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:

STXBP1-Related Disorders: Clinical Presentation, Molecular Function, Treatment, and Future Directions
Alexander Freibauer, Mikayla Wohlleben, Cyrus Boelman
Genes (2023) Vol. 14, Iss. 12, pp. 2179-2179
Open Access | Times Cited: 8

Showing 8 citing articles:

Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine
Hannah R. Snyder, Puneet Jain, Rajesh RamachandranNair, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 266-266
Open Access | Times Cited: 6

4-Phenylbutyrate for STXBP1 and SLC6A1. Safety, tolerability, seizure, and EEG outcomes. A case series at 2 centers.
Zachary M. Grinspan, Jacqueline Burré, Jennifer Cross, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

STXBP1 Syndrome: Biotechnological Advances, Challenges, and Perspectives in Gene Therapy, Experimental Models, and Translational Research
Silvestre Ruano-Rodríguez, Mar Navarro-Alonso, Benito Domínguez-Velasco, et al.
BioTech (2025) Vol. 14, Iss. 1, pp. 11-11
Open Access

Neural Excitatory/Inhibitory Imbalance in Motor Aging: From Genetic Mechanisms to Therapeutic Challenges
Xuhui Chen, Ya Wang, Yongning Zhang, et al.
Biology (2025) Vol. 14, Iss. 3, pp. 272-272
Open Access

Exploring potential key genes and disease mechanisms in Εarly-onset genetic epilepsy via integrated bioinformatics analysis
Vasiliki Boulaki, Spiros Efthimiopoulos, Nicholas Κ. Moschonas, et al.
Neurobiology of Disease (2025), pp. 106888-106888
Open Access

Case reports of identical twins with developmental and epileptic encephalopathy with STXBP1 gene mutations for whom different CBD supplementations were markedly effective
Yuji Masataka, Nobuhiro Miki, Kozo Akino, et al.
Epilepsy & Behavior Reports (2024) Vol. 28, pp. 100720-100720
Open Access | Times Cited: 1

A novel clinical approach to abnormal head movements in children: an expert review
Maher A. Khalifa, Mai M. Abou Heikal, Yasser Ragab
Alexandria Journal of Pediatrics (2024) Vol. 37, Iss. 2, pp. 83-88
Closed Access

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