Publikationen von Bernd Timmermann
Alle Typen
Zeitschriftenartikel (134)
101.
Zeitschriftenartikel
41 (6), S. 3518 - 3531 (2013)
Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells. Nucleic Acids Research (London) 102.
Zeitschriftenartikel
10 (4), S. 339 - 342 (2013)
A Y2H-seq approach defines the human protein methyltransferase interactome. Nature methods 103.
Zeitschriftenartikel
280 (5), S. 1249 - 66 (2013)
Anterior gradient 2 and 3--two prototype androgen-responsive genes transcriptionally upregulated by androgens and by oestrogens in prostate cancer cells. FEBS Journal 104.
Zeitschriftenartikel
9 (2), S. e1003250 - e1003250 (2013)
DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer. PLoS Genetics 105.
Zeitschriftenartikel
12 (5), S. 411 - 21 (2013)
Genomics and epigenomics: new promises of personalized medicine for cancer patients. Briefings in Functional Genomics 106.
Zeitschriftenartikel
91 (6), S. 1022 - 1031 (2012)
Deleterious- and Disease-Allele Prevalence in Healthy Individuals: Insights from Current Predictions, Mutation Databases, and Population-Scale Resequencing. The American Journal of Human Genetics 107.
Zeitschriftenartikel
7 (12), e44591 (2012)
Mutations of the EPHB6 receptor tyrosine kinase induce a pro-metastatic phenotype in non-small cell lung cancer. PLoS One 108.
Zeitschriftenartikel
51 (12), S. 1114 - 1124 (2012)
Involvement of the MLL gene in adult T-lymphoblastic leukemia. Genes, Chromosomes and Cancer 109.
Zeitschriftenartikel
491 (7422), S. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature 110.
Zeitschriftenartikel
2 (11), S. 1024 - 1035 (2012)
Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation. Cancer Discovery 111.
Zeitschriftenartikel
91 (4), S. 629 - 635 (2012)
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus. American Journal of Human Genetics 112.
Zeitschriftenartikel
18 (5), S. 504 - 507 (2012)
Genomanalyse von Modellorganismen: Saccharomyces cerevisiae. Biospektrum 113.
Zeitschriftenartikel
2 (8), 120093 (2012)
The Saccharomyces cerevisiae W303-K6001 cross-platform genome sequence: insights into ancestry and physiology of a laboratory mutt. Open Biology 114.
Zeitschriftenartikel
9 (5), S. 459 - 462 (2012)
The 1000 Genomes Project: data management and community access. Nature methods 115.
Zeitschriftenartikel
335 (6070), S. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 116.
Zeitschriftenartikel
7 (12), e1002304 (2011)
Combinatorial binding in human and mouse embryonic stem cells identifies conserved enhancers active in early embryonic development. PLoS Comput Biol 117.
Zeitschriftenartikel
4, S. 68 (2011)
Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity. BMC Med Genomics 118.
Zeitschriftenartikel
25 (12), S. 1840 - 8 (2011)
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 119.
Zeitschriftenartikel
29 (9), S. 1338 - 48 (2011)
Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming. Stem Cells 120.
Zeitschriftenartikel
30 (2), S. 199 - 210 (2011)
The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations. Cancer Metastasis Reviews