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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:

Epileptogenesis in tuberous sclerosis complex-related developmental and epileptic encephalopathy
Eleonora Aronica, Nicola Specchio, Mark J. Luinenburg, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 2694-2710
Open Access | Times Cited: 37

Showing 1-25 of 37 citing articles:

New GABA-Targeting Therapies for the Treatment of Seizures and Epilepsy: I. Role of GABA as a Modulator of Seizure Activity and Recently Approved Medications Acting on the GABA System
Emilio Perucca, Meir Bialer, H. Steve White
CNS Drugs (2023) Vol. 37, Iss. 9, pp. 755-779
Open Access | Times Cited: 41
mTOR and neuroinflammation in epilepsy: implications for disease progression and treatment
Teresa Ravizza, Mirte Scheper, Rossella Di Sapia, et al.
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 5, pp. 334-350
Closed Access | Times Cited: 28
Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy
Nicola Specchio, Rima Nabbout, Eleonora Aronica, et al.
European Journal of Paediatric Neurology (2023) Vol. 47, pp. 25-34
Open Access | Times Cited: 27
An overview of the value of mTOR inhibitors to the treatment of epilepsy: the evidence to date
Patrick B. Moloney, Norman Delanty
Expert Review of Neurotherapeutics (2025)
Closed Access | Times Cited: 1
The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
Nicola Specchio, Valentina Di Micco, Eleonora Aronica, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Retrospective analysis of presymptomatic treatment in Sturge–Weber syndrome
Chelsea B. Valery, Isabelle Iannotti, Eric H. Kossoff, et al.
Annals of the Child Neurology Society (2024) Vol. 2, Iss. 1, pp. 60-72
Open Access | Times Cited: 7
Is tuberous sclerosis complex-associated autism a preventable and treatable disorder?
Paolo Curatolo, Mirte Scheper, Leonardo Emberti Gialloreti, et al.
World Journal of Pediatrics (2023) Vol. 20, Iss. 1, pp. 40-53
Closed Access | Times Cited: 13
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: 5
Astroglial calcium signaling and homeostasis in tuberous sclerosis complex
Alessia Romagnolo, Giulia Dematteis, Mirte Scheper, et al.
Acta Neuropathologica (2024) Vol. 147, Iss. 1
Open Access | Times Cited: 5
The expanding field of genetic developmental and epileptic encephalopathies: current understanding and future perspectives
Nicola Specchio, Marina Trivisano, Eleonora Aronica, et al.
The Lancet Child & Adolescent Health (2024) Vol. 8, Iss. 11, pp. 821-834
Closed Access | Times Cited: 5
Exhaustive clinical examination of etiology and initial response to first‐line treatment in 577 children with infantile epileptic spasm syndrome children: A 5‐year retrospective observational study
Lin Wan, Wenrong Ge, Guoyin Liu, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 8, pp. 2049-2062
Open Access | Times Cited: 4
Therapeutic Approaches to Tuberous Sclerosis Complex: From Available Therapies to Promising Drug Targets
Elena Conte, Brigida Boccanegra, Giorgia Dinoi, et al.
Biomolecules (2024) Vol. 14, Iss. 9, pp. 1190-1190
Open Access | Times Cited: 4
Distinct peripheral pro‐inflammatory profile associated with tuberous sclerosis complex and epilepsy
Renaud Balthazard, Rose‐Marie Drouin‐Engler, S. Bertrand, et al.
Epilepsia (2025)
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
Intellectual disability and autistic behavior and their modifying factors in children with tuberous sclerosis complex
Sergiusz Jóźwiak, Paolo Curatolo, Katarzyna Kotulska
Brain and Development (2025) Vol. 47, Iss. 2, pp. 104322-104322
Closed Access
Multi-parametric diffusion spectrum imaging in tuberous sclerosis complex: Assessing cortical tubers and predicting genotypes
Hui Sun, Zhiping Yan, Jiawei Gao, et al.
European Journal of Radiology (2025) Vol. 184, pp. 111963-111963
Closed Access
Altered cortical excitability in tuberous sclerosis and the effect of mTOR inhibitors: An intracranial electrical stimulation study
Kishore Vedala, Gewalin Aungaroon, David M. Ritter, et al.
Clinical Neurophysiology (2025) Vol. 172, pp. 1-9
Closed Access
Investigation of Gait Characteristics and Kinematic Deviations in Rare Genetic Disorders with Instrumented Gait Analysis
Esra Kınacı‐Biber, Lis Gys, Anna Jansen, et al.
Journal of Intellectual Disability Research (2025)
Open Access
The clinical interface of tuberous sclerosis complex and autism spectrum disorder: insights and future directions
R. Ramani, B Fatima, Anower Hussain, et al.
Neurological Sciences (2025)
Closed Access
Interictal paroxysmal fast activity and functional connectivity in steroid responsive and non-responsive Lennox-Gastaut syndrome
Zongpu Zhou, Pan Gong, Xianru Jiao, et al.
European Journal of Paediatric Neurology (2025) Vol. 55, pp. 38-46
Closed Access
Improved pre-surgical localization of epileptogenic tubers in pediatric tuberous sclerosis complex using mean apparent propagator MRI
Hui Sun, Zhiping Yan, Jiawei Gao, et al.
Neurosurgical Review (2025) Vol. 48, Iss. 1
Closed Access
Development of a Nomogram for Predicting Tuberous Sclerosis Complex Genotypes in Children Using Advanced Diffusion MRI and Clinical Data
Hui Sun, Zhiping Yan, Jiawei Gao, et al.
Academic Radiology (2025)
Closed Access
Identification of hub genes significantly linked to tuberous sclerosis related-epilepsy and lipid metabolism via bioinformatics analysis
Wang Weiliang, Ren Yinghao, Hou Weiliang, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 2
Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C N‐methyl‐D‐aspartate receptors
Louison Pineau, Emmanuelle Buhler, Sarah Tarhini, et al.
Epilepsia (2024) Vol. 65, Iss. 7, pp. 2111-2126
Open Access | Times Cited: 2
Dementia in Rare Genetic Neurodevelopmental Disorders
Hadassa Kwetsie, Malu van Schaijk, Sven J. van der Lee, et al.
Neurology (2024) Vol. 102, Iss. 11
Open Access | Times Cited: 2
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