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Orthogonal arrangement of rhythm-generating microcircuits in the hippocampus

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.903390204openalex-snapshot

The hippocampal CA3 network: An in vivo intracellular labeling study

inferredcites →https://doi.org/10.1002/hipo.450030307openalex-snapshot

Phase relationship between hippocampal place units and the EEG theta rhythm

inferredcites →https://doi.org/10.1007/bf00234087openalex-snapshot

Lamellar organization of hippocampal excitatory pathways

inferredcites →https://doi.org/10.1016/0013-4694(62)90030-5openalex-snapshot

The significance of the rabbit's septum as a relay station between the midbrain and the hippocampus I. The control of hippocampus arousal activity by the septum cells

inferredcites →https://doi.org/10.1016/0165-0173(83)90037-1openalex-snapshot

Cellular bases of hippocampal EEG in the behaving rat

inferredcites →https://doi.org/10.1016/0306-4522(90)90055-9openalex-snapshot

Coherence of compound field potentials reveals discontinuities in the CA1-subiculum of the hippocampus in freely-moving rats

inferredcites →https://doi.org/10.1016/j.tins.2003.09.016openalex-snapshot

Interneuron Diversity series: Inhibitory interneurons and network oscillations in vitro

inferredcites →https://doi.org/10.1016/s0896-6273(02)00586-xopenalex-snapshot

Theta Oscillations in the Hippocampus

inferredcites →https://doi.org/10.1016/s0896-6273(02)01169-8openalex-snapshot

Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat

inferredcites →https://doi.org/10.1038/28179openalex-snapshot

Cholinergic induction of network oscillations at 40 Hz in the hippocampus in vitro

inferredcites →https://doi.org/10.1038/35049047openalex-snapshot

Interneurons unbound

inferredcites →https://doi.org/10.1038/373612a0openalex-snapshot

Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation

inferredcites →https://doi.org/10.1038/45154openalex-snapshot

Distribution of spatial and nonspatial information in dorsal hippocampus

inferredcites →https://doi.org/10.1038/84032openalex-snapshot

Rapid feature selective neuronal synchronization through correlated latency shifting

inferredcites →https://doi.org/10.1038/nature01374openalex-snapshot

Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo

inferredcites →https://doi.org/10.1038/nature01834openalex-snapshot

Organization of cell assemblies in the hippocampus

inferredcites →https://doi.org/10.1093/oso/9780195104912.001.0001openalex-snapshot

Biophysics of Computation

inferredcites →https://doi.org/10.1097/00000539-200110000-00032openalex-snapshot

Practical Issues in Bispectral Analysis of Electroencephalographic Signals

inferredcites →https://doi.org/10.1113/jphysiol.1952.sp004764openalex-snapshot

A quantitative description of membrane current and its application to conduction and excitation in nerve

inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021397openalex-snapshot

Analysis of gamma rhythms in the rat hippocampus in vitro and in vivo.

inferredcites →https://doi.org/10.1113/jphysiol.2002.024588openalex-snapshot

A Model of Atropine‐Resistant Theta Oscillations in Rat Hippocampal Area CA1

inferredcites →https://doi.org/10.1113/jphysiol.2003.046177openalex-snapshot

Active dendrites and spike propagation in multicompartment models of oriens‐lacunosum/moleculare hippocampal interneurons

inferredcites →https://doi.org/10.1113/jphysiol.2004.071191openalex-snapshot

α5 subunit‐containing GABA A receptors affect the dynamic range of mouse hippocampal kainate‐induced gamma frequency oscillations in vitro

inferredcites →https://doi.org/10.1113/jphysiol.2004.073007openalex-snapshot

Differential involvement of oriens/pyramidale interneurones in hippocampal network oscillations in vitro

inferredcites →https://doi.org/10.1126/science.1099745openalex-snapshot

Neuronal Oscillations in Cortical Networks

inferredcites →https://doi.org/10.1126/science.2218534openalex-snapshot

The Primate Hippocampal Formation: Evidence for a Time-Limited Role in Memory Storage

inferredcites →https://doi.org/10.1137/1.9780898718195openalex-snapshot

Simulating, Analyzing, and Animating Dynamical Systems

inferredcites →https://doi.org/10.1146/annurev.ne.13.030190.001151openalex-snapshot

Postembryonic Neuronal Plasticity And Its Hormonal Control During Insect Metamorphosis

inferredcites →https://doi.org/10.1152/jn.00957.2004openalex-snapshot

Slow and Fast Inhibition and an H-Current Interact to Create a Theta Rhythm in a Model of CA1 Interneuron Network

inferredcites →https://doi.org/10.1152/jn.1988.60.4.1481openalex-snapshot

Spread of synchronous firing in longitudinal slices from the CA3 region of the hippocampus

inferredcites →https://doi.org/10.1162/089892903321107891openalex-snapshot

Book Review

inferredcites →https://doi.org/10.1515/revneuro.2002.13.2.183openalex-snapshot

The Longitudinal Axis of the Hippocampal Formation: Its Anatomy, Circuitry, and Role in Cognitive Function

inferredcites →https://doi.org/10.1523/jneurosci.15-01-00047.1995openalex-snapshot

Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat

inferredcites →https://doi.org/10.1523/jneurosci.15-10-06651.1995openalex-snapshot

Hippocampal CA1 interneurons: an in vivo intracellular labeling study

inferredcites →https://doi.org/10.1523/jneurosci.17-21-08427.1997openalex-snapshot

Synaptic Communication among Hippocampal Interneurons: Properties of Spontaneous IPSCs in Morphologically Identified Cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Human cerebrospinal fluid promotes spontaneous gamma oscillations in the hippocampus in vitro

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Theta and alpha oscillations in human hippocampus and medial parietal cortex support the formation of location‐based representations

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Individual NMDA receptor GluN2 subunit signaling domains differentially regulate the postnatal maturation of hippocampal excitatory synaptic transmission and plasticity but not dendritic morphology

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Gamma and Theta Rhythms in Biophysical Models of Hippocampal Circuits

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Morphology of Hippocampal Neurons

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Neuronal Activity Patterns During Hippocampal Network Oscillations In Vitro

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Hippocampal Theta, Gamma, and Theta/Gamma Network Models

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Hippocampal Theta, Gamma, and Theta/Gamma Network Models

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Hippocampus, Model Inhibitory Cells

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Theta, Gamma, and Cross-Frequency Coupling in the Hippocampus

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Hippocampus, Theta, Gamma, and Cross-Frequency Coupling

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Discrete Modeling for a Minimal Circuit in the Hippocampus

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Morphology of Hippocampal Neurons

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Modelling Epileptic Activity in Hippocampal CA3

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Cell Type-Specific Activity During Hippocampal Network Oscillations In Vitro

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The GABAA receptor-mediated recurrent inhibition in ventral compared with dorsal CA1 hippocampal region is weaker, decays faster and lasts less

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Phase resetting reduces theta–gamma rhythmic interaction to a one-dimensional map

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The voltage and spiking responses of subthreshold resonant neurons to structured and fluctuating inputs: persistence and loss of resonance and variability

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The ventral hippocampus is necessary for expressing a spatial memory

inferred← citeshttps://doi.org/10.1007/s10827-012-0426-4openalex-snapshot

Modulation of hippocampal rhythms by subthreshold electric fields and network topology

inferred← citeshttps://doi.org/10.1007/s10827-016-0632-6openalex-snapshot

The shaping of intrinsic membrane potential oscillations: positive/negative feedback, ionic resonance/amplification, nonlinearities and time scales

inferred← citeshttps://doi.org/10.1016/b978-0-12-819410-2.00012-6openalex-snapshot

General principles of brain electromagnetic rhythmic oscillations and implications for neuroplasticity

inferred← citeshttps://doi.org/10.1016/j.biosystems.2006.02.017openalex-snapshot

Oscillations and waves in the models of interactive neural populations

inferred← citeshttps://doi.org/10.1016/j.brainres.2008.07.030openalex-snapshot

Cross-frequency phase coupling of brain rhythms during the orienting response

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Effects of XE991, retigabine, losigamone and ZD7288 on kainate-induced theta-like and gamma network oscillations in the rat hippocampus in vitro

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Hippocampal neurodegeneration and rhythms mirror each other during acute spinal cord injury in male rats

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Hippocampal Interneuronal α7 nAChRs Modulate Theta Oscillations in Freely Moving Mice

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Human NMDAR autoantibodies disrupt excitatory-inhibitory balance, leading to hippocampal network hypersynchrony

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Increase of theta/gamma ratio is associated with memory impairment

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The hippocampal learning-behavior translation and the functional significance of hippocampal dysfunction in schizophrenia

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Volume-transmitted GABA waves pace epileptiform rhythms in the hippocampal network

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Spike timing-dependent plasticity is affected by the interplay of intrinsic and network oscillations

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Increased inhibitory input to CA1 pyramidal cells alters hippocampal gamma frequency oscillations in the MK-801 model of acute psychosis

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Functional role of gamma and theta oscillations in episodic memory

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Switching between gamma and theta: Dynamic network control using subthreshold electric fields

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Two forms of feedback inhibition determine the dynamical state of a small hippocampal network

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Directional spike propagation in a recurrent network: Dynamical firewall as anisotropic recurrent inhibition

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Modulation of spike and burst rate in a minimal neuronal circuit with feed-forward inhibition

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Synchronized Activity between the Ventral Hippocampus and the Medial Prefrontal Cortex during Anxiety

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The Theta-Gamma Neural Code

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Beyond the Connectome: The Dynome

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Parvalbumin Interneurons of Hippocampus Tune Population Activity at Theta Frequency

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Gamma Oscillation Dysfunction in mPFC Leads to Social Deficits in Neuroligin 3 R451C Knockin Mice

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C-type natriuretic peptide decreases hippocampal network oscillations in adult rats in vitro

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Nicotine induction of theta frequency oscillations in rodent hippocampus in vitro

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No evidence for role of extracellular choline-acetyltransferase in generation of gamma oscillations in rat hippocampal slices in vitro

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Cell Type-specific Intrinsic Perithreshold Oscillations in Hippocampal GABAergic Interneurons

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Statistical mechanics of the neocortex

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The alpha2 nicotinic acetylcholine receptor, a subunit with unique and selective expression in inhibitory interneurons associated with principal cells

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The Continuity of Context: A Role for the Hippocampus

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Neural Cross-Frequency Coupling: Connecting Architectures, Mechanisms, and Functions

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Deconstructing Circadian Rhythmicity with Models and Manipulations

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Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I

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OLM interneurons differentially modulate CA3 and entorhinal inputs to hippocampal CA1 neurons

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Hippocampal theta rhythms follow the beat of their own drum

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Long-Lasting Increase of Corticosterone After Fear Memory Reactivation: Anxiolytic Effects and Network Activity Modulation in the Ventral Hippocampus

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Distance-dependent inhibition facilitates focality of gamma oscillations in the dentate gyrus

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Hypomyelination in autism-associated neuroligin-3 mutant mice impairs parvalbumin interneuron excitability, gamma oscillations, and sensory discrimination

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Brain slice on a chip: opportunities and challenges of applying microfluidic technology to intact tissues

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On the formation of gamma-coherent cell assemblies by oriens lacunosum-moleculare interneurons in the hippocampus

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Impaired hippocampal rhythmogenesis in a mouse model of mesial temporal lobe epilepsy

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Hippocampal theta rhythm and its coupling with gamma oscillations require fast inhibition onto parvalbumin-positive interneurons

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GABA B autoreceptor-mediated cell type-specific reduction of inhibition in epileptic mice

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Coexisting fast–slow dendritic traveling waves in a 3D-array electric field coupled neuronal network

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Cortical Oscillations in Health and Disease

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inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.002.0005openalex-snapshot

Epigraphs

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.002.0006openalex-snapshot

Preface

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.002.0009openalex-snapshot

Glossary of abbreviations

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0001openalex-snapshot

Introduction

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0002openalex-snapshot

Historical Prelude

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0003openalex-snapshot

Overview of In Vivo Cortical Oscillations

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Epilepsy

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Parkinson’s Disease

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Schizophrenia

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0007openalex-snapshot

Cerebellar Ataxia

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Cortical Neurons and Their Models

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0009openalex-snapshot

Gap Junctions and the Notion of Electrical Coupling Between Axons

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0010openalex-snapshot

Very Fast Oscillations

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0011openalex-snapshot

Beta-2 Oscillations

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0012openalex-snapshot

Persistent Gamma Oscillations

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0013openalex-snapshot

Epileptiform Discharges In Vitro

inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195342796.003.0014openalex-snapshot

Conclusion

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Ordering Information in Working Memory and Modulation of Gamma by Theta Oscillations in Humans

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Phase Gradients and Anisotropy of the Suprachiasmatic Network

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Theta and alpha oscillations in human hippocampus and medial parietal cortex support the formation of location-based representations

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Theta-Gamma Phase-Amplitude Coupling Supports Working Memory Performance in the Human Hippocampus

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δ-containing GABA A receptors on parvalbumin interneurons modulate neuronal excitability and network dynamics in the mouse medial prefrontal cortex

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The Role of Feedforward and Feedback Inhibition in Modulating Theta-Gamma Cross-Frequency Interactions

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Lag synchrony measures dynamical processes underlying progression of seizure states

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Modeling rhythmic patterns in the hippocampus

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Kalman filter tracking of intracellular neuronal voltage and current

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Classifying cross-frequency coupling pattern in epileptogenic tissues by convolutional neural network

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Shaping spiking patterns through synaptic parameters revealed by wavelet bifurcation analysis

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On the Biological Plausibility of Orthogonal Initialisation for Solving Gradient Instability in Deep Neural Networks

inferred← citeshttps://doi.org/10.1109/ner.2013.6696053openalex-snapshot

Propagation of epileptiform activity in the hippocampus can be driven by non-synaptic mechanisms

inferred← citeshttps://doi.org/10.1111/ejn.12739openalex-snapshot

Beta2 oscillations (23–30 Hz) in the mouse hippocampus during novel object recognition

inferred← citeshttps://doi.org/10.1111/epi.16903openalex-snapshot

Neural recruitment by ephaptic coupling in epilepsy

inferred← citeshttps://doi.org/10.1111/j.1460-9568.2007.05462.xopenalex-snapshot

Effects of the GABAA receptor antagonists bicuculline and gabazine on stimulus‐induced sharp wave‐ripple complexes in adult rat hippocampus in vitro

inferred← citeshttps://doi.org/10.1111/j.1460-9568.2009.06771.xopenalex-snapshot

Comparison between spontaneous and kainate‐induced gamma oscillations in the mouse hippocampus in vitro

inferred← citeshttps://doi.org/10.1111/j.1460-9568.2011.07682.xopenalex-snapshot

Characterization of orderly spatiotemporal patterns of clock gene activation in mammalian suprachiasmatic nucleus

inferred← citeshttps://doi.org/10.1111/j.1460-9568.2012.08132.xopenalex-snapshot

The role of inhibition in oscillatory wave dynamics in the cortex

inferred← citeshttps://doi.org/10.1111/j.1528-1167.2007.01300.xopenalex-snapshot

Cholinergic Dysfunction in Temporal Lobe Epilepsy

inferred← citeshttps://doi.org/10.1111/j.1528-1167.2011.03125.xopenalex-snapshot

Orthogonal wave propagation of epileptiform activity in the planar mouse hippocampus in vitro

inferred← citeshttps://doi.org/10.1126/sciadv.adj7427openalex-snapshot

Gamma oscillation plasticity is mediated via parvalbumin interneurons

inferred← citeshttps://doi.org/10.1140/epjs/s11734-023-00781-0openalex-snapshot

Shaping spiking patterns through synaptic parameters as revealed by conventional and wavelet-based bifurcation analysis

inferred← citeshttps://doi.org/10.1152/jn.00026.2017openalex-snapshot

Disharmony in neural oscillations

inferred← citeshttps://doi.org/10.1152/jn.00160.2023openalex-snapshot

Simulations predict differing phase responses to excitation vs. inhibition in theta-resonant pyramidal neurons

inferred← citeshttps://doi.org/10.1152/jn.00495.2024openalex-snapshot

δ-Containing GABA A receptors on parvalbumin interneurons modulate neuronal excitability and network dynamics in the mouse medial prefrontal cortex

inferred← citeshttps://doi.org/10.1152/jn.00636.2018openalex-snapshot

Theta-gamma cascades and running speed

inferred← citeshttps://doi.org/10.1152/jn.00957.2004openalex-snapshot

Slow and Fast Inhibition and an H-Current Interact to Create a Theta Rhythm in a Model of CA1 Interneuron Network

inferred← citeshttps://doi.org/10.1152/jn.01105.2006openalex-snapshot

Beta Rhythms (15–20 Hz) Generated by Nonreciprocal Communication in Hippocampus

inferred← citeshttps://doi.org/10.1152/jn.01306.2006openalex-snapshot

Local Generation of Theta-Frequency EEG Activity in the Parasubiculum

inferred← citeshttps://doi.org/10.1152/jn.90846.2008openalex-snapshot

Theta and Gamma Coherence Along the Septotemporal Axis of the Hippocampus

inferred← citeshttps://doi.org/10.11575/prism/2082openalex-snapshot

Synaptic regulation of intrinsic dynamics in ell pyramidal cells

inferred← citeshttps://doi.org/10.1162/neco_a_00458openalex-snapshot

The Role of Extracellular Conductivity Profiles in Compartmental Models for Neurons: Particulars for Layer 5 Pyramidal Cells

inferred← citeshttps://doi.org/10.1162/neco_a_01369openalex-snapshot

Flexible Frequency Switching in Adult Mouse Visual Cortex Is Mediated by Competition Between Parvalbumin and Somatostatin Expressing Interneurons

inferred← citeshttps://doi.org/10.1172/jci71472openalex-snapshot

Changes in neural network homeostasis trigger neuropsychiatric symptoms

inferred← citeshttps://doi.org/10.1186/1471-2202-11-96openalex-snapshot

Imbalanced pattern completion vs. separation in cognitive disease: network simulations of synaptic pathologies predict a personalized therapeutics strategy

inferred← citeshttps://doi.org/10.1186/1471-2202-15-s1-p42openalex-snapshot

Network models provide insight into how oriens-lacunosum-moleculare (OLM) and bistratified cell (BSC) interactions influence local CA1 theta rhythms

inferred← citeshttps://doi.org/10.1186/1471-2202-9-s1-p8openalex-snapshot

Electric field modulation of theta and gamma rhythms: probe into network connectivity

inferred← citeshttps://doi.org/10.1186/s12868-017-0372-1openalex-snapshot

A single pyramidal-cell and network computational model of the hippocampal CA3 region

inferred← citeshttps://doi.org/10.1186/s12868-017-0398-4openalex-snapshot

A gradient of frequency-dependent synaptic properties along the longitudinal hippocampal axis

inferred← citeshttps://doi.org/10.1203/pdr.0b013e31815586a1openalex-snapshot

Frequency Domain Analyses of Neonatal Flash VEP

inferred← citeshttps://doi.org/10.1371/journal.pbio.1000089openalex-snapshot

From Rapid Place Learning to Behavioral Performance: A Key Role for the Intermediate Hippocampus

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1000169openalex-snapshot

Rhythm Generation through Period Concatenation in Rat Somatosensory Cortex

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004880openalex-snapshot

Hippocampal CA1 Ripples as Inhibitory Transients

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1005467openalex-snapshot

ARACHNE: A neural-neuroglial network builder with remotely controlled parallel computing

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1009235openalex-snapshot

Theta-gamma coupling emerges from spatially heterogeneous cholinergic neuromodulation

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1010942openalex-snapshot

Theta-gamma phase amplitude coupling in a hippocampal CA1 microcircuit

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1013363openalex-snapshot

The role of feedforward and feedback inhibition in modulating theta-gamma cross-frequency interactions in neural circuits

inferred← citeshttps://doi.org/10.1371/journal.pone.0046652openalex-snapshot

Ion Channel Gradients in the Apical Tuft Region of CA1 Pyramidal Neurons

inferred← citeshttps://doi.org/10.1371/journal.pone.0074910openalex-snapshot

Synconset Waves and Chains: Spiking Onsets in Synchronous Populations Predict and Are Predicted by Network Structure

inferred← citeshttps://doi.org/10.1371/journal.pone.0121676openalex-snapshot

Electrographic Waveform Structure Predicts Laminar Focus Location in a Model of Temporal Lobe Seizures In Vitro

inferred← citeshttps://doi.org/10.1371/journal.pone.0123636openalex-snapshot

Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities

inferred← citeshttps://doi.org/10.1371/journal.pone.0182648openalex-snapshot

An integrative model of the intrinsic hippocampal theta rhythm

inferred← citeshttps://doi.org/10.1371/journal.pone.0206237openalex-snapshot

Integrated information in the EEG of preterm infants increases with family nurture intervention, age, and conscious state

inferred← citeshttps://doi.org/10.14232/phd.10280openalex-snapshot

The impact of stimulus modality on the EEG-correlates of associative learning and the connected memory processes

inferred← citeshttps://doi.org/10.14336/ad.2022.0906openalex-snapshot

Toward the Identification of Neurophysiological Biomarkers for Alzheimer’s Disease in Down Syndrome: A Potential Role for Cross-Frequency Phase-Amplitude Coupling Analysis

inferred← citeshttps://doi.org/10.1515/revneuro.2007.18.3-4.253openalex-snapshot

Toward an Integrative Perspective on Hippocampal Function: From the Rapid Encoding of Experience to Adaptive Behavior

inferred← citeshttps://doi.org/10.1523/eneuro.0078-21.2021openalex-snapshot

Phase Gradients and Anisotropy of the Suprachiasmatic Network: Discovery of Phaseoids

inferred← citeshttps://doi.org/10.1523/eneuro.0142-19.2019openalex-snapshot

Methodological Considerations on the Use of Different Spectral Decomposition Algorithms to Study Hippocampal Rhythms

inferred← citeshttps://doi.org/10.1523/eneuro.0308-24.2024openalex-snapshot

GABA-Induced Seizure-Like Events Caused by Multi-ionic Interactive Dynamics

inferred← citeshttps://doi.org/10.1523/hon.009007openalex-snapshot

Nancy Kopell

inferred← citeshttps://doi.org/10.1523/jneurosci.1193-20.2020openalex-snapshot

Comprehensive Estimates of Potential Synaptic Connections in Local Circuits of the Rodent Hippocampal Formation by Axonal-Dendritic Overlap

inferred← citeshttps://doi.org/10.1523/jneurosci.1361-11.2012openalex-snapshot

Spike Resonance Properties in Hippocampal O-LM Cells Are Dependent on Refractory Dynamics

inferred← citeshttps://doi.org/10.1523/jneurosci.1370-11.2011openalex-snapshot

Fast and Slow Gamma Rhythms Are Intrinsically and Independently Generated in the Subiculum

inferred← citeshttps://doi.org/10.1523/jneurosci.1580-06.2006openalex-snapshot

Synaptic Currents in Anatomically Identified CA3 Neurons during Hippocampal Gamma Oscillations In Vitro

inferred← citeshttps://doi.org/10.1523/jneurosci.3005-07.2007openalex-snapshot

The Source of Afterdischarge Activity in Neocortical Tonic–Clonic Epilepsy

inferred← citeshttps://doi.org/10.1523/jneurosci.3573-11.2011openalex-snapshot

Terminal Field and Firing Selectivity of Cholecystokinin-Expressing Interneurons in the Hippocampal CA3 Area

inferred← citeshttps://doi.org/10.1523/jneurosci.3575-07.2007openalex-snapshot

Neurotech for Neuroscience: Unifying Concepts, Organizing Principles, and Emerging Tools

inferred← citeshttps://doi.org/10.1523/jneurosci.3693-08.2008openalex-snapshot

Neural-Activity-Dependent Release of S100B from Astrocytes Enhances Kainate-Induced Gamma OscillationsIn Vivo

inferred← citeshttps://doi.org/10.1523/jneurosci.3757-16.2017openalex-snapshot

Strength and Diversity of Inhibitory Signaling Differentiates Primate Anterior Cingulate from Lateral Prefrontal Cortex

inferred← citeshttps://doi.org/10.1523/jneurosci.3877-13.2014openalex-snapshot

Propagation of Epileptiform Activity Can Be Independent of Synaptic Transmission, Gap Junctions, or Diffusion and Is Consistent with Electrical Field Transmission

inferred← citeshttps://doi.org/10.1523/jneurosci.4122-11.2012openalex-snapshot

Cross-Frequency Phase–Phase Coupling between Theta and Gamma Oscillations in the Hippocampus

inferred← citeshttps://doi.org/10.17169/refubium-16824openalex-snapshot

Post-transcriptional modification of gephyrin and glycine receptor messenger RNA in temporal lobe epilepsy

inferred← citeshttps://doi.org/10.17169/refubium-5264openalex-snapshot

Disease-related posttranscriptional modifications of glycine receptor mRNA under physiological and pathophysiological conditions

inferred← citeshttps://doi.org/10.31234/osf.io/ushkaopenalex-snapshot

The Continuity of Context: A Role for the Hippocampus

inferred← citeshttps://doi.org/10.3233/jad-2008-14303openalex-snapshot

Cerebrovascular Disease and Hippocampal Atrophy Are Differently Linked to Functional Coupling of Brain Areas: An EEG Coherence Study in MCI Subjects

inferred← citeshttps://doi.org/10.32469/10355/88874openalex-snapshot

Biophysical modeling to reverse engineer two mammalian neural circuits lower urinar Y tract and hippocampus

inferred← citeshttps://doi.org/10.3389/fncel.2013.00117openalex-snapshot

Amyloid-β induces synaptic dysfunction through G protein-gated inwardly rectifying potassium channels in the fimbria-CA3 hippocampal synapse

inferred← citeshttps://doi.org/10.3389/fncel.2020.00277openalex-snapshot

Integration of Within-Cell Experimental Data With Multi-Compartmental Modeling Predicts H-Channel Densities and Distributions in Hippocampal OLM Cells

inferred← citeshttps://doi.org/10.3389/fncel.2020.554405openalex-snapshot

Alterations in Intrinsic and Synaptic Properties of Hippocampal CA1 VIP Interneurons During Aging

inferred← citeshttps://doi.org/10.3389/fncir.2012.00102openalex-snapshot

Updating the Lamellar Hypothesis of Hippocampal Organization

inferred← citeshttps://doi.org/10.3389/fncir.2021.643360openalex-snapshot

A Hypothesis for Theta Rhythm Frequency Control in CA1 Microcircuits

inferred← citeshttps://doi.org/10.3389/fncom.2011.00024openalex-snapshot

Robust Transient Dynamics and Brain Functions

inferred← citeshttps://doi.org/10.3389/fncom.2017.00061openalex-snapshot

Transition Dynamics of a Dentate Gyrus-CA3 Neuronal Network during Temporal Lobe Epilepsy

inferred← citeshttps://doi.org/10.3389/fncom.2021.630271openalex-snapshot

Effects of Several Classes of Voltage-Gated Ion Channel Conductances on Gamma and Theta Oscillations in a Hippocampal Microcircuit Model

inferred← citeshttps://doi.org/10.3389/fnhum.2010.00187openalex-snapshot

Are Different Rhythms Good for Different Functions?

inferred← citeshttps://doi.org/10.3389/fnhum.2010.00198openalex-snapshot

Computational Modeling of Distinct Neocortical Oscillations Driven by Cell-Type Selective Optogenetic Drive: Separable Resonant Circuits Controlled by Low-Threshold Spiking and Fast-Spiking Interneurons

inferred← citeshttps://doi.org/10.3389/fnhum.2019.00023openalex-snapshot

Direct Stimulation of Human Hippocampus During Verbal Associative Encoding Enhances Subsequent Memory Recollection

inferred← citeshttps://doi.org/10.3389/fninf.2011.00011openalex-snapshot

GenNet: A Platform for Hybrid Network Experiments

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