Publications

Max Planck Institute for Molecular Genetics

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

Börno, S.; Fischer, A.; Kerick, M.; Falth, M.; Laible, M.; Brase, J. C.; Kuner, R.; Dahl, A.; Grimm, C.; Sayanjali, B. et al.; Isau, M.; Röhr, C.; Wunderlich, A.; Timmermann, B.; Claus, R.; Plass, C.; Graefen, M.; Simon, R.; Demichelis, F.; Rubin, M. A.; Sauter, G.; Schlomm, T.; Sültmann, H.; Lehrach, H.; Schweiger, M. R.: Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation. Cancer Discovery 2 (11), pp. 1024 - 1035 (2012)

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Fischer, B.; Dimopoulou, A.; Egerer, J.; Gardeitchik, T.; Kidd, A.; Jost, D.; Kayserili, H.; Alanay, Y.; Tantcheva-Poor, I.; Mangold, E. et al.; Daumer-Haas, C.; Phadke, S.; Peirano, R. I.; Heusel, J.; Desphande, C.; Gupta, N.; Nanda, A.; Felix, E.; Berry-Kravis, E.; Kabra, M.; Wevers, R. A.; van Maldergem, L.; Mundlos, S.; Morava, E.; Kornak, U.: Further characterization of ATP6V0A2-related autosomal recessive cutis laxa. Human Genetics 131 (11), pp. 1761 - 1773 (2012)

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Hucho, T.; Suckow, V.; Joseph, E. K.; Kuhn, J.; Schmoranzer, J.; Dina, O. A.; Chen, X.; Karst, M.; Bernateck, M.; Levine, J. D. et al.; Ropers, H.-H.: Ca++/CaMKII switches nociceptor-sensitizing stimuli into desensitizing stimuli. Journal of Neurochemistry: official journal of the International Society for Neurochemistry 123 (4), pp. 589 - 601 (2012)

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Sharma, M.; Ioannidis, J. P.; Aasly, J. O.; Annesi, G.; Brice, A.; Bertram, L.; Bozi, M.; Barcikowska, M.; Crosiers, D.; Clarke, C. E. et al.; Facheris, M. F.; Farrer, M.; Garraux, G.; Gispert, S.; Auburger, G.; Vilarino-Guell, C.; Hadjigeorgiou, G. M.; Hicks, A. A.; Hattori, N.; Jeon, B. S.; Jamrozik, Z.; Krygowska-Wajs, A.; Lesage, S.; Lill, C. M.; Lin, J. J.; Lynch, T.; Lichtner, P.; Lang, A. E.; Libioulle, C.; Murata, M.; Mok, V.; Jasinska-Myga, B.; Mellick, G. D.; Morrison, K. E.; Meitnger, T.; Zimprich, A.; Opala, G.; Pramstaller, P. P.; Pichler, I.; Park, S. S.; Quattrone, A.; Rogaeva, E.; Ross, O. A.; Stefanis, L.; Stockton, J. D.; Satake, W.; Silburn, P. A.; Strom, T. M.; Theuns, J.; Tan, E. K.; Toda, T.; Tomiyama, H.; Uitti, R. J.; Van Broeckhoven, C.; Wirdefeldt, K.; Wszolek, Z.; Xiromerisiou, G.; Yomono, H. S.; Yueh, K. C.; Zhao, Y.; Gasser, T.; Maraganore, D.; Krüger, R.: A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics (London) 49 (11), pp. 721 - 726 (2012)

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Sudheer, S.; Bhushan, R.; Fauler, B.; Lehrach, H.; Adjaye, J.: FGF inhibition directs BMP4-mediated differentiation of human embryonic stem cells to syncytiotrophoblast. Stem Cells and Development 21 (16), pp. 2987 - 3000 (2012)

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Wollrab, C.; Heitkam, T.; Holtgrawe, D.; Weisshaar, B.; Minoche, A. E.; Dohm, J. C.; Himmelbauer, H.; Schmidt, T.: Evolutionary reshuffling in the Errantivirus lineage Elbe within the Beta vulgaris genome. The Plant Journal 72 (4), pp. 636 - 51 (2012)

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McCall, C.; Tipper, C. M.; Blascovich, J.; Grafton, S. T.: Attitudes trigger motor behavior through conditioned associations: Neural and behavioral evidence. Social Cognitive and Affective Neuroscience 7 (7), pp. 841 - 849 (2012)

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Kamburov, A.; Grossmann, A.; Herwig, R.; Stelzl, U.: Cluster-based assessment of protein-protein interaction confidence. BMC Bioinformatics, p. 13:262 - 13:262 (2012)

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Rubelt, F.; Sievert, V.; Knaust, F.; Diener, C.; Lim, T. S.; Klipp, E.; Reinhardt, R.; Lehrach, H.; Konthur, Z.: Onset of Immune Senescence Defined by Unbiased Pyrosequencing of Human Immunoglobulin mRNA Repertoires. PLoS One (accepted)

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Berillo, O.; Khailenko, V.; Ivashchenko, A.; Perlmuter-Shoshany, L.; Bolshoy, A.: miRNA and tropism of human parvovirus B19. Computational Biology and Chemistry 40 (0), pp. 1 - 6 (2012)

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El Khassawna, T.; Toben, D.; Kolanczyk, M.; Schmidt-Bleek, K.; Koennecke, I.; Schell, H.; Mundlos, S.; Duda, G. N.: Deterioration of fracture healing in the mouse model of NF1 long bone dysplasia. Bone 51 (4), pp. 651 - 660 (2012)

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Geffers, L.; Herrmann, B. G.; Eichele, G.: Web-based digital gene expression atlases for the mouse. Mammalian Genome 23, pp. 525 - 538 (2012)

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Mangold, E.; Reutter, H.; Leon-Cachon, R. B.; Ludwig, K. U.; Herms, S.; Chacon-Camacho, O.; Ortiz-Lopez, R.; Paredes-Zenteno, M.; Arizpe-Cantu, A.; Munoz-Jimenez, S. G. et al.; Nowak, S.; Kramer, F. J.; Wienker, T. F.; Nothen, M. M.; Knapp, M.; Rojas-Martinez, A.: Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate. European Journal of Oral Science 120 (5), pp. 373 - 377 (2012)

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Moschidou, D.; Mukherjee, S.; Blundell, M. P.; Drews, K.; Jones, G. N.; Abdulrazzak, H.; Nowakowska, B.; Phoolchund, A.; Lay, K.; Ramasamy, T. S. et al.; Cananzi, M.; Nettersheim, D.; Sullivan, M.; Frost, J.; Moore, G.; Vermeesch, J. R.; Fisk, N. M.; Thrasher, A. J.; Atala, A.; Adjaye, J.; Schorle, H.; De Coppi, P.; Guillot, P. V.: Valproic acid confers functional pluripotency to human amniotic fluid stem cells in a transgene-free approach. Molecular Therapy 20 (10), pp. 1953 - 1967 (2012)

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Peifer, M.; Fernandez-Cuesta, L.; Sos, M. L.; George, J.; Seidel, D.; Kasper, L. H.; Plenker, D.; Leenders, F.; Sun, R.; Zander, T. et al.; Menon, R.; Koker, M.; Dahmen, I.; Muller, C.; Di Cerbo, V.; Schildhaus, H. U.; Altmuller, J.; Baessmann, I.; Becker, C.; de Wilde, B.; Vandesompele, J.; Bohm, D.; Ansen, S.; Gabler, F.; Wilkening, I.; Heynck, S.; Heuckmann, J. M.; Lu, X.; Carter, S. L.; Cibulskis, K.; Banerji, S.; Getz, G.; Park, K. S.; Rauh, D.; Grutter, C.; Fischer, M.; Pasqualucci, L.; Wright, G.; Wainer, Z.; Russell, P.; Petersen, I.; Chen, Y.; Stoelben, E.; Ludwig, C.; Schnabel, P.; Hoffmann, H.; Muley, T.; Brockmann, M.; Engel-Riedel, W.; Muscarella, L. A.; Fazio, V. M.; Groen, H.; Timens, W.; Sietsma, H.; Thunnissen, E.; Smit, E.; Heideman, D. A.; Snijders, P. J.; Cappuzzo, F.; Ligorio, C.; Damiani, S.; Field, J.; Solberg, S.; Brustugun, O. T.; Lund-Iversen, M.; Sanger, J.; Clement, J. H.; Soltermann, A.; Moch, H.; Weder, W.; Solomon, B.; Soria, J. C.; Validire, P.; Besse, B.; Brambilla, E.; Brambilla, C.; Lantuejoul, S.; Lorimier, P.; Schneider, P. M.; Hallek, M.; Pao, W.; Meyerson, M.; Sage, J.; Shendure, J.; Schneider, R.; Buttner, R.; Wolf, J.; Nurnberg, P.; Perner, S.; Heukamp, L. C.; Brindle, P. K.; Haas, S.; Thomas, R. K.: Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer. Nature Genetics 44 (10), pp. 1104 - 1110 (2012)

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Spielmann, M.; Brancati, F.; Krawitz, P. M.; Robinson, P. N.; Ibrahim, D. M.; Franke, M.; Hecht, J.; Lohan, S.; Dathe, K.; Nardone, A. M. et al.; Ferrari, P.; Landi, A.; Wittler, L.; Timmermann, B.; Chan, D.; Mennen, U.; Klopocki, E.; Mundlos, S.: Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus. American Journal of Human Genetics 91 (4), pp. 629 - 635 (2012)

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Huang, L.; Jolly, L. A.; Willis-Owen, S.; Gardner, A.; Kumar, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M. et al.; Hackett, A.; Field, M.; Froyen, G.; Hu, H. C.; Haas, S.; Ropers, H.-H.; Kalscheuer, V. M.; Corbett, M. A.; Gecz, J.: A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability. The American Journal of Human Genetics 91 (4), pp. 694 - 702 (2012)

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Kämpjärvi, K.; Mäkinen, N.; Kilpivaara, O.; Arola, J.; Heinonen, H.-R.; Böhm, J.; Abdel-Wahab, O.; Lehtonen, H. J.; Pelttari, L. M.; Mehine, M. et al.; Schrewe, H.; Nevanlinna, H.; Levine, R. L.; Hokland, P.; Böhling, T.; Mecklin, J.-P.; Bützow, R.; Aaltonen, L. A.; Vahteristo, P.: Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. British Journal of Cancer 107, pp. 1761 - 1765 (2012)

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Wittler, L.; Hilger, A.; Proske, J.; Pennimpede, T.; Draaken, M.; Ebert, A.-K.; Rösch, W.; Stein, R.; Nöthen, M. M.; Reutter, H. et al.; Ludwig, M.: Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene 506 (2), pp. 392 - 395 (2012)

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Parsons, M. J.; Grimm, C.; Paya-Cano, J. L.; Fernandes, C.; Liu, L.; Philip, V. M.; Chesler, E. J.; Nietfeld, W.; Lehrach, H.; Schalkwyk, L. C.: Genetic variation in hippocampal microRNA expression differences in C57BL/6 J X DBA/2 J (BXD) recombinant inbred mouse strains. BMC Genomics 13, p. 476 (2012)

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