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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

Jones, D. T.; Hutter, B.; Jager, N.; Korshunov, A.; Kool, M.; Warnatz, H. J.; Zichner, T.; Lambert, S. R.; Ryzhova, M.; Quang, D. A. et al.; Fontebasso, A. M.; Stutz, A. M.; Hutter, S.; Zuckermann, M.; Sturm, D.; Gronych, J.; Lasitschka, B.; Schmidt, S.; Seker-Cin, H.; Witt, H.; Sultan, M.; Ralser, M.; Northcott, P. A.; Hovestadt, V.; Bender, S.; Pfaff, E.; Stark, S.; Faury, D.; Schwartzentruber, J.; Majewski, J.; Weber, U. D.; Zapatka, M.; Raeder, B.; Schlesner, M.; Worth, C. L.; Bartholomae, C. C.; von Kalle, C.; Imbusch, C. D.; Radomski, S.; Lawerenz, C.; van Sluis, P.; Koster, J.; Volckmann, R.; Versteeg, R.; Lehrach, H.; Monoranu, C.; Winkler, B.; Unterberg, A.; Herold-Mende, C.; Milde, T.; Kulozik, A. E.; Ebinger, M.; Schuhmann, M. U.; Cho, Y. J.; Pomeroy, S. L.; von Deimling, A.; Witt, O.; Taylor, M. D.; Wolf, S.; Karajannis, M. A.; Eberhart, C. G.; Scheurlen, W.; Hasselblatt, M.; Ligon, K. L.; Kieran, M. W.; Korbel, J. O.; Yaspo, M. L.; Brors, B.; Felsberg, J.; Reifenberger, G.; Collins, V. P.; Jabado, N.; Eils, R.; Lichter, P.; Pfister, S. M.: Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma. Nature Genetics 45 (8), pp. 927 - 32 (2013)

Kalsoom, U. E.; Klopocki, E.; Wasif, N.; Tariq, M.; Khan, S.; Hecht, J.; Krawitz, P.; Mundlos, S.; Ahmad, W.: Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A. Journal of Medical Genetics 50 (1), pp. 47 - 53 (2013)

Kamburov, A.; Stelzl, U.; Lehrach, H.; Herwig, R.: The ConsensusPathDB interaction database: 2013 update. Nucleic Acids Research (London) 41 (Database issue), pp. D793 - 800 (2013)

Klatt, S.; Hartl, D.; Fauler, B.; Gagoski, D.; Castro-Obregon, S.; Konthur, Z.: Generation and Characterization of a Leishmania tarentolae Strain for Site-Directed in Vivo Biotinylation of Recombinant Proteins. Journal of Proteome Research 12 (12), pp. 5512 - 5519 (2013)