Stacher, E.; Boldt, V.; Leibl, S.; Halbwedl, I.; Popper, H. H.; Ullmann, R.; Tavassoli, F. A.; Moinfar, F.: Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias of the breast. Histopathology 59 (3), pp. 549 - 55 (2011)

Stanke, F.; Becker, T.; Kumar, V.; Hedtfeld, S.; Becker, C.; Cuppens, H.; Tamm, S.; Yarden, J.; Laabs, U.; Siebert, B. et al.; Fernandez, L.; Macek, M.; Radojkovic, D.; Ballmann, M.; Greipel, J.; Cassiman, J. J.; Wienker, T. F.; Tummler, B.: Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet 48 (1), pp. 24 - 31 (2011)

Stehr, H.; Jang, S. H.; Duarte, J. M.; Wierling, C.; Lehrach, H.; Lappe, M.; Lange, B. M.: The structural impact of cancer-associated missense mutations in oncogenes and tumor suppressors. Molecular Cancer 10, p. 54 (2011)

Steininger, A.; Mobs, M.; Ullmann, R.; Kochert, K.; Kreher, S.; Lamprecht, B.; Anagnostopoulos, I.; Hummel, M.; Richter, J.; Beyer, M. et al.; Janz, M.; Klemke, C. D.; Stein, H.; Dorken, B.; Sterry, W.; Schrock, E.; Mathas, S.; Assaf, C.: Genomic loss of the putative tumor suppressor gene E2A in human lymphoma. J Exp Med 208 (8), pp. 1585 - 93 (2011)

Stricker, S.; Mathia, S.; Haupt, J.; Seemann, P.; Meier, J.; Mundlos, S.: Odd-Skipped Related Genes Regulate Differentiation of Embryonic Limb Mesenchyme and Bone Marrow Mesenchymal Stromal Cells. Stem Cells Dev (2011)

Stricker, S.; Mundlos, S.: FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development. Curr Top Dev Biol 97, pp. 179 - 206 (2011)

Stricker, S.; Mundlos, S.: Mechanisms of digit formation: Human malformation syndromes tell the story. Dev Dyn 240 (5), pp. 990 - 1004 (2011)

Strobl-Wildemann, G.; Kalscheuer, V. M.; Hu, H.; Wrogemann, K.; Ropers, H. H.; Tzschach, A.: Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability. Am J Med Genet A 155A (12), pp. 3067 - 70 (2011)

Suk, E. K.; McEwen, G. K.; Duitama, J.; Nowick, K.; Schulz, S.; Palczewski, S.; Schreiber, S.; Holloway, D. T.; McLaughlin, S.; Peckham, H. et al.; Lee, C.; Huebsch, T.; Hoehe, M. R.: A comprehensively molecular haplotype-resolved genome of a European individual. Genome Research 21 (10), pp. 1672 - 85 (2011)

Szczurek, E.; Markowetz, F.; Gat-Viks, I.; Biecek, P.; Tiuryn, J.; Vingron, M.: Deregulation upon DNA damage revealed by joint analysis of context-specific perturbation data. BMC Bioinformatics 12, p. 249 (2011)

Thomas-Chollier, M.; Defrance, M.; Medina-Rivera, A.; Sand, O.; Herrmann, C.; Thieffry, D.; van Helden, J.: RSAT 2011: regulatory sequence analysis tools. Nucleic Acids Res 39 (Web Server issue), pp. W86 - 91 (2011)

Thomas-Chollier, M.; Herrmann, C.; Defrance, M.; Sand, O.; Thieffry, D.; van Helden, J.: RSAT peak-motifs: motif analysis in full-size ChIP-seq datasets. Nucleic Acids Res (2011)

Thomas-Chollier, M.; Hufton, A.; Heinig, M.; O'Keeffe, S.; Masri, N. E.; Roider, H. G.; Manke, T.; Vingron, M.: Transcription factor binding predictions using TRAP for the analysis of ChIP-seq data and regulatory SNPs. Nat Protoc 6 (12), pp. 1860 - 9 (2011)

Thormann, A.; Rasche, A.: Functional Context Network of T2DM, Medical Complications of Type 2 Diabetes. Intech Publishing (2011)

Turkmen, S.; Riehn, M.; Klopocki, E.; Molkentin, M.; Reinhardt, R.; Burmeister, T.: A BACH2-BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE-1. Genes Chromosomes Cancer 50 (6), pp. 389 - 96 (2011)

Tzschach, A.; Ullmann, R.; Ahmed, A.; Martin, T.; Weber, G.; Decker-Schwering, O.; Pauly, F.; Shamdeen, M. G.; Reith, W.; Oehl-Jaschkowitz, B.: Christianson syndrome in a patient with an interstitial Xq26.3 deletion. Am J Med Genet A 155A (11), pp. 2771 - 4 (2011)

Vilardell, M.; Rasche, A.; Thormann, A.; Maschke-Dutz, E.; Perez-Jurado, L. A.; Lehrach, H.; Herwig, R.: Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processes. BMC Genomics 12, p. 229 (2011)

Vinayagam, A.; Stelzl, U.; Foulle, R.; Plassmann, S.; Zenkner, M.; Timm, J.; Assmus, H. E.; Andrade-Navarro, M. A.; Wanker, E. E.: A directed protein interaction network for investigating intracellular signal transduction. Sci Signal 4 (189), p. rs8 (2011)

Viswanathan, J.; Haapasalo, A.; Bottcher, C.; Miettinen, R.; Kurkinen, K. M.; Lu, A.; Thomas, A.; Maynard, C. J.; Romano, D.; Hyman, B. T. et al.; Berezovska, O.; Bertram, L.; Soininen, H.; Dantuma, N. P.; Tanzi, R. E.; Hiltunen, M.: Alzheimer's disease-associated ubiquilin-1 regulates presenilin-1 accumulation and aggresome formation. Traffic 12 (3), pp. 330 - 48 (2011)

von Keyserling, H.; Bergmann, T.; Schuetz, M.; Schiller, U.; Stanke, J.; Hoffmann, C.; Schneider, A.; Lehrach, H.; Dahl, A.; Kaufmann, A. M.: Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure. International Journal of Gynecological Cancer: Official Journal of the International Gynecological Cancer Society 21 (9), pp. 1664 - 71 (2011)