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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:

Architecture of the Mouse Brain Synaptome
Fei Zhu, Mélissa Cizeron, Zhen Qiu, et al.
Neuron (2018) Vol. 99, Iss. 4, pp. 781-799.e10
Open Access | Times Cited: 219

Showing 1-25 of 219 citing articles:

The synapse in traumatic brain injury
Aimun A. B. Jamjoom, Jonathan Rhodes, Peter Andrews, et al.
Brain (2020) Vol. 144, Iss. 1, pp. 18-31
Open Access | Times Cited: 173
A brainwide atlas of synapses across the mouse life span
Mélissa Cizeron, Zhen Qiu, Babis Koniaris, et al.
Science (2020) Vol. 369, Iss. 6501, pp. 270-275
Open Access | Times Cited: 164
Synapse pathology in Alzheimer’s disease
Jessica Griffiths, Seth G. N. Grant
Seminars in Cell and Developmental Biology (2022) Vol. 139, pp. 13-23
Open Access | Times Cited: 112
Recent advances on the molecular mechanisms of exercise-induced improvements of cognitive dysfunction
Yi Lü, Faqian Bu, Fang Wang, et al.
Translational Neurodegeneration (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 54
Droplet-based transcriptome profiling of individual synapses
Muchun Niu, Wenjian Cao, Yongcheng Wang, et al.
Nature Biotechnology (2023) Vol. 41, Iss. 9, pp. 1332-1344
Closed Access | Times Cited: 44
A large-scale nanoscopy and biochemistry analysis of postsynaptic dendritic spines
Martin S. Helm, Tal M. Dankovich, Sunit Mandad, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 8, pp. 1151-1162
Closed Access | Times Cited: 97
Similar Microglial Cell Densities across Brain Structures and Mammalian Species: Implications for Brain Tissue Function
Sandra Esmeralda Dos Santos, Marcelle Medeiros, Jairo Porfírio, et al.
Journal of Neuroscience (2020) Vol. 40, Iss. 24, pp. 4622-4643
Open Access | Times Cited: 82
Multiplexed peroxidase-based electron microscopy labeling enables simultaneous visualization of multiple cell types
Qiyu Zhang, Wei-Chung Allen Lee, David L. Paul, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 5, pp. 828-839
Open Access | Times Cited: 81
BraInMap Elucidates the Macromolecular Connectivity Landscape of Mammalian Brain
Mohammad Reza Pourhaghighi, Peter E.A. Ash, Sadhna Phanse, et al.
Cell Systems (2020) Vol. 10, Iss. 4, pp. 333-350.e14
Open Access | Times Cited: 71
A brain atlas of synapse protein lifetime across the mouse lifespan
Edita Bulovaite, Zhen Qiu, Maximilian Kratschke, et al.
Neuron (2022) Vol. 110, Iss. 24, pp. 4057-4073.e8
Open Access | Times Cited: 67
GluD1 is a signal transduction device disguised as an ionotropic receptor
Jinye Dai, Christopher Patzke, Kifayathullah Liakath‐Ali, et al.
Nature (2021) Vol. 595, Iss. 7866, pp. 261-265
Open Access | Times Cited: 64
Visualizing synaptic plasticity in vivo by large-scale imaging of endogenous AMPA receptors
Austin R Graves, Richard H. Roth, Han L. Tan, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 63
Selective vulnerability of inhibitory networks in multiple sclerosis
Lida Zoupi, Sam A. Booker, Dimitri Eigel, et al.
Acta Neuropathologica (2021) Vol. 141, Iss. 3, pp. 415-429
Open Access | Times Cited: 61
Revealing nanostructures in brain tissue via protein decrowding by iterative expansion microscopy
Deblina Sarkar, Jinyoung Kang, Asmamaw T. Wassie, et al.
Nature Biomedical Engineering (2022) Vol. 6, Iss. 9, pp. 1057-1073
Open Access | Times Cited: 61
Merged magnetic resonance and light sheet microscopy of the whole mouse brain
G. Allan Johnson, Yuqi Tian, David G. Ashbrook, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 17
Open Access | Times Cited: 36
The in-tissue molecular architecture of β-amyloid pathology in the mammalian brain
Conny Leistner, Martin Wilkinson, Ailidh Burgess, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 32
Brain high-throughput multi-omics data reveal molecular heterogeneity in Alzheimer’s disease
Abdallah M. Eteleeb, Brenna C. Novotny, Carolina Soriano‐Tárraga, et al.
PLoS Biology (2024) Vol. 22, Iss. 4, pp. e3002607-e3002607
Open Access | Times Cited: 12
Integrated multi-omic characterizations of the synapse reveal RNA processing factors and ubiquitin ligases associated with neurodevelopmental disorders
Mei Yuan, Maya L. Gosztyla, Xinzhu Tan, et al.
Cell Systems (2025), pp. 101204-101204
Open Access | Times Cited: 1
Locating the engram: Should we look for plastic synapses or information-storing molecules?
Jesse J. Langille, C. R. Gallistel
Neurobiology of Learning and Memory (2020) Vol. 169, pp. 107164-107164
Closed Access | Times Cited: 61
Synapse diversity and synaptome architecture in human genetic disorders
Seth G. N. Grant
Human Molecular Genetics (2019) Vol. 28, Iss. R2, pp. R219-R225
Open Access | Times Cited: 60
Steps towards standardized quantification of adult neurogenesis
Xinyu Zhao, Henriette van Praag
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 59
Artificial selection on brain size leads to matching changes in overall number of neurons
Lucie Marhounová, Alexander Kotrschal, Kristina Kverková, et al.
Evolution (2019) Vol. 73, Iss. 9, pp. 2003-2012
Open Access | Times Cited: 57
Synaptic FUS accumulation triggers early misregulation of synaptic RNAs in a mouse model of ALS
Sonu Sahadevan, Katharina Hembach, Elena Tantardini, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 55
Estimation of the number of synapses in the hippocampus and brain-wide by volume electron microscopy and genetic labeling
Andrea Santuy, Laura Tomás‐Roca, José‐Rodrigo Rodríguez, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 54
Synapse type-specific proteomic dissection identifies IgSF8 as a hippocampal CA3 microcircuit organizer
Nuno Apóstolo, Samuel N. Smukowski, Jeroen Vanderlinden, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 51
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