Nils Winkelmann

ORCID: 0000-0001-7772-8225
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About
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Research Areas
  • Chronic Lymphocytic Leukemia Research
  • Acute Myeloid Leukemia Research
  • Chronic Myeloid Leukemia Treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Hematopoietic Stem Cell Transplantation
  • Lymphoma Diagnosis and Treatment
  • Epigenetics and DNA Methylation
  • Acute Lymphoblastic Leukemia research
  • Immunodeficiency and Autoimmune Disorders
  • Microbial infections and disease research
  • Infections and bacterial resistance
  • Nuclear Structure and Function
  • Connective tissue disorders research
  • Wound Healing and Treatments
  • Autoimmune and Inflammatory Disorders Research
  • Childhood Cancer Survivors' Quality of Life
  • T-cell and B-cell Immunology
  • Respiratory viral infections research
  • Testicular diseases and treatments
  • Skin and Cellular Biology Research
  • CNS Lymphoma Diagnosis and Treatment
  • CAR-T cell therapy research
  • Protein Degradation and Inhibitors
  • Cancer-related gene regulation
  • Pneumonia and Respiratory Infections

Jena University Hospital
2010-2020

Klinikum Magdeburg
2016-2017

Wessex Regional Genetics Laboratory
2011-2015

Salisbury District Hospital
2012-2015

Salisbury NHS Foundation Trust
2013

Johannes Gutenberg University Mainz
2003-2005

Klinik und Poliklinik für Psychosomatische Medizin und Psychotherapie
2001

Summary Whole exome sequencing was performed in a patient with myelodysplastic syndrome before and after progression to acute myeloid leukaemia. Mutations several genes, including SETBP 1 , were identified following leukaemic transformation. Screening of 328 patients disorders revealed mutations 14 (4·3%), 7 whom had −7/del(7q) 3 i(17)(q10), cytogenetic markers associated shortened overall survival increased risk evolution. frequently acquired at the time evolution, coinciding increase...

10.1111/bjh.12491 article EN British Journal of Haematology 2013-07-24

Fusion genes involving the catalytic domain of tyrosine kinases (TKs) play an important role in pathogenesis hematological malignancies and solid tumors. In BCR-ABL1-negative myeloproliferative neoplasms (MPNs) several different kinase fusion events have been described, most commonly encoding platelet-derived growth factor receptor alpha (PDGFRA) or beta (PDGFRB). Since introduction small molecule inhibitors, TK fusions emerged as prime therapeutic targets. Here, we report a recurrent...

10.3109/10428194.2012.753544 article EN Leukemia & lymphoma/Leukemia and lymphoma 2012-11-27

Abstract Background Community‐acquired respiratory viruses (CARV) cause upper and lower tract infections (URTI/LRTI) may be life‐threatening for recipients of an allogeneic stem cell transplantation (allo‐SCT). Methods In a prospective study encompassing 4 winter‐seasons, we collected throat gargles (TG) at random time points from allo‐SCT (patients) controls followed them up least 3 weeks including repetitive sampling documentation symptoms. A Multiplex‐PCR system to identify 20 CARV...

10.1111/tid.13415 article EN Transplant Infectious Disease 2020-07-13

Infectious complications such as invasive aspergillosis or infection with <i>Stenotrophomonas maltophilia</i> (SM) in immunocompromised patients are associated a high mortality rate. Our report concerns 40-year-old male newly diagnosed very severe aplastic anemia (vSAA) who consequence of mosquito bite was suffering from skin lesion and consecutive soft tissue phlegmon subsequent to the administration antithymocyte globulin; full-thickness autologous meshed graft successfully...

10.1159/000495878 article EN cc-by-nc Case Reports in Oncology 2019-01-04

Abstract Atypical Chronic Myeloid Leukemia (aCML) is a heterogeneous disorder belonging to the group of myelodysplastic/myeloproliferative (MDS/MPN) syndromes. The molecular pathogenesis this disease still unclear and outcome poor with no improvement over last 20 years. We applied whole exome sequencing approach in 9 aCML patient samples order identify possible recurrent alterations. analysis revealed presence unique mutations 70 genes 3 cases SETBP1 Some identified as mutated initial set...

10.1158/1538-7445.am2013-2993 article EN Cancer Research 2013-04-01
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