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Oskar Haas
Oskar Haas
CCRI
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Year
Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: results in 3184 patients of the …
V Conter, CR Bartram, MG Valsecchi, A Schrauder, R Panzer-Grümayer, ...
Blood, The Journal of the American Society of Hematology 115 (16), 3206-3214, 2010
9462010
MDR1 gene expression and treatment outcome in acute myeloid leukemia
R Pirker, J Wallner, K Geissler, W Linkesch, OA Haas, P Bettelheim, ...
JNCI: Journal of the National Cancer Institute 83 (10), 708-712, 1991
4741991
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome
D Bercovich, I Ganmore, LM Scott, G Wainreb, Y Birger, A Elimelech, ...
The Lancet 372 (9648), 1484-1492, 2008
3952008
Aneurysmal Bone Cyst: A Population Based Epidemiologic Study and Literature Review.
A Leithner, R Windhager, S Lang, OA Haas, F Kainberger, R Kotz
Clinical Orthopaedics and Related Research (1976-2007) 363, 176-179, 1999
3481999
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
L Rainis, D Bercovich, S Strehl, A Teigler-Schlegel, B Stark, J Trka, ...
Blood 102 (3), 981-986, 2003
3182003
Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with at (X; 11)(q13; q23)
A Borkhardt, R Repp, OA Haas, T Leis, J Harbott, J Kreuder, ...
Oncogene 14 (2), 195-202, 1997
3041997
Prognostic impact of specific chromosomal aberrations in a large group of pediatric patients with acute myeloid leukemia treated uniformly according to trial AML-BFM 98
C Von Neuhoff, D Reinhardt, A Sander, M Zimmermann, J Bradtke, ...
Journal of clinical oncology 28 (16), 2682-2689, 2010
2912010
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
RJ Jaju, C Fidler, OA Haas, AJ Strickson, F Watkins, K Clark, NCP Cross, ...
Blood, The Journal of the American Society of Hematology 98 (4), 1264-1267, 2001
2792001
IKZF1plus Defines a New Minimal Residual Disease–Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia
M Stanulla, E Dagdan, M Zaliova, A Möricke, C Palmi, G Cazzaniga, ...
Journal of Clinical Oncology 36 (12), 1240-1249, 2018
2572018
Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia
K Nebral, D Denk, A Attarbaschi, M König, G Mann, OA Haas, S Strehl
Leukemia 23 (1), 134-143, 2009
2532009
Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options
U Fischer, M Forster, A Rinaldi, T Risch, S Sungalee, HJ Warnatz, ...
Nature genetics 47 (9), 1020-1029, 2015
2432015
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
T Akasaka, T Balasas, LJ Russell, K Sugimoto, A Majid, R Walewska, ...
Blood 109 (8), 3451-3461, 2007
2332007
Diagnostic tool for the identification of MLL rearrangements including unknown partner genes
C Meyer, B Schneider, M Reichel, S Angermueller, S Strehl, S Schnittger, ...
Proceedings of the National Academy of Sciences 102 (2), 449-454, 2005
2262005
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21
JD McKay, F Lesueur, L Jonard, A Pastore, J Williamson, L Hoffman, ...
The American Journal of Human Genetics 69 (2), 440-446, 2001
2242001
Mutational Analysis of the SOX9 Gene in Campomelic Dysplasia and Autosomal Sex Reversal: Lack of Genotype/Phenotype Correlations
J Meyer, P Südbeck, M Held, T Wagner, ML Schmitz, F Dagna Bricarelli, ...
Human molecular genetics 6 (1), 91-98, 1997
2191997
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
E Forestier, S Izraeli, B Beverloo, O Haas, A Pession, K Michalová, ...
Blood, The Journal of the American Society of Hematology 111 (3), 1575-1583, 2008
1952008
KIT activating mutations: incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication
A Beghini, CB Ripamonti, R Cairoli, G Cazzaniga, P Colapietro, F Elice, ...
haematologica 89 (8), 920-925, 2004
1932004
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27
E Salzer, S Daschkey, S Choo, M Gombert, E Santos-Valente, S Ginzel, ...
haematologica 98 (3), 473, 2013
1832013
Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance
J Drach, J Angerler, J Schuster, C Rothermundt, R Thalhammer, OA Haas, ...
1811995
Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study
H Hasle, TA Alonzo, A Auvrignon, C Behar, M Chang, U Creutzig, ...
Blood, The Journal of the American Society of Hematology 109 (11), 4641-4647, 2007
1692007
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