Publications

Journal Article

Bertram, L.: Alzheimer's genetics in the GWAS era: a continuing story of 'replications and refutations'. Current Neurology and Neuroscience Reports 11 (3), pp. 246 - 53 (2011)

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Journal Article

Bertram, L.; Hampel, H.: The role of genetics for biomarker development in neurodegeneration. Progress in Neurobiology 95 (4), pp. 501 - 4 (2011)

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Journal Article

Bhushan, S.; Hoffmann, T.; Seidelt, B.; Frauenfeld, J.; Mielke, T.; Berninghausen, O.; Wilson, D. N.; Beckmann, R.: SecM-stalled ribosomes adopt an altered geometry at the peptidyl transferase center. PLoS Biology 9 (1), p. e1000581 (2011)

MPG.PuRe

Journal Article

Blau, O.; Baldus, C. D.; Hofmann, W. K.; Thiel, G.; Nolte, F.; Burmeister, T.; Turkmen, S.; Benlasfer, O.; Schumann, E.; Sindram, A. et al.; Molkentin, M.; Mundlos, S.; Keilholz, U.; Thiel, E.; Blau, I. W.: Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts. Blood 118 (20), pp. 5583 - 92 (2011)

MPG.PuRe

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Bluemlein, K.; Gruning, N. M.; Feichtinger, R. G.; Lehrach, H.; Kofler, B.; Ralser, M.: No evidence for a shift in pyruvate kinase PKM1 to PKM2 expression during tumorigenesis. Oncotarget 2 (5), pp. 393 - 400 (2011)

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Bluemlein, K.; Ralser, M.: Monitoring protein expression in whole-cell extracts by targeted label- and standard-free LC-MS/MS. Nature Protocols 6 (6), pp. 859 - 69 (2011)

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Bordlein, A.; Scherthan, H.; Nelkenbrecher, C.; Molter, T.; Bosl, M. R.; Dippold, C.; Birke, K.; Kinkley, S.; Staege, H.; Will, H. et al.; Winterpacht, A.: SPOC1 (PHF13) is required for spermatogonial stem cell differentiation and sustained spermatogenesis. J Cell Sci 124 (Pt 18), pp. 3137 - 48 (2011)

MPG.PuRe

Journal Article

Bormann, F.; Sers, C.; Seliger, B.; Handke, D.; Bergmann, T.; Seibt, S.; Lehrach, H.; Dahl, A.: Methylation-specific ligation detection reaction (msLDR): a new approach for multiplex evaluation of methylation patterns. Molecular Genetics and Genomics: MGG 286 (3-4), pp. 279 - 91 (2011)

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Borodina, T.; Adjaye, J.; Sultan, M.: A strand-specific library preparation protocol for RNA sequencing. Methods in Enzymology 500, pp. 79 - 98 (2011)

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Brameier, M.; Herwig, A.; Reinhardt, R.; Walter, L.; Gruber, J.: Human box C/D snoRNAs with miRNA like functions: expanding the range of regulatory RNAs. Nucleic Acids Research 39 (2), pp. 675 - 686 (2011)

MPG.PuRe

DOI

Journal Article

Braunholz, D.; Hullings, M.; Gil-Rodriguez, M. C.; Fincher, C. T.; Mallozzi, M. B.; Loy, E.; Albrecht, M.; Kaur, M.; Limon, J.; Rampuria, A. et al.; Clark, D.; Kline, A.; Dalski, A.; Eckhold, J.; Tzschach, A.; Hennekam, R.; Gillessen-Kaesbach, G.; Wierzba, J.; Krantz, I. D.; Deardorff, M. A.; Kaiser, F. J.: Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. Eur J Hum Genet (2011)

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Journal Article

Brinkmeyer, J.; Mobascher, A.; Musso, F.; Schmitz, M.; Wagner, M.; Frommann, I.; Grunder, G.; Spreckelmeyer, K. N.; Wienker, T.; Diaz-Lacava, A. et al.; Holler, D.; Dahmen, N.; Thuerauf, N.; Clepce, M.; Kiefer, F.; de Millas, W.; Gallinat, J.; Winterer, G.: P50 sensory gating and smoking in the general population. Addict Biol 16 (3), pp. 485 - 98 (2011)

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Journal Article

Budkevich, T.; Giesebrecht, J.; Altman, R. B.; Munro, J. B.; Mielke, T.; Nierhaus, K. H.; Blanchard, S. C.; Spahn, C. M.: Structure and dynamics of the mammalian ribosomal pretranslocation complex. Mol Cell 44 (2), pp. 214 - 24 (2011)

MPG.PuRe

Journal Article

Budkevich, T.; Giesebrecht, J.; Altman, R. B.; Munro, J. B.; Mielke, T.; Nierhaus, K. H.; Blanchard, S. C.; Spahn, C. M.: Structure and dynamics of the mammalian ribosomal pretranslocation complex. Molecular Cell 44 (2), pp. 214 - 24 (2011)

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Journal Article

Buonincontri, R.; Bache, I.; Silahtaroglu, A.; Elbro, C.; Nielsen, A. M.; Ullmann, R.; Arkesteijn, G.; Tommerup, N.: A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1. Behav Genet 41 (1), pp. 125 - 33 (2011)

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Journal Article

Busche, A.; Graul-Neumann, L. M.; Zweier, C.; Rauch, A.; Klopocki, E.; Horn, D.: Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature. Eur J Med Genet 54 (3), pp. 256 - 61 (2011)

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Journal Article

Cavill, R.; Kamburov, A.; Ellis, J. K.; Athersuch, T. J.; Blagrove, M. S.; Herwig, R.; Ebbels, T. M.; Keun, H. C.: Consensus-phenotype integration of transcriptomic and metabolomic data implies a role for metabolism in the chemosensitivity of tumour cells. PLoS Computational Biology 7 (3), p. e1001113 (2011)

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Journal Article

Chatzinasiou, F.; Lill, C. M.; Kypreou, K.; Stefanaki, I.; Nicolaou, V.; Spyrou, G.; Evangelou, E.; Roehr, J. T.; Kodela, E.; Katsambas, A. et al.; Tsao, H.; Ioannidis, J. P.; Bertram, L.; Stratigos, A. J.: Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. Journal of the National Cancer Institute 103 (16), pp. 1227 - 35 (2011)

MPG.PuRe

Journal Article

Cichon, S.; Muhleisen, T. W.; Degenhardt, F. A.; Mattheisen, M.; Miro, X.; Strohmaier, J.; Steffens, M.; Meesters, C.; Herms, S.; Weingarten, M. et al.; Priebe, L.; Haenisch, B.; Alexander, M.; Vollmer, J.; Breuer, R.; Schmal, C.; Tessmann, P.; Moebus, S.; Wichmann, H. E.; Schreiber, S.; Muller-Myhsok, B.; Lucae, S.; Jamain, S.; Leboyer, M.; Bellivier, F.; Etain, B.; Henry, C.; Kahn, J. P.; Heath, S.; Hamshere, M.; O'Donovan, M. C.; Owen, M. J.; Craddock, N.; Schwarz, M.; Vedder, H.; Kammerer-Ciernioch, J.; Reif, A.; Sasse, J.; Bauer, M.; Hautzinger, M.; Wright, A.; Mitchell, P. B.; Schofield, P. R.; Montgomery, G. W.; Medland, S. E.; Gordon, S. D.; Martin, N. G.; Gustafsson, O.; Andreassen, O.; Djurovic, S.; Sigurdsson, E.; Steinberg, S.; Stefansson, H.; Stefansson, K.; Kapur-Pojskic, L.; Oruc, L.; Rivas, F.; Mayoral, F.; Chuchalin, A.; Babadjanova, G.; Tiganov, A. S.; Pantelejeva, G.; Abramova, L. I.; Grigoroiu-Serbanescu, M.; Diaconu, C. C.; Czerski, P. M.; Hauser, J.; Zimmer, A.; Lathrop, M.; Schulze, T. G.; Wienker, T. F.; Schumacher, J.; Maier, W.; Propping, P.; Rietschel, M.; Nothen, M. M.: Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 88 (3), pp. 372 - 81 (2011)

MPG.PuRe

Journal Article

Cingoz, S.; Bache, I.; Bjerglund, L.; Ropers, H. H.; Tommerup, N.; Jensen, H.; Brondum-Nielsen, K.; Tumer, Z.: Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects. Am J Med Genet A 155A (1), pp. 203 - 6 (2011)

MPG.PuRe

Journal Article (247)