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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 vectors displaying bispecific DARPins enable dual-control targeted gene delivery
Samuel A. Theuerkauf, Elena Herrera-Carrillo, F. Atkins John, et al.
Biomaterials (2023) Vol. 303, pp. 122399-122399
Open Access | Times Cited: 11

Showing 11 citing articles:

Advancements and challenges in developing in vivo CAR T cell therapies for cancer treatment
Thuỳ Anh Bùi, Haoqi Mei, Rui Sang, et al.
EBioMedicine (2024) Vol. 106, pp. 105266-105266
Open Access | Times Cited: 15
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
T-cell specific in vivo gene delivery with DART-AAVs targeted to CD8
Muhammed Burak Demircan, Luca J. Zinser, Alexander Michels, et al.
Molecular Therapy (2024) Vol. 32, Iss. 10, pp. 3470-3484
Open Access | Times Cited: 4
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
Molecular Engineering of Virus Tropism
Bo He, Belinda A. Wilson, Shih‐Heng Chen, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 20, pp. 11094-11094
Open Access | Times Cited: 3
A facile chemical strategy to synthesize precise AAV-protein conjugates for targeted gene delivery
Quan Pham, Jake Glicksman, Sadegh Shahraeini, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 2
Adeno-associated Virus (AAV) vectors - a target of cellular and humoral immunity – are expanding their reach towards hematopoietic stem cell modification and immunotherapies
Angela E. Araujo, Martin Bentler, Xabier Perez Garmendia, et al.
Human Gene Therapy (2024) Vol. 35, Iss. 17-18, pp. 586-603
Closed Access | Times Cited: 2
Genome Editing Therapy for the Blood: Ex Vivo Success and In Vivo Prospects
Christy A. George, Srishti U. Sahu, Lorena de Oñate, et al.
The CRISPR Journal (2024)
Closed Access | Times Cited: 2
Nanoscale synthetic biology with innovative medicinal applications
Jingsen Ji, Li Li, Weisheng Guo, et al.
Fundamental Research (2024)
Open Access | Times Cited: 2
The Rise of Cochlear Gene Therapy
Lukas D. Landegger, Ellen Reisinger, François Lallemend, et al.
Molecular Therapy (2024)
Open Access | Times Cited: 1
Molecular concepts for pandemic viruses : membrane fusion assays and targeting of reservoir cells
Samuel A. Theuerkauf
(2024)
Open Access
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