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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:

Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice
Ariadna Amador, Christopher D. Bostick, Heather E. Olson, et al.
Brain (2020) Vol. 143, Iss. 7, pp. 2039-2057
Open Access | Times Cited: 73

Showing 1-25 of 73 citing articles:

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Kasper B. Hansen, Lonnie P. Wollmuth, Derek Bowie, et al.
Pharmacological Reviews (2021) Vol. 73, Iss. 4, pp. 1469-1658
Open Access | Times Cited: 461
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
Current practice in diagnostic genetic testing of the epilepsies
Ilona Krey, Konrad Platzer, Alina Esterhuizen, et al.
Epileptic Disorders (2022) Vol. 24, Iss. 5, pp. 765-786
Open Access | Times Cited: 67
Modelling epilepsy in the mouse: challenges and solutions
Grant F. Marshall, Alfredo Gonzalez-Sulser, Catherine M. Abbott
Disease Models & Mechanisms (2021) Vol. 14, Iss. 3
Open Access | Times Cited: 57
L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null Variants
Ilona Krey, Sarah von Spiczak, Katrine M. Johannesen, et al.
Neurotherapeutics (2022) Vol. 19, Iss. 1, pp. 334-341
Open Access | Times Cited: 40
Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients
Linnea Herzog, Lei Wang, Eunah Yu, et al.
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 30
Mechanisms of NMDA receptor regulation
Laétitia Mony, Pierre Paoletti
Current Opinion in Neurobiology (2023) Vol. 83, pp. 102815-102815
Open Access | Times Cited: 29
De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor
Yuchen Xu, Rui Song, Riley E. Perszyk, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 9
Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights
Andy Cheuk‐Him Ng, Mohamed Chahine, Morris H. Scantlebury, et al.
Journal of Neurology (2024) Vol. 271, Iss. 6, pp. 3063-3094
Closed Access | Times Cited: 9
Progress report on new medications for seizures and epilepsy: A summary of the 17th Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVII). II. Drugs in more advanced clinical development
Meir Bialer, Svein I. Johannessen, Matthias J. Koepp, et al.
Epilepsia (2024) Vol. 65, Iss. 10, pp. 2858-2882
Open Access | Times Cited: 9
Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs
Tim A. Benke, Kristen Park, Ilona Krey, et al.
Neuropharmacology (2021) Vol. 199, pp. 108805-108805
Open Access | Times Cited: 51
The role of NMDA receptor and neuroligin rare variants in synaptic dysfunction underlying neurodevelopmental disorders
Marta Vieira, Jae‐Hoon Jeong, Katherine W. Roche
Current Opinion in Neurobiology (2021) Vol. 69, pp. 93-104
Open Access | Times Cited: 45
Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons
Chad R. Camp, Anna Vlachos, Chiara Klöckner, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 19
The epilepsy–autism spectrum disorder phenotype in the era of molecular genetics and precision therapy
Nicola Specchio, Valentina Di Micco, Marina Trivisano, et al.
Epilepsia (2021) Vol. 63, Iss. 1, pp. 6-21
Closed Access | Times Cited: 35
Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-function
Scott J. Myers, Hongjie Yuan, Riley E. Perszyk, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 19, pp. 2857-2871
Open Access | Times Cited: 16
Sigma-1 receptor and seizures
Edijs Vavers, Liga Zvejniece, Maija Dambrova
Pharmacological Research (2023) Vol. 191, pp. 106771-106771
Open Access | Times Cited: 14
Recurrent seizure‐related GRIN1 variant: Molecular mechanism and targeted therapy
Yuchen Xu, Rui Song, Wenjuan Chen, et al.
Annals of Clinical and Translational Neurology (2021) Vol. 8, Iss. 7, pp. 1480-1494
Open Access | Times Cited: 30
Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2a K1422E mice
Dennis M. Echevarria-Cooper, Nicole A. Hawkins, Sunita N. Misra, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. 17, pp. 2964-2988
Open Access | Times Cited: 20
Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes
Kathryn J. Peall, Michael J. Owen, Jérémy Hall
Nature Reviews Neurology (2023) Vol. 20, Iss. 1, pp. 7-21
Closed Access | Times Cited: 13
Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency
Sarah A. Dugger, Ryan S. Dhindsa, Gabriela Louise de Almeida Sampaio, et al.
PLoS Genetics (2023) Vol. 19, Iss. 10, pp. e1010952-e1010952
Open Access | Times Cited: 12
Genetic diagnostics in epilepsies: recommendations of the Commission Epilepsy and Genetics of German Society of Epileptology (German ILAE Chapter)
Christian M. Boßelmann, Ingo Borggräfe, Walid Fazeli, et al.
Deleted Journal (2023) Vol. 36, Iss. 3, pp. 224-237
Open Access | Times Cited: 11
Disease-Associated Variants in GRIN1, GRIN2A and GRIN2B genes: Insights into NMDA Receptor Structure, Function, and Pathophysiology
Michal Korinek, M C Serra, Fes Abdel Rahman, et al.
Physiological Research (2024), Iss. Suppl 1, pp. S413-S434
Open Access | Times Cited: 4
Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies
Isabel Haviland, Carolyn I. Daniels, Caitlin Greene, et al.
Pediatric Neurology (2022) Vol. 138, pp. 71-80
Open Access | Times Cited: 19
The dysfunctionality of hippocampal synapses may be directly related to PM-induced impairments in spatial learning and memory in juvenile rats
Jianxiong Gui, Jie Liu, Ziyao Han, et al.
Ecotoxicology and Environmental Safety (2023) Vol. 254, pp. 114729-114729
Open Access | Times Cited: 10
NMDAR dysfunction in autism spectrum disorders: Lessons learned from 10 years of study
Soowon Lee, Heera Moon, Eunjoon Kim
Current Opinion in Neurobiology (2025) Vol. 92, pp. 103023-103023
Open Access
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