Modelling and analysis of local field potentials for studying the function of cortical circuits

By Gaute T. Einevoll, Christoph Kayser, Nikos K. Logothetis, Stefano Panzeri. Nature Reviews Neuroscience, 2013

802 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience, Electrical and Electronic Engineering

View Paper: https://www.semanticscholar.org/paper/4be8cc4e9e9ea7c7879b6d4fd7f0207dbb582966

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In Cellular and Molecular Neuroscience

In Cognitive Neuroscience

In Electrical and Electronic Engineering

Citations in the corpus

Revealing neuronal function through microelectrode array recordings (2015, neutral): “We refer the reader to Einevoll et al.’s extensive review on the modeling and analysis of LFPs for further details (Einevoll et al., 2013).”
Identifying and Quantifying Multisensory Integration: A Tutorial Review (2014, background): “…across the cell membrane, which is measured as sources and sinks and helps to index subthreshold synaptic processing in a layer specific manner in various cortical areas and also has much less spatial spread than LFP signals (Kajikawa and Schroeder 2011; Lakatos et al. 2007; Einevoll et al. 2013).”
Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models (2015, methodology): “Note that this spatial scale is similar to the size of the neuronal pool contributing to the recorded LFP, the so-called spatial reach, in the case of uncorrelated synaptic activity driving a neuronal population [20,21,35], and resulted in a neuronal density consistent with known estimates of 50000 ”
Distinct laminar origins of sensory-evoked high-gamma and low-frequency ECoG signals revealed by optogenetics (2026, unknown): “How different layers and cell types contribute to CSEP magnitude and frequency depends on biophysical factors for each cell type including distance to the surface electrode, number of cells of a given type, size, and alignment of each cell’s electrical dipole, and population synchrony (2, 22–24).”
Neural representations of visual memory in inferotemporal cortex reveal a generalizable framework for translating between spikes and field potentials (2026, unknown): “While the LFP has historically been viewed as reflecting summed synapto-dendritic activity [10–12], several studies have established that the amplitude of high-frequency activity of the LFP, high-gamma activity (HGA; 50-150Hz), correlates with the activity of single neurons and local neuronal…”
Distinct laminar origins of high-gamma and low-frequency ECoG signals revealed by optogenetics (2025, unknown): “How different layers and cell types contribute to CSEP magnitude and frequency depends on biophysical factors for each cell type including distance to the surface electrode, number of cells of a given type, size and alignment of each cell's electrical dipole, and population synchrony 2,22–24 .”
Frequency Coding of Multisensory Integration in the Local Field Potentials of the Medial Pulvinar (2024, unknown): “The single-unit neuronal data is already reported in Vittek et al. (2023).”
Intracranial neural representation of phenomenal and access consciousness in the human brain (2024, background): “The biological characteristics of LFP polarity are not yet clearly understood (Einevoll et al., 2013).”
The involvement of the human prefrontal cortex in the emergence of visual awareness (2023, background): “Since it is not clearly understood so far regarding the biological characteristics of LFP polarity ( Einevoll et al., 2013 ), to simplify such complex issue, we consider the change in magnitude of LFP during delay period in our task is awareness related activity, regardless its actual value being…”