Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia
Schnittger, Susanne, Bacher, Ulrike, Haferlach, Torsten, Wendland, Nicole, Ulke, Madlen, Dicker, Frank, Grossmann, Vera, Haferlach, Claudia, Kern, Wolfgang
Published in Blood (29.03.2012)
Published in Blood (29.03.2012)
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Journal Article
Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases
SCHNITTGER, Susanne, BACHER, Ulrike, KERN, Wolfgang, HAFERLACH, Claudia, HAFERLACH, Torsten, ALPERMANN, Tamara, REITER, Andreas, ULKE, Madlen, DICKER, Frank, EDER, Christiane, KOHLMANN, Alexander, GROSSMANN, Vera, KOWARSCH, Andreas
Published in Haematologica (Roma) (01.12.2012)
Published in Haematologica (Roma) (01.12.2012)
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Journal Article
IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status
Schnittger, Susanne, Haferlach, Claudia, Ulke, Madlen, Alpermann, Tamara, Kern, Wolfgang, Haferlach, Torsten
Published in Blood (16.12.2010)
Published in Blood (16.12.2010)
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Journal Article
Targeting Genomic Heterogeneity of Adult Acute Lymphoblastic Leukemia
Fasan, Annette, Zenger, Melanie, Ulke, Madlen, Kern, Wolfgang, Haferlach, Torsten, Haferlach, Claudia, Schnittger, Susanne
Published in Blood (06.12.2014)
Published in Blood (06.12.2014)
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Journal Article
IKZF1 deletions Are Detected In 40.3% Of 270 Adult B-Precursor-ALL and Are Independently Associated With BCR-ABL1 Positivity and Inferior Outcome
Fasan, Annette, Haferlach, Claudia, Ulke, Madlen, Kern, Wolfgang, Haferlach, Torsten, Schnittger, Susanne
Published in Blood (15.11.2013)
Published in Blood (15.11.2013)
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Journal Article
WT1 Mutations Are Secondary Events In AML and Show Varying Frequencies Within Genetic Subgroups and Different Impact On Prognosis
Schnittger, Susanne, Eder, Christiane, Alpermann, Tamara, Dicker, Frank, Ulke, Madlen, Kohlmann, Alexander, Kuznia, Sabrina, Kern, Wolfgang, Haferlach, Torsten, Haferlach, Claudia
Published in Blood (15.11.2013)
Published in Blood (15.11.2013)
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Journal Article
Development and Validation of a Real Time Quantification Assay to Detect and Monitor BRAFV600E-Mutations in Hairy Cell Leukemia
Schnittger, Susanne, Haferlach, Torsten, Wendland, Nicole, Ulke, Madlen, Grossmann, Vera, Haferlach, Claudia, Kern, Wolfgang
Published in Blood (18.11.2011)
Published in Blood (18.11.2011)
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Journal Article
IDH1 Mutations Are Detected in 9.3% of All AML and Are Strongly Associated with Intermediate Risk Karyotype and Unfavourable Prognosis: a Study of 999 Patients
Schnittger, Susanne, Haferlach, Claudia, Ulke, Madlen, Kaya, Leyla, Weiss, Tamara, Kern, Wolfgang, Haferlach, Torsten
Published in Blood (20.11.2009)
Published in Blood (20.11.2009)
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Journal Article
CBL Mutations Are Correlated with CMML, Frequently Associated with RUNX1 but Mutually Exclusive of JAK2V617F Mutations
Schnittger, Susanne, Reiter, Andreas, Ulke, Madlen, Spiel, Alexandra, Dicker, Frank, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten
Published in Blood (20.11.2009)
Published in Blood (20.11.2009)
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Journal Article
Analysis of Genetic Variants and Expression Levels of Human Organic Cation Transporter 1 (HOCT1) and Genetic Variants in MDR1 in CML: Weak Associations Were Detected but a Major Role in Clinical Response to Imatinib Resistance Is Unlikely
Schnittger, Susanne, Rauhut, Sonja, Tschulik, Claudia, Ulke, Madlen, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten
Published in Blood (16.11.2008)
Published in Blood (16.11.2008)
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Journal Article