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Journal Articles

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

Susanne Schnittger, PhD, Sonja Rauhut, Claudia Tschulik, Madlen Ulke, Wolfgang Kern, MD, Claudia Haferlach, MD, Torsten Haferlach, MD

Blood (2008) 112 (11): 3203.

https://doi.org/10.1182/blood.V112.11.3203.3203

Published: 2008

Journal Articles

A Distinct Pattern of Additional Aberrations and Novel Mechanisms of MLL Rearrangements Are Detectable in AML with 11q23 Aberrations Using SNP Arrays

Claudia Haferlach, MD, Alexander Kohlmann, PhD, Sonja Rauhut, Frank Dicker, PhD, Wolfgang Kern, MD, Susanne Schnittger, PhD, Torsten Haferlach, MD

Blood (2008) 112 (11): 4143.

https://doi.org/10.1182/blood.V112.11.4143.4143

Published: 2008

Journal Articles

Deciphering the Heterogeneity of 13q Deletions in CLL on the Cytogenetic and Molecular Level by SNP Arrays: In 49% of Cases Deletion Breakpoints Cluster in a 200 Kb Sized Region on the Centromeric Side and in a 300 Kb Sized Region on the Telomeric Side

Claudia Haferlach, MD, Alexander Kohlmann, PhD, Sonja Rauhut, Frank Dicker, PhD, Wolfgang Kern, MD, Susanne Schnittger, PhD, Torsten Haferlach, MD

Blood (2008) 112 (11): 3147.

https://doi.org/10.1182/blood.V112.11.3147.3147

Published: 2008

Journal Articles

Recurrent Additional Genetic Aberrations and a Novel Mechanism of CBFB - MYH11 -Rearrangement in AML M4eo Are Detected Using High-Resolution Genome-Wide Single Nucleotide Polymorphisms (SNPs) Microarrays

Alexander Kohlmann, PhD, Sonja Rauhut, Frank Dicker, PhD, Susanne Schnittger, PhD, Wolfgang Kern, MD, Torsten Haferlach, MD, Claudia Haferlach, MD

Blood (2008) 112 (11): 3115.

https://doi.org/10.1182/blood.V112.11.3115.3115

Published: 2008

Journal Articles

Gain of the Short Arm of Chromosome 2 Is a New Recurring Chromosome Aberration in CLL Which Is Significantly Associated with an Unmutated IgGVH Status and a Complex Aberrant Karyotype and Leads to a Higher Expression of Genes Located on 2P.

Claudia Haferlach, MD, Sonja Rauhut, Sylvia Merk, MD, Frank Dicker, PhD, Susanne Schnittger, PhD, Wolfgang Kern, MD, Martin Dugas, MD, Torsten Haferlach, MD

Blood (2007) 110 (11): 2075.

https://doi.org/10.1182/blood.V110.11.2075.2075

Published: 2007

Journal Articles

Intraplatform Reproducibility and Technical Precision of Gene Expression Profiling in Four Laboratories Investigating 112 Leukemia Samples: The DACH Study.

Alexander Kohlmann, PhD, Elisabeth Haschke-Becher, MD, Barbara Wimmer, PhD, Ariana Huber-Wechselberger, PhD, Sandrine Meyer-Monard, MD, Heike Huxol, Uwe Siegler, PhD, Michel Rossier, PhD, Thomas Matthes, MD, Michela Rebsamen, PhD, Adeline Diemand, Alberto Chiappe, Sonja Rauhut, Wei-min Liu, PhD, Andrea Johnson, PhD, Lothar Wieczorek, PhD, Torsten Haferlach, MD

Blood (2007) 110 (11): 2383.

https://doi.org/10.1182/blood.V110.11.2383.2383

Published: 2007

Journal Articles

An Approach to Virtual Karyotyping for Unbalanced Rearrangements Based on Gene Expression Data.

Claudia Haferlach, MD, Sylvia Merk, MD, Sonja Rauhut, Susanne Schnittger, PhD, Wolfgang Kern, MD, Martin Dugas, MD, Torsten Haferlach, MD

Blood (2007) 110 (11): 885.

https://doi.org/10.1182/blood.V110.11.885.885

Published: 2007

Journal Articles

Translocation t(14;19)(q32;q13) Is a Rare Abnormality in CLL and Associated with Trisomy 12, an Unmutated IgVH Status and a Distinct Gene Expression Profile.

Claudia Haferlach, MD, Sonja Rauhut, Sylvia Merk, MD, Frank Dicker, PhD, Susanne Schnittger, PhD, Wolfgang Kern, MD, Martin Dugas, MD, Torsten Haferlach, MD

Blood (2007) 110 (11): 4703.

https://doi.org/10.1182/blood.V110.11.4703.4703

Published: 2007

Journal Articles

5q Deletions Can Be Identified Based on the Expression Level of 5q Genes: A Study on 49 Cases with MDS or AML Analysed in Parallel by Gene Expression Profiling and Genomic Arrays.

Claudia Schoch, MD, Sonja Rauhut, Susanne Schnittger, PhD, Frank Dicker, PhD, Wolfgang Kern, MD, Torsten Haferlach, MD

Blood (2006) 108 (11): 2642.

https://doi.org/10.1182/blood.V108.11.2642.2642

Published: 2006

Journal Articles

Individual Gene Expression Profiling of Bone Marrow CD34 Cells in Acquired Severe Aplastic Anemia (aSAA) in Children.

Bernd Hubner, Sylvia Merk, Sonja Rauhut, Martin Dugas, Torsten Haferlach, Monika Fuehrer, Arndt Borkhardt

Blood (2006) 108 (11): 978.

https://doi.org/10.1182/blood.V108.11.978.978

Published: 2006

Journal Articles

Further Insights into the Pathogenesis of AML with Complex Aberrant Karyotype by Performing a Combination of Conventional CGH, Gene Expression and Genomic Array Analysis.

Claudia Schoch, MD, Alexander Kohlmann, PhD, Sonja Rauhut, Frank Dicker, PhD, Susanne Schnittger, PhD, Wolfgang Kern, MD, Torsten Haferlach, MD

Blood (2005) 106 (11): 758.

https://doi.org/10.1182/blood.V106.11.758.758

Published: 2005

Journal Articles

Mutations of the TP53 Gene Play an Important Role in the Pathogenesis of Acute Myeloid Leukemia with Complex Aberrant Karyotype.

Claudia Schoch, MD, Frank Dicker, PhD, Alexander Kohlmann, Sonja Rauhut, Wolfgang Hiddemann, MD, Susanne Schnittger, PhD, Wolfgang Kern, MD, Torsten Haferlach, MD8

Blood (2004) 104 (11): 63.

https://doi.org/10.1182/blood.V104.11.63.63

Published: 2004

NARROW

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

A Distinct Pattern of Additional Aberrations and Novel Mechanisms of MLL Rearrangements Are Detectable in AML with 11q23 Aberrations Using SNP Arrays

Deciphering the Heterogeneity of 13q Deletions in CLL on the Cytogenetic and Molecular Level by SNP Arrays: In 49% of Cases Deletion Breakpoints Cluster in a 200 Kb Sized Region on the Centromeric Side and in a 300 Kb Sized Region on the Telomeric Side

Recurrent Additional Genetic Aberrations and a Novel Mechanism of CBFB - MYH11 -Rearrangement in AML M4eo Are Detected Using High-Resolution Genome-Wide Single Nucleotide Polymorphisms (SNPs) Microarrays

Gain of the Short Arm of Chromosome 2 Is a New Recurring Chromosome Aberration in CLL Which Is Significantly Associated with an Unmutated IgGVH Status and a Complex Aberrant Karyotype and Leads to a Higher Expression of Genes Located on 2P.

Intraplatform Reproducibility and Technical Precision of Gene Expression Profiling in Four Laboratories Investigating 112 Leukemia Samples: The DACH Study.

An Approach to Virtual Karyotyping for Unbalanced Rearrangements Based on Gene Expression Data.

Translocation t(14;19)(q32;q13) Is a Rare Abnormality in CLL and Associated with Trisomy 12, an Unmutated IgVH Status and a Distinct Gene Expression Profile.

5q Deletions Can Be Identified Based on the Expression Level of 5q Genes: A Study on 49 Cases with MDS or AML Analysed in Parallel by Gene Expression Profiling and Genomic Arrays.

Individual Gene Expression Profiling of Bone Marrow CD34 Cells in Acquired Severe Aplastic Anemia (aSAA) in Children.

Further Insights into the Pathogenesis of AML with Complex Aberrant Karyotype by Performing a Combination of Conventional CGH, Gene Expression and Genomic Array Analysis.

Mutations of the TP53 Gene Play an Important Role in the Pathogenesis of Acute Myeloid Leukemia with Complex Aberrant Karyotype.

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ASH Publications

American Society of Hematology

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ASH Publications

American Society of Hematology

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