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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:

Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome
Sang Soo Seo, Susana R. Louros, Natasha Anstey, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Non-ionotropic signaling through the NMDA receptor GluN2B carboxy-terminal domain drives dendritic spine plasticity and reverses fragile X phenotypes
Stephanie A. Barnes, Aurore Thomazeau, Peter S.B. Finnie, et al.
Cell Reports (2025), pp. 115311-115311
Open Access | Times Cited: 2
The Trail of axonal protein Synthesis: Origins and current functional Landscapes
Joaquín Garat, Andrés Di Paolo, Guillermo Eastman, et al.
Neuroscience (2025)
Closed Access | Times Cited: 1
mRNA transport, translation, and decay in adult mammalian central nervous system axons
Jane Jung, Jiyeon Ohk, Hye Young Kim, et al.
Neuron (2022) Vol. 111, Iss. 5, pp. 650-668.e4
Open Access | Times Cited: 38
Specialized Ribosomes in Health and Disease
Sarah Miller, Clinton C. MacDonald, Morgana K. Kellogg, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6334-6334
Open Access | Times Cited: 21
Proteomics insights into fragile X syndrome: Unraveling molecular mechanisms and therapeutic avenues
Diana A. Abbasi, Elizabeth Berry‐Kravis, Xinyu Zhao, et al.
Neurobiology of Disease (2024) Vol. 194, pp. 106486-106486
Open Access | Times Cited: 5
Dysregulated cholesterol metabolism, aberrant excitability and altered cell cycle of astrocytes in fragile X syndrome
Baiyan Ren, Maria Burkovetskaya, Yoosun Jung, et al.
Glia (2023) Vol. 71, Iss. 5, pp. 1176-1196
Open Access | Times Cited: 12
Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice
Francesco Longo, Sameer Aryal, Paul G. Anastasiades, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112901-112901
Open Access | Times Cited: 12
Fragile X mental retardation protein modulates translation of proteins with predicted tendencies for liquid-liquid phase separation
Omar Jurado, Marco V. José, Eugenio Frixione
Biosystems (2025), pp. 105405-105405
Closed Access
The Fragile X Messenger Ribonucleoprotein 1 Regulates the Morphology and Maturation of Human and Rat Oligodendrocytes
Vidya Ramesh, Eleni Tsoukala, Ioanna Kougianou, et al.
Glia (2025)
Open Access
Genetic and Pharmacological Inhibition of Metabotropic Glutamate Receptor Signalling Extends Lifespan in Drosophila
Cui Guan, Abigail Otchere, Mihails Laskovs, et al.
Aging Cell (2025)
Open Access
Dysregulation of the actin cytoskeleton and FMRP causes polar body protrusion defects in human fragile X premutation and aged oocytes
Kelly McCarter, Madhura Deshpande, Phillip A. Romanski, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Excessive proteostasis contributes to pathology in fragile X syndrome
Susana R. Louros, Sang Soo Seo, Beatriz Maio, et al.
Neuron (2022) Vol. 111, Iss. 4, pp. 508-525.e7
Open Access | Times Cited: 17
Syngap+/- CA1 pyramidal neurons exhibit upregulated translation of long mRNAs associated with LTP
Aditi Singh, Manuela Rizzi, Sang Soo Seo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Translational modulator ISRIB alleviates synaptic and behavioral phenotypes in Fragile X syndrome
Rochelle L. Coulson, Valentina Frattini, Caitlin E. Moyer, et al.
iScience (2024) Vol. 27, Iss. 4, pp. 109259-109259
Open Access | Times Cited: 3
Sex-specific perturbations of neuronal development caused by mutations in the autism risk gene DDX3X
Adele Mossa, Lauren Dierdorff, Jerónimo Lukin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
FMRP-dependent production of large dosage-sensitive proteins is highly conserved
Keegan Flanagan, Alireza Baradaran‐Heravi, Qi Yin, et al.
Genetics (2022) Vol. 221, Iss. 4
Open Access | Times Cited: 13
Dysregulated ribosome quality control in human diseases
Tom McGirr, Okan Onar, Seyed Mehdi Jafarnejad
FEBS Journal (2024)
Open Access | Times Cited: 2
DDX3X syndrome: From clinical phenotypes to biological insights
Alexa von Mueffling, Marta García-Forn, Silvia De Rubeis
Journal of Neurochemistry (2024)
Closed Access | Times Cited: 2
Enrichment of the Local Synaptic Translatome for Genetic Risk Associated With Schizophrenia and Autism Spectrum Disorder
Nicholas E. Clifton, Julie Qiaojin Lin, Christine E. Holt, et al.
Biological Psychiatry (2023) Vol. 95, Iss. 9, pp. 888-895
Open Access | Times Cited: 5
Hippocampal proteome comparison of infant and adult Fmr1 deficiency mice reveals adult-related changes associated with postsynaptic density
Cui Yang, Yu-Ting Huang, Yi-Fei Yao, et al.
Journal of Proteomics (2024) Vol. 303, pp. 105202-105202
Closed Access | Times Cited: 1
Crosstalk between ubiquitination and translation in neurodevelopmental disorders
Nagore Elu, Srividya Subash, Susana R. Louros
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 1
Construction destruction: Contribution of dyregulated proteostasis to neurodevelopmental disorders
Kellen D. Winden, Juan Pablo Ruíz, Mustafa Şahin
Current Opinion in Neurobiology (2024) Vol. 90, pp. 102934-102934
Closed Access | Times Cited: 1
Nmnat1 Deficiency Causes Mitoribosome Excess in Diabetic Nephropathy Mediated by Transcriptional Repressor HIC1
Kazuhiro Hasegawa, Masanori Tamaki, Yusuke Sakamaki, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 12, pp. 6384-6384
Open Access | Times Cited: 1
Novel presynaptic assay system revealed that metformin ameliorates exaggerated synaptic release and Munc18-1 accumulation in presynapses of neurons from Fragile X syndrome mouse model
Renoma Takeda, Rie Ishii, Shumaia Parvin, et al.
Neuroscience Letters (2023) Vol. 810, pp. 137317-137317
Open Access | Times Cited: 2
Suppression of astrocyte BMP signaling improves fragile X syndrome molecular signatures and functional deficits
James Deng, Lara Labarta-Bajo, Ashley N. Brandebura, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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