Michael Kazinski

Papers

1

Total Citations

35

H-Index

1

About

Michael Kazinski is a pioneering figure in functional genomics, with a primary focus on cellular stress responses and neuroprotection. His most influential work centers on developing high-throughput genetic screening methodologies to identify genes that mitigate oxidative stress—a key driver of neurodegeneration. In his landmark 2004 study, Kazinski introduced a novel approach by transfecting individual clones from an expression library into separate cell populations, enabling the systematic discovery of human genes that ameliorate toxicity in neuronal HT-22 cells. This paper, cited 35 times, laid the groundwork for integrating functional genomics with experimental validation, bridging the gap between large-scale data and biological relevance. Kazinski’s contributions have provided critical insights into the molecular mechanisms underlying oxidative damage, offering potential therapeutic targets for diseases like Alzheimer’s and Parkinson’s. His work is notable for its methodological innovation, demonstrating how high-throughput screens can be harnessed to uncover protective pathways in neurons. For students and researchers, Kazinski’s research exemplifies the power of combining computational and experimental approaches to tackle complex biological questions, making him a key figure in advancing our understanding of cellular resilience and stress biology.

Research Focus

Key Achievements

1
H-Index
1
Papers
35
Total Citations
35
Avg Citations/Paper
🏆 Most Cited Paper
High-throughput Functional Genomics Identifies Genes That Ameliorate Toxicity Due to Oxidative Stress in Neuronal HT-22 Cells
35 citations · 2004
📈 Most Prolific Year: 2004 (1 Papers)
🤝 Key Collaborators: 8

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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