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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:

ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins
Hourinaz Behesti, Taylor R. Fore, Peter Wu, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 41
Open Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Prediction signals in the cerebellum: Beyond supervised motor learning
Court Hull
eLife (2020) Vol. 9
Open Access | Times Cited: 159
Genetics of glutamate and its receptors in autism spectrum disorder
Sabah Nisar, Ajaz A. Bhat, Tariq Masoodi, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 5, pp. 2380-2392
Open Access | Times Cited: 102
Relating enhancer genetic variation across mammals to complex phenotypes using machine learning
Irene M. Kaplow, Alyssa J. Lawler, Daniel E. Schäffer, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 44
Structurally divergent and recurrently mutated regions of primate genomes
Yafei Mao, William T. Harvey, David Porubský, et al.
Cell (2024) Vol. 187, Iss. 6, pp. 1547-1562.e13
Open Access | Times Cited: 41
Persistence of spike protein at the skull-meninges-brain axis may contribute to the neurological sequelae of COVID-19
Zhouyi Rong, Hongcheng Mai, Gregor Ebert, et al.
Cell Host & Microbe (2024) Vol. 32, Iss. 12, pp. 2112-2130.e10
Open Access | Times Cited: 11
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder
Itaru Kushima, Masahiro Nakatochi, Branko Aleksić, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 362-374
Open Access | Times Cited: 35
RAB3 phosphorylation by pathogenic LRRK2 impairs trafficking of synaptic vesicle precursors
Dan Dou, Jayne Aiken, Erika L.F. Holzbaur
The Journal of Cell Biology (2024) Vol. 223, Iss. 6
Open Access | Times Cited: 7
Genetic Risk Factors in Drug‐Induced Liver Injury Due to Isoniazid‐Containing Antituberculosis Drug Regimens
Paola Nicoletti, Harshad Devarbhavi, Ashish Goel, et al.
Clinical Pharmacology & Therapeutics (2020) Vol. 109, Iss. 4, pp. 1125-1135
Open Access | Times Cited: 46
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia
Weilai Dong, Sheng Chih Jin, August Allocco, et al.
iScience (2020) Vol. 23, Iss. 10, pp. 101552-101552
Open Access | Times Cited: 41
Elucidating the relationship between migraine risk and brain structure using genetic data
Brittany L. Mitchell, Santiago Diaz‐Torres, Svetlana Bivol, et al.
Brain (2022) Vol. 145, Iss. 9, pp. 3214-3224
Open Access | Times Cited: 21
Autism common variants associated with white matter alterations at birth: cross-sectional fixel-based analyses of 221 European term-born neonates from the developing human connectome project
Hai Le, Alexandra F. Bonthrone, Alena Uus, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
A cross-generational methylomic signature of infant maltreatment in newborn rhesus macaques
Roy Lardenoije, Michelle N C A Smulders, Elyse L. Morin, et al.
Biological Psychiatry (2025)
Closed Access
Normal hearing function genetics: have you heard all about it? An integrated approach of genome-wide association studies and transcriptome-wide association studies in three Italian cohorts
Aurora Santin, Giulia Pianigiani, Alessandro Gialluisi, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Transcription factors in neurodevelopmental and associated psychiatric disorders: A potential convergence for genetic and environmental risk factors
Júlio Santos‐Terra, Iohanna Deckmann, Mellanie Fontes‐Dutra, et al.
International Journal of Developmental Neuroscience (2021) Vol. 81, Iss. 7, pp. 545-578
Open Access | Times Cited: 19
A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort
Chun’e Li, Xiao Liang, Shiqiang Cheng, et al.
Journal of Psychiatric Research (2022) Vol. 147, pp. 59-66
Closed Access | Times Cited: 13
Whole-genome sequencing reveals the genetic mechanisms of domestication in classical inbred mice
Ming Liu, Caixia Yu, Zhichao Zhang, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 13
Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose
Olivia Corradin, Richard Sallari, An T. Hoang, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 4, pp. 2158-2170
Open Access | Times Cited: 12
Structurally divergent and recurrently mutated regions of primate genomes
Yafei Mao, William T. Harvey, David Porubský, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Genetic Alterations in a Large Population of Italian Patients Affected by Neurodevelopmental Disorders
Annaluisa Ranieri, Ilaria La Monica, Maria Rosaria Di Iorio, et al.
Genes (2024) Vol. 15, Iss. 4, pp. 427-427
Open Access | Times Cited: 2
STED Imaging of Vesicular Endocytosis in the Synapse
Shaoqin Hu, Zhenli Xie, Bianbian Wang, et al.
Neuroscience Bulletin (2024) Vol. 40, Iss. 9, pp. 1379-1395
Closed Access | Times Cited: 2
Deciphering the Effect of Different Genetic Variants on Hippocampal Subfield Volumes in the General Population
Kevin Kirchner, Linda Garvert, Katharina Wittfeld, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1120-1120
Open Access | Times Cited: 6
Astrotactin 2 (ASTN2) regulates emotional and cognitive functions by affecting neuronal morphogenesis and monoaminergic systems
Takahiro Ito, Mikio Yoshida, Tomomi Aida, et al.
Journal of Neurochemistry (2023) Vol. 165, Iss. 2, pp. 211-229
Closed Access | Times Cited: 6
Mice lackingAstn2have ASD-like behaviors and altered cerebellar circuit properties
Michalina Hanzel, Kayla Fernando, Susan E. Maloney, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations
Timuçin Avşar, Seyma Calis, Baran Yılmaz, et al.
TURKISH JOURNAL OF BIOLOGY (2020) Vol. 44, Iss. 6, pp. 449-456
Open Access | Times Cited: 15
Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis
Guodong Chen, Lin Han, Senwei Tan, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2022) Vol. 49, Iss. 9, pp. 881-890
Closed Access | Times Cited: 10
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