Liu, C.; Young, A. L.; Starling-Windhof, A.; Bracher, A.; Saschenbrecker, S.; Rao, B. V.; Rao, K. V.; Berninghausen, O.; Mielke, T.; Hartl, F. U. et al.; Beckmann, R.; Hayer-Hartl, M.: Coupled chaperone action in folding and assembly of hexadecameric Rubisco. Nature 463 (7278), S. 197 - 202 (2010)

Gruning, N. M.; Lehrach, H.; Ralser, M.: Regulatory crosstalk of the metabolic network. Trends in Biochemical Sciences 35 (4), S. 220 - 227 (2010)

Albrecht, M.; Sharma, C. M.; Reinhardt, R.; Vogel, J.; Rudel, T.: Deep sequencing-based discovery of the Chlamydia trachomatis transcriptome. Nucleic Acids Research 38 (3), S. 868 - 877 (2010)

Attarbaschi, A.; Pisecker, M.; Inthal, A.; Mann, G.; Janousek, D.; Dworzak, M.; Pötschger, U.; Ullmann, R.; Schrappe, M.; Gadner, H. et al.; Haas, O. A.; Panzer-Grümayer, R.; Strehl, S.: Prognostic relevance of TLX3 (HOX11L2) expression in childhood T-cell acute lymphoblastic leukaemia treated with Berlin–Frankfurt–Münster (BFM) protocols containing early and late re-intensification elements. British Journal of Hematology 148 (2), S. 293 - 300 (2010)

Bertram, L.; Tanzi, R. E.: Alzheimer disease: new light on an old CLU. Nature Reviews Neurology 6 (1), S. 11 - 13 (2010)

Chen, W.; Ullmann, R.; Langnick, C.; Menzel, C.; Wotschofsky, Z.; Hu, H.; Döring, A.; Hu, Y.; Kang, H.; Tzschach, A. et al.; Hoeltzenbein, M.; Neitzel, H.; Markus, S.; Wiedersberg, E.; Kistner, G.; van Ravenswaaij-Arts, C. M. A.; Kleefstra, T.; Kalscheuer, V. M.; Ropers, H.-H.: Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing. European Journal of Human Genetics (2010)

Córdova-Fletes, C.; Rademacher, N.; Müller, I.; Mundo-Ayala, J. N.; Morales-Jeanhs, E. A.; García-Ortiz, J. E.; León-Gil, A.; Rivera, H.; Domínguez, M. G.; Kalscheuer, V. M.: CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndrome. Clinical Genetics 77 (1), S. 92 - 96 (2010)

Dahl, A.; Mertes, F.; Marchfelder, U.; Boerno, S.; Fischer, A.; Schweiger, M.; Lehrach, H.: Bewertung der SOLiD-Sequenzierungsplattform aus Nutzerperspektive. Laborwelt 11 (1), S. 8 - 10 (2010)

Di Stefano, B.; Buecker, C.; Ungaro, F.; Prigione, A.; Chen, H. H.; Welling, M.; Eijpe, M.; Mostoslavsky, G.; Tesar, P.; Adjaye, J. et al.; Geijsen, N.; Broccoli, V.: An ES-like pluripotent state in FGF-dependent murine iPS cells. PLoS ONE 5 (12), S. e16092 - e16092 (2010)

Dolan, S. M.; Hollegaard, M. V.; Merialdi, M.; Betran, A. P.; Allen, T.; Abelow, C.; Nace, J.; Lin, B. K.; Khoury, M. J.; Ioannidis, J. P. et al.; Bagade, S.; Zheng, X.; Dubin, R. A.; Bertram, L.; Velez Edwards, D. R.; Menon, R.: Synopsis of preterm birth genetic association studies: the preterm birth genetics knowledge base (PTBGene). Public Health Genomics 13 (7-8), S. 514 - 523 (2010)

Emde, A. K.; Grunert, M.; Weese, D.; Reinert, K.; Sperling, S. R.: MicroRazerS: rapid alignment of small RNA reads. Bioinformatics 26 (1), S. 123 - 124 (2010)

Endele, S.; Rosenberger, G.; Geider, K.; Popp, B.; Tamer, C.; Stefanova, I.; Milh, M.; Kortum, F.; Fritsch, A.; Pientka, F. K. et al.; Hellenbroich, Y.; Kalscheuer, V. M.; Kohlhase, J.; Moog, U.; Rappold, G.; Rauch, A.; Ropers, H. H.; von Spiczak, S.; Tonnies, H.; Villeneuve, N.; Villard, L.; Zabel, B.; Zenker, M.; Laube, B.; Reis, A.; Wieczorek, D.; Van Maldergem, L.; Kutsche, K.: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet 42 (11), S. 1021 - 6 (2010)

Groth, D.; Hartmann, S.; Friemel, M.; Hill, N.; Muller, S.; Poustka, A. J.; Panopoulou, G.: Data integration using scanners with SQL output--the bioscanners project at sourceforge. Journal of Integrative Bioinformatics 7 (3), S. e122 - e122 (2010)

Hache, H.; Wierling, C.: Computerprogramme zur Modellierung genregulatorischer Netzwerke. Laborwelt 1, S. 31 - 32 (2010)

Harhausen, D.; Khojasteh, U.; Stahel, P. F.; Morgan, B. P.; Nietfeld, W.; Dirnagl, U.; Trendelenburg, G.: Membrane attack complex inhibitor CD59a protects against focal cerebral ischemia in mice. Journal of Neuroinflammation 7, S. 7:15 - 7:15 (2010)

Kim, G.-J.; Georg, I.; Scherthan, H.; Merkenschlager, M.; Guillou, F.; Scherer, G.; Barrionuevo, F.: Dicer is required for Sertoli cell function and survival. International Journal of Developmental Biology 54, S. 867 - 875 (2010)

Konrad, K.; Dempfle, A.; Friedel, S.; Heiser, P.; Holtkamp, K.; Walitza, S.; Sauer, S.; Warnke, A.; Remschmidt, H.; Gilsbach, S. et al.; Schäfer, H.; Hinney, A.; Hebebrand, J.; Herpertz-Dahlmann, B.: Familiality and molecular genetics of attention networks in ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (1), S. 148 - 158 (2010)

Köster, D. M.; Wild, R.: Arrays, Sequenzer und funktionelle Genomik im Focus. Laborwelt 11 (2), S. 29 - 30 (2010)

Krawitz, P.; Rödelsperger, C.; Jäger, M.; Jostins, L.; Bauer, S.; Robinson, P. N.: Microindel detection in short-read sequence data. Bioinformatics 26 (6), S. 722 - 729 (2010)

Lambert, J. C.; Sleegers, K.; Gonzalez-Perez, A.; Ingelsson, M.; Beecham, G. W.; Hiltunen, M.; Combarros, O.; Bullido, M. J.; Brouwers, N.; Bettens, K. et al.; Berr, C.; Pasquier, F.; Richard, F.; Dekosky, S. T.; Hannequin, D.; Haines, J. L.; Tognoni, G.; Fievet, N.; Dartigues, J. F.; Tzourio, C.; Engelborghs, S.; Arosio, B.; Coto, E.; De Deyn, P.; Del Zompo, M.; Mateo, I.; Boada, M.; Antunez, C.; Lopez-Arrieta, J.; Epelbaum, J.; Schjeide, B. M.; Frank-Garcia, A.; Giedraitis, V.; Helisalmi, S.; Porcellini, E.; Pilotto, A.; Forti, P.; Ferri, R.; Delepine, M.; Zelenika, D.; Lathrop, M.; Scarpini, E.; Siciliano, G.; Solfrizzi, V.; Sorbi, S.; Spalletta, G.; Ravaglia, G.; Valdivieso, F.; Vepsalainen, S.; Alvarez, V.; Bosco, P.; Mancuso, M.; Panza, F.; Nacmias, B.; Bossu, P.; Hanon, O.; Piccardi, P.; Annoni, G.; Mann, D.; Marambaud, P.; Seripa, D.; Galimberti, D.; Tanzi, R. E.; Bertram, L.; Lendon, C.; Lannfelt, L.; Licastro, F.; Campion, D.; Pericak-Vance, M. A.; Soininen, H.; Van Broeckhoven, C.; Alperovitch, A.; Ruiz, A.; Kamboh, M. I.; Amouyel, P.: The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. J Alzheimers Dis 22 (1), S. 247 - 255 (2010)