Christa Fonatsch

Christa Fonatsch

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Christa Fonatsch

Christa Fonatsch

Publications by authors named "Christa Fonatsch"

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61Publications

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Clinical utility gene card for: tuberous sclerosis complex (TSC1, TSC2).

Eur J Hum Genet 2014 Feb 12;22(2). Epub 2013 Jun 12.

Department Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1038/ejhg.2013.129DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895647PMC
February 2014

The role of chromosome 21 in hematology and oncology.

Authors:
Christa Fonatsch

Genes Chromosomes Cancer 2010 Jun;49(6):497-508

Institute of Human Genetics, Medical University of Vienna, Währinger Strasse 10, Vienna, Austria.

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http://dx.doi.org/10.1002/gcc.20764DOI Listing
June 2010

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

Hum Mol Genet 2010 Apr 21;19(8):1507-14. Epub 2010 Jan 21.

Department of Clinical Genetics, University and Regional Laboratories, Lund University Hospital, Lund University, Lund, Sweden.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddq024DOI Listing
April 2010

DNA repair polymorphisms associated with cytogenetic subgroups in B-cell chronic lymphocytic leukemia.

Genes Chromosomes Cancer 2009 Sep;48(9):760-7

Department of Medical Genetics, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1002/gcc.20680DOI Listing
September 2009

Idiopathic cytopenia of undetermined significance (ICUS) versus low risk MDS: the diagnostic interface.

Leuk Res 2007 Nov 16;31(11):1461-8. Epub 2007 May 16.

Department of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1016/j.leukres.2007.03.015DOI Listing
November 2007

A patient with de novo AML M1 and t(16;21) with karyotype evolution.

Leuk Res 2007 Sep 28;31(9):1319-21. Epub 2006 Nov 28.

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http://dx.doi.org/10.1016/j.leukres.2006.10.010DOI Listing
September 2007

Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndrome.

Am J Med Genet A 2007 Sep;143A(17):2065-9

Biochemical and Paediatric Genetics, Department of General Paediatrics, University Children's Hospital, Medical University Vienna, Vienna, Austria.

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http://dx.doi.org/10.1002/ajmg.a.31792DOI Listing
September 2007

GAB2 is a novel target of 11q amplification in AML/MDS.

Genes Chromosomes Cancer 2006 Sep;45(9):798-807

Abteilung für Humangenetik, Klinisches Institut für Medizinische und Chemische Labor Diagnostik (KIMCL), Medizinische Universität Wien, Währinger Strasse 10, A-1090 Vienna, Austria.

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http://dx.doi.org/10.1002/gcc.20344DOI Listing
September 2006

Silver-Russell syndrome-like features in a patient carrying a novel NF1 mutation.

Pediatr Res 2005 Dec;58(6):1265-8

Department of Human Genetics, Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Vienna, Austria.

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http://dx.doi.org/10.1203/01.pdr.0000183661.81772.f8DOI Listing
December 2005

An unusual case of myelodysplastic syndrome with prolonged clonal stability, indolent clinical course over a decade, and spontaneous regression of AML in the terminal phase.

Eur J Haematol 2005 Jul;75(1):73-7

Division of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria.

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http://dx.doi.org/10.1111/j.1600-0609.2005.00423.xDOI Listing
July 2005

[Tumor cytogenetics].

Wien Med Wochenschr 2005 Jun;155(11-12):281-8

Abteilung für Humangenetik, Klinisches Institut für Medizinische und Chemische Labordiagnostik, Medizinische Universität Wien, Wien, Osterreich.

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June 2005

Highly refractory acute myeloid leukemia.

Wien Klin Wochenschr 2004 Aug;116(15-16):561-4

Division of Hematology and Hemostaseology, The University of Vienna, Austria.

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August 2004

Normal bone marrow function over 6 years in a patient with dysplastic hematopoiesis and a complex karyotype.

Leuk Res 2004 Jun;28(6):651-5

Department of Internal Medicine I, University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria.

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http://dx.doi.org/10.1016/j.leukres.2003.10.023DOI Listing
June 2004

A novel effective and safe consolidation for patients over 60 years with acute myeloid leukemia: intermediate dose cytarabine (2 x 1 g/m2 on days 1, 3, and 5).

Clin Cancer Res 2004 Jun;10(12 Pt 1):3965-71

Department of Internal Medicine I, Division of Hematology & Hemostaseology, Institute of Medical Biology, and Institute of Medical and Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1158/1078-0432.CCR-04-0185DOI Listing
June 2004

Unusual karyotype aberrations involving 2p12, 3q27, 18q21, 8q24, and 14q32 in a patient with non-Hodgkin lymphoma/acute lymphoblastic leukemia.

Cancer Genet Cytogenet 2003 Apr;142(1):60-4

Institut für Medizinische Biologie der Universität Wien, 1090 Vienna, Austria.

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http://dx.doi.org/10.1016/s0165-4608(02)00801-4DOI Listing
April 2003

Mutational and expression analysis of the NF1 gene argues against a role as tumor suppressor in sporadic pilocytic astrocytomas.

J Neuropathol Exp Neurol 2002 Oct;61(10):896-902

Institut für Medizinische Biologie, Universität Wien, Vienna, Austria.

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http://dx.doi.org/10.1093/jnen/61.10.896DOI Listing
October 2002