Christopher E. Nelson
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Assistant Professor
Also affiliated: Dartmouth College (1994–1998); University of North Carolina at Chapel Hill (2024); Rutherford Appleton Laboratory (2020); Oak Ridge National Laboratory (2025); Intel (United States) (2016); North Carolina State University (2024); Lawrence Berkeley National Laboratory (2002–2015); Cooperative Institute for Research in Environmental Sciences (1998); Duke University (2014–2021); Iowa State University (1991); University of Colorado Boulder (1998–2004); Vanderbilt University (2011–2016); Battery Park (1938); Miller Group (Canada) (1952); Center for Nanoscale Science and Technology (2013); Kemin (Belgium) (1993); Capital Meeting Planning (1963); Tashkent Institute of Irrigation and Agricultural Mechanization Engineers (1960); Duke Medical Center (2015–2017); Dow Chemical (United States) (1951–2023); Institute for Soil Sciences (1953); Applied Genetic Technologies (United States) (2019); Nashville Oncology Associates (2014–2015); Northwest Irrigation and Soils Research Laboratory (1953); Genetic Technologies (Australia) (2021); Vanderbilt Health (2015); Hartford Financial Services (United States) (1998); KLA (United States) (1999–2007); Washington State University (1967–1983); Morehouse College (1989); Michigan State University (2002); Atlanta University Center (1989)
Faculty Researcher
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Christopher E. Nelson's research focuses on gene editing technologies, particularly CRISPR-Cas9, and their application in treating genetic disorders. His work investigates the challenges and optimization strategies for delivering these gene editing tools, with a significant emphasis on Duchenne muscular dystrophy. Nelson has published on preclinical development for exon skipping in Duchenne muscular dystrophy and explored the delivery mechanisms for CRISPR-Cas9 genome editing for this condition.
His research also delves into the immune responses to gene therapy vectors, such as adeno-associated virus (AAV), in preclinical models. Nelson has received federal funding for projects exploring the genomic and cellular factors influencing gene therapy durability and for developing non-viral delivery methods for CRISPR/Cas9. He also contributes to research on extracellular matrix biomaterials and has investigated markers for colorectal tumor progression. With a substantial publication record and high citation count, Nelson leads an active research group at the University of Arkansas at Fayetteville and collaborates with several colleagues within the institution.
Metrics
- h-index: 38
- Publications: 145
- Citations: 5,874
Selected Publications
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Targeting mitochondrial dynamics via OPA1 overexpression and BNIP3 knockdown confers protection against pancreatic cancer induced muscle dysfunction (2026)
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OPTIMIZATION OF PRODUCTION, QUANTIFICATION, AND QUALIFICATION OF LENTIVIRAL VECTORS (2026)
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Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy (2025)
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Standardizing a Protocol for Streamlined Synthesis and Characterization of Lipid Nanoparticles to Enable Preclinical Research and Education (2025)
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A dual-fluorescence assay for gene delivery vehicle screening in macrophages with an inflammation-inducible reporter construct (2025)
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Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping (2025)
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Resistance to Acetyl Coenzyme A Carboxylase (ACCase) Inhibitor in Lolium multiflorum: Effect of Multiple Target-Site Mutations (2024)
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Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci (2024)
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Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing (2024)
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Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci (2024)
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PINE-TREE enables efficient enrichment of prime-edited hPSCs (2023)
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Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy (2023)
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Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies (2022)
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Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies (2022)
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Gene delivery into cells and tissues (2020)
Federal Grants 3 $1,036,213 total
Exploring genomic and cellular determinants of gene therapy durability
Non-viral delivery of CRISPR/Cas9 for targeted gene replacement
Collaboration Network
Top Collaborators
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping
Showing 5 of 9 shared publications
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping
Showing 5 of 6 shared publications
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- PINE-TREE enables efficient enrichment of prime-edited hPSCs
- Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Standardizing a Protocol for Streamlined Synthesis and Characterization of Lipid Nanoparticles to Enable Preclinical Research and Education
- A dual-fluorescence assay for gene delivery vehicle screening in macrophages with an inflammation-inducible reporter construct
- Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- A dual-fluorescence assay for gene delivery vehicle screening in macrophages with an inflammation-inducible reporter construct
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
- Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Longitudinal examination of perfusion and angiogenesis markers in primary colorectal tumors shows distinct signatures for metronomic and maximum-tolerated dose strategies
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- A dual-fluorescence assay for gene delivery vehicle screening in macrophages with an inflammation-inducible reporter construct
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
- Beyond the Cut: Long-read sequencing reveals complex genomic and transcriptomic changes in AAV-CRISPR therapy for Duchenne Muscular Dystrophy
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Optimizing Recombinant Cas9 Expression: Insights from E. coli BL21(DE3) Strains for Enhanced Protein Purification and Genome Editing
- Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
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