Publications

Journal Article

Lai, F.; Ørom, U. A.; Cesaroni, M.; Beringer, M.; Taatjes, D. J.; Blobel, G. A.; Shiekhattar, R.: Activating RNAs associate with Mediator to enhance chromatin architecture and transcription. Nature 494 (7438), pp. 497 - 501 (2013)

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Feldmann, R.; Geikowski, A.; Weidner, C.; Witzke, A.; Kodelja, V.; Schwarz, T.; Gabriel, M.; Erker, T.; Sauer, S.: Foam cell specific LXRalpha ligand. PLoS One 8 (2), p. e57311 - e57311 (2013)

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Zerck, A.; Nordhoff, E.; Lehrach, H.; Reinert, K.: Optimal precursor ion selection for LC-MALDI MS/MS. BMC Bioinformatics 14, p. 14:56 - 14:56 (2013)

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Grimm, C.; Chavez, L.; Vilardell, M.; Farrall, A.; Tierling, S.; Böhm, J. W.; Grote, P.; Lienhard, M.; Dietrich, J.; Timmermann, B. et al.; Walter, J.; Schweiger, M. R.; Lehrach, H.; Herwig, R.; Herrmann, B. G.; Morkel, M.: DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer. PLoS Genetics 9 (2), p. e1003250 - e1003250 (2013)

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Bainbridge, M. N.; Hu, H.; Muzny, D. M.; Musante, L.; Lupski, J. R.; Graham, B. H.; Chen, W.; Gripp, K. W.; Jenny, K.; Wienker, T. F. et al.; Yang, Y.; Sutton, V. R.; Gibbs, R. A.; Ropers, H. H.: De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine 5 (2), p. 5:11 - 5:11 (2013)

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Demetrius, L.; Legendre, S.: Evolutionary entropy predicts the outcome of selection: Competition for resources that vary in abundance and diversity. Theoretical Population Biology 83, pp. 39 - 54 (2013)

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Suter, B.; Fontaine, J. F.; Yildirimman, R.; Rasko, T.; Schaefer, M. H.; Rasche, A.; Porras, P.; Vazquez-Alvarez, B. M.; Russ, J.; Rau, K. et al.; Foulle, R.; Zenkner, M.; Saar, K.; Herwig, R.; Andrade-Navarro, M. A.; Wanker, E. E.: Development and application of a DNA microarray-based yeast two-hybrid system. Nucleic Acids Research (London) 41 (3), pp. 1496 - 1507 (2013)

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Weirauch, M. T.; Cote, A.; Norel, R.; Annala, M.; Zhao, Y.; Riley, T. R.; Saez-Rodriguez, J.; Cokelaer, T.; Vedenko, A.; Talukder, S. et al.; Consortium, D.; Agius, P.; Arvey, A.; Bucher, P.; Callan, C. G.,. J.; Chang, C. W.; Chen, C. Y.; Chen, Y. S.; Chu, Y. W.; Grau, J.; Grosse, I.; Jagannathan, V.; Keilwagen, J.; Kielbasa, S. M.; Kinney, J. B.; Klein, H.; Kursa, M. B.; Lahdesmaki, H.; Laurila, K.; Lei, C.; Leslie, C.; Linhart, C.; Murugan, A.; Mysickova, A.; Noble, W. S.; Nykter, M.; Orenstein, Y.; Posch, S.; Ruan, J.; Rudnicki, W. R.; Schmid, C. D.; Shamir, R.; Sung, W. K.; Vingron, M.; Zhang, Z.; Bussemaker, H. J.; Morris, Q. D.; Bulyk, M. L.; Stolovitzky, G.; Hughes, T. R.: Evaluation of methods for modeling transcription factor sequence specificity. Nature biotechnology 31 (2), pp. 126 - 34 (2013)

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Grote, P.; Wittler, L.; Hendrix, D.; Währisch, S.; Beisaw, A.; Macura, K.; Bläss, G.; Kellis, M.; Werber, M.; Herrmann, B. G.: The tissue-specific IncRNA Fendrr is an essential regulator of heart and body wall development in the mouse. Developmental Cell 24 (2), pp. 206 - 214 (2013)

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Tosato, V.; Grüning, N.-M.; Breitenbach, M.; Arnak, R.; Ralser, M.; Bruschi, C. V.: Warburg effect and translocation-induced genomic instability: two yeast models for cancer cells. Frontiers in Oncology 2, 212 (2013)

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Lill, C. M.; Schjeide, B.-M.; Graetz, C.; Liu, T.; Damotte, V.; Akkad, D. A.; Blaschke, P.; Gerdes, L. A.; Kroner, A.; Luessi, F. et al.; Cournu-Rebeix, I.; Hoffjan, S.; Winkelmann, A.; Touze, E.; Pico, F.; Corcia, P.; Otaegui, D.; Antiguedad, A.; Alcina, A.; Comabella, M.; Montalban, X.; Olascoaga, J.; Matesanz, F.; Dorner, T.; Li, S. C.; Steinhagen-Thiessen, E.; Lindenberger, U.; Chan, A.; Rieckmann, P.; Hartung, H. P.; Aktas, O.; Lohse, P.; Buttmann, M.; Kumpfel, T.; Kubisch, C.; Zettl, U. K.; Epplen, J. T.; Fontaine, B.; Zipp, F.; Vandenbroeck, K.; Bertram, L.: Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Journal of Medical Genetics (London) 50 (3), pp. 140 - 143 (2013)

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Al-Nbaheen, M.; Vishnubalaji, R.; Ali, D.; Bouslimi, A.; Al-Jassir, F.; Megges, M.; Prigione, A.; Adjaye, J.; Kassem, M.; Aldahmash, A.: Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential. Stem Cell Reviews 9 (1), pp. 32 - 43 (2013)

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Barann, M.; Esser, D.; Klostermeier, U. C.; Lappalainen, T.; Luzius, A.; Kuiper, J. W. P.; Ammerpohl, O.; Vater, I.; Siebert, R.; Amstislavskiy, V. et al.; Sudbrak, R.; Lehrach, H.; Schreiber, S.; Rosenstiel, P.: Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 29 (13), pp. 1600 - 1606 (2013)

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Bertram, L.; Parrado, A. R.; Tanzi, R. E.: TREM2 and Neurodegenerative Disease. The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 369 (16), p. 1565 - 1565 (2013)

MPG.PuRe

correspondence

Journal Article

Broer, L.; Lill, C.; Schuur, M.; Amin, N.; Roehr, C.; Bertram, L.; Ioannidis, J. P. A.; van Duijn, C. M.: Distinguishing true from false positives in genomic studies: p values. European Journal of Epidemiology 28 (2), pp. 131 - 138 (2013)

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Doktorova, T. Y.; Yildirimman, R.; Vinken, M.; Vilardell, M.; Vanhaecke, T.; Gmuender, H.; Bort, R.; Brolen, G.; Holmgren, G.; Li, R. et al.; Chesne, C.; van Delft, J.; Kleinjans, J.; Castell, J.; Bjorquist, P.; Herwig, R.; Rogiers, V.: Transcriptomic responses generated by hepatocarcinogens in a battery of liver-based in vitro models. Carcinogenesis 34 (6), pp. 1393 - 402 (2013)

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Fogeron, M.-L.; Müller, H.; Schade, S.; Dreher, F.; Lehmann, V.; Kühnel, A.; Scholz, A. K.; Kashofer, K.; Zerck, A.; Fauler, B. et al.; Lurz, R.; Herwig, R.; Zatloukal, K.; Lehrach, H.; Gobom, J.; Nordhoff, E.; Lange, B.: LGALS3BP regulates centriole biogenesis and centrosome hypertrophy in cancer cells. Nature Communications 4, p. 4:1531 - 4:1531 (2013)

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Hoffer, J. L.; Fryssira, H.; Konstantinidou, A.; Ropers, H.-H.; Tzschach, A.: Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical Genetics: an international journal of genetics in medicine 83 (1), pp. 92 - 95 (2013)

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Jager, N.; Schlesner, M.; Jones, D. T.; Raffel, S.; Mallm, J. P.; Junge, K. M.; Weichenhan, D.; Bauer, T.; Ishaque, N.; Kool, M. et al.; Northcott, P. A.; Korshunov, A.; Drews, R. M.; Koster, J.; Versteeg, R.; Richter, J.; Hummel, M.; Mack, S. C.; Taylor, M. D.; Witt, H.; Swartman, B.; Schulte-Bockholt, D.; Sultan, M.; Yaspo, M. L.; Lehrach, H.; Hutter, B.; Brors, B.; Wolf, S.; Plass, C.; Siebert, R.; Trumpp, A.; Rippe, K.; Lehmann, I.; Lichter, P.; Pfister, S. M.; Eils, R.: Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 155 (3), pp. 567 - 81 (2013)

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Jankowski, V.; Schulz, A.; Kretschmer, A.; Mischak, H.; Boehringer, F.; van der Giet, M.; Janke, D.; Schuchardt, M.; Herwig, R.; Zidek, W. et al.; Jankowski, J.: The enzymatic activity of the VEGFR2 receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine-JMM 91 (9), pp. 1095 - 107 (2013)

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Journal Article (148)