Starokadomskyy, P.; Gluck, N.; Li, H.; Chen, B.; Wallis, M.; Maine, G. N.; Mao, X.; Zaidi, I. W.; Hein, M. Y.; McDonald, F. J. et al.; Lenzner, S.; Zecha, A.; Ropers, H. H.; Kuss, A. W.; McGaughran, J.; Gecz, J.; Burstein, E.: CCDC22 deficiency in humans blunts activation of proinflammatory NF-kappaB signaling. The Journal of Clinical Investigation 123 (5), S. 2244 - 2256 (2013)

Gilling, M.; Rasmussen, H. B.; Calloe, K.; Sequeira, A. F.; Baretto, M.; Oliveira, G.; Almeida, J.; Lauritsen, M. B.; Ullmann, R.; Boonen, S. E. et al.; Brondum-Nielsen, K.; Kalscheuer, V. M.; Tumer, Z.; Vicente, A. M.; Schmitt, N.; Tommerup, N.: Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders. Frontiers in Genetics 4, S. 4:54 - 4:54 (2013)

Vogl, M. R.; Reiprich, S.; Küspert, M.; Kosian, T.; Schrewe, H.; Nave, K.-A.; Wegner, M.: Sox10 cooperates with the mediator subunit 12 during terminal differentiation of myelinating glia. The Journal of Neuroscience: the Official Journal of the Society for Neuroscience 33 (15), S. 6679 - 6690 (2013)

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), S. 367 - 372 (2013)

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), S. 3518 - 3531 (2013)

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), S. 3518 - 3531 (2013)

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), S. 461 - 471 (2013)

Schulz, E. G.; Heard, E.: Role and control of X chromosome dosage in mammalian development. Current Opinion in Genetics & Development 23 (2), S. 109 - 115 (2013)

Siragusa, E.; Weese, D.; Reinert, K.: Fast and accurate read mapping with approximate seeds and multiple backtracking. Nucleic Acids Research (London) 41 (7), S. e78 - e78 (2013)

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), S. 339 - 342 (2013)

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), S. e59976 - e59976 (2013)

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), S. 73 - 74 (2013)

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), S. 1249 - 66 (2013)

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), S. 133 - 139 (2013)

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), S. 294 - 300 (2013)

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), S. 113 - 117 (2013)

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), S. 113 - 117 (2013)

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), S. 1535 - 1543 (2013)

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), S. 497 - 501 (2013)

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), S. e57311 - e57311 (2013)