Neurophysiological investigation of the basis of the fMRI signal

Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.

Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212

Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization.

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Neuronal Synchrony: A Versatile Code for the Definition of Relations?

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Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1

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Stimulus-specific neuronal oscillations in orientation columns of cat visual cortex

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Coherent oscillations: A mechanism of feature linking in the visual cortex?

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Time course EPI of human brain function during task activation

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Multi-planar image formation using NMR spin echoes

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Synchronization of cortical activity and its putative role in information processing and learning

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Dynamics of blood flow and oxygenation changes during brain activation: the Balloon model

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Prediction of Forelimb Reach Results From Motor Cortex Activities Based on Calcium Imaging and Deep Learning

Li, C., Chan, D. C. W., Yang, X., Ke, Y., & Yung, W. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00088 · Cited by 20

Glutamatergic response to a low load working memory paradigm in the left dorsolateral prefrontal cortex in patients with mild cognitive impairment: a functional magnetic resonance spectroscopy study

Vijayakumari, A. A., Menon, R. N., Thomas, B., Arun, T. M., Mohanan, N., & Kesavadas, C. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00122-7 · Cited by 20

Temporal tuning of repetition suppression across the visual cortex

Fritsche, M., Lawrence, S. J. D., & de Lange, F. P. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00582.2019 · Cited by 20

Mapping language from MEG beta power modulations during auditory and visual naming

Youssofzadeh, V., Stout, J. D., Ustine, C., Gross, W. L., Conant, L. L., Humphries, C., Binder, J. R., & Raghavan, M. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117090 · Cited by 21

Intraoperative mapping of executive function using electrocorticography for patients with low-grade gliomas

Erez, Y., Assem, M., Coelho, P., Romero-García, R., Owen, M., McDonald, A., Woodberry, E., Morris, R. C., Price, S. J., Suckling, J., et al. (2020) · Acta Neurochirurgica · doi:10.1007/s00701-020-04646-6 · Cited by 21

Altered Spontaneous Brain Activity Patterns and Functional Connectivity in Adults With Intermittent Exotropia: A Resting-State fMRI Study

He, X., Hong, J., Wang, Q., Guo, Y., Li, T., Qu, X., Liu, J., Li, W., Zhang, L., Fu, J. H., et al. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.746882 · Cited by 20

Cortical depth-dependent human fMRI of resting-state networks using EPIK

Pais‐Roldán, P., Yun, S. D., Palomero‐Gallagher, N., & Shah, N. J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1151544 · Cited by 20

pyElectrode: An open-source tool using structural MRI for electrode positioning and neuron mapping

Daye, P. M., Monosov, I. E., Hikosaka, O., Leopold, D. A., & Optican, L. M. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.12.012 · Cited by 20

Increased neural correlations in primate auditory cortex during slow-wave sleep

Issa, E. B., & Wang, X. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00695.2012 · Cited by 20

Synthesis of monodisperse and single-crystal Fe3O4 hollow spheres by a solvothermal approach

Shen, W., Chen, X., Shi, Y., Shi, M., & Chen, H. (2012) · Materials Chemistry and Physics · doi:10.1016/j.matchemphys.2011.12.046 · Cited by 20

Autism spectrum disorder, functional MRI and MR spectroscopy: possibilities and challenges

Hugdahl, K., Beyer, M. K., Brix, M. K., & Ersland, L. (2012) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v23i0.18960 · Cited by 20

Contour extracting networks in early extrastriate cortex

Dumoulin, S. O., Hess, R. F., May, K. A., Harvey, B. M., Rokers, B., & Barendregt, M. (2014) · Journal of Vision · doi:10.1167/14.5.18 · Cited by 20

Time-dependent effects of hyperoxia on the BOLD fMRI signal in primate visual cortex and LGN

Wibral, M., Muckli, L. F., Melnikovic, K., Scheller, B., Alink, A., Singer, W., & Munk, M. H. J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.039 · Cited by 20

Investigation of Cross-Species Translatability of Pharmacological MRI in Awake Nonhuman Primate - A Buprenorphine Challenge Study

Seah, S., Asad, A. B. A., Baumgartner, R., Dai, F., Williams, D. S., Manigbas, E., Beaver, J. D., Reese, T., Henry, B., Evelhoch, J. L., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110432 · Cited by 20

Measuring diffusion parameters in the brain: comparing the real‐time iontophoretic method and diffusion‐weighted magnetic resonance

Vorisek, I., & Syková, E. (2008) · Acta Physiologica · doi:10.1111/j.1748-1716.2008.01924.x · Cited by 20

Bridging the gap between physiology and behavior: Evidence from the sSoTS model of human visual attention.

Mavritsaki, E., Heinke, D. G., Allen, H. A., Deco, G., & Humphreys, G. W. (2011) · Psychological Review · doi:10.1037/a0021868 · Cited by 21

Investigations on spinal cord fMRI of cats under ketamine

Cohen‐Adad, J., Hoge, R. D., Leblond, H., Xie, G., Beaudoin, G., SONG, A., KRUEGER, G., Doyon, J., Benali, H., & Rossignol, S. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.023 · Cited by 20

Estimation of Optimal Location of EEG Reference Electrode for Motor Imagery Based BCI Using fMRI

Choi, S. H., Lee, M.-H., Wang, Y., & Hong, B. (2006) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.2006.260270 · Cited by 20

Identification of Cerebral Networks by Classification of the Shape of BOLD Responses

d’Avossa, G., Shulman, G. L., & Corbetta, M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01040.2002 · Cited by 20

Neuroplasticity: An Appreciation From Synapse to System

Gillick, B. T., & Zirpel, L. (2012) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2012.04.026 · Cited by 20

Probing Intrinsic Resting-State Networks in the Infant Rat Brain

Bajic, D., Craig, M. M., Borsook, D., & Becerra, L. R. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00192 · Cited by 21

Altered Default Mode Network on Resting-State fMRI in Children with Infantile Spasms

Wang, Y., Li, Y., Wang, H., Chen, Y., & Huang, W. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00209 · Cited by 20

Atlas of Morphology and Functional Anatomy of the Brain

Scarabino, T., & Salvolini, U. (2006) · Springer eBooks · doi:10.1007/3-540-29943-2 · Cited by 20

Frontal gamma-band activity in magnetoencephalogram during auditory oddball processing

Kaiser, J., & Lutzenberger, W. (2004) · Neuroreport · doi:10.1097/00001756-200410050-00008 · Cited by 20

Changes in BOLD transients with visual stimuli across 1–44Hz

Emir, U. E., Bayraktaroğlu, Z., Öztürk, C., Ademoğlu, A., & Demıralp, T. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.03.021 · Cited by 20

Information transfer rate in fMRI experiments measured using mutual information theory

Ward, B. D., & Mazaheri, Y. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.06.027 · Cited by 20

Correlation of Functional MR Imaging Activation Data with Simple Reaction Times

Oğuz, K. K., Browner, N., Calhoun, V. D., Wu, C. O., Kraut, M. A., & Yousem, D. M. (2003) · Radiology · doi:10.1148/radiol.2261020141 · Cited by 20

Functional magnetic resonance imaging in stroke recovery

Cramer, S. C. (2003) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/s1047-9651(02)00053-0 · Cited by 20

Further steps toward direct magnetic resonance (MR) imaging detection of neural action currents: Optimization of MR sensitivity to transient and weak currents in a conductor

Pell, G. S., Abbott, D. F., Fleming, S. W., Prichard, J. W., & Jackson, G. D. (2006) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20857 · Cited by 20

Neural systems underlying affective disorders

Surguladze, S., Keedwell, P. A., & Phillips, M. L. (2003) · Advances in Psychiatric Treatment · doi:10.1192/apt.9.6.446 · Cited by 20

Neurovascular coupling develops alongside neural circuits in the postnatal brain

Kozberg, M. G., & Hillman, E. M. C. (2016) · Neurogenesis · doi:10.1080/23262133.2016.1244439 · Cited by 20

Co-localization of theta-band activity and hemodynamic responses during face perception: simultaneous electroencephalography and functional near-infrared spectroscopy recordings

Dravida, S., Ono, Y., Noah, J. A., Zhang, X. Z., & Hirsch, J. (2019) · Neurophotonics · doi:10.1117/1.nph.6.4.045002 · Cited by 19

FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity

Fracasso, A., Gaglianese, A., Vansteensel, M. J., Aarnoutse, E. J., Ramsey, N. F., Dumoulin, S. O., & Petridou, N. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02342-4 · Cited by 19

Task-Related Modulation of Sensorimotor GABA+ Levels in Association with Brain Activity and Motor Performance: A Multimodal MRS–fMRI Study in Young and Older Adults

Maes, C., Cuypers, K., Peeters, R. R., Sunaert, S. G., Edden, R. A. E., Gooijers, J., & Swinnen, S. P. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1154-21.2021 · Cited by 19

Associations of lesion location, structural disconnection, and functional diaschisis with depressive symptoms post stroke

Klingbeil, J., Brandt, M.-L., Stockert, A., Baum, P., Hoffmann, K., Saur, D., & Wawrzyniak, M. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1144228 · Cited by 19

The transitive inference task to study the neuronal correlates of memory-driven decision making: A monkey neurophysiology perspective

Ramawat, S., Marc, I. B., Ceccarelli, F., Ferrucci, L., Bardella, G., Ferraina, S., Pani, P., & Brunamonti, E. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105258 · Cited by 19

Behavioral Economics and Neuroeconomics of Environmental Values

Koundouri, P., Hammer, B., Kuhl, U., & Velias, A. (2023) · Annual Review of Resource Economics · doi:10.1146/annurev-resource-101722-082743 · Cited by 19

MEBRAINS 1.0: A new population-based macaque atlas

Balan, P. F., Zhu, Q., Li, X., Niu, M., Rapan, L., Funck, T., Wang, H., Bakker, R., Palomero‐Gallagher, N., & Vanduffel, W. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00077 · Cited by 19

Rat superior colliculus encodes the transition between static and dynamic vision modes

Gil, R., Valente, M., & Shemesh, N. (2024) · Nature Communications · doi:10.1038/s41467-024-44934-8 · Cited by 19

Hippocampal replay sequence governed by spontaneous brain-wide dynamics

Yang, Y., Leopold, D. A., Duyn, J. H., & Liu, X. (2024) · PNAS Nexus · doi:10.1093/pnasnexus/pgae078 · Cited by 20

Changes in high-frequency aperiodic 1/f slope and periodic activity reflect post-stimulus functional inhibition in the visual cortex

Manyukhina, V. O., Prokofyev, A. O., Obukhova, T. S., Stroganova, T. A., & Orekhova, E. V. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00146 · Cited by 19

Neuroimaging Databases as a Resource for Scientific Discovery

Horn, J. D. V., Wolfe, J., Agnoli, A., Woodward, J. B., Schmitt, M. N., Dobson, J. E., Schumacher, S., & Vance, B. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)66002-3 · Cited by 19

Application of Partial Directed Coherence to the Analysis of Resting-State EEG-fMRI Data

Biazoli, C. E., Sturzbecher, M. J., White, T. P., Onias, H., Andrade, K. C., de Araújo, D. B., & Sato, J. R. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0135 · Cited by 19

Dynamic correlations between hemodynamic, metabolic, and neuronal responses to acute whole‐brain ischemia

Taylor, J. M., Zhu, X., Zhang, Y., & Chen, W. (2015) · NMR in Biomedicine · doi:10.1002/nbm.3408 · Cited by 19

Pattern motion representation in primary visual cortex is mediated by transcortical feedback

Schmidt, K. E., Lomber, S. G., Payne, B. R., & Galuske, R. A. W. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.017 · Cited by 19

Complex relationship between BOLD-fMRI and electrophysiological signals in different olfactory bulb layers

Li, B., Gong, L., Wu, R., Li, A., & Xu, F. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.052 · Cited by 19

Spatial homogeneity and task-synchrony of the trial-related hemodynamic signal

Sirotin, Y. B., Cardoso, M. M. B., Lima, B., & Das, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.019 · Cited by 19

Integration of fMRI, NIROT and ERP for studies of human brain function

Gore, J. C., Horovitz, S. G., Cannistraci, C. J., & Skudlarski, P. (2006) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2005.12.039 · Cited by 19

Assessment of rodent brain activity using combined [15O]H2O-PET and BOLD-fMRI

Wehrl, H. F., Martirosian, P., Schick, F., Reischl, G., & Pichler, B. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.044 · Cited by 19

The relation between functional magnetic resonance imaging activations and single-cell selectivity in the macaque intraparietal sulcus

Dromme, I. C. V., Vanduffel, W., & Janssen, P. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.03.023 · Cited by 19

Spatial attention enhances object coding in local and distributed representations of the lateral occipital complex

Guggenmos, M., Thoma, V., Haynes, J., Richardson‐Klavehn, A., Cichy, R. M., & Sterzer, P. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.004 · Cited by 19

Increased local synchronization of resting-state fMRI signal after episodic memory encoding reflects off-line memory consolidation

Wang, D.-Y., Liu, D., Li, S., & Zang, Y. (2012) · Neuroreport · doi:10.1097/wnr.0b013e3283587c96 · Cited by 20

Turning visual shapes into sounds: Early stages of reading acquisition revealed in the ventral occipitotemporal cortex

Perrone‐Bertolotti, M., Vidal, J. R., Palma, L. D., Hamamé, C. M., Ossandón, T., Kahane, P., Minotti, L., Bertrand, O., & Lachaux, J.-P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.12.027 · Cited by 20

Ultra high resolution fMRI at ultra-high field

Harel, N. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.018 · Cited by 20

MRI for coma emergence and recovery

Stevens, R. D., Hannawi, Y., & Puybasset, L. (2014) · Current Opinion in Critical Care · doi:10.1097/mcc.0000000000000069 · Cited by 19

Using an achiasmic human visual system to quantify the relationship between the fMRI BOLD signal and neural response

Bao, P., Purington, C. J., & Tjan, B. S. (2015) · eLife · doi:10.7554/elife.09600 · Cited by 20

Comprehending auditory speech: previous and potential contributions of functional MRI

Evans, S., & McGettigan, C. (2017) · Language Cognition and Neuroscience · doi:10.1080/23273798.2016.1272703 · Cited by 19

Mathematical analysis of the influence of brain metabolism on the BOLD signal in Alzheimer’s disease

Winter, F., Bludszuweit-Philipp, C., & Wolkenhauer, O. (2017) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x17693024 · Cited by 19

Tonotopic organisation of the auditory cortex in sloping sensorineural hearing loss

Wolak, T. P., Cieśla, K., Lorens, A., Kochanek, K., Lewandowska, M., Rusiniak, M., Pluta, A., Wójcik, J., & Skarżyńśki, H. (2017) · Hearing Research · doi:10.1016/j.heares.2017.09.012 · Cited by 19

Development of human electrophysiological brain networks

Briley, P. M., Liddle, E. B., Groom, M. J., Smith, H. J. F., Morris, P. G., Colclough, G. L., Brookes, M. J., & Liddle, P. F. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00293.2018 · Cited by 19

Imbalance of Functional Connectivity and Temporal Entropy in Resting-State Networks in Autism Spectrum Disorder: A Machine Learning Approach

Smith, R. X., Jann, K., Dapretto, M., & Wang, D. J. J. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00869 · Cited by 20

The relationship between negative BOLD responses and ERS and ERD of alpha/beta oscillations in visual and motor cortex

Wilson, R., Mullinger, K. J., Francis, S., & Mayhew, S. D. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.009 · Cited by 19

Single-cell selectivity and functional architecture of human lateral occipital complex

Decramer, T., Premereur, E., Uytterhoeven, M., Paesschen, W. V., Loon, J. V., Janssen, P., & Theys, T. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000280 · Cited by 22

Regional Spontaneous Neural Activity Alterations in Type 2 Diabetes Mellitus: A Meta-Analysis of Resting-State Functional MRI Studies

Liu, J., Li, Y., Yang, X., Xu, H., Ren, J., & Zhou, P. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.678359 · Cited by 19

Functional MRI of Awake Behaving Macaques Using Standard Equipment

Vanduffel, W., & Farivar, R. (2014) · InTech eBooks · doi:10.5772/58281 · Cited by 19

Comparative neuroimaging in children with cerebral palsy using fMRI and a novel EEG-based brain mapping during a motor task – A preliminary investigation

Lee, J. J., Lee, D. R., Shin, Y. K., Lee, N. G., Han, B. S., & You, S. H. (2013) · Neurorehabilitation · doi:10.3233/nre-130845 · Cited by 19

An Introduction to Magnetic Resonance Imaging: From Image Acquisition to Clinical Diagnosis

Revett, K. (2011) · Studies in computational intelligence · doi:10.1007/978-3-642-17934-1_7 · Cited by 19

Pattern‐motion selective responses in MT, MST and the pulvinar of humans

Villeneuve, M. Y., Thompson, B. S., Hess, R. F., & Casanova, C. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08205.x · Cited by 19

Physiological monitoring of small animals during magnetic resonance imaging

Mirsattari, S. M., Bihari, F., Leung, L.-W. S., Menon, R. S., Wang, Z., Ives, J. R., & Bartha, R. (2005) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2004.11.019 · Cited by 19

Illusions of Visual Motion Elicited by Electrical Stimulation of Human MT Complex

Rauschecker, A. M., Dastjerdi, M., Weiner, K. S., Witthoft, N., Chen, J., Selimbeyoglu, A., & Parvizi, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021798 · Cited by 19

Localization of MEG human brain responses to retinotopic visual stimuli with contrasting source reconstruction approaches

Cicmil, N., Bridge, H., Parker, A. J., Woolrich, M. W., & Krug, K. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00127 · Cited by 19

Neuronal synchronization in human parietal cortex during saccade planning

van der Werf, J., Buchholz, V. N., Jensen, O. B., & Medendorp, W. P. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.06.011 · Cited by 20

Fast (100–175 ms) components elicited bilaterally by language production as measured by three-wavelength optical imaging

Kubota, M., Inouchi, M., Dan, I., Tsuzuki, D., Ishikawa, A., & Scovel, T. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.079 · Cited by 19

Simultaneous VEP and transcranial Doppler ultrasound recordings to investigate activation-flow coupling in humans

Rosengarten, B., Molnar, S., Trautmann, J., & Kaps, M. (2006) · Ultrasound in Medicine & Biology · doi:10.1016/j.ultrasmedbio.2006.04.016 · Cited by 19

Modeling Mind and Matter: Reductionism and Psychological Measurement in Cognitive Neuroscience

Kievit, R., Romeijn, J., Waldorp, L., Wicherts, J. M., Scholte, H. S., & Borsboom, D. (2011) · Psychological Inquiry · doi:10.1080/1047840x.2011.567962 · Cited by 21

Social Neuroscience: A Role for Brain Imaging

Raichle, M. E. (2003) · Political Psychology · doi:10.1046/j.1467-9221.2003.00351.x · Cited by 19

Optogenetic auditory fMRI reveals the effects of visual cortical inputs on auditory midbrain response

Leong, A. T. L., Dong, C. M., Gao, P. P., Chan, R. W., To, A., Sanes, D. H., & Wu, E. X. (2018) · Scientific Reports · doi:10.1038/s41598-018-26568-1 · Cited by 20

Physiological Considerations of Functional Magnetic Resonance Imaging in Animal Models

Sumiyoshi, A., Keeley, R. J., & Lu, H. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.08.002 · Cited by 19

Recent developments in oximetry and perfusion-based mapping techniques and their role in the surgical treatment of neocortical epilepsy

Shariff, S., Suh, M., Zhao, M., Ma, H., & Schwartz, T. H. (2006) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2005.11.006 · Cited by 19

Quantitative Comparison Between Functional Imaging and Single-Unit Spiking in Rat Somatosensory Cortex

Masino, S. A. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00860.2002 · Cited by 19

Predator odor-evoked BOLD activation in the awake rat: Modulation by oxytocin and V1a vasopressin receptor antagonists

Reed, M. D., Price, K. E., Archbold, J., Moffa, A., & Febo, M. (2012) · Brain Research · doi:10.1016/j.brainres.2012.11.045 · Cited by 18

Cerebral blood flow in 5‐ to 8‐month‐olds: Regional tissue maturity is associated with infant affect

Camacho, M. C., King, L. S., Ojha, A., Garcia, C. M., Sisk, L. M., Cichocki, A. C., Humphreys, K. L., & Gotlib, I. H. (2019) · Developmental Science · doi:10.1111/desc.12928 · Cited by 18

Toward Studying Cognition in a Dish

Rouleau, N., Murugan, N. J., & Kaplan, D. L. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.01.005 · Cited by 19

Detection of prenatal alcohol exposure using machine learning classification of resting-state functional network connectivity data

Rodriguez, C. I., Vergara, V. M., Davies, S., Calhoun, V. D., Savage, D. D., & Hamilton, D. A. (2021) · Alcohol · doi:10.1016/j.alcohol.2021.03.001 · Cited by 18

A method for diagnosis support of mild cognitive impairment through EEG rhythms source location during working memory tasks

San-Martin, R., Johns, E. K., Mamani, G. Q., Tavares, G., Phillips, N. A., & Fraga, F. J. (2021) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2021.102499 · Cited by 19

Correlated functional connectivity and glucose metabolism in brain white matter revealed by simultaneous MRI/positron emission tomography

Guo, B., Zhou, F., Li, M., Gore, J. C., & Ding, Z. (2021) · Magnetic Resonance in Medicine · doi:10.1002/mrm.29107 · Cited by 18

Relationships between correlated spikes, oxygen and LFP in the resting-state primate

Li, J. M., Acland, B. T., Brenner, A. S., Bentley, W. J., & Snyder, L. H. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118728 · Cited by 18

Proceedings of the Second International Workshop on Advances in Electrocorticography

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Regional hypothalamic, amygdala, and midbrain periaqueductal gray matter recruitment during acute pain in awake humans: A 7-Tesla functional magnetic resonance imaging study

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Bimodal EEG-fNIRS in Neuroergonomics. Current Evidence and Prospects for Future Research

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Functional MRI reveals brain-wide actions of thalamically-initiated oscillatory activities on associative memory consolidation

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Neurovascular effects of cocaine: relevance to addiction

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Neural activation signatures in individuals with subclinical depression: A task-fMRI meta-analysis

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Simultaneous epidural functional near-infrared spectroscopy and cortical electrophysiology as a tool for studying local neurovascular coupling in primates

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Can you hear me yet? An intracranial investigation of speech and non-speech audiovisual interactions in human cortex

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BOLD fMRI study of ultrahigh frequency encoding in the inferior colliculus

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Concordance of MEG and fMRI patterns in adolescents during verb generation

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Controlling ferrofluid permeability across the blood–brain barrier model

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Intracranial EEG evaluation of relationship within a resting state network

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The role of sub-second neural events in spontaneous brain activity

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The neural basis of the blood-oxygen-level-dependent functional magnetic resonance imaging signal.

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Neurophysiology of the BOLD fMRI Signal in Awake Monkeys

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Summary

Goense, J. B. M., & Logothetis, N. K. (2013)

Locally Measured Neuronal Correlates of Functional MRI Signals

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Close correlation between fMRI signals and neural activity…or not?

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