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
Vilardell, M.; Civit, S.; Herwig, R.: An integrative computational analysis provides evidence for FBN1-associated network de-regulation in trisomy 21. Biology Open 2 (8), pp. 771 - 778 (2013)
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Engert, V.; Efanov, S. I.; Duchesne, A.; Vogel, S.; Corbo, V.; Pruessner, J. C.: Differentiating anticipatory from reactive cortisol responses to psychosocial stress. Psychoneuroendocrinology 38 (8), pp. 1328 - 1337 (2013)
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Jankowski, A.; Szczurek, E.; Jauch, R.; Tiuryn, J.; Prabhakar, S.: Comprehensive prediction in 78 human cell lines reveals rigidity and compactness of transcription factor dimers. Genome Research 23 (8), pp. 1307 - 1318 (2013)
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Puettmann, L.; Stehr, H.; Garshasbi, M.; Hu, H.; Kahrizi, K.; Lipkowitz, B.; Jamali, P.; Tzschach, A.; Najmabadi, H.; Ropers, H. H. et al.; Musante, L.; Kuss, A. W.: A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. American Journal of Medical Genetics Part A 161A (8), pp. 1915 - 1922 (2013)
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Rump, A.; Hildebrand, L.; Tzschach, A.; Ullmann, R.; Schrock, E.; Mitter, D.: A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (8), pp. 887 - 890 (2013)
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Sauer, S.: Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 10 (4), pp. 305 - 307 (2013)
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Weidner, C.; Wowro, S. J.; Freiwald, A.; Kawamoto, K.; Witzke, A.; Kliem, M.; Siems, K.; Müller-Kuhrt, L.; Schroeder, F. C.; Sauer, S.: Amorfrutin B is an efficient natural peroxisome proliferator-activated receptor gamma (PPARgamma) agonist with potent glucose-lowering properties. Diabetologia 56 (8), pp. 1802 - 1812 (2013)
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Mason, M.; Brown, K.; Mar, R. A.; Smallwood, J.: Driver of discontent or escape vehicle: The affective consequences of mindwandering. Frontiers in Psychology 4, 477 (2013)
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Engen, H.; Kanske, P.: How working memory training improves emotion regulation: Neural efficiency, effort and transfer effects. The Journal of Neuroscience 33 (30), pp. 12152 - 12153 (2013)
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Kube, M.; Chernikova, T. N.; Al-Ramahi, Y.; Beloqui, A.; Lopez-Cortez, N.; Guazzaroni, M.-E.; Heipieper, H. J.; Klages, S.; Kotsyurbenko, O. R.; Langer, I. et al.; Nechitaylo, T. Y.; Lünsdorf, H.; Fernández, M.; Juárez, S.; Ciordia, S.; Singer, A.; Kagan, O.; Egorova, O.; Alain Petit, P.; Stogios, P.; Kim, Y.; Tchigvintsev, A.; Flick, R.; Denaro, R.; Genovese, M.; Albar, J. P.; Reva, O. N.; Martínez-Gomariz, M.; Tran, H.; Ferrer, M.; Savchenko, A.; Yakunin, A. F.; Yakimov, M. M.; Golyshina, O. V.; Reinhardt, R.; Golyshin, P. N.: Genome sequence and functional genomic analysis of the oil-degrading bacterium Oleispira antarctica. Nature Communications 4, 4:2156 (2013)
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Hartl, D.; Klatt, S.; Roch, M.; Konthur, Z.; Klose, J.; Willnow, T. E.; Rohe, M.: Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS One 8 (6) (2013)
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Röhr, C.; Kerick, M.; Fischer, A.; Kuehn, A.; Kashofer, K.; Timmermann, B.; Daskalaki, A.; Meinel, T.; Drichel, D.; Börno, S. et al.; Nowka, A.; Krobitsch, S.; McHardy, A. C.; Kratsch, C.; Becker, T.; Wunderlich, A.; Barmeyer, C.; Viertler, C.; Zatloukal, K.; Wierling, C.; Lehrach, H.; Schweiger, M.-R.: High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications. PLoS One 8 (7), p. e67461 - e67461 (2013)
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Baud, A.; Hermsen, R.; Guryev, V.; Stridh, P.; Graham, D.; McBride, M. W.; Foroud, T.; Calderari, S.; Diez, M.; Ockinger, J. et al.; Beyeen, A. D.; Gillett, A.; Abdelmagid, N.; Guerreiro-Cacais, A. O.; Jagodic, M.; Tuncel, J.; Norin, U.; Beattie, E.; Huynh, N.; Miller, W. H.; Koller, D. L.; Alam, I.; Falak, S.; Osborne-Pellegrin, M.; Martinez-Membrives, E.; Canete, T.; Blazquez, G.; Vicens-Costa, E.; Mont-Cardona, C.; Diaz-Moran, S.; Tobena, A.; Hummel, O.; Zelenika, D.; Saar, K.; Patone, G.; Bauerfeind, A.; Bihoreau, M. T.; Heinig, M.; Lee, Y. A.; Rintisch, C.; Schulz, H.; Wheeler, D. A.; Worley, K. C.; Muzny, D. M.; Gibbs, R. A.; Lathrop, M.; Lansu, N.; Toonen, P.; Ruzius, F. P.; de Bruijn, E.; Hauser, H.; Adams, D. J.; Keane, T.; Atanur, S. S.; Aitman, T. J.; Flicek, P.; Malinauskas, T.; Jones, E. Y.; Ekman, D.; Lopez-Aumatell, R.; Dominiczak, A. F.; Johannesson, M.; Holmdahl, R.; Olsson, T.; Gauguier, D.; Hubner, N.; Fernandez-Teruel, A.; Cuppen, E.; Mott, R.; Flint, J.: Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. Nature Genetics 45 (7), pp. 767 - 775 (2013)
Journal Article
Depienne, C.; Bugiani, M.; Dupuits, C.; Galanaud, D.; Touitou, V.; Postma, N.; van Berkel, C.; Polder, E.; Tollard, E.; Darios, F. et al.; Brice, A.; de Die-Smulders, C. E.; Vles, J. S.; Vanderver, A.; Uziel, G.; Yalcinkaya, C.; Frints, S. G.; Kalscheuer, V. M.; Klooster, J.; Kamermans, M.; Abbink, T. E.; Wolf, N. I.; Sedel, F.; van der Knaap, M. S.: Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study. Lancet Neurology 12 (7), pp. 659 - 668 (2013)
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Hendrickx, J. J.; Huyghe, J. R.; Topsakal, V.; Demeester, K.; Wienker, T. F.; Laer, L. V.; Eyken, E. V.; Fransen, E.; Maki-Torkko, E.; Hannula, S. et al.; Parving, A.; Jensen, M.; Tropitzsch, A.; Bonaconsa, A.; Mazzoli, M.; Espeso, A.; Verbruggen, K.; Huyghe, J.; Huygen, P. L.; Kremer, H.; Kunst, S. J.; Diaz-Lacava, A. N.; Steffens, M.; Pyykko, I.; Dhooge, I.; Stephens, D.; Orzan, E.; Pfister, M. H.; Bille, M.; Sorri, M.; Cremers, C. W.; Camp, G. V.; de Heyning, P. V.: Familial aggregation of pure tone hearing thresholds in an aging European population. Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 34 (5), pp. 838 - 844 (2013)
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Isrie, M.; Kalscheuer, V. M.; Holvoet, M.; Fieremans, N.; Van Esch, H.; Devriendt, K.: HUWE1 mutation explains phenotypic severity in a case of familial idiopathic intellectual disability. European Journal of Medical Genetics 56 (7), pp. 379 - 382 (2013)
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Meierhofer, D.; Weidner, C.; Hartmann, L.; Mayr, J. A.; Han, C.-T.; Schroeder, F. C.; Sauer, S.: Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics 12 (7), pp. 1965 - 1979 (2013)
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Mugal, C. F.; Arndt, P. F.; Ellegren, H.: Twisted signatures of GC-biased gene conversion embedded in an evolutionary stable karyotype. Molecular Biology and Evolution 30 (7), pp. 1700 - 1712 (2013)
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Göke, J.; Chan, Y. S.; Yan, J. L.; Vingron, M.; Ng, H. H.: Genome-wide Kinase-Chromatin Interactions Reveal the Regulatory Network of ERK Signaling in Human Embryonic Stem Cells. Molecular Cell 50 (6), pp. 844 - 855 (2013)
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Haddad, D. M.; Vilain, S.; Vos, M.; Esposito, G.; Matta, S.; Kalscheuer, V. M.; Craessaerts, K.; Leyssen, M.; Nascimento, R. M.; Vianna-Morgante, A. M. et al.; De Strooper, B.; Van Esch, H.; Morais, V. A.; Verstreken, P.: Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy. Molecular Cell 50 (6), pp. 831 - 843 (2013)
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