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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:

Functional screening of GATOR1 complex variants reveals a role for mTORC1 deregulation in FCD and focal epilepsy
Ruby Dawson, Alvaro F. Nieto Guil, Louise J. Robertson, et al.
Neurobiology of Disease (2019) Vol. 134, pp. 104640-104640
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Epilepsy in the mTORopathies: opportunities for precision medicine
Patrick B. Moloney, Gianpiero L. Cavalleri, Norman Delanty
Brain Communications (2021) Vol. 3, Iss. 4
Open Access | Times Cited: 87
Antisense oligonucleotide therapy for KCNT1 encephalopathy
Lisseth Estefania Burbano, Melody Li, Nikola Jancovski, et al.
JCI Insight (2022) Vol. 7, Iss. 23
Open Access | Times Cited: 42
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
Convergent and Divergent Mechanisms of Epileptogenesis in mTORopathies
Lena H. Nguyen, Angélique Bordey
Frontiers in Neuroanatomy (2021) Vol. 15
Open Access | Times Cited: 55
DEPDC5-related epilepsy: A comprehensive review
Debopam Samanta
Epilepsy & Behavior (2022) Vol. 130, pp. 108678-108678
Closed Access | Times Cited: 37
Prevention of premature death and seizures in a Depdc5 mouse epilepsy model through inhibition of mTORC1
Lindsay K. Klofas, Brittany Short, Chengwen Zhou, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 8, pp. 1365-1377
Open Access | Times Cited: 33
Everolimus precision therapy for the GATOR1‐related epilepsies: A case series
Patrick B. Moloney, Hugh Kearney, Katherine A. Benson, et al.
European Journal of Neurology (2023) Vol. 30, Iss. 10, pp. 3341-3346
Open Access | Times Cited: 13
Acute knockdown of Depdc5 leads to synaptic defects in mTOR-related epileptogenesis
Antonio De Fusco, Maria Sabina Cerullo, Antonella Marte, et al.
Neurobiology of Disease (2020) Vol. 139, pp. 104822-104822
Open Access | Times Cited: 29
DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect
Liu Liu, Zirong Chen, Hai-Qing Xu, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 29
SUDEP risk and autonomic dysfunction in genetic epilepsies
Ahmed N. Sahly, Michael Shevell, Lynette G. Sadleir, et al.
Autonomic Neuroscience (2021) Vol. 237, pp. 102907-102907
Closed Access | Times Cited: 24
Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery
Hao Wang, Wenwei Liu, Yuehua Zhang, et al.
Epilepsia Open (2023) Vol. 8, Iss. 3, pp. 969-979
Open Access | Times Cited: 10
Neuronal cell type specific roles for Nprl2 in neurodevelopmental disorder-relevant behaviors
Brianne Dentel, Lidiette Angeles-Perez, Abigail Y. Flores, et al.
Neurobiology of Disease (2025) Vol. 205, pp. 106790-106790
Open Access
4E-BP2–dependent translation in parvalbumin neurons controls epileptic seizure threshold
Vijendra Sharma, Rapita Sood, Danning Lou, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 15
Open Access | Times Cited: 22
Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE)
Stefka Mincheva-Tasheva, Alvaro F. Nieto Guil, Claire C. Homan, et al.
Molecular Neurobiology (2021) Vol. 58, Iss. 5, pp. 2005-2018
Closed Access | Times Cited: 21
Current Review in Basic Science: Animal Models of Focal Cortical Dysplasia and Epilepsy
Lena H. Nguyen, Angélique Bordey
Epiliepsy currents/Epilepsy currents (2022) Vol. 22, Iss. 4, pp. 234-240
Open Access | Times Cited: 15
GATOR1 Mutations Impair PI3 Kinase-Dependent Growth Factor Signaling Regulation of mTORC1
Maéline Muller, Jasmine Bélanger, Imane Hadj-Aissa, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2068-2068
Open Access | Times Cited: 3
Unraveling the genetic basis of epilepsy: Recent advances and implications for diagnosis and treatment
Rekha Dwivedi, Meenakshi Kaushik, Manjari Tripathi, et al.
Brain Research (2024) Vol. 1843, pp. 149120-149120
Closed Access | Times Cited: 3
DEPDC5 haploinsufficiency drives increased mTORC1 signaling and abnormal morphology in human iPSC-derived cortical neurons
Lindsay K. Klofas, Brittany Short, John P. Snow, et al.
Neurobiology of Disease (2020) Vol. 143, pp. 104975-104975
Open Access | Times Cited: 19
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy
Shiyue Du, Sheng Zeng, Song Li, et al.
Science China Life Sciences (2023) Vol. 66, Iss. 9, pp. 2152-2166
Closed Access | Times Cited: 5
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
Athina Ververi, Sara Zagaglia, Lara Menzies, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 4, pp. 580-594
Open Access | Times Cited: 8
Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties
Stefka Mincheva-Tasheva, Chandran Pfitzner, Raman Kumar, et al.
Open Biology (2024) Vol. 14, Iss. 4
Open Access | Times Cited: 1
Identifying the Pathogenicity of a Novel NPRL3 Missense Mutation Using Personalized Cortical Organoid Model of Focal Cortical Dysplasia
Rongrong Lu, Ying Xu, Hao Li, et al.
Journal of Molecular Neuroscience (2024) Vol. 75, Iss. 1
Closed Access | Times Cited: 1
Antisense oligonucleotide therapy forKCNT1encephalopathy
Lisseth Estefania Burbano, Melody Li, Nikola Jancovski, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 10
Corrigendum: Convergent and Divergent Mechanisms of Epileptogenesis in mTORopathies
Lena H. Nguyen, Angélique Bordey
Frontiers in Neuroanatomy (2021) Vol. 15
Open Access | Times Cited: 6
Phenotypic and Genotypic Characterization of NPRL2-Related Epilepsy: Two Case Reports and Literature Review
Yulin Sun, Lin Wan, Huimin Yan, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 6
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