Clara M. Stiefel

Researcher

Last publication 2024 Last refreshed 2026-05-16

unknown

4 h-index 5 pubs 137 cited

Biography and Research Information

OverviewAI-generated summary

Clara M. Stiefel's research investigates the molecular mechanisms underlying DNA double-strand break repair and the consequences of genomic instability, particularly in the context of trisomy syndromes. Her work has identified the APE2 nuclease as essential for microhomology-mediated end joining, a critical pathway for repairing DNA breaks. Additionally, her studies explore how genotoxic stress in constitutive trisomies triggers cellular responses like autophagy and the innate immune system through the cGAS-STING pathway. She also examines the functional impact of genetic variations, such as a rare SNP in the HELB gene that interferes with RPA interaction and cellular function. Stiefel collaborates with researchers at the University of Arkansas for Medical Sciences, including Maroof K. Zafar, Eric J. Enemark, Alicia K. Byrd, and Matthew D. Thompson. Her scholarly contributions are reflected in a h-index of 4, with 5 publications and 133 citations.

Metrics

  • h-index: 4
  • Publications: 5
  • Citations: 137

Selected Publications

  • Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2024)
  • Consequences of chromosome gain: A new view on trisomy syndromes (2022)
    39 citations DOI OpenAlex
  • The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining (2022)
    5 citations DOI OpenAlex

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Collaboration Network

32 Collaborators 10 Institutions 3 Countries

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