Publications 2011

Year
21.
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), 279-91 (2011)
22.
Borodina, T.; Adjaye, J.; Sultan, M.;
A strand-specific library preparation protocol for RNA sequencing. Methods in Enzymology 500, 79-98 (2011)
23.
Braig, F.;
A novel approach for the generation of full Ig-repertoire-based antibody phage display libraries. Universität Potsdam, Potsdam.
24.
Braunholz, D.; Hullings, M.; Gil-Rodriguez, M. C.; Fincher, C. T.; Mallozzi, M. B.; Loy, E.; Albrecht, M.; Kaur, M.; Limon, J.; Rampuria, A.; 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)
25.
Brinkmeyer, J.; Mobascher, A.; Musso, F.; Schmitz, M.; Wagner, M.; Frommann, I.; Grunder, G.; Spreckelmeyer, K. N.; Wienker, T.; Diaz-Lacava, A.; 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), 485-98 (2011)
26.
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), 214-24 (2011)
27.
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), 214-24 (2011)
28.
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), 125-33 (2011)
29.
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), 256-61 (2011)
30.
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), e1001113 (2011)
31.
Chatzinasiou, F.; Lill, C. M.; Kypreou, K.; Stefanaki, I.; Nicolaou, V.; Spyrou, G.; Evangelou, E.; Roehr, J. T.; Kodela, E.; Katsambas, A.; 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), 1227-35 (2011)
32.
Chavez, L.;
Epigenetic Analysis of Human Embryonic Stem Cells- Basics, Computational Methods, Applications. Book, 140 (2011)
33.
Cichon, S.; Muhleisen, T. W.; Degenhardt, F. A.; Mattheisen, M.; Miro, X.; Strohmaier, J.; Steffens, M.; Meesters, C.; Herms, S.; Weingarten, M.; 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), 372-81 (2011)
34.
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), 203-6 (2011)
35.
Clark, M. S.;
Long-term survival of hydrated resting eggs from Brachionus plicatilis. PLoS ONE, (2011)
36.
Clement, Y.; Arndt, P. F.;
Substitution patterns are under different influences in primates and rodents. Genome Biol Evol 3, 236-45 (2011)
37.
Conrad, D. F.; Keebler, J. E.; DePristo, M. A.; Lindsay, S. J.; Zhang, Y.; Casals, F.; Idaghdour, Y.; Hartl, C. L.; Torroja, C.; Garimella, K. V.; Zilversmit, M.; Cartwright, R.; Rouleau, G. A.; Daly, M.; Stone, E. A.; Hurles, M. E.; Awadalla, P.;
Variation in genome-wide mutation rates within and between human families. Nature Genetics 43 (7), 712-4 (2011)
38.
Cusack, B. P.; Arndt, P. F.; Duret, L.; Roest Crollius, H.;
Preventing dangerous nonsense: selection for robustness to transcriptional error in human genes. PLoS Genet 7 (10), e1002276 (2011)
39.
Czeko, E.; Seizl, M.; Augsberger, C.; Mielke, T.; Cramer, P.;
Iwr1 directs RNA polymerase II nuclear import. Molecular Cell 42 (2), 261-6 (2011)
40.
Danecek, P.; Auton, A.; Abecasis, G.; Albers, C. A.; Banks, E.; DePristo, M. A.; Handsaker, R. E.; Lunter, G.; Marth, G. T.; Sherry, S. T.; McVean, G.; Durbin, R.;
The variant call format and VCFtools. Bioinformatics 27 (15), 2156-8 (2011)
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