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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:

Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derivedNRXN1-mutant neurons
ChangHui Pak, Tamás Dankó, Vincent R. Mirabella, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 22
Open Access | Times Cited: 62

Showing 1-25 of 62 citing articles:

The cell biology of synapse formation
Thomas C. Südhof
The Journal of Cell Biology (2021) Vol. 220, Iss. 7
Open Access | Times Cited: 250
Neurodevelopmental disturbances in schizophrenia: evidence from genetic and environmental factors
Andrea Schmitt, Peter Falkai, Sergi Papiol
Journal of Neural Transmission (2022) Vol. 130, Iss. 3, pp. 195-205
Open Access | Times Cited: 48
Modeling gene × environment interactions in PTSD using human neurons reveals diagnosis-specific glucocorticoid-induced gene expression
Carina Seah, Michael S. Breen, Tom Rusielewicz, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 11, pp. 1434-1445
Open Access | Times Cited: 41
Neurexin-2: An inhibitory neurexin that restricts excitatory synapse formation in the hippocampus
Pei-Yi Lin, Lulu Y. Chen, Man Jiang, et al.
Science Advances (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 29
Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids
Rebecca Sebastian, Kang Jin, Narciso Pavon, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 28
The molecular pathology of schizophrenia: an overview of existing knowledge and new directions for future research
Takumi Nakamura, Atsushi Takata
Molecular Psychiatry (2023) Vol. 28, Iss. 5, pp. 1868-1889
Open Access | Times Cited: 27
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100356-100356
Open Access | Times Cited: 24
Schizophrenia genomics: genetic complexity and functional insights
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 11
Astrocytic-supplied cholesterol drives synaptic gene expression programs in developing neurons and downstream astrocytic transcriptional programs
Emilia Vartiainen, Dhara Liyanage, Illinca Mazureac, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disorders
Katelyn Cuttler, Maryam Hassan, Jonathan Carr, et al.
Open Biology (2021) Vol. 11, Iss. 10
Open Access | Times Cited: 46
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: 30
Genetic Mechanisms Underlying the Evolution of Connectivity in the Human Cortex
Ewoud R.E. Schmidt, Franck Polleux
Frontiers in Neural Circuits (2022) Vol. 15
Open Access | Times Cited: 29
Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders
David Exposito-Alonso, Beatriz Rico
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 391-422
Closed Access | Times Cited: 28
Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons
Siwei Zhang, Hanwen Zhang, Marc P. Forrest, et al.
Cell Genomics (2023) Vol. 3, Iss. 9, pp. 100399-100399
Open Access | Times Cited: 17
A fast and responsive voltage indicator with enhanced sensitivity for unitary synaptic events
Yukun Hao, Sungmoo Lee, Richard H. Roth, et al.
Neuron (2024)
Closed Access | Times Cited: 7
Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism
Le Wang, Vincent R. Mirabella, Rujia Dai, et al.
Molecular Psychiatry (2022) Vol. 29, Iss. 6, pp. 1620-1635
Open Access | Times Cited: 24
Neurexin dysfunction in neurodevelopmental and neuropsychiatric disorders: a PRIMSA-based systematic review through iPSC and animal models
Dan Shan, Yuming Song, Yanyi Zhang, et al.
Frontiers in Behavioral Neuroscience (2024) Vol. 18
Open Access | Times Cited: 5
Unraveling the potential of neuroinflammation and autophagy in schizophrenia
Hongxia Tao, Cheng‐Xiang Wang, Chuan Zou, et al.
European Journal of Pharmacology (2025) Vol. 997, pp. 177469-177469
Closed Access
Bridging the translational gap: what can synaptopathies tell us about autism?
Ciara J. Molloy, Jennifer Cooke, Nicholas J. F. Gatford, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 12
FOXG1 drives transcriptomic networks to specify principal neuron subtypes during the development of the medial pallium
Ru Ba, Lin Yang, Baoshen Zhang, et al.
Science Advances (2023) Vol. 9, Iss. 7
Open Access | Times Cited: 11
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice
Bing Xu, Yugong Ho, Maria Fasolino, et al.
PLoS Genetics (2023) Vol. 19, Iss. 2, pp. e1010659-e1010659
Open Access | Times Cited: 11
Current Best Practices for Analysis of Dendritic Spine Morphology and Number in Neurodevelopmental Disorder Research
Ben‐Zheng Li, Anna Sumera, Sam A. Booker, et al.
ACS Chemical Neuroscience (2023) Vol. 14, Iss. 9, pp. 1561-1572
Open Access | Times Cited: 11
Genetics of Suicide
M. Khalil, Anıl Kalyoncu, Alfredo Bellon
Genes (2025) Vol. 16, Iss. 4, pp. 428-428
Open Access
Phenotypic complexities of rare heterozygous neurexin-1 deletions
Michael B. Fernando, Yu Fan, Yanchun Zhang, et al.
Nature (2025)
Closed Access
Targeted splicing approach for alleviation of a neurexin 1 haploinsufficiency model
H. Peter Lu, Kyle M. Roddick, Yuan Ge, et al.
Molecular Psychiatry (2025)
Closed Access
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