Mller, R. S.; Kübart, S.; Hoeltzenbein, M.; Heye, B.; Vogel, I.; Hansen, C. P.; Menzel, C.; Ullmann, R.; Tommerup, N.; Ropers, H.-H. et al.; Tümer, Z.; Kalscheuer, V. M.: Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly. The American Journal of Human Genetics 82 (5), pp. 1165 - 1170 (2008)

Mayr, J. A.; Meierhofer, D.; Zimmermann, F.; Feichtinger, R.; Kögler, C.; Ratschek, M.; Schmeller, N.; Sperl, W.; Kofler, B.: Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 14 (8), pp. 2270 - 2275 (2008)

Frints, S. G. M.; Lenzner, S.; Bauters, M.; Jensen, L. R.; Van Esch, H.; des Portes, V.; Moog, U.; Macville, M. V. E.; van Roozendaal, K.; Schrander-Stumpel, C. T. R. M. et al.; Tzschach, A.; Marynen, P.; Fryns, J.-P.; Hame, B.; van Bokhoven, H.; Chelly, J.; Beldjord, C.; Turner, G.; Gecz, J.; Moraine, C.; Raynaud, M.; Ropers, H. H.; Froyen, G.; Kuss, A. W.: MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression. European Journal of Human Genetics 16 (9), pp. 1029 - 1037 (2008)

Choudhurya, K.; Zander, D.; Kube, M.; Reinhardt, R.; Clos, J.: Identification of a Leishmania infantum gene mediating resistance to miltefosine and SbIII. International Journal for Parasitology 38 (12), pp. 1411 - 1423 (2008)

Toenjes, M.; Schueler, M.; Hammer, S.; Pape, U. J.; Fischer, J. J.; Felix Berger, F.; Vingron, M.; Sperling, S.: Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes. Molecular BioSystems: A New High Quality Chemical Biology Journal with A Particular Focus on the Interface between Chemistry and the -Omic Sciences and Systems Biology 4 (6), pp. 589 - 598 (2008)

Burmeister, T.; Reinhardt, R.: A multiplex PCR for improved detection of typical and atypical BCR-ABL fusion transcripts. Leukemea Research 32 (4), pp. 579 - 585 (2008)

Friedländer, M. R.; Chen, W.; Adamidi, C.; Maaskola, J.; Einspanier, R.; Knespel, S.; Rajewsky, N.: Discovering microRNAs from deep sequencing data using miRDeep. Nature Biotechnology 26 (4), pp. 407 - 415 (2008)

Guo, G.; Bauer, S.; Hecht, J.; Schulz, M. H.; Busche, A.; Robinson, P. N.: A short ultraconserved sequence drives transcription from an alternate FBN1 promoter. The International Journal of Biochemistry & Cell Biology 40 (4), pp. 638 - 650 (2008)

Menzel, C.; Schirrmann, T.; Konthur, Z.; Jostock, T.; Dübel, S.: Human antibody RNase fusion protein targeting CD30+ lymphomas. Blood 111 (7), pp. 3830 - 3837 (2008)

Nogai, H.; Rosowski, M.; Grün, J.; Rietz, A.; Debus, N.; Schmidt, G.; Lauster, C.; Janitz, M.; Vortkamp, A.; Lauster, R.: Follistatin antagonizes transforming growth factor-β3-induced epithelial–mesenchymal transition in vitro: implications for murine palatal development supported by microarray analysis. Differentiation 76 (4), pp. 404 - 416 (2008)

Türkmen, S.; Hoffmann, K. ..; Demirhan, O.; Aruoba, D.; Humphrey, N.; Mundlos, S.: Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene. European Journal of Human Genetics 16, pp. 1070 - 1074 (2008)

Hecht, J.; Stricker, S.; Wiecha, U.; Stiege, A.; Panopoulou, G.; Podsiadlowski, L.; Poustka, A. J.; Dieterich, C.; Ehrich, S.; Suvorova, J. et al.; Mundlos, S.; Seitz, V.: Evolution of a core gene network for skeletogenesis in chordates. PLoS Genetics 4 (3), p. e1000025 - e1000025 (2008)

Manke, T.; Roider, H. G.; Vingron, M.: Statistical Modeling of Transcription Factor Binding Affinities Predicts Regulatory Interactions. PLoS Computational Biology 4 (3), p. e1000039 - e1000039 (2008)

Raz, R.; Stricker, S.; Elizabetta Gazzerro, E.; Clor, J. L.; Witte, F.; Nistala, H.; Zabski, S.; Pereira, R. C.; Stadmeyer, L.; Wang, X. et al.; Gowen, L.; Sleeman, M. W.; Yancopoulos, G. D.; Canalis, E.; Mundlos, S.; Valenzuela, D. M. V.; Economides, A. N.: The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome. Development 135 (9), pp. 1713 - 1723 (2008)

Fuhrmann, C.; Schmidt-Kittler, O.; Stoecklein, N. H.; Petat-Dutter, K.; Vay, C.; Bockler, K.; Reinhardt, R.; Ragg, T.; Klein, C. A.: High-resolution array comparative genomic hybridization of single micrometastatic tumor cells. Nucleic Acids Research 36 (7), p. e39 - e39 (2008)

Grunwald, S.; Speer, A.; Ackermann, J.; Koch, I.: Petri net modelling of gene regulation of the Duchenne muscular dystrophy. Biosystems 92 (2), pp. 189 - 205 (2008)

Chen, W.; Kalscheuer, V.; Tzschach, A.; Menzel, C.; Ullmann, R.; Schulz, M. H.; Erdogan, F.; Na, L.; Kijas, Z.; Arkesteijn, G. et al.; Pajares, I. L.; Goetz-Sothmann, M.; Heinrich, U.; Rost, I.; Dufke, A.; Grasshoff, U.; Glaeser, B.; Vingron, M.; Ropers, H. H.: Mapping translocation breakpoints by next-generation sequencing. Genome Research 18 (7), pp. 1143 - 1149 (2008)

Deutsch, E. W.; Ball, C. A.; Berman, J. J.; Bova, G. S.; Brazma, A.; Bumgarner, R. E.; Campbell, D.; Causton, H. C.; Christiansen, J. H.; Daian, F. et al.; Dauga, D.; Davidson, D. R.; Gimenez, G.; Goo, Y. A.; Grimmond, S.; Henrich, T.; Herrmann, B. G.; Johnson, M. H.; Korb, M.; Mills, J. C.; Oudes, A. J.; Parkinson, H. E.; Pascal, L. E.; Pollet, N.; Quackenbush, J.; Ramialison, M.; Ringwald, M.; Salgado, D.; Sansone, S.-A.; Sherlock, G.; Stoeckert Jr, C. J.; Swedlow, J.; Taylor, R. C.; Walashek, L.; Warford, A.; Wilkinson, D. G.; Zhou, Y.; Zon, L. I.; Liu, A. Y.; True, L. D.: Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE). Nature Biotechnology 26, pp. 305 - 312 (2008)

Graeber, I.; Kaesler, I.; Borchert, M. S.; Dieckmann, R.; Pape, T.; Lurz, R.; Nielsen, P.; von Döhren, H.; Michaelis, W.; Szewzyk, U.: Spongiibacter marinus gen. nov., sp. nov., a halophilic marine bacterium isolated from the boreal sponge Haliclona sp. 1. International Journal of Sytematic and Evolutionary Micro 58 (Pt 3), pp. 585 - 590 (2008)

Kirov, G.; Gumus, D.; Chen, W.; Norton, N.; Georgieva, L.; Sari, M.; O’Donovan, M. C.; Erdogan, F.; Owen, M. J.; Ropers, H.-H. et al.; Ullmann, R.: Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics 17 (3), pp. 458 - 465 (2008)