Publikationen von A. Fischer

S. Börno, A. Fischer, M. Kerick, M. Falth, M. Laible, J. C. Brase, R. Kuner, A. Dahl, C. Grimm, B. Sayanjali, M. Isau, C. Röhr, A. Wunderlich, B. Timmermann, R. Claus, C. Plass, M. Graefen, R. Simon, F. Demichelis, M. A. Rubin, G. Sauter, T. Schlomm, H. Sültmann, H. Lehrach, and M. R. Schweiger, "Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation," Cancer Discovery 2 (11), 1024-1035 (2012).

Robert Querfurth, Axel Fischer, Michal R. Schweiger, Hans Lehrach, and Florian Mertes, "Creation and application of immortalized bait libraries for targeted enrichment and next-generation sequencing," Biotechniques 52 (6), 375-380 (2012).

A. Pangrazio, B. Cassani, M. M. Guerrini, J. C. Crockett, V. Marrella, L. Zammataro, D. Strina, A. Schulz, C. Schlack, U. Kornak, D. J. Mellis, A. Duthie, M. H. Helfrich, A. Durandy, D. Moshous, A. Vellodi, R. Chiesa, P. Veys, N. L. Iacono, P. Vezzoni, A. Fischer, A. Villa, and C. Sobacchi, "RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations," J Bone Miner Res (2011).

B. Timmermann, M. Kerick, C. Roehr, A. Fischer, M. Isau, S. T. Boerno, A. Wunderlich, C. Barmeyer, P. Seemann, J. Koenig, M. Lappe, A. W. Kuss, M. Garshasbi, L. Bertram, K. Trappe, M. Werber, B. G. Herrmann, K. Zatloukal, H. Lehrach, and M. R. Schweiger (ed), "Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis," PLoS ONE 5 (12), e15661-e15661 (2010).

P. M. Krawitz, M. R. Schweiger, C. Rödelsperger, C. Marcelis, U. Kölsch, C. Meisel, F. Stephani, T. Kinoshita, Y. Murakami, S. Bauer, M. Isau, A. Fischer, A. Dahl, M. Kerick, J. Hecht, S. Köhler, M. Jager, J. Grünhagen, B. J. de Condor, S. Doelken, H. G. Brunner, P. Meinecke, E. Passarge, M. D. Thompson, D. E. Cole, D. Horn, T. Roscioli, S. Mundlos, and P. N. Robinson, "Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.," Nature Genetics 42 (10), 827-829 (2010).

P. M. Krawitz, M. R. Schweiger, C. Rödelsperger, C. Marcelis, U. Kölsch, C. Meisel, F. Stephani, T. Kinoshita, Y. Murakami, S. Bauer, M. Isau, A. Fischer, A. Dahl, M. Kerick, J. Hecht, S. Köhler, M. Jager, J. Grünhagen, B. J. de Condor, S. Doelken, H. G. Brunner, P. Meinecke, E. Passarge, M. D. Thompson, D. E. Cole, D. Horn, T. Roscioli, S. Mundlos, and P. N. Robinson, "Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.," Nature Genetics 42 (10), 827-829 (2010).

P. M. Krawitz, M. R. Schweiger, C. Rödelsperger, C. Marcelis, U. Kölsch, C. Meisel, F. Stephani, T. Kinoshita, Y. Murakami, S. Bauer, M. Isau, A. Fischer, A. Dahl, M. Kerick, J. Hecht, S. Köhler, M. Jager, J. Grünhagen, B. J. de Condor, S. Doelken, H. G. Brunner, P. Meinecke, E. Passarge, M. D. Thompson, D. E. Cole, D. Horn, T. Roscioli, S. Mundlos, and P. N. Robinson, "Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.," Nature Genetics 42 (10), 827-829 (2010).

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