Synapse Pathology in Psychiatric and Neurologic Disease
Open accessAbstract
Inhibitory and excitatory synapses play a fundamental role in information processing in the brain. Excitatory synapses usually are situated on dendritic spines, small membrane protrusions that harbor glutamate receptors and postsynaptic density components and help transmit electrical signals. In recent years, it has become evident that spine morphology is intimately linked to synapse function--smaller spines have smaller synapses and support reduced synaptic transmission. The relationship between synaptic signaling, spine shape, and brain function is never more apparent than when the brain becomes dysfunctional. Many psychiatric and neurologic disorders, ranging from mental retardation and autism to Alzheimer's disease and addiction, are accompanied by alterations in spine morphology and synapse number. In this review, we highlight the structure and molecular organization of synapses and discuss functional effects of synapse pathology in brain disease.
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
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?
Changes in morphological complexity, dendritic spine number, shape and plasticity are associated with several neuropsychiatric and neurological disorders, including schizophrenia, autism spectrum disorder, intellectual disability and epilepsy.
“changes in morphological complexity, dendritic spine number, shape and plasticity are associated with several neuropsychiatric and neurological disorders, including SCZ, ASD, ID and epilepsy.16, 17, 18, 19”
From The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines (2014) · cites this paper as [19]
The Introduction (page unavailable) links abnormal dendritic spine density and morphology and aberrant synaptic plasticity to neuropsychiatric diseases, including schizophrenia, autism, and intellectual disability. The Conclusions (page unavailable) link epilepsy to disrupted excitatory–inhibitory synaptic balance, but do not specifically associate it with the claimed changes in dendritic morphology or spines. The copy also does not clearly address changes in overall morphological complexity. (LLM, conf=0.85)
Experimental — accuracy not yet measuredDisruption in dendritic morphogenesis, synaptogenesis or activity-dependent remodelling produces network-wide deficits in neuronal connectivity.
“A disruption in any of these processes produces network-wide deficits in neuronal connectivity”
From The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines (2014) · cites this paper as [19]
The Introduction (page not provided) says that loss of synaptic stability may disrupt neuronal circuits, supporting the general connection. It does not establish that disruption of any of the three named processes necessarily produces network-wide connectivity deficits; the claim is more categorical and specific than the source. (LLM, conf=0.85)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Alzheimer's Disease Is a Synaptic Failure
Selkoe, D. J. (2002) · Science · doi:10.1126/science.1074069 · Cited by 4,420 · see citing works
Shankar, G. M., Li, S., Mehta, T. H., Garcia-Munoz, A., Shepardson, N. E., Smith, I., Brett, F. M., Farrell, M. A., Rowan, M. J., Lemere, C. A., et al. (2008) · Nature Medicine · doi:10.1038/nm1782 · Cited by 3,685 · see citing works
AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588 · see citing works
Südhof, T. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131412 · Cited by 2,491 · see citing works
Experience-dependent structural synaptic plasticity in the mammalian brain
Holtmaat, A., & Svoboda, K. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2699 · Cited by 1,934 · see citing works
Advances in autism genetics: on the threshold of a new neurobiology
Abrahams, B. S., & Geschwind, D. H. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2346 · Cited by 1,866 · see citing works
Neuroligins and neurexins link synaptic function to cognitive disease
Südhof, T. C. (2008) · Nature · doi:10.1038/nature07456 · Cited by 1,849 · see citing works
Amyloid-β Dynamics Are Regulated by Orexin and the Sleep-Wake Cycle
Kang, J.-E., Lim, M. M., Bateman, R. J., Lee, J. J., Smyth, L. P., Cirrito, J. R., Fujiki, N., Nishino, S., & Holtzman, D. M. (2009) · Science · doi:10.1126/science.1180962 · Cited by 1,565 · see citing works
Synaptic plasticity and addiction
Kauer, J. A., & Malenka, R. C. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2234 · Cited by 1,397 · see citing works
The glutamate homeostasis hypothesis of addiction
Kalivas, P. W. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2515 · Cited by 1,350 · see citing works
Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269 · see citing works
NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders
Lau, C. G., & Zukin, R. S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2153 · Cited by 1,159 · cited 1× · see citing works
“Moreover, alterations in synaptic receptor trafficking, abnormal spine morphology, and defects in synaptic function have been reported in animal models of neuropsychiatric disorders including addiction and schizophrenia [8, 34 ], as well as in models of mental retardation, such as FXS [35].”
BackgroundFragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Bassell, G. J., & Warren, S. T. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.004 · Cited by 1,051 · see citing works
AMPAR Removal Underlies Aβ-Induced Synaptic Depression and Dendritic Spine Loss
Hsieh, H., Boehm, J., Sato, C., Iwatsubo, T., Tomita, T., Sisodia, S., & Malinow, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.035 · Cited by 1,042 · see citing works
X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor
Sobolevsky, A. I., Rosconi, M. P., & Gouaux, E. (2009) · Nature · doi:10.1038/nature08624 · Cited by 1,027 · see citing works
The Postsynaptic Architecture of Excitatory Synapses: A More Quantitative View
Sheng, M., & Hoogenraad, C. C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060805.160029 · Cited by 1,003 · see citing works
Self-citationA Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
Tabuchi, K., Blundell, J., Etherton, M. R., Hammer, R. E., Liu, X., Powell, C. M., & Südhof, T. C. (2007) · Science · doi:10.1126/science.1146221 · Cited by 997 · see citing works
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., et al. (2009) · Nature · doi:10.1038/nature07999 · Cited by 989 · see citing works
Balancing Structure and Function at Hippocampal Dendritic Spines
Bourne, J. N., & Harris, K. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125646 · Cited by 916 · see citing works
Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice
Welch, J. M., Lu, J., Rodriguiz, R. M., Trotta, N. C., Peca, J., Ding, J.-D., Feliciano, C., Chen, M., Adams, J. P., Luo, J., et al. (2007) · Nature · doi:10.1038/nature06104 · Cited by 852 · see citing works
Structure-stability-function relationships of dendritic spines
Kasai, H., Matsuzaki, M., Noguchi, J., Yasumatsu, N., & Nakahara, H. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00162-0 · Cited by 847 · see citing works
Synaptic plasticity and dysconnection in schizophrenia
Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841 · see citing works
GABAA receptor trafficking and its role in the dynamic modulation of neuronal inhibition
Jacob, T. C., Moss, S. J., & Jurd, R. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2370 · Cited by 695 · see citing works
Animal models of Alzheimer's disease and frontotemporal dementia
Götz, J., & Ittner, L. M. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2420 · Cited by 676 · see citing works
Dynamic microtubules regulate dendritic spine morphology and synaptic plasticity
Jaworski, J., Kapitein, L. C., Gouveia, S. M., Dortland, B. R., Wulf, P. S., Grigoriev, I., Camera, P., Spangler, S. A., Di Stefano, P., Demmers, J., et al. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.013 · Cited by 643 · see citing works
Self-citationEndocytosis Is Required for Synaptic Activity-Dependent Release of Amyloid-β In Vivo
Cirrito, J. R., Kang, J.-E., Lee, J., Stewart, F. R., Verges, D. K., Silverio, L. M., Bu, G., Mennerick, S., & Holtzman, D. M. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.003 · Cited by 635 · see citing works
Molecular mechanisms of dendritic spine morphogenesis
Tada, T., & Sheng, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.12.001 · Cited by 615 · see citing works
Lord, C., Cook, E. H., Leventhal, B. L., & Amaral, D. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00115-x · Cited by 555 · see citing works
Myosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity
Wang, Z., Edwards, J. G., Riley, N., Provance, D. W., Karcher, R., Li, X.-D., Davison, I. G., Ikebe, M., Mercer, J. A., Kauer, J. A., et al. (2008) · Cell · doi:10.1016/j.cell.2008.09.057 · Cited by 470 · see citing works
Failure of neuronal homeostasis results in common neuropsychiatric phenotypes
Ramocki, M. B., & Zoghbi, H. Y. (2008) · Nature · doi:10.1038/nature07457 · Cited by 399 · see citing works
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
Zalfa, F., Eleuteri, B., Dickson, K. S., Mercaldo, V., Rubeis, S. D., di Penta, A., Tabolacci, E., Chiurazzi, P., Neri, G., Grant, S. G. N., et al. (2007) · Nature Neuroscience · doi:10.1038/nn1893 · Cited by 364 · see citing works
Rho GTPases, dendritic structure, and mental retardation
Newey, S. E., Velamoor, V., Govek, E., & Van Aelst, L. (2005) · Journal of Neurobiology · doi:10.1002/neu.20153 · Cited by 351 · see citing works
Calabresi, P., Picconi, B., Parnetti, L., & Filippo, M. D. (2006) · The Lancet Neurology · doi:10.1016/s1474-4422(06)70600-7 · Cited by 337 · see citing works
Dendritic spine formation and stabilization
Yoshihara, Y., De Roo, M., & Muller, D. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.05.013 · Cited by 292 · see citing works
In Vivo Cocaine Experience Generates Silent Synapses
Huang, Y. H., Lin, Y., Mu, P., Lee, B. R., Brown, T. E., Wayman, G. A., Marie, H., Liu, W., Yan, Z., Sorg, B. A., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.007 · Cited by 290 · see citing works
Organization of the core structure of the postsynaptic density
Chen, X., Winters, C. A., Azzam, R. N., Li, X., Galbraith, J. A., Leapman, R. D., & Reese, T. S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800897105 · Cited by 290 · see citing works
Cadherins and catenins at synapses: Roles in synaptogenesis and synaptic plasticity.
Arikkath, J., & Reichardt, L. F. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.07.001 · Cited by 289 · see citing works
Integration of biochemical signalling in spines
Kennedy, M. B., Beale, H. C., Carlisle, H. J., & Washburn, L. R. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1685 · Cited by 286 · see citing works
Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome
Dölen, G., & Bear, M. F. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.150722 · Cited by 278 · see citing works
Molecular mechanisms of α-synuclein neurodegeneration
Waxman, E. A., & Giasson, B. I. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.09.013 · Cited by 241 · see citing works
The State of Synapses in Fragile X Syndrome
Pfeiffer, B. E., & Huber, K. M. (2009) · The Neuroscientist · doi:10.1177/1073858409333075 · Cited by 214 · see citing works
Molecular Mechanisms of Presynaptic Differentiation
Jin, Y., & Garner, C. C. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123417 · Cited by 184 · see citing works
Blanpied, T. A., & Ehlers, M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.10.006 · Cited by 179 · see citing works
Control of neuronal polarity and plasticity – a renaissance for microtubules?
Hoogenraad, C. C., & Bradke, F. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.08.006 · Cited by 173 · see citing works
Self-citationHow to build a central synapse: clues from cell culture
Craig, A. M., Graf, E. R., & Linhoff, M. W. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.11.002 · Cited by 168 · see citing works
Microsatellite repeat instability and neurological disease
Brouwer, J. R., Willemsen, R., & Oostra, B. A. (2009) · BioEssays · doi:10.1002/bies.080122 · Cited by 137 · see citing works
Recent advances in fragile X: a model for autism and neurodegeneration
Hagerman, R. J., Ono, M. Y., & Hagerman, P. J. (2005) · Current Opinion in Psychiatry · doi:10.1097/01.yco.0000179485.39520.b0 · Cited by 116 · see citing works
LIMK1 and CLIP‐115: linking cytoskeletal defects to Williams syndrome
Hoogenraad, C. C., Akhmanova, A. S., Galjart, N., & Zeeuw, C. I. D. (2004) · BioEssays · doi:10.1002/bies.10402 · Cited by 107 · see citing works
Self-citationBasic mechanisms for recognition and transport of synaptic cargos
Schlager, M. A., & Hoogenraad, C. C. (2009) · Molecular Brain · doi:10.1186/1756-6606-2-25 · Cited by 94 · see citing works
Self-citationMolecular dynamics of postsynaptic receptors and scaffold proteins
Renner, M. L., Specht, C. G., & Triller, A. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.09.009 · Cited by 91 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease
Petzinger, G. M., Fisher, B. E., McEwen, S., Beeler, J. A., Walsh, J. P., & Jakowec, M. W. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70123-6 · Cited by 798 · see citing works
The Indispensable Roles of Microglia and Astrocytes during Brain Development
Reemst, K., Noctor, S. C., Lucassen, P. J., & Hol, E. M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00566 · Cited by 516 · see citing works
Tau Protein Modifications and Interactions: Their Role in Function and Dysfunction
Mietelska‐Porowska, A., Wasik, U., Goras, M., Filipek, A., & Niewiadomska, G. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15034671 · Cited by 407 · see citing works
Raven, F., Van der Zee, E. A., Meerlo, P., & Havekes, R. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2017.05.002 · Cited by 331 · see citing works
Sphingolipids: membrane microdomains in brain development, function and neurological diseases
Olsen, A. S. B., & Færgeman, N. J. (2017) · Open Biology · doi:10.1098/rsob.170069 · Cited by 312 · see citing works
Masini, E., Loi, E., Vega-Benedetti, A. F., Carta, M., Doneddu, G., Fadda, R., & Zavattari, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218290 · Cited by 293 · see citing works
The role of glutamate signaling in the pathogenesis and treatment of obsessive-compulsive disorder
Wu, K., Hanna, G. L., Rosenberg, D. R., & Arnold, P. D. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.10.007 · Cited by 264 · see citing works
Brain IL-6 elevation causes neuronal circuitry imbalances and mediates autism-like behaviors
Wei, H., Chadman, K. K., McCloskey, D. P., Sheikh, A. M., Malik, M. N., Brown, W. T., & Li, X. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.01.011 · Cited by 257 · see citing works
Which way to go? Cytoskeletal organization and polarized transport in neurons
Kapitein, L. C., & Hoogenraad, C. C. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.015 · Cited by 246 · see citing works
Self-citationCranial irradiation compromises neuronal architecture in the hippocampus
Parihar, V. K., & Limoli, C. L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307301110 · Cited by 240 · see citing works
Briner, A., Nikonenko, I., Roo, M. D., Dayer, A. G., Müller, D., & Vutskits, L. (2011) · Anesthesiology · doi:10.1097/aln.0b013e318221fbbd · Cited by 236 · see citing works
Infectious Agents and Neurodegeneration
Chiara, G. D., Marcocci, M. E., Sgarbanti, R., Civitelli, L., Ripoli, C., Piacentini, R., Garaci, E., Grassi, C., & Palamara, A. T. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8320-7 · Cited by 231 · see citing works
Developmental origins of brain disorders: roles for dopamine
Money, K. M., & Stanwood, G. D. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00260 · Cited by 221 · see citing works
What happens to your brain on the way to Mars
Parihar, V. K., Allen, B., Tran, K. K., Macaraeg, T. G., Chu, E. M., Kwok, S. F., Chmielewski, N. N., Craver, B. M., Baulch, J. E., Acharya, M. M., et al. (2015) · Science Advances · doi:10.1126/sciadv.1400256 · Cited by 217 · see citing works
RBFOX1 regulates both splicing and transcriptional networks in human neuronal development
Fogel, B. L., Wexler, E., Wahnich, A., Friedrich, T., Vijayendran, C., Gao, F., Parikshak, N., Konopka, G., & Geschwind, D. H. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds240 · Cited by 216 · see citing works
Targeting ligand-operated chaperone sigma-1 receptors in the treatment of neuropsychiatric disorders
Hayashi, T., Tsai, S., Mori, T., Fujimoto, M., & Su, T. (2011) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2011.560837 · Cited by 206 · see citing works
Toxoplasma gondii‐induced neuronal alterations
Parlog, A., Schlüter, D., & Dunay, I. R. (2014) · Parasite Immunology · doi:10.1111/pim.12157 · Cited by 199 · see citing works
Structural and functional plasticity of dendritic spines – root or result of behavior?
Gipson, C. D., & Olive, M. F. (2016) · Genes Brain & Behavior · doi:10.1111/gbb.12324 · Cited by 192 · see citing works
Pathania, M., Davenport, E. C., Muir, J., Sheehan, D. F., López-Doménech, G., & Kittler, J. T. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.16 · Cited by 189 · see citing works
A pivotal role of GSK-3 in synaptic plasticity
Bradley, C. A., Peineau, S., Taghibiglou, C., Nicolas, C. S., Whitcomb, D. J., Bortolotto, Z. A., Kaang, B., Cho, K., Wang, Y. T., & Collingridge, G. L. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00013 · Cited by 189 · see citing works
RhoA-ROCK Signaling as a Therapeutic Target in Traumatic Brain Injury
Mulherkar, S., & Tolias, K. F. (2020) · Cells · doi:10.3390/cells9010245 · Cited by 179 · see citing works
Actin Out: Regulation of the Synaptic Cytoskeleton
Spence, E. F., & Soderling, S. H. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.r115.655118 · Cited by 171 · see citing works
Persistent changes in neuronal structure and synaptic plasticity caused by proton irradiation
Parihar, V. K., Pasha, J., Tran, K. K., Craver, B. M., Acharya, M. M., & Limoli, C. L. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0709-9 · Cited by 165 · see citing works
Fitting, S., Ignatowska-Jankowska, B. M., Bull, C., Skoff, R. P., Lichtman, A. H., Wise, L. E., Fox, M. A., Su, J., Medina, A. E., Krahe, T. E., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.026 · Cited by 162 · see citing works
Synucleins Have Multiple Effects on Presynaptic Architecture
Vargas, K. J., Schrod, N., Davis, T., Fernández‐Busnadiego, R., Taguchi, Y. V., Laugks, U., Lučić, V., & Chandra, S. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.023 · Cited by 160 · see citing works
AMPA receptors as drug targets in neurological disease—advantages, caveats, and future outlook
Chang, P. K. ‐., Verbich, D., & McKinney, R. A. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08165.x · Cited by 155 · see citing works
Insights into Rapid Modulation of Neuroplasticity by Brain Estrogens
Srivastava, D. P., Woolfrey, K. M., & Penzes, P. (2013) · Pharmacological Reviews · doi:10.1124/pr.111.005272 · Cited by 138 · see citing works
PET imaging of synaptic density: A new tool for investigation of neuropsychiatric diseases
Cai, Z., Li, S., Matuskey, D., Nabulsi, N., & Huang, Y. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2018.07.038 · Cited by 131 · see citing works
Rapid Estrogen Signaling in the Brain: Implications for the Fine-Tuning of Neuronal Circuitry
Srivastava, D. P., Waters, E. M., Mermelstein, P. G., Kramár, E. A., Shors, T. J., & Liu, F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4097-11.2011 · Cited by 137 · see citing works
Increased expression of miRNA-146a in Alzheimer's disease transgenic mouse models
Li, Y. Y., Cui, J. G., Hill, J. M., Bhattacharjee, S., Zhao, Y., & Lukiw, W. J. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2010.09.079 · Cited by 112 · see citing works
Kaphzan, H., Buffington, S. A., Jung, J. I., Rasband, M. N., & Klann, E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4162-11.2011 · Cited by 129 · see citing works
Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders
Penzes, P., Buonanno, A., Passafaro, M., Sala, C., & Sweet, R. A. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12261 · Cited by 125 · see citing works
Changes in Plasticity Across the Lifespan
Oberman, L. M., & Pascual‐Leone, Á. (2013) · Progress in brain research · doi:10.1016/b978-0-444-63327-9.00016-3 · Cited by 125 · see citing works
Maiti, P., Manna, J., Ilavazhagan, G., Rossignol, J., & Dunbar, G. L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.09.020 · Cited by 118 · see citing works
Weston, M. C., Chen, H., & Swann, J. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1283-12.2012 · Cited by 121 · see citing works
Spooren, W., Lindemann, L., Ghosh, A., & Santarelli, L. (2012) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2012.09.004 · Cited by 119 · see citing works
de Waal, H., Stam, C. J., Lansbergen, M. M., Wieggers, R. L., Kamphuis, P. J. G. H., Scheltens, P., Maestú, F., & van Straaten, E. C. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086558 · Cited by 119 · see citing works
Inhibitory Basal Ganglia Inputs Induce Excitatory Motor Signals in the Thalamus
Kim, J.-J., Kim, Y., Nakajima, R., Shin, A., Jeong, M., Park, A. H., Jeong, Y., Jo, S., Yang, S., Park, H., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.08.028 · Cited by 119 · see citing works
Synapses and Dendritic Spines as Pathogenic Targets in Alzheimer’s Disease
Yu, W., & Lu, B. (2012) · Neural Plasticity · doi:10.1155/2012/247150 · Cited by 119 · see citing works
Jeyabalan, N., & Clement, J. P. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00032 · Cited by 118 · see citing works
Cytoplasmic dynein in neurodegeneration
Eschbach, J., & Dupuis, L. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.03.004 · Cited by 114 · see citing works
Fiumelli, H., Briner, A., Puskarjov, M., Blaesse, P., Belem, B. J., Dayer, A. G., Kaila, K., Martin, J., & Vutskits, L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs027 · Cited by 115 · see citing works
Hochstenbach, R., Buizer‐Voskamp, J. E., Vorstman, J. A. S., & Ophoff, R. A. (2011) · Cytogenetic and Genome Research · doi:10.1159/000332928 · Cited by 110 · see citing works
Toxoplasmosis: A pathway to neuropsychiatric disorders
Tyebji, S., Seizova, S., Hannan, A. J., & Tonkin, C. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.11.012 · Cited by 111 · see citing works
Ribosomal biogenesis as an emerging target of neurodevelopmental pathologies
Hetman, M., & Słomnicki, Ł. P. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14576 · Cited by 110 · see citing works
Eph receptors and ephrins in neuron–astrocyte communication at synapses
Murai, K. K., & Pasquale, E. B. (2011) · Glia · doi:10.1002/glia.21226 · Cited by 109 · see citing works
Perineuronal Nets and Their Role in Synaptic Homeostasis
Bosiacki, M., Gąssowska-Dobrowolska, M., Kojder, K., Fabiańska, M., Jeżewski, D., Gutowska, I., & Lubkowska, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174108 · Cited by 107 · see citing works
Sun, F., Guo, W., Zheng, D.-H., Zhang, C., Li, S., Liu, S., Yin, Q., Yang, H., & Shu, H. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9878-2 · Cited by 106 · see citing works
Stem Cell Transplantation Reverses Chemotherapy-Induced Cognitive Dysfunction
Acharya, M. M., Martirosian, V., Chmielewski, N. N., Hanna, N. M., Tran, K. K., Liao, A. C., Christie, L., Parihar, V. K., & Limoli, C. L. (2015) · Cancer Research · doi:10.1158/0008-5472.can-14-2237 · Cited by 104 · see citing works
Dzyubenko, E., Rozenberg, A., Hermann, D. M., & Faissner, A. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.09.001 · Cited by 98 · see citing works
Higdon, R., Earl, R. K., Stanberry, L. I., Hudac, C. M., Montague, E., Stewart, E., Janko, I., Choiniere, J., Broomall, W., Kolker, N., et al. (2015) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2015.0020 · Cited by 103 · see citing works
Villalba, R. M., & Smith, Y. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.011 · Cited by 94 · see citing works
Presynaptic function in health and disease
Waites, C. L., & Garner, C. C. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.03.004 · Cited by 94 · see citing works
Behavioral and neurochemical effects of proline
Wyse, Â. T. D. S., & Netto, C. A. (2011) · Metabolic Brain Disease · doi:10.1007/s11011-011-9246-x · Cited by 92 · see citing works
Zada, D., Tovin, A., Lerer-Goldshtein, T., Vatine, G. D., & Appelbaum, L. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004615 · Cited by 92 · see citing works
Molecular signature of rapid estrogen regulation of synaptic connectivity and cognition
Sellers, K. J., Raval, P., & Srivastava, D. P. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.08.001 · Cited by 89 · see citing works
Ng, L. H. L., Huang, Y., Han, L., Chang, R. C.-C., Chan, Y. S., & Lai, C. S. W. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0321-5 · Cited by 82 · see citing works
Electrochemistry at the Synapse
Shin, M., Wang, Y., Borgus, J. R., & Venton, B. (2019) · Annual Review of Analytical Chemistry · doi:10.1146/annurev-anchem-061318-115434 · Cited by 63 · see citing works
Electron tomographic analysis of synaptic ultrastructure
Burette, A. C., Lesperance, T., Crum, J., Martone, M., Volkmann, N., Ellisman, M. H., & Weinberg, R. J. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23067 · Cited by 85 · see citing works
Modulation of synaptic plasticity by exercise
Bettio, L. E. B., Thacker, J. S., Hutton, C. P., & Christie, B. R. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.07.002 · Cited by 82 · see citing works
Gąssowska-Dobrowolska, M., Baranowska‐Bosiacka, I., Moczydłowska, J., Frontczak‐Baniewicz, M., Gewartowska, M., Strużyńska, L., Gutowska, I., Chlubek, D., & Adamczyk, A. (2016) · Toxicology · doi:10.1016/j.tox.2016.10.014 · Cited by 80 · see citing works
Neuregulin 3 promotes excitatory synapse formation on hippocampal interneurons
Müller, T. H., Braud, S., Jüttner, R., Voigt, B. C., Paulick, K., Sheean, M. E., Klisch, C., Güneykaya, D., Rathjen, F. G., Geiger, J. R., et al. (2018) · The EMBO Journal · doi:10.15252/embj.201798858 · Cited by 77 · see citing works
Control of dendritic spine morphological and functional plasticity by small GTPases.
Woolfrey, K. M., & Srivastava, D. P. (2016) · Neural Plasticity · doi:10.1155/2016/3025948 · Cited by 76 · see citing works
Eph receptors at synapses: Implications in neurodegenerative diseases
Chen, Y., Fu, A. K. Y., & Ip, N. Y. (2011) · Cellular Signalling · doi:10.1016/j.cellsig.2011.11.016 · Cited by 75 · see citing works
Neurobiology of autism gene products: towards pathogenesis and drug targets
Kleijer, K. T. E., Schmeißer, M. J., Krueger‐Burg, D., Boeckers, T. M., Scheiffele, P., Bourgeron, T., Brose, N., & Burbach, J. P. H. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3403-3 · Cited by 75 · see citing works
Martín‐Montañez, E., Millón, C., Boraldi, F., García-Guirado, F., Pedraza, C., Lara, E., Santín, L. J., Pavı́a, J., & Garcia‐Fernandez, M. I. (2017) · Redox Biology · doi:10.1016/j.redox.2017.05.012 · Cited by 74 · see citing works
The structure and function of actin cytoskeleton in mature glutamatergic dendritic spines
Bellot, A., Guivernau, B., Tajes, M., Bosch-Morató, M., Valls-Comamala, V., & Muñoz, F. J. (2014) · Brain Research · doi:10.1016/j.brainres.2014.05.024 · Cited by 74 · see citing works
Imaging Synaptic Density: The Next Holy Grail of Neuroscience?
Serrano, M. E., Kim, E., Petrinovic, M. M., Turkheimer, F., & Cash, D. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.796129 · Cited by 67 · see citing works
Ribarič, S. (2023) · Biomedicines · doi:10.3390/biomedicines11020355 · Cited by 66 · see citing works
Sumoylation in Synaptic Function and Dysfunction
Schorova, L., & Martin, S. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00009 · Cited by 68 · see citing works
Afroz, S., Parato, J., Shen, H., & Smith, S. S. (2016) · eLife · doi:10.7554/elife.15106 · Cited by 68 · see citing works
Adams, D. J., Arthur, C. P., & Stowell, M. H. B. (2015) · Scientific Reports · doi:10.1038/srep13659 · Cited by 68 · see citing works
EphBs: an integral link between synaptic function and synaptopathies
Sheffler-Collins, S. I., & Dalva, M. B. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.03.003 · Cited by 67 · see citing works
Bawari, S., Tewari, D., Argüelles, S., Sah, A. N., Nabavi, S. F., Xu, S., Vacca, R. A., Nabavi, S. M., & Shirooie, S. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.104458 · Cited by 68 · see citing works
Space–brain: The negative effects of space exposure on the central nervous system
Limoli, C., Jandial, R., Hoshide, R., & Waters, J. (2018) · Surgical Neurology International · doi:10.4103/sni.sni_250_17 · Cited by 66 · see citing works
Eps8 controls dendritic spine density and synaptic plasticity through its actin‐capping activity
Menna, E., Zambetti, S., Morini, R., Donzelli, A., Disanza, A., Calvigioni, D., Braida, D., Nicolini, C., Orlando, M., Fossati, G., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.107 · Cited by 64 · see citing works
Targets for Drug Therapy for Autism Spectrum Disorder: Challenges and Future Directions
Lacivita, E., Perrone, R., Margari, L., & Leopoldo, M. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00965 · Cited by 66 · see citing works
Li, S., Cai, Z., Zhang, W., Holden, D., Lin, S.-F., Finnema, S. J., Shirali, A., Ropchan, J., Carre, S., Mercier, J., et al. (2019) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-019-04357-w · Cited by 59 · see citing works
Mitigation of helium irradiation-induced brain injury by microglia depletion
Allen, B. D., Syage, A. R., Maroso, M., Baddour, A. A. D., Luong, V., Minasyan, H., Giedzinski, E., West, B. L., Soltész, I., Limoli, C. L., et al. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01790-9 · Cited by 61 · see citing works
Prince, S., Paulson, A. L., Jeong, N., Zhang, L., Amigues, S., & Singer, A. C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109008 · Cited by 58 · see citing works
Yadav, R., Hillman, B. G., Gupta, S. C., Suryavanshi, P. S., Bhatt, J. M., Pavuluri, R., Stairs, D. J., & Dravid, S. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060785 · Cited by 62 · see citing works
Zinc in Cognitive Impairment and Aging
Sun, R., Wang, J., Feng, J., & Cao, B. (2022) · Biomolecules · doi:10.3390/biom12071000 · Cited by 61 · see citing works
Imaging Chemical Neurotransmission with Genetically Encoded Fluorescent Sensors
Liang, R., Broussard, G. J., & Tian, L. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500280k · Cited by 61 · see citing works
Khanal, P., & Hotulainen, P. (2021) · Cells · doi:10.3390/cells10092392 · Cited by 60 · see citing works
Ramalho, R. M., Nunes, A. F., Dias, R. B., Amaral, J. D., Lo, A. C., D’Hooge, R., Sebastião, A. M., & Rodrigues, C. M. P. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.04.018 · Cited by 60 · see citing works
Workman, J. L., Manny, N., Walton, J. C., & Nelson, R. J. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.07.021 · Cited by 60 · see citing works
Srivastava, A., Das, B., Yao, A. Y., & Yan, R. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-201146 · Cited by 57 · see citing works
Treatment of actinic keratoses with sequential use of photodynamic therapy; and imiquimod 5% cream.
Shaffelburg, M. (2009) · PubMed · Cited by 56 · see citing works
Identification of novel genomic risk loci shared between common epilepsies and psychiatric disorders
Karadag, N., Shadrin, A. A., O’Connell, K. S., Hindley, G., Rahman, Z., Parker, N., Bahrami, S., Fominykh, V., Cheng, W., Holen, B., et al. (2023) · Brain · doi:10.1093/brain/awad038 · Cited by 57 · see citing works
Destination Brain: the Past, Present, and Future of Therapeutic Gene Delivery
Joshi, C. R., Labhasetwar, V., & Ghorpade, A. (2017) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-016-9724-3 · Cited by 55 · see citing works
Wei, H., Dobkin, C., Sheikh, A. M., Malik, M. N., Brown, W. T., & Li, X. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036981 · Cited by 55 · see citing works
Mencer, S., Kartawy, M., Lendenfeld, F. V., Soluh, H., Tripathi, M. K., Халиулин, И. Г., & Amal, H. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01578-2 · Cited by 55 · see citing works
Zebrafish as a model for studying the developmental neurotoxicity of propofol
Guo, P., Huang, Z., Tao, T., Chen, X., Zhang, W., Zhang, Y., & Lin, C. (2015) · Journal of Applied Toxicology · doi:10.1002/jat.3183 · Cited by 54 · see citing works
Vutskits, L. (2012) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e31826a1178 · Cited by 53 · see citing works
The DISC1 promoter: characterization and regulation by FOXP2
Walker, R. M., Hill, A. E., Newman, A. C., Hamilton, G., Torrance, H. S., Anderson, S. M., Ogawa, F., Deriziotis, P., Nicod, J., Vernes, S. C., et al. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds111 · Cited by 54 · see citing works
Waltereit, R., Leimer, U., Halbach, O. V. B. U., Panke, J., Hölter, S. M., Garrett, L., Wittig, K., Schneider, M., Schmitt, C., Calzada‐Wack, J., et al. (2012) · The FASEB Journal · doi:10.1096/fj.11-202317 · Cited by 54 · see citing works
Repetto, D., Camera, P., Melani, R., Morello, N., Russo, I., Calcagno, E., Tomasoni, R., Bianchi, F. T., Berto, G. E., Giustetto, M., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2341-13.2014 · Cited by 53 · see citing works
Regulation of Dendritic Spine Morphology in Hippocampal Neurons by Copine-6
Burk, K., Ramachandran, B., Ahmed, S., Hurtado-Zavala, J. I., Awasthi, A., Benito, E., Faram, R., Ahmad, H., Swaminathan, A., McIlhinney, J., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx009 · Cited by 52 · see citing works
Actin Capping Protein Is Required for Dendritic Spine Development and Synapse Formation
Fan, Y., Tang, X., Vitriol, E. A., Chen, G., & Zheng, J. Q. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0115-11.2011 · Cited by 52 · see citing works
Iasevoli, F., Tomasetti, C., Marmo, F., Bravi, D., Arnt, J., & de Bartolomeis, A. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1954-0 · Cited by 49 · see citing works
- Authors
- van Spronsen, M., & Hoogenraad, C. C.
- Affiliations
- Erasmus MC (NL)
- Corresponding author
- Hoogenraad, Casper C.
- Venue
- Current Neurology and Neuroscience Reports
- Published
- 2010-03-18
- Volume
- 10
- Issue
- 3
- Pages
- 207-214
- ISSN
- 1528-4042 (ISSN-L)
- 1534-6293
- PMC
- PMC2857788
- OpenAlex
- W2098229885
- Cited by
- 345
- References
- 50
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 13 · 2023: 16 · 2022: 22 · 2021: 18 · 2020: 21 · 2019: 20 · 2018: 29 · 2017: 21 · 2016: 25 · 2015: 26 · 2014: 22 · 2013: 24 · 2012: 38
- FWCI
- 2.66
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- Current Neurology and Neuroscience Reports (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion, other-oa)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- RePub (Erasmus University Rotterdam) (submittedVersion)
- Funders
- ZonMw
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Keywords
- dendritic spines, dendritic spine morphology, excitatory synapses, inhibitory synapses, synaptic transmission, postsynaptic density, glutamate receptors, mental illness, neurological disorders, autism spectrum disorder, intellectual disability, Alzheimer's disease, addiction, synapse number
- MeSH terms
- Mental Disorders, Humans, Models, Biological, Nervous System Diseases, Neuronal Plasticity, Neurons, Synapses, Dendritic Spines
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