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), S. 771 - 778 (2013)

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), S. 1328 - 1337 (2013)

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), S. 1307 - 1318 (2013)

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), S. 1915 - 1922 (2013)

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), S. 887 - 890 (2013)

Sauer, S.: Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 10 (4), S. 305 - 307 (2013)

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), S. 1802 - 1812 (2013)

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)

Engen, H.; Kanske, P.: How working memory training improves emotion regulation: Neural efficiency, effort and transfer effects. The Journal of Neuroscience 33 (30), S. 12152 - 12153 (2013)

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)

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)

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), S. e67461 - e67461 (2013)

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), S. 767 - 775 (2013)

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), S. 659 - 668 (2013)

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), S. 838 - 844 (2013)

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), S. 379 - 382 (2013)

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), S. 1965 - 1979 (2013)

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), S. 1700 - 1712 (2013)

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), S. 844 - 855 (2013)

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), S. 831 - 843 (2013)