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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:

The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons
Mattéa J. Finelli, Davide Aprile, Enrico Castroflorio, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 4, pp. 584-597
Open Access | Times Cited: 51

Showing 1-25 of 51 citing articles:

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: 94
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: 20
Presynaptic dysfunction in neurodevelopmental disorders: Insights from the synaptic vesicle life cycle
Katherine Bonnycastle, Elizabeth C. Davenport, Michael A. Cousin
Journal of Neurochemistry (2020) Vol. 157, Iss. 2, pp. 179-207
Open Access | Times Cited: 68
Synaptic genes and neurodevelopmental disorders: From molecular mechanisms to developmental strategies of behavioral testing
Caterina Michetti, Antonio Falace, Fabio Benfenati, et al.
Neurobiology of Disease (2022) Vol. 173, pp. 105856-105856
Open Access | Times Cited: 31
Human V-ATPase function is positively and negatively regulated by TLDc proteins
Rebecca A. Oot, Stephan Wilkens
Structure (2024) Vol. 32, Iss. 7, pp. 989-1000.e6
Closed Access | Times Cited: 7
TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model
Kevin Lüthy, Davide Mei, Baptiste Fischer, et al.
Brain (2019) Vol. 142, Iss. 8, pp. 2319-2335
Open Access | Times Cited: 53
The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviour
Enrico Castroflorio, Joery den Hoed, Daria M. Dolmatova, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 7, pp. 3503-3524
Open Access | Times Cited: 33
Paroxysmal Movement Disorders
Susan Harvey, Mary D. King, Kathleen M. Gorman
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 28
CryoEM of endogenous mammalian V-ATPase interacting with the TLDc protein mEAK-7
Yong Zi Tan, Y.M. Abbas, Jing Wu, et al.
Life Science Alliance (2022) Vol. 5, Iss. 11, pp. e202201527-e202201527
Open Access | Times Cited: 22
Synaptic Vesicle Recycling and the Endolysosomal System: A Reappraisal of Form and Function
Daniela Ivanova, Michael A. Cousin
Frontiers in Synaptic Neuroscience (2022) Vol. 14
Open Access | Times Cited: 19
Familiar case of a small TBC1D24 and ATP6V0C-containing microdeletion associated with developmental delay, microcephaly, and seizures
Catarina Macedo, Raquel Rodrigues, José Paulo Monteiro, et al.
Clinical Dysmorphology (2025)
Closed Access
Incomplete Trisomy Rescue Reveals the Mechanism Underlying Discordance Between Noninvasive Prenatal Screening and Prenatal Diagnosis
Yanan Wang, Yong Zhou, Yuqiong Chai, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 3
Open Access
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons
Davide Aprile, Floriana Fruscione, Sımona Baldassari, et al.
Cell Death and Differentiation (2019) Vol. 26, Iss. 11, pp. 2464-2478
Open Access | Times Cited: 33
The axonal endolysosomal and autophagic systems
Marijn Kuijpers, Domenico Azarnia Tehran, Volker Haucke, et al.
Journal of Neurochemistry (2020) Vol. 158, Iss. 3, pp. 589-602
Open Access | Times Cited: 30
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
The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy
Risa Tona, Wenqian Chen, Yoko Nakano, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 9, pp. 1530-1547
Open Access | Times Cited: 28
DOORS syndrome and a recurrent truncating ATP6V1B2 variant
Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 149-154
Open Access | Times Cited: 25
The evolutionary conserved TLDc domain defines a new class of (H+)V-ATPase interacting proteins
Amity F. Eaton, Dennis Brown, Maria Merkulova
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 22
Oxidation resistance 1 regulates post-translational modifications of peroxiredoxin 2 in the cerebellum
Daria M. Dolmatova, Jillian N. Simon, Elzbieta Rembeza, et al.
Free Radical Biology and Medicine (2018) Vol. 130, pp. 151-162
Open Access | Times Cited: 26
Frontrunner in Translation: Progressive Supranuclear Palsy
Ali Shoeibi, Nahid Olfati, Irene Litvan
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 25
Microtubule Dynamics and Neuronal Excitability: Advances on Cytoskeletal Components Implicated in Epileptic Phenomena
Giuditta Gambino, Valerio Rizzo, Giuseppe Giglia, et al.
Cellular and Molecular Neurobiology (2020) Vol. 42, Iss. 3, pp. 533-543
Open Access | Times Cited: 20
IbTLD modulates reactive oxygen species scavenging and DNA protection to confer salinity stress tolerance in tobacco
Tsung-Chi Chen, Si-Yun Chou, Ming‐Cheng Chen, et al.
Plant Science (2022) Vol. 323, pp. 111415-111415
Closed Access | Times Cited: 11
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness
Risa Tona, Iván A. López, Cristina Fenollar‐Ferrer, et al.
Genes (2020) Vol. 11, Iss. 10, pp. 1122-1122
Open Access | Times Cited: 18
A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial–temporal regulation of histone arginine methylation in neurodevelopment
Xiaolin Lin, Wei Wang, Mingyi Yang, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 6
The epilepsy and intellectual disability-associated protein TBC1D24 regulates the maintenance of excitatory synapses and animal behaviors
Lian-Feng Lin, Q Lyu, Pui‐Yi Kwan, et al.
PLoS Genetics (2020) Vol. 16, Iss. 1, pp. e1008587-e1008587
Open Access | Times Cited: 16
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