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:

Engineered AAVs for non-invasive gene delivery to rodent and non-human primate nervous systems
Xinhong Chen, Sripriya Ravindra Kumar, Cameron D. Adams, et al.
Neuron (2022) Vol. 110, Iss. 14, pp. 2242-2257.e6
Open Access | Times Cited: 82

Showing 1-25 of 82 citing articles:

AAV-based in vivo gene therapy for neurological disorders
Qinglan Ling, Jessica A. Herstine, Allison M. Bradbury, et al.
Nature Reviews Drug Discovery (2023) Vol. 22, Iss. 10, pp. 789-806
Closed Access | Times Cited: 77

Adeno-associated viral vectors for functional intravenous gene transfer throughout the non-human primate brain
Miguel R. Chuapoco, Nicholas C. Flytzanis, Nick Goeden, et al.
Nature Nanotechnology (2023) Vol. 18, Iss. 10, pp. 1241-1251
Open Access | Times Cited: 47

The nature and neurobiology of fear and anxiety: State of the science and opportunities for accelerating discovery
Shannon E. Grogans, Eliza Bliss‐Moreau, Kristin A. Buss, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 151, pp. 105237-105237
Closed Access | Times Cited: 39

Functional gene delivery to and across brain vasculature of systemic AAVs with endothelial-specific tropism in rodents and broad tropism in primates
Xinhong Chen, Damien A. Wolfe, Dhanesh Sivadasan Bindu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 39

Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders
Jihad El Andari, Edith Renaud-Gabardos, Warut Tulalamba, et al.
Science Advances (2022) Vol. 8, Iss. 38
Open Access | Times Cited: 40

Spatial transcriptomics for profiling the tropism of viral vectors in tissues
Min Jee Jang, Gerard Michael Coughlin, Cameron Jackson, et al.
Nature Biotechnology (2023) Vol. 41, Iss. 9, pp. 1272-1286
Open Access | Times Cited: 29

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: 27

Molecular and cognitive signatures of ageing partially restored through synthetic delivery of IL2 to the brain
Pierre Lemaître, Samar Tareen, Emanuela Pasciuto, et al.
EMBO Molecular Medicine (2023) Vol. 15, Iss. 5
Open Access | Times Cited: 26

Primate-conserved carbonic anhydrase IV and murine-restricted LY6C1 enable blood-brain barrier crossing by engineered viral vectors
Timothy F. Shay, Erin E. Sullivan, Xiaozhe Ding, et al.
Science Advances (2023) Vol. 9, Iss. 16
Open Access | Times Cited: 25

Micro/nanosystems for controllable drug delivery to the brain
Mingzhen Tian, Zhichao Ma, Guang‐Zhong Yang
The Innovation (2023) Vol. 5, Iss. 1, pp. 100548-100548
Open Access | Times Cited: 24

Advances in AAV technology for delivering genetically encoded cargo to the nonhuman primate nervous system
Lillian J. Campos, Cynthia M. Arokiaraj, Miguel R. Chuapoco, et al.
Current Research in Neurobiology (2023) Vol. 4, pp. 100086-100086
Open Access | Times Cited: 21

The role of cellular and molecular neuroimmune crosstalk in gut immunity
Daping Yang, Nicole Almanzar, Isaac M. Chiu
Cellular and Molecular Immunology (2023) Vol. 20, Iss. 11, pp. 1259-1269
Open Access | Times Cited: 21

Transcriptional reprogramming restores UBE3A brain-wide and rescues behavioral phenotypes in an Angelman syndrome mouse model
Henriette O’Geen, Ulrika Beitnere, Miranda S. Garcia, et al.
Molecular Therapy (2023) Vol. 31, Iss. 4, pp. 1088-1105
Open Access | Times Cited: 19

Gene therapy and other novel treatment approaches for Charcot-Marie-Tooth disease
Chiara Pisciotta, Davide Pareyson
Neuromuscular Disorders (2023) Vol. 33, Iss. 8, pp. 627-635
Closed Access | Times Cited: 19

Natural Adeno-Associated Virus Serotypes and Engineered Adeno-Associated Virus Capsid Variants: Tropism Differences and Mechanistic Insights
Estrella López-Gordo, Kyle Chamberlain, Jalish M. Riyad, et al.
Viruses (2024) Vol. 16, Iss. 3, pp. 442-442
Open Access | Times Cited: 10

The menace of severe adverse events and deaths associated with viral gene therapy and its potential solution
Artyom Kachanov, Anastasiya Kostyusheva, Sergey Brezgin, et al.
Medicinal Research Reviews (2024) Vol. 44, Iss. 5, pp. 2112-2193
Closed Access | Times Cited: 8

An innate immune response to adeno-associated virus genomes decreases cortical dendritic complexity and disrupts synaptic transmission
Christos Michael Suriano, Neerav Kumar, Jessica L. Verpeut, et al.
Molecular Therapy (2024) Vol. 32, Iss. 6, pp. 1721-1738
Open Access | Times Cited: 6

Probing neural circuit mechanisms in Alzheimer’s disease using novel technologies
Steven F. Grieco, Todd C. Holmes, Xiangmin Xu
Molecular Psychiatry (2023) Vol. 28, Iss. 10, pp. 4407-4420
Open Access | Times Cited: 17

Charcot–Marie–Tooth neuropathies: Current gene therapy advances and the route toward translation
Marina Stavrou, Alexia Kagiava, Irene Sargiannidou, et al.
Journal of the Peripheral Nervous System (2023) Vol. 28, Iss. 2, pp. 150-168
Open Access | Times Cited: 14

Synthetic dosage-compensating miRNA circuits for quantitative gene therapy
Michael Flynn, A. Mayfield, Rongrong Du, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Highly conserved brain vascular receptor ALPL mediates transport of engineered viral vectors across the blood-brain barrier
Tyler C. Moyer, Brett Hoffman, Weitong Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Multimodal evaluation of network activity and optogenetic interventions in human hippocampal slices
John P. Andrews, Jinghui Geng, Kateryna Voitiuk, et al.
Nature Neuroscience (2024)
Closed Access | Times Cited: 5

Adeno-associated virus–based gene therapy treats inflammatory kidney disease in mice
Guochao Wu, Shuya Liu, Julia Hagenstein, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 17
Open Access | Times Cited: 4

Routes of administration for adeno-associated viruses carrying gene therapies for brain diseases
Kai Zhou, Jinming Han, Yafeng Wang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 23

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