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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:

CDKL5 deficiency disorder: molecular insights and mechanisms of pathogenicity to fast-track therapeutic development
Nicole J. Van Bergen, Sean Massey, Anita Quigley, et al.
Biochemical Society Transactions (2022) Vol. 50, Iss. 4, pp. 1207-1224
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

The gut-brain connection: Exploring the influence of the gut microbiota on neuroplasticity and neurodevelopmental disorders
Francesca Damiani, Sara Cornuti, Paola Tognini
Neuropharmacology (2023) Vol. 231, pp. 109491-109491
Open Access | Times Cited: 38
A systematic literature review on the global epidemiology of Dravet syndrome and Lennox–Gastaut syndrome: Prevalence, incidence, diagnosis, and mortality
Joseph Sullivan, Arturo Benítez, Jeannine Roth, et al.
Epilepsia (2024) Vol. 65, Iss. 5, pp. 1240-1263
Open Access | Times Cited: 15
De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms
Ali Hosseini Bereshneh, Jonathan C. Andrews, Daniel F. Eberl, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
Serious Games in the new era of digital-health interventions: A narrative review of their therapeutic applications to manage neurobehavior in neurodevelopmental disorders
Rosa Anna Vacca, Agnese Augello, Luigi Gallo, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 149, pp. 105156-105156
Open Access | Times Cited: 21
Cell type-specific expression, regulation and compensation of CDKL5 activity in mouse brain
Margaux Silvestre, Kelvin Dempster, Simeon R. Mihaylov, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 6, pp. 1844-1856
Open Access | Times Cited: 8
Sex Differences in Brain Disorders
Małgorzata Ziemka‐Nałęcz, Paulina Pawelec, Karolina Ziąbska, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 14571-14571
Open Access | Times Cited: 15
Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies
Antonino Zito, Jeannie T. Lee
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 4
Unveiling Molecular Dynamics of MeCp2, CDKL5 and BDNF in the Hippocampus of Individuals With Intractable Mesial Temporal Lobe Epilepsy
NoorMohammad Meshkinkhood, Parastoo Barati Dowom, Farshid Noorbakhsh, et al.
Journal of Cellular and Molecular Medicine (2025) Vol. 29, Iss. 3
Open Access
Navigating Uncertainty: Assessing Variants of Uncertain Significance in the CDKL5 Gene for Developmental and Epileptic Encephalopathy Using In Silico Prediction Tools and Computational Analysis
Özlem Yalçın Çapan
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 1
Closed 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
A phylogenetic analysis of the CDKL protein family unravels its evolutionary history and supports the Drosophila model of CDKL5 deficiency disorder
María del Carmen Martín-Carrascosa, Christian Palacios-Martínez, Máximo Ibo Galindo
Frontiers in Cell and Developmental Biology (2025) Vol. 13
Open Access
Preclinical studies of gene replacement therapy for CDKL5 deficiency disorder
Gregory Voronin, Jana Narasimhan, Jamila Gittens, et al.
Molecular Therapy (2024) Vol. 32, Iss. 10, pp. 3331-3345
Closed Access | Times Cited: 3
The natural history of CDKL5 deficiency disorder into adulthood
Ángel Aledo‐Serrano, David Lewis‐Smith, Helen Leonard, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Epilepsy-linked kinase CDKL5 phosphorylates voltage-gated calcium channel Cav2.3, altering inactivation kinetics and neuronal excitability
Marisol Sampedro Castañeda, Lucas L. Baltussen, André T. Lopes, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
A review of CDKL: An underestimated protein kinase family
Chenrui Li, Yan Liu, Shilu Luo, et al.
International Journal of Biological Macromolecules (2024) Vol. 277, pp. 133604-133604
Open Access | Times Cited: 2
Autistic‐relevant behavioral phenotypes of a mouse model of cyclin‐dependent kinase‐like 5 deficiency disorder
Nicola Mottolese, Oceane Coiffard, Celeste Ferraguto, et al.
Autism Research (2024) Vol. 17, Iss. 9, pp. 1742-1759
Open Access | Times Cited: 2
Rett and Rett-related disorders: Common mechanisms for shared symptoms?
Santosh R. D’Mello
Experimental Biology and Medicine (2023)
Open Access | Times Cited: 6
CDKL5 regulates p62-mediated selective autophagy and confers protection against neurotropic viruses
Josephine Thinwa, Zhongju Zou, Emily Parks, et al.
Journal of Clinical Investigation (2023) Vol. 134, Iss. 1
Open Access | Times Cited: 5
CDKL5 Deficiency Disorder: Some Lessons Learned 20 Years After the First Description
Elia M. Pestana-Knight, Heather E. Olson
American Journal on Intellectual and Developmental Disabilities (2024) Vol. 129, Iss. 2, pp. 101-109
Closed Access | Times Cited: 1
Drug repurposing in Rett and Rett-like syndromes: a promising yet underrated opportunity?
Claudia Fuchs, Peter A.C. ‘t Hoen, Annelieke R. Müller, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access | Times Cited: 1
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced Neurons
Madison R. Glass, Dosh Whye, Nickesha C. Anderson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder
Hanzhe Kuang, Yunlong Li, Yixuan Wang, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113445-113445
Open Access | Times Cited: 3
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: A Calcium Channelopathy?
Carl E. Stafstrom
Epiliepsy currents/Epilepsy currents (2024) Vol. 24, Iss. 3, pp. 191-193
Open Access
A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism
Antonietta Lombardo, Lorenzo Sinibaldi, Silvia Genovese, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 13, pp. 6912-6912
Open Access
Novel CDKL5 targets identified in human iPSC-derived neurons
Sean Massey, Ching‐Seng Ang, N. Davidson, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access
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