Hemodynamic Signals Correlate Tightly with Synchronized Gamma Oscillations

Neurophysiological investigation of the basis of the fMRI signal

Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,542 · see citing works

Brain magnetic resonance imaging with contrast dependent on blood oxygenation.

Ogawa, S., Lee, T. M., Kay, A. R., & Tank, D. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9868 · Cited by 6,483 · see citing works

An Energy Budget for Signaling in the Grey Matter of the Brain

Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543 · see citing works

Dynamic predictions: Oscillations and synchrony in top–down processing

Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454 · see citing works

Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention

Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786 · see citing works

Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1

Boynton, G., Engel, S., Glover, G., & Heeger, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04207.1996 · Cited by 2,522 · see citing works

Neural foundations of imagery

Kosslyn, S. M., Ganis, G., & Thompson, W. L. (2001) · Nature Reviews Neuroscience · doi:10.1038/35090055 · Cited by 1,894 · see citing works

Increased Activity in Human Visual Cortex during Directed Attention in the Absence of Visual Stimulation

Kastner, S., Pinsk, M. A., De Weerd, P., Desimone, R., & Ungerleider, L. G. (1999) · Neuron · doi:10.1016/s0896-6273(00)80734-5 · Cited by 1,622 · see citing works

Brain magnetic resonance imaging with contrast-dependent oxygenation

Ogawa, S. (1990) · Medical Entomology and Zoology · Cited by 1,367 · see citing works

Sleep and arousal: thalamocortical mechanisms

McCormick, D. A., & Bal, T. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.185 · Cited by 1,267 · see citing works

Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals.

Frostig, R. D., Lieke, E. E., Ts’o, D. Y., & Grinvald, A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6082 · Cited by 948 · see citing works

A mechanism for generation of long-range synchronous fast oscillations in the cortex

Traub, R. D., Whittington, M. A., Stanford, I. M., & Jefferys, J. G. R. (1996) · Nature · doi:10.1038/383621a0 · Cited by 701 · see citing works

A direct quantitative relationship between the functional properties of human and macaque V5

Rees, G. E., Friston, K. J., & Christof Koch, A. (2000) · Nature Neuroscience · doi:10.1038/76673 · Cited by 656 · see citing works

Cortical GABA Interneurons in Neurovascular Coupling: Relays for Subcortical Vasoactive Pathways

Cauli, B., Tong, X., Rancillac, A., Serluca, N., Lambolez, B., Rossier, J., & Hamel, É. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3065-04.2004 · Cited by 568 · see citing works

Cellular Mechanisms Contributing to Response Variability of Cortical NeuronsIn Vivo

Azouz, R., & Gray, C. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02209.1999 · Cited by 408 · see citing works

How well do we understand the neural origins of the fMRI BOLD signal?

Arthurs, O. J., & Boniface, S. J. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01995-0 · Cited by 376 · see citing works

Modification of activity‐dependent increases of cerebral blood flow by excitatory synaptic activity and spikes in rat cerebellar cortex

Mathiesen, C., Caesar, K., Akgören, N., & Lauritzen, M. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.555be.x · Cited by 375 · see citing works

Arousal--Revisiting the Reticular Activating System

Steriade, M. (1996) · Science · doi:10.1126/science.272.5259.225 · Cited by 350 · see citing works

Cerebral energetics and spiking frequency: The neurophysiological basis of fMRI

Smith, A. J., Blumenfeld, H., Behar, K. L., Rothman, D. L., Shulman, R. G., & Hyder, F. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.132272199 · Cited by 349 · see citing works

Modulation of induced gamma band activity in the human EEG by attention and visual information processing

Müller, M. M., Gruber, T., & Keil, A. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(00)00171-9 · Cited by 272 · see citing works

Reading vascular changes in brain imaging: is dendritic calcium the key?

Lauritzen, M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1589 · Cited by 266 · see citing works

Prominent excitatory pathways in the cat visual cortex (A 17 and A 18): A current source density analysis of electrically evoked potentials

Mitzdorf, U., & Singer, W. (1978) · Experimental Brain Research · doi:10.1007/bf00235560 · Cited by 250 · see citing works

Short- and long-term effects of cholinergic modulation on gamma oscillations and response synchronization in the visual cortex

Rodriguez, R., Kallenbach, U., Singer, W., & Munk, M. H. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1839-04.2004 · Cited by 246 · see citing works

Precisely Synchronized Oscillatory Firing Patterns Require Electroencephalographic Activation

Herculano‐Houzel, S., Munk, M. H. J., Neuenschwander, S., & Singer, W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03992.1999 · Cited by 241 · see citing works

Neurons in rat cerebral cortex that synthesize nitric oxide: NADPH diaphorase histochemistry, NOS immunocytochemistry, and colocalization with GABA

Valtschanoff, J. G., Weinberg, R. J., Kharazia, V., et al. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90726-2 · Cited by 206 · see citing works

Modification of discharge patterns of neocortical neurons by induced oscillations of the membrane potential

Volgushev, M., Chistiakova, M., & Singer, W. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00380-1 · Cited by 176 · see citing works

Oscillatory synchrony and human visual cognition

Tallon‐Baudry, C. (2003) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2003.09.009 · Cited by 145 · see citing works

Linear coupling between functional magnetic resonance imaging and evoked potential amplitude in human somatosensory cortex

Arthurs, O. J., Williams, E. J., Carpenter, T. A., Pickard, J. D., & Boniface, S. J. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00511-x · Cited by 135 · see citing works

Evaluation of coupling between optical intrinsic signals and neuronal activity in rat somatosensory cortex

Sheth, S. A., Nemoto, M., Guiou, M., Walker, M. A., Pouratian, N., & Toga, A. W. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00086-7 · Cited by 132 · see citing works

A Comparison of Hemodynamic and Neural Responses in Cat Visual Cortex Using Complex Stimuli

Kayser, C. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh047 · Cited by 110 · see citing works

Spatial/temporal correlation of BOLD and optical intrinsic signals in humans

Pouratian, N., Sicotte, N. L., Rex, D., Martin, N. A., Becker, D., Cannestra, A. F., & Toga, A. W. (2002) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10096 · Cited by 68 · see citing works

Processing Deficits in Primary Visual Cortex of Amblyopic Cats

Schmidt, K. E., Singer, W., & Galuske, R. A. W. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00878.2003 · Cited by 28 · 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

High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex

Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works

Neural synchrony in brain disorders: Relevance for cognitive dysfunctions and pathophysiology

Uhlhaas, P. J., & Singer, W. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.020 · Cited by 2,194 · see citing works

Low-frequency neuronal oscillations as instruments of sensory selection

Schroeder, C. E., & Lakatos, P. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.012 · Cited by 1,528 · see citing works

Visual areas exert feedforward and feedback influences through distinct frequency channels

Bastos, A. M., Vezoli, J., Bosman, C. A., Schoffelen, J.-M., Oostenveld, R., Dowdall, J. R., De Weerd, P., Kennedy, H., & Fries, P. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.018 · Cited by 1,320 · see citing works

Cortical oscillations and sensory predictions

Arnal, L. H., & Giraud, A.-L. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.05.003 · Cited by 1,114 · see citing works

Network abnormalities and interneuron dysfunction in Alzheimer disease

Palop, J. J., & Mucke, L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.141 · Cited by 1,022 · see citing works

Neural basis of global resting-state fMRI activity

Schölvinck, M. L., Maier, A., Ye, F. Q., Duyn, J. H., & Leopold, D. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913110107 · Cited by 939 · see citing works

Negative functional MRI response correlates with decreases in neuronal activity in monkey visual area V1

Shmuel, A., Augath, M., Oeltermann, A., & Logothetis, N. K. (2006) · Nature Neuroscience · doi:10.1038/nn1675 · Cited by 898 · see citing works

Adolescence as a neurobiological critical period for the development of higher-order cognition

Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853 · see citing works

Neural Correlates of High-Gamma Oscillations (60–200 Hz) in Macaque Local Field Potentials and Their Potential Implications in Electrocorticography

Ray, S., Crone, N. E., Niebur, E., Franaszczuk, P. J., & Hsiao, S. S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2848-08.2008 · Cited by 722 · see citing works

White matter maturation reshapes structural connectivity in the late developing human brain

Hagmann, P., Sporns, O., Madan, N., Cammoun, L., Pienaar, R., Wedeen, V. J., Meuli, R., Thiran, J.-P., & Grant, P. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009073107 · Cited by 700 · see citing works

Electrophysiological correlates of the brain's intrinsic large-scale functional architecture

He, B. J., Snyder, A. Z., Zempel, J. M., Smyth, M. D., & Raichle, M. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807010105 · Cited by 670 · see citing works

Promises and limitations of human intracranial electroencephalography

Parvizi, J., & Kastner, S. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0108-2 · Cited by 631 · see citing works

Coupling between Neuronal Firing Rate, Gamma LFP, and BOLD fMRI Is Related to Interneuronal Correlations

Nir, Y., Fisch, L., Mukamel, R., Gelbard-Sagiv, H., Arieli, A., Fried, I., & Malach, R. (2007) · Current Biology · doi:10.1016/j.cub.2007.06.066 · Cited by 621 · see citing works

Slow cortical dynamics and the accumulation of information over long timescales

Honey, C. J., Thesen, T., Donner, T. H., Silbert, L. J., Carlson, C. E., Devinsky, O., Doyle, W. K., Rubin, N., Heeger, D. J., & Hasson, U. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.011 · Cited by 532 · see citing works

The default-mode, ego-functions and free-energy: a neurobiological account of Freudian ideas

Carhart-Harris, R. L., & Friston, K. J. (2010) · Brain · doi:10.1093/brain/awq010 · Cited by 574 · see citing works

Neural synchrony and the development of cortical networks

Uhlhaas, P. J., Roux, F., Rodriguez, E., Rotarska-Jagiela, A., & Singer, W. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.12.002 · Cited by 532 · see citing works

Alterations in Cortical Network Oscillations and Parvalbumin Neurons in Schizophrenia

Gonzalez-Burgos, G., Cho, R. Y., & Lewis, D. A. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.010 · Cited by 497 · see citing works

Concurrent TMS-fMRI and Psychophysics Reveal Frontal Influences on Human Retinotopic Visual Cortex

Ruff, C. C., Blankenburg, F., Bjoertomt, O., Bestmann, S., Freeman, E., Haynes, J.-D., Rees, G., Josephs, O., Deichmann, R., & Driver, J. (2006) · Current Biology · doi:10.1016/j.cub.2006.06.057 · Cited by 514 · see citing works

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

Travis, F., & Shear, J. (2010) · Consciousness and Cognition · doi:10.1016/j.concog.2010.01.007 · Cited by 522 · see citing works

Single-trial EEG–fMRI reveals the dynamics of cognitive function

Debener, S., Ullsperger, M., Siegel, M., & Engel, A. K. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.09.010 · Cited by 428 · see citing works

Energy-Efficient Action Potentials in Hippocampal Mossy Fibers

Alle, H., Roth, A., & Geiger, J. R. P. (2009) · Science · doi:10.1126/science.1174331 · Cited by 429 · see citing works

Rolandic alpha and beta EEG rhythms' strengths are inversely related to fMRI‐BOLD signal in primary somatosensory and motor cortex

Ritter, P., Moosmann, M., & Villringer, A. (2009) · Human Brain Mapping · doi:10.1002/hbm.20585 · Cited by 400 · see citing works

Neurometabolic coupling in cerebral cortex reflects synaptic more than spiking activity

Viswanathan, A., & Freeman, R. D. (2007) · Nature Neuroscience · doi:10.1038/nn1977 · Cited by 397 · see citing works

Frontal theta EEG activity correlates negatively with the default mode network in resting state

Scheeringa, R., Bastiaansen, M. C. M., Petersson, K. M., Oostenveld, R., Norris, D. G., & Hagoort, P. (2008) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2007.05.017 · Cited by 400 · see citing works

Transitions in neural oscillations reflect prediction errors generated in audiovisual speech

Arnal, L. H., Wyart, V., & Giraud, A.-L. (2011) · Nature Neuroscience · doi:10.1038/nn.2810 · Cited by 353 · see citing works

The development of neural synchrony reflects late maturation and restructuring of functional networks in humans

Uhlhaas, P. J., Roux, F., Singer, W., Haenschel, C., Sireteanu, R., & Rodriguez, E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900390106 · Cited by 356 · see citing works

Recent advances in the neuropsychopharmacology of serotonergic hallucinogens

Halberstadt, A. L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.016 · Cited by 312 · see citing works

Highly energized inhibitory interneurons are a central element for information processing in cortical networks.

Kann, O., Papageorgiou, I. E., & Draguhn, A. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.104 · Cited by 295 · see citing works

Entrainment of Arteriole Vasomotor Fluctuations by Neural Activity Is a Basis of Blood-Oxygenation-Level-Dependent “Resting-State” Connectivity

Mateo, C., Knutsen, P. M., Tsai, P. S., Shih, A. Y., & Kleinfeld, D. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.012 · Cited by 303 · see citing works

Movement related activity in the high gamma range of the human EEG

Ball, T., Demandt, E., Mutschler, I., Neitzel, E., Mehring, C., Vogt, K., Aertsen, A., & Schulze-Bonhage, A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.02.032 · Cited by 274 · see citing works

Alterations of cortical GABA neurons and network oscillations in schizophrenia

Gonzalez-Burgos, G., Hashimoto, T., & Lewis, D. A. (2010) · Current Psychiatry Reports · doi:10.1007/s11920-010-0124-8 · Cited by 260 · see citing works

Ketamine has distinct electrophysiological and behavioral effects in depressed and healthy subjects

Nugent, A. C., Ballard, E. D., Gould, T. D., Park, L. T., Moaddel, R., Brutsche, N. E., & Zarate, C. A. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0028-2 · Cited by 250 · see citing works

Primary visual cortex activity along the apparent-motion trace reflects illusory perception

Muckli, L., Kohler, A., Kriegeskorte, N., & Singer, W. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030265 · Cited by 225 · see citing works

Spatiotemporal dynamics of electrocorticographic high gamma activity during overt and covert word repetition

Pei, X., Leuthardt, E. C., Gaona, C. M., Brunner, P., Wolpaw, J. R., & Schalk, G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.029 · Cited by 204 · see citing works

Endogenous brain oscillations and related networks detected by surface EEG‐combined fMRI

Laufs, H. (2008) · Human Brain Mapping · doi:10.1002/hbm.20600 · Cited by 194 · see citing works

Learning what to expect (in visual perception)

Seriès, P., & Seitz, A. R. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00668 · Cited by 194 · see citing works

The relationship between oscillatory EEG activity and the laminar-specific BOLD signal

Scheeringa, R., Koopmans, P. J., van Mourik, T., Jensen, O., & Norris, D. G. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522577113 · Cited by 162 · see citing works

Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria

Kann, O., Huchzermeyer, C., Kovács, R., Wirtz, S., & Schuelke, M. (2011) · Brain · doi:10.1093/brain/awq333 · Cited by 189 · see citing works

Dissociation of broadband high-frequency activity and neuronal firing in the neocortex

Leszczyński, M., Barczak, A., Kajikawa, Y., Ulbert, I., Falchier, A. Y., Tal, I., Haegens, S., Melloni, L., Knight, R. T., & Schroeder, C. E. (2020) · Science Advances · doi:10.1126/sciadv.abb0977 · Cited by 188 · see citing works

Local field potential reflects perceptual suppression in monkey visual cortex

Wilke, M., Logothetis, N. K., & Leopold, D. A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604673103 · Cited by 187 · see citing works

Electrophysiological correlates of the BOLD signal for EEG-informed fMRI

Murta, T., Leite, M., Carmichael, D. W., Figueiredo, P., & Lemieux, L. (2015) · Human Brain Mapping · doi:10.1002/hbm.22623 · Cited by 165 · 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

Electrophysiological Low-Frequency Coherence and Cross-Frequency Coupling Contribute to BOLD Connectivity

Wang, L., Saalmann, Y. B., Pinsk, M. A., Arcaro, M. J., & Kastner, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.033 · Cited by 158 · see citing works

Direct electrophysiological measurement of human default network areas

Miller, K. J., Weaver, K. E., & Ojemann, J. G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902071106 · Cited by 149 · see citing works

The Entwined Mysteries of Anesthesia and Consciousness: Is There a Common Underlying Mechanism?

Hameroff, S. R. (2006) · Anesthesiology · doi:10.1097/00000542-200608000-00024 · Cited by 129 · see citing works

fMRI evidence for multisensory recruitment associated with rapid eye movements during sleep.

Hong, C. C., Harris, J. C., Pearlson, G. D., Kim, J., Calhoun, V. D., Fallon, J. H., Golay, X., Gillen, J. S., Simmonds, D. J., van Zijl, P. C. M., et al. (2009) · Human Brain Mapping · doi:10.1002/hbm.20635 · Cited by 124 · see citing works

Local hippocampal fast gamma rhythms precede brain-wide hyperemic patterns during spontaneous rodent REM sleep

Bergel, A., Deffieux, T., Demené, C., Tanter, M., & Cohen, I. (2018) · Nature Communications · doi:10.1038/s41467-018-07752-3 · Cited by 117 · see citing works

Emotional Automaticity Is a Matter of Timing

Luo, Q., Holroyd, T., Majestic, C., Cheng, X., Schechter, J., & Blair, R. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.bc-5668-09.2010 · Cited by 118 · see citing works

Broadband Electrophysiological Dynamics Contribute to Global Resting-State fMRI Signal

Wen, H., & Liu, Z. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0187-16.2016 · Cited by 100 · see citing works

Estimating the transfer function from neuronal activity to BOLD using simultaneous EEG-fMRI

Rosa, M. J., Kilner, J., Blankenburg, F., Josephs, O., & Penny, W. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.011 · Cited by 105 · see citing works

MR connectomics: a conceptual framework for studying the developing brain

Hagmann, P., Grant, P. E., & Fair, D. A. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00043 · Cited by 96 · see citing works

fMRI–EEG integrated cortical source imaging by use of time-variant spatial constraints

Liu, Z., & He, B. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.003 · Cited by 103 · see citing works

On the relationship between slow cortical potentials and BOLD signal changes in humans

Khader, P., Schicke, T., Röder, B., & Rösler, F. (2008) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2007.05.018 · Cited by 99 · see citing works

Heterogeneous Single-Unit Selectivity in an fMRI-Defined Body-Selective Patch

Popivanov, I. D., Jastorff, J., Vanduffel, W., & Vogels, R. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2748-13.2014 · Cited by 90 · see citing works

Cortical layers, rhythms and BOLD signals

Scheeringa, R., & Fries, P. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.002 · Cited by 88 · see citing works

A trio of concerns

Kagan, J. (2007) · Perspectives on Psychological Science · doi:10.1111/j.1745-6916.2007.00049.x · Cited by 84 · see citing works

Oxygen Consumption Rates during Three Different Neuronal Activity States in the Hippocampal CA3 Network

Huchzermeyer, C., Berndt, N., Holzhütter, H.-G., & Kann, O. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.165 · Cited by 81 · see citing works

Neuroelectromagnetic correlates of perceptual closure processes

Grutzner, C., Uhlhaas, P. J., Genc, E., Kohler, A., Singer, W., & Wibral, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5434-09.2010 · Cited by 77 · see citing works

Gradual emergence of spontaneous correlated brain activity during fading of general anesthesia in rats: evidences from fMRI and local field potentials

Bettinardi, R. G., Tort-Colet, N., Ruiz-Mejias, M., Sanchez-Vives, M. V., & Deco, G. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.03.037 · Cited by 68 · see citing works

Population receptive fields in nonhuman primates from whole-brain fMRI and large-scale neurophysiology in visual cortex

Klink, P. C., Chen, X., Vanduffel, W., & Roelfsema, P. R. (2021) · eLife · doi:10.7554/elife.67304 · Cited by 63 · see citing works

Fast oscillatory activity in the anterior cingulate cortex: dopaminergic modulation and effect of perineuronal net loss

Steullet, P., Cabungcal, J.-H., Cuénod, M., & Do, K. Q. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00244 · Cited by 49 · see citing works

Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states

Natsubori, A., Tsunematsu, T., Karashima, A., Imamura, H., Kabe, N., Trevisiol, A., Hirrlinger, J., Kodama, T., Sanagi, T., Masamoto, K., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-01215-6 · Cited by 54 · see citing works

Executive functions and prefrontal cortex: a matter of persistence?

Ball, G., Stokes, P. R., Rhodes, R. A., Bose, S. K., Rezek, I., Wink, A.-M., Lord, L.-D., Mehta, M. A., Grasby, P. M., & Turkheimer, F. E. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00003 · Cited by 50 · see citing works

Intrinsic Connectivity Networks of Glutamate-Mediated Antidepressant Response: A Neuroimaging Review

Demchenko, I., Tassone, V. K., Kennedy, S. H., Dunlop, K., & Bhat, V. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.864902 · Cited by 29 · see citing works

Untitled work

Theriault (n.d.) · doi:10.31234/osf.io/pkzr8 · Cited by 51 · see citing works

Plastic vasomotion entrainment

Sasaki, D., Imai, K., Ikoma, Y., & Matsui, K. (2024) · eLife · doi:10.7554/elife.93721.3 · Cited by 6 · see citing works

Response Properties of Local Field Potentials and Neighboring Single Neurons in Awake Primary Visual Cortex

Lashgari, R., Li, X., Chen, Y., Kremkow, J., Bereshpolova, Y., Swadlow, H. A., & Alonso, J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0429-12.2012 · Cited by 46 · see citing works

LFP Power Spectra in V1 Cortex: The Graded Effect of Stimulus Contrast

Henrie, J. A., & Shapley, R. M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00919.2004 · Cited by 425 · see citing works

Local Origin of Field Potentials in Visual Cortex

Katzner, S., Nauhaus, I., Benucci, A., Bonin, V., Ringach, D. L., & Carandini, M. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.016 · Cited by 552 · see citing works

Spatial Spread of the Local Field Potential and its Laminar Variation in Visual Cortex

Xing, D., Yeh, C.-I., & Shapley, R. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2573-09.2009 · Cited by 246 · see citing works

Spectral Analysis of Local Field Potentials from Rat Primary Visual Cortex (V1)

Ad, A. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/conf.fncom.2012.55.00087