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
Drews, K.; Jozefczuk, J.; Prigione, A.; Adjaye, J.: Human induced pluripotent stem cells--from mechanisms to clinical applications. Journal of Molecular Medicine-JMM 90 (7), pp. 735 - 745 (2012)
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Kamburov, A.; Stelzl, U.; Herwig, R.: IntScore: a web tool for confidence scoring of biological interactions. Nucleic Acids Research (London) 40 (Web Server issue), pp. W140 - W146 (2012)
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Ott, C. E.; Hein, H.; Lohan, S.; Hoogeboom, J.; Foulds, N.; Grunhagen, J.; Stricker, S.; Villavicencio-Lorini, P.; Klopocki, E.; Mundlos, S.: Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia. Journal of Medical Genetics (London) 49 (7), pp. 437 - 441 (2012)
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Ropers, H.-H.: On the future of genetic risk assessment. Journal of Community Genetics 3 (3), pp. 229 - 236 (2012)
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Rosenfeld, J. A.; Traylor, R. N.; Schaefer, G. B.; McPherson, E. W.; Ballif, B. C.; Klopocki, E.; Mundlos, S.; Shaffer, L. G.; Aylsworth, A. S.: Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 20 (7), pp. 754 - 761 (2012)
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Schimek, M. G.; Mysickova, A.; Budinská, E.: An Inference and Integration Approach for the Consolidation of Ranked Lists. Communications in Statistics - Simulation and Computation 41 (7), pp. 1152 - 1166 (2012)
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Wallace, B. C.; Small, K.; Brodley, C. E.; Lau, J.; Schmid, C. H.; Bertram, L.; Lill, C. M.; Cohen, J. T.; Trikalinos, T. A.: Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining. GENETICS IN MEDICINE 14 (7), pp. 663 - 669 (2012)
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Abu Dawud, R.; Schreiber, K.; Schomburg, D.; Adjaye, J.: Human embryonic stem cells and embryonal carcinoma cells have overlapping and distinct metabolic signatures. PLoS One 7 (6), p. e39896 - e39896 (2012)
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Pin, P. A.; Zhang, W.; Vogt, S. H.; Dally, N.; Büttner, B.; Schulze-Buxloh, G.; Jelly, N. S.; Chia, T. Y.P.; Mutasa-Gottgens, E. S.; Dohm, J. C. et al.; Himmelbauer, H.; Weisshaar, B.; Kraus, J.; Gielen, J. J.L.; Lommel, M.; Weyens, G.; Wahl, B.; Schechert, A.; Nilsson, O.; Jung, C.; Kraft, T.; Müller, A. E.: The role of a pseudo-response regulator gene in life cycle adaptation and domestication of beet. Current Biology 22 (12), pp. 1095 - 1101 (2012)
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Sultan, M.; Dokel, S.; Amstislavskiy, V.; Wuttig, D.; Sultmann, H.; Lehrach, H.; Yaspo, M. L.: A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods. Biochemical and Biophysical Research Communications 422 (4), pp. 643 - 646 (2012)
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Ni, S.; Vingron, M.: R2KS: a novel measure for comparing gene expression based on ranked gene lists. Journal of Computational Biology 19 (6), pp. 766 - 775 (2012)
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Drews, K.; Tavernier, G.; Demeester, J.; Lehrach, H.; de Smedt, S. C.; Rejman, J.; Adjaye, J.: The cytotoxic and immunogenic hurdles associated with non-viral mRNA-mediated reprogramming of human fibroblasts. Biomaterials 33 (16), pp. 4059 - 4068 (2012)
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Kliem, M.; Sauer, S.: The essence on mass spectrometry based microbial diagnostics. Current Opinion in Microbiology 15 (3), pp. 397 - 402 (2012)
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Klopocki, E.; Kaehler, C.; Foulds, N.; Shah, H.; Joseph, B.; Vogel, H.; Luttgen, S.; Bald, R.; Besoke, R.; Held, K. et al.; Mundlos, S.; Kurth, I.: Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 20 (6), pp. 705 - 708 (2012)
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Lill, C. M.; Zipp, F.: [The genetic profile of multiple sclerosis: risk genes and the "dark matter"]. Der Nervenarzt 83 (6), pp. 705 - 713 (2012)
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Querfurth, R.; Fischer, A.; Schweiger, M. R.; Lehrach, H.; Mertes, F.: Creation and application of immortalized bait libraries for targeted enrichment and next-generation sequencing. Biotechniques 52 (6), pp. 375 - 380 (2012)
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Welzel, F.; Kaehler, C.; Isau, M.; Hallen, L.; Lehrach, H.; Krobitsch, S.: FOX-2 dependent splicing of ataxin-2 transcript is affected by ataxin-1 overexpression. PLoS One 7 (5), p. e37985 - e37985 (2012)
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Ziv, L.; Muto, A.; Schoonheim, P. J.; Meijsing, S. H.; Strasser, D.; Ingraham, H. A.; Schaaf, M. J.; Yamamoto, K. R.; Baier, H.: An affective disorder in zebrafish with mutation of the glucocorticoid receptor. Molecular Psychiatry 18 (6), pp. 681 - 91 (2012)
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Nora, E. P.; Lajoie, B. R.; Schulz, E. G.; Giorgetti, L.; Okamoto, I.; Servant, N.; Piolot, T.; van Berkum, N. L.; Meisig, J.; Sedat, J. et al.; Gribnau, J.; Barillot, E.; Blüthgen, N.; Dekker, J.; Heard, E.: Spatial partitioning of the regulatory landscape of the X-inactivation centre. Nature 485 (7398), pp. 381 - 385 (2012)
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Dreher, F.; Kreitler, T.; Hardt, C.; Kamburov, A.; Yildirimman, R.; Schellander, K.; Lehrach, H.; Lange, B. M. H.; Herwig, R.: DIPSBC--data integration platform for systems biology collaborations. BMC Bioinformatics 13, 13:85 (2012)
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