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BOLD signatures of sleep
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archpsyc.1969.01740140118016openalex-snapshot
A Manual of Standardized Terminology, Techniques and Scoring System for Sleep Stages of Human Subjects.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19971103)387:4<588::aid-cne8>3.0.co;2-zopenalex-snapshot
Multiarchitectonic and stereotactic atlas of the human thalamus
inferredcites →https://doi.org/10.1002/1522-2594(200007)44:1<162::aid-mrm23>3.0.co;2-eopenalex-snapshot
Image-based method for retrospective correction of physiological motion effects in fMRI: RETROICOR
inferredcites →https://doi.org/10.1002/hbm.20428openalex-snapshot
Low frequency BOLD fluctuations during resting wakefulness and light sleep: A simultaneous EEG‐fMRI study
inferredcites →https://doi.org/10.1002/hbm.22623openalex-snapshot
Electrophysiological correlates of the BOLD signal for EEG-informed fMRI
inferredcites →https://doi.org/10.1006/nimg.2000.0630openalex-snapshot
Nonlinear Responses in fMRI: The Balloon Model, Volterra Kernels, and Other Hemodynamics
inferredcites →https://doi.org/10.1006/nimg.2000.0657openalex-snapshot
Spontaneous Low Frequency Oscillations of Cerebral Hemodynamics and Metabolism in Human Adults
inferredcites →https://doi.org/10.1007/978-3-540-29678-2_6166openalex-snapshot
Two-Process Model of Sleep Regulation
inferredcites →https://doi.org/10.1016/0006-8993(82)91252-5openalex-snapshot
Slow rhythmic rate fluctuations of cat midbrain reticular neurons in synchronized sleep and waking
inferredcites →https://doi.org/10.1016/0006-8993(83)90153-1openalex-snapshot
Slow rhythmic oscillations of EEG slow-wave amplitudes and their relations to midbrain reticular discharge
inferredcites →https://doi.org/10.1016/0013-4694(49)90066-8openalex-snapshot
Brain stem reticular formation and activation of the EEG
inferredcites →https://doi.org/10.1016/0013-4694(49)90219-9openalex-snapshot
Brain stem reticular formation and activation of the EEG
inferredcites →https://doi.org/10.1016/0013-4694(62)90004-4openalex-snapshot
Reticular facilitation of responses to acoustic stimuli
inferredcites →https://doi.org/10.1016/0013-4694(75)90227-8openalex-snapshot
Evolution of sleep spindles in childhood
inferredcites →https://doi.org/10.1016/j.brainres.2010.12.035openalex-snapshot
Infraslow EEG oscillations organize large-scale cortical–subcortical interactions during sleep: A combined EEG/fMRI study
inferredcites →https://doi.org/10.1016/j.clinph.2011.06.018openalex-snapshot
Functional MRI of sleep spindles and K-complexes
inferredcites →https://doi.org/10.1016/j.conb.2014.09.001openalex-snapshot
The thalamocortical network as a single slow wave-generating unit
inferredcites →https://doi.org/10.1016/j.conb.2017.03.021openalex-snapshot
Wake–sleep circuitry: an overview
inferredcites →https://doi.org/10.1016/j.cub.2007.06.066openalex-snapshot
Coupling between Neuronal Firing Rate, Gamma LFP, and BOLD fMRI Is Related to Interneuronal Correlations
inferredcites →https://doi.org/10.1016/j.cub.2015.11.062openalex-snapshot
Local Slow Waves in Superficial Layers of Primary Cortical Areas during REM Sleep
inferredcites →https://doi.org/10.1016/j.dcn.2014.10.004openalex-snapshot
Frequency of spontaneous BOLD signal shifts during infancy and correlates with cognitive performance
inferredcites →https://doi.org/10.1016/j.mri.2009.02.004openalex-snapshot
Sources of functional magnetic resonance imaging signal fluctuations in the human brain at rest: a 7 T study
inferredcites →https://doi.org/10.1016/j.neubiorev.2018.03.027openalex-snapshot
Dynamic coupling between the central and autonomic nervous systems during sleep: A review
inferredcites →https://doi.org/10.1016/j.neures.2003.10.014openalex-snapshot
Stimulus frequency dependence of the linear relationship between local cerebral blood flow and field potential evoked by activation of rat somatosensory cortex
inferredcites →https://doi.org/10.1016/j.neuroimage.2003.10.018openalex-snapshot
Spatial relationship between neuronal activity and BOLD functional MRI
inferredcites →https://doi.org/10.1016/j.neuroimage.2006.01.021openalex-snapshot
An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest
inferredcites →https://doi.org/10.1016/j.neuroimage.2007.07.037openalex-snapshot
Low-frequency fluctuations in the cardiac rate as a source of variance in the resting-state fMRI BOLD signal
inferredcites →https://doi.org/10.1016/j.neuroimage.2008.05.055openalex-snapshot
Stereotaxic probabilistic maps of the magnocellular cell groups in human basal forebrain
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.01.045openalex-snapshot
A probabilistic MR atlas of the human cerebellum
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.10.042openalex-snapshot
A mean three-dimensional atlas of the human thalamus: Generation from multiple histological data
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.05.077openalex-snapshot
A theoretical framework for estimating cerebral oxygen metabolism changes using the calibrated-BOLD method: Modeling the effects of blood volume distribution, hematocrit, oxygen extraction fraction, and tissue signal properties on the BOLD signal
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.07.013openalex-snapshot
MRI atlas of the human hypothalamus
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.09.013openalex-snapshot
To wake or not to wake? The two-sided nature of the human K-complex
inferredcites →https://doi.org/10.1016/j.neuroimage.2012.06.036openalex-snapshot
Automatic sleep staging using fMRI functional connectivity data
inferredcites →https://doi.org/10.1016/j.neuroimage.2013.04.068openalex-snapshot
Correlated slow fluctuations in respiration, EEG, and BOLD fMRI
inferredcites →https://doi.org/10.1016/j.neuroimage.2013.09.029openalex-snapshot
Quasi-periodic patterns (QPP): Large-scale dynamics in resting state fMRI that correlate with local infraslow electrical activity
inferredcites →https://doi.org/10.1016/j.neuroimage.2013.10.044openalex-snapshot
Direct, intraoperative observation of ~ 0.1 Hz hemodynamic oscillations in awake human cortex: Implications for fMRI
inferredcites →https://doi.org/10.1016/j.neuroimage.2014.12.012openalex-snapshot
BOLD fractional contribution to resting-state functional connectivity above 0.1 Hz
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.04.042openalex-snapshot
A computational atlas of the hippocampal formation using ex vivo, ultra-high resolution MRI: Application to adaptive segmentation of in vivo MRI
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.12.034openalex-snapshot
Progression to deep sleep is characterized by changes to BOLD dynamics in sensory cortices
inferredcites →https://doi.org/10.1016/j.neuroimage.2016.11.010openalex-snapshot
Spatiotemporal characteristics of sleep spindles depend on cortical location
inferredcites →https://doi.org/10.1016/j.neuroimage.2017.01.059openalex-snapshot
On the detection of high frequency correlations in resting state fMRI
inferredcites →https://doi.org/10.1016/j.neuron.2006.10.023openalex-snapshot
Integration and Segregation of Activity in Entorhinal-Hippocampal Subregions by Neocortical Slow Oscillations
inferredcites →https://doi.org/10.1016/j.neuron.2011.02.043openalex-snapshot
Regional Slow Waves and Spindles in Human Sleep
inferredcites →https://doi.org/10.1016/j.neuron.2013.02.008openalex-snapshot
Visceral Influences on Brain and Behavior
inferredcites →https://doi.org/10.1016/j.neuron.2013.12.025openalex-snapshot
Sleep and the Price of Plasticity: From Synaptic and Cellular Homeostasis to Memory Consolidation and Integration
inferredcites →https://doi.org/10.1016/j.neuron.2014.03.020openalex-snapshot
Decoding Wakefulness Levels from Typical fMRI Resting-State Data Reveals Reliable Drifts between Wakefulness and Sleep
inferredcites →https://doi.org/10.1016/j.neuron.2016.03.036openalex-snapshot
Network Homeostasis and State Dynamics of Neocortical Sleep
inferredcites →https://doi.org/10.1016/j.neuron.2017.01.014openalex-snapshot
Neural Circuitry of Wakefulness and Sleep
inferredcites →https://doi.org/10.1016/j.neuron.2017.10.012openalex-snapshot
Entrainment of Arteriole Vasomotor Fluctuations by Neural Activity Is a Basis of Blood-Oxygenation-Level-Dependent “Resting-State” Connectivity
inferredcites →https://doi.org/10.1016/j.neuron.2018.01.025openalex-snapshot
Ultra-Slow Single-Vessel BOLD and CBV-Based fMRI Spatiotemporal Dynamics and Their Correlation with Neuronal Intracellular Calcium Signals
inferredcites →https://doi.org/10.1016/j.nlm.2018.12.008openalex-snapshot
Coupling of autonomic and central events during sleep benefits declarative memory consolidation
inferredcites →https://doi.org/10.1016/j.sleep.2017.11.212openalex-snapshot
Sleep and cortical maturation: slow and fast sleep spindles in the first 4 years of life
inferredcites →https://doi.org/10.1016/j.tins.2009.11.002openalex-snapshot
Recovery of consciousness after brain injury: a mesocircuit hypothesis
inferredcites →https://doi.org/10.1016/s0031-9384(99)00049-9openalex-snapshot
A Comparison of Period Amplitude Analysis and FFT Power Spectral Analysis of All-Night Human Sleep EEG
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)00186-3openalex-snapshot
Low-frequency (<1Hz) oscillations in the human sleep electroencephalogram
inferredcites →https://doi.org/10.1016/s0896-6273(02)00569-xopenalex-snapshot
Whole Brain Segmentation
inferredcites →https://doi.org/10.1017/s0012162206001654openalex-snapshot
A neurophysiological perspective on sleep and its maturation
inferredcites →https://doi.org/10.1037/0735-7044.121.1.1openalex-snapshot
Sleep spindles and learning potential.
inferredcites →https://doi.org/10.1038/35084005openalex-snapshot
Neurophysiological investigation of the basis of the fMRI signal
inferredcites →https://doi.org/10.1038/jcbfm.2008.25openalex-snapshot
Metabolic Origin of Bold Signal Fluctuations in the Absence of Stimuli
inferredcites →https://doi.org/10.1038/nature18933openalex-snapshot
A multi-modal parcellation of human cerebral cortex
inferredcites →https://doi.org/10.1038/ncomms15930openalex-snapshot
Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource
inferredcites →https://doi.org/10.1038/nmeth.2855openalex-snapshot
Sleep-spindle detection: crowdsourcing and evaluating performance of experts, non-experts and automated methods
inferredcites →https://doi.org/10.1038/nn.3671openalex-snapshot
Spontaneous fluctuations in neural responses to heartbeats predict visual detection
inferredcites →https://doi.org/10.1038/nn1758openalex-snapshot
Arm immobilization causes cortical plastic changes and locally decreases sleep slow wave activity
inferredcites →https://doi.org/10.1038/s41467-017-02815-3openalex-snapshot
Subcortical evidence for a contribution of arousal to fMRI studies of brain activity
inferredcites →https://doi.org/10.1038/srep29671openalex-snapshot
The occurrence of individual slow waves in sleep is predicted by heart rate
inferredcites →https://doi.org/10.1046/j.1365-2869.1997.00046.xopenalex-snapshot
Topographic distribution of sleep spindles in young healthy subjects
inferredcites →https://doi.org/10.1046/j.1365-2869.1997.d01-36.xopenalex-snapshot
Fronto‐occipital EEG power gradients in human sleep
inferredcites →https://doi.org/10.1073/pnas.0305375101openalex-snapshot
Infraslow oscillations modulate excitability and interictal epileptic activity in the human cortex during sleep
inferredcites →https://doi.org/10.1073/pnas.0700668104openalex-snapshot
Electrophysiological signatures of resting state networks in the human brain
inferredcites →https://doi.org/10.1073/pnas.0703084104openalex-snapshot
Hemodynamic cerebral correlates of sleep spindles during human non-rapid eye movement sleep
inferredcites →https://doi.org/10.1073/pnas.0801819105openalex-snapshot
Spontaneous neural activity during human slow wave sleep
inferredcites →https://doi.org/10.1073/pnas.0807933106openalex-snapshot
Source modeling sleep slow waves
inferredcites →https://doi.org/10.1073/pnas.0900924106openalex-snapshot
Cortical network functional connectivity in the descent to sleep
inferredcites →https://doi.org/10.1073/pnas.0901435106openalex-snapshot
Decoupling of the brain's default mode network during deep sleep
inferredcites →https://doi.org/10.1073/pnas.0905509106openalex-snapshot
Spatiotemporal precision and hemodynamic mechanism of optical point spreads in alert primates
inferredcites →https://doi.org/10.1073/pnas.0909710107openalex-snapshot
Thalamic deactivation at sleep onset precedes that of the cerebral cortex in humans
inferredcites →https://doi.org/10.1073/pnas.1111133109openalex-snapshot
Hierarchical clustering of brain activity during human nonrapid eye movement sleep
inferredcites →https://doi.org/10.1073/pnas.1217691110openalex-snapshot
Rhythmic alternating patterns of brain activity distinguish rapid eye movement sleep from other states of consciousness
inferredcites →https://doi.org/10.1073/pnas.1410800111openalex-snapshot
Low-frequency calcium oscillations accompany deoxyhemoglobin oscillations in rat somatosensory cortex
inferredcites →https://doi.org/10.1073/pnas.1608117113openalex-snapshot
Fast fMRI can detect oscillatory neural activity in humans
inferredcites →https://doi.org/10.1089/brain.2015.0369openalex-snapshot
Propofol-Induced Frontal Cortex Disconnection: A Study of Resting-State Networks, Total Brain Connectivity, and Mean BOLD Signal Oscillation Frequencies
inferredcites →https://doi.org/10.1093/brain/awm084openalex-snapshot
'Brain activation and hypothalamic functional connectivity during human non-rapid eye movement sleep: an EEG/fMRI study'--its limitations and an alternative approach
inferredcites →https://doi.org/10.1093/cercor/bhs397openalex-snapshot
Connectivity-Based Functional Analysis of Dopamine Release in the Striatum Using Diffusion-Weighted MRI and Positron Emission Tomography
inferredcites →https://doi.org/10.1093/cercor/bhu089openalex-snapshot
Robust Long-Range Coordination of Spontaneous Neural Activity in Waking, Sleep and Anesthesia
inferredcites →https://doi.org/10.1093/sleep/30.12.1643openalex-snapshot
Sleep Homeostasis and Cortical Synchronization: III. A High-Density EEG Study of Sleep Slow Waves in Humans
inferredcites →https://doi.org/10.1093/sleep/34.2.181openalex-snapshot
The Sleep EEG as a Marker of Intellectual Ability in School Age Children
inferredcites →https://doi.org/10.1093/sleep/34.3.283openalex-snapshot
Propofol Anesthesia and Sleep: A High-Density EEG Study
inferredcites →https://doi.org/10.1097/00004647-200209000-00002openalex-snapshot
Effect of Basal Conditions on the Magnitude and Dynamics of the Blood Oxygenation Level-Dependent fMRI Response
inferredcites →https://doi.org/10.1098/rsta.2015.0182openalex-snapshot
Delay-correlation landscape reveals characteristic time delays of brain rhythms and heart interactions
inferredcites →https://doi.org/10.1098/rsta.2015.0188openalex-snapshot
Brain–heart interactions: challenges and opportunities with functional magnetic resonance imaging at ultra-high field
inferredcites →https://doi.org/10.1111/j.1365-2869.1993.tb00074.xopenalex-snapshot
Period‐amplitude analysis and power spectral analysis: a comparison based on all‐night sleep EEG recordings
inferredcites →https://doi.org/10.1111/j.1365-2869.2005.00472.xopenalex-snapshot
Prediction of general mental ability based on neural oscillation measures of sleep
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04694.xopenalex-snapshot
Sleep spindle‐related activity in the human EEG and its relation to general cognitive and learning abilities
inferredcites →https://doi.org/10.1111/j.1460-9568.2011.07877.xopenalex-snapshot
Stimulus‐induced dissociation of neuronal firing rates and local field potential gamma power and its relationship to the blood oxygen level‐dependent signal in macaque primary visual cortex
inferredcites →https://doi.org/10.1111/j.1469-7793.2000.t01-1-00235.xopenalex-snapshot
Temporal coupling between neuronal activity and blood flow in rat cerebellar cortex as indicated by field potential analysis
inferredcites →https://doi.org/10.1111/jsr.12371openalex-snapshot
The two‐process model of sleep regulation: a reappraisal
inferredcites →https://doi.org/10.1111/psyp.12508openalex-snapshot
Heartbeat‐related EEG amplitude and phase modulations from wakefulness to deep sleep: Interactions with sleep spindles and slow oscillations
inferredcites →https://doi.org/10.1152/jn.00014.2006openalex-snapshot
Hippocampal Sharp Wave-Ripples Linked to Slow Oscillations in Rat Slow-Wave Sleep
inferredcites →https://doi.org/10.1152/jn.00804.2013openalex-snapshot
Lag structure in resting-state fMRI
inferredcites →https://doi.org/10.1152/jn.1960.23.6.602openalex-snapshot
UNSPECIFIC SYSTEMS OF INHIBITION AND FACILITATION OF POTENTIALS EVOKED BY INTERMITTENT LIGHT
inferredcites →https://doi.org/10.1152/jn.1987.57.1.260openalex-snapshot
The deafferented reticular thalamic nucleus generates spindle rhythmicity
inferredcites →https://doi.org/10.1152/jn.2000.84.2.1076openalex-snapshot
Spiking-Bursting Activity in the Thalamic Reticular Nucleus Initiates Sequences of Spindle Oscillations in Thalamic Networks
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/physrev.00032.2012openalex-snapshot
About Sleep's Role in Memory
inferredcites →https://doi.org/10.1176/ajp.2007.164.3.483openalex-snapshot
Reduced Sleep Spindle Activity in Schizophrenia Patients
inferredcites →https://doi.org/10.1196/annals.1417.024openalex-snapshot
Why Does Consciousness Fade in Early Sleep?
inferredcites →https://doi.org/10.1371/journal.pone.0084279openalex-snapshot
BOLD Granger Causality Reflects Vascular Anatomy
inferredcites →https://doi.org/10.1523/eneuro.0293-18.2018openalex-snapshot
Human Rapid Eye Movement Sleep Shows Local Increases in Low-Frequency Oscillations and Global Decreases in High-Frequency Oscillations Compared to Resting Wakefulness
inferredcites →https://doi.org/10.1523/jneurosci.0763-12.2013openalex-snapshot
The Impact of Visual Perceptual Learning on Sleep and Local Slow-Wave Initiation
inferredcites →https://doi.org/10.1523/jneurosci.0796-14.2014openalex-snapshot
Development of Thalamocortical Connectivity during Infancy and Its Cognitive Correlations
inferredcites →https://doi.org/10.1523/jneurosci.1296-11.2011openalex-snapshot
Anatomical and Functional Assemblies of Brain BOLD Oscillations
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.1318-04.2004openalex-snapshot
The Sleep Slow Oscillation as a Traveling Wave
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.2241-17.2018openalex-snapshot
Heterogeneous Origins of Human Sleep Spindles in Different Cortical Layers
inferredcites →https://doi.org/10.1523/jneurosci.2339-11.2011openalex-snapshot
Properties of Slow Oscillation during Slow-Wave Sleep and Anesthesia in Cats
inferredcites →https://doi.org/10.1523/jneurosci.2604-11.2011openalex-snapshot
Sleep Spindles in Humans: Insights from Intracranial EEG and Unit Recordings
inferredcites →https://doi.org/10.1523/jneurosci.3218-16.2017openalex-snapshot
Are the Neural Correlates of Consciousness in the Front or in the Back of the Cerebral Cortex? Clinical and Neuroimaging Evidence
inferredcites →https://doi.org/10.1523/jneurosci.3787-14.2015openalex-snapshot
A Critical Role for Purinergic Signalling in the Mechanisms Underlying Generation of BOLD fMRI Responses
inferredcites →https://doi.org/10.1523/jneurosci.4460-13.2014openalex-snapshot
Global Intracellular Slow-Wave Dynamics of the Thalamocortical System
inferredcites →https://doi.org/10.1523/jneurosci.4567-14.2015openalex-snapshot
Neural and Behavioral Correlates of Extended Training during Sleep Deprivation in Humans: Evidence for Local, Task-Specific Effects
inferredcites →https://doi.org/10.3389/fneur.2012.00100openalex-snapshot
EEG-fMRI Methods for the Study of Brain Networks during Sleep
inferredcites →https://doi.org/10.3389/fnhum.2018.00248openalex-snapshot
Local and Widespread Slow Waves in Stable NREM Sleep: Evidence for Distinct Regulation Mechanisms
inferredcites →https://doi.org/10.3389/fnins.2016.00313openalex-snapshot
Systemic Low-Frequency Oscillations in BOLD Signal Vary with Tissue Type
inferredcites →https://doi.org/10.3389/fnsys.2014.00083openalex-snapshot
Intralaminar and medial thalamic influence on cortical synchrony, information transmission and cognition
inferredcites →https://doi.org/10.3389/fnsys.2014.00208openalex-snapshot
Enhancement of sleep slow waves: underlying mechanisms and practical consequences
inferredcites →https://doi.org/10.3389/fpsyg.2013.00542openalex-snapshot
Assessing sleep consciousness within subjects using a serial awakening paradigm
inferredcites →https://doi.org/10.5664/jcsm.5.2s.s6openalex-snapshot
Regulation and Functional Correlates of Slow Wave Sleep
inferredcites →https://doi.org/10.5665/sleep.1290openalex-snapshot
Fast and Slow Spindles during the Sleep Slow Oscillation: Disparate Coalescence and Engagement in Memory Processing
inferredcites →https://doi.org/10.5665/sleep.3422openalex-snapshot
Decreased Connectivity between the Thalamus and the Neocortex during Human Nonrapid Eye Movement Sleep
inferredcites →https://doi.org/10.7554/elife.27602openalex-snapshot
Cortex-wide BOLD fMRI activity reflects locally-recorded slow oscillation-associated calcium waves
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Brain–stomach coupling: Anatomy, functions, and future avenues of research
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Linking the nature and functions of sleep: insights from multimodal imaging of the sleeping brain
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Modeling regional changes in dynamic stability during sleep and wakefulness
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Modular slowing of resting-state dynamic functional connectivity as a marker of cognitive dysfunction induced by sleep deprivation
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Capturing the non-stationarity of whole-brain dynamics underlying human brain states
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Ultra-slow fMRI fluctuations in the fourth ventricle as a marker of drowsiness
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New Cognitive Neurotechnology Facilitates Studies of Cortical–Subcortical Interactions
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Dynamic functional connectivity as a marker of pathological and cognitive changes in Alzheimer's disease
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