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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.

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Showing 13 citing articles:

Loss of Slc35a2 alters development of the mouse cerebral cortex
Soad Elziny, Sahibjot Sran, Hyojung Yoon, et al.
Neuroscience Letters (2024) Vol. 836, pp. 137881-137881
Open Access | Times Cited: 9
Somatic variants in SLC35A2 leading to defects in N-glycosylation in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Xianyu Liu, Qi Tang, Xiaoqian Xia, et al.
Acta Neuropathologica (2025) Vol. 149, Iss. 1
Closed Access | Times Cited: 1
Mild Malformation of Cortical Development With Oligodendroglial Hyperplasia and Epilepsy
Yixin Zhan, Shijia Chen, Zhenghan Jin, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Closed Access
Glycosphingolipid synthesis is impaired in SLC35A2-CDG and improves with galactose supplementation
Andrea Jáñez Pedrayes, Sam De Craemer, Jakub Idkowiak, et al.
Research Square (Research Square) (2025)
Closed Access
Human brain tissue with MOGHE carrying somatic SLC35A2 variants reveal aberrant protein expression and protein loss in the white matter
Erica Cecchini, Simon Geffers, Roland Coras, et al.
Acta Neuropathologica (2025) Vol. 149, Iss. 1
Open Access
Genetic testing in children enrolled in epilepsy surgery program. A real-life study
Barbora Straka, Barbora Splítková, Markéta Vlčková, et al.
European Journal of Paediatric Neurology (2023) Vol. 47, pp. 80-87
Closed Access | Times Cited: 9
Identification and treatment of surgically-remediable causes of infantile epileptic spasms syndrome
Emma Macdonald‐Laurs, Winston Dzau, Aaron E. L. Warren, et al.
Expert Review of Neurotherapeutics (2024) Vol. 24, Iss. 7, pp. 661-680
Closed Access | Times Cited: 3
Multiparametric Characterization of Focal Cortical Dysplasia Using 3D MR Fingerprinting
Ting‐Yu Su, Joon Yul Choi, Siyuan Hu, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 944-957
Open Access | Times Cited: 1
Neuropathology of focal epilepsy: the promise of AI and digital Neuropathology 3.0
Ingmar Blümcke, Jörg Vorndran
Pathology (2024)
Open Access | Times Cited: 1
Precision medicine approaches in epilepsy: A systematic review of genetic markers and personalized treatment strategies
Aman Agarwal, Ravneet Kaur, Faiza Ashfaque, et al.
Precision Medical Sciences (2024) Vol. 13, Iss. 2, pp. 72-83
Open Access | Times Cited: 1
A deep‐learning‐based histopathology classifier for focal cortical dysplasia (FCD) unravels a complex scenario of comorbid FCD subtypes
Jörg Vorndran, Ingmar Blümcke
Epilepsia (2024)
Open Access | Times Cited: 1
Technological and computational approaches to detect somatic mosaicism in epilepsy
Christian M. Boßelmann, Costin Leu, Dennis Lal
Neurobiology of Disease (2023) Vol. 184, pp. 106208-106208
Open Access | Times Cited: 3
SLC35A2 loss of function variants affect glycomic signatures, neuronal fate, and network dynamics
Dulcie Lai, Paulina Sosicka, Damian J. Williams, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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