Menzel, G.; Krebs, C.; Diez, M.; Holtgrawe, D.; Weisshaar, B.; Minoche, A. E.; Dohm, J. C.; Himmelbauer, H.; Schmidt, T.: Survey of sugar beet (Beta vulgaris L.) hAT transposons and MITE-like hATpin derivatives. Plant Molecular Biology 78 (4-5), pp. 393 - 405 (2012)

Hegele, A.; Kamburov, A.; Großmann, A.; Sourlis, C.; Wowro, S. J.; Weimann, M.; Will, C. L.; Pena, V.; Lührmann, R.; Stelzel, U.: Dynamic protein-protein interaction wiring of the human spliceosome. Molecular Cell 45 (4), pp. 567 - 580 (2012)

Murakami, Y.; Kanzawa, N.; Saito, K.; Krawitz, P. M.; Mundlos, S.; Robinson, P. N.; Karadimitris, A.; Maeda, Y.; Kinoshita, T.: Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome. The Journal of Biological Chemistry 287 (9), pp. 6318 - 6325 (2012)

MacArthur, D. G.; Balasubramanian, S.; Frankish, A.; 1000 Genomes Project, C.; Sudbrak, R.; Albrecht , M. W.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A. et al.; Herwig, R.; Marquardt, P.; Mertes, F.; Nietfeld, W.; Parkhomchuk, D.; Soldatov, A.; Timmermann, B.; Tolzmann, M.; Lehrach, H.: A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 335 (6070), pp. 823 - 828 (2012)

Wagner, M.; Schulze-Rauschenbach, S.; Petrovsky, N.; Brinkmeyer, J.; von der Goltz, C.; Grunder, G.; Spreckelmeyer, K. N.; Wienker, T.; Diaz-Lacava, A.; Mobascher, A. et al.; Dahmen, N.; Clepce, M.; Thuerauf, N.; Kiefer, F.; de Millas, J. W.; Gallinat, J.; Winterer, G.: Neurocognitive impairments in non-deprived smokers-results from a population-based multi-center study on smoking-related behavior. Addiction Biology 2012, p. e - e (2012)

Klopocki, E.; Lohan, S.; Doelken, S. C.; Stricker, S.; Ockeloen, C. W.; Soares Thiele de Aguiar, R.; Lezirovitz, K.; Netto, M.; Jamsheer, A.; Shah, H. et al.; Kurth, I.; Habenicht, R.; Warman, M.; Devriendt, K.; Kordass, U.; Hempel, M.; Rajab, A.; Makitie, O.; Naveed, M.; Radhakrishna, U.; Antonarakis, S. E.; Horn, D.; Mundlos, S.: Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics (London) 49 (2), pp. 119 - 125 (2012)

Schueler, M.; Zhang, Q.; Schlesinger, J.; Tönjes, M.; Sperling, S.: Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse. Molecular BioSystems 8 (2), pp. 495 - 503 (2012)

Haupt, A.; Joberty, G.; Bantscheff, M.; Fröhlich, H.; Stehr, H.; Schweiger, M. R.; Fischer, A.; Kerick, M.; Boerno, S. T.; Dahl, A. et al.; Lappe, M.; Lehrach, H.; Gonzalez, C.; Drewes, G.; Lange, B. M.: Hsp90 inhibition differentially destabilises MAP kinase and TGF-beta signalling components in cancer cells revealed by kinase-targeted chemoproteomics. BMC Cancer 12 (12), p. 38 (2012)

Schwaerzer, G. K.; Hiepen, C.; Schrewe, H.; Nickel, J.; Ploeger, F.; Sebald, W.; Mueller, T.; Knaus, P.: New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): mutation within the GDF5 knuckle epitope causes noggin-resistance. Journal of Bone and Mineral Research 27 (2), pp. 429 - 442 (2012)

Mysickova, A.; Vingron, M.: Detection of interacting transcription factors in human tissues using predicted DNA binding affinity. BMC Genomics 13 Suppl 1, p. S2 - S2 (2012)

Arnold, H.; Wienker, T. F.; Hoffmann, M. M.; Scheuerbrandt, G.; Kemp, K.; Bugert, P.: High levels of brain-type creatine kinase activity in human platelets and leukocytes: a genetic anomaly with autosomal dominant inheritance. Blood Cells Molecules and Diseases 48 (1), pp. 62 - 67 (2012)

Huppke, P.; Brendel, C.; Kalscheuer, V.; Korenke, G. C.; Marquardt, I.; Freisinger, P.; Christodoulou, J.; Hillebrand, M.; Pitelet, G.; Wilson, C. et al.; Gruber-Sedlmayr, U.; Ullmann, R.; Haas, S.; Elpeleg, O.; Nürnberg, G.; Nürnberg, P.; Dad, S.; Møller, L. B.; Kaler, S. G.; Gärtner, J.: Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin. The American Journal of Human Genetics 90 (1), pp. 61 - 8 (2012)

Li, J.; Pandey, V.; Kessler, T.; Lehrach, H.; Wierling, C.: Modeling of miRNA and drug action in the EGFR signaling pathway. PLoS One 7 (1), e30140 (2012)

Adams, D.; Altucci, L.; Antonarakis, S. E.; Ballesteros, J.; Beck, S.; Bird, A.; Bock, C.; Boehm, B.; Campo, E.; Caricasole, A. et al.; Dahl, F.; Dermitzakis, E. T.; Enver, T.; Esteller, M.; Estivill, X.; Ferguson-Smith, A.; Fitzgibbon, J.; Flicek, P.; Giehl, C.; Graf, T.; Grosveld, F.; Guigo, R.; Gut, I.; Helin, K.; Jarvius, J.; Kuppers, R.; Lehrach, H.; Lengauer, T.; Lernmark, A.; Leslie, D.; Loeffler, M.; Macintyre, E.; Mai, A.; Martens, J. H.; Minucci, S.; Ouwehand, W. H.; Pelicci, P. G.; Pendeville, H.; Porse, B.; Rakyan, V.; Reik, W.; Schrappe, M.; Schubeler, D.; Seifert, M.; Siebert, R.; Simmons, D.; Soranzo, N.; Spicuglia, S.; Stratton, M.; Stunnenberg, H. G.; Tanay, A.; Torrents, D.; Valencia, A.; Vellenga, E.; Vingron, M.; Walter, J.; Willcocks, S.: BLUEPRINT to decode the epigenetic signature written in blood. Nature biotechnology 30 (3), pp. 224 - 226 (2012)

Braunholz, D.; Hullings, M.; Gil-Rodriguez, M. C.; Fincher, C. T.; Mallozzi, M. B.; Loy, E.; Albrecht, M.; Kaur, M.; Limon, J.; Rampuria, A. et al.; Clark, D.; Kline, A.; Dalski, A.; Eckhold, J.; Tzschach, A.; Hennekam, R.; Gillessen-Kaesbach, G.; Wierzba, J.; Krantz, I. D.; Deardorff, M. A.; Kaiser, F. J.: Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 20 (3), pp. 271 - 276 (2012)

Clark, M. S.; Denekamp, N. Y.; Thorne, M. A.; Reinhardt, R.; Drungowski, M.; Albrecht, M.; Klages, S.; Beck, A.; Kube, M.; Lubzens, E.: Long-term survival of hydrated resting eggs from Brachionus plicatilis. PLoS One 7 (1), p. e29365 - e29365 (2012)

Diedrichs, F.; Mlody, B.; Matz, P.; Fuchs, H.; Chavez, L.; Drews, K.; Adjaye, J.: Comparative molecular portraits of human unfertilized oocytes and primordial germ cells at 10 weeks of gestation. International Journal of Developmental Biology 56 (10-11-12), pp. 789 - 797 (2012)

Dreher, F.; Kamburov, A.; Herwig, R.: Construction of a pig physical interactome using sequence homology and a comprehensive reference human interactome. Evolutionary Bioinformatics 8, pp. 119 - 126 (2012)

Emde, A. K.; Schulz, M. H.; Weese, D.; Sun, R.; Vingron, M.; Kalscheuer, V. M.; Haas, S.; Reinert, K.: Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. Bioinformatics 28 (5), pp. 619 - 27 (2012)

Göke, J.; Schulz, M. H.; Lasserre, J.; Vingron, M.: Estimation of pairwise sequence similarity of mammalian enhancers with word neighbourhood counts. Bioinformatics 28 (5), pp. 656 - 63 (2012)