List of works - Stephan Bartels

Absence of MGMT promoter methylation in diffuse midline glioma, H3 K27M-mutant

scientific article published on 15 December 2017

Activating human epidermal growth factor receptor 2 (HER2) gene mutation in bone metastases from breast cancer

scientific article published on 09 August 2018

Analysis of Mutational Hotspots in Routinely Processed Bone Marrow Trephines by Pyrosequencing®.

scientific article

Archival bone marrow trephines are suitable for high-throughput mutation analysis using next generation sequencing technology

scientific article published on September 2013

CDKN2A loss and PIK3CA mutation in myoepithelial-like metaplastic breast cancer.

scientific article published on 30 April 2018

Chromosome 2q gain and epigenetic silencing of GATA3 in microglandular adenosis of the breast

scientific article published on 31 December 2020

Comprehensive Molecular Profiling of Archival Bone Marrow Trephines Using a Commercially Available Leukemia Panel and Semiconductor-Based Targeted Resequencing

scientific article published on 29 July 2015

Comprehensive mutation profiling and mRNA expression analysis in atypical chronic myeloid leukemia in comparison with chronic myelomonocytic leukemia

scientific article published on 11 January 2019

De novo CSF3R mutation associated with transformation of myeloproliferative neoplasm to atypical CML

scientific article published on 14 April 2015

E-cadherin to P-cadherin switching in lobular breast cancer with tubular elements

scientific article published on 22 June 2020

ERBB2 mutation frequency in lobular breast cancer with pleomorphic histology or high-risk characteristics by molecular expression profiling

scientific article published on 07 January 2019

Estrogen receptor (ESR1) mutation in bone metastases from breast cancer

scientific article published on 11 August 2017

Evolution of chronic myelomonocytic leukemia to myeloproliferative neoplasm.

scientific article

Fibrotic progression in Polycythemia vera is associated with early concomitant driver-mutations besides JAK2.

scientific article published on 22 September 2017

Genome-wide DNA methylation profiling is able to identify prefibrotic PMF cases at risk for progression to myelofibrosis

scientific article published on 04 February 2021

Hotspot mutations in cancer genes may be missed in routine diagnostics due to neighbouring sequence variants

scientific article published on 27 May 2018

Molecular Analysis of Circulating Cell-Free DNA from Lung Cancer Patients in Routine Laboratory Practice: A Cross-Platform Comparison of Three Different Molecular Methods for Mutation Detection

scientific article

Molecular defects in BRAF wild-type ameloblastomas and craniopharyngiomas-differences in mutation profiles in epithelial-derived oropharyngeal neoplasms

scientific article published on 15 March 2018

Mutations associated with age-related clonal hematopoiesis in PMF patients with rapid progression to myelofibrosis

scientific article published on 27 November 2019

Next-Generation Sequencing Analysis of Laser-Microdissected Formalin-Fixed and Paraffin-Embedded (FFPE) Tissue Specimens

scientific article published in January 2018

RNA-binding protein (RBFOX1) inherited polymorphism rs8051518 is not associated with splice factor mutations in myelodysplastic syndromes and myeloproliferative neoplasms

scientific article published on 29 August 2018

Routine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms

scientific article published on 23 March 2016

SRSF2 and U2AF1 mutations in primary myelofibrosis are associated with JAK2 and MPL but not calreticulin mutation and may independently reoccur after allogeneic stem cell transplantation

scientific article published on 18 September 2014

SRSF2 mutation is present in the hypercellular and prefibrotic stage of primary myelofibrosis

scientific article published in May 2013

Subclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinoma

scientific article published on 19 July 2017

[Liquid biopsy in tumor diagnostics : Applications, perspectives, and limitations of the "cancer liquidome"]

scientific article published on 01 May 2019

List of works by Stephan Bartels

Absence of MGMT promoter methylation in diffuse midline glioma, H3 K27M-mutant

Activating human epidermal growth factor receptor 2 (HER2) gene mutation in bone metastases from breast cancer

Analysis of Mutational Hotspots in Routinely Processed Bone Marrow Trephines by Pyrosequencing®.

Archival bone marrow trephines are suitable for high-throughput mutation analysis using next generation sequencing technology

CDKN2A loss and PIK3CA mutation in myoepithelial-like metaplastic breast cancer.

Chromosome 2q gain and epigenetic silencing of GATA3 in microglandular adenosis of the breast

Comprehensive Molecular Profiling of Archival Bone Marrow Trephines Using a Commercially Available Leukemia Panel and Semiconductor-Based Targeted Resequencing

Comprehensive mutation profiling and mRNA expression analysis in atypical chronic myeloid leukemia in comparison with chronic myelomonocytic leukemia

De novo CSF3R mutation associated with transformation of myeloproliferative neoplasm to atypical CML

E-cadherin to P-cadherin switching in lobular breast cancer with tubular elements

ERBB2 mutation frequency in lobular breast cancer with pleomorphic histology or high-risk characteristics by molecular expression profiling

Estrogen receptor (ESR1) mutation in bone metastases from breast cancer

Evolution of chronic myelomonocytic leukemia to myeloproliferative neoplasm.

Fibrotic progression in Polycythemia vera is associated with early concomitant driver-mutations besides JAK2.

Genome-wide DNA methylation profiling is able to identify prefibrotic PMF cases at risk for progression to myelofibrosis

Hotspot mutations in cancer genes may be missed in routine diagnostics due to neighbouring sequence variants

Molecular Analysis of Circulating Cell-Free DNA from Lung Cancer Patients in Routine Laboratory Practice: A Cross-Platform Comparison of Three Different Molecular Methods for Mutation Detection

Molecular defects in BRAF wild-type ameloblastomas and craniopharyngiomas-differences in mutation profiles in epithelial-derived oropharyngeal neoplasms

Mutations associated with age-related clonal hematopoiesis in PMF patients with rapid progression to myelofibrosis

Next-Generation Sequencing Analysis of Laser-Microdissected Formalin-Fixed and Paraffin-Embedded (FFPE) Tissue Specimens

RNA-binding protein (RBFOX1) inherited polymorphism rs8051518 is not associated with splice factor mutations in myelodysplastic syndromes and myeloproliferative neoplasms

Routine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms

SRSF2 and U2AF1 mutations in primary myelofibrosis are associated with JAK2 and MPL but not calreticulin mutation and may independently reoccur after allogeneic stem cell transplantation

SRSF2 mutation is present in the hypercellular and prefibrotic stage of primary myelofibrosis

Subclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinoma

[Liquid biopsy in tumor diagnostics : Applications, perspectives, and limitations of the "cancer liquidome"]