The DOI matches its Crossref record; 118 of the 118 references it cites were found in a registry or an index.
Astrocyte Ca2+ signalling: an unexpected complexity
Open accessAbstract
Astrocyte Ca(2+) signalling has been proposed to link neuronal information in different spatial-temporal dimensions to achieve a higher level of brain integration. However, some discrepancies in the results of recent studies challenge this view and highlight key insufficiencies in our current understanding. In parallel, new experimental approaches that enable the study of astrocyte physiology at higher spatial-temporal resolution in intact brain preparations are beginning to reveal an unexpected level of compartmentalization and sophistication in astrocytic Ca(2+) dynamics. This newly revealed complexity needs to be attentively considered in order to understand how astrocytes may contribute to brain information processing.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“astrocyte interactions with synaptic circuits are multimodal and multiscale, occur under physiological conditions 2-5 and contribute to behavior 6-8 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [5]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474
Calcium signalling: dynamics, homeostasis and remodelling
Berridge, M. J., Bootman, M. D., & Roderick, H. L. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1155 · Cited by 5,719
Fluorescent indicators for Ca2+based on green fluorescent proteins and calmodulin
Miyawaki, A., Llopis, J. L., Heim, R., McCaffery, J. M., Adams, J. A., Ikura, M., & Tsien, R. Y. (1997) · Nature · doi:10.1038/42264 · Cited by 3,250
Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators
Tian, L., Hires, S. A., Mao, T., Huber, D., Chiappe, M. E., Chalasani, S. H., Petreanu, L., Akerboom, J., McKinney, S. A., Schreiter, E. R., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1398 · Cited by 1,967
Calcium oscillations increase the efficiency and specificity of gene expression
Dolmetsch, R. E., Xu, K., & Lewis, R. S. (1998) · Nature · doi:10.1038/31960 · Cited by 1,896
Astrocytes, from brain glue to communication elements: the revolution continues
Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,837
Self-citationTripartite synapses: astrocytes process and control synaptic information
Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820
Glutamate-mediated astrocyte–neuron signalling
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K., Jeftinija, S., & Haydon, P. G. (1994) · Nature · doi:10.1038/369744a0 · Cited by 1,768
Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains
Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578
Grienberger, C., & Konnerth, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.011 · Cited by 1,459
Flagged first, then by citations
Research works printed but not linked: 1
- Volterra, A. in Neuroglia (eds Kettenmann, H. & Ransom, B. R.) 816–823 (Oxford Univ. Press, 2013).
Cited by
Sorted by citations
Items 201–300 of 442
Multiplexed calcium imaging of single-synapse activity and astroglial responses in the intact brain
Reynolds, J. R., Zheng, K., & Rusakov, D. A. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.06.024 · Cited by 23
Kidins220/ARMS controls astrocyte calcium signaling and neuron–astrocyte communication
Jaudon, F., Chiacchiaretta, M., Albini, M., Ferroni, S., Benfenati, F., & Cesca, F. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0431-5 · Cited by 24
Yamaguchi, K., Kitamura, R., Kawakami, R., Otomo, K., & Nemoto, T. (2020) · PLoS ONE · doi:10.1371/journal.pone.0237230 · Cited by 23
Vellucci, L., Mazza, B., Barone, A., Nasti, A., Simone, G. D., Iasevoli, F., & de Bartolomeis, A. (2025) · Biomolecules · doi:10.3390/biom15050615 · Cited by 23
A functional perspective on astrocyte heterogeneity
Kwon, W., Williamson, M. R., & Deneen, B. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.06.009 · Cited by 22
Kelly, P., Sanchez-Mico, M. V., Hou, S. S., Whiteman, S. T., Russ, A., Hudry, E., Arbel‐Ornath, M., Greenberg, S. M., & Bacskai, B. J. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1988-22.2023 · Cited by 23
Njau, S. N., Joshi, S. H., Leaver, A. M., Vasavada, M. M., Fleet, J. V., Espinoza, R. T., & Narr, K. L. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.05.012 · Cited by 26
Puma, D. D. L., Marcocci, M. E., Lazzarino, G., Chiara, G. D., Tavazzi, B., Palamara, A. T., Piacentini, R., & Grassi, C. (2020) · Glia · doi:10.1002/glia.23895 · Cited by 22
An analog astrocyte–neuron interaction circuit for neuromorphic applications
Ranjbar, M., & Amiri, M. (2015) · Journal of Computational Electronics · doi:10.1007/s10825-015-0703-3 · Cited by 22
Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex
Henriques, V. J., Chiavegato, A., Carmignoto, G., & Gómez‐Gonzalo, M. (2022) · Cells · doi:10.3390/cells11091400 · Cited by 21
Neuron–Glia Interactions and Brain Circuits
Linne, M., Aćimović, J., Saudargienė, A., & Manninen, T. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-89439-9_4 · Cited by 21
Mechanisms of Activation of Brain’s Drainage during Sleep: The Nightlife of Astrocytes
Postnov, D. E., Semyachkina-Glushkovskaya, O. V., Litvinenko, E., Kurths, J., & Penzel, T. (2023) · Cells · doi:10.3390/cells12222667 · Cited by 23
Владимирович, М. В., Gordleeva, S. Y., Boldyreva, N., Ben‐Jacob, E., Kazantsev, V., & Pittà, M. D. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_6 · Cited by 21
A Compartmental Model to Investigate Local and Global Ca2+ Dynamics in Astrocytes
Cresswell-Clay, E., Crock, N., Tabak, J., & Erlebacher, G. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00094 · Cited by 21
Spatiotemporal model of tripartite synapse with perinodal astrocytic process
Lorenzo, J., Vuillaume, R., Binczak, S., & Jacquir, S. (2019) · Journal of Computational Neuroscience · doi:10.1007/s10827-019-00734-4 · Cited by 21
Na+–Ca2+ exchanger mediates ChR2-induced [Ca2+]i elevation in astrocytes
Yang, J., Yu, H. Q., Zhou, D., Zhu, K., Lou, H., Duan, S., & Wang, H. (2015) · Cell Calcium · doi:10.1016/j.ceca.2015.06.008 · Cited by 21
Gray, S. R., Ye, L., Ye, J. Y., & Paukert, M. (2021) · Science Advances · doi:10.1126/sciadv.abk1378 · Cited by 24
GABAρ subunits confer a bicuculline-insensitive component to GFAP + cells of cerebellum
Pétriz, A., Reyes‐Haro, D., González‐González, M. A., Miledi, R., & Martínez‐Torres, A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419632111 · Cited by 20
IP 3 R2 null mice display a normal acquisition of somatic and neurological development milestones
Guerra‐Gomes, S., Cunha‐Garcia, D., Nascimento, D. S. M., Duarte‐Silva, S., Loureiro‐Campos, E., Sardinha, V. M., Viana, J. F., Sousa, N., Maciel, P., Pinto, L., et al. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14724 · Cited by 20
Chemogenetic manipulation of astrocytic activity: Is it possible to reveal the roles of astrocytes?
Shen, W., Chen, S., Liu, Y., Han, P., Ma, T., & Zeng, L. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114457 · Cited by 21
Li, J., Du, M., Wang, R., Lei, J., & Wu, Y. (2016) · International Journal of Bifurcation and Chaos · doi:10.1142/s0218127416501388 · Cited by 20
Statistical Mechanics of Neocortical Interactions: Large-Scale EEG Influences on Molecular ProcessesPreprint
Ingber, L. (2015) · SSRN Electronic Journal · doi:10.1016/j.jtbi.2016.02.003 · Cited by 20
Rethinking intellectual disability from neuro- to astro-pathology.
Fernández-Blanco, Á., & Dierssen, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239039 · Cited by 19
Calcium‐Dependent Signaling in Astrocytes: Downstream Mechanisms and Implications for Cognition
Veiga, A., Abreu, D. S., Dias, J. D., Azenha, P., Barsanti, S., & Oliveira, J. F. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70019 · Cited by 21
Probing nano‐organization of astroglia with multi‐color super‐resolution microscopy
Heller, J. P., Michaluk, P., Sugao, K., & Rusakov, D. A. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24026 · Cited by 19
A common role for astrocytes in rhythmic behaviours?
Broadhead, M. J., & Miles, G. B. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102052 · Cited by 19
Pittà, M. D. (2020) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_100691-1 · Cited by 21
Glia plasma membrane transporters: Key players in glutamatergic neurotransmission
Flores‐Méndez, M., Méndez-Flores, O. G., & Ortega, A. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.04.004 · Cited by 18
Tyurikova, O., Zheng, K., Rings, A., Drews, A., Klenerman, D., & Rusakov, D. A. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.12.007 · Cited by 18
Moshkforoush, A., Balachandar, L., Moncion, C., Santana, J., & Riera, J. J. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008648 · Cited by 18
ARACHNE: A neural-neuroglial network builder with remotely controlled parallel computing
Aleksin, S. G., Zheng, K., Rusakov, D. A., & Savtchenko, L. P. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005467 · Cited by 18
Lim, D., Mapelli, L., Canonico, P. L., Moccia, F. D., & Genazzani, A. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102997 · Cited by 18
Héja, L., Simon, Á., Szabó, Z. M., & Kardos, J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.05.006 · Cited by 18
26th Annual Computational Neuroscience Meeting (CNS*2017): Part 2
Rubchinsky, L. L., Ahn, S., Klijn, W., Cumming, B., Yates, S., Karakasis, V., Peyser, A., Woodman, M., Diaz-Pier, S., Deraeve, J., et al. (2017) · BMC Neuroscience · doi:10.1186/s12868-017-0371-2 · Cited by 17
Astrocyte Calcium Signaling Shifts the Polarity of Presynaptic Plasticity
Letellier, M., & Goda, Y. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.05.032 · Cited by 18
Optogenetic and chemogenetic approaches for modeling neurological disorders in vivo
Krut’, V. G., Kalinichenko, A. L., Maltsev, D. I., Jappy, D., Shevchenko, E. K., Podgorny, O. V., & Belousov, V. V. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102600 · Cited by 17
Autoimmune inflammation triggers aberrant astrocytic calcium signaling to impair synaptic plasticity
Baraibar, A. M., Colomer, T., Moreno‐García, A., Bernal‐Chico, A., Sánchez-Martín, E., Utrilla, C., Serrat, R., Gómez, E. S., Rodríguez-Antigüedad, A., Araque, A., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.010 · Cited by 18
Adenosine‐Dependent Arousal Induced by Astrocytes in a Brainstem Circuit
Zhu, Y., Ma, J., Li, Y., Gu, M.-Y., Feng, X., Shao, Y., Tan, L., Lou, H., Sun, L., Liu, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202407706 · Cited by 17
Subcellular calcium dynamics during juvenile development in mouse hippocampal astrocytes
Nakayama, R., Sasaki, T., Tanaka, K. F., & Ikegaya, Y. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13188 · Cited by 17
Savtchouk, I., Carriero, G., & Volterra, A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00098 · Cited by 17
Self-citationCrapart, C. C., Scott, Z. C., Konno, T., Sharma, A., Parutto, P., Bailey, D. M., Westrate, L. M., Avezov, E., & Koslover, E. F. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2312172121 · Cited by 16
Calcium signaling at the interface between astrocytes and brain inflammation
Novakovic, M. M., & Prakriya, M. (2024) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2024.102940 · Cited by 16
Dynamic Transitions in Neuronal Network Firing Sustained by Abnormal Astrocyte Feedback
Yu, Y., Yuan, Z., Fan, Y., Li, J., & Wu, Y. (2020) · Neural Plasticity · doi:10.1155/2020/8864246 · Cited by 16
Schnell, C., Negm, M., Driehaus, J., Scheller, A., & Hülsmann, S. (2015) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2015.10.008 · Cited by 16
Duan, J., Navarro‐Dorado, J., Clark, J. H., Kinnear, N. P., Meinke, P., Schirmer, E. C., & Evans, A. M. (2019) · Nature Communications · doi:10.1038/s41467-019-10055-w · Cited by 17
Direct monitoring of ER Ca2+ dynamics reveals that Ca2+ entry induces ER-Ca2+ release in astrocytes
Rodríguez-Prados, M., Rojo‐Ruiz, J., Garcı́a-Sancho, J., & Alonso, M. T. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02364-7 · Cited by 16
Lactate release from astrocytes to neurons contributes to cocaine memory formation
Boury‐Jamot, B., Halfon, O., Magistretti, P. J., & Boutrel, B. (2016) · BioEssays · doi:10.1002/bies.201600118 · Cited by 16
Raos, B. J., Simpson, M. C., Doyle, C., Murray, A. F., Graham, E. S., & Unsworth, C. P. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aaae1d · Cited by 15
Manninen, T., Havela, R., & Linne, M. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_16 · Cited by 15
Piccialli, I., Tedeschi, V., Boscia, F., Ciccone, R., Casamassa, A., de Rosa, V., Grieco, P., Secondo, A., & Pannaccione, A. (2020) · Toxins · doi:10.3390/toxins13010020 · Cited by 14
General anesthetic agents induce neurotoxicity through astrocytes
Yang, Y., Liu, T., Li, ., Yan, D., Hu, Y., Wu, P., Fang, F., McQuillan, P. M., Hang, W., Leng, J., et al. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.385857 · Cited by 14
Takizawa, M., Harada, K., Nakamura, K., & Tsuboi, T. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.05.097 · Cited by 14
Photonics tools begin to clarify astrocyte calcium transients
Gorzo, K. A., & Gordon, G. R. (2022) · Neurophotonics · doi:10.1117/1.nph.9.2.021907 · Cited by 14
Do Astrocytes Respond To Dopamine ?
Jennings, A., & Rusakov, D. A. (2016) · Russian Agency for Digital Standardization · doi:10.20388/omp2016.001.0017 · Cited by 14
Spatiotemporal control of mitochondrial network dynamics in astroglial cells
Göbel, J., Motori, E., & Bergami, M. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.06.191 · Cited by 15
Astrocyte Viability and Functionality in Spatially Confined Microcavitation Zone
Chen, B., Tjahja, J., Malla, S., Liebman, C., & Cho, M. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b21410 · Cited by 14
The Astrogenic Balance in the Aging Brain
Andromidas, F., Atashpanjeh, S., Myers, A. J., MacKinnon, B., Shaffer, M. M., & Koob, A. O. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210420095118 · Cited by 13
Huguet, J. E., Gómez, E. S., & Grandes, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413231 · Cited by 14
Amyloid pathology disrupts gliotransmitter release in astrocytes
Pillai, A. G., & Nadkarni, S. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010334 · Cited by 15
Rózsa, M., Baka, J., Bordé, S., Rózsa, B. J., Katona, G., & Tamás, G. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1166-9 · Cited by 14
G Protein-Coupled Receptor-Mediated Calcium Signaling in Astrocytes
Pittà, M. D., Ben‐Jacob, E., & Berry, H. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_5 · Cited by 15
A Neuron–Glial Perspective for Computational Neuroscience
Pittà, M. D., & Berry, H. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_1 · Cited by 13
Noriega‐Prieto, J. A., Falcón‐Moya, R., Noeker, J. A., Cai, R. H. Y. M., Fundazuri, U. B., Eraso‐Pichot, A., Cai, S., Guttipatti, P., Belisle, L., Antonio, R.-M., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02148-1 · Cited by 12
Linne, M. (2024) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102838 · Cited by 12
Estradiol Mediates Astrocyte-Neuron Communication in the Hippocampus
Goenaga, J. G., Nanclares, C., Hall, M. A. L., Kofuji, P., Mermelstein, P. G., & Araque, A. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04905-6 · Cited by 13
From Pathology to Physiology of Calcineurin Signalling in Astrocytes
Lim, D., Rocchio, F., Mapelli, L., & Moccia, F. D. (2016) · Russian Agency for Digital Standardization · doi:10.20388/omp2016.002.0029 · Cited by 12
Astroglial Vesicular Trafficking in Neurodegenerative Diseases
Zorec, R., Parpura, V., & Verkhratsky, A. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2055-1 · Cited by 13
Tsai, Y.-L., Yen, C.-T., & Wang, Y. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220218 · Cited by 12
Thapaliya, P. K., Pape, N., Rose, C. R., & Ullah, G. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1035553 · Cited by 12
Glycine Receptor Activation Impairs ATP-Induced Calcium Transients in Cultured Cortical Astrocytes
Morais, T. P., Correia-Coelho, D. A., Vaz, S. H., Sebastião, A. M., & Valente, C. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00444 · Cited by 12
Balderas, P. M. D. O., & Balderas, H. M. D. O. (2018) · BMC Biophysics · doi:10.1186/s13628-018-0043-3 · Cited by 12
Schweigmann, M., Caudal, L. C., Stopper, G., Scheller, A., Koch, K. P., & Kirchhoff, F. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.720675 · Cited by 12
Li, J., Song, J., Tan, N., Cao, C., Du, M., Xu, S., & Wu, Y. (2021) · Nonlinear Dynamics · doi:10.1007/s11071-021-06737-0 · Cited by 12
Nanosecond UV lasers stimulate transient Ca 2+ elevations in human hNT astrocytes
Raos, B. J., Graham, E. S., & Unsworth, C. P. (2017) · Journal of Neural Engineering · doi:10.1088/1741-2552/aa5f27 · Cited by 12
Yamamoto, M., & Takano, T. (2025) · Cells · doi:10.3390/cells14241936 · Cited by 12
Aghighi, Z., Ghorbani, Z., Moghaddam, M. H., Fathi, M., Abdollahifar, M., Soleimani, M., Karimzadeh, F., Rasoolijazi, H., & Aliaghaei, A. (2022) · Neuropeptides · doi:10.1016/j.npep.2022.102295 · Cited by 11
Previdi, A., Borghi, F., Profumo, F., Schulte, C., Piazzoni, C., Lamanna, J., Racchetti, G., Malgaroli, A., & Milani, P. (2023) · Cells · doi:10.3390/cells12020293 · Cited by 11
Shining the Light on Astrocytic Ensembles
Delgado, L., & Navarrete, M. (2023) · Cells · doi:10.3390/cells12091253 · Cited by 12
Raman, S., Srinivasan, G. R., Brookhouser, N., Nguyen, T., Henson, T., Morgan, D., Cutts, J., & Brafman, D. A. (2020) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.0c00067 · Cited by 11
Transmembrane Prolyl 4-Hydroxylase is a Novel Regulator of Calcium Signaling in Astrocytes
Byts, N., Sharma, S., Laurila, J., Paudel, P., Miinalainen, I., Ronkainen, V., Hinttala, R., Törnquist, K., Koivunen, P., & Myllyharju, J. (2020) · eNeuro · doi:10.1523/eneuro.0253-20.2020 · Cited by 11
Introducing Astrocytes on a Neuromorphic Processor
Tang, G., Polykretis, I., Ivanov, V. A., Shah, A., & Michmizos, K. P. (2019) · Neuro Inspired Computational Elements Conference (NICE) · doi:10.1145/3320288.3320302 · Cited by 11
Morita, M., Nakane, A., Maékawa, S., & Kudo, Y. (2015) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2015.08.004 · Cited by 10
Guerrero, A. A., & Turrigiano, G. G. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0807-25.2025 · Cited by 12
Novel therapeutic modulators of astrocytes for hydrocephalus
Yang, Y., Wang, C., Chen, R., Wang, Y.-C., Tan, C., Liu, J., Zhang, Q., & Xiao, G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.932955 · Cited by 10
Chemogenetic manipulation of astrocyte activity at the synapse— a gateway to manage brain disease
Pereira, M. J., Ayana, R., Holt, M. G., & Arckens, L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1193130 · Cited by 10
Deng, Q., Parker, E., Wu, C., Zhu, L., Liu, T. C., Duan, R., & Yang, L. (2024) · Aging and Disease · doi:10.14336/ad.2024.0239 · Cited by 10
Conceptual Network Model From Sensory Neurons to Astrocytes of the Human Nervous System
Yang, Y., & Yeo, C. K. (2015) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2015.2405549 · Cited by 10
Spontaneous Ultraslow Na+ Fluctuations in the Neonatal Mouse Brain
Felix, L., Ziemens, D., Seifert, G., & Rose, C. R. (2019) · Cells · doi:10.3390/cells9010102 · Cited by 10
Paniccia, J. E., Otis, J. M., & Scofield, M. D. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.07.052 · Cited by 13
Butcher, J. B., Sims, R. E., Ngum, N., Bazzari, A. H., Jenkins, S. I., King, M. C., Hill, E. J., Nagel, D. A., Fox, K. D., Parri, H. R., et al. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.905285 · Cited by 10
Sugimoto, H., Sato, M., Nakai, J., & Kawakami, K. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.12848 · Cited by 9
Khananshvili, D. (2023) · Cell Calcium · doi:10.1016/j.ceca.2023.102818 · Cited by 9
Mongrédien, R., Anésio, A., Fernandes, G. J. D., Eagle, A. L., Maldera, S., Pham, C., Robert, S., Bezerra, F. R., Vilette, A., Bianchi, P. C., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.02.904 · Cited by 11
Shakhidzhanov, S. S., Balabin, F. A., Obydennyi, S. I., Атауллаханов, Ф. И., & Sveshnikova, A. N. (2018) · Physics-Uspekhi · doi:10.3367/ufne.2018.05.038335 · Cited by 9
Astrocyte Bioenergetics and Major Psychiatric Disorders
Maly, I. V., Morales, M. J., & Pletnikov, M. V. (2021) · Advances in neurobiology · doi:10.1007/978-3-030-77375-5_9 · Cited by 10
The Mandala of the Present Moment
Gordon, W. V., Shonin, E., & García‐Campayo, J. (2017) · Mindfulness · doi:10.1007/s12671-017-0779-x · Cited by 10
Role of dysregulated calcium homeostasis in astrocytes in neurodegenerative disorders
Sanchez-Mico, M. V., Calvo-Rodríguez, M., & Bacskai, B. J. (2026) · Nature reviews. Neuroscience · doi:10.1038/s41583-026-01032-6 · Cited by 9
Chen, Y., Du, T., Peng, L., Gibbs, M. E., & Hertz, L. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00067 · Cited by 8
Elucidating regulators of astrocytic Ca 2+ signaling via multi‐threshold event detection ( MTED )
Müller, F. E., Cherkas, V., Stopper, G., Caudal, L. C., Stopper, L., Kirchhoff, F., Henneberger, C., Ponimaskin, E. G., & Zeug, A. (2021) · Glia · doi:10.1002/glia.24070 · Cited by 8
Venugopal, S., Srinivasan, R., & Khakh, B. S. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_17 · Cited by 8
Metadata
- Authors
- Volterra, A., Liaudet, N., & Savtchouk, I.
- Affiliations
- University of Lausanne (CH)
- Corresponding author
- Volterra, Andrea
- Venue
- Nature Reviews Neuroscience
- Published
- 2014-04-17
- Volume
- 15
- Issue
- 5
- Pages
- 327-335
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W1972077052
- Cited by
- 446
- References
- 117
- Citations by year
- 2026: 15 · 2025: 32 · 2024: 27 · 2023: 32 · 2022: 27 · 2021: 43 · 2020: 44 · 2019: 52 · 2018: 50 · 2017: 37 · 2016: 38 · 2015: 43 · 2014: 6
- FWCI
- 4.66
- Type
- journal article
- Language
- en
- Open access
- green
- iris.unil.ch
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- SERVAL (Université de Lausanne) (submittedVersion, other-oa)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (140999, 31003A)
- FP7 Ideas: European Research Council (340368)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- astrocytes, calcium signaling, calcium dynamics, synaptic function, brain information processing, astrocyte-neuron interaction, brain integration
- MeSH terms
- Animals, Astrocytes, Brain, Calcium, Humans, Synapses, Calcium Signaling
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review