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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:

AAV capsid design: A Goldilocks challenge
Sergei Zolotukhin, Luk H. Vandenberghe
Trends in Molecular Medicine (2022) Vol. 28, Iss. 3, pp. 183-193
Closed Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

Gene therapy for liver diseases — progress and challenges
Nerea Zabaleta, Carmen Unzu, Nicholas D. Weber, et al.
Nature Reviews Gastroenterology & Hepatology (2023) Vol. 20, Iss. 5, pp. 288-305
Closed Access | Times Cited: 42
Brainwide silencing of prion protein by AAV-mediated delivery of an engineered compact epigenetic editor
Edwin N. Neumann, Tessa M. Bertozzi, Elaine Wu, et al.
Science (2024) Vol. 384, Iss. 6703
Closed Access | Times Cited: 22
Understanding AAV vector immunogenicity: from particle to patient
Bijay Dhungel, Ian Winburn, Candida da Fonseca Pereira, et al.
Theranostics (2024) Vol. 14, Iss. 3, pp. 1260-1288
Open Access | Times Cited: 15
Fantastic AAV Gene Therapy Vectors and How to Find Them—Random Diversification, Rational Design and Machine Learning
Jonas Becker, Julia Fakhiri, Dirk Grimm
Pathogens (2022) Vol. 11, Iss. 7, pp. 756-756
Open Access | Times Cited: 53
AAV Engineering for Improving Tropism to the Central Nervous System
Muhammad S Ghauri, Li Ou
Biology (2023) Vol. 12, Iss. 2, pp. 186-186
Open Access | Times Cited: 30
Precision RNA base editing with engineered and endogenous effectors
Laura S. Pfeiffer, Thorsten Stafforst
Nature Biotechnology (2023) Vol. 41, Iss. 11, pp. 1526-1542
Closed Access | Times Cited: 30
Cell and gene therapy for kidney disease
Jennifer L. Peek, Matthew H. Wilson
Nature Reviews Nephrology (2023) Vol. 19, Iss. 7, pp. 451-462
Open Access | Times Cited: 29
Advances in AAV technology for delivering genetically encoded cargo to the nonhuman primate nervous system
Lillian Campos, Cynthia M. Arokiaraj, Miguel R. Chuapoco, et al.
Current Research in Neurobiology (2023) Vol. 4, pp. 100086-100086
Open Access | Times Cited: 23
An adeno-associated virus variant enabling efficient ocular-directed gene delivery across species
Shuang Luo, Hao Jiang, Qingwei Li, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Artificial Intelligence‐Based Approaches for AAV Vector Engineering
Fangzhi Tan, Yue Dong, Jieyu Qi, et al.
Advanced Science (2025)
Open Access | Times Cited: 1
Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing
Trevor J. Gonzalez, Katherine E. Simon, Leo O. Blondel, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 35
Tumor antigen-loaded AAV vaccine drives protective immunity in a melanoma animal model
Karina Krotova, Hisae Kuoch, Colin Caine, et al.
Molecular Therapy — Methods & Clinical Development (2023) Vol. 28, pp. 301-311
Open Access | Times Cited: 16
Chemical approaches to probe and engineer AAV vectors
Quan Pham, Jake Glicksman, Abhishek Chatterjee
Nanoscale (2024) Vol. 16, Iss. 29, pp. 13820-13833
Open Access | Times Cited: 6
Structure-guided AAV capsid evolution strategies for enhanced CNS gene delivery
Trevor J. Gonzalez, Aaron Mitchell-Dick, Leo O. Blondel, et al.
Nature Protocols (2023) Vol. 18, Iss. 11, pp. 3413-3459
Closed Access | Times Cited: 13
An engineered adeno-associated virus mediates efficient blood-brain barrier penetration with enhanced neurotropism and reduced hepatotropism
Nengsong Luo, Kunzhang Lin, Yuxiang Cai, et al.
Journal of Controlled Release (2025) Vol. 379, pp. 303-315
Open Access
Approaches and applications in transdermal and transpulmonary gene drug delivery
Anni Zhang, Xuran Zhang, Jiahui Chen, et al.
Frontiers in Bioengineering and Biotechnology (2025) Vol. 12
Open Access
Adeno-Associated Virus Vectors: Principles, Practices, and Prospects in Gene Therapy
Limor Zwi‐Dantsis, Saira Mohamed, Giulia Massaro, et al.
Viruses (2025) Vol. 17, Iss. 2, pp. 239-239
Open Access
Loss of Golga7 Suppresses Oncogenic Nras‐Driven Leukemogenesis without Detectable Toxicity in Adult Mice
Bo Jiao, Lei Yan, Rui Zhang, et al.
Advanced Science (2025)
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
Characterization of the humanized FRG mouse model and development of an AAV-LK03 variant with improved liver lobular biodistribution
Marti Cabanes‐Creus, Renina Gale Navarro, Sophia H.Y. Liao, et al.
Molecular Therapy — Methods & Clinical Development (2023) Vol. 28, pp. 220-237
Open Access | Times Cited: 12
Computer-Aided Directed Evolution Generates Novel AAV Variants with High Transduction Efficiency
Zengpeng Han, Nengsong Luo, Fei Wang, et al.
Viruses (2023) Vol. 15, Iss. 4, pp. 848-848
Open Access | Times Cited: 12
Drug product formulation and fill/finish manufacturing process considerations for AAV-based genomic medicines
Madhura Som, Benson Gikanga, Varna Kanapuram, et al.
Journal of Pharmaceutical Sciences (2024) Vol. 113, Iss. 7, pp. 1711-1725
Closed Access | Times Cited: 4
Probing recombinant AAV capsid integrity and genome release after thermal stress by mass photometry
Eduard H.T.M. Ebberink, Alisa Ruisinger, Markus Nuebel, et al.
Molecular Therapy — Methods & Clinical Development (2024) Vol. 32, Iss. 3, pp. 101293-101293
Open Access | Times Cited: 4
The Expression and Function of the Small Nonstructural Proteins of Adeno-Associated Viruses (AAVs)
Çağla Aksu Küz, Shane McFarlin, Jianming Qiu
Viruses (2024) Vol. 16, Iss. 8, pp. 1215-1215
Open Access | Times Cited: 3
Human cell surface-AAV interactomes identify LRP6 as blood-brain barrier transcytosis receptor and immune cytokine IL3 as AAV9 binder
Timothy F. Shay, Seongmin Jang, Tyler J. Brittain, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
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