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
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Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2024)
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Consequences of chromosome gain: A new view on trisomy syndromes (2022)
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The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining (2022)
Collaboration Network
Top Collaborators
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Genotoxic stress in constitutive trisomies induces autophagy and the innate immune response via the cGAS-STING pathway
- Consequences of chromosome gain: A new view on trisomy syndromes
- Genotoxic stress in constitutive trisomies induces autophagy and the innate immune response via the cGAS-STING pathway
- Consequences of chromosome gain: A new view on trisomy syndromes
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining
- The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining
- Genotoxic stress in constitutive trisomies induces autophagy and the innate immune response via the cGAS-STING pathway
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