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Lange, B.M.H.; Schweiger, R.M.; Lehrach, H.: Global molecular and cellular measurement technologies. book chapter. Editors, Cesario A Marcus F B City: Heidelberg, New York (Book Title: Cancer Systems Biology, Bioinformatics and Medicine), pp. 97 - 126 (2011)

Lange, C.; Li, C.; Manjubala, I.; Wagermaier, W.; Kuhnisch, J.; Kolanczyk, M.; Mundlos, S.; Knaus, P.; Fratzl, P.: Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatite. J Struct Biol 176 (2), pp. 159 - 67 (2011)

Lehrach, H.: ITFoM - The IT Future of Medicine. Procedia Computer Science 7, pp. 26 - 29 (2011)

Lesch, K. P.; Selch, S.; Renner, T. J.; Jacob, C.; Nguyen, T. T.; Hahn, T.; Romanos, M.; Walitza, S.; Shoichet, S.; Dempfle, A. et al.; Heine, M.; Boreatti-Hummer, A.; Romanos, J.; Gross-Lesch, S.; Zerlaut, H.; Wultsch, T.; Heinzel, S.; Fassnacht, M.; Fallgatter, A.; Allolio, B.; Schafer, H.; Warnke, A.; Reif, A.; Ropers, H. H.; Ullmann, R.: Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. Mol Psychiatry 16 (5), pp. 491 - 503 (2011)

Leushacke, M.; Sporle, R.; Bernemann, C.; Brouwer-Lehmitz, A.; Fritzmann, J.; Theis, M.; Buchholz, F.; Herrmann, B. G.; Morkel, M.: An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression. PLoS ONE 6 (8), p. e23381 - e23381 (2011)

Lill, C. M.; Abel, O.; Bertram, L.; Al-Chalabi, A.: Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases. Amyotrophic Lateral Sclerosis: Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 12 (4), pp. 238 - 49 (2011)

Lill, C. M.; Bertram, L.: Towards unveiling the genetics of neurodegenerative diseases. Seminars in Neurology 31 (5), pp. 531 - 41 (2011)

Lim, T. S.; Schutze, T.; Lehrach, H.; Glokler, J.; Konthur, Z.: Diversity visualization by endonuclease: a rapid assay to monitor diverse nucleotide libraries. Analytical Biochemistry 411 (1), pp. 16 - 21 (2011)

Lin, S.; Haas, S.; Zemojtel, T.; Xiao, P.; Vingron, M.; Li, R.: Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators. Gene 473 (2), pp. 139 - 49 (2011)

Lindblom, A.; Robinson, P. N.: Bioinformatics for human genetics: promises and challenges. Hum Mutat 32 (5), pp. 495 - 500 (2011)

Lindenberg, A.; Brinkmeyer, J.; Dahmen, N.; Gallinat, J.; de Millas, W.; Mobascher, A.; Wagner, M.; Schulze-Rauschenbach, S.; Grunder, G.; Spreckelmeyer, K. N. et al.; Clepce, M.; Thurauf, N.; von der Goltz, C.; Kiefer, F.; Steffens, M.; Holler, D.; Diaz-Lacava, A.; Wienker, T.; Winterer, G.: The German multi-centre study on smoking-related behavior-description of a population-based case-control study. Addict Biol 16 (4), pp. 638 - 53 (2011)

Liu, Z.; Fusi, A.; Klopocki, E.; Schmittel, A.; Tinhofer, I.; Nonnenmacher, A.; Keilholz, U.: Negative enrichment by immunomagnetic nanobeads for unbiased characterization of circulating tumor cells from peripheral blood of cancer patients. J Transl Med 9, p. 70 (2011)

Llorens, F.; Hummel, M.; Pastor, X.; Ferrer, A.; Pluvinet, R.; Vivancos, A.; Castillo, E.; Iraola, S.; Mosquera, A. M.; Gonzalez, E. et al.; Lozano, J.; Ingham, M.; Dohm, J. C.; Noguera, M.; Kofler, R.; del Rio, J. A.; Bayes, M.; Himmelbauer, H.; Sumoy, L.: Multiple platform assessment of the EGF dependent transcriptome by microarray and deep tag sequencing analysis. BMC Genomics 12, p. 326 (2011)

Love, M. I.; Mysickova, A.; Sun, R.; Kalscheuer, V. M.; Vingron, M.; Haas, S. A.: Modeling read counts for CNV detection in exome sequencing data. Statistical Applications in Genetics and Molecular Biology 10 (1) (2011)

Mah, N.; Wang, Y.; Liao, M. C.; Prigione, A.; Jozefczuk, J.; Lichtner, B.; Wolfrum, K.; Haltmeier, M.; Flottmann, M.; Schaefer, M. et al.; Hahn, A.; Mrowka, R.; Klipp, E.; Andrade-Navarro, M. A.; Adjaye, J.: Molecular insights into reprogramming-initiation events mediated by the OSKM gene regulatory network. PLoS ONE 6 (8), p. e24351 (2011)

Manolopoulos, V. G.; Dechairo, B.; Huriez, A.; Kuhn, A.; Llerena, A.; van Schaik, R. H.; Yeo, K. T.; Ragia, G.; Siest, G.: Pharmacogenomics and personalized medicine in clinical practice. Pharmacogenomics 12 (5), pp. 597 - 610 (2011)

Marchal, J. A.; Ghani, M.; Schindler, D.; Gavvovidis, I.; Winkler, T.; Esquitino, V.; Sternberg, N.; Busche, A.; Krawitz, P.; Hecht, J. et al.; Robinson, P.; Mundlos, S.; Graul-Neumann, L.; Sperling, K.; Trimborn, M.; Neitzel, H.: Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly. Cell Cycle 10 (17), pp. 2967 - 77 (2011)

Marklein, B.; Konthur, Z.; Häupl, T.; Shlomchik, M.; Burmester, G.; Skriner, K.: Toll-like receptor (TLR-7/9), MYOD88, TIR8, dependent and independent autoantigens. Annals of the Rheumatic Diseases 69 (Suppl 2), pp. A1 - A76 (2011)

Matrai, J.; Cantore, A.; Bartholomae, C. C.; Annoni, A.; Wang, W.; Acosta-Sanchez, A.; Samara-Kuko, E.; De Waele, L.; Ma, L.; Genovese, P. et al.; Damo, M.; Arens, A.; Goudy, K.; Nichols, T. C.; von Kalle, C.; MK, L. C.; Roncarolo, M. G.; Schmidt, M.; Vandendriessche, T.; Naldini, L.: Hepatocyte-targeted expression by integrase-defective lentiviral vectors induces antigen-specific tolerance in mice with low genotoxic risk. Hepatology 53 (5), pp. 1696 - 707 (2011)