Publications of B. Timmermann
All genres
Journal Article (130)
101.
Journal Article
12 (5), pp. 411 - 21 (2013)
Genomics and epigenomics: new promises of personalized medicine for cancer patients. Briefings in Functional Genomics 102.
Journal Article
91 (6), pp. 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 103.
Journal Article
7 (12), e44591 (2012)
Mutations of the EPHB6 receptor tyrosine kinase induce a pro-metastatic phenotype in non-small cell lung cancer. PLoS One 104.
Journal Article
51 (12), pp. 1114 - 1124 (2012)
Involvement of the MLL gene in adult T-lymphoblastic leukemia. Genes, Chromosomes and Cancer 105.
Journal Article
491 (7422), pp. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature 106.
Journal Article
2 (11), pp. 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 107.
Journal Article
91 (4), pp. 629 - 635 (2012)
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus. American Journal of Human Genetics 108.
Journal Article
18 (5), pp. 504 - 507 (2012)
Genomanalyse von Modellorganismen: Saccharomyces cerevisiae. Biospektrum 109.
Journal Article
2 (8), 120093 (2012)
The Saccharomyces cerevisiae W303-K6001 cross-platform genome sequence: insights into ancestry and physiology of a laboratory mutt. Open Biology 110.
Journal Article
9 (5), pp. 459 - 462 (2012)
The 1000 Genomes Project: data management and community access. Nature methods 111.
Journal Article
335 (6070), pp. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 112.
Journal Article
7 (12), e1002304 (2011)
Combinatorial binding in human and mouse embryonic stem cells identifies conserved enhancers active in early embryonic development. PLoS Comput Biol 113.
Journal Article
4, p. 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 114.
Journal Article
25 (12), pp. 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 115.
Journal Article
29 (9), pp. 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 116.
Journal Article
30 (2), pp. 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 117.
Journal Article
5 (12), p. e15661 - e15661 (2010)
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS ONE 118.
Journal Article
31 (suppl 2), pp. 255 - 257 (2010)
High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue. Pathologe 119.
Journal Article
20, pp. 1441 - 1450 (2010)
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage. Genome Research 120.
Journal Article
2 (8), pp. 475 - 486 (2010)
A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging. Aging (Albany NY)