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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:

Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains
Sharon A. Swanger, Wenjuan Chen, Gordon Wells, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 6, pp. 1261-1280
Open Access | Times Cited: 166

Showing 1-25 of 166 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: 445
GRIN2Bencephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
Konrad Platzer, Hongjie Yuan, Hannah M. Schutz, et al.
Journal of Medical Genetics (2017) Vol. 54, Iss. 7, pp. 460-470
Open Access | Times Cited: 218
Human GRIN2B variants in neurodevelopmental disorders
Chun Hu, Wenjuan Chen, Scott J. Myers, et al.
Journal of Pharmacological Sciences (2016) Vol. 132, Iss. 2, pp. 115-121
Open Access | Times Cited: 205
GRIN2A-related disorders: genotype and functional consequence predict phenotype
Vincent Strehlow, Henrike Heyne, Danique R.M. Vlaskamp, et al.
Brain (2018) Vol. 142, Iss. 1, pp. 80-92
Open Access | Times Cited: 181
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation
Joshua L. Traynelis, Michael Silk, Quanli Wang, et al.
Genome Research (2017) Vol. 27, Iss. 10, pp. 1715-1729
Open Access | Times Cited: 174
Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry
Jesse E. Hanson, Hongjie Yuan, Riley E. Perszyk, et al.
Neuropsychopharmacology (2023) Vol. 49, Iss. 1, pp. 51-66
Open Access | Times Cited: 54
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: 16
Distinct roles of GRIN2A and GRIN2B variants in neurological conditions
Scott J. Myers, Hongjie Yuan, Jing‐Qiong Kang, et al.
F1000Research (2019) Vol. 8, pp. 1940-1940
Open Access | Times Cited: 126
Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology
Kevin K. Ogden, Wenjuan Chen, Sharon A. Swanger, et al.
PLoS Genetics (2017) Vol. 13, Iss. 1, pp. e1006536-e1006536
Open Access | Times Cited: 125
De novo mutations and rare variants occurring in NMDA receptors
Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan
Current Opinion in Physiology (2017) Vol. 2, pp. 27-35
Open Access | Times Cited: 123
Regulation of NMDA glutamate receptor functions by the GluN2 subunits
Marta Vieira, Xuan Ling Hilary Yong, Katherine W. Roche, et al.
Journal of Neurochemistry (2020) Vol. 154, Iss. 2, pp. 121-143
Open Access | Times Cited: 112
Synaptic GluN2A-Containing NMDA Receptors: From Physiology to Pathological Synaptic Plasticity
Luca Franchini, Nicolò Carrano, Mónica Di Luca, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 4, pp. 1538-1538
Open Access | Times Cited: 96
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
Andrew E. Fry, Katherine A. Fawcett, Nathanel Zelnik, et al.
Brain (2017) Vol. 141, Iss. 3, pp. 698-712
Open Access | Times Cited: 91
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: 39
GRIN2B-related neurodevelopmental disorder: current understanding of pathophysiological mechanisms
Shasta L. Sabo, Jessica M. Lahr, Madelyn Offer, et al.
Frontiers in Synaptic Neuroscience (2023) Vol. 14
Open Access | Times Cited: 37
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
L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study
Natalia Juliá‐Palacios, Mireia Olivella, Mariya Sigatullina Bondarenko, et al.
Brain (2024) Vol. 147, Iss. 5, pp. 1653-1666
Closed Access | Times Cited: 8
GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function
Wenjuan Chen, Christine Shieh, Sharon A. Swanger, et al.
Journal of Human Genetics (2017) Vol. 62, Iss. 6, pp. 589-597
Open Access | Times Cited: 76
Disease-associated missense mutations in GluN2B subunit alter NMDA receptor ligand binding and ion channel properties
Laura Fedele, Joseph Newcombe, Maya Topf, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 74
Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy
Wenjuan Chen, Anel Tankovic, Pieter B. Burger, et al.
Molecular Pharmacology (2017) Vol. 91, Iss. 4, pp. 317-330
Open Access | Times Cited: 73
A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density
Shuxi Liu, Liang Zhou, Hongjie Yuan, et al.
Journal of Neuroscience (2017) Vol. 37, Iss. 15, pp. 4093-4102
Open Access | Times Cited: 71
De novoGRINvariants in NMDA receptor M2 channel pore‐forming loop are associated with neurological diseases
Jia Li, Jin Zhang, Weiting Tang, et al.
Human Mutation (2019) Vol. 40, Iss. 12, pp. 2393-2413
Open Access | Times Cited: 60
Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy
Wenshu XiangWei, Varun Kannan, Yuchen Xu, et al.
Brain (2019) Vol. 142, Iss. 10, pp. 3009-3027
Open Access | Times Cited: 60
Characterization of intellectual disability and autism comorbidity through gene panel sequencing
Maria Cristina Aspromonte, Mariagrazia Bellini, Alessandra Gasparini, et al.
Human Mutation (2019) Vol. 40, Iss. 9, pp. 1346-1363
Open Access | Times Cited: 57
Architecture and function of NMDA receptors: an evolutionary perspective
David Stroebel, Pierre Paoletti
The Journal of Physiology (2020) Vol. 599, Iss. 10, pp. 2615-2638
Open Access | Times Cited: 56
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