On the public citation graph

The corticothalamic system in sleep

0 signed · 575 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/cne.903440203openalex-snapshot

Pedunculopontine nucleus in the squirrel monkey: Distribution of cholinergic and monoaminergic neurons in the mesopontine tegmentum with evidence for the presence of glutamate in cholinergic neurons

inferredcites →https://doi.org/10.1007/978-1-4615-6622-9openalex-snapshot

Normal and Altered States of Function

inferredcites →https://doi.org/10.1007/978-1-4757-4669-3openalex-snapshot

Brainstem Control of Wakefulness and Sleep

inferredcites →https://doi.org/10.1007/978-3-642-91118-7_33openalex-snapshot

„Innere Hemmung“der bedingten Reflexe und der Schlaf — ein und derselbe Prozess

inferredcites →https://doi.org/10.1007/bf00238096openalex-snapshot

Firing rates and patterns of midbrain reticular neurons during steady and transitional states of the sleep-waking cycle

inferredcites →https://doi.org/10.1016/0006-8993(83)91264-7openalex-snapshot

Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat

inferredcites →https://doi.org/10.1016/0006-8993(92)90522-bopenalex-snapshot

Cerebral glucose utilization during stage 2 sleep in man

inferredcites →https://doi.org/10.1016/0006-8993(92)91559-wopenalex-snapshot

The time course of σ activity and slow-wave activity during NREMS in cortical and thalamic EEG of the cat during baseline and after 12 hours of wakefulness

inferredcites →https://doi.org/10.1016/0013-4694(53)90072-8openalex-snapshot

Atlas of electroencephalography

inferredcites →https://doi.org/10.1016/0301-0082(92)90012-4openalex-snapshot

Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity

inferredcites →https://doi.org/10.1016/0304-3940(90)90497-wopenalex-snapshot

Pacemaker-like and other types of spontaneous membrane potential oscillations of thalamocortical cells

inferredcites →https://doi.org/10.1016/0306-4522(88)90006-1openalex-snapshot

Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey

inferredcites →https://doi.org/10.1016/0306-4522(91)90374-wopenalex-snapshot

Thalamic oscillations and signaling

inferredcites →https://doi.org/10.1016/0306-4522(92)90464-dopenalex-snapshot

Voltage-dependent fast (20–40 Hz) oscillations in long-axoned neocortical neurons

inferredcites →https://doi.org/10.1016/0306-4522(93)90474-topenalex-snapshot

Spindle rhythmicity in the reticularis thalami nucleus: Synchronization among mutually inhibitory neurons

inferredcites →https://doi.org/10.1016/0306-4522(95)00523-4openalex-snapshot

Differential effects of α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid and N-methyl-d-aspartate receptor antagonists applied to the basal forebrain on cortical acetylcholine release and electroencephalogram desynchronization

inferredcites →https://doi.org/10.1016/0361-9230(91)90286-sopenalex-snapshot

Sigma (12–15 Hz) and Delta (0.3–3 Hz) EEG oscillate reciprocally within NREM sleep

inferredcites →https://doi.org/10.1016/b0-72-160797-7/50018-5openalex-snapshot

Basic Mechanisms of Sleep-Wake States

inferredcites →https://doi.org/10.1016/s0013-4694(98)00051-0openalex-snapshot

Electrophysiological correlates of sleep delta waves

inferredcites →https://doi.org/10.1016/s0306-4522(00)00353-5openalex-snapshot

Corticothalamic resonance, states of vigilance and mentation

inferredcites →https://doi.org/10.1016/s0306-4522(97)00167-xopenalex-snapshot

Modulation of cholinergic nucleus basalis neurons by acetylcholine and N-methyl-d-aspartate

inferredcites →https://doi.org/10.1016/s0896-6273(00)80161-0openalex-snapshot

What Stops Synchronized Thalamocortical Oscillations?

inferredcites →https://doi.org/10.1016/s0896-6273(00)80994-0openalex-snapshot

Periodicity of Thalamic Synchronized Oscillations: the Role of Ca2+-Mediated Upregulation of Ih

inferredcites →https://doi.org/10.1016/s1472-9288(01)00004-8openalex-snapshot

Contribution of intrinsic and synaptic factors in the desynchronization of thalamic oscillatory activity

inferredcites →https://doi.org/10.1038/79848openalex-snapshot

Cellular and network mechanisms of rhythmic recurrent activity in neocortex

inferredcites →https://doi.org/10.1038/81756openalex-snapshot

Visual discrimination learning requires sleep after training

inferredcites →https://doi.org/10.1038/81881openalex-snapshot

Early sleep triggers memory for early visual discrimination skills

inferredcites →https://doi.org/10.1046/j.1365-2869.1997.00033.xopenalex-snapshot

Event‐related potentials to tones in the absence and presence of sleep spindles

inferredcites →https://doi.org/10.1053/smrv.2001.0181openalex-snapshot

The functional significance of K-complexes

inferredcites →https://doi.org/10.1073/pnas.041430398openalex-snapshot

Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: An intracellular study

inferredcites →https://doi.org/10.1073/pnas.061013698openalex-snapshot

Differences in quantal amplitude reflect GluR4- subunit number at corticothalamic synapses on two populations of thalamic neurons

inferredcites →https://doi.org/10.1073/pnas.47.4.427openalex-snapshot

CHAIRMAN'S OPENING REMARKS

inferredcites →https://doi.org/10.1073/pnas.79.19.6102openalex-snapshot

Sleep-promoting effects of muramyl peptides.

inferredcites →https://doi.org/10.1073/pnas.80.10.3121openalex-snapshot

Sleep-promoting effects of muramyl peptides

inferredcites →https://doi.org/10.1073/pnas.88.10.4396openalex-snapshot

Fast oscillations (20-40 Hz) in thalamocortical systems and their potentiation by mesopontine cholinergic nuclei in the cat.

inferredcites →https://doi.org/10.1073/pnas.88.3.897openalex-snapshot

In vitro neurons in mammalian cortical layer 4 exhibit intrinsic oscillatory activity in the 10- to 50-Hz frequency range.

inferredcites →https://doi.org/10.1073/pnas.98.4.1924openalex-snapshot

Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: An intracellular study

inferredcites →https://doi.org/10.1093/cercor/11.4.360openalex-snapshot

Relationship between EEG Potentials and Intracellular Activity of Striatal and Cortico-striatal Neurons: an In Vivo Study under Different Anesthetics

inferredcites →https://doi.org/10.1093/oso/9780198542667.003.0001openalex-snapshot

Parallel activation of thalamic and cortical neurons by brainstem and basal forebrain cholinergic systems

inferredcites →https://doi.org/10.1093/sleep/27.2.344openalex-snapshot

Neuronal Substrates of Sleep and Epilepsy

inferredcites →https://doi.org/10.1097/00001756-199411000-00003openalex-snapshot

Modeling the control of reticular thalamic oscillations by neuromodulators

inferredcites →https://doi.org/10.1097/00013414-200206000-00011openalex-snapshot

The Intact and Sliced Brain.

inferredcites →https://doi.org/10.1111/j.1748-1716.1923.tb00808.xopenalex-snapshot

„Innere Hemmung” der bedingten Reflexe und der Schlaf—ein und derselbe Prozeß1

inferredcites →https://doi.org/10.1113/jphysiol.1990.sp018331openalex-snapshot

Properties of a hyperpolarization‐activated cation current and its role in rhythmic oscillation in thalamic relay neurones.

inferredcites →https://doi.org/10.1113/jphysiol.1991.sp018744openalex-snapshot

Low‐frequency oscillatory activities intrinsic to rat and cat thalamocortical cells.

inferredcites →https://doi.org/10.1113/jphysiol.1992.sp018999openalex-snapshot

Electrophysiology of a slow (0.5‐4 Hz) intrinsic oscillation of cat thalamocortical neurones in vivo.

inferredcites →https://doi.org/10.1113/jphysiol.1995.sp020611openalex-snapshot

Subthreshold oscillations and resonant frequency in guinea‐pig cortical neurons: physiology and modelling.

inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021488openalex-snapshot

Mechanisms of long‐lasting hyperpolarizations underlying slow sleep oscillations in cat corticothalamic networks.

inferredcites →https://doi.org/10.1126/science.274.5288.771openalex-snapshot

Control of Spatiotemporal Coherence of a Thalamic Oscillation by Corticothalamic Feedback

inferredcites →https://doi.org/10.1126/science.8392750openalex-snapshot

Cellular Mechanisms of a Synchronized Oscillation in the Thalamus

inferredcites →https://doi.org/10.1152/ajplegacy.1943.138.2.297openalex-snapshot

MECHANISM OF THALAMOCORTICAL AUGMENTATION AND REPETITION

inferredcites →https://doi.org/10.1152/jn.0871.2002openalex-snapshot

Electrophysiological Properties and Input-Output Organization of Callosal Neurons in Cat Association Cortex

inferredcites →https://doi.org/10.1152/jn.1969.32.2.251openalex-snapshot

Responsiveness of thalamic and cortical motor relays during arousal and various stages of sleep.

inferredcites →https://doi.org/10.1152/jn.1974.37.5.1065openalex-snapshot

Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. I. Background firing and responsiveness of pyramidal tract neurons and interneurons.

inferredcites →https://doi.org/10.1152/jn.1985.54.6.1473openalex-snapshot

Abolition of spindle oscillations in thalamic neurons disconnected from nucleus reticularis thalami

inferredcites →https://doi.org/10.1152/jn.1988.59.2.424openalex-snapshot

Multiple potassium conductances and their functions in neurons from cat sensorimotor cortex in vitro

inferredcites →https://doi.org/10.1152/jn.1988.59.2.450openalex-snapshot

Slow conductances in neurons from cat sensorimotor cortex in vitro and their role in slow excitability changes

inferredcites →https://doi.org/10.1152/jn.1991.65.3.393openalex-snapshot

Short-lasting nicotinic and long-lasting muscarinic depolarizing responses of thalamocortical neurons to stimulation of mesopontine cholinergic nuclei

inferredcites →https://doi.org/10.1152/jn.1994.72.2.803openalex-snapshot

A model of spindle rhythmicity in the isolated thalamic reticular nucleus

inferredcites →https://doi.org/10.1152/jn.1994.72.3.1109openalex-snapshot

Synchronization properties of spindle oscillations in a thalamic reticular nucleus model

inferredcites →https://doi.org/10.1152/jn.1994.72.5.1-aopenalex-snapshot

Synchronization properties of spindle oscillations in a thalamic reticular nucleus model

inferredcites →https://doi.org/10.1152/jn.1995.74.3.1301openalex-snapshot

Spindle waves are propagating synchronized oscillations in the ferret LGNd in vitro

inferredcites →https://doi.org/10.1152/jn.1996.76.6.4152openalex-snapshot

Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats

inferredcites →https://doi.org/10.1152/jn.1998.79.1.483openalex-snapshot

Dynamic Properties of Corticothalamic Neurons and Local Cortical Interneurons Generating Fast Rhythmic (30–40 Hz) Spike Bursts

inferredcites →https://doi.org/10.1152/jn.1998.79.5.2716openalex-snapshot

Cellular Mechanisms Underlying Intrathalamic Augmenting Responses of Reticular and Relay Neurons

inferredcites →https://doi.org/10.1152/jn.1998.79.5.2730openalex-snapshot

Cellular and Network Models for Intrathalamic Augmenting Responses During 10-Hz Stimulation

inferredcites →https://doi.org/10.1152/jn.2001.85.3.1346openalex-snapshot

Extracellular Calcium Fluctuations and Intracellular Potentials in the Cortex During the Slow Sleep Oscillation

inferredcites →https://doi.org/10.1152/jn.2001.85.5.1969openalex-snapshot

Natural Waking and Sleep States: A View From Inside Neocortical Neurons

inferredcites →https://doi.org/10.1152/jn.2001.86.1.1openalex-snapshot

Impact of Network Activities on Neuronal Properties in Corticothalamic Systems

inferredcites →https://doi.org/10.1152/jn.2001.86.4.1884openalex-snapshot

Focal Synchronization of Ripples (80–200 Hz) in Neocortex and Their Neuronal Correlates

inferredcites →https://doi.org/10.1152/physrev.1989.69.2.605openalex-snapshot

Endogenous sleep-promoting substances and sleep regulation

inferredcites →https://doi.org/10.1176/ajp.148.7.944openalex-snapshot

Brainstem Control of Wakefulness and Sleep

inferredcites →https://doi.org/10.1212/wnl.16.11.1053openalex-snapshot

Acetylcholine released from cerebral cortex in relation to state of activation

inferredcites →https://doi.org/10.1523/jneurosci.02-10-01387.1982openalex-snapshot

Discharge rate and excitability of cortically projecting intralaminar thalamic neurons during waking and sleep states

inferredcites →https://doi.org/10.1523/jneurosci.06-01-00068.1986openalex-snapshot

Reticularis thalami neurons revisited: activity changes during shifts in states of vigilance

inferredcites →https://doi.org/10.1523/jneurosci.10-08-02541.1990openalex-snapshot

Neuronal activities in brain-stem cholinergic nuclei related to tonic activation processes in thalamocortical systems

inferredcites →https://doi.org/10.1523/jneurosci.10-08-02560.1990openalex-snapshot

Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves

inferredcites →https://doi.org/10.1523/jneurosci.11-10-03200.1991openalex-snapshot

Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortically induced synchronization and brainstem cholinergic suppression

inferredcites →https://doi.org/10.1523/jneurosci.13-08-03252.1993openalex-snapshot

A novel slow (< 1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components

inferredcites →https://doi.org/10.1523/jneurosci.15-01-00604.1995openalex-snapshot

Cellular basis of EEG slow rhythms: a study of dynamic corticothalamic relationships

inferredcites →https://doi.org/10.1523/jneurosci.15-05-03526.1995openalex-snapshot

Contribution of the circadian pacemaker and the sleep homeostat to sleep propensity, sleep structure, electroencephalographic slow waves, and sleep spindle activity in humans

inferredcites →https://doi.org/10.1523/jneurosci.15-06-04658.1995openalex-snapshot

Disconnection of intracortical synaptic linkages disrupts synchronization of a slow oscillation

inferredcites →https://doi.org/10.1523/jneurosci.16-01-00169.1996openalex-snapshot

In vivo, in vitro, and computational analysis of dendritic calcium currents in thalamic reticular neurons

inferredcites →https://doi.org/10.1523/jneurosci.16-01-00392.1996openalex-snapshot

Synchronization of fast (30-40 Hz) spontaneous cortical rhythms during brain activation

inferredcites →https://doi.org/10.1523/jneurosci.16-07-02397.1996openalex-snapshot

The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons

inferredcites →https://doi.org/10.1523/jneurosci.16-08-02767.1996openalex-snapshot

Spatiotemporal properties of short-term plasticity sensorimotor thalamocortical pathways of the rat

inferredcites →https://doi.org/10.1523/jneurosci.16-08-02788.1996openalex-snapshot

Synchronization of fast (30-40 Hz) spontaneous oscillations in intrathalamic and thalamocortical networks

inferredcites →https://doi.org/10.1523/jneurosci.16-23-07742.1996openalex-snapshot

Cellular Mechanisms of the Augmenting Response: Short-Term Plasticity in a Thalamocortical Pathway

inferredcites →https://doi.org/10.1523/jneurosci.17-03-01179.1997openalex-snapshot

Spatiotemporal Patterns of Spindle Oscillations in Cortex and Thalamus

inferredcites →https://doi.org/10.1523/jneurosci.17-08-02807.1997openalex-snapshot

Functional Neuroanatomy of Human Slow Wave Sleep

inferredcites →https://doi.org/10.1523/jneurosci.17-10-03778.1997openalex-snapshot

Short-Term Plasticity during Intrathalamic Augmenting Responses in Decorticated Cats

inferredcites →https://doi.org/10.1523/jneurosci.17-12-04800.1997openalex-snapshot

Regional Cerebral Blood Flow Changes as a Function of Delta and Spindle Activity during Slow Wave Sleep in Humans

inferredcites →https://doi.org/10.1523/jneurosci.18-16-06444.1998openalex-snapshot

Computational Models of Thalamocortical Augmenting Responses

inferredcites →https://doi.org/10.1523/jneurosci.21-16-06430.2001openalex-snapshot

Cortical Slow Oscillatory Activity Is Reflected in the Membrane Potential and Spike Trains of Striatal Neurons in Rats with Chronic Nigrostriatal Lesions

inferredcites →https://doi.org/10.7551/mitpress/3822.001.0001openalex-snapshot

The Intact and Sliced Brain

What points at this work

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

inferred← citeshttps://doi.org/10.1093/jmammal/gyad122zenodo-depositor-declared

Noninvasive EEG measurement of sleep in the family cat and comparison with the dog

inferred← citeshttps://doi.org/10.1001/archpsyc.62.4.387openalex-snapshot

Alterations in Regional Cerebral Glucose Metabolism Across Waking and Non–Rapid Eye Movement Sleep in Depression

inferred← citeshttps://doi.org/10.1002/9780470101001.hcn051openalex-snapshot

Sedatives and Hypnotics

inferred← citeshttps://doi.org/10.1002/9780471740360.ebs1096openalex-snapshot

Sleep

inferred← citeshttps://doi.org/10.1002/9781118133880.hop203013openalex-snapshot

Sleep and Biological Rhythms

inferred← citeshttps://doi.org/10.1002/aur.2875openalex-snapshot

Increased resting‐state thalamocortical functional connectivity in children and young adults with autism spectrum disorder

inferred← citeshttps://doi.org/10.1002/bies.201700105openalex-snapshot

Ca2+‐Dependent Hyperpolarization Pathways in Sleep Homeostasis and Mental Disorders

inferred← citeshttps://doi.org/10.1002/brb3.1557openalex-snapshot

Nonrapid eye movement sleep and risk for autism spectrum disorder in early development: A topographical electroencephalogram pilot study

inferred← citeshttps://doi.org/10.1002/hbm.20525openalex-snapshot

Late evening brain activation patterns and their relation to the internal biological time, melatonin, and homeostatic sleep debt

inferred← citeshttps://doi.org/10.1002/hbm.22581openalex-snapshot

Evoked effective connectivity of the human neocortex

inferred← citeshttps://doi.org/10.1002/hbm.24590openalex-snapshot

Instability of brain connectivity during nonrapid eye movement sleep reflects altered properties of information integration

inferred← citeshttps://doi.org/10.1002/hipo.20121openalex-snapshot

The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme

inferred← citeshttps://doi.org/10.1002/hipo.20585openalex-snapshot

Genetic ablation of tenascin‐C expression leads to abnormal hippocampal CA1 structure and electrical activity in vivo

inferred← citeshttps://doi.org/10.1002/hipo.22494openalex-snapshot

Oscillatory patterns in hippocampus under light and deep isoflurane anesthesia closely mirror prominent brain states in awake animals

inferred← citeshttps://doi.org/10.1002/wcs.52openalex-snapshot

Sleep and cognition

inferred← citeshttps://doi.org/10.1007/3-7643-7440-3openalex-snapshot

Clinical Pharmacology of Sleep

inferred← citeshttps://doi.org/10.1007/3-7643-7440-3_7openalex-snapshot

Sleep disturbances in affective disorders

inferred← citeshttps://doi.org/10.1007/7854_2014_326openalex-snapshot

Neuroimaging Studies of Sleep and Memory in Humans

inferred← citeshttps://doi.org/10.1007/7854_2014_366openalex-snapshot

Sleep and Plasticity in Schizophrenia

inferred← citeshttps://doi.org/10.1007/978-0-306-48526-8_1openalex-snapshot

Brain Death

inferred← citeshttps://doi.org/10.1007/978-0-387-38977-6_3openalex-snapshot

Conceptual Approach to Human Death on Neurological Grounds

inferred← citeshttps://doi.org/10.1007/978-0-387-46526-5_9openalex-snapshot

Central Cholinergic Nervous System and Its Correlates

inferred← citeshttps://doi.org/10.1007/978-1-0716-0653-7_9openalex-snapshot

Sleep Oscillations and Psychiatric Disorders

inferred← citeshttps://doi.org/10.1007/978-1-4614-9087-6_15openalex-snapshot

Noise-Induced Sleep Deprivation: Toward Sleeping Soundly on Noisy Nights

inferred← citeshttps://doi.org/10.1007/978-3-030-10620-1_15openalex-snapshot

The Sixth Sense: Let Your Mind Go to Sleep

inferred← citeshttps://doi.org/10.1007/978-3-031-06413-5_2openalex-snapshot

Covering the Gap Between Sleep and Cognition – Mechanisms and Clinical Examples

inferred← citeshttps://doi.org/10.1007/978-3-031-06447-0_3openalex-snapshot

Atypical Sleep and Pathologic Wakefulness

inferred← citeshttps://doi.org/10.1007/978-3-031-07121-8_16openalex-snapshot

Sleep

inferred← citeshttps://doi.org/10.1007/978-3-031-16770-6_7openalex-snapshot

Is Free Energy an Organizational Principle in Spiking Neural Networks?

inferred← citeshttps://doi.org/10.1007/978-3-319-45066-7_12openalex-snapshot

Neuronal Oscillations and Reactivation Subserving Memory Consolidation

inferred← citeshttps://doi.org/10.1007/978-3-319-59740-9_40openalex-snapshot

Circadian Modulation of Sleep-Wake Dynamics Evaluated by Transition Probabilities

inferred← citeshttps://doi.org/10.1007/978-3-540-71905-2_35openalex-snapshot

Transkranielle Magnetstimulation und Elektroenzephalografie

inferred← citeshttps://doi.org/10.1007/978-3-540-87919-0_14openalex-snapshot

Sleep

inferred← citeshttps://doi.org/10.1007/978-3-642-54672-3_194-1openalex-snapshot

Schlafregulation

inferred← citeshttps://doi.org/10.1007/978-3-642-54672-3_957-1openalex-snapshot

Lokaler Schlaf

inferred← citeshttps://doi.org/10.1007/978-3-642-75837-9_10openalex-snapshot

Cytokines and Sleep

inferred← citeshttps://doi.org/10.1007/978-3-662-43850-3_6openalex-snapshot

Time–Frequency Analysis of EEG: From Theory to Practice

inferred← citeshttps://doi.org/10.1007/978-3-662-65186-5_194openalex-snapshot

Schlafregulation

inferred← citeshttps://doi.org/10.1007/978-3-662-65186-5_957openalex-snapshot

Lokaler Schlaf

inferred← citeshttps://doi.org/10.1007/s00018-009-0019-1openalex-snapshot

Memory processes during sleep: beyond the standard consolidation theory

inferred← citeshttps://doi.org/10.1007/s00018-011-0631-8openalex-snapshot

The waking brain: an update

inferred← citeshttps://doi.org/10.1007/s00114-006-0120-3openalex-snapshot

Do birds sleep in flight?

inferred← citeshttps://doi.org/10.1007/s00213-007-0866-0openalex-snapshot

Short-term treatment with gaboxadol improves sleep maintenance and enhances slow wave sleep in adult patients with primary insomnia

inferred← citeshttps://doi.org/10.1007/s00415-010-5517-4openalex-snapshot

How vital is sleep in Huntington’s disease?

inferred← citeshttps://doi.org/10.1007/s00424-014-1477-3openalex-snapshot

Role for T-type Ca2+ channels in sleep waves

inferred← citeshttps://doi.org/10.1007/s00429-017-1559-zopenalex-snapshot

Modulation of thalamocortical oscillations by TRIP8b, an auxiliary subunit for HCN channels

inferred← citeshttps://doi.org/10.1007/s10072-023-06982-8openalex-snapshot

Association between lesion location and sensorimotor rhythms in stroke – a systematic review with narrative synthesis

inferred← citeshttps://doi.org/10.1007/s10827-013-0493-1openalex-snapshot

A thalamo-cortical neural mass model for the simulation of brain rhythms during sleep

inferred← citeshttps://doi.org/10.1007/s10827-017-0658-4openalex-snapshot

Stimulus-induced transitions between spike-wave discharges and spindles with the modulation of thalamic reticular nucleus

inferred← citeshttps://doi.org/10.1007/s10827-020-00754-5openalex-snapshot

Optogenetic activation of corticogeniculate feedback stabilizes response gain and increases information coding in LGN neurons

inferred← citeshttps://doi.org/10.1007/s11325-005-0010-5openalex-snapshot

Injection of glutamate into the pedunculopontine tegmental nuclei of anesthetized rat causes respiratory dysrhythmia and alters EEG and EMG power

inferred← citeshttps://doi.org/10.1007/s11325-010-0327-6openalex-snapshot

Coupling changes in cortical and pontine sigma and theta frequency oscillations following monoaminergic lesions in rat

inferred← citeshttps://doi.org/10.1007/s11325-019-01951-yopenalex-snapshot

Differences in electroencephalographic spectra during pre-sleep wakefulness, N1, and R sleep between comorbid insomnia and obstructive sleep apnea

inferred← citeshttps://doi.org/10.1007/s11818-009-0423-7openalex-snapshot

Schlafregulation

inferred← citeshttps://doi.org/10.1007/s11818-015-0697-xopenalex-snapshot

Individual stability of sleep spindle characteristics in healthy young males

inferred← citeshttps://doi.org/10.1007/s12017-015-8355-9openalex-snapshot

Neuronal Network Oscillations in Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.1007/s12035-020-02264-yopenalex-snapshot

Metabolic Changes in Brain Slices over Time: a Multiplatform Metabolomics Approach

inferred← citeshttps://doi.org/10.1007/s13246-024-01428-7openalex-snapshot

SPINDILOMETER: a model describing sleep spindles on EEG signals for polysomnography

inferred← citeshttps://doi.org/10.1007/s13534-023-00298-4openalex-snapshot

Modulation of sleep using noninvasive stimulations during sleep

inferred← citeshttps://doi.org/10.1007/s40675-024-00291-yopenalex-snapshot

Electrophysiological Mechanisms of Memory Consolidation in Human Non-rapid Eye Movement Sleep

inferred← citeshttps://doi.org/10.1016/b0-72-160797-7/50016-1openalex-snapshot

Brain Electrical Activity and Sensory Processing during Waking and Sleep States

inferred← citeshttps://doi.org/10.1016/b0-72-160797-7/50040-9openalex-snapshot

Sleep Homeostasis and Models of Sleep Regulation

inferred← citeshttps://doi.org/10.1016/b978-0-12-374168-4.00008-3openalex-snapshot

Sleep and Dreaming

inferred← citeshttps://doi.org/10.1016/b978-0-12-374168-4.00028-9openalex-snapshot

The Neurology of Consciousness: An Overview

inferred← citeshttps://doi.org/10.1016/b978-0-12-375073-0.50019-1openalex-snapshot

Cytokines and other Neuromodulators

inferred← citeshttps://doi.org/10.1016/b978-0-12-378610-4.00097-8openalex-snapshot

Basic Sleep–Wake Mechanisms

inferred← citeshttps://doi.org/10.1016/b978-0-12-384995-3.00004-6openalex-snapshot

Genetic Mechanisms Underlying Rhythmic EEG Activity during Sleep

inferred← citeshttps://doi.org/10.1016/b978-0-12-387003-2.00009-4openalex-snapshot

From Genetics to Structure to Function: Exploring Sleep in Drosophila

inferred← citeshttps://doi.org/10.1016/b978-0-12-415804-7.00021-6openalex-snapshot

Consciousness and Subcortical Arousal Systems

inferred← citeshttps://doi.org/10.1016/b978-0-12-800948-2.00007-8openalex-snapshot

Sleep and Dreaming

inferred← citeshttps://doi.org/10.1016/b978-0-12-800948-2.00009-1openalex-snapshot

Consciousness and Anesthesia

inferred← citeshttps://doi.org/10.1016/b978-0-12-800948-2.00025-xopenalex-snapshot

The Neurology of Consciousness

inferred← citeshttps://doi.org/10.1016/b978-0-12-813743-7.00012-8openalex-snapshot

Genes and Ion Channels in the Circadian and Homeostatic Regulation of Sleep

inferred← citeshttps://doi.org/10.1016/b978-0-12-822963-7.00219-xopenalex-snapshot

Local circuits: the fundamental minimal unit for emergent sleep

inferred← citeshttps://doi.org/10.1016/b978-0-12-822963-7.00312-1openalex-snapshot

Neuroinflammation, sleep, and autoimmune disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-822963-7.20012-1openalex-snapshot

Basic sleep–wake mechanisms

inferred← citeshttps://doi.org/10.1016/b978-0-323-24288-2.00007-6openalex-snapshot

Neural Control of Sleep in Mammals

inferred← citeshttps://doi.org/10.1016/b978-0-323-24288-2.00166-5openalex-snapshot

Cardiopulmonary Coupling Sleep Spectrograms

inferred← citeshttps://doi.org/10.1016/b978-0-443-06959-8.00011-xopenalex-snapshot

Sleep, Memory, and Consciousness

inferred← citeshttps://doi.org/10.1016/b978-0-443-33651-5.00016-1openalex-snapshot

The effects of sound stimulation on slow waves

inferred← citeshttps://doi.org/10.1016/b978-0-444-52007-4.00018-7openalex-snapshot

Fatal familial insomnia and the role of the thalamus in sleep regulation

inferred← citeshttps://doi.org/10.1016/b978-0-444-52898-8.00019-7openalex-snapshot

Sleep and epilepsy

inferred← citeshttps://doi.org/10.1016/b978-0-444-53839-0.00007-7openalex-snapshot

Slow oscillations orchestrating fast oscillations and memory consolidation

inferred← citeshttps://doi.org/10.1016/b978-008045046-9.00036-xopenalex-snapshot

Sleep and Sleep States: Cytokines and Neuromodulation

inferred← citeshttps://doi.org/10.1016/b978-1-4160-6645-3.00007-4openalex-snapshot

Neural Control of Sleep in Mammals

inferred← citeshttps://doi.org/10.1016/j.alcohol.2008.08.001openalex-snapshot

Effects of adolescent ethanol exposure on sleep in adult rats

inferred← citeshttps://doi.org/10.1016/j.anclin.2012.05.003openalex-snapshot

Interfaces of Sleep and Anesthesia

inferred← citeshttps://doi.org/10.1016/j.bbamem.2003.10.023openalex-snapshot

Electrical synapses: a dynamic signaling system that shapes the activity of neuronal networks

inferred← citeshttps://doi.org/10.1016/j.bbi.2008.02.001openalex-snapshot

Sleep-wake behavior and responses to sleep deprivation of mice lacking both interleukin-1β receptor 1 and tumor necrosis factor-α receptor 1

inferred← citeshttps://doi.org/10.1016/j.bbr.2006.07.028openalex-snapshot

Precise rhythmicity in activity of neocortical, thalamic and brain stem neurons in behaving cats and rabbits

inferred← citeshttps://doi.org/10.1016/j.bbr.2013.07.047openalex-snapshot

Topography of the sleep/wake states related EEG microstructure and transitions structure differentiates the functionally distinct cholinergic innervation disorders in rat

inferred← citeshttps://doi.org/10.1016/j.bbr.2014.09.008openalex-snapshot

Role of slow oscillatory activity and slow wave sleep in consolidation of episodic-like memory in rats

inferred← citeshttps://doi.org/10.1016/j.bnd.2024.07.001openalex-snapshot

Synchronization-suppressing stimulation of the amygdala circuitry reduces pathological anxiety in sub-chronic stress rat model

inferred← citeshttps://doi.org/10.1016/j.bpsc.2019.04.012openalex-snapshot

Increased Thalamocortical Connectivity in Schizophrenia Correlates With Sleep Spindle Deficits: Evidence for a Common Pathophysiology

inferred← citeshttps://doi.org/10.1016/j.bpsc.2021.07.013openalex-snapshot

The Feature of Sleep Spindle Deficits in Patients With Schizophrenia With and Without Auditory Verbal Hallucinations

inferred← citeshttps://doi.org/10.1016/j.brainres.2005.05.022openalex-snapshot

Theta activity in the waking EEG is a marker of sleep propensity in the rat

inferred← citeshttps://doi.org/10.1016/j.brainres.2005.06.052openalex-snapshot

Unilateral cortical application of tumor necrosis factor α induces asymmetry in Fos- and interleukin-1β-immunoreactive cells within the corticothalamic projection

inferred← citeshttps://doi.org/10.1016/j.brainres.2025.149973openalex-snapshot

Resting EEG partial coherence demonstrates increased γ range central functional connectivity in amnestic mild cognitive impairment

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2003.09.004openalex-snapshot

Sleep and synaptic homeostasis: a hypothesis

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2005.11.002openalex-snapshot

Evolution of slow-wave sleep and palliopallial connectivity in mammals and birds: A hypothesis

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2007.02.010openalex-snapshot

Response to commentary on evolution of slow-wave sleep and palliopallial connectivity in mammals and birds: A hypothesis

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2010.01.006openalex-snapshot

The effects of morning training on night sleep: A behavioral and EEG study

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2018.07.002openalex-snapshot

Sleep and brain infections

inferred← citeshttps://doi.org/10.1016/j.brainresrev.2004.04.003openalex-snapshot

Brain inhibitory mechanisms involved in basic and higher integrated sleep processes

inferred← citeshttps://doi.org/10.1016/j.brs.2013.05.006openalex-snapshot

No Effects of Slow Oscillatory Transcranial Direct Current Stimulation (tDCS) on Sleep-Dependent Memory Consolidation in Healthy Elderly Subjects

inferred← citeshttps://doi.org/10.1016/j.cbpa.2007.02.020openalex-snapshot

Topographical distribution of the locus coeruleus and raphe nuclei in the lizard Ctenosaura pectinata: Functional implications on sleep

inferred← citeshttps://doi.org/10.1016/j.ceca.2006.04.022openalex-snapshot

Thalamic T-type Ca2+ channels and NREM sleep

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112200openalex-snapshot

Thalamic control of sensory processing and spindles in a biophysical somatosensory thalamoreticular circuit model of wakefulness and sleep

inferred← citeshttps://doi.org/10.1016/j.cels.2019.03.007openalex-snapshot

Reduced Repertoire of Cortical Microstates and Neuronal Ensembles in Medically Induced Loss of Consciousness

inferred← citeshttps://doi.org/10.1016/j.chaos.2025.117081openalex-snapshot

Network motifs in talamocortical system model responsible for delta-rhythm generation

inferred← citeshttps://doi.org/10.1016/j.chest.2017.01.002openalex-snapshot

Sleep and Neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.clinph.2004.05.029openalex-snapshot

Night terrors associated with thalamic lesion

inferred← citeshttps://doi.org/10.1016/j.clinph.2005.09.019openalex-snapshot

Sources of cortical rhythms change as a function of cognitive impairment in pathological aging: a multicenter study

inferred← citeshttps://doi.org/10.1016/j.clinph.2007.07.001openalex-snapshot

Cyclic alternating pattern sequences and non-cyclic alternating pattern periods in human sleep

inferred← citeshttps://doi.org/10.1016/j.clinph.2010.04.027openalex-snapshot

Resting state eyes-closed cortical rhythms in patients with locked-in-syndrome: An eeg study

inferred← citeshttps://doi.org/10.1016/j.clinph.2012.07.023openalex-snapshot

Effects of pharmacological agents, sleep deprivation, hypoxia and transcranial magnetic stimulation on electroencephalographic rhythms in rodents: Towards translational challenge models for drug discovery in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.clinph.2013.06.016openalex-snapshot

Altered resting state effective connectivity in long-standing vegetative state patients: An EEG study

inferred← citeshttps://doi.org/10.1016/j.clinph.2014.01.024openalex-snapshot

Cortical sources of resting-state EEG rhythms in “experienced” HIV subjects under antiretroviral therapy

inferred← citeshttps://doi.org/10.1016/j.clinph.2015.05.029openalex-snapshot

Cortical sources of resting state electroencephalographic rhythms differ in relapsing–remitting and secondary progressive multiple sclerosis

inferred← citeshttps://doi.org/10.1016/j.clinph.2015.12.007openalex-snapshot

Abnormal cortical sources of resting state electroencephalographic rhythms in single treatment-naïve HIV individuals: A statistical z-score index

inferred← citeshttps://doi.org/10.1016/j.clinph.2018.08.009openalex-snapshot

When is “brainstem death” brain death? The case for ancillary testing in primary infratentorial brain lesion

inferred← citeshttps://doi.org/10.1016/j.clinph.2024.08.002openalex-snapshot

Altered sleep onset transition in depression: Evidence from EEG activity and EEG functional connectivity analyses

inferred← citeshttps://doi.org/10.1016/j.concog.2010.01.007openalex-snapshot

Focused attention, open monitoring and automatic self-transcending: Categories to organize meditations from Vedic, Buddhist and Chinese traditions

inferred← citeshttps://doi.org/10.1016/j.coph.2005.10.001openalex-snapshot

Unravelling the brain targets of γ-hydroxybutyric acid

inferred← citeshttps://doi.org/10.1016/j.crvi.2004.05.009openalex-snapshot

Neural reapportionment: an hypothesis to account for the function of sleep

inferred← citeshttps://doi.org/10.1016/j.cub.2015.01.016openalex-snapshot

Sleep Interacts with Aβ to Modulate Intrinsic Neuronal Excitability

inferred← citeshttps://doi.org/10.1016/j.cub.2026.01.075openalex-snapshot

Sleep spindles promote hippocampal network downregulation during sleep

inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2006.01.003openalex-snapshot

NMDA-NR1 and AMPA-GluR4 receptor subunit immunoreactivities in the absence epileptic WAG/Rij rat

inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2022.106999openalex-snapshot

Role of anterior thalamic circuitry during sleep

inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.02.007openalex-snapshot

Lesion of the pedunculopontine tegmental nucleus in rat augments cortical activation and disturbs sleep/wake state transitions structure

inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114775openalex-snapshot

Mice harboring the T316N variant in the GABAAR γ2 subunit exhibit sleep-related hypermotor epilepsy phenotypes and hypersynchronization in the thalamocortical pathway

inferred← citeshttps://doi.org/10.1016/j.heares.2020.108003openalex-snapshot

Mechanisms of GABAergic and cholinergic neurotransmission in auditory thalamus: Impact of aging

inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2015.02.008openalex-snapshot

Brain neural synchronization and functional coupling in Alzheimer's disease as revealed by resting state EEG rhythms

inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2025.113205openalex-snapshot

Missing what's right under your nose: Failed appetitive and aversive audio-olfactory conditioning in humans

inferred← citeshttps://doi.org/10.1016/j.intell.2018.11.004openalex-snapshot

The associations between spindle characteristics and cognitive ability in a large adolescent birth cohort

inferred← citeshttps://doi.org/10.1016/j.isci.2025.111904openalex-snapshot

A design principle for neuronal firing with up-down oscillation through Na+ dynamics

inferred← citeshttps://doi.org/10.1016/j.jneumeth.2008.11.006openalex-snapshot

The individual adjustment method of sleep spindle analysis: Methodological improvements and roots in the fingerprint paradigm

inferred← citeshttps://doi.org/10.1016/j.jneumeth.2015.06.002openalex-snapshot

Physiologically based arousal state estimation and dynamics

inferred← citeshttps://doi.org/10.1016/j.jsmc.2019.11.001openalex-snapshot

You Snooze, You Win? An Ecological Dynamics Framework Approach to Understanding the Relationships Between Sleep and Sensorimotor Performance in Sport

inferred← citeshttps://doi.org/10.1016/j.jtbi.2018.10.013openalex-snapshot

Nonlinear harmonic generation in the corticothalamic system

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2005.11.012openalex-snapshot

The somatotropic axis in sleep and thermoregulation: A tribute to Ferenc Obál, Jr. (1948–2004)

inferred← citeshttps://doi.org/10.1016/j.nbd.2025.107081openalex-snapshot

Thalamocortical dysrhythmia-related sleep spindle desynchronization in patients with tinnitus

inferred← citeshttps://doi.org/10.1016/j.ncl.2012.08.001openalex-snapshot

Neurobiological Aspects of Sleep Physiology

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2014.10.021openalex-snapshot

The nonspecific thalamus: A place in a wedding bed for making memories last?

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2022.104765openalex-snapshot

Sleep as a window to target traumatic memories

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2005.03.004openalex-snapshot

Age-related attenuation of the evening circadian arousal signal in humans

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2008.09.020openalex-snapshot

Cortical sources of resting EEG rhythms in mild cognitive impairment and subjective memory complaint

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2016.04.016openalex-snapshot

Corticothalamic network dysfunction and behavioral deficits in a mouse model of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2021.03.003openalex-snapshot

EEG measures for clinical research in major vascular cognitive impairment: recommendations by an expert panel

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2005.05.028openalex-snapshot

Cerebral correlates of delta waves during non-REM sleep revisited

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2005.08.030openalex-snapshot

Genotype (cystatin C) and EEG phenotype in Alzheimer disease and mild cognitive impairment: A multicentric study

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2006.02.015openalex-snapshot

Donepezil effects on sources of cortical rhythms in mild Alzheimer's disease: Responders vs. Non-Responders

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.01.033openalex-snapshot

The human brain pacemaker: Synchronized infra-slow neurovascular coupling in patients undergoing non-pulsatile cardiopulmonary bypass

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.07.057openalex-snapshot

Heterogeneity of arousals in human sleep: A stereo-electroencephalographic study

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.116490openalex-snapshot

Memory quality modulates the effect of aging on memory consolidation during sleep: Reduced maintenance but intact gain

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117587openalex-snapshot

The laminar profile of sleep spindles in humans

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119325openalex-snapshot

Thalamic activity during scalp slow waves in humans

inferred← citeshttps://doi.org/10.1016/j.neurom.2025.08.414openalex-snapshot

Distinct Patterns of Temporally Coded Electrical Stimulation Interfere With Long-Range Interhemispheric Coupling in a Focal Model of Epilepsy

inferred← citeshttps://doi.org/10.1016/j.neuron.2014.11.010openalex-snapshot

Wireless Neurosensor for Full-Spectrum Electrophysiology Recordings during Free Behavior

inferred← citeshttps://doi.org/10.1016/j.neuron.2016.02.032openalex-snapshot

Involvement of Ca2+-Dependent Hyperpolarization in Sleep Duration in Mammals

inferred← citeshttps://doi.org/10.1016/j.neuron.2023.07.007openalex-snapshot

A common thalamic hub for general and defensive arousal control

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2004.08.001openalex-snapshot

Pentobarbital induces thalamic oscillations in brain slices, modulated by GABA and glycine receptors

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2025.110721openalex-snapshot

Receptor-specific noradrenergic modulation of oscillatory dynamics during non-rapid eye movement sleep in adult male rats

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2006.08.049openalex-snapshot

Conversion from mild cognitive impairment to Alzheimer’s disease is predicted by sources and coherence of brain electroencephalography rhythms

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.03.081openalex-snapshot

Normal sleep homeostasis and lack of epilepsy phenotype in GABAA receptor α3 subunit-knockout mice

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.01.049openalex-snapshot

Anandamide activation of CB1 receptors increases spontaneous bursting and oscillatory activity in the thalamus

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.12.007openalex-snapshot

Regulation of neuron–astrocyte metabolic coupling across the sleep–wake cycle

inferred← citeshttps://doi.org/10.1016/j.nlm.2006.10.006openalex-snapshot

Neural representations during sleep: From sensory processing to memory traces

inferred← citeshttps://doi.org/10.1016/j.nlm.2012.07.002openalex-snapshot

Offline consolidation of memory varies with time in slow wave sleep and can be accelerated by cuing memory reactivations

inferred← citeshttps://doi.org/10.1016/j.patbio.2014.07.003openalex-snapshot

Insomnia and sleep misperception

inferred← citeshttps://doi.org/10.1016/j.physbeh.2006.04.009openalex-snapshot

The effect of transdermal nicotine patches on sleep and dreams

inferred← citeshttps://doi.org/10.1016/j.physbeh.2006.09.009openalex-snapshot

Circadian rhythms in cognitive performance: Methodological constraints, protocols, theoretical underpinnings

inferred← citeshttps://doi.org/10.1016/j.physbeh.2012.11.007openalex-snapshot

The administration of endocannabinoid uptake inhibitors OMDM-2 or VDM-11 promotes sleep and decreases extracellular levels of dopamine in rats

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2013.10.001openalex-snapshot

Neurophysiology of HCN channels: From cellular functions to multiple regulations

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102589openalex-snapshot

Fundamentals of sleep regulation: Model and benchmark values for fractal and oscillatory neurodynamics

inferred← citeshttps://doi.org/10.1016/j.reia.2025.202538openalex-snapshot

EEG spectral characteristics and asymmetry in pre-school children with autism in awake and sleep stages

inferred← citeshttps://doi.org/10.1016/j.schres.2015.06.012openalex-snapshot

Topographic deficits in alpha-range resting EEG activity and steady state visual evoked responses in schizophrenia

inferred← citeshttps://doi.org/10.1016/j.schres.2019.05.027openalex-snapshot

Thalamus-related anomalies as candidate mechanism-based biomarkers for psychosis

inferred← citeshttps://doi.org/10.1016/j.schres.2020.03.025openalex-snapshot

Slow wave oscillations in Schizophrenia First-Degree Relatives: A confirmatory analysis and feasibility study on slow wave traveling

inferred← citeshttps://doi.org/10.1016/j.schres.2024.05.008openalex-snapshot

Overview on cognitive impairment in psychotic disorders: From impaired microcircuits to dysconnectivity

inferred← citeshttps://doi.org/10.1016/j.sleep.2007.10.003openalex-snapshot

Suprachiasmatic nucleus in sleep–wake regulation

inferred← citeshttps://doi.org/10.1016/j.sleep.2013.10.002openalex-snapshot

Relationship between delta power and the electrocardiogram-derived cardiopulmonary spectrogram: possible implications for assessing the effectiveness of sleep

inferred← citeshttps://doi.org/10.1016/j.sleep.2017.05.013openalex-snapshot

Electrophysiological and microstructural features of sleep in children at high risk for depression: a preliminary study

inferred← citeshttps://doi.org/10.1016/j.sleep.2021.07.028openalex-snapshot

Focal limbic sources create the large slow oscillations of the EEG in human deep sleep

inferred← citeshttps://doi.org/10.1016/j.sleep.2025.106519openalex-snapshot

Day–night hyperarousal in tinnitus patients

inferred← citeshttps://doi.org/10.1016/j.smrv.2004.03.003openalex-snapshot

Advancing the neurobiology of insomnia, a commentary on: “Functional imaging of the sleeping brain” by Drummond et al.

inferred← citeshttps://doi.org/10.1016/j.smrv.2005.01.002openalex-snapshot

Cytokines and sleep

inferred← citeshttps://doi.org/10.1016/j.smrv.2005.04.003openalex-snapshot

K-complex, a reactive EEG graphoelement of NREM sleep: an old chap in a new garment

inferred← citeshttps://doi.org/10.1016/j.smrv.2005.05.002openalex-snapshot

Sleep function and synaptic homeostasis

inferred← citeshttps://doi.org/10.1016/j.smrv.2011.02.003openalex-snapshot

Cyclic alternating pattern (CAP): The marker of sleep instability

inferred← citeshttps://doi.org/10.1016/j.smrv.2011.08.001openalex-snapshot

Does abnormal non-rapid eye movement sleep impair declarative memory consolidation?

inferred← citeshttps://doi.org/10.1016/j.smrv.2015.12.005openalex-snapshot

Top-down control of arousal and sleep: Fundamentals and clinical implications

inferred← citeshttps://doi.org/10.1016/j.smrv.2019.101252openalex-snapshot

REM sleep vs exploratory wakefulness: Alternatives within adult ‘sleep debt’?

inferred← citeshttps://doi.org/10.1016/j.smrv.2020.101304openalex-snapshot

Episodic memory consolidation during sleep in healthy aging

inferred← citeshttps://doi.org/10.1016/j.smrv.2022.101605openalex-snapshot

A systematic scoping review of the effects of central nervous system active drugs on sleep spindles and sleep-dependent memory consolidation

inferred← citeshttps://doi.org/10.1016/j.smrv.2026.102321openalex-snapshot

Assessing the effects of non-invasive transcranial electrical stimulation (tACS and tDCS) on electrophysiological sleep parameters - a systematic review

inferred← citeshttps://doi.org/10.1016/j.spen.2023.101087openalex-snapshot

Sleep and Epilepsy

inferred← citeshttps://doi.org/10.1016/j.tics.2011.05.008openalex-snapshot

The hippocampus: hub of brain network communication for memory

inferred← citeshttps://doi.org/10.1016/j.tics.2013.12.005openalex-snapshot

Sleep, synaptic connectivity, and hippocampal memory during early development

inferred← citeshttps://doi.org/10.1016/j.tins.2006.06.013openalex-snapshot

Slow-waves in the olfactory system: an olfactory perspective on cortical rhythms

showing the first 200 of 480

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.