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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:

Reversibility and therapeutic development for neurodevelopmental disorders, insights from genetic animal models
Platon Megagiannis, Rahul Suresh, Guy A. Rouleau, et al.
Advanced Drug Delivery Reviews (2022) Vol. 191, pp. 114562-114562
Closed Access | Times Cited: 10

Showing 10 citing articles:

Presynaptic perspective: Axonal transport defects in neurodevelopmental disorders
Gui-Jing Xiong, Zu‐Hang Sheng
The Journal of Cell Biology (2024) Vol. 223, Iss. 6
Open Access | Times Cited: 4
The role of prickle proteins in vertebrate development and pathology
Katarzyna Anna Radaszkiewicz, Marie Šulcová, E. Kohoutkova, et al.
Molecular and Cellular Biochemistry (2023) Vol. 479, Iss. 5, pp. 1199-1221
Open Access | Times Cited: 10
Transition from Animal-Based to Human Induced Pluripotent Stem Cells (iPSCs)-Based Models of Neurodevelopmental Disorders: Opportunities and Challenges
Sara Guerreiro, Patrı́cia Maciel
Cells (2023) Vol. 12, Iss. 4, pp. 538-538
Open Access | Times Cited: 5
Neurological Disease Modeling Using Pluripotent and Multipotent Stem Cells: A Key Step towards Understanding and Treating Mucopolysaccharidoses
Sofia Carvalho, Juliana Inês Santos, Luciana Moreira, et al.
Biomedicines (2023) Vol. 11, Iss. 4, pp. 1234-1234
Open Access | Times Cited: 4
CRISPR-Cas9 Direct Fusions for Improved Genome Editing via Enhanced Homologous Recombination
Tahmina Tabassum, Giovanni Pietrogrande, Michael D. Healy, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 14701-14701
Open Access | Times Cited: 4
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Research Square (Research Square) (2024)
Open Access
Early Screen Exposure and Developmental Abnormalities: Understanding the Trepidations of “Virtual Autism”
Shreya Detroja, Gayatri Bhatia
Indian Journal of Psychological Medicine (2024)
Open Access
CRISPR/Cas9-based genetic engineering for translational research in neurological disorders
Platon Megagiannis, Guy A. Rouleau, Yang Zhou
Elsevier eBooks (2024), pp. 187-206
Closed Access
Drug Delivery Systems for Treating NeuroDevelopmental Disorders
Boaz Barak, Paolo Decuzzi
Advanced Drug Delivery Reviews (2024), pp. 115473-115473
Closed Access
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
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