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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:

Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 433-513
Open Access | Times Cited: 91

Showing 1-25 of 91 citing articles:

Developmental and epileptic encephalopathies
Ingrid E. Scheffer, Sameer M. Zuberi, Heather C. Mefford, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 16
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study
Benedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1248-1248
Open Access | Times Cited: 8
Thalamocortical circuits in generalized epilepsy: Pathophysiologic mechanisms and therapeutic targets
Britta E. Lindquist, Clare Timbie, Yuliya Voskobiynyk, et al.
Neurobiology of Disease (2023) Vol. 181, pp. 106094-106094
Open Access | Times Cited: 19
Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies
Luigi Vetri, Francesco Calı̀, Salvatore Saccone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1146-1146
Open Access | Times Cited: 6
Severity of GNAO1‐Related Disorder Correlates with Changes in G‐Protein Function
J. Domínguez-Carral, W.H. Ludlam, Mar Junyent Segarra, et al.
Annals of Neurology (2023) Vol. 94, Iss. 5, pp. 987-1004
Open Access | Times Cited: 15
An update on the seizures beget seizures theory
Přemysl Jiruška, Dean R. Freestone, Vadym Gnatkovsky, et al.
Epilepsia (2023) Vol. 64, Iss. S3
Open Access | Times Cited: 13
Developmental and Epileptic Encephalopathy: Pathogenesis of Intellectual Disability Beyond Channelopathies
Alexandra D. Medyanik, Polina E. Anisimova, Angelina Kustova, et al.
Biomolecules (2025) Vol. 15, Iss. 1, pp. 133-133
Open Access
To what extent does status epilepticus contribute to brain damage in the developmental and epileptic Encephalopathies
Nicola Specchio, Stéphane Auvin
Epilepsy & Behavior (2025) Vol. 164, pp. 110271-110271
Closed 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
Expanding the phenotypic spectrum of DNM1-related disorders: novel GTPase domain variants and their diverse neurological outcomes
Juan Liu, Jihong Hu, Yaqin Duan, et al.
Neurological Sciences (2025)
Closed Access
Expert-Agreed Practical Recommendations on the Use of Fenfluramine in Developmental and Epileptic Encephalopathies Based on Clinical Experience and Literature Review
Vicente Villanueva, Víctor Soto Insuga, Patricia Smeyers, et al.
Neurology and Therapy (2025)
Open Access
Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality
Lara Pizzamiglio, Fabrizio Capitano, Evgeniia Rusina, et al.
Neurobiology of Disease (2025) Vol. 207, pp. 106853-106853
Open Access
MOTOR PHENOTYPING IN A GREEK COHORT OF PATIENTS WITH NEONATAL AND INFANTILE ONSET DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY
Elissavet Kollia, Eleftheria Kokkinou, Chrysa Outsika, et al.
European Journal of Paediatric Neurology (2025) Vol. 55, pp. 1-8
Closed Access
Comorbidity Between Mental and Physical Disorders in Children and Adolescents: Identification, Management, and Treatment
Daniele Marcotulli, Anna Salvalaggio, Anita Zardini, et al.
(2025), pp. 275-298
Closed Access
A Novel YWHAG Variant L173S Causes Developmental and Epileptic Encephalopathy by Disrupting the Hydrophobic Internal Protein Structure
Jin Yuan, Qian Niu, S. Liang, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 4
Open Access
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy?
Raffaele Falsaperla, Annamaria Sapuppo, Xena Giada Pappalardo, et al.
Molecular and Cellular Pediatrics (2025) Vol. 12, Iss. 1
Open Access
Neonate with developmental and epileptic encephalopathy 81 (DEE81): lessons learnt and future implications
Anshika Mishra, Prerna Priyadarshini, Shalini Tripathi, et al.
BMJ Case Reports (2025) Vol. 18, Iss. 4, pp. e260508-e260508
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
RNF13 Variants L311S and L312P Associated with Developmental Epileptic Encephalopathy Alter Dendritic Organization in Hippocampal Neurons
Valérie C. Cabana, Marc Lussier
IBRO Neuroscience Reports (2025)
Open Access
Revisiting the concept of drug‐resistant epilepsy: A TASK1 report of the ILAE/AES Joint Translational Task Force
Stéphane Auvin, Aristea S. Galanopoulou, Solomon L. Moshé, et al.
Epilepsia (2023) Vol. 64, Iss. 11, pp. 2891-2908
Closed Access | Times Cited: 12
Steps to Improve Precision Medicine in Epilepsy
Simona Balestrini, Davide Mei, Sanjay M. Sisodiya, et al.
Molecular Diagnosis & Therapy (2023) Vol. 27, Iss. 6, pp. 661-672
Open Access | Times Cited: 11
Long‐term effectiveness and tolerability of ketogenic diet therapy in patients with genetic developmental and epileptic encephalopathy onset within the first 6 months of life
Tianyu Song, Jie Deng, Chun‐Hong Chen, et al.
Epilepsia Open (2024) Vol. 9, Iss. 2, pp. 643-652
Open Access | Times Cited: 4
The Neurovascular Unit Dysfunction in the Molecular Mechanisms of Epileptogenesis and Targeted Therapy
Xiuxiu Liu, Ying Zhang, Yanming Zhao, et al.
Neuroscience Bulletin (2024) Vol. 40, Iss. 5, pp. 621-634
Open Access | Times Cited: 4
Preictal dysfunctions of inhibitory interneurons paradoxically lead to their rebound hyperactivity and to low-voltage-fast onset seizures in Dravet syndrome
Fabrizio Capitano, Mathieu Kuchenbuch, Jennifer Lavigne, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 23
Open Access | Times Cited: 4
Unveiling the disease progression in developmental and epileptic encephalopathies: Insights from EEG and neuropsychology
Paolo Surdi, Marina Trivisano, Angela De Dominicis, et al.
Epilepsia (2024) Vol. 65, Iss. 11, pp. 3279-3292
Open Access | Times Cited: 4
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