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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:

Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans
Felicia Mermer, Sarah Poliquin, Shuizhen Zhou, et al.
Neurobiology of Disease (2022) Vol. 172, pp. 105810-105810
Open Access | Times Cited: 22

Showing 22 citing articles:

Astrocytes as a target for therapeutic strategies in epilepsy: current insights
Nihan Çarçak, Filiz Onat, Evgenia Sitnikova
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 29
Glial regulation of critical period plasticity
Jacob Starkey, Eric J. Horstick, Sarah D. Ackerman
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 15
4-Phenylbutyrate restored GABA uptake, mitigated seizures in SLC6A1 and SLC6A11 Microdeletions/ 3p- Syndrome: from Cellular Models to Human Patients
Melissa B. DeLeeuw, Wangzhen Shen, Tian Xiaojuan, et al.
Epilepsy Research (2025) Vol. 210, pp. 107514-107514
Open Access
Disrupted astrocyte-neuron signaling reshapes brain activity in epilepsy and Alzheimer’s disease
Mengjie Wu, Ruonan Zhang, Peng Fu, et al.
Neuroscience (2025)
Closed Access
Dynamics and conditions for inhibitory synaptic current to induce bursting and spreading depolarization in pyramidal neurons
Hongtao Hua, Huaguang Gu, Kaihua Ma, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Update on Inherited Disorders of GABA Metabolism
Phillip L. Pearl, Phillip L. Pearl
European Journal of Paediatric Neurology (2025) Vol. 56, pp. 10-16
Closed Access
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
Benedetta Kassabian, Christina Fenger, Marjolaine Willems, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
γ-Aminobutyric acid transporter and GABAA receptor mechanisms in Slc6a1+/A288V and Slc6a1+/S295L mice associated with developmental and epileptic encephalopathies
Wangzhen Shen, Gerald Nwosu, Michael Honer, et al.
Brain Communications (2024) Vol. 6, Iss. 2
Open Access | Times Cited: 3
Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet Syndrome
Sarah Poliquin, Gerald Nwosu, Karishma Randhave, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4601-4601
Open Access | Times Cited: 3
A transporter’s doom or destiny: SLC6A1 in health and disease, novel molecular targets and emerging therapeutic prospects
Nikita Shah, Ameya Kasture, Florian P. Fischer, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 3
Astrocyte dysregulation as an epileptogenic factor: a systematic review
Komang Trisna Sumadewi, Bryan Gervais de Liyis, Ni Made Linawati, et al.
The Egyptian Journal of Neurology Psychiatry and Neurosurgery (2024) Vol. 60, Iss. 1
Open Access | Times Cited: 2
AAV9/SLC6A1 gene therapy rescues abnormal EEG patterns and cognitive behavioral deficiencies in Slc6a1-/- mice
Weirui Guo, Matthew Rioux, Frances C. Shaffo, et al.
Journal of Clinical Investigation (2024) Vol. 135, Iss. 3
Open Access | Times Cited: 2
State-of-the-art Application of Artificial Intelligence to Transporter-centered Functional and Pharmaceutical Research
Jiayi Yin, Nanxin You, Fengcheng Li, et al.
Current Drug Metabolism (2023) Vol. 24, Iss. 3, pp. 162-174
Closed Access | Times Cited: 4
4‐Phenylbutyrate promoted wild‐type γ‐aminobutyric acid type A receptor trafficking, reduced endoplasmic reticulum stress, and mitigated seizures in Gabrg2+/Q390X mice associated with Dravet syndrome
Wangzhen Shen, Carson Flamm, Aiden J. Delahanty, et al.
Epilepsia (2023) Vol. 65, Iss. 1, pp. 204-217
Open Access | Times Cited: 4
Experimental and Bioinformatic Insights into the Effects of Epileptogenic Variants on the Function and Trafficking of the GABA Transporter GAT-1
Dolores Piniella, Ania Canseco-Rodríguez, Silvia M. Vidal, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 955-955
Open Access | Times Cited: 3
GABAA Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome
Gerald Nwosu, Wangzhen Shen, Kirill Zavalin, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8458-8458
Open Access | Times Cited: 3
Myoclonic-Atonic Epilepsy Caused by a Novel de Novo Heterozygous Missense Variant in the SLC6A1 Gene: Brief Discussion of the Literature and Detailed Case Description of a Severely Intellectually Disabled Adult Male Patient
W.M.A. Verhoeven, José Zuijdam, Anneke Scheick, et al.
International Medical Case Reports Journal (2022) Vol. Volume 15, pp. 753-759
Open Access | Times Cited: 5
Genetic mechanisms in generalized epilepsies
Xiaoqian Wang, Xueyi Rao, Jia Zhang, et al.
Acta Epileptologica (2023) Vol. 5, Iss. 1
Open Access | Times Cited: 2
Heterozygous GABAA receptor β3 subunit N110D knock‐in mice have epileptic spasms
Shimian Qu, Laurel G. Jackson, Chengwen Zhou, et al.
Epilepsia (2022) Vol. 64, Iss. 4, pp. 1061-1073
Open Access | Times Cited: 4
Resolution of SLC6A1 variable expressivity in a multi-generational family using deep clinical phenotyping and Drosophila models
Kristy L. Jay, Nikhita Gogate, Kim Ezell, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
SLC6A1 Related Disorder: Clinical Manifestations, Management, and Prognosis
Neelan Pillay, Gurjot Brar, Niamh Mulryan
(2024), pp. 1-9
Closed Access
Patient‐derived SLC6A1 variant S295L results in an epileptic phenotype similar to haploinsufficient mice
Britta E. Lindquist, Yuliya Voskobiynyk, Kimberly Goodspeed, et al.
Epilepsia (2023) Vol. 64, Iss. 10
Open Access | Times Cited: 1
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