Publikationen von B. Timmermann

A. Kohlmann, H. U. Klein, S. Weissmann, S. Bresolin, T. Chaplin, H. Cuppens, E. Haschke-Becher, B. Garicochea, V. Grossmann, B. Hanczaruk, K. Hebestreit, C. Gabriel, I. Iacobucci, J. H. Jansen, G. te Kronnie, L. van de Locht, G. Martinelli, K. McGowan, M. R. Schweiger, B. Timmermann, P. Vandenberghe, B. D. Young, M. Dugas, and T. Haferlach, "The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories," Leukemia: Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K 25 (12), 1840-8 (2011).

A. Prigione, B. Lichtner, H. Kuhl, E. A. Struys, M. Wamelink, H. Lehrach, M. Ralser, B. Timmermann, and J. Adjaye, "Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming," Stem Cells 29 (9), 1338-48 (2011).

M. R. Schweiger, M. Kerick, B. Timmermann, and M. Isau, "The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations," Cancer Metastasis Reviews 30 (2), 199-210 (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).

M. Kerick, B. Timmermann, and M. R. Schweiger, "High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue," Pathologe 31 (suppl 2), 255-257 (2010).

L. Chavez, J. Jozefczuk, C. Grimm, J. Dietrich, B. Timmermann, H. Lehrach, R. Herwig, and J. Adjaye, "Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage," Genome Research 20, 1441-1450 (2010).

B. Timmermann, S. Jarolim, H. Russmayer, M. Kerick, S. Michel, A. Krüger, K. Bluemlein, P. Laun, J. Grillari, H. Lehrach, M. Breitenbach, and M. Ralser, "A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging.," Aging (Albany NY) 2 (8), 475-486 (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).

Anja Weise, Bernd Timmermann, Manfred Grabherr, Martin Werber, Patricia Heyn, Nadezdaa Kosyakova, Thomas Liehr, Heidemarie Neitzel, Kateryna Konrat, Christiane Bommer, Carola Dietrich, Anna Rajab, Richard Reinhardt, Stefan Mundlos, Tom H. Lindner, and Katrin Hoffmann, "High-throughput sequencing of microdissected chromosomal regions.," European Journal of Human Genetics , 1-6 (2009).

Michal R. Schweiger, Martin Kerick, Bernd Timmermann, Marcus W. Albrecht, Tatjana Borodina, Dmitri Parkhomchuk, Kurt Zatloukal, and Hans Lehrach, "Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis.," PLoS ONE 4 (5), e5548-e5548 (2009).

Markus Ralser, Almut Nebel, Rabea Kleindorp, Sylvia Krobitsch, Hans Lehrach, Stefan Schreiber, Richard Reinhardt, and Bernd Timmermann, "Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans," BMC Genetics 9, 9:38-9:38 (2008).

Markus Ralser, Almut Nebel, Rabea Kleindorp, Sylvia Krobitsch, Hans Lehrach, Stefan Schreiber, Richard Reinhardt, and Bernd Timmermann, "Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans," BMC Genetics 9, 9:38-9:38 (2008).

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

Bernd Timmermann, Sascha Sauer, Heymut Omran, Ralf Sudbrak, and Richard Reinhardt, "Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG," GenomXPress: Informationen aus der Deutschen Genomforschung 2004 (1), 17-19 (2004).

Margret R. Hoehe, Bernd Timmermann, and Hans Lehrach, "Human inter-individual DNA sequence variation in candidate genes, drug targets, the importance of haplotypes and pharmacogenomics," Current Pharmaceutical Biotechnology 4 (6), 351-378 (2003).

Andreas Busjahn, Kristina Freier, Hans-Dieter Faulhaber, Guo-Hua Li, Magda Rosenthal, Jens Jordan, Margret R. Hoehe, Bernd Timmermann, and Friedrich C. Luft, "Beta-2 Adrenergic receptor gene variations and coping styles in twins," Biological Psychology 61 (1 - 2), 97-109 (2002).

Margret R. Hoehe, Bernd Timmermann, and Hans Lehrach, "Haplotypen und die systematische Analyse genetischer Variation: Krankheitsgene, „Drug Targets“ und Pharmakogenomik," Proteomics & Drug Development , 478-485 (2002).

Mike Bridavsky, Heiner Kuhl, Arthur Woodruff, Uwe Kornak, Bernd Timmermann, Norbert Mages, 99 Lives Consortium, Dario G. Lupiáñez, Orsolya Symmons, and Daniel M. Ibrahim, "Crowdfunded whole-genome sequencing of the celebrity cat Lil BUB identifies causal mutations for her osteopetrosis and polydactyly", in bioRxiv: the preprint server for biology, (Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 2019).

Matthias Lienhard, Twan van den Beucken, Bernd Timmermann, Myriam Hochradel, Stefan Boerno, Florian Caiment, Martin Vingron, and Ralf Herwig, "Long-read transcriptome sequencing analysis with IsoTools", in bioRxiv, (2021).

S. Smajić, C. A. Prada-Medina, Z. Landoulsi​, C. Dietrich, J. Jarazo, J. Henck, S. Balachandran, S. Pachchek, C. M. Morris, P. Antony, B. Timmermann, S. Sauer, J. C. Schwamborn, P. May, A. Grünewald, and M. Spielmann, "Single-cell sequencing of the human midbrain reveals glial activation and a neuronal state specific to Parkinson’s disease", in medRxiv, (2020).