Inga Nagel

Summary

Affiliation: University of Kiel
Country: Germany

Publications

  1. pmc Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature
    Maryam Maghbool
    Department of Molecular Pathology, Dr Daneshbod Pathology Laboratory, Shiraz, Iran
    BMC Clin Pathol 13:17. 2013
  2. pmc Identification of the gene encoding cyclin E1 (CCNE1) as a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphoma
    Inga Nagel
    Institute of Human Genetics, University Hospital Schleswig Holstein, Campus Kiel, 24105 Kiel, Germany
    Haematologica 94:1020-3. 2009
  3. doi Deregulation of the telomerase reverse transcriptase (TERT) gene by chromosomal translocations in B-cell malignancies
    Inga Nagel
    Institute of Human Genetics, Christian Albrechts University Kiel and University Hospital Schleswig Holstein, Campus Kiel, Kiel, Germany
    Blood 116:1317-20. 2010
  4. doi Clinical and pathological features of Burkitt lymphoma showing expression of BCL2--an analysis including gene expression in formalin-fixed paraffin-embedded tissue
    Neus Masqué-Soler
    Department of Pathology, Haematopathology Section and Lymph Node Registry, University Hospital Schleswig Holstein, Campus Kiel Christian Albrecht University, Kiel, Germany
    Br J Haematol 171:501-8. 2015
  5. doi A familial disorder of altered DNA-methylation
    Almuth Caliebe
    Institute of Human Genetics, University Hospital Schleswig Holstein Campus Kiel Christian Albrechts University Kiel, Kiel, Germany
    J Med Genet 51:407-12. 2014
  6. pmc A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms
    Jose I Martin-Subero
    Institute of Human Genetics, Christian Albrechts University, Kiel, Germany
    PLoS ONE 4:e6986. 2009
  7. doi ALK-positive primary cutaneous T-cell-lymphoma (CTCL) with unusual clinical presentation and aggressive course
    Ulrike Wehkamp
    Department of Dermatology, University of Kiel, Kiel, Germany
    J Cutan Pathol 42:870-7. 2015
  8. doi Genes encoding members of the JAK-STAT pathway or epigenetic regulators are recurrently mutated in T-cell prolymphocytic leukaemia
    Cristina Lopez
    Institute for Human Genetics, Christian Albrechts University Kiel and University Hospital Schleswig Holstein, Kiel, Germany
    Br J Haematol 173:265-73. 2016
  9. doi Microdeletion 5q14.3 and anomalies of brain development
    Alrun Hotz
    Institute of Human Genetics, Albert Ludwigs University Medical Centre Freiburg, Freiburg, Germany
    Am J Med Genet A 161:2124-33. 2013
  10. pmc Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case report
    Christel Eckmann-Scholz
    Department of Gynecology and Obstetrics, University Hospital Schleswig Holstein, Campus Kiel and Christian Albrechts University Kiel, Kiel, Germany
    Mol Cytogenet 3:16. 2010

Collaborators

Detail Information

Publications10

  1. pmc Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature
    Maryam Maghbool
    Department of Molecular Pathology, Dr Daneshbod Pathology Laboratory, Shiraz, Iran
    BMC Clin Pathol 13:17. 2013
    ..Primary adenocarcinoma of thymus is extremely rare...
  2. pmc Identification of the gene encoding cyclin E1 (CCNE1) as a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphoma
    Inga Nagel
    Institute of Human Genetics, University Hospital Schleswig Holstein, Campus Kiel, 24105 Kiel, Germany
    Haematologica 94:1020-3. 2009
    ..These data indicate that cyclin E1 may act as a novel oncogene in B-cell lymphomagenesis...
  3. doi Deregulation of the telomerase reverse transcriptase (TERT) gene by chromosomal translocations in B-cell malignancies
    Inga Nagel
    Institute of Human Genetics, Christian Albrechts University Kiel and University Hospital Schleswig Holstein, Campus Kiel, Kiel, Germany
    Blood 116:1317-20. 2010
    ..These data suggest that deregulation of TERT gene by chromosomal abnormalities leading to increased telomerase activity might contribute to B-cell lymphomagenesis...
  4. doi Clinical and pathological features of Burkitt lymphoma showing expression of BCL2--an analysis including gene expression in formalin-fixed paraffin-embedded tissue
    Neus Masqué-Soler
    Department of Pathology, Haematopathology Section and Lymph Node Registry, University Hospital Schleswig Holstein, Campus Kiel Christian Albrecht University, Kiel, Germany
    Br J Haematol 171:501-8. 2015
    ..The four lymphomas diagnosed molecularly as intermediates did not differ in clinical presentation and outcome from molecularly defined BL. ..
  5. doi A familial disorder of altered DNA-methylation
    Almuth Caliebe
    Institute of Human Genetics, University Hospital Schleswig Holstein Campus Kiel Christian Albrechts University Kiel, Kiel, Germany
    J Med Genet 51:407-12. 2014
    ..In a subset of imprinting disorders caused by epimutations, multiple imprinted loci are affected. Familial occurrence of multilocus imprinting disorders is rare...
  6. pmc A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms
    Jose I Martin-Subero
    Institute of Human Genetics, Christian Albrechts University, Kiel, Germany
    PLoS ONE 4:e6986. 2009
    ..However, most epigenetic studies in hematologic neoplasms (HNs) have focused either on the analysis of few candidate genes or many genes and few HN entities, and comprehensive studies are required...
  7. doi ALK-positive primary cutaneous T-cell-lymphoma (CTCL) with unusual clinical presentation and aggressive course
    Ulrike Wehkamp
    Department of Dermatology, University of Kiel, Kiel, Germany
    J Cutan Pathol 42:870-7. 2015
    ..In contrast to its role in systemic ALCL as favorable prognostic marker, ALK expression here was associated with an aggressive course...
  8. doi Genes encoding members of the JAK-STAT pathway or epigenetic regulators are recurrently mutated in T-cell prolymphocytic leukaemia
    Cristina Lopez
    Institute for Human Genetics, Christian Albrechts University Kiel and University Hospital Schleswig Holstein, Kiel, Germany
    Br J Haematol 173:265-73. 2016
    ..These findings complement the mutational spectrum of secondary aberrations in T-PLL and underscore the potential therapeutical relevance of epigenetic regulators in T-PLL. ..
  9. doi Microdeletion 5q14.3 and anomalies of brain development
    Alrun Hotz
    Institute of Human Genetics, Albert Ludwigs University Medical Centre Freiburg, Freiburg, Germany
    Am J Med Genet A 161:2124-33. 2013
    ..3q15, did not detect any additional mutations, allowing us to conclude that 5q14.3 deletion syndrome is a rare cause of microcephaly with simplified gyral pattern...
  10. pmc Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case report
    Christel Eckmann-Scholz
    Department of Gynecology and Obstetrics, University Hospital Schleswig Holstein, Campus Kiel and Christian Albrechts University Kiel, Kiel, Germany
    Mol Cytogenet 3:16. 2010
    ..Postnatal chromosome analysis in lymphocytes of the infant revealed complex mosaicism with four cell lines. By arrayCGH the sSMC was provisionally described as derivative chromosome 21 which was confirmed by targeted FISH experiments...