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)

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Engen, H. G.; Singer, T.: Empathy circuits. Current Opinion in Neurobiology 23 (2), pp. 275 - 282 (2013)
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Arelin, M.; Schulze, B.; Muller-Myhsok, B.; Horn, D.; Diers, A.; Uhlenberg, B.; Nurnberg, P.; Nurnberg, G.; Becker, C.; Mundlos, S. et al.; Lindner, T. H.; Sperling, K.; Hoffmann, K.: Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (4), pp. 367 - 372 (2013)
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Feldmann, R.; Fischer, C.; Kodelja, V.; Behrens, S.; Haas, S.; Vingron, M.; Timmermann, B.; Geikowski, A.; Sauer, S.: Genome-wide analysis of LXRalpha activation reveals new transcriptional networks in human atherosclerotic foam cells. Nucleic Acids Research (London) 41 (6), pp. 3518 - 3531 (2013)
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Feldmann, R.; Fischer, C.; Kodelja, V.; Behrens, S.; Haas, S.; Vingron, M.; Timmermann, B.; Geikowski, A.; Sauer, S.: Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells. Nucleic Acids Research (London) 41 (6), pp. 3518 - 3531 (2013)
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Kunde, S.-A.; Rademacher, N.; Tzschach, A.; Wiedersberg, E.; Ullmann, R.; Kalscheuer, V. M.; Shoichet, S. A.: Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients. Human Genetics 132 (4), pp. 461 - 471 (2013)
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Schulz, E. G.; Heard, E.: Role and control of X chromosome dosage in mammalian development. Current Opinion in Genetics & Development 23 (2), pp. 109 - 115 (2013)
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Siragusa, E.; Weese, D.; Reinert, K.: Fast and accurate read mapping with approximate seeds and multiple backtracking. Nucleic Acids Research (London) 41 (7), p. e78 - e78 (2013)
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Smallwood, J.; Tipper, C.; Brown, K.; Baird, B.; Engen, H.; Michaels, J. R.; Grafton, S.; Schooler, J. W.: Escaping the here and now: Evidence for a role of the default mode network in perceptually decoupled thought. NeuroImage 69, pp. 120 - 125 (2013)
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Weimann, M.; Grossmann, A.; Woodsmith, J.; Özkan, Z.; Birth, P.; Meierhofer, D.; Benlasfer, N.; Valovka, T.; Timmermann, B.; Wanker, E. E. et al.; Sauer, S.; Stelzl, U.: A Y2H-seq approach defines the human protein methyltransferase interactome. Nature methods 10 (4), pp. 339 - 342 (2013)
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Kacprzyk, L. A.; Laible, M.; Andrasiuk, T.; Brase, J. C.; Börno, S.; Falth, M.; Kuner, R.; Lehrach, H.; Schweiger, M. R.; Sultmann, H.: ERG Induces Epigenetic Activation of Tudor Domain-Containing Protein 1 (TDRD1) in ERG Rearrangement-Positive Prostate Cancer. PLoS One 8 (3), p. e59976 - e59976 (2013)
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Barrett, H. C.; Broesch, T.; Scott, R. M.; He, Z.; Baillargeon, R.; Wu, D.; Bolz, M.; Henrich, J.; Setoh, P.; Wang, J. et al.; Laurence, S.: Early false-belief understanding in traditional non-Western societies. Proceedings of the Royal Society B: Biological Sciences 280 (1755), 20122654 (2013)
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Bolshoy, A.: Modeling of DNA curvature: comment on "Sequence-dependent collective properties of DNAs and their role in biological systems" by Pasquale De Santis and Anita Scipioni. Physics of Life Reviews 10 (1), pp. 73 - 74 (2013)
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Bu, H.; Schweiger, M. R.; Manke, T.; Wunderlich, A.; Timmermann, B.; Kerick, M.; Pasqualini, L.; Shehu, E.; Fuchsberger, C.; Cato, A. C. et al.; Klocker, H.: Anterior gradient 2 and 3--two prototype androgen-responsive genes transcriptionally upregulated by androgens and by oestrogens in prostate cancer cells. FEBS Journal 280 (5), pp. 1249 - 66 (2013)
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Draaken, M.; Mughal, S. S.; Pennimpede, T.; Wolter, S.; Wittler, L.; Ebert, A.-K.; Rösch, W.; Stein, R.; Bartels, E.; Schmidt, D. et al.; Boemers, T. M.; Schmiedeke, E.; Hoffmann, P.; Moebus, S.; Herrmann, B. G.; Nöthen, M. M.; Reutter, H.; Ludwig, M.: Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Research, Part A: Clinical and Molecular Teratology 97 (3), pp. 133 - 139 (2013)
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Full, G. E.; Walach, H.; Trautwein, M.: Meditation-induced changes in perception: An interview study with expert meditators (Sotapannas) in Burma. Mindfulness 4 (1), pp. 55 - 63 (2013)
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Meyer, T.; Ruppert, V.; Ackermann, S.; Richter, A.; Perrot, A.; Sperling, S.; Posch, M. G.; Maisch, B.; Pankuweit, S.: Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (3), pp. 294 - 300 (2013)
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Smallwood, J.: Penetrating the fog of the decoupled mind: The effects of visual salience in the sustained attention to response task. Canadian Journal of Experimental Psychology 67 (1), pp. 32 - 40 (2013)
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van Engelen, K.; Postma, A. V.; van de Meerakker, J. B. A.; Roos-Hesselink, J. W.; Helderman-van den Enden, A. T. J. M.; Vliegen, H. W.; Rahman, T.; Baars, M. J. H.; Sels, J.-W.; Bauer, U. et al.; Pickardt, T.; Sperling, S.; Moorman, A. F. M.; Keavney, B.; Goodship, J.; Klaassen, S.; Mulder, B. J. M.: Ebstein´s anomaly may be caused by mutations in the sarcomere protein gene MYH7. Netherlands Heart Journal 21 (3), pp. 113 - 117 (2013)
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van Engelen, K.; Postma, A. V.; van de Meerakker, J. B. A.; Roos-Hesselink, J. W.; Helderman-van den Enden, A. T. J. M.; Vliegen, H. W.; Rahman, T.; Baars, M. J. H.; Sels, J. W.; Bauer, U. et al.; Pickardt, T.; Sperling, S.; Moorman, A. F. M.; Keavney, B.; Goodship, J.; Klaassen, S.; Mulder, B. J. M.: Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7. Netherlands Heart Journal 21 (3), pp. 113 - 117 (2013)
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de Groot, J. C.; Weidner, C.; Krausze, J.; Kawamoto, K.; Schroeder, F. C.; Sauer, S.; Büssow, K.: Structural Characterization of Amorfrutins Bound to the Peroxisome Proliferator-Activated Receptor gamma. Journal of Medicinal Chemistry 56 (4), pp. 1535 - 1543 (2013)
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