Hans A. Kestler
Hans A. Kestler
Professor, Institute of Medical Systems Biology, Ulm University
Verified email at uni-ulm.de - Homepage
Title
Cited by
Cited by
Year
Sequelae of acute myocardial infarction regarding cardiac structure and function and their prognostic significance as assessed by magnetic resonance imaging
V Hombach, O Grebe, N Merkle, S Waldenmaier, M Höher, M Kochs, ...
European heart journal 26 (6), 549-557, 2005
5562005
Three learning phases for radial-basis-function networks
F Schwenker, HA Kestler, G Palm
Neural networks 14 (4-5), 439-458, 2001
5072001
MYC stimulates EZH2 expression by repression of its negative regulator miR-26a
S Sander, L Bullinger, K Klapproth, K Fiedler, HA Kestler, TFE Barth, ...
Blood, The Journal of the American Society of Hematology 112 (10), 4202-4212, 2008
3932008
An expanded genome-wide association study of type 2 diabetes in Europeans
RA Scott, LJ Scott, R Mägi, L Marullo, KJ Gaulton, M Kaakinen, ...
Diabetes 66 (11), 2888-2902, 2017
3322017
BoolNet—an R package for generation, reconstruction and analysis of Boolean networks
C Müssel, M Hopfensitz, HA Kestler
Bioinformatics 26 (10), 1378-1380, 2010
3002010
A differentiation checkpoint limits hematopoietic stem cell self-renewal in response to DNA damage
J Wang, Q Sun, Y Morita, H Jiang, A Groß, A Lechel, K Hildner, ...
Cell 148 (5), 1001-1014, 2012
2832012
Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations
C Schwaenen, M Nessling, S Wessendorf, T Salvi, G Wrobel, ...
Proceedings of the National Academy of Sciences 101 (4), 1039-1044, 2004
2732004
NF-κB controls the global pro-inflammatory response in endothelial cells: evidence for the regulation of a pro-atherogenic program
S Kempe, H Kestler, A Lasar, T Wirth
Nucleic acids research 33 (16), 5308-5319, 2005
2692005
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ...
Nature genetics 47 (12), 1415-1425, 2015
2572015
From individual Wnt pathways towards a Wnt signalling network
HA Kestler, M Kuehl
Philosophical Transactions of the Royal Society B: Biological Sciences 363 …, 2008
2242008
A canonical to non-canonical Wnt signalling switch in haematopoietic stem-cell ageing
MC Florian, KJ Nattamai, K Dörr, G Marka, B Überle, V Vas, C Eckl, ...
Nature 503 (7476), 392-396, 2013
2092013
Transcriptome analysis of microdissected pancreatic intraepithelial neoplastic lesions
M Buchholz, M Braun, A Heidenblut, HA Kestler, G Klöppel, W Schmiegel, ...
Oncogene 24 (44), 6626-6636, 2005
1952005
Genomic DNA-chip hybridization reveals a higher incidence of genomic amplifications in pancreatic cancer than conventional comparative genomic hybridization and leads to the …
K Holzmann, H Kohlhammer, C Schwaenen, S Wessendorf, HA Kestler, ...
Cancer Research 64 (13), 4428-4433, 2004
1732004
Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization
FG Rucker, L Bullinger, C Schwaenen, DB Lipka, S Wessendorf, ...
J Clin Oncol 24 (24), 3887-3894, 2006
1712006
β-Catenin signaling contributes to stemness and regulates early differentiation in murine embryonic stem cells
R Anton, HA Kestler, M Kühl
FEBS letters 581 (27), 5247-5254, 2007
1462007
Lifestyle impacts on the aging‐associated expression of biomarkers of DNA damage and telomere dysfunction in human blood
Z Song, G Von Figura, Y Liu, JM Kraus, C Torrice, P Dillon, ...
Aging cell 9 (4), 607-615, 2010
1442010
Generalized Venn diagrams: a new method of visualizing complex genetic set relations
HA Kestler, A Müller, TM Gress, M Buchholz
Bioinformatics 21 (8), 1592-1595, 2005
1442005
Genomic DNA-chip hybridization in t (11; 14)-positive mantle cell lymphomas shows a high frequency of aberrations and allows a refined characterization of consensus regions
H Kohlhammer, C Schwaenen, S Wessendorf, K Holzmann, HA Kestler, ...
Blood 104 (3), 795-801, 2004
1402004
RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features
VI Gaidzik, V Teleanu, E Papaemmanuil, D Weber, P Paschka, J Hahn, ...
Leukemia 30 (11), 2160-2168, 2016
1302016
Insights into sex chromosome evolution and aging from the genome of a short-lived fish
K Reichwald, A Petzold, P Koch, BR Downie, N Hartmann, S Pietsch, ...
Cell 163 (6), 1527-1538, 2015
1252015
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