Journal Article (40)
21.
Journal Article
4 (68) (2011)
Technical Challenges of targeted DNA Enrichment to identify Geneic Variations in Cancer Patiens. BMC Medical Genomics 22.
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 23.
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 24.
Journal Article
15 (2), pp. 311 - 24 (2011)
The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response. Antioxidants & Redox Signaling 25.
Journal Article
RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. J Bone Miner Res (2011)
26.
Journal Article
27 (6), pp. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 27.
Journal Article
27 (6), pp. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 28.
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 29.
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 30.
Journal Article
31 (suppl 2), pp. 255 - 257 (2010)
High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue. Pathologe 31.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 32.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 33.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 34.
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) 35.
Journal Article
2 (2), pp. 199 - 207 (2010)
Next-generation sequencing technologies for DNA methylation analyses in cancer genomics. Epigenomics 36.
Journal Article
11 (1), pp. 8 - 10 (2010)
Bewertung der SOLiD-Sequenzierungsplattform aus Nutzerperspektive. Laborwelt 37.
Journal Article
33 (suppl 2), pp. 115 - 128 (2010)
The genome maintenance and transcriptional regulation mechanisms of human high risk papillomaviruses as target points for antiviral treatment and cervical cancer prevention. Onkologie 38.
Journal Article
4 (5), p. e5548 - e5548 (2009)
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 39.
Journal Article
5 (2), pp. 82 - 84 (2008)
From Bench to Bedside: New Technologies for Cancer Diagnosis and Treatment. Journal of International Biotechnology Law 40.
Journal Article
359 (3), pp. 574 - 579 (2007)
TLR2 has a detrimental role in mouse transient focal cerebral ischemia. Biochemical and Biophysical Research Communications (Orlando, FL)