OA Haas

St Anna Children's Hospital — Austria

Medicine · Health Sciences

16h-index1.2kcitations22works0.02yr avg
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Research Topics

Acute Myeloid Leukemia Research(10), Acute Lymphoblastic Leukemia research(8), Chronic Myeloid Leukemia Treatments(5), Genomic variations and chromosomal abnormalities(4), Hematopoietic Stem Cell Transplantation(3)

Publications22 total

Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia
Klinische Pädiatrie·2009· 65 cited
Möglichkeiten, Grenzen und Konsequenzen der genetischen Diagnostik im medizinischen Kontext
Journal für Kardiologie (Krause & Pachernegg GmbH)·2006Open Access
MRD levels during the first months of treatment indicate relapses in children with t(12;21)-positive ALL
Leukemia·2000· 6 cited
Allogeneic bone marrow transplantation for juvenile myelomonocytic leukaemia: a single centre experience and review of the literature
Bone Marrow Transplantation·2000· 51 cited
Drug resistance factors in acute myeloid leukemia: a comparative analysis
Leukemia·2000· 61 cited
Monitoring of minimal residual leukemia in patients with MLL-AF9 positive acute myeloid leukemia by RT-PCR
Leukemia·1999· 47 cited
Post-transplant acute myeloid leukemia (PT-AML)
Leukemia·1999· 41 cited
Detection of the WT1 transcript by RT-PCR in complete remission has no prognostic relevance in de novo acute myeloid leukemia
Leukemia·1998· 83 cited
Hematologic malignancies with t(4;11)(q21;q23) – a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases
Leukemia·1998· 150 cited
Comparative genomic hybridization as part of a new diagnostic strategy in childhood hyperdiploid acute lymphoblastic leukemia
Leukemia·1998· 28 cited
Leukemia-free survival and mortality in patients with refractory or relapsed acute leukemia given marrow transplants from sibling and unrelated donors
Bone Marrow Transplantation·1998· 35 cited
Prognostic significance of WT1 gene expression at diagnosis in adult de novo acute myeloid leukemia
Leukemia·1997· 112 cited
Pathogenesis, biology, and management of myelodysplastic syndromes in children.
PubMed·1996· 29 cited
Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance
Blood·1995· 140 citedOpen Access
Increase of bcr-abl chimeric mRNA expression in tumor cells of patients with chronic myeloid leukemia precedes disease progression
Blood·1995· 163 citedOpen Access
Heterogeneity of the T-cell receptor delta gene indicating subclone formation in acute precursor B-cell leukemias
Blood·1995· 37 citedOpen Access
Are ABL and BCR imprinted? No definitive answers, but more questions.
PubMed·1995· 3 cited
Peripheral blood hematopoietic progenitor cells of cytokine-stimulated healthy donors as an alternative for allogeneic transplantation [letter]
Blood·1994Open Access
Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
PubMed·1993· 16 cited
The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young children
Blood·1992· 116 citedOpen Access
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Frequent Co-authors

Klaus Lechner(7), Christine Mannhalter(6), Klaus Geißler(4), Gerlinde Mitterbauer(4), Alexander Gaiger(3), Ulrich Jäger(3), Thomas Lion(3), Peter Kalhs(3), Georg Mann(3), Christa Fonatsch(3), Helmut Gadner(3), Traudl Henn(2), Hildegard Greinix(2), Jochen Harbott(2), Élise Bannier(2), J. Ritterbach(2), Momcilo Jankovic(2), F. M. Fink(2), A Stojimirovic(2), J. Herrmann(2)