OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
CRISPR-Cas9 homology-independent targeted integration of exons 1–19 restores full-length dystrophin in mice
Anthony A. Stephenson, Stefan Nicolau, Tatyana A. Vetter, et al.
Molecular Therapy — Methods & Clinical Development (2023) Vol. 30, pp. 486-499
Open Access | Times Cited: 8
Anthony A. Stephenson, Stefan Nicolau, Tatyana A. Vetter, et al.
Molecular Therapy — Methods & Clinical Development (2023) Vol. 30, pp. 486-499
Open Access | Times Cited: 8
Showing 8 citing articles:
biGMamAct: efficient CRISPR/Cas9-mediated docking of large functional DNA cargoes at the ACTB locus
Martin Pelosse, Marco Marcia
Synthetic Biology (2025) Vol. 10, Iss. 1
Open Access
Martin Pelosse, Marco Marcia
Synthetic Biology (2025) Vol. 10, Iss. 1
Open Access
Establishing a semi-homology-directed recombination method for precision gene integration in axolotls
Liqun Wang, Yan Hu, Yuanhui Qiu, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2025)
Open Access
Liqun Wang, Yan Hu, Yuanhui Qiu, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2025)
Open Access
Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping
Made Harumi Padmaswari, Shilpi Agrawal, Christopher E. Nelson
Journal of Neuromuscular Diseases (2025)
Closed Access
Made Harumi Padmaswari, Shilpi Agrawal, Christopher E. Nelson
Journal of Neuromuscular Diseases (2025)
Closed Access
Post-cleavage target residence determines asymmetry in non-homologous end joining of Cas12a-induced DNA double strand breaks
Ruo-Dan Chen, Yi Yang, Kun-Ming Liu, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
Ruo-Dan Chen, Yi Yang, Kun-Ming Liu, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
biGMamAct: efficient CRISPR/Cas9-mediated docking of large functional DNA cargoes at theACTBlocus
Martin Pelosse, Marco Marcia
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
Martin Pelosse, Marco Marcia
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
Viral and nonviral nanocarriers for in vivo CRISPR-based gene editing
Zhongyuan Guo, Audrey T. Zhu, Ronnie H. Fang, et al.
Nano Research (2024) Vol. 17, Iss. 10, pp. 8904-8925
Closed Access | Times Cited: 1
Zhongyuan Guo, Audrey T. Zhu, Ronnie H. Fang, et al.
Nano Research (2024) Vol. 17, Iss. 10, pp. 8904-8925
Closed Access | Times Cited: 1
Single-stranded DNA with internal base modifications mediates highly efficient knock-in in primary cells using CRISPR-Cas9
Karen L Kanke, Rachael E. Rayner, Jack Bozik, et al.
Nucleic Acids Research (2024)
Open Access | Times Cited: 1
Karen L Kanke, Rachael E. Rayner, Jack Bozik, et al.
Nucleic Acids Research (2024)
Open Access | Times Cited: 1
Precision and efficacy of RNA-guided DNA integration in high-expressing muscle loci
Made Harumi Padmaswari, Gabrielle N Bulliard, Shilpi Agrawal, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 4, pp. 102320-102320
Open Access
Made Harumi Padmaswari, Gabrielle N Bulliard, Shilpi Agrawal, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 4, pp. 102320-102320
Open Access
Lipid Nanoparticles Enable Efficient In Vivo DNA Knock-In via HITI-Mediated Genome Editing
Jun Hirose, Emi Aizawa, Shogo Yamamoto, et al.
Biomolecules (2024) Vol. 14, Iss. 12, pp. 1558-1558
Open Access
Jun Hirose, Emi Aizawa, Shogo Yamamoto, et al.
Biomolecules (2024) Vol. 14, Iss. 12, pp. 1558-1558
Open Access
