Locally Synchronized Synaptic Inputs

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483

Memory of sequential experience in the hippocampus during slow wave sleep

Lee, A. K., & Wilson, M. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)01096-6 · Cited by 1,296

A new cellular mechanism for coupling inputs arriving at different cortical layers

Larkum, M. E., Zhu, J. J., & Sakmann, B. (1999) · Nature · doi:10.1038/18686 · Cited by 1,180

DENDRITIC COMPUTATION

London, M., & Häusser, M. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135703 · Cited by 1,149

Synfire Chains and Cortical Songs: Temporal Modules of Cortical Activity

Ikegaya, Y., Aaron, G., Cossart, R., Aronov, D., Lampl, I., Ferster, D., & Yuste, R. (2004) · Science · doi:10.1126/science.1093173 · Cited by 838

NMDA spikes in basal dendrites of cortical pyramidal neurons

Schiller, J., Major, G., Koester, H. J., & Schiller, Y. (2000) · Nature · doi:10.1038/35005094 · Cited by 720

Integrative Properties of Radial Oblique Dendrites in Hippocampal CA1 Pyramidal Neurons

Losonczy, A., & Magee, J. C. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.016 · Cited by 641

Locally dynamic synaptic learning rules in pyramidal neuron dendrites

Harvey, C. D., & Svoboda, K. (2007) · Nature · doi:10.1038/nature06416 · Cited by 625

Compartmentalized dendritic plasticity and input feature storage in neurons

Losonczy, A., Makara, J. K., & Magee, J. C. (2008) · Nature · doi:10.1038/nature06725 · Cited by 598

Local, persistent activation of Rho GTPases during plasticity of single dendritic spines

Murakoshi, H., Wang, H., & Yasuda, R. (2011) · Nature · doi:10.1038/nature09823 · Cited by 564

Imaging Calcium in Neurons

Grienberger, C., & Konnerth, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.011 · Cited by 1,459

Sustained rescue of prefrontal circuit dysfunction by antidepressant-induced spine formation

Moda-Sava, R. N., Murdock, M. H., Parekh, P. K., Fetcho, R. N., Huang, B. S., Huynh, T. N., Witztum, J., Shaver, D. C., Rosenthal, D. L., Alway, E. J., et al. (2019) · Science · doi:10.1126/science.aat8078 · Cited by 643

Dendritic integration: 60 years of progress

Stuart, G. J., & Spruston, N. (2015) · Nature Neuroscience · doi:10.1038/nn.4157 · Cited by 516

Dendritic Spines: The Locus of Structural and Functional Plasticity

Sala, C., & Segal, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00012.2013 · Cited by 491

Active properties of neocortical pyramidal neuron dendrites

Major, G., Larkum, M. E., & Schiller, J. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150343 · Cited by 443

Dendritic spines: from structure to in vivo function

Rochefort, N. L., & Konnerth, A. (2012) · The EMBO Reports · doi:10.1038/embor.2012.102 · Cited by 299

Illuminating dendritic function with computational models

Poirazi, P., & Papoutsi, A. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0301-7 · Cited by 313

Astrocytes Modulate Neural Network Activity by Ca 2+ -Dependent Uptake of Extracellular K +

Wang, F., Smith, N., Xu, Q., Fujita, T., Baba, A., Matsuda, T., Takano, T., Bekar, L. K., & Nedergaard, M. (2012) · Science Signaling · doi:10.1126/scisignal.2002334 · Cited by 304

Higher-Order Thalamocortical Inputs Gate Synaptic Long-Term Potentiation via Disinhibition

Williams, L. E., & Holtmaat, A. J. D. G. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.049 · Cited by 282

Orientation selectivity and the functional clustering of synaptic inputs in primary visual cortex

Wilson, D. E., Whitney, D. E., Scholl, B., & Fitzpatrick, D. (2016) · Nature Neuroscience · doi:10.1038/nn.4323 · Cited by 271

Genetically Encoded Green Fluorescent Ca2+ Indicators with Improved Detectability for Neuronal Ca2+ Signals

Ohkura, M., Sasaki, T., Sadakari, J., Gengyo‐Ando, K., Kagawa‐Nagamura, Y., Kobayashi, C., Ikegaya, Y., & Nakai, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051286 · Cited by 267

Hippocampal ripples down-regulate synapses

Norimoto, H., Makino, K., Gao, M., Shikano, Y., Okamoto, K., Ishikawa, T., Sasaki, T., Hioki, H., Fujisawa, S., & Ikegaya, Y. (2018) · Science · doi:10.1126/science.aao0702 · Cited by 262

Power-efficient neural network with artificial dendrites

Li, X., Tang, J., Zhang, Q., Gao, B., Yang, J. J., Song, S., Wu, W., Zhang, W., Yao, P., Deng, N., et al. (2020) · Nature Nanotechnology · doi:10.1038/s41565-020-0722-5 · Cited by 262

Synaptic organization of visual space in primary visual cortex

Iacaruso, M. F., Gasler, I. T., & Hofer, S. B. (2017) · Nature · doi:10.1038/nature23019 · Cited by 249

Synaptic Computation and Sensory Processing in Neocortical Layer 2/3

Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 249

Operation and plasticity of hippocampal CA3 circuits: implications for memory encoding

Rebola, N., Carta, M., & Mulle, C. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.10 · Cited by 221

Toward a Neurocentric View of Learning

Titley, H. K., Brunel, N., & Hansel, C. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.021 · Cited by 209

Biochemical Computation for Spine Structural Plasticity

Nishiyama, J., & Yasuda, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.043 · Cited by 199

Local translation in neuronal compartments: how local is local?

Rangaraju, V., Dieck, S. T., & Schuman, E. M. (2017) · EMBO Reports · doi:10.15252/embr.201744045 · Cited by 203

Synaptic clustering within dendrites: An emerging theory of memory formation

Kastellakis, G., Cai, D. J., Mednick, S. C., Silva, A. J., & Poirazi, P. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.12.002 · Cited by 198

Structured Synaptic Connectivity between Hippocampal Regions

Druckmann, S., Feng, L., Lee, B., Yook, C., Zhao, T., Magee, J. C., & Kim, J. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.026 · Cited by 188

The developmental stages of synaptic plasticity

Löhmann, C., & Kessels, H. W. H. G. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.235119 · Cited by 195

Spontaneous Activity Drives Local Synaptic Plasticity In Vivo

Winnubst, J., Cheyne, J. E., Niculescu, D., & Lohmann, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.029 · Cited by 180

Hotspots of dendritic spine turnover facilitate clustered spine addition and learning and memory

Frank, A. C., Huang, S., Zhou, M., Gdalyahu, A., Kastellakis, G., Silva, T. K., Lu, E. D., Wen, X., Poirazi, P., Trachtenberg, J. T., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02751-2 · Cited by 187

Contribution of sublinear and supralinear dendritic integration to neuronal computations

Tran-Van-Minh, A., Cazé, R. D., Abrahamsson, T., Cathala, L., Gutkin, B. S., & DiGregorio, D. A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00067 · Cited by 171

Structured dendritic inhibition supports branch-selective integration in CA1 pyramidal cells

Bloss, E. B., Cembrowski, M. S., Karsh, B., Colonell, J., Fetter, R. D., & Spruston, N. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.029 · Cited by 164

Docosanoids and elovanoids from omega-3 fatty acids are pro-homeostatic modulators of inflammatory responses, cell damage and neuroprotection

Bazan, N. G. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.09.003 · Cited by 148

Beyond von Neumann Architecture: Brain‐Inspired Artificial Neuromorphic Devices and Integrated Computing

Seok, H., Lee, D., Son, S., Choi, H., Kim, G., & Kim, T. (2024) · Advanced Electronic Materials · doi:10.1002/aelm.202300839 · Cited by 153

A highly sensitive fluorescent indicator dye for calcium imaging of neural activity in vitro and in vivo

Tada, M., Takeuchi, A., Hashizume, M., Kitamura, K., & Kano, M. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12476 · Cited by 148

Correlated Synaptic Inputs Drive Dendritic Calcium Amplification and Cooperative Plasticity during Clustered Synapse Development

Lee, K. F. H., Soares, C., Thivierge, J., & Béïque, J.-C. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.012 · Cited by 137

Single excitatory axons form clustered synapses onto CA1 pyramidal cell dendrites

Bloss, E. B., Cembrowski, M. S., Karsh, B., Colonell, J. I., Fetter, R. D., & Spruston, N. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0084-6 · Cited by 134

Compartment-specific tuning of dendritic feature selectivity by intracellular Ca 2+ release

O’Hare, J. K., Gonzalez, K. C., Herrlinger, S. A., Hirabayashi, Y., Hewitt, V. L., Blockus, H., Szoboszlay, M., Rolotti, S. V., Geiller, T., Negrean, A., et al. (2022) · Science · doi:10.1126/science.abm1670 · Cited by 123

Synaptic retinoic acid signaling and homeostatic synaptic plasticity

Chen, L., Lau, A. G., & Sarti, F. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.12.004 · Cited by 134

Stress-primed secretory autophagy promotes extracellular BDNF maturation by enhancing MMP9 secretion

Martinelli, S., Anderzhanova, E. A., Bajaj, T., Wiechmann, S., Dethloff, F., Weckmann, K., Heinz, D. E., Ebert, T., Hartmann, J., Geiger, T. M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24810-5 · Cited by 136

Local Order within Global Disorder: Synaptic Architecture of Visual Space

Scholl, B., Wilson, D. E., & Fitzpatrick, D. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.017 · Cited by 116

Deprivation-Induced Homeostatic Spine Scaling In Vivo Is Localized to Dendritic Branches that Have Undergone Recent Spine Loss

Barnes, S. J., Franzoni, E., Jacobsen, R. I., Erdélyi, F., Szabó, G., Clopath, C., Keller, G. B., & Keck, T. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.052 · Cited by 125

Variable Dendritic Integration in Hippocampal CA3 Pyramidal Neurons

Makara, J. K., & Magee, J. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.033 · Cited by 117

Artificial Association of Pre-stored Information to Generate a Qualitatively New Memory

Ohkawa, N., Saitoh, Y., Suzuki, A. Z., Tsujimura, S., Murayama, E., Kosugi, S., Nishizono, H., Matsuo, M., Takahashi, Y., Nagase, M., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.03.017 · Cited by 129

Global and Multiplexed Dendritic Computations under In Vivo-like Conditions

Ujfalussy, B. B., Makara, J. K., Lengyel, M., & Branco, T. (2018) · Neuron · doi:10.1016/j.neuron.2018.08.032 · Cited by 114

Location-dependent synaptic plasticity rules by dendritic spine cooperativity

Weber, J. P., Andrásfalvy, B. K., Polito, M., Magó, Á., Ujfalussy, B. B., & Makara, J. K. (2016) · Nature Communications · doi:10.1038/ncomms11380 · Cited by 114

A BDNF-Mediated Push-Pull Plasticity Mechanism for Synaptic Clustering

Niculescu, D., Michaelsen‐Preusse, K., Güner, Ü., van Dorland, R., Wierenga, C. J., & Löhmann, C. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.073 · Cited by 106

SK2 Channel Modulation Contributes to Compartment-Specific Dendritic Plasticity in Cerebellar Purkinje Cells

Ohtsuki, G., Piochon, C., Adelman, J. P., & Hansel, C. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.025 · Cited by 108

Selective activation of parvalbumin interneurons prevents stress-induced synapse loss and perceptual defects

Chen, C.-C., Lu, J., Yang, R., Ding, J., & Zuo, Y. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.159 · Cited by 107

Fast 3D Imaging of Spine, Dendritic, and Neuronal Assemblies in Behaving Animals

Szalay, G., Judák, L., Katona, G., Ócsai, K., Juhász, G., Veress, M., Szadai, Z., Fehér, A., Tompa, T., Chiovini, B., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.002 · Cited by 110

Dendritic Spikes Induce Ripples in Parvalbumin Interneurons during Hippocampal Sharp Waves

Chiovini, B., Turi, G. F., Katona, G., Kaszás, A., Pálfi, D., Maák, P. A., Szalay, G., Szabó, M. F., Szabó, G., Szadai, Z., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.004 · Cited by 101

Elimination of Dendritic Spines with Long-Term Memory Is Specific to Active Circuits

Sanders, J. D., Cowansage, K. K., Baumgärtel, K., & Mayford, M. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1131-12.2012 · Cited by 101

PKCα integrates spatiotemporally distinct Ca2+ and autocrine BDNF signaling to facilitate synaptic plasticity

Colgan, L. A., Hu, M., Misler, J. A., Parra-Bueno, P., Moran, C., Leitges, M., & Yasuda, R. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0184-3 · Cited by 100

Dendritic NMDA spikes are necessary for timing-dependent associative LTP in CA3 pyramidal cells

Brandalise, F., Carta, S., Helmchen, F., Lisman, J. E., & Gerber, U. R. (2016) · Nature Communications · doi:10.1038/ncomms13480 · Cited by 100

Dendritic function in vivo

Grienberger, C., Chen, X., & Konnerth, A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.002 · Cited by 107

An Augmented Two-Layer Model Captures Nonlinear Analog Spatial Integration Effects in Pyramidal Neuron Dendrites

Jadi, M. P., Behabadi, B. F., Poleg-Polsky, A., Schiller, J., & Mel, B. W. (2014) · Proceedings of the IEEE · doi:10.1109/jproc.2014.2312671 · Cited by 96

Astrocytic Coverage of Dendritic Spines, Dendritic Shafts, and Axonal Boutons in Hippocampal Neuropil

Игоревич, Г. Н., Golyagina, I., Brazhe, A., Scimemi, A., Турлапов, В., & Semyanov, A. V. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00248 · Cited by 91

Synaptic Clustering and Memory Formation

Kastellakis, G., & Poirazi, P. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00300 · Cited by 92

The computational power of astrocyte mediated synaptic plasticity

Min, R., Santello, M., & Nevian, T. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00093 · Cited by 100

Learning binds new inputs into functional synaptic clusters via spinogenesis

Hedrick, N. G., Lu, Z., Bushong, E. A., Singhi, S., Nguyen, P., Magaña, Y., Jilani, S., Lim, B. K., Ellisman, M. H., & Komiyama, T. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01086-6 · Cited by 96

Synapse rearrangements upon learning: from divergent–sparse connectivity to dedicated sub-circuits

Caroni, P., Chowdhury, A., & Lahr, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.08.011 · Cited by 85

Local resources of polyribosomes and SER promote synapse enlargement and spine clustering after long-term potentiation in adult rat hippocampus

Chirillo, M. A., Waters, M. S., Lindsey, L. F., Bourne, J. N., & Harris, K. M. (2019) · Scientific Reports · doi:10.1038/s41598-019-40520-x · Cited by 84

Inhibitory Regulation of Dendritic Activity in vivo

Palmer, L. M., Murayama, M., & Larkum, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00026 · Cited by 88

Reading out a spatiotemporal population code by imaging neighbouring parallel fibre axons in vivo

Wilms, C. D., & Häusser, M. (2015) · Nature Communications · doi:10.1038/ncomms7464 · Cited by 83

Are Dendrites Conceptually Useful?

Larkum, M. E. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.03.008 · Cited by 84

Translocation of CaMKII to dendritic microtubules supports the plasticity of local synapses

Lemieux, M., Labrecque, S., Tardif, C., Labrie-Dion, É., LeBel, É., & Koninck, P. D. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201202058 · Cited by 82

Interaction of nNOS with PSD-95 Negatively Controls Regenerative Repair after Stroke

Luo, C., Lin, Y., Qian, X., Tang, Y., Zhou, H.-H., Jin, X., Ni, H., Zhang, F., Qin, C., Li, F., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1305-14.2014 · Cited by 82

Optical inactivation of synaptic AMPA receptors erases fear memory

Takemoto, K., Iwanari, H., Tada, H., Suyama, K., Sano, A., Nagai, T., Hamakubo, T., & Takahashi, T. (2016) · Nature Biotechnology · doi:10.1038/nbt.3710 · Cited by 83

A metaplasticity view of the interaction between homeostatic and Hebbian plasticity

Yee, A. X., Hsu, Y., & Chen, L. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0155 · Cited by 85

Retrograde Synaptic Signaling Mediated by K+ Efflux through Postsynaptic NMDA Receptors

Shih, P., Savtchenko, L. P., Kamasawa, N., Dembitskaya, Y., McHugh, T. J., Rusakov, D. A., Shigemoto, R., & Semyanov, A. V. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.10.026 · Cited by 72

Photoactivatable CaMKII induces synaptic plasticity in single synapses

Shibata, A. C. E., Ueda, H. H., Eto, K., Onda, M., Sato, A., Ohba, T., Nabekura, J., & Murakoshi, H. (2021) · Nature Communications · doi:10.1038/s41467-021-21025-6 · Cited by 74

Thalamocortical input onto layer 5 pyramidal neurons measured using quantitative large-scale array tomography

Rah, J., Bas, E., Colonell, J. I., Mishchenko, Y., Karsh, B., Fetter, R. D., Myers, E. W., Chklovskii, D. B., Svoboda, K., Harris, T. D., et al. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00177 · Cited by 74

Emergence of local and global synaptic organization on cortical dendrites

Kirchner, J. H., & Gjorgjieva, J. (2021) · Nature Communications · doi:10.1038/s41467-021-23557-3 · Cited by 74

Shaping inhibition: activity dependent structural plasticity of GABAergic synapses

Flores, C. E., & Méndez, P. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00327 · Cited by 74

Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons

Ju, N., Li, Y., Liu, F., Jiang, H., Macknik, S. L., Martínez‐Conde, S., & Tang, S. (2020) · Nature Communications · doi:10.1038/s41467-020-14501-y · Cited by 63

Linear integration of spine Ca 2+ signals in layer 4 cortical neurons in vivo

Jia, H., Varga, Z., Sakmann, B. J., & Konnerth, A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1408525111 · Cited by 67

Synaptic modifications in learning and memory – A dendritic spine story

Ma, S., & Zuo, Y. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.05.015 · Cited by 66

Active dendrites enable strong but sparse inputs to determine orientation selectivity

Goetz, L., Roth, A., & Häusser, M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017339118 · Cited by 75

A low-power vertical dual-gate neurotransistor with short-term memory for high energy-efficient neuromorphic computing

Han, X., Shang, D., Luo, Q., An, J., Li, Y., Wu, S., Yao, Z., Zhang, W., Xu, X., Dou, C., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42172-y · Cited by 68

Co-dependent excitatory and inhibitory plasticity accounts for quick, stable and long-lasting memories in biological networks

Agnes, E. J., & Vogels, T. P. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01597-4 · Cited by 69

Sublinear integration underlies binocular processing in primary visual cortex

Longordo, F., To, M., Ikeda, K., & Stuart, G. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3394 · Cited by 67

LOTOS-based two-photon calcium imaging of dendritic spines in vivo

Chen, X., Leischner, U., Varga, Z., Jia, H., Deca, D., Rochefort, N. L., & Konnerth, A. (2012) · Nature Protocols · doi:10.1038/nprot.2012.106 · Cited by 62

Input transformation by dendritic spines of pyramidal neurons

Araya, R. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00141 · Cited by 63

Impact of functional synapse clusters on neuronal response selectivity

Ujfalussy, B. B., & Makara, J. K. (2020) · Nature Communications · doi:10.1038/s41467-020-15147-6 · Cited by 56

Integrin adhesion in brain assembly: From molecular structure to neuropsychiatric disorders

Jaudon, F., Thalhammer, A., & Cingolani, L. A. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14859 · Cited by 59

Differential Dendritic Integration of Synaptic Potentials and Calcium in Cerebellar Interneurons

Tran-Van-Minh, A., Abrahamsson, T., Cathala, L., & DiGregorio, D. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.029 · Cited by 63

White Matter Plasticity Keeps the Brain in Tune: Axons Conduct While Glia Wrap

Chorghay, Z., Káradóttir, R. T., & Ruthazer, E. S. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00428 · Cited by 66

Beyond the Patch Clamp: Nanotechnologies for Intracellular Recording

Kruskal, P. B., Jiang, Z., Gao, T., & Lieber, C. M. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.004 · Cited by 59

Synaptic clustering during development and learning: the why, when, and how

Winnubst, J., & Löhmann, C. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00070 · Cited by 60

How do neurons operate on sparse distributed representations? A mathematical theory of sparsity, neurons and active dendritesPreprint

Ahmad, S., & Hawkins, J. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1601.00720 · Cited by 82

Catching the engram: strategies to examine the memory trace

Sakaguchi, M., & Hayashi, Y. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-32 · Cited by 58

Clusters of synaptic inputs on dendrites of layer 5 pyramidal cells in mouse visual cortex

Gökçe, O., Bonhoeffer, T., & Scheuß, V. (2016) · eLife · doi:10.7554/elife.09222 · Cited by 56

The emerging use of bioluminescence in medical research

Sharifian, S., Homaei, A. A., Hemmati, R., Luwor, R. B., & Khajeh, K. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.02.065 · Cited by 53

Functional Synaptic Architecture of Callosal Inputs in Mouse Primary Visual Cortex

Lee, K.-S., Vandemark, K., Mezey, D., Shultz, N., & Fitzpatrick, D. (2018) · Neuron · doi:10.1016/j.neuron.2018.12.005 · Cited by 55

Thalamus and claustrum control parallel layer 1 circuits in retrosplenial cortex

Brennan, E. K. W., Jedrasiak‐Cape, I., Kailasa, S., Rice, S. P., Sudhakar, S., & Ahmed, O. J. (2021) · eLife · doi:10.7554/elife.62207 · Cited by 58

Sensory-evoked synaptic integration in cerebellar and cerebral cortical neurons

Chadderton, P. T., Schaefer, A. T., Williams, S. R., & Margrie, T. W. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3648 · Cited by 53

Selective Memory Generalization by Spatial Patterning of Protein Synthesis

O’Donnell, C., & B, T. J. S. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.028 · Cited by 51

Targeted axon-attached recording with fluorescent patch-clamp pipettes in brain slices

Sasaki, T., Matsuki, N., & Ikegaya, Y. (2012) · Nature Protocols · doi:10.1038/nprot.2012.061 · Cited by 52

Redundancy in synaptic connections enables neurons to learn optimally

Hiratani, N., & Fukai, T. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1803274115 · Cited by 58

Actin remodeling, the synaptic tag and the maintenance of synaptic plasticity

Pinho, J., Marcut, C. F., & Fonseca, R. (2020) · IUBMB Life · doi:10.1002/iub.2261 · Cited by 50

Effects of Axonal Topology on the Somatic Modulation of Synaptic Outputs

Sasaki, T., Matsuki, N., & Ikegaya, Y. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5365-11.2012 · Cited by 48

Morphologic evidence for spatially clustered spines in apical dendrites of monkey neocortical pyramidal cells

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