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:

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

Showing 1-25 of 29 citing articles:

Neurodevelopmental Disorders: From Genetics to Functional Pathways
Ilaria Parenti, Luis G. Rabaneda, Hanna Schoen, et al.
Trends in Neurosciences (2020) Vol. 43, Iss. 8, pp. 608-621
Open Access | Times Cited: 428

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: 96

Advances in Zebrafish as a Comprehensive Model of Mental Disorders
Lei Wang, Fan Liu, Yimeng Fang, et al.
Depression and Anxiety (2023) Vol. 2023, pp. 1-48
Open Access | Times Cited: 26

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

Interplay of epilepsy and long-term potentiation: implications for memory
Luis A. Marín-Castañeda, Gerónimo Pacheco Aispuro, Guillermo Gonzalez-Garibay, et al.
Frontiers in Neuroscience (2025) Vol. 18
Open Access

Hippocampal astrocytic neogenin regulating glutamate uptake, a critical pathway for preventing epileptic response
Dong Sun, Zhibing Tan, Xiangdong Sun, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 16
Open Access | Times Cited: 20

Cardiac Investigations in Sudden Unexpected Death in DEPDC5‐Related Epilepsy
Alexandre Bacq, Delphine Roussel, Thomas Bonduelle, et al.
Annals of Neurology (2021) Vol. 91, Iss. 1, pp. 101-116
Open Access | Times Cited: 20

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

Dorsal telencephalon-specific Nprl2- and Nprl3-knockout mice: novel mouse models for GATORopathy
Saeko Ishida, Di Zhao, Yuta Sawada, et al.
Human Molecular Genetics (2021) Vol. 31, Iss. 9, pp. 1519-1530
Open Access | Times Cited: 16

DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature
Chunyu Gu, Xinping Wei, Dandan Yan, et al.
Epileptic Disorders (2024) Vol. 26, Iss. 3, pp. 341-349
Closed Access | Times Cited: 2

Loss of POGZ alters neural differentiation of human embryonic stem cells
Lu Deng, Sandra P. Mojica-Perez, Ruth D. Azaria, et al.
Molecular and Cellular Neuroscience (2022) Vol. 120, pp. 103727-103727
Open Access | Times Cited: 10

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

Fine-tuning of mTOR signaling by the UBE4B-KLHL22 E3 ubiquitin ligase cascade in brain development
Xiangxing Kong, Xin Shu, Jiachuan Wang, et al.
Development (2022) Vol. 149, Iss. 24
Open Access | Times Cited: 7

Increased glycine contributes to synaptic dysfunction and early mortality in Nprl2 seizure model
Brianne Dentel, Lidiette Angeles-Perez, Chongyu Ren, et al.
iScience (2022) Vol. 25, Iss. 5, pp. 104334-104334
Open Access | Times Cited: 6

Exploring Dendritic and Spine Structural Profiles in Epilepsy: Insights From Human Studies and Experimental Animal Models
Shikha Kumari, Amy L. Brewster
Epiliepsy currents/Epilepsy currents (2023) Vol. 24, Iss. 1, pp. 40-46
Open Access | Times Cited: 2

Neurophysiological assessment of cortical activity in DEPDC5- and NPRL3-related epileptic mTORopathies
Madora Mabika, Kristian Agbogba, Samantha Côté, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 1

Modeling genetic mosaicism of the mammalian target of rapamycin pathway in the cerebral cortex
David M. Feliciano
Frontiers in Mammal Science (2023) Vol. 2
Open Access | Times Cited: 1

Pathogenic genes implicated in sleep-related hypermotor epilepsy: a research progress update
Yufang Yang, Jinmei Tuo, Jun Zhang, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access

Familial Focal Epilepsy with Variable Foci: A Novel DEPDC5 Gene Mutation
Özlem Akdoğan, Şahin Avcı, Peter Bauer, et al.
Neurological Sciences and Neurophysiology (2024) Vol. 41, Iss. 2, pp. 118-120
Open Access

Neuropathology and epilepsy surgery
Lucas Hoffmann, Ingmar Blümcke
Current Opinion in Neurology (2022) Vol. 35, Iss. 2, pp. 202-207
Closed Access | Times Cited: 2

What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report
Chunyu Gu, Xiaowei Lu, Jinhui Ma, et al.
BMC Pediatrics (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 2

Getting Sucker Punched by Depdc5 Really Hurts
Matthew C. Weston
Epiliepsy currents/Epilepsy currents (2020) Vol. 20, Iss. 6, pp. 378-380
Open Access | Times Cited: 1

Cutting-Edge Classification of Focal Cortical Dysplasia for Epilepsy Surgery
David G. Vossler
Epiliepsy currents/Epilepsy currents (2021) Vol. 22, Iss. 1, pp. 48-50
Open Access | Times Cited: 1

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