Simone Feurstein

Employment

Employment history is unavailable.

Education

• Hannover Medical School M.D.
  2006 - 2013
• Hannover Medical School Ph.D.
  ? - 2015

Projects & Funding

Projects & funding information is unavailable.

Publications (26)

• Germline predisposition to myeloid neoplasms: Characteristics and management of high versus variable penetrance disorders.
  Best practice & research. Clinical haematology 2024 DOI: 10.1016/j.beha.2024.101537
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• Germline and somatic drivers in inherited hematologic malignancies.
  Frontiers in oncology 2023 DOI: 10.3389/fonc.2023.1205855
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• Emerging bone marrow failure syndromes- new pieces to an unsolved puzzle.
  Frontiers in oncology 2023 DOI: 10.3389/fonc.2023.1128533
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• Familial Myeloid Neoplasms—When to Suspect and What to Do?
  Cancer Consult: Neoplastic Hematology & Cell Therapy 2 2023
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• Germ line predisposition variants occur in myelodysplastic syndrome patients of all ages
  Blood 2022 DOI: 10.1182/blood.2022015790
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• Functional genomics for curation of variants in telomere biology disorder associated genes: A systematic review.
  Genetics in medicine : official journal of the American College of Medical Genetics 2022 DOI: 10.1016/j.gim.2022.11.021
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• Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior—A case report
  eJHaem 2022 DOI: 10.1002/jha2.555
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• Significance of hereditary gene alterations for the pathogenesis of adult bone marrow failure versus myeloid neoplasia.
  Leukemia 2022 DOI: 10.1038/s41375-022-01729-4
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• Revision of RUNX1 variant curation rules
  Blood Advances 2022 DOI: 10.1182/bloodadvances.2022008017
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• A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias.
  Genetics in medicine : official journal of the American College of Medical Genetics 2022 DOI: 10.1016/j.gim.2021.12.008
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• Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
  Deepak Singhal, Christopher Norman Hahn, Simone K. Feurstein +22 more
  Leukemia 2021 DOI: 10.1038/s41375-021-01246-w
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• GATA2 deficiency syndrome: A decade of discovery.
  Claire C. Homan, Parvathy Venugopal, Peer Arts

  +10 more

  • Nur Hezrin Shahrin
  • Simone K. Feurstein
  • Lesley H. Rawlings
  • David Lawrence
  • James Andrews
  • +5 more
  Human Mutation 2021 DOI: 10.1002/humu.24288
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• Germline predisposition to hematopoietic malignancies.
  Human molecular genetics 2021 DOI: 10.1093/hmg/ddab141
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• Germline variants drive myelodysplastic syndrome in young adults
  Leukemia 2021 DOI: 10.1038/s41375-021-01137-0
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• Accurate germline RUNX1 variant interpretation and its clinical significance
  Blood Advances 2020 DOI: 10.1182/bloodadvances.2020003304
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• Heterozygous germ line CSF3R variants as risk alleles for development of hematologic malignancies
  Blood Advances 2020 DOI: 10.1182/bloodadvances.2020002013
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• Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations
  Blood Advances 2020 DOI: 10.1182/bloodadvances.2020001721
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• How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline predisposition to myeloid malignancies.
  Haematologica 2020 DOI: 10.3324/haematol.2018.214221
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• ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
  Blood advances 2019 DOI: 10.1182/bloodadvances.2019000644
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• Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q Deletion.
  International journal of molecular sciences 2018 DOI: 10.3390/ijms19103269
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