Renzhi Han
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
134
Citations
4,750
Est. group size
—
Recurring co-author estimate
Active years
43
Publishing since 1984
Renzhi Han studies gene and genome editing therapies for inherited and metabolic diseases, with a strong focus on Duchenne muscular dystrophy (a genetic muscle-wasting disorder) and related heart complications. The work uses tools such as CRISPR-based editing, base and epigenome editing, and viral gene delivery (for example AAV vectors) in animal models to restore missing proteins or lower disease-causing factors like blood cholesterol and lipids.
Publication activity has been fairly steady across the past decade, averaging about 7-8 papers per year over the last five years with some year-to-year fluctuation.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- In vivo base editing of Asgr1 reduces blood lipids in mice
Molecular Therapy · 2026
- A Virtual Peer Mentor to Enhance Social Presence in VR Rehabilitation for Recovering Heart-Attack Patients
IEEE Transactions on Visualization and Computer Graphics · 2026
- Therapeutic Gene Editing: DNA Repair Pathways, Emerging Editors, and Clinical Progress
iNew Medicine · 2026
- Dystrophin rescue in the brain for DMD
Molecular Therapy — Nucleic Acids · 2026
- Factor VIII originates primarily from anatomically distinct subsets of liver sinusoidal endothelial cells
Blood Advances · 2026
- Sproutfit: an immersive seed-planting virtual reality game to enhance patient motivation for performing exercises for the prevention of venous thromboembolism through loss and avoidance gamification
Virtual Reality · 2025
- An approximate analytical method for evaluating the first-crossing probability of base-isolated structures subjected to stochastic pulse-like ground motions
2025
- Recent advances in therapeutic gene-editing technologies
Molecular Therapy · 2025
- IDOL Deficiency Inhibits Cholesterol-Rich Diet–Induced Atherosclerosis in Rabbits
Arteriosclerosis Thrombosis and Vascular Biology · 2025
- Promotion or inhibition? This is a question in gene editing
Molecular Therapy · 2025
- An oversized AAV8 vector to deliver CPS1
Molecular Therapy — Nucleic Acids · 2025
- Systemic Delivery of Full-Length Dystrophin in DMD Mice
Research Square · 2024
- Systemic delivery of full-length dystrophin in Duchenne muscular dystrophy mice
Nature Communications · 2024
- High Resolution Sequence Stratigraphy Constrained Precise Palaeogene Reservoir Prediction
2024
- Cardiomyopathy in Duchenne Muscular Dystrophy and the Potential for Mitochondrial Therapeutics to Improve Treatment Response
Cells · 2024
- Molecular Therapy×12
- Research Square×6
- Figshare×6
- Molecular Therapy — Nucleic Acids×4
- Nature Communications×3
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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