Publikationen von A. Dahl

V. Colonna, Q. Ayub, Y. Chen, L. Pagani, P. Luisi, M. Pybus, E. Garrison, Y. Xue, C. Tyler-Smith, Consortium 1000 Genomes Project, R. Sudbrak, M. Albrecht, V. Amstislavskiy, T. A. Borodina, A. Dahl, A. Davydov, R. Herwig, P. Marquardt, F. Mertes, W. Nietfeld, D. Parkhomchuk, A. V. Soldatov, B. Timmermann, M. Tolzmann, H. Lehrach, and M. L. Yaspo, "Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences," Genome Biology: Biology for the Post-Genomic Era 15 (6), R88 (2014).

The 1000 Genomes Project Consortium, Ralf Sudbrak, Marcus Albrecht, Vyacheslav Amstislavskiy, Tatiana A. Borodina, Andreas Dahl, Alexey Davydov, Ralf Herwig, Peter Marquardt, Florian Mertes, Wilfried Nietfeld, Dmitri Parkhomchuk, Aleksey Soldatov, Bernd Timmermann, Marius Tolzmann, and Hans Lehrach, "The 1000 Genomes Project: data management and community access," Nature methods 9 (5), 459-462 (2012).

D. G. MacArthur, S. Balasubramanian, A. Frankish, Consortium 1000 Genomes Project, R. Sudbrak, M. W. Albrecht , V. Amstislavskiy, T. A. Borodina, Andreas Dahl, A. Davydov, R. Herwig, P. Marquardt, F. Mertes, W. Nietfeld, D. Parkhomchuk, A. Soldatov, B. Timmermann, M. Tolzmann, and H. Lehrach, "A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes," Science 335 (6070), 823-828 (2012).

F. Bormann, C. Sers, B. Seliger, D. Handke, T. Bergmann, S. Seibt, H. Lehrach, and A. Dahl, "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).

H. von Keyserling, T. Bergmann, M. Schuetz, U. Schiller, J. Stanke, C. Hoffmann, A. Schneider, H. Lehrach, A. Dahl, and A. M. Kaufmann, "Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure," International Journal of Gynecological Cancer: Official Journal of the International Gynecological Cancer Society 21 (9), 1664-71 (2011).

F. Mertes, K. Biens, H. Lehrach, M. Wagner, and A. Dahl, "High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR.," J Microbiol Methods 83 (2), 217-223 (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, B. Timmermann, and H. Lehrach, "The application of massively parallel sequencing technologies in diagnostics," F1000 Biology Reports 2, 2:59-2:59 (2010).

Anne-Kathrin Scholz, Bert M. Klebl, Markus Morkel, Hans Lehrach, Andreas Dahl, and Bodo M.H. Lange, "A Flexible Multiwell Format for Immunofluorescence Screening Microscopy of Small-Molecule Inhibitors.," Assay and Drug Development Technologies. 8 (5), 571-580 (2010).

T. A. McMeekin, C. Hill, M. Wagner, A. Dahl, and T. Ross, "Ecophysiology of food-borne pathogens: Essential knowledge to improve food safety.," International Journal of Food Microbiology 139 (Suppl 1), S64-78 (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).

Pamela Kepper, Richard Reinhardt, Andreas Dahl, Hans Lehrach, and Sascha Sauer, "Matrix-Assisted Laser Desorption/Ionization Mass Spectrometric Analysis of DNA on Microarrays," Clinical Chemistry: International Journal of Molecular Diagnostics and Laboratory Medicine 52 (7), 1303-1310 (2007).

Andreas Dahl, Marc Sultan, Alexander Jung, Regine Schwartz, Matthias Lange, Michael Steinwand, Kenneth J. Livak, Hans Lehrach, and Lajos Nyarsik, "Quantitative PCR based expression analysis on a nanoliter scale using polymer nano-well chips," Biomedical Microdevices 9 (3), 307-314 (2007).

Sascha Sauer, Pamela Kepper, Anett Smyra, Andreas Dahl, Falk-Thilo Ferse, Hans Lehrach, and Richard Reinhardt, "Automated solid-phase extraction for purification of single nucleotide polymorphism genotyping products prior to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometric analysis," Journal of Chromatography A 1049 (1-2), 9-16 (2004).

Bernd Timmermann, Sascha Sauer, Andreas Dahl, and Richard Reinhardt, "Genetische Variabilität des Menschen: Hochdurchsatz- Technologien und Datenanalyse," Laborwelt 5 (5), 31-32 (2004).

Andreas Dahl, Development of a miniaturised platform for PCR based assays with application in gene expression analysis and SNP genotyping, PhD Thesis, Freie Universität, 2007.