Schnittger S - Search Results

1

A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controls.

Schnittger S, Bacher U, Eder C, Lohse P, Haferlach C, Kern W, Haferlach T. Schnittger S, et al. Exp Hematol. 2011 Jan;39(1):87-94. doi: 10.1016/j.exphem.2010.09.009. Epub 2010 Oct 1. Exp Hematol. 2011. PMID: 20888888

2

Further correlations of morphology according to FAB and WHO classification to cytogenetics in de novo acute myeloid leukemia: a study on 2,235 patients.

Bacher U, Kern W, Schnittger S, Hiddemann W, Schoch C, Haferlach T. Bacher U, et al. Among authors: schnittger s. Ann Hematol. 2005 Nov;84(12):785-91. doi: 10.1007/s00277-005-1099-0. Epub 2005 Nov 12. Ann Hematol. 2005. PMID: 16132906

3

D324N single-nucleotide polymorphism in the FLT3 gene is associated with higher risk of myeloid leukemias.

Schnittger S, Kohl TM, Leopold N, Schoch C, Wichmann HE, Kern W, Lohse P, Hiddemann W, Haferlach T, Spiekermann K. Schnittger S, et al. Genes Chromosomes Cancer. 2006 Apr;45(4):332-7. doi: 10.1002/gcc.20294. Genes Chromosomes Cancer. 2006. PMID: 16320249

4

Implications of NRAS mutations in AML: a study of 2502 patients.

Bacher U, Haferlach T, Schoch C, Kern W, Schnittger S. Bacher U, et al. Among authors: schnittger s. Blood. 2006 May 15;107(10):3847-53. doi: 10.1182/blood-2005-08-3522. Epub 2006 Jan 24. Blood. 2006. PMID: 16434492 Free article.

5

Insight into the molecular pathogenesis of myeloid malignancies.

Haferlach T, Bacher U, Haferlach C, Kern W, Schnittger S. Haferlach T, et al. Among authors: schnittger s. Curr Opin Hematol. 2007 Mar;14(2):90-7. doi: 10.1097/MOH.0b013e3280168490. Curr Opin Hematol. 2007. PMID: 17255785 Review.

6

Diagnostic pathways in acute leukemias: a proposal for a multimodal approach.

Haferlach T, Bacher U, Kern W, Schnittger S, Haferlach C. Haferlach T, et al. Among authors: schnittger s. Ann Hematol. 2007 May;86(5):311-27. doi: 10.1007/s00277-007-0253-2. Epub 2007 Feb 14. Ann Hematol. 2007. PMID: 17375301 Review.

7

The diagnosis of BCR/ABL-negative chronic myeloproliferative diseases (CMPD): a comprehensive approach based on morphology, cytogenetics, and molecular markers.

Haferlach T, Bacher U, Kern W, Schnittger S, Haferlach C. Haferlach T, et al. Among authors: schnittger s. Ann Hematol. 2008 Jan;87(1):1-10. doi: 10.1007/s00277-007-0403-6. Epub 2007 Oct 16. Ann Hematol. 2008. PMID: 17938925 Free PMC article. Review.

8

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 S, Haferlach C, Ulke M, Alpermann T, Kern W, Haferlach T. Schnittger S, et al. Blood. 2010 Dec 16;116(25):5486-96. doi: 10.1182/blood-2010-02-267955. Epub 2010 Aug 30. Blood. 2010. PMID: 20805365 Free article.

9

RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis.

Schnittger S, Dicker F, Kern W, Wendland N, Sundermann J, Alpermann T, Haferlach C, Haferlach T. Schnittger S, et al. Blood. 2011 Feb 24;117(8):2348-57. doi: 10.1182/blood-2009-11-255976. Epub 2010 Dec 9. Blood. 2011. PMID: 21148331 Free article.

10

Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology.

Grossmann V, Schnittger S, Schindela S, Klein HU, Eder C, Dugas M, Kern W, Haferlach T, Haferlach C, Kohlmann A. Grossmann V, et al. Among authors: schnittger s. J Mol Diagn. 2011 Mar;13(2):129-36. doi: 10.1016/j.jmoldx.2010.09.001. J Mol Diagn. 2011. PMID: 21354046 Free PMC article.

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