiro, P.; Carracedo, A.; Bertram, L.: Databases for neurogenetics: Introduction, overview, and challenges. Human Mutation 33 (9), pp. 1311 - 1314 (2012)
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Odoardi, F.; Sie, C.; Streyl, K.; Ulaganathan, V. K.; Schlaeger, C.; Lodygin, D.; Heckelsmiller, K.; Nietfeld, W.; Ellwart, J.; Klinkert, W. E. F. et al.; Lottaz, C.; Nosov, M.; Brinkmann, V.; Spang, R.; Lehrach, H.; Vingron, M.; Wekerle, H.; Fluegel-Koch, C.; Fluegel, A.: T cells become licensed in the lung to enter the central nervous system. Nature 488 (7413), pp. 675 - 679 (2012)
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Ralser, M.; Timmermann, B.: Genomanalyse von Modellorganismen: Saccharomyces cerevisiae. Biospektrum 18 (5), pp. 504 - 507 (2012)
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Cohrs, S.; Rodenbeck, A.; Riemann, D.; Szagun, B.; Jaehne, A.; Brinkmeyer, J.; Grunder, G.; Wienker, T.; Diaz-Lacava, A.; Mobascher, A. et al.; Dahmen, N.; Thuerauf, N.; Kornhuber, J.; Kiefer, F.; Gallinat, J.; Wagner, M.; Kunz, D.; Grittner, U.; Winterer, G.: Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine Dependence. Addiction Biology 2012, p. e - e (2012)
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Wierling, C.; Kühn, A.; Hache, H.; Daskalaki, A.; Maschke-Dutz, E.; Peycheva, S.; Li, J.; Herwig, R.; Lehrach, H.: Prediction in the face of uncertainty: a Monte Carlo-based approach for systems biology of cancer treatment. Mutation Research-Genetic Toxixology and Environmental Mutagenesis 746 (2), pp. 163 - 170 (2012)
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Sharma, M.; Ioannidis, J. P.; Aasly, J. O.; Annesi, G.; Brice, A.; Van Broeckhoven, C.; Bertram, L.; Bozi, M.; Crosiers, D.; Clarke, C. et al.; Facheris, M.; Farrer, M.; Garraux, G.; Gispert, S.; Auburger, G.; Vilarino-Guell, C.; Hadjigeorgiou, G. M.; Hicks, A. A.; Hattori, N.; Jeon, B.; Lesage, S.; Lill, C. M.; Lin, J. J.; Lynch, T.; Lichtner, P.; Lang, A. E.; Mok, V.; Jasinska-Myga, B.; Mellick, G. D.; Morrison, K. E.; Opala, G.; Pramstaller, P. P.; Pichler, I.; Park, S. S.; Quattrone, A.; Rogaeva, E.; Ross, O. A.; Stefanis, L.; Stockton, J. D.; Satake, W.; Silburn, P. A.; Theuns, J.; Tan, E. K.; Toda, T.; Tomiyama, H.; Uitti, R. J.; Wirdefeldt, K.; Wszolek, Z.; Xiromerisiou, G.; Yueh, K. C.; Zhao, Y.; Gasser, T.; Maraganore, D.; Krüger, R.: Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 79 (7), pp. 659 - 667 (2012)
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Ralser, M.; Kuhl, H.; Ralser, M.; Werber, M.; Lehrach, H.; Breitenbach, M.; Timmermann, B.: The Saccharomyces cerevisiae W303-K6001 cross-platform genome sequence: insights into ancestry and physiology of a laboratory mutt. Open Biology 2 (8), 120093 (2012)
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Thomas-Chollier, M.; Darbo, E.; Herrmann, C.; Defrance, M.; Thieffry, D.; van Helden, J.: A complete workflow for the analysis of full-size ChIP-seq (and similar) data sets using peak-motifs. Nature Protocols 7 (8), pp. 1551 - 1568 (2012)
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Klatt, S.; Konthur, Z.: Secretory signal peptide modification for optimized antibody-fragment expression-secretion in Leishmania tarentolae. Microbial Cell Factories 11, 11:97 (2012)
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Habermann, K.; Lange, B. M. H.: New insights into subcomplex assembly and modifications of centrosomal proteins. Cell Division 7 (1), 7:17 (2012)
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Kim, H.-G.; Kim, H. T.; Leach, N. T.; Lan, F.; Ullmann, R.; Silahtaroglu, A.; Kurth, I.; Nowka, A.; Seong, I. S.; Shen, Y. et al.; Talkowski, M. E.; Ruderfer, D.; Lee, J. H.; Glotzbach, C.; Ha, K.; Kjaergaard, S.; Levin, A. V.; Romeike, B. F.; Kleefstra, T.; Bartsch, O.; Elsea, S. H.; Jabs, E. W.; Macdonald, M. E.; Harris, D. J.; Quade, B. J.; Ropers, H.-H.; Shaffer, L. G.; Kutsche, K.; Layman, L. C.; Tommerup, N.; Kalscheuer, V. M.; Shi, Y.; Morton, C. C.; Kim, C. H.; Gusella, J. F.: Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies. The American Journal of Human Genetics 91 (1), pp. 56 - 72 (2012)
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Krawitz, P. M.; Murakami, Y.; Hecht, J.; Kruger, U.; Holder, S. E.; Mortier, G. R.; Delle Chiaie, B.; De Baere, E.; Thompson, M. D.; Roscioli, T. et al.; Kielbasa, S. M.; Kinoshita, T.; Mundlos, S.; Robinson, P. N.; Horn, D.: Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation. American Journal of Human Genetics 91 (1), pp. 146 - 151 (2012)
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Zi, Z.; Chapnick, D. A.; Liu, X.: Dynamics of TGF-β/Smad signaling. FEBS Letters 586 (14), pp. 1921 - 1928 (2012)
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