A synaptic organizing principle for cortical neuronal groups
By Rodrigo Perin, Thomas K. Berger, Henry Markram. 2011
724 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- Wulfram Gerstner
- Henry Markram
- Michael Häusser
- Arnd Roth
- Per Jesper Sjöström
- Sarah Rieubland
- E. Bullmore
- Eörs Szathmáry
In Cognitive Neuroscience
- Wulfram Gerstner
- Henry Markram
- E. Bullmore
- Michael Häusser
- Olaf Sporns
- Arnd Roth
- Jay N. Giedd
- Per Jesper Sjöström
Citations in the corpus
- Predictive Processing: A Canonical Cortical Computation (2018, neutral): “A number of plausible mechanisms have been proposed for the persistence of neural activity, including strong and selective recurrent excitation between coactive neuronal assemblies within the cortex (Cossell et al., 2015; Li et al., 2016; Perin et al., 2011; Song et al., 2005), or via thalamocortica”
- A History of Spike-Timing-Dependent Plasticity (2011, background): “In fact, we also know from paired recordings that synaptic connectivity often clusters, showing higher reciprocal coupling than expected from random uniform distributions (Markram et al., 1997a; Song et al., 2005; Perin et al., 2011).”
- Structured Connectivity in Cerebellar Inhibitory Networks (2014, methodology): “These studies have investigated connectivity between principal cells of the same type (Ko et al., 2011; Perin et al., 2011; Song et al., 2005), where nonrandom features and clustering are present, and between different types of principal cells, where cortical layer specificity governs connectivity…”
- Neuronal circuits underlying persistent representations despite time varying activity. (2012, result): “They occur in the sparse FEVER network nearly five times as often as would be expected by chance (Figure 4B, see the Experimental Procedures), compared with four times in the cortical network data [29, 41, 43, 44].”
- Cliques of Neurons Bound into Cavities Provide a Missing Link between Structure and Function (2016, background): “Sub-sampling networks of neurons experimentally has revealed small motifs of synaptic connectivity, but not large cliques of neurons (Song et al., 2005; Perin et al., 2011).”
- In Vivo Monosynaptic Excitatory Transmission between Layer 2 Cortical Pyramidal Neurons (2015, background): “, 2005), and previous studies have identified non-randompatterns of connectivity betweenpyramidal neurons in some cortical regions (Cossell et al., 2015; Ko et al., 2011; Markram et al., 1997; Perin et al., 2011; Song et al., 2005).”
- Neural Elements for Predictive Coding (2016, background): “There are indications that CC and CS neurons form intermingled local networks and subnets (Song et al., 2005; Perin et al., 2011; Zarrinpar and Callaway, 2016), that may receive selective contacts from separate networks in layer 2/3 (Kampa et al., 2006).”
- Control Principles of Complex Networks (2015, background): “Similarly, neuronal connections (synapses) in our brains can strengthen or weaken, and form in response to changes in brain activity, a phenomenon called synaptic plasticity (Bayati and Valizadeh, 2012; Perin et al., 2011).”
- Synchronization from Second Order Network Connectivity Statistics (2011, result): “Studies have also found that the frequencies of other patterns of connections differ from the independent model prediction (Song et al., 2005; Perin et al., 2011).”
- Reconstruction and Simulation of Neocortical Microcircuitry. (2015, background): “The reconstruction also allows studies of neurons involved in polysynaptic pathways (see NMC Portal) forming known motifs (Honey et al., 2007; Perin et al., 2011; Silberberg, 2008; Sporns and Kötter, 2004).”
- Revealing neuronal function through microelectrode array recordings (2015, neutral): “…bulkiness of current micromanipulators and patch-clamp systems together with the necessity for accurate and precise control have limited simultaneous patch-clamp recordings to a few—maximum of four and twelve for in vivo (Kodandaramaiah et al., 2014) and in vitro (Perin et al., 2011), respectively.”
- Selectionist and Evolutionary Approaches to Brain Function: A Critical Appraisal (2012, background): “However, we note that whether we are referring to the primary repertoire of assemblies, or the secondary repertoire of super assemblies (Perin et al., 2011), there is no replication of these forms at either level in NGS.”
- A Complete Electron Microscopy Volume of the Brain of Adult Drosophila melanogaster (2017, background): “Updated forms of this approach remain important to this day (e.g. Wertz et al., 2015; Wolff et al., 2015), as do electrophysiological measurements of connectivity between small groups of neurons (Ko et al., 2011; Perin et al., 2011; Song et al., 2005).”