The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (160)

Journal Article
Banerjee, A.: Structural distance and evolutionary relationship of networks. Biosystems 107 (3), pp. 186 - 196 (2012)
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Eberl, M.; Klingler, S.; Mangelberger, D.; Loipetzberger, A.; Damhofer, H.; Zoidl, K.; Schnidar, H.; Hache, H.; Bauer, H. C.; Solca, F. et al.; Hauser-Kronberger, C.; Ermilov, A. N.; Verhaegen, M. E.; Bichakjian, C. K.; Dlugosz, A. A.; Nietfeld, W.; Sibilia, M.; Lehrach, H.; Wierling, C.; Aberger, F.: Hedgehog-EGFR cooperation response genes determine the oncogenic phenotype of basal cell carcinoma and tumour-initiating pancreatic cancer cells. EMBO Molecular Medicine 4 (3), pp. 218 - 233 (2012)
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Geay, F.; Zambonino-Infante, J.; Reinhardt, R.; Kuhl, H.; Santigosa, E.; Cahu, C.; Mazurais, D.: Characteristics of fads2 gene expression and putative promoter in European sea bass (Dicentrarchus labrax): Comparison with salmonid species and analysis of CpG methylation. Marine Genomics 5, pp. 7 - 13 (2012)
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Heinrich, V.; Stange, J.; Dickhaus, T.; Imkeller, P.; Kruger, U.; Bauer, S.; Mundlos, S.; Robinson, P. N.; Hecht, J.; Krawitz, P. M.: The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process. Nucleic Acids Research (London) 40 (6), pp. 2426 - 2431 (2012)
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Lasserre, J.; Arnold, S.; Vingron, M.; Reinke, P.; Hinrichs, C.: Predicting the outcome of renal transplantation. Journal of the American Medical Informatics Association 19 (2), pp. 255 - 262 (2012)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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Smallwood, J.; Brown, K.; Baird, B.; Schooler, J. W.: Cooperation between the default mode network and the frontal-parietal network in the production of an internal train of thought. Brain Research 1428, pp. 60 - 70 (2012)
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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)
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