Publications

Journal Article

Bernal Ulloa, S. M.; Heinzmann, J.; Herrmann, D.; Timmermann, B.; Baulain, U.; Großfeld, R.; Diederich, M.; Lucas-Hahn, A.; Niemann, H.: Effects of different oocyte retrieval and in vitro maturation systems on bovine embryo development and quality. Zygote 23 (3), pp. 367 - 377 (2015)

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Journal Article

Emmerich, D.; Zemojtel, T.; Hecht, J.; Krawitz, P.; Spielmann, M.; Kühnisch, J.; Kobus, K.; Oßwald, M.; Heinrich, V.; Berlien, P. et al.; Müller, U.; Mautner, V.-F.; Wimmer, K.; Robinson, P. N.; Vingron, M.; Tinschert, S.; Mundlos, S.; Kolanczyk, M.: Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient. European journal of human genetics 23 (6), pp. 1870 - 1873 (2015)

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Journal Article

Grote, P.; Herrmann, B. G.: Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics 31 (6), pp. 329 - 335 (2015)

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Journal Article

Hossini, A. M.; Megges, M.; Prigione, A.; Lichtner, B.; Toliat, M. R.; Wruck, W.; Schröter, F.; Nuernberg, P.; Kroll, H.; Makrantonak, E. et al.; Zoubouli, C. C.; Adjaye, J.: Erratum: Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer's disease donor as a model for investigating AD-associated gene regulatory networks. BMC Genomics 16, p. 84 (2015)

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Journal Article

Maass, P. G.; Aydin, A.; Luft, F. C.; Schachterle, C.; Weise, A.; Stricker, S.; Lindschau, C.; Vaegler, M.; Qadri, F.; Toka, H. R. et al.; Schulz, H.; Krawitz, P. M.; Parkhomchuk, D.; Hecht, J.; Hollfinger, I.; Wefeld-Neuenfeld, Y.; Bartels-Klein, E.; Muhl, A.; Kann, M.; Schuster, H.; Chitayat, D.; Bialer, M. G.; Wienker, T. F.; Ott, J.; Rittscher, K.; Liehr, T.; Jordan, J.; Plessis, G.; Tank, J.; Mai, K.; Naraghi, R.; Hodge, R.; Hopp, M.; Hattenbach, L. O.; Busjahn, A.; Rauch, A.; Vandeput, F.; Gong, M.; Ruschendorf, F.; Hübner, N.; Haller, H.; Mundlos, S.; Bilginturan, N.; Movsesian, M. A.; Klussmann, E.; Toka, O.; Bahring, S.: PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics 47 (6), pp. 647 - 653 (2015)

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Journal Article

Shaw, M.; Yap, T. Y.; Henden, L.; Bahlo, M.; Gardner, A.; Kalscheuer, V. M.; Haan, E.; Christie, L.; Hackett, A.; Gecz, J.: Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics 58 (6-7), pp. 364 - 368 (2015)

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Journal Article

Starick, S. R.; Ibn-Salem, J.; Jurk, M.; Hernandez, C.; Love, M. I.; Chung, H.-R.; Vingron, M.; Thomas-Chollier, M.; Meijsing, S. H.: ChIP-exo signal associated with DNA-binding motifs provides insight into the genomic binding of the glucocorticoid receptor and cooperating transcription factors. Genome Res 25 (6), pp. 825 - 835 (2015)

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Journal Article

Sukalo, M.; Tilsen, F.; Kayserili, H.; Muller, D.; Tuysuz, B.; Ruddy, D. M.; Wakeling, E.; Orstavik, K. H.; Snape, K. M.; Trembath, R. et al.; De Smedt, M.; van der Aa, N.; Skalej, M.; Mundlos, S.; Wuyts, W.; Southgate, L.; Zenker, M.: DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. Human Mutations 36 (6), pp. 593 - 598 (2015)

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Valk, S. L.; DiMartino, A.; Milham, M.i.; Bernhardt, B. C.: Multi-center mapping of structural network alterations in autism. Human Brain Mapping 36 (6), pp. 2364 - 2373 (2015)

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Wessa, M.; Kollmann, B.; Linke, J.; Schönfelder, S.; Kanske, P.: Increased impulsivity as a vulnerability marker for bipolar disorder: Evidence from self-report and experimental measures in two high-risk populations. Journal of Affective Disorders 178, pp. 18 - 24 (2015)

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Journal Article

Schafer, S.; Adami, E.; Heinig, M.; Rodrigues, K. E.; Kreuchwig, F.; Silhavy, J.; van Heesch, S.; Simaite, D.; Rajewsky, N.; Cuppen, E. et al.; Pravenec, M.; Vingron, M.; Cook, S. A.; Hubner, N.: Translational regulation shapes the molecular landscape of complex disease phenotypes. Nat Commun 6, 6:7200 (2015)

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Journal Article

Fuhr, L.; Rousseau, M.; Plauth, A.; Schroeder, F. C.; Sauer, S.: Amorfrutins Are Natural PPARgamma Agonists with Potent Anti-inflammatory Properties. Journal of Natural Products 78 (5), pp. 1160 - 1164 (2015)

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Lupiáñez, D. G.; Kraft, K.; Heinrich, V.; Krawitz, P.; Brancati, F.; Klopocki, E.; Horn, D.; Kayserili, H.; Opitz, J. M.; Laxova, R. et al.; Santos-Simarro, F.; Gilbert-Dussardier, B.; Wittler, L.; Borschiwer, M.; Haas, S. A.; Osterwalder, M.; Franke, M.; Timmermann, B.; Hecht, J.; Spielmann, M.; Visel, A.; Mundlos, S.: Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions. Cell 161 (5), pp. 1012 - 1025 (2015)

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Journal Article

Milenkovic, A.; Brandl, C.; Milenkovic, V. M.; Jendryke, T.; Sirianant, L.; Wanitchakool, P.; Zimmermann, S.; Reiff, C. M.; Horling, F.; Schrewe, H. et al.; Schreiber, R.; Kunzelmann, K.; Wetzel, C. H.; Weber, B. H. F.: Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells. Proceedings of the National Academy of Sciences of the United States of America 112 (20), pp. E2630 - E2639 (2015)

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Journal Article

Kähler, C.; Guenther, A.; Uhlich, A.; Krobitsch, S.: PRMT1-mediated arginine methylation controls ATXN2L localization. Experimental Cell Research 334 (1), pp. 114 - 125 (2015)

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Journal Article

Pajtler, K. W.; Witt, H.; Sill, M.; Jones, D. T.; Hovestadt, V.; Kratochwil, F.; Wani, K.; Tatevossian, R.; Punchihewa, C.; Johann, P. et al.; Reimand, J.; Warnatz, H.-J.; Ryzhova, M.; Mack, S.; Ramaswamy, V.; Capper, D.; Schweizer, L.; Sieber, L.; Wittmann, A.; Huang, Z.; van Sluis, P.; Volckmann, R.; Koster, J.; Versteeg, R.; Fults, D.; Toledano, H.; Avigad, S.; Hoffman, L. M.; Donson, A. M.; Foreman, N.; Hewer, E.; Zitterbart, K.; Gilbert, M.; Armstrong, T. S.; Gupta, N.; Allen, J. C.; Karajannis, M. A.; Zagzag, D.; Hasselblatt, M.; Kulozik, A. E.; Witt, O.; Collins, V. P.; von Hoff, K.; Rutkowski, S.; Pietsch, T.; Bader, G.; Yaspo, M. L.; von Deimling, A.; Lichter, P.; Taylor, M. D.; Gilbertson, R.; Ellison, D. W.; Aldape, K.; Korshunov, A.; Kool, M.; Pfister, S. M.: Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups. Cancer Cell 27 (5), pp. 728 - 743 (2015)

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Behrmann, E.; Loerke, J.; Budkevich, T. .; Yamamoto, K.; Schmidt, A.; Penczek, P. .; Vos, M. .; Bürger, J.; Mielke, T.; Scheerer, P. et al.; Spahn, C. . T.: Structural Snapshots of Actively Translating Human Ribosomes. Cell 161 (4), pp. 845 - 857 (2015)

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Journal Article

Redmer, T.; Welte, Y.; Behrens, D.; Fichtner, I.; Przybilla, D.; Wruck, W.; Yaspo, M. L.; Lehrach, H.; Schäfer, R.; Regenbrecht, C. R.: The nerve growth factor receptor CD271 is crucial to maintain tumorigenicity and stem-like properties of melanoma cells. PLoS One 9 (5), e92596 (2015)

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Journal Article

Etchegaray, J. P.; Chavez, L.; Huang, Y.; Ross, K. N.; Choi, J.; Martinez-Pastor, B.; Walsh, R. M.; Sommer, C. A.; Lienhard, M.; Gladden, A. et al.; Kugel, S.; Silberman, D. M.; Ramaswamy, S.; Mostoslavsky, G.; Hochedlinger, K.; Goren, A.; Rao, A.; Mostoslavsky, R.: The histone deacetylase SIRT6 controls embryonic stem cell fate via TET-mediated production of 5-hydroxymethylcytosine. Nature Cell Biology 17 (5), pp. 545 - 557 (2015)

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