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Cortex: Statistics and Geometry of Neuronal Connectivity
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“This is because the high levels of recurrent connectivity in the source area (Braitenberg and Schüz 1998; Markov et al. 2011) can lead to labeled axon terminals in the vicinity of the retrogradely labeled cells that can be mistaken for long-distance anterograde labeling from the injected target area.”
From A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex (2014) · cites this paper as Braitenberg and Schüz 1998
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Local versus global scales of organization in auditory cortex
Kanold, P. O., Nelken, I., & Polley, D. B. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.06.003 · Cited by 121
Topology and dynamics of the canonical circuit of cat V1
Binzegger, T., Douglas, R. J., & Martin, K. A. C. (2009) · Neural Networks · doi:10.1016/j.neunet.2009.07.011 · Cited by 108
“Overall, the vast majority of cortical excitatory synapses and almost all inhibitory synapses, originate from neurons within cortex (Braitenberg & Schüz, 1998).”
InfluentialCrossNets: High‐Performance Neuromorphic Architectures for CMOL Circuits
LIKHAREV, K., MAYR, A., MUCKRA, I., & TÜREL, Ö. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1292.010 · Cited by 121
An algorithm to predict the connectome of neural microcircuits
Reimann, M., King, J. G., Muller, E. B., Ramaswamy, S., & Markram, H. (2015) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2015.00120 · Cited by 117
“, 1979) have been generalized in rules stating that connections are untargeted, that the fraction of axo-dendritic appositions forming synapses is constant, and that most connections are formed of only one synapse (Braitenberg and Schüz, 1998; Braitenberg, 2001).”
BackgroundMethodInfluentialBoucsein, C. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00032 · Cited by 125
“…with radius d as N d f h P s sdsdcon E( ) ( )= ∫2 0πρ , with ρ = 60,000/mm3 (black trace) defining the cell density per cortex volume, fE = 0.85 representing the relative fraction of excitatory connections (Braitenberg and Schüz, 1998), and h = 1.3 mm defining the thickness of the gray matter.”
BackgroundInfluentialGyrification and neural connectivity in schizophrenia
White, T. J. H., & Hilgetag, C. C. (2011) · Development and Psychopathology · doi:10.1017/s0954579410000842 · Cited by 121
Why Bilateral Damage Is Worse than Unilateral Damage to the Brain
Schapiro, A. C., McClelland, J. L., Welbourne, S. R., Rogers, T. T., & Ralph, M. A. L. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00441 · Cited by 117
Neuromorphic architectures for nanoelectronic circuits
Türel, Ö., Lee, J. H., Ma, X., & Likharev, K. K. (2004) · International Journal of Circuit Theory and Applications · doi:10.1002/cta.282 · Cited by 116
The Interscutularis Muscle Connectome
Lu, J., Tapia, J. C., White, O. L., & Lichtman, J. W. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000032 · Cited by 117
“This method assumes that connectional specificity at the level of classes of cells suffices to account for the properties of circuits [7–9].”
MethodGonchar, Y., & Burkhalter, A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10904.2003 · Cited by 114
“The preference for PV neurons over other types of interneurons argues against an interareal connectivity that is strictly determined by axonal density (Braitenberg and Schüz, 1998; Traczy-Hornoch et al., 1999).”
BackgroundFledgling pathoconnectomics of psychiatric disorders
Rubinov, M., & Bullmore, E. T. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.10.007 · Cited by 118
Basselin, M., Chang, L., Bell, J. M., & Rapoport, S. I. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300920 · Cited by 114
“This interpretation is consistent with evidence that glutamatergic receptors constitute about 75% of the synapses in the mammalian cortex, and that many of these synapses include NMDARs (Braitenberg and Schüz, 1998; Fonnum, 1984; Raichle and Gusnard, 2002).”
ResultPattern formation in intracortical neuronal fields
Hutt, A., Bestehorn, M., & Wennekers, T. (2003) · Network Computation in Neural Systems · doi:10.1088/0954-898x_14_2_310 · Cited by 114
“The existence of a fixed point in the active part of the sigmoid function yields the restriction ae > ai (figure 1). There are indications that inhibitory gain factors can exceed excitatory gain factors [ 31 ], which might lead to ae ai for the rest of the paper.”
BackgroundHow do general anaesthetics work?
Antkowiak, B. (2001) · Die Naturwissenschaften · doi:10.1007/s001140100230 · Cited by 111
“Neocortical cells are covered by as many as 2,000–10,000 synapses that originate from more than 500–5,000 presynaptic cells (Braitenberg 1978; Braitenberg and Schüz 1998).”
BackgroundFriedemann Pulvermüller, A., Юрьевич, Ш. Ю., & Ilmoniemi, R. J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00356-2 · Cited by 109
“The newly available information about the temporal structure of the activation of cortical areas may be relevant for future theorizing about the brain basis of language and cognition ( Braitenberg, 1997; Pulvermu ¨ller, 2003).”
BackgroundWeisenburger, S., & Vaziri, A. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031458 · Cited by 110
Spatial embedding of structural similarity in the cerebral cortex
Song, H. F., Kennedy, H., & Wang, X. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414153111 · Cited by 104
“These results shed light on how the brain may be wired consistently through a combination of specific patterning and general connection rules (31).”
BackgroundMotor cognition–motor semantics: Action perception theory of cognition and communication
Friedemann Pulvermüller, A., Moseley, R. L., Egorova, N., Shebani, Z., & Véronique Boulenger, A. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.12.002 · Cited by 117
“As such they provide a mechanism for what Braitenberg and Schüz consider the primary function of the neocortex, namely " information mixing " , that is the joining together of specific information across modalities (Braitenberg & Schüz, 1998).”
BackgroundInfluentialMicromechanics of diffuse axonal injury: influence of axonal orientation and anisotropy
Cloots, R. R., van Dommelen, J. V., Nyberg, T., Kleiven, S., & Geers, M. (2011) · Biomechanics and Modeling in Mechanobiology · doi:10.1007/s10237-010-0243-5 · Cited by 112
“…about 5–10% consists of glial processes, 60–70% of neuronal processes (including their boutons and spines), 10–20% of somata and blood vessels, and the remaining part is the extracellular space (Fenstermacher et al. 1970; Braitenberg and Schüz 1998; Ventura and Harris 1999; Chklovskii et al. 2002).”
BackgroundCell-type specific innervation of cortical pyramidal cells at their apical dendrites
Karimi, A., Odenthal, J., Drawitsch, F., Boergens, K. M., & Helmstaedter, M. (2020) · eLife · doi:10.7554/elife.46876 · Cited by 103
“For this analysis, we identified putative inhibitory versus excitatory synapses by their location on den- dritic shafts versus spines (See Materials and methods, [Braitenberg and Schüz, 1998; Kubota et al., 2016]).”
MethodConservation of Regional Gene Expression in Mouse and Human Brain
Strand, A. D., Aragaki, A. K., Baquet, Z. C., Hodges, A., Cunningham, P., Holmans, P., Jones, K. R., Jones, L., Kooperberg, C. L., & Olson, J. M. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030059 · Cited by 106
“brain structure and conservation of cell types within comparable regions [18,19].”
BackgroundCortical Oscillations in Health and Disease
Traub, R. D., & Whittington, M. A. (2010) · doi:10.1093/acprof:oso/9780195342796.001.0001 · Cited by 108
Roudi, Y., & Latham, P. E. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030141 · Cited by 107
“Second, connectivity is all to all, which is inconsistent with the sparse connectivity seen in cortex [47].”
BackgroundA Bayesian approach for inferring neuronal connectivity from calcium fluorescent imaging data
Mishchenko, Y., Vogelstein, J. T., & Paninski, L. (2011) · The Annals of Applied Statistics · doi:10.1214/09-aoas303 · Cited by 104
Liska, A., Bertero, A., Gomolka, R. S., Sabbioni, M., Galbusera, A., Barsotti, N., Panzeri, S., Scattoni, M. L., Pasqualetti, M., & Gozzi, A. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx022 · Cited by 106
Kaiser, M., Hilgetag, C., & van Ooyen, A. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp071 · Cited by 110
“The distance between spines on the dendritic tree, however, is significantly smaller than this search space, with typically two spines/µm for dendritic segments of cortical pyramidal cells (Braitenberg and Schuez, 1998).”
BackgroundMethodKühn, B., Denk, W. T., & Bruno, R. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802462105 · Cited by 102
Automated Tracing of Neurites from Light Microscopy Stacks of Images
Chothani, P., Mehta, V., & Stepanyants, A. (2011) · Neuroinformatics · doi:10.1007/s12021-011-9121-2 · Cited by 94
“As the average axon length per neuron in mouse neocortex is about 40 mm (Braitenberg and Schüz 1998), the above error-rate is sufficiently low, making reconstructions suitable for circuit level analyses of connectivity.”
Abeysuriya, R., Hadida, J., Sotiropoulos, S. N., Jbabdi, S., Becker, R., Hunt, B. A. E., Brookes, M. J., & Woolrich, M. W. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006007 · Cited by 96
Anatomy of a cortical simulator
Ananthanarayanan, R., & Modha, D. S. (2007) · ACM/IEEE Conference on Supercomputing (SC) · doi:10.1145/1362622.1362627 · Cited by 101
“Roughly, 80% of the cortical neurons are excitatory [3].”
BackgroundMethodInfluentialAlterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors
Ballesteros-Yáñez, I., Benavides-Piccione, R., Bourgeois, J.-P., Changeux, J.-P., & DeFelipe, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006269107 · Cited by 96
EM connectomics reveals axonal target variation in a sequence-generating network
Kornfeld, J. M. R., Benezra, S. E., Narayanan, R. T., Svara, F., Egger, R., Oberlaender, M., Denk, W. T., & Long, M. A. (2017) · eLife · doi:10.7554/elife.24364 · Cited by 97
“Instead, the architecture we observed may arise naturally from a pattern that initially follows Peters’ rule (Braitenberg and Schüz, 1998), which predicts synaptic connections between cell types with intermingled axonal and dendritic arbors (Rees et al., 2017), but is then refined as the Video 4.”
BackgroundFriedemann Pulvermüller, A., & Knoblauch, A. (2009) · Neural Networks · doi:10.1016/j.neunet.2009.01.009 · Cited by 99
Synaptic Clustering and Memory Formation
Kastellakis, G., & Poirazi, P. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00300 · Cited by 92
“Synapses can be scattered, seemingly randomly in dendrites, with the location of synapses being determined by anatomy (Braitenberg and Schüz, 2013).”
BackgroundPrinciples of recovery from traumatic brain injury: Reorganization of functional networks
Castellanos, N. P., Leyva, I., Buldú, J. M., Bajo, R., Paúl, N., Cuesta, P., Ordóñez, V. E., Pascua, C. L., Boccaletti, S., Maestú, F., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.12.046 · Cited by 96
“Individual or assemblies of physically close neurons have a higher probability of being connected than spatially remote neurons or regions (Braitenberg and Schüz, 1998; Hellwig, 2000; Cherniak, 1994).”
Rewiring neural interactions by micro-stimulation
Rebesco, J. M. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00039 · Cited by 94
Spikes, BOLD, Attention, and Awareness: A comparison of electrophysiological and fMRI signals in V1
Boynton, G. M. (2011) · Journal of Vision · doi:10.1167/11.5.12 · Cited by 97
Influence of Wiring Cost on the Large-Scale Architecture of Human Cortical Connectivity
Samu, D., Seth, A. K., & Nowotny, T. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003557 · Cited by 95
Knight, J. C., & Nowotny, T. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00941 · Cited by 95
“achieve a realistic number of incoming connections per neuron of ≈ 10000 (Braitenberg and Schüz, 2013) 323 with a biologically plausible connection probability of ≈ 0.”
BackgroundFunctional connectomics reveals general wiring rule in mouse visual cortex
Ding, Z., Fahey, P. G., Papadopoulos, S., Wang, E. Y., Celii, B., Papadopoulos, C., Chang, A., Kunin, A. B., Tran, D., Fu, J., et al. (2025) · Nature · doi:10.1038/s41586-025-08840-3 · Cited by 114
Connecting Mean Field Models of Neural Activity to EEG and fMRI Data
Bojak, I., Oostendorp, T. F., Reid, A., & Kötter, R. (2010) · Brain Topography · doi:10.1007/s10548-010-0140-3 · Cited by 94
Ashby, M. C., & Isaac, J. T. R. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.057 · Cited by 100
“The majority of synaptic inputs onto neurons in the neocortex originate from nearby neurons within the same cortical area, producing local microcircuits that are ubiquitous in neocortex (Braitenberg and Schüz, 1998; Douglas and Martin, 2004; White, 2007).”
Mishchenko, Y. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.09.006 · Cited by 73
“(Compare this with 5-10mm of axonal wire present in a typical cube of mammalian neuropil of 1000μm(3) and 20-40mm of axonal wire in a typical axonal arbor of single pyramidal neuron (Braitenberg and Schuz, 1998).”
Berger, T. K., Perin, R., Silberberg, G., & Markram, H. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.176552 · Cited by 96
“(Braitenberg & Schüz, 1998), and the distribution of many though not all visualizable molecular markers is relatively homogeneous (Dong, 2007).”
BackgroundSpiegler, A., Hansen, E. C. A., Bernard, C., McIntosh, A. R., & Jirsa, V. (2016) · eNeuro · doi:10.1523/eneuro.0068-16.2016 · Cited by 96
“5), which is in keeping with known statistics of synapses within a population, namely 50% of intracortical and 50% of corticocortical fibers (Braitenberg and Schüz, 1998).”
BackgroundЮрьевич, Ш. Ю., & Friedemann Pulvermüller, A. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.10.1633 · Cited by 96
“…of 20 msec between superior temporal and inferior frontal cortices may be caused by the conduction of action potentials through the most common myelinated cortico-cortical fibers (Braitenberg & Schüz, 1998; Aboitiz, Scheibel, Fisher, & Zaidel, 1992), possibly in the arcuate and uncinate fasciculi.”
BackgroundResolving Structural Variability in Network Models and the Brain
Klimm, F., Bassett, D. S., Carlson, J. M., & Mucha, P. J. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003491 · Cited by 89
“Although a homogeneous random distribution of links has been suggested to characterize the small-scale structure of neuron-to-neuron connections [89,90], the large-scale structure of human and animal brains instead displays heterogeneous connectivity [67].”
BackgroundA Unified Dynamic Model for Learning, Replay, and Sharp-Wave/Ripples
Jahnke, S., Timme, M., & Memmesheimer, R.-M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3977-14.2015 · Cited by 90
“However, since cortical neural networks are overall sparse (Braitenberg and Schüz, 1998; Holmgren et al., 2003), we may also expect some level of dilution for embedded feedforward chains.”
BackgroundSengupta, B., Laughlin, S. B., & Niven, J. E. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003263 · Cited by 96
“A single cortical neuron makes recurrent excitatory synaptic connections with many other cortical neurons, of which about 85% of the synapses are with other excitatory neurons [2,3,55,56].”
BackgroundCommunication through Resonance in Spiking Neuronal Networks
Hahn, G., Bujan, A. F., Frégnac, Y., Aertsen, A., & Kumar, A. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003811 · Cited by 97
“However, biological neuronal networks are typically neither densely connected nor have strong synapses [11] and therefore the mechanisms that govern the propagation of neuronal activity in dense/strong FFNs are not always applicable.”
BackgroundGeometric Effects on Complex Network Structure in the Cortex
Henderson, J. A., & Robinson, P. A. (2011) · Physical Review Letters · doi:10.1103/physrevlett.107.018102 · Cited by 90
Nielsen, K. J., Logothetis, N. K., & Rainer, G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2273-06.2006 · Cited by 88
“It is estimated that between 60 and 70% of excitatory connections of a given pyramidal cell remain local and only between 30 and 40% project to other cortical area (Braitenberg and Schüz, 1998; Binzegger et al., 2004).”
BackgroundCellular pathways of energy metabolism in the brain: Is glucose used by neurons or astrocytes?
Nehlig, A., & Coles, J. A. (2007) · Glia · doi:10.1002/glia.20376 · Cited by 91
Suter, B. A., Migliore, M., & Shepherd, G. M. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs184 · Cited by 87
Molecular Profiles of Pyramidal Neurons in the Superior Temporal Cortex in Schizophrenia
Pietersen, C. Y., Mauney, S. A., Kim, S. S., Lim, M. P., Rooney, R. J., Goldstein, J. M., Petryshen, T. L., Seidman, L. J., Shenton, M. E., McCarley, R. W., et al. (2014) · Journal of Neurogenetics · doi:10.3109/01677063.2014.882918 · Cited by 87
“…dendrites and dendritic spines, and vascular elements such as blood vessels and related cellular components, including endothelial cells and various blood cells (Braitenberg & Schuz, 1998), and the abundance of many transcripts can vary in a compartment-specifi c manner (Cajigas et al., 2012).”
Optimal Information Storage in Noisy Synapses under Resource Constraints
Varshney, L. R., Sjöström, P. J., & Chklovskii, D. B. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.017 · Cited by 88
Glial Glutamine Homeostasis in Health and Disease
Andersen, J. V., & Schousboe, A. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03771-1 · Cited by 92
Lampinen, B., Szczepankiewicz, F., Mårtensson, J., van Westen, D., Hansson, O., Westin, C., & Nilsson, M. (2020) · Magnetic Resonance in Medicine · doi:10.1002/mrm.28216 · Cited by 86
Integrate-and-Fire Neurons Driven by Correlated Stochastic Input
Salinas, E., & Sejnowski, T. J. (2002) · Neural Computation · doi:10.1162/089976602320264024 · Cited by 85
Pleßer, H. E., Eppler, J. M., Morrison, A., Diesmann, M., & Gewaltig, M.-O. (2007) · Lecture notes in computer science · doi:10.1007/978-3-540-74466-5_71 · Cited by 87
“Just 1 mm(3) cortex contains some 10(5) neurons with 10(9) connections [1].”
BackgroundNeurobiological Mechanisms for Semantic Feature Extraction and Conceptual Flexibility
Friedemann Pulvermüller, A. (2018) · Topics in Cognitive Science · doi:10.1111/tops.12367 · Cited by 85
Coupling between neuronal activity and microcirculation: Implications for functional brain imaging
Vanzetta, I., & Grinvald, A. (2008) · HFSP journal · doi:10.2976/1.2889618 · Cited by 87
“…vessel “senses” not one neuron, but many [capillary length 150–500 µm (Hudetz, 1997); median capillary length and distance 110 and 25 µm, respectively (Pawlik et al., 1981), whereas interneuronal distance is 30 µm and neuronal density is 40,000/mm3 (Abeles, 1991; Braitenberg and Schüz, 1998)].”
BackgroundScaling of Brain Metabolism and Blood Flow in Relation to Capillary and Neural Scaling
Karbowski, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026709 · Cited by 88
“Cortical volume data (for 2 hemispheres) are taken from [52,41,81].”
BackgroundMethodInfluentialMota, B., & Herculano‐Houzel, S. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00127 · Cited by 89
Butz, M., & van Ooyen, A. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003259 · Cited by 88
“The mircocircuit is represented by a two dimensional recurrent network of 400 neurons, of which 80% are excitatory and 20% inhibitory [53].”
BackgroundComplex Receptive Fields in Primary Visual Cortex
Martı́nez, L. M., & Alonso, J. (2003) · The Neuroscientist · doi:10.1177/1073858403252732 · Cited by 82
“Cortical neurons (simple or complex) receive abundant input from other cortical neurons both inhibitory and excitatory (e.g., Ahmed and others 1994; Callaway 1998; Fitzpatrick 1996; Braitenberg and Schuz 1998).”
BackgroundPhysiologically based arousal state estimation and dynamics
Abeysuriya, R., RENNIE, C. J., & Robinson, P. A. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.06.002 · Cited by 82
The impact of neuron morphology on cortical network architecture
Udvary, D., Harth, P., Macke, J. H., Hege, H., de Kock, C. P. J., Sakmann, B. J., & Oberlaender, M. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110677 · Cited by 76
Pyatigorskaya, N., Bihan, D. L., Reynaud, O., & Ciobanu, L. (2013) · Magnetic Resonance in Medicine · doi:10.1002/mrm.24921 · Cited by 80
A modeler's view on the spatial structure of intrinsic horizontal connectivity in the neocortex
Voges, N., Schüz, A., Aertsen, A., & Rotter, S. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.05.001 · Cited by 77
“The study by Kisvárday and Eysel (1992, cat area 17) was based on extracellular injections, but they were able to reconstruct the axonal and dendritic arborization of 10 individual PCs.”
InfluentialSelf-citationJones, M. S., & Barth, D. S. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.1016 · Cited by 81
Visual physiology of the layer 4 cortical circuit in silico
Arkhipov, A. S., Gouwens, N. W., Billeh, Y. N., Gratiy, S. L., Iyer, R., Wei, Z., Xu, Z., Abbasi-Asl, R., Berg, J., Buice, M. A., et al. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006535 · Cited by 80
Kumarasinghe, K., Kasabov, N. K., & Taylor, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-81805-4 · Cited by 81
The Circuit Architecture of Whole Brains at the Mesoscopic Scale
Mitra, P. P. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.055 · Cited by 77
Mota, B., & Herculano‐Houzel, S. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00003 · Cited by 80
“The factor of 2 is due to the fact that we expect the vast majority of fibers in the WM to be cortico-cortical (Braitenberg and Schüz, 1998) and thus cross the WM–GM interface twice, coming in and out of the WM as they connect different areas of the cortical GM. Notice that because any deviation of…”
BackgroundParcellation and Area-Area Connectivity as a Function of Neocortex Size
Changizi, M. A., & Shinsuke Shimojo, A. (2005) · Brain Behavior and Evolution · doi:10.1159/000085942 · Cited by 80
“This may be called the ‘square root compartment invariance’, a version which was fi rst conjectured by Braitenberg [1978, 2001] and Braitenberg and Schuz [1998] .”
Abnormalities of cortical minicolumnar organization in the prefrontal lobes of autistic patients
Casanova, M. F., van Kooten, I. A. J., Switala, A. E., van Engeland, H., Heinsen, H., Steinbusch, H. W. M., Hof, P. R., & Schmitz, C. (2006) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2006.06.003 · Cited by 80
Interpreting neurodynamics: concepts and facts
Harald Atmanspacher, A., & Rotter, S. (2008) · Cognitive Neurodynamics · doi:10.1007/s11571-008-9067-8 · Cited by 79
Davis, Z. W., Benigno, G., Fletterman, C., Desbordes, T., Steward, C., B, T. J. S. A., Reynolds, J. H., & Muller, L. (2021) · Nature Communications · doi:10.1038/s41467-021-26175-1 · Cited by 80
Scaling laws in the mammalian neocortex: Does form provide clues to function?
Harrison, K. H., Hof, P. R., & Wang, S. S.-H. (2002) · Journal of Neurocytology · doi:10.1023/a:1024178127195 · Cited by 78
Topology and computational performance of attractor neural networks
McGraw, P. N., & Menzinger, M. (2003) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.68.047102 · Cited by 78
“[7] The networks compared are: (1) a regular one-dimensional ring of nodes, each connected to its 50 nearest neighbors, (2) a random (Erd˝os-Renyi[17]) network, (3) a small world ( Wemeasured two aspects of the performance of the associative memory networks: the stability of the memorized patterns…”
BackgroundMoseley, R. L., & Friedemann Pulvermüller, A. (2017) · Cortex · doi:10.1016/j.cortex.2017.11.019 · Cited by 81
Neurophysiological changes with age probed by inverse modeling of EEG spectra
van Albada, S. J., Kerr, C. C., Chiang, A. K., RENNIE, C. J., & Robinson, P. A. (2009) · Clinical Neurophysiology · doi:10.1016/j.clinph.2009.09.021 · Cited by 76
From Functional Architecture to Functional Connectomics
Reid, R. C. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.031 · Cited by 80
Propagating Waves Can Explain Irregular Neural Dynamics
Keane, A., & Gong, P. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1669-14.2015 · Cited by 73
“Each neuron receives the same number of connections (i.e., 316 excitatory connections and 180 inhibitory connections, approximately one-tenth of the average number of connections found in the cortex) (Braitenberg and Schüz, 1998).”
BackgroundA Connectomic Hypothesis for the Hominization of the Brain
Changeux, J., Goulas, A., & Hilgetag, C. C. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa365 · Cited by 80
Neural anatomy and optical microscopy (NAOMi) simulation for evaluating calcium imaging methods
Song, A. K., Gauthier, J. L., Pillow, J. W., Tank, D. W., & Charles, A. S. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109173 · Cited by 78
Brain Computations and Connectivity
Rolls, E. T. (2023) · doi:10.1093/oso/9780198887911.001.0001 · Cited by 78
Derivation and Analysis of Basic Computational Operations of Thalamocortical Circuits
Rodriguez, A., Whitson, J., & Granger, R. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904970690 · Cited by 78
“An average neocortical pyramidal cell in humans reportedly receives 25,000 to 80,000 such afferents (Braitenberg & Schüz, 1998, pp. 190–191; Rockel et al., 1980; Cragg, 1967) (with a few notable exceptions such as area 17, which has an unusually high density of neurons per square millimeter and a…”
BackgroundInfluentialKasabov, N. K., Doborjeh, M., & Doborjeh, Z. (2016) · IEEE Transactions on Neural Networks and Learning Systems · doi:10.1109/tnnls.2016.2612890 · Cited by 73
Coherent Oscillations in Neuronal Activity of the Supplementary Motor Area during a Visuomotor Task
Lee, D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06798.2003 · Cited by 76
“The number of neurons contributing synaptic inputs to a given cortical neuron is large, and many such inputs arise locally or from neighboring cortical columns with similar functional properties (Breitenberg and Schüz, 1998).”
BackgroundOweiss, K. G. (2006) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2006.873749 · Cited by 74
“This is considered a modest number considering that approximately 30 000 neurons and synapses (assuming 8000 synapse/neuron) may exist in a cubic millimeter of cortex tissue [11].”
BackgroundResultAnalyzing the structure and function of neuronal circuits in zebrafish
Friedrich, R. W., Genoud, C., & Wanner, A. A. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00071 · Cited by 77
“Zebrafish therefore allow for the sampling of neuronal activity across a large fraction of neurons in many brain areas.”
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Bennett, M. R. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.01.001 · Cited by 79
“…and Holz (1975) Total Pyramidal 5613 5613 Rat hippocampus CA1 Pokorny and Yamamoto (1981a,b) Basalar Pyramidal 2621 4886 Rat hippocampus CA1 Braitenberg and Schuz (1998) 0.9 Rat hippocampus CA1 Trommald et al. (1995) Basalar Pyramidal 4524 11900 0.73 Mean SD Human cortex 5200 1544 Mean SD…”
InfluentialAn Energy Budget for the Olfactory Glomerulus
Nawroth, J. C., Greer, C. A., Chen, W. R., Laughlin, S. B., & Shepherd, G. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1415-07.2007 · Cited by 78
“This value is almost 100 times greater than the average cell density in the neocortex (Braitenberg and Schuez, 1998).”
BackgroundInterpreting BOLD: towards a dialogue between cognitive and cellular neuroscience
Hall, C. N., Howarth, C., Kurth-Nelson, Z. L., & Mishra, A. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0348 · Cited by 80
Engines of the brain: The computational instruction set of human cognition
Granger, R. (2006) · Cited by 73
Effects of the anesthetic agent propofol on neural populations
Hutt, A., & Longtin, A. (2009) · Cognitive Neurodynamics · doi:10.1007/s11571-009-9092-2 · Cited by 72
“For example, the dendritic branches around pyramidal cells are very diverse in geometry and spatial spread and are not known in detail for each neuron (Braitenberg and Schütz, 1998; Mell and Schiller, 2004).”
BackgroundMitochondria in Myelinating Oligodendrocytes: Slow and Out of Breath?
Meyer, N., & Rinholm, J. E. (2021) · Metabolites · doi:10.3390/metabo11060359 · Cited by 78
Friedemann Pulvermüller, A., & Garagnani, M. (2014) · Cortex · doi:10.1016/j.cortex.2014.02.015 · Cited by 74
Metadata
- Authors
- Braitenberg, V., & Schüz, A.
- Affiliations
- Max Planck Society (DE)
- Venue
- Springer eBooks
- Publisher
- Springer Berlin Heidelberg
- Published
- 1998
- OpenAlex
- W1603661052
- Cited by
- 1,178
- References
- 0
- Citations by year
- 2026: 14 · 2025: 30 · 2024: 38 · 2023: 62 · 2022: 38 · 2021: 54 · 2020: 34 · 2019: 57 · 2018: 49 · 2017: 44 · 2016: 42 · 2015: 57 · 2014: 53 · 2013: 51 · 2012: 64
- FWCI
- 4.64
- Type
- book
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Springer eBooks (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- cerebral cortex, neuronal connectivity, cortical networks, mouse cortex, cortical geometry, corticocortical connections
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