Made Harumi Padmaswari Data-verified

Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.

Researcher

Last publication 2025 Last refreshed 2026-05-16

unknown

2 h-index 6 pubs 26 cited

Biography and Research Information

OverviewAI-generated summary

Made Harumi Padmaswari's research focuses on the preclinical development of genome editing strategies for Duchenne muscular dystrophy. Her work investigates the delivery challenges associated with CRISPR-Cas9 technology for this genetic disorder, exploring methods to optimize its efficacy in treating muscle disease. Padmaswari has published research on improving recombinant Cas9 expression for enhanced protein purification and genome editing applications. She also studies the precision and efficacy of RNA-guided DNA integration in muscle tissue and the complex genomic and transcriptomic changes that can occur with AAV-CRISPR therapy. Her publications include work on exon skipping as a therapeutic approach for Duchenne muscular dystrophy. Padmaswari collaborates with researchers at the University of Arkansas at Fayetteville, including Christopher E. Nelson and Shilpi Agrawal, with whom she has co-authored multiple publications.

Metrics

  • h-index: 2
  • Publications: 6
  • Citations: 26

Selected Publications

  • Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy (2025)
  • Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping (2025)
    2 citations DOI OpenAlex
  • Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci (2024)
    2 citations DOI OpenAlex
  • Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing (2024)
    5 citations DOI OpenAlex
  • Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci (2024)
    2 citations DOI OpenAlex
  • Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy (2023)
    10 citations DOI OpenAlex

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Collaboration Network

12 Collaborators 3 Institutions 1 Country

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