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OpenAlex Citation Counts

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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:

Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophy
Christiano R. R. Alves, Leillani L. Ha, Rebecca Yaworski, et al.
Nature Biomedical Engineering (2023)
Open Access | Times Cited: 18

Showing 18 citing articles:

Advanced Delivery Systems for Gene Editing: A Comprehensive Review from the GenE-HumDi COST Action Working group
Alessia Cavazza, Francisco J Molina-Estévez, Álvaro Plaza Reyes, et al.
Molecular Therapy — Nucleic Acids (2025) Vol. 36, Iss. 1, pp. 102457-102457
Open Access | Times Cited: 2
Selective haematological cancer eradication with preserved haematopoiesis
Simon Garaudé, Romina Marone, Rosalba Lepore, et al.
Nature (2024) Vol. 630, Iss. 8017, pp. 728-735
Open Access | Times Cited: 13
CHANGE-seq-BE enables simultaneously sensitive and unbiasedin vitroprofiling of base editor genome-wide activity
Cícera R. Lazzarotto, Varun Katta, Yichao Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Treating neuromuscular diseases: unveiling gene therapy breakthroughs and pioneering future applications
Yu‐Fu Wu, Jun‐An Chen, Yuh‐Jyh Jong
Journal of Biomedical Science (2025) Vol. 32, Iss. 1
Open Access
Preparation of high-purity RNPs of CRISPR-based DNA base editors
Mitchell J. McAndrew, Madeleine B. King, Audronė Lapinaitė
Methods in enzymology on CD-ROM/Methods in enzymology (2025), pp. 277-315
Closed Access
Improving adenine base editing precision by enlarging the recognition domain of CRISPR-Cas9
Shuliang Gao, Benson Weng, Douglas Wich, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Selict-seq profiles genome-wide off-target effects in adenosine base editing
Kexin Yuan, Xi Xin, Shaoqing Han, et al.
Nucleic Acids Research (2025) Vol. 53, Iss. 7
Open Access
Prenatal gene editing for neurodevelopmental diseases: Ethical considerations
Rami Major, Eric T. Juengst
The American Journal of Human Genetics (2025)
Open Access
CRISPR-dependent base editing as a therapeutic strategy for rare monogenic disorders
Júlia-Jié Cabré-Romans, Raquel Cuella-Martin
Frontiers in Genome Editing (2025) Vol. 7
Open Access
Engineering adeno-associated viral vectors for CRISPR/Cas based in vivo therapeutic genome editing
Buhle Moyo, Leo D. Brown, Ishika I Khondaker, et al.
Biomaterials (2025), pp. 123314-123314
Closed Access
Crispr-Based Editing of Human Pluripotent Stem Cells for Disease Modeling
Yun Chang, Feng Lan, Yongshuai Zhang, et al.
Stem Cell Reviews and Reports (2024) Vol. 20, Iss. 5, pp. 1151-1161
Closed Access | Times Cited: 2
Microglial Replacement and COURIER or SPIT for Neuronal Gene Editing
Michael Renteln
(2024)
Open Access | Times Cited: 1
Improvement of TaC9‐ABE mediated correction of human SMN2 gene
Xiaohua Peng, Yue Chi, Jinling Wang, et al.
Biotechnology and Bioengineering (2024) Vol. 121, Iss. 10, pp. 3059-3067
Closed Access | Times Cited: 1
Management and Therapeutic Strategies for Spinal Muscular Atrophy
Kochumon Sheena P, Nair Cherupally Krishnan Krishnan
Journal of Genetic Medicine and Gene Therapy (2024) Vol. 7, Iss. 1, pp. 001-007
Open Access
New Perspectives in Human Embryology [Working Title]

Obstetrics and gynecology. (2024)
Closed Access
The research progress of correcting pathogenic mutations by base editing
Guanglei Li, Yu Zhang, Xingxu Huang
IntechOpen eBooks (2024)
Open Access
The severe von Willebrand Disease variant p.M771V leads to impaired anterograde trafficking of Von Willebrand factor in patient-derived and base-edited ECFCs
Ilana Bar, Allison Barraclough, Petra E. Bürgisser, et al.
Journal of Thrombosis and Haemostasis (2024)
Closed Access
Mutation corrections in spinal muscular atrophy
Andrew Portell, Prashant Mali
Nature Biomedical Engineering (2023) Vol. 8, Iss. 2, pp. 111-113
Closed Access
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