The Phase of Thalamic Alpha Activity Modulates Cortical Gamma-Band Activity: Evidence from Resting-State MEG Recordings

On Information and Sufficiency

Kullback, S., & Leibler, R. A. (1951) · The Annals of Mathematical Statistics · doi:10.1214/aoms/1177729694 · Cited by 20,193 · see citing works

A default mode of brain function

Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works

FieldTrip: open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data

Oostenveld, R., Fries, P., Maris, E., & Schoffelen, J.-M. (2011) · Computational Intelligence and Neuroscience · doi:10.1155/2011/156869 · Cited by 10,323 · see citing works

An Information-Maximization Approach to Blind Separation and Blind Deconvolution

Bell, A. J., & Sejnowski, T. J. (1995) · Neural Computation · doi:10.1162/neco.1995.7.6.1129 · Cited by 8,986 · see citing works

Nonparametric statistical testing of EEG- and MEG-data

Maris, E., & Oostenveld, R. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.03.024 · Cited by 8,496 · see citing works

The precuneus: a review of its functional anatomy and behavioural correlates

Cavanna, A. E., & Trimble, M. R. (2006) · Brain · doi:10.1093/brain/awl004 · Cited by 5,128 · see citing works

Über das Elektrenkephalogramm des Menschen

Berger, H. (1929) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf01797193 · Cited by 4,266 · see citing works

The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes

Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works

Estimating mutual information

Kraskov, A., Stögbauer, H., & Grassberger, P. (2004) · Physical Review E · doi:10.1103/physreve.69.066138 · Cited by 4,157 · see citing works

EEG alpha oscillations: The inhibition–timing hypothesis

Klimesch, W., Sauseng, P., & Hanslmayr, S. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.06.003 · Cited by 3,890 · see citing works

Searching for a baseline: Functional imaging and the resting human brain

Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371 · see citing works

Shaping Functional Architecture by Oscillatory Alpha Activity: Gating by Inhibition

Jensen, O., & Mazaheri, A. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00186 · Cited by 3,237 · see citing works

Localization of brain electrical activity via linearly constrained minimum variance spatial filtering

Van Veen, B. D., Van Drongelen, W., Yuchtman, M., & Suzuki, A. (1997) · IEEE Transactions on Biomedical Engineering · doi:10.1109/10.623056 · Cited by 2,561 · see citing works

A default mode of brain function: a brief history of an evolving idea

Raichle, M. E., & Snyder, A. Z. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.041 · Cited by 2,173 · see citing works

Oscillatory gamma activity in humans and its role in object representation

Tallon‐Baudry, C. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01299-1 · Cited by 2,111 · see citing works

Dynamic imaging of coherent sources: studying neural interactions in the human brain

Gross, J., Kujala, J., Hämäläinen, M., Timmermann, L., Schnitzler, A., & Salmelin, R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.694 · Cited by 1,810 · see citing works

THE BERGER RHYTHM: POTENTIAL CHANGES FROM THE OCCIPITAL LOBES IN MAN

ADRIAN, E. D., & MATTHEWS, B. H. C. (1934) · Brain · doi:10.1093/brain/57.4.355 · Cited by 1,396 · see citing works

Measuring Phase-Amplitude Coupling Between Neuronal Oscillations of Different Frequencies

Tort, A. B. L., Komorowski, R. W., Eichenbaum, H., & Kopell, N. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00106.2010 · Cited by 1,365 · see citing works

The magnetic lead field theorem in the quasi-static approximation and its use for magnetoencephalography forward calculation in realistic volume conductors.

Nolte, G. (2003) · Physics in Medicine and Biology · doi:10.1088/0031-9155/48/22/002 · Cited by 1,140 · see citing works

Ionic basis for the electro‐responsiveness and oscillatory properties of guinea‐pig thalamic neurones in vitro.

Jahnsen, H., & Llinas, R. H. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015154 · Cited by 1,081 · see citing works

The pulvinar regulates information transmission between cortical areas based on attention demands

Saalmann, Y. B., Pinsk, M. A., Wang, L., Li, X., & Kastner, S. (2012) · Science · doi:10.1126/science.1223082 · Cited by 1,016 · see citing works

Transfer entropy—a model-free measure of effective connectivity for the neurosciences

Vicente, R., Wibral, M., Lindner, M., & Pipa, G. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0262-3 · Cited by 1,009 · see citing works

Spectral Analysis for Physical Applications: Multitaper and Conventional Univariate Techniques.

DSS, Percival, D. B., & Walden, A. T. (1997) · Journal of the American Statistical Association · doi:10.2307/2965609 · Cited by 975 · see citing works

Broadband Shifts in Local Field Potential Power Spectra Are Correlated with Single-Neuron Spiking in Humans

Manning, J. R., Jacobs, J., Fried, I., & Kahana, M. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2041-09.2009 · Cited by 973 · see citing works

Cross-frequency coupling supports multi-item working memory in the human hippocampus

Axmacher, N., Henseler, M. M., Jensen, O. B., Weinreich, I., Elger, C. E., & Fell, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911531107 · Cited by 929 · see citing works

α-Oscillations in the monkey sensorimotor network influence discrimination performance by rhythmical inhibition of neuronal spiking

Haegens, S., Nácher, V., Luna, R., Romo, R., & Jensen, O. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117190108 · Cited by 738 · see citing works

Brain Oscillatory Substrates of Visual Short-Term Memory Capacity

Sauseng, P., Klimesch, W., Heise, K.-F., Gruber, W. R., Holz, E. M., Karim, A. A., Glennon, M., Gerloff, C. P., Birbaumer, N., & Hummel, F. C. (2009) · Current Biology · doi:10.1016/j.cub.2009.08.062 · Cited by 707 · see citing works

Is perception discrete or continuous?

VanRullen, R., & Koch, C. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(03)00095-0 · Cited by 662 · see citing works

Thalamic Mechanisms of EEG Alpha Rhythms and Their Pathological Implications

Hughes, S. W., & Crunelli, V. (2005) · The Neuroscientist · doi:10.1177/1073858405277450 · Cited by 565 · see citing works

Magnetic field tomography of coherent thalamocortical 40-Hz oscillations in humans.

Ribary, U., Ioannides, A. A., Singh, K. D., Hasson, R., Bolton, J. P., Lado, F. A., Mogilner, A. Y., & Llinas, R. H. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.24.11037 · Cited by 541 · see citing works

Physiological Basis of the Alpha Rhythm

Andersen, P. N., & Andersson, S. A. (1968) · Medical Entomology and Zoology · Cited by 540 · see citing works

A review of systems and networks of the limbic forebrain/limbic midbrain

Morgane, P. J., Galler, J. R., & Mokler, D. J. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.01.001 · Cited by 497 · see citing works

An oscillatory mechanism for prioritizing salient unattended stimuli

Jensen, O. B., Bonnefond, M., & Rufin Vanrullen, A. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.03.002 · Cited by 449 · see citing works

Neuronal Mechanisms and Attentional Modulation of Corticothalamic Alpha Oscillations

Bollimunta, A., Mo, J., Schroeder, C. E., & Ding, M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5580-10.2011 · Cited by 441 · see citing works

Neuronal Mechanisms of Cortical Alpha Oscillations in Awake-Behaving Macaques

Bollimunta, A., Chen, Y., Schroeder, C. E., & Ding, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-08.2008 · Cited by 434 · see citing works

Relative contributions of intracortical and thalamo-cortical processes in the generation of alpha rhythms, revealed by partial coherence analysis

Lopes, F. H. D. S., Vos, J. E., Mooibroek, J. J., & van Rotterdam, A. (1980) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(80)90011-5 · Cited by 425 · see citing works

Shifts in gamma phase–amplitude coupling frequency from theta to alpha over posterior cortex during visual tasks

Voytek, B. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00191 · Cited by 401 · see citing works

Layer-Specific Entrainment of Gamma-Band Neural Activity by the Alpha Rhythm in Monkey Visual Cortex

Spaak, E., Bonnefond, M., Maier, A., Leopold, D. A., & Jensen, O. (2012) · Current Biology · doi:10.1016/j.cub.2012.10.020 · Cited by 385 · see citing works

Frequency-Band Coupling in Surface EEG Reflects Spiking Activity in Monkey Visual Cortex

Whittingstall, K., & Logothetis, N. K. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.016 · Cited by 364 · see citing works

The phase of ongoing oscillations mediates the causal relation between brain excitation and visual perception.

Dugué, L., Marque, P., & VanRullen, R. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1161-11.2011 · Cited by 364 · see citing works

Exploring the Thalamus

(2001) · Elsevier eBooks · doi:10.1016/b978-0-12-305460-9.x5013-8 · Cited by 355 · see citing works

Thalamic circuitry and thalamocortical synchrony

Jones, E. G. (2002) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1168 · Cited by 340 · see citing works

Sex Differences in Regional Cerebral Glucose Metabolism During a Resting State

Gur, R. C., Mozley, L. H., Mozley, P. D., Resnick, S. M., Karp, J. S., Alavi, A. A., Arnold, S. E., & Gur, R. E. (1995) · Science · doi:10.1126/science.7824953 · Cited by 340 · see citing works

Gamma Power Is Phase-Locked to Posterior Alpha Activity

Osipova, D. V., Hermes, D., & Jensen, O. B. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003990 · Cited by 329 · see citing works

Organization of thalamic and cortical alpha rhythms: Spectra and coherences

Lopes, F. H. D. S., van Lierop, T. H. M. T., Schrijer, C. F., & van Leeuwen, W. S. (1973) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(73)90216-2 · Cited by 326 · see citing works

Temporal Framing of Thalamic Relay-Mode Firing by Phasic Inhibition during the Alpha Rhythm

Lörincz, M. L., Kékesi, K. A., Juhász, G. D., Crunelli, V., & Hughes, S. W. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.012 · Cited by 326 · see citing works

Perceptual framing and cortical alpha rhythm

Valera, F. J., Toro, A., John, E. R., & Schwartz, E. (1981) · Neuropsychologia · doi:10.1016/0028-3932(81)90005-1 · Cited by 290 · see citing works

Coherent neural representation of hand speed in humans revealed by MEG imaging

Jerbi, K., Lachaux, J.-P., N′Diaye, K., Pantazis, D., Leahy, R. M., Garnero, L., & Baillet, S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609632104 · Cited by 289 · see citing works

Measuring Information-Transfer Delays

Wibral, M., Pampu, N. C., Priesemann, V., Siebenhühner, F., Seiwert, H., Lindner, M., Lizier, J. T., & Vicente, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055809 · Cited by 286 · see citing works

Sensitivity of MEG and EEG to Source Orientation

Hämäläinen, M., Ahlfors, S. P., Han, J., & Belliveau, J. W. (2010) · Digital Access to Scholarship at Harvard (DASH) (Harvard University) · Cited by 265 · see citing works

TRENTOOL: A Matlab open source toolbox to analyse information flow in time series data with transfer entropy

Lindner, M., Vicente, R., Priesemann, V., & Wibral, M. (2011) · BMC Neuroscience · doi:10.1186/1471-2202-12-119 · Cited by 231 · see citing works

Inferring Spike Trains From Local Field Potentials

Rasch, M. J., Gretton, A., Murayama, Y., Maass, W., & Logothetis, N. K. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00919.2007 · Cited by 210 · see citing works

EEG Alpha Power Modulation of fMRI Resting-State Connectivity

Scheeringa, R., Petersson, K. M., Kleinschmidt, A. K., Jensen, O. B., & BASTIAANSEN, M. C. M. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0088 · Cited by 204 · see citing works

Good Vibrations: Cross-frequency Coupling in the Human Nucleus Accumbens during Reward Processing

Cohen, M. X., Axmacher, N., Lenartz, D., Elger, C. E., Sturm, V., & Schlaepfer, T. E. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21062 · Cited by 197 · see citing works

Asymptotic SNR of Scalar and Vector Minimum-Variance Beamformers for Neuromagnetic Source Reconstruction

Sekihara, K., Nagarajan, S. S., Poeppel, D., & Marantz, A. (2004) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2004.827926 · Cited by 193 · see citing works

Dysfunctions in Multiple Interrelated Systems as the Neurobiological Bases of Schizophrenic Symptom Clusters

O’Donnell, P., & Grace, A. A. (1998) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a033325 · Cited by 191 · see citing works

Thalamic model of awake alpha oscillations and implications for stimulus processing

Vijayan, S., & Kopell, N. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215385109 · Cited by 171 · see citing works

A Golgi analysis of the primate globus pallidus. II. Quantitative morphology and spatial orientation of dendritic arborizations

Yelnik, J., Percheron, G., & François, C. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902270206 · Cited by 161 · see citing works

Gain control in the visual thalamus during perception and cognition

Saalmann, Y. B., & Kastner, S. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.05.007 · Cited by 156 · see citing works

Broadband Spectral Change: Evidence for a Macroscale Correlate of Population Firing Rate?: Figure 1.

Miller, K. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6401-09.2010 · Cited by 154 · see citing works

Markov models from data by simple nonlinear time series predictors in delay embedding spaces

Ragwitz, M., & Kantz, H. (2002) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.65.056201 · Cited by 136 · see citing works

Modulation of Visually Evoked Cortical fMRI Responses by Phase of Ongoing Occipital Alpha Oscillations

Scheeringa, R., Mazaheri, A., Bojak, I., Norris, D. G., & Kleinschmidt, A. K. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4697-10.2011 · Cited by 136 · see citing works

Regulation of Motor Representation by Phase–Amplitude Coupling in the Sensorimotor Cortex

Yanagisawa, T., Yamashita, O., Hirata, M., Kishima, H., Saitoh, Y., Goto, T., Yoshimine, T., & Kamitani, Y. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2929-12.2012 · Cited by 134 · see citing works

Interactions between Core and Matrix Thalamocortical Projections in Human Sleep Spindle Synchronization

Bonjean, M., Baker, T. I., Bazhenov, M., Cash, S. S., Halgren, E., & B, T. J. S. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6141-11.2012 · Cited by 107 · see citing works

Dysfunctional Thalamus-Related Networks in Schizophrenia

Pinault, D. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq165 · Cited by 105 · see citing works

Resting oscillations and cross-frequency coupling in the human posteromedial cortex

Foster, B. L., & Parvizi, J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.019 · Cited by 102 · see citing works

The 3D topography of MEG source localization accuracy: effects of conductor model and noise

Tarkiainen, A., Liljeström, M., Seppä, M., & Salmelin, R. H. (2003) · Clinical Neurophysiology · doi:10.1016/s1388-2457(03)00195-0 · Cited by 81 · see citing works

Dynamic Modulation of Local Population Activity by Rhythm Phase in Human Occipital Cortex During a Visual Search Task

Miller, K. J., Hermes, D., Honey, C. J., Sharma, M., Rao, R. P. N., den Nijs, M., Fetz, E. E., B, T. J. S. A., Hebb, A. O., Ojemann, J. G., et al. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00197 · Cited by 68 · see citing works

Hippocampal Theta-Phase Modulation of Replay Correlates with Configural-Relational Short-Term Memory Performance: Figure 1.

Poch, C., Fuentemilla, L., Barnes, G. R., & Düzel, E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6305-10.2011 · Cited by 62 · see citing works

Memory signals from the thalamus: Early thalamocortical phase synchronization entrains gamma oscillations during long-term memory retrieval

Staudigl, T., Zaehle, T., Voges, J., Hanslmayr, S., Esslinger, C., Hinrichs, H., Schmitt, F. C., Heinze, H., & Richardson‐Klavehn, A. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.08.023 · Cited by 61 · see citing works

Cross-frequency coupling within and between the human thalamus and neocortex

FitzGerald, T. H. B. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00084 · Cited by 60 · see citing works

Non-invasive imaging of neuronal population dynamics in human thalamus

Tesche, C. D. (1996) · Brain Research · doi:10.1016/0006-8993(96)00555-0 · Cited by 47 · see citing works

Coherence in consciousness: Paralimbic gamma synchrony of self‐reference links conscious experiences

Lou, H. C., Groß, J., Biermann‐Ruben, K., Kjær, T. W., & Schnitzler, A. (2009) · Human Brain Mapping · doi:10.1002/hbm.20855 · Cited by 35 · see citing works

How to Detect Amygdala Activity with Magnetoencephalography using Source Imaging

Balderston, N. L., Schultz, D. H., Baillet, S., & Helmstetter, F. J. (2013) · Journal of Visualized Experiments · doi:10.3791/50212 · Cited by 30 · see citing works

Phase shift detection in thalamocortical oscillations using magnetoencephalography in humans

Bish, J. P., Martin, T., Houck, J. M., Ilmoniemi, R. J., & Tesche, C. D. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.02.032 · Cited by 23 · see citing works

Amplitude modulation of gamma band oscillations at alpha frequency produced by photic driving

Chorlian, D. B., Bernice Porjesz, A., & Begleiter, H. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.11.002 · Cited by 17 · see citing works

MEG imaging of neuronal population dynamics in the human thalamus.

Tesche, C. D. (1996) · PubMed · Cited by 16 · see citing works

Sensitivity of MEG and EEG to source orientation

Ahlfors, S. P., Han, J., Belliveau, J. W., & Hämäläinen, M. S. (2010) · Brain Topography · doi:10.1007/s10548-010-0154-x · Cited by 1 · see citing works

High-resolution intersubject averaging and a coordinate system for the cortical surface

Fischl, B., Sereno, M. I., Tootell, R. B. H., & Dale, A. M. (1999) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1999)8:4

Magnetoencephalography for Brain Electrophysiology and Imaging

Baillet, S. (2017) · Nature Neuroscience · doi:10.1038/nn.4504 · Cited by 992 · see citing works

Working memory and neural oscillations: alpha–gamma versus theta–gamma codes for distinct WM information?

Roux, F., & Uhlhaas, P. J. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.10.010 · Cited by 865 · see citing works

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

Hyafil, A., Giraud, A., Fontolan, L., & Gutkin, B. S. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.09.001 · Cited by 498 · see citing works

Cerebral hierarchies: predictive processing, precision and the pulvinar

Kanai, R., Komura, Y., Shipp, S., & Friston, K. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0169 · Cited by 432 · see citing works

The Speed of Alpha-Band Oscillations Predicts the Temporal Resolution of Visual Perception

Samaha, J., & Postle, B. R. (2015) · Current Biology · doi:10.1016/j.cub.2015.10.007 · Cited by 467 · see citing works

Brain Networks and α-Oscillations: Structural and Functional Foundations of Cognitive Control

Sadaghiani, S., & Kleinschmidt, A. K. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.09.004 · Cited by 447 · see citing works

The generation and propagation of the human alpha rhythm

Halgren, M., Ulbert, I., Bastuji, H., Fabó, D., Erőss, L., Rey, M. F., Devinsky, O., Doyle, W., Mak-McCully, R. A., Halgren, E., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913092116 · Cited by 418 · see citing works

Temporal coding organized by coupled alpha and gamma oscillations prioritize visual processing

Jensen, O., Gips, B., Bergmann, T. O., & Bonnefond, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.04.001 · Cited by 389 · see citing works

Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks

Vidaurre, D., Hunt, L. T., Quinn, A. J., Hunt, B. A. E., Brookes, M. J., Nobre, A. C., & Woolrich, M. W. (2018) · Nature Communications · doi:10.1038/s41467-018-05316-z · Cited by 363 · see citing works

Subcortical electrophysiological activity is detectable with high-density EEG source imaging

Seeber, M., Cantonas, L.-M., Hoevels, M., Sesia, T., Visser-Vandewalle, V. E. R. M., & Michel, C. M. (2019) · Nature Communications · doi:10.1038/s41467-019-08725-w · Cited by 294 · see citing works

Oscillations and Neuronal Dynamics in Schizophrenia: The Search for Basic Symptoms and Translational Opportunities

Uhlhaas, P. J., & Singer, W. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.11.019 · Cited by 243 · see citing works

Electrophysiological Brain Connectivity: Theory and Implementation

He, B., Laura Astolfi, A., Valdes-Sosa, P. A., Marinazzo, D., Palva, S., Bénar, C., Michel, C. M., & Koenig, T. W. (2019) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2019.2913928 · Cited by 236 · see citing works

Cortical alpha oscillations as a tool for auditory selective inhibition

Strauß, A., Wöstmann, M., & Obleser, J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00350 · Cited by 227 · see citing works

Phase-amplitude coupling at the organism level: The amplitude of spontaneous alpha rhythm fluctuations varies with the phase of the infra-slow gastric basal rhythm

Richter, C. G., Babo-Rebelo, M., Schwartz, D., & Tallon-Baudry, C. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.043 · Cited by 151 · see citing works

Ketamine Dysregulates the Amplitude and Connectivity of High-Frequency Oscillations in Cortical–Subcortical Networks in Humans: Evidence From Resting-State Magnetoencephalography-Recordings

Rivolta, D., Heidegger, T., Scheller, B., Sauer, A., Schaum, M., Birkner, K., Singer, W., Wibral, M., & Uhlhaas, P. J. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv051 · Cited by 145 · see citing works

Relating resting-state fMRI and EEG whole-brain connectomes across frequency bands

Deligianni, F., Centeno, M., Carmichael, D. W., & Clayden, J. D. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00258 · Cited by 136 · see citing works

Increased thalamic resting‐state connectivity as a core driver of LSD‐induced hallucinations

Müller, F., Lenz, C., Dolder, P. C., Lang, U. E., Schmidt, A., Liechti, M. E., & Borgwardt, S. (2017) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12818 · Cited by 137 · see citing works

Efficient Transfer Entropy Analysis of Non-Stationary Neural Time Series

Wollstadt, P., Martínez‐Zarzuela, M., Vicente, R., Pernas, F. J. D., & Wibral, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102833 · Cited by 133 · see citing works

Gamma Activity Coupled to Alpha Phase as a Mechanism for Top-Down Controlled Gating

Bonnefond, M., & Jensen, O. B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128667 · Cited by 128 · see citing works

Tactile remapping: from coordinate transformation to integration in sensorimotor processing

Heed, T., Buchholz, V. N., Engel, A. K., & Röder, B. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.03.001 · Cited by 126 · see citing works

Current findings and perspectives on aberrant neural oscillations in schizophrenia

Hirano, Y., & Uhlhaas, P. J. (2021) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13300 · Cited by 121 · see citing works

Enhanced Gamma Activity and Cross-Frequency Interaction of Resting-State Electroencephalographic Oscillations in Patients with Alzheimer’s Disease

Wang, J., Fang, Y., Wang, X., Yang, H., Yu, X., & Wang, H. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00243 · Cited by 122 · see citing works

Functional topography of the thalamocortical system in human

Yuan, R., Di, X., Taylor, P. A., Gohel, S., Tsai, Y., & Biswal, B. B. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1018-7 · Cited by 123 · see citing works

Neuronal Oscillations with Non-sinusoidal Morphology Produce Spurious Phase-to-Amplitude Coupling and Directionality

Lozano‐Soldevilla, D., ter Huurne, N., & Oostenveld, R. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00087 · Cited by 120 · see citing works

Measuring directionality between neuronal oscillations of different frequencies

Jiang, H., Bahramisharif, A., van Gerven, M. A. J., & Jensen, O. B. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.05.044 · Cited by 119 · see citing works

Genuine cross-frequency coupling networks in human resting-state electrophysiological recordings

Siebenhühner, F., Wang, S. H., Arnulfo, G., Lampinen, A., Nobili, L., Palva, J. M., & Palva, S. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000685 · Cited by 101 · see citing works

Thalamocortical excitability modulation guides human perception under uncertainty

Kosciessa, J. Q., Lindenberger, U., & Garrett, D. D. (2021) · Nature Communications · doi:10.1038/s41467-021-22511-7 · Cited by 101 · see citing works

Alpha Oscillatory Dynamics Index Temporal Expectation Benefits in Working Memory

Wilsch, A., Henry, M. J., Herrmann, B., Maeß, B., & Obleser, J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu004 · Cited by 100 · see citing works

Brainstorm Pipeline Analysis of Resting-State Data From the Open MEG Archive

Niso, G., Tadel, F., Bock, E. A., Cousineau, M., Santos, A., & Baillet, S. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00284 · Cited by 99 · see citing works

Alpha and theta brain oscillations index dissociable processes in spoken word recognition

Strauß, A., Kotz, S. A., Scharinger, M., & Obleser, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.005 · Cited by 98 · see citing works

Review of electroencephalography signals approaches for mental stress assessment

Attar, E. T. (2022) · Neurosciences · doi:10.17712/nsj.2022.4.20220025 · Cited by 98 · see citing works

Brain Functional Connectivity Through Phase Coupling of Neuronal Oscillations: A Perspective From Magnetoencephalography

Marzetti, L., Basti, A., Chella, F., D’Andrea, A., Syrjälä, J., & Pizzella, V. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00964 · Cited by 88 · see citing works

Neuropathic pain and pain interference are linked to alpha-band slowing and reduced beta-band magnetoencephalography activity within the dynamic pain connectome in patients with multiple sclerosis

Kim, J. A., Bosma, R. L., Hemington, K. S., Rogachov, A., Osborne, N. R., Cheng, J. C., Oh, J., Crawley, A. P., Dunkley, B. T., & Davis, K. D. (2018) · Pain · doi:10.1097/j.pain.0000000000001391 · Cited by 81 · see citing works

40-Hz Auditory Steady-State Responses Characterize Circuit Dysfunctions and Predict Clinical Outcomes in Clinical High-Risk for Psychosis Participants: A Magnetoencephalography Study

Grent-‘t-Jong, T., Gajwani, R., Groß, J., Gumley, A. I., Krishnadas, R., Lawrie, S. M., Schwannauer, M., Schultze‐Lutter, F., & Uhlhaas, P. J. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.03.018 · Cited by 79 · see citing works

Oscillatory Mechanisms of Stimulus Processing and Selection in the Visual and Auditory Systems: State-of-the-Art, Speculations and Suggestions

Zoefel, B., & Rufin Vanrullen, A. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00296 · Cited by 79 · see citing works

Non-linear auto-regressive models for cross-frequency coupling in neural time series

la Tour, T. D., Tallot, L., Grabot, L., Doyère, V., van Wassenhove, V., Grenier, Y., & Gramfort, A. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005893 · Cited by 76 · see citing works

Data-Driven Topological Filtering Based on Orthogonal Minimal Spanning Trees: Application to Multigroup Magnetoencephalography Resting-State Connectivity

Dimitriadis, S. I., Antonakakis, M., Simos, P. G., Fletcher, J. M., & Papanicolaou, A. C. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0512 · Cited by 71 · see citing works

Acute ketamine dysregulates task-related gamma-band oscillations in thalamo-cortical circuits in schizophrenia

Grent-‘t-Jong, T., Rivolta, D., Groß, J., Gajwani, R., Lawrie, S. M., Schwannauer, M., Heidegger, T., Wibral, M., Singer, W., Sauer, A., et al. (2018) · Brain · doi:10.1093/brain/awy175 · Cited by 66 · see citing works

Measuring transient phase-amplitude coupling using local mutual information

Martínez-Cancino, R., Heng, J., Arnaud Delorme, A., Kreutz-Delgado, K., Sotero, R. C., & Makeig, S. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.034 · Cited by 64 · see citing works

Toward understanding thalamocortical dysfunction in schizophrenia through computational models of neural circuit dynamics

Murray, J. D., & Anticevic, A. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.10.021 · Cited by 62 · see citing works

Revealing Cross-Frequency Causal Interactions During a Mental Arithmetic Task Through Symbolic Transfer Entropy: A Novel Vector-Quantization Approach

Dimitriadis, S. I., Sun, Y., Laskaris, N., Thakor, N. V., & Bezerianos, A. (2016) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2016.2516107 · Cited by 60 · see citing works

Reduced predictable information in brain signals in autism spectrum disorder

Gómez, C., Lizier, J. T., Schaum, M., Wollstadt, P., Grützner, C., Uhlhaas, P., Freitag, C. M., Schlitt, S., Bölte, S., Hornero, R., et al. (2014) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2014.00009 · Cited by 59 · see citing works

Data-driven causal analysis of observational biological time series

Yuan, A. E., & Shou, W. (2022) · eLife · doi:10.7554/elife.72518 · Cited by 58 · see citing works

Abnormal alpha band power in the dynamic pain connectome is a marker of chronic pain with a neuropathic component

Kisler, L. B., Kim, J. A., Hemington, K. S., Rogachov, A., Cheng, J. C., Bosma, R. L., Osborne, N. R., Dunkley, B. T., Inman, R. D., & Davis, K. D. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102241 · Cited by 58 · see citing works

Oscillatory brain activity in the alpha range is modulated by the content of word‐prompted mental imagery

Bartsch, F., Hamuni, G., Miskovic, V., Lang, P. J., & Keil, A. (2015) · Psychophysiology · doi:10.1111/psyp.12405 · Cited by 57 · see citing works

Cell-specific abnormalities of glutamate transporters in schizophrenia: sick astrocytes and compensating relay neurons?

McCullumsmith, R. E., O'Donovan, S. M., Drummond, J. B., Benesh, F., Simmons, M. S., Roberts, R. C., Lauriat, T. L., Haroutunian, V. H., & Meador‐Woodruff, J. H. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.148 · Cited by 56 · see citing works

Low-frequency alternating current stimulation rhythmically suppresses gamma-band oscillations and impairs perceptual performance

Herring, J., Esterer, S., Marshall, T. R., Jensen, O. B., & Bergmann, T. O. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.047 · Cited by 54 · see citing works

A thalamocortical pathway for fast rerouting of tactile information to occipital cortex in congenital blindness

Mueller, F., Niso, G., Samiee, S., Ptito, M., Baillet, S., & Kupers, R. C. (2019) · Nature Communications · doi:10.1038/s41467-019-13173-7 · Cited by 56 · see citing works

Pulvino-cortical interaction: An integrative role in the control of attention

Bourgeois, A., Guedj, C., Carrera, E., & Vuilleumier, P. O. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.005 · Cited by 55 · see citing works

High gamma cortical processing of continuous speech in younger and older listeners

Kulasingham, J. P., Brodbeck, C. J., Presacco, A., Kuchinsky, S. E., Anderson, S., & Simon, J. Z. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117291 · Cited by 52 · see citing works

Enriched Environment and Social Isolation Affect Cognition Ability via Altering Excitatory and Inhibitory Synaptic Density in Mice Hippocampus

Wang, H., Xu, X., Xu, X., Gao, J., & Zhang, T. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03102-2 · Cited by 48 · see citing works

Laminar Distribution of Phase-Amplitude Coupling of Spontaneous Current Sources and Sinks

Sotero, R. C., Bortel, A. B., Naaman, S., Mocanu, V. M., Kropf, P., Villeneuve, M. Y., & Shmuel, A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00454 · Cited by 47 · see citing works

Using generative models to make probabilistic statements about hippocampal engagement in MEG

Meyer, S. S., Rossiter, H. E., Brookes, M. J., Woolrich, M. W., Bestmann, S., & Barnes, G. R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.029 · Cited by 47 · see citing works

Magnetoencephalography as a Tool in Psychiatric Research: Current Status and Perspective

Uhlhaas, P. J., Liddle, P. F., Linden, D. E. J., Nobre, A. C., Singh, K. D., & Groß, J. (2017) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2017.01.005 · Cited by 46 · see citing works

Top-down control of cortical gamma-band communication via pulvinar induced phase shifts in the alpha rhythm

Quax, S. C., Jensen, O. B., & Tiesinga, P. H. E. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005519 · Cited by 47 · see citing works

Gamma oscillations modulate working memory recall precision

Thompson, L., Khuc, J., Saccani, M. S., Zokaei, N., & Cappelletti, M. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06051-6 · Cited by 44 · see citing works

A biologically plausible mechanism for neuronal coding organized by the phase of alpha oscillations

Gips, B., van der Eerden, J. P. J. M., & Jensen, O. B. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13318 · Cited by 42 · see citing works

Thalamo-cortical communication, glutamatergic neurotransmission and neural oscillations: A unique window into the origins of ScZ?

Pratt, J. A., Dawson, N., Morris, B. J., Grent-‘t-Jong, T., Roux, F., & Uhlhaas, P. J. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.05.013 · Cited by 40 · see citing works

Alpha oscillations control cortical gain by modulating excitatory-inhibitory background activityPreprint

Peterson, E. J., & Voytek, B. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/185074 · Cited by 42 · see citing works

The Functional Role of Thalamocortical Coupling in the Human Motor Network

Opri, E., Cernera, S., Okun, M. S., Foote, K. D., & Gunduz, A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1153-19.2019 · Cited by 40 · see citing works

Exploring sex differences in alpha brain activity as a potential neuromarker associated with neuropathic pain

Fauchon, C., Kim, J. A., El‐Sayed, R., Osborne, N. R., Rogachov, A., Cheng, J. C., Hemington, K. S., Bosma, R. L., Dunkley, B. T., Oh, J., et al. (2021) · Pain · doi:10.1097/j.pain.0000000000002491 · Cited by 38 · see citing works

Formation of visual memories controlled by gamma power phase-locked to alpha oscillations

Park, H., Lee, D. S., Kang, E., Kang, H., Hahm, J., Kim, J. S., Chung, C. K., Jiang, H., Groß, J., & Jensen, O. B. (2016) · Scientific Reports · doi:10.1038/srep28092 · Cited by 38 · see citing works

Intrinsic frequency biases and profiles across human cortex

Mellem, M. S., Wohltjen, S., Gotts, S. J., Ghuman, A. S., & Martin, A. D. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00061.2017 · Cited by 35 · see citing works

Magnetoencephalography: physics, techniques, and applications in the basic and clinical neurosciences

Kim, J. A., & Davis, K. D. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00530.2020 · Cited by 35 · see citing works

Excitation-Inhibition Imbalance in Migraine: From Neurotransmitters to Brain Oscillations

O’Hare, L., Tarasi, L., Asher, J. M., Hibbard, P. B., & Romei, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210093 · Cited by 35 · see citing works

Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS

Schoonhoven, D. N., Fraschini, M., Tewarie, P. K. B., Uitdehaag, B. M. J., Eijlers, A. J. C., Geurts, J. J. G., Hillebrand, A., Schoonheim, M. M., Stam, C. J., & Strijbis, E. M. M. (2018) · Multiple Sclerosis Journal · doi:10.1177/1352458518810260 · Cited by 34 · see citing works

Effects of Task Complexity on Motor Imagery-Based Brain–Computer Interface

Mashat, M. E. M., Lin, C., & Zhang, D. (2019) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2019.2936987 · Cited by 32 · see citing works

Top–Down Control of Alpha Phase Adjustment in Anticipation of Temporally Predictable Visual Stimuli

Solís‐Vivanco, R., Jensen, O. B., & Bonnefond, M. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01280 · Cited by 32 · see citing works

Reduction of somatosensory functional connectivity by transcranial alternating current stimulation at endogenous mu-frequency

Gundlach, C., Müller, M. M., Hoff, M., Ragert, P., Nierhaus, T., Villringer, A., & Sehm, B. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117175 · Cited by 32 · see citing works

Resting-State Electroencephalography for Prognosis in Disorders of Consciousness Following Traumatic Brain Injury

Pauli, R., O’Donnell, A., & Cruse, D. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.586945 · Cited by 31 · see citing works

Anterior Thalamic High Frequency Band Activity Is Coupled with Theta Oscillations at Rest

Sweeney‐Reed, C. M., Zaehle, T., Voges, J., Schmitt, F. C., Buentjen, L., Borchardt, V., Walter, M., Hinrichs, H., Heinze, H., Rugg, M. D., et al. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00358 · Cited by 30 · see citing works

Multi-modal and multi-model interrogation of large-scale functional brain networks

Castaldo, F., dos Santos, F. P., Timms, R. C., Cabral, J., Vohryzek, J., Deco, G., Woolrich, M. W., Friston, K. J., Verschure, P. F. M. J., & Vladimir Litvak, A. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120236 · Cited by 30 · see citing works

Neural oscillations as a translational tool in schizophrenia research: Rationale, paradigms and challenges

Phillips, K. G., & Uhlhaas, P. J. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881114562093 · Cited by 29 · see citing works

EEG Phase-Amplitude Coupling Strength and Phase Preference: Association with Age over the First Three Years after Birth

Mariscal, M. G., Levin, A. R., Gabard-Durnam, L. J., Xie, W., Tager-Flusberg, H. B., & Nelson, C. A. (2021) · eNeuro · doi:10.1523/eneuro.0264-20.2021 · Cited by 35 · see citing works

Metacognition of attention during tactile discrimination

Whitmarsh, S., Oostenveld, R., Almeida, R., & Lundqvist, D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.070 · Cited by 26 · see citing works

Generators and Connectivity of the Early Auditory Evoked Gamma Band Response

Polomac, N., Leicht, G., Nolte, G., Andreou, C., Schneider, T. R., Steinmann, S., Engel, A. K., & Mulert, C. (2015) · Brain Topography · doi:10.1007/s10548-015-0434-6 · Cited by 24 · see citing works

Overview of MEG

Ahlfors, S. P., & Mody, M. (2016) · Organizational Research Methods · doi:10.1177/1094428116676344 · Cited by 27 · see citing works

Dynamic spatiotemporal variability of alpha-BOLD relationships during the resting-state and task-evoked responses

Mayhew, S. D., & Bagshaw, A. P. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.04.051 · Cited by 25 · see citing works

The prognostic value of resting-state EEG in acute post-traumatic unresponsive states

O’Donnell, A., Pauli, R., Banellis, L., Sokoliuk, R., Hayton, T., Sturman, S., Veenith, T., Yakoub, K. M., Belli, A., Chennu, S., et al. (2021) · Brain Communications · doi:10.1093/braincomms/fcab017 · Cited by 24 · see citing works

Functional role of induced gamma oscillatory responses in processing noxious and innocuous sensory events in humans

Liu, C. C., Chien, J. H., Chang, Y. W., Kim, J. H., Anderson, W. S., & Lenz, F. A. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.047 · Cited by 23 · see citing works

(Neural) Syntax

Boeckx, C. A., & Theofanopoulou, C. (2018) · Cambridge University Press eBooks · doi:10.1017/9781316591529.016 · Cited by 22 · see citing works

Thalamocortical dysrhythmia in patients with schizophrenia spectrum disorder and individuals at clinical high risk for psychosis

Kim, M., Lee, T. H., Park, H., Moon, S., Lho, S. K., & Kwon, J. S. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01180-6 · Cited by 22 · see citing works

Light modulates task-dependent thalamo-cortical connectivity during an auditory attentional task

Paparella, I., Campbell, I., Sharifpour, R., Beckers, E., Berger, A., Aizpurua, J. F. B., Koshmanova, E., Mortazavi, N., Talwar, P., Degueldre, C., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05337-5 · Cited by 22 · see citing works

Alpha-gamma phase amplitude coupling subserves information transfer during perceptual sequence learning

Tzvi, E., Bauhaus, L. J., Kessler, T. U., Liebrand, M., Wöstmann, M., & Krämer, U. M. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.02.019 · Cited by 21 · see citing works

A Neurophysiological Perspective on a Preventive Treatment against Schizophrenia Using Transcranial Electric Stimulation of the Corticothalamic Pathway

Pinault, D. (2017) · Brain Science · doi:10.3390/brainsci7040034 · Cited by 22 · see citing works

The Functional Alterations in Top-Down Attention Streams of Parkinson’s disease Measured by EEG

Yoo, H. B., de la Concha, E. O., Ridder, D. D., Pickut, B. A., & Vanneste, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-29036-y · Cited by 21 · see citing works

Modelling the effects of ongoing alpha activity on visual perception: The oscillation-based probability of response

Zazio, A., Schreiber, M., Miniussi, C., & Bortoletto, M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.037 · Cited by 20 · see citing works

A neural mass model of phase–amplitude coupling

Chehelcheraghi, M., Nakatani, C., Steur, E., & van Leeuwen, C. (2016) · Biological Cybernetics · doi:10.1007/s00422-016-0687-5 · Cited by 18 · see citing works

The Early Subcortical Response at the Fundamental Frequency of Speech Is Temporally Separated from Later Cortical Contributions

Schüller, A., Schilling, A., Krauß, P., & Reichenbach, T. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02103 · Cited by 18 · see citing works

Phase-Amplitude Coupling of Neural Oscillations Can Be Effectively Probed with Concurrent TMS-EEG

Glim, S., Okazaki, Y. O., Nakagawa, Y., Mizuno, Y., Hanakawa, T., & Kitajo, K. (2019) · Neural Plasticity · doi:10.1155/2019/6263907 · Cited by 18 · see citing works

Efficacy of an Integrative Treatment for Tinnitus Combining Music and Cognitive-Behavioral Therapy—Assessed With Behavioral and EEG Data

Feng, T., Wang, M., Xiong, H., Zheng, Y., & Yang, H. (2020) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2020.00012 · Cited by 18 · see citing works

Magnetoencephalography detects phase-amplitude coupling in Parkinson’s disease

Tanaka, M., Yanagisawa, T., Fukuma, R., Tani, N., Oshino, S., Mihara, M., Hattori, N., Kajiyama, Y., Hashimoto, R., Ikeda, M., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-05901-9 · Cited by 17 · see citing works

Parietal alpha underlies slower cognitive responses during interference processing in adolescents

Mo, Z., Grennan, G., Kulkarni, A., Ramanathan, D., Balasubramani, P. P., & Mishra, J. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114356 · Cited by 16 · see citing works

High-gamma activity in an attention network predicts individual differences in elderly adults' behavioral performance

Akimoto, Y., Nozawa, T., Kanno, A., Ihara, M., Goto, T., Ogawa, T., Kambara, T., Sugiura, M., Okumura, E., & Kawashima, R. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.037 · Cited by 16 · see citing works

Prospects for Future Methodological Development and Application of Magnetoencephalography Devices in Psychiatry

Hironaga, N., Takei, Y., Mitsudo, T., Kimura, T., & Hirano, Y. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00863 · Cited by 17 · see citing works

Cortical oscillatory dysfunction in Parkinson disease during movement activation and inhibition

Disbrow, E. A., Glassy, N., Dressler, E. M., Russo, K., Franz, E. A., Turner, R. S., Ventura, M. I., Hinkley, L. B. N., Zweig, R. M., Nagarajan, S. S., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0257711 · Cited by 15 · see citing works

Theta–Alpha Connectivity in the Hippocampal–Entorhinal Circuit Predicts Working Memory Load

Li, J., Cao, D., Yu, S. P., Wang, H., Imbach, L., Stieglitz, L. H., Sarnthein, J., & Jiang, T. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0398-23.2023 · Cited by 17 · see citing works

Infragranular layers lead information flow during slow oscillations according to information directionality indicators

Amigó, J. M., Monetti, R., Tort‐Colet, N., & Sanchez-Vives, M. V. (2015) · Journal of Computational Neuroscience · doi:10.1007/s10827-015-0563-7 · Cited by 15 · see citing works

Single unit activities recorded in the thalamus and the overlying parietal cortex of subjects affected by disorders of consciousness

Magrassi, L., Zippo, A. G., Azzalin, A., Bastianello, S., Imberti, R., & Biella, G. E. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0205967 · Cited by 15 · see citing works

Successful Object Encoding Induces Increased Directed Connectivity in Presymptomatic Early-Onset Alzheimer’s Disease

Ochoa, J. F., Alonso, J. F., Duque, J. E., Tobón, C., Mañanas, M. Á., Lopera, F. J., & Hernández, A. M. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160803 · Cited by 15 · see citing works

Behavioral/Cognitive The Phase of Thalamic Alpha Activity Modulates Cortical Gamma-Band Activity: Evidence from Resting-State MEG Recordings

Wibral, M., Singer, W., Aru, J., & Uhlhaas, P. J. (2016)

doi: 10.3389/fnhum.2014.00187 Thalamo-cortical cross-frequency coupling detected

van Wijk, B. C. M., & FitzGerald, T. H. B. (2014)

Gamma Activity Coupled to Alpha Phase as a Mechanism for Top-Down Controlled Gating

Bonnefond, M., & Jensen, O. B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128667 · Cited by 128 · see citing works

RESEARCH ARTICLE Gamma Activity Coupled to Alpha Phase as a Mechanism for Top-Down Controlled Gating

Bonnefond, M., & Jensen, O. B. (2016)

Gamma amplitude coupled with alpha phase represents motor information before actual movements

Yanagisawa, T., Yamashita, O., Hirata, M., Kishima, H., Saitoh, Y., Goto, T., Yoshimine, T., & Kamitani, Y. (2011) · Neuroscience Research · doi:10.1016/j.neures.2011.07.419