Linear and nonlinear relationships between visual stimuli, EEG and BOLD fMRI signals
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In the present study, the cascaded interactions between stimuli and neural and hemodynamic responses were modeled using linear systems. These models provided the theoretical hypotheses that were tested against the electroencephalography (EEG) and blood oxygen level dependent (BOLD) functional magnetic resonance imaging (fMRI) data recorded from human subjects during prolonged periods of repeated visual stimuli with a variable setting of the inter-stimulus interval (ISI) and visual contrast. Our results suggest that (1) neural response is nonlinear only when ISI<0.2 s, (2) BOLD response is nonlinear with an exclusively vascular origin when 0.25<ISI<4.2 s, (3) vascular response nonlinearity reflects a refractory effect, rather than a ceiling effect, and (4) there is a strong linear relationship between the BOLD effect size and the integrated power of event-related synaptic current activity, after modeling and taking into account the vascular refractory effect. These conclusions offer important insights into the origins of BOLD nonlinearity and the nature of neurovascular coupling, and suggest an effective means to quantitatively interpret the BOLD signal in terms of neural activity. The validated cross-modal relationship between fMRI and EEG may provide a theoretical basis for the integration of these two modalities.
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In event-related or block designs, the size of the BOLD response to repeated stimuli over long intervals is roughly proportional to the integrated power of stimulus-evoked synaptic activity in the brief period after each stimulus.
“For event-related or block-design paradigms, it has been shown that the BOLD effect size given repeated stimuli in a long time-scale is approximately proportional to the integral of the power of stimulus-evoked synaptic activity in a short period following each stimulus (151).”
From Electrophysiological source imaging: A noninvasive window to brain dynamics (2018) · cites this paper as [151]
This relationship provides a quantitative model linking fMRI to EEG/MEG and allows a more principled use of fMRI to constrain the EEG/MEG inverse solution for stimulus-evoked responses.
“This relationship yields a quantitative model to relate fMRI to EEG/MEG, enabling a more principled way for using fMRI to constrain the EEG/MEG inverse solution for stimulus-evoked responses (150–152).”
From Electrophysiological source imaging: A noninvasive window to brain dynamics (2018) · cites this paper as [151]
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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
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 · see citing works
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681 · see citing works
What we can do and what we cannot do with fMRI
Logothetis, N. K. (2008) · Nature · doi:10.1038/nature06976 · Cited by 3,612 · 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
Time course EPI of human brain function during task activation
Bandettini, P. A., Wong, E. C., Hinks, R. S., Tikofsky, R. S., & Hyde, J. S. (1992) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910250220 · Cited by 1,935 · see citing works
Analysis of functional MRI time‐series
Friston, K. J., Jezzard, P., & Turner, R. (1994) · Human Brain Mapping · doi:10.1002/hbm.460010207 · Cited by 1,835 · see citing works
Raichle, M. E., & Mintun, M. A. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112819 · Cited by 1,630 · see citing works
A Method for Removing Imaging Artifact from Continuous EEG Recorded during Functional MRI
Allen, P. J., Josephs, O., & Turner, R. (2000) · NeuroImage · doi:10.1006/nimg.2000.0599 · Cited by 1,301 · see citing works
Modeling the hemodynamic response to brain activation
Buxton, R. B., Uludaǧ, K., Dubowitz, D. J., & Liu, T. T. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.013 · Cited by 1,222 · see citing works
Nonlinear Responses in fMRI: The Balloon Model, Volterra Kernels, and Other Hemodynamics
Friston, K. J., Mechelli, A., Turner, R., & Price, C. J. (2000) · NeuroImage · doi:10.1006/nimg.2000.0630 · Cited by 1,131 · see citing works
Goebel, R., Esposito, F., & Formisano, E. (2006) · Human Brain Mapping · doi:10.1002/hbm.20249 · Cited by 1,053 · see citing works
Selective averaging of rapidly presented individual trials using fMRI
Dale, A. M., & Buckner, R. L. (1997) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1997)5:5 · Cited by 1,028 · see citing works
Coupling Between Neuronal Firing, Field Potentials, and fMRI in Human Auditory Cortex
Mukamel, R., Gelbard, H., Arieli, A., Hasson, U., Fried, I., & Malach, R. (2005) · Science · doi:10.1126/science.1110913 · Cited by 1,023 · see citing works
The neural basis of functional brain imaging signals
Attwell, D., & Iadecola, C. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02264-6 · Cited by 957 · see citing works
Allen, P. J., Polizzi, G., Krakow, K., Fish, D. R., & Lemieux, L. (1998) · NeuroImage · doi:10.1006/nimg.1998.0361 · Cited by 914 · see citing works
Parametric Analysis of fMRI Data Using Linear Systems Methods
Cohen, M. S. (1997) · NeuroImage · doi:10.1006/nimg.1997.0278 · Cited by 723 · 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
Rapid Adaptation in Visual Cortex to the Structure of Images
Müller, J. R., Metha, A. B., Krauskopf, J., & Lennie, P. (1999) · Science · doi:10.1126/science.285.5432.1405 · Cited by 458 · 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
Devor, A., Dunn, A. K., Andermann, M. L., Ulbert, I., Boas, D. A., & Dale, A. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00403-3 · Cited by 387 · see citing works
Spikes versus BOLD: what does neuroimaging tell us about neuronal activity?
Heeger, D. J., Huk, A. C., Geisler, W. S., & Albrecht, D. G. (2000) · Nature Neuroscience · doi:10.1038/76572 · Cited by 364 · see citing works
Nonlinear Aspects of the BOLD Response in Functional MRI
Vazquez, A. L., & Noll, D. C. (1998) · NeuroImage · doi:10.1006/nimg.1997.0316 · Cited by 364 · see citing works
Budd, T. W., Barry, R. J., Gordon, E., RENNIE, C. J., & Michie, P. T. (1998) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(98)00040-3 · Cited by 353 · 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
Sheth, S. A., Nemoto, M., Guiou, M., Walker, M., Pouratian, N., & Toga, A. W. (2004) · Neuron · doi:10.1016/s0896-6273(04)00221-1 · Cited by 308 · see citing works
Identification of the neural sources of the pattern-reversal VEP
Russo, F. D., Pitzalis, S., Spitoni, G. F., Aprile, T., Patria, F., Donatella Spinelli, A., & Hillyard, S. A. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.09.029 · Cited by 269 · see citing works
Ogawa, S., Lee, T.-M., Stepnoski, R. A., Chen, W., Zhu, X., & Uǧurbil, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.20.11026 · Cited by 265 · see citing works
Self-citationRelationship of spikes, synaptic activity, and local changes of cerebral blood flow
Lauritzen, M. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200112000-00001 · Cited by 253 · see citing works
Stimulus rate determines regional brain blood flow in striate cortex
Fox, P. T., & Raichle, M. E. (1985) · Annals of Neurology · doi:10.1002/ana.410170315 · Cited by 237 · see citing works
Evidence for a Refractory Period in the Hemodynamic Response to Visual Stimuli as Measured by MRI
Huettel, S. A., & McCarthy, G. (2000) · NeuroImage · doi:10.1006/nimg.2000.0553 · Cited by 149 · see citing works
Vanni, S., Warnking, J. M., Michel Dojat, D., Delon‐Martin, C., Bullier, J., & Segebarth, C. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.10.047 · Cited by 138 · see citing works
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
The Hemodynamic Impulse Response to a Single Neural Event
Martindale, J., Mayhew, J. E., Berwick, J., Jones, M., Martin, C. J., Johnston, D., Redgrave, P., & Zheng, Y. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000058871.46954.2b · Cited by 133 · see citing works
Huttunen, J. K., Gröhn, O. H. J., & Penttonen, M. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.06.042 · Cited by 121 · see citing works
Bruhn, H., Kleinschmidt, A. K., Boecker, H., Merboldt, K., Hänicke, W., & Frahm, J. (1994) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1994.95 · Cited by 112 · 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
Self-citationCortical dynamics of visual motion perception: Short-range and long-range apparent motion.
Grossberg, S., & Rudd, M. E. (1992) · Psychological Review · doi:10.1037/0033-295x.99.1.78 · Cited by 93 · see citing works
Muthukumaraswamy, S. D., & Singh, K. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.052 · Cited by 91 · see citing works
Wan, X., Riera, J. J., Iwata, K., Takahashi, M. K., Wakabayashi, T., & Kawashima, R. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.03.040 · Cited by 87 · see citing works
Nonlinear Neurovascular Coupling in Rat Sensory Cortex by Activation of Transcallosal Fibers
Hoffmeyer, H. W., Enager, P., Thomsen, K. J., & Lauritzen, M. (2006) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600372 · Cited by 84 · see citing works
Refractory Periods Observed by Intrinsic Signal and Fluorescent Dye Imaging
Cannestra, A. F., Pouratian, N., Shomer, M. H., & Toga, A. W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1522 · Cited by 84 · see citing works
Further nonlinearities in neurovascular coupling in rodent barrel cortex
Hewson-Stoate, N., Jones, M., Martindale, J., Berwick, J., & Mayhew, J. E. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.08.040 · Cited by 78 · see citing works
Coupling between somatosensory evoked potentials and hemodynamic response in the rat
Franceschini, M. A., Nissila, I. T., Wu, W., Diamond, S. G., Bonmassar, G., & Boas, D. A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.02.061 · Cited by 74 · see citing works
The effect of stimulus duty cycle and “off” duration on BOLD response linearity
Birn, R. M., & Bandettini, P. A. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.03.040 · Cited by 71 · see citing works
Hemodynamic nonlinearities affect BOLD fMRI response timing and amplitude
de Zwart, J. A., van Gelderen, P., Jansma, J. M., Fukunaga, M., Bianciardi, M., & Duyn, J. H. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.001 · Cited by 63 · see citing works
Zhang, N., Zhu, X. H., & Chen, W. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.06.033 · Cited by 52 · see citing works
Self-citationWanmei Ou, A., Nissila, I. T., Radhakrishnan, H., Boas, D. A., Hämäläinen, M., & Franceschini, M. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.03.008 · Cited by 52 · see citing works
Cerebral oxygen demand for short‐lived and steady‐state events
Hermán, P., Sanganahalli, B. G., Blumenfeld, H., & Hyder, F. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.05844.x · Cited by 41 · see citing works
Mapping the bilateral visual integration by EEG and fMRI
Liu, Z., Zhang, N., Chen, W., & He, B. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.03.028 · Cited by 37 · see citing works
Self-citationNoninvasive Study of Neurovascular Coupling during Graded Neuronal Suppression
Zhang, N., Liu, Z., He, B., & Chen, W. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600531 · Cited by 30 · see citing works
Self-citationNangini, C., Tam, F., & Graham, S. J. (2007) · Human Brain Mapping · doi:10.1002/hbm.20361 · Cited by 17 · see citing works
Norcia, A. M., McKee, S. P., Bonneh, Y. S., & Pettet, M. W. (2005) · Journal of Vision · doi:10.1167/5.1.4 · Cited by 9 · see citing works
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Electrophysiological source imaging: A noninvasive window to brain dynamics
He, B., Sohrabpour, A., Brown, E., & Liu, Z. (2018) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-062117-120853 · Cited by 297 · see citing works
Self-citationElectrophysiological Imaging of Brain Activity and Connectivity—Challenges and Opportunities
He, B., Yang, L., Wilke, C., & Yuan, H. (2011) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2011.2139210 · Cited by 300 · see citing works
Self-citationFast fMRI can detect oscillatory neural activity in humans
Lewis, L. D., Setsompop, K., Rosen, B. R., & Polimeni, J. R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608117113 · Cited by 189 · see citing works
Macroscopic resting-state brain dynamics are best described by linear models
Nozari, E., Bertolero, M. A., Stiso, J., Caciagli, L., Cornblath, E. J., He, X., Mahadevan, A. S., Pappas, G. J., & Bassett, D. S. (2023) · Nature Biomedical Engineering · doi:10.1038/s41551-023-01117-y · Cited by 178 · see citing works
EEG–fMRI integration for the study of human brain function
Jorge, J., van der Zwaag, W., & Figueiredo, P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.114 · Cited by 172 · see citing works
Analysis of Multimodal Neuroimaging Data
Bießmann, F., Plis, S., Meinecke, F. C., Eichele, T., & Müller, K. (2011) · IEEE Reviews in Biomedical Engineering · doi:10.1109/rbme.2011.2170675 · Cited by 156 · see citing works
Mullinger, K. J., Mayhew, S. D., Bagshaw, A. P., Bowtell, R. W., & Francis, S. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.02.029 · Cited by 154 · see citing works
Advances in Multimodal Emotion Recognition Based on Brain–Computer Interfaces
He, Z., Li, Z., Yang, F., Wang, L., Li, J., Zhou, C., & Pan, J. (2020) · Brain Sciences · doi:10.3390/brainsci10100687 · Cited by 157 · see citing works
The time-course and spatial distribution of brain activity associated with sentence processing
Brennan, J., & Liina Pylkkänen, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.030 · Cited by 124 · see citing works
Usefulness of simultaneous EEG–NIRS recording in language studies
Wallois, F., Mahmoudzadeh, M., Patil, A., & Grebe, R. (2011) · Brain and Language · doi:10.1016/j.bandl.2011.03.010 · Cited by 115 · see citing works
Event-related fMRI in cognition
Huettel, S. A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.113 · Cited by 114 · see citing works
Bimodal BCI Using Simultaneously NIRS and EEG
Tomita, Y., Vialatte, F., Dreyfus, G., Mitsukura, Y., Bakardjian, H., & Cichocki, A. S. (2014) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2014.2300492 · Cited by 110 · see citing works
Imaging faster neural dynamics with fast fMRI: A need for updated models of the hemodynamic response
Polimeni, J. R., & Lewis, L. D. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102174 · Cited by 104 · see citing works
A personalized history of EEG–fMRI integration
Laufs, H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.039 · Cited by 103 · see citing works
Vazquez, A. L., Fukuda, M., Crowley, J. C., & Kim, S.-G. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht147 · Cited by 85 · see citing works
Millin, R., Arman, A. C., Chung, S. T. L., & Tjan, B. S. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht159 · Cited by 85 · see citing works
Lewis, L. D., Setsompop, K., Rosen, B. R., & Polimeni, J. R. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.06.056 · Cited by 81 · see citing works
Quantitative theory of driven nonlinear brain dynamics
Roberts, J. A., & Robinson, P. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.054 · Cited by 77 · see citing works
Is it a face of a woman or a man? Visual mismatch negativity is sensitive to gender category
Kecskés‐Kovács, K., Sulykos, I., & Czigler, I. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00532 · Cited by 63 · see citing works
Functional MRI and multivariate autoregressive models
Rogers, B. P., Katwal, S. B., Morgan, V. L., Asplund, C. L., & Gore, J. C. (2010) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2010.03.002 · Cited by 61 · see citing works
Simultaneous GCaMP6-based fiber photometry and fMRI in rats
Liang, Z., Ma, Y., Watson, G. D. R., & Zhang, N. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.07.002 · Cited by 59 · see citing works
Self-citationCollins, E., Robinson, A. K., & Behrmann, M. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.06.080 · Cited by 54 · see citing works
Schönwiesner, M., Dechent, P., Voit, D., Petkov, C. I., & Krumbholz, K. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu124 · Cited by 49 · see citing works
Complex discharge‐affecting networks in juvenile myoclonic epilepsy: A simultaneous EEG‐fMRI study
Dong, L., Luo, C., Zhu, Y., Hou, C., Jiang, S., Wang, P., Biswal, B. B., & Yao, D. (2016) · Human Brain Mapping · doi:10.1002/hbm.23256 · Cited by 45 · see citing works
Face-Evoked Steady-State Visual Potentials: Effects of Presentation Rate and Face Inversion
Gruss, L. F., Wieser, M. J., Schweinberger, S. R., & Keil, A. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00316 · Cited by 42 · see citing works
Bernstein, L. E., Jordan, N., Auer, E. T., & Eberhardt, S. P. (2022) · American Journal of Audiology · doi:10.1044/2021_aja-21-00112 · Cited by 39 · see citing works
Martin, C. J. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00211 · Cited by 37 · see citing works
Mapping interictal epileptic discharges using mutual information between concurrent EEG and fMRI
Caballero‐Gaudes, C., Ville, D. V. D., Grouiller, F., Thornton, R., Lemieux, L., Seeck, M., Lazeyras, F., & Vulliémoz, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.011 · Cited by 37 · see citing works
Paired pulse depression in the somatosensory cortex: Associations between MEG and BOLD fMRI
Stevenson, C. M., Wang, F., Brookes, M. J., Zumer, J. M., Francis, S., & Morris, P. G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.037 · Cited by 34 · see citing works
Dong, L., Gong, D., Valdes-Sosa, P. A., Xia, Y., Luo, C., Xu, P., & Yao, D. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.029 · Cited by 33 · see citing works
Moradi, F., & Buxton, R. B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.110 · Cited by 31 · see citing works
Chen, J. J., & Gauthier, C. J. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.657362 · Cited by 30 · see citing works
Chen, J. E., Glover, G. H., Fultz, N. E., Rosen, B. R., Polimeni, J. R., & Lewis, L. D. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118658 · Cited by 29 · see citing works
Gastric stimulation drives fast BOLD responses of neural origin
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Self-citationAnalysis of Time and Space Invariance of BOLD Responses in the Rat Visual System
Bailey, C. J., Sanganahalli, B. G., Hermán, P., Blumenfeld, H., GJEDDE, A. H., & Hyder, F. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs008 · Cited by 28 · see citing works
Stability of representational geometry across a wide range of fMRI activity levels
Arbuckle, S. A., Yokoi, A., Pruszynski, J. A., & Diedrichsen, J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.11.002 · Cited by 31 · see citing works
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Cao, J., Huppert, T. J., Grover, P., & Kainerstorfer, J. M. (2021) · Neurophotonics · doi:10.1117/1.nph.8.1.015002 · Cited by 23 · see citing works
Lin, F., Polimeni, J. R., Lin, J.-F. L., Tsai, K. W., Chu, Y.-H., Wu, P., Li, Y.-T., Hsu, Y.-C., Tsai, S., & Kuo, W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.041 · Cited by 23 · see citing works
Bao, P., Purington, C. J., & Tjan, B. S. (2015) · eLife · doi:10.7554/elife.09600 · Cited by 19 · see citing works
Large-scale dynamic modeling of task-fMRI signals via subspace system identification
Becker, C. O., Bassett, D. S., & Preciado, V. M. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aad8c7 · Cited by 16 · see citing works
Brain-wide ongoing activity is responsible for significant cross-trial BOLD variability
Zhang, Q., Cramer, S. R., Ma, Z., Turner, K. L., Gheres, K. W., Liu, Y., Drew, P. J., & Zhang, N. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac016 · Cited by 17 · see citing works
Self-citationKim, J. H., Taylor, A. J., Himmelbach, M., Hagberg, G. E., Scheffler, K., & Ress, D. B. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1009295 · Cited by 16 · see citing works
Sensitivity of BOLD response to increasing visual contrast: Spin echo versus gradient echo EPI
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Volumetric Spatial Correlations of Neurovascular Coupling Studied using Single Pulse Opto-fMRI
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Mangalathu-Arumana, J., Liebenthal, E., & Beardsley, S. A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00013 · Cited by 11 · see citing works
Comparing hand movement rate dependence of cerebral blood volume and BOLD responses at 7T
de Oliveira, I. A. F., van der Zwaag, W., Raimondo, L., Dumoulin, S. O., & Siero, J. C. W. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117623 · Cited by 11 · see citing works
Stimulus-specific information is represented as local activity patterns across the brain
Sadoun, A., Chauhan, T., Mameri, S., Zhang, Y. F., Barone, P., Déguine, O., & Strelnikov, K. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117326 · Cited by 10 · see citing works
de la Rosa, N., Ress, D. B., Taylor, A. J., & Kim, J. H. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00676.2020 · Cited by 9 · see citing works
Zhang, X., Pan, W., & Keilholz, S. D. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01126 · Cited by 10 · see citing works
Hemodynamic characteristics for improvement of EEG-BCI performance
Tomita, Y., & Mitsukura, Y. (2013) · Conference on Human System Interactions · doi:10.1109/hsi.2013.6577871 · Cited by 9 · see citing works
Bernstein, L. E., Auer, E. T., & Eberhardt, S. P. (2021) · American Journal of Audiology · doi:10.1044/2021_aja-21-00034 · Cited by 9 · see citing works
Zuo, N., Song, M., Fan, L., Eickhoff, S. B., & Jiang, T. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13112 · Cited by 9 · see citing works
Strelnikov, K., & Barone, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033462 · Cited by 9 · see citing works
Multi-study fMRI outlooks on subcortical BOLD responses in the stop-signal paradigmPreprint
Isherwood, S. J., Kemp, S. A., Miletić, S., Stevenson, N., Bazin, P., & Forstmann, B. U. (2023) · eLife · doi:10.7554/elife.88652.4 · Cited by 8 · see citing works
EEG and fMRI coupling and decoupling based on joint independent component analysis (jICA)
Heugel, N., Beardsley, S. A., & Liebenthal, E. (2022) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2022.109477 · Cited by 8 · see citing works
Tan, A., Hu, L., Tu, Y., Chen, R., Hung, Y. S., & Zhang, Z. (2016) · Brain Connectivity · doi:10.1089/brain.2016.0418 · Cited by 7 · see citing works
Ahmed, S., & Nozari, E. (2022) · IEEE Conference on Decision and Control (CDC) · doi:10.1109/cdc51059.2022.9993260 · Cited by 7 · see citing works
Meng, L., & Yang, C. (2023) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn54540.2023.10191903 · Cited by 7 · see citing works
Mode-locking dynamics of corticothalamic system responses to periodic external stimuli
Alinejad, H., Yang, D., & Robinson, P. A. (2019) · Physica D Nonlinear Phenomena · doi:10.1016/j.physd.2019.132231 · Cited by 7 · see citing works
Bondi, E., Ding, Y., Zhang, Y., Maggioni, E., & He, B. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121311 · Cited by 6 · see citing works
Self-citationMeng, L., & Yang, C. (2024) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2024.3377698 · Cited by 6 · see citing works
Si, J., Zhang, X., Li, Y., Zhang, Y., Zuo, N., & Jiang, T. (2016) · Journal of Biomedical Optics · doi:10.1117/1.jbo.21.9.091315 · Cited by 6 · see citing works
Yamamoto, H., Kita, Y., Kobayashi, T., Yamazaki, H., Kaga, M., Hoshino, H., Hanakawa, T., Yamamoto, H., & Inagaki, M. (2013) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2013.32017 · Cited by 4 · see citing works
Integration of EEG-FMRI in an Auditory Oddball Paradigm Using Joint Independent Component Analysis
Arumana, J. M. (2012) · Cited by 3 · see citing works
The paradoxical brain – so what?
Kapur, N., Manly, T., Cole, J. D., & Pascual‐Leone, Á. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511978098.026 · Cited by 3 · see citing works
Strelnikov, K., & Barone, P. (2013) · Journal of Neuroscience and Neuroengineering · doi:10.1166/jnsne.2013.1086 · Cited by 3 · see citing works
Naming disorders anomic aphasia.
Lorwatanapongsa, P. (2005) · PubMed · Cited by 3 · see citing works
Experimental Design and Data Analysis Strategies
Wirsich, J., Bagshaw, A. P., Guye, M., Lemieux, L., & Bénar, C. (2022) · Springer eBooks · doi:10.1007/978-3-031-07121-8_12 · Cited by 3 · see citing works
On the Linearizing Effect of Temporal Averaging in Nonlinear Dynamical Systems
Ahmed, S., & Nozari, E. (2023) · Proceedings of the ... American Control Conference/Proceedings of the American Control Conference · doi:10.23919/acc55779.2023.10155808 · Cited by 3 · see citing works
A novel piecewise-linear method for detecting associations between variables
Wang, P., & Zhang, J. (2023) · PLoS ONE · doi:10.1371/journal.pone.0290280 · Cited by 3 · see citing works
Bernstein, L. E., Auer, E. T., & Eberhardt, S. P. (2023) · Brain Sciences · doi:10.3390/brainsci13071008 · Cited by 3 · see citing works
Wahl, T., Riedinger, J., Duprez, M., & Hutt, A. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1183670 · Cited by 2 · see citing works
Reconstruction of natural images from human fMRI using a three-stage multi-level deep fusion model
Meng, L., Tang, Z., & Liu, Y. (2024) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2024.110269 · Cited by 2 · see citing works
Decoding with Purpose: Improving Image Reconstruction from fMRI with Multitask Learning
Lad, A., & Patel, R. (2021) · IEEE International Conference on Computing, Power and Communication Technologies (IC2PCT) · doi:10.1109/gucon50781.2021.9573575 · Cited by 2 · see citing works
Electrophysiological Measures of Age‐Related Cognitive Impairment In Humans
Anderson, D. E., & Taraschenko, O. D. (2018) · doi:10.1002/9781118772034.ch10 · Cited by 1 · see citing works
Multi-study fMRI outlooks on subcortical BOLD responses in the stop-signal paradigmPreprint
Isherwood, S. J., Kemp, S. A., Miletić, S., Stevenson, N., Bazin, P., & Forstmann, B. U. (2024) · eLife · doi:10.7554/elife.88652.2 · Cited by 1 · see citing works
Multi-study fMRI outlooks on subcortical BOLD responses in the stop-signal paradigmPreprint
Isherwood, S. J., Kemp, S. A., Miletić, S., Stevenson, N., Bazin, P., & Forstmann, B. U. (2025) · eLife · doi:10.7554/elife.88652.3 · Cited by 1 · see citing works
Korkmaz, G., Lorenzi, R. M., Ravera, F., Alahmadi, A. A. S., Monteverdi, A., Kanber, B., Prados, F., D'Angelo, E. U., Palesi, F., Toosy, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.03.692031 · Cited by 1 · see citing works
Simultaneous EEG-Correlated Noninvasive Imaging of Epilepsy Using Fast Diffuse Optical Tomography
Jiang, R., Ji, L., Zhou, J., Jiang, M. S., Yuan, Z., Zhang, Q., Carney, P. R., & Jiang, H. (2012) · Biomedical Optics and 3-D Imaging · doi:10.1364/biomed.2012.btu3a.47
Current Awareness in NMR in Biomedicine
(2010) · NMR in Biomedicine · doi:10.1002/nbm.1457
Becker, R., Mayhew, S. D., Ritter, P., & Villringer, A. (2022) · Springer eBooks · doi:10.1007/978-3-031-07121-8_23
Brain Visual Stimulus Reconstruction Using a Three-Stage Multilevel Deep Fusion Model
Meng, L., & Tang, Z. (2023) · IEEE International Conference on Computer and Communications (ICCC) · doi:10.1109/iccc59590.2023.10507552
Does the Cortical-Depth Dependence of the Hemodynamic Response Function Differ Between Age Groups?
Raimondo, L., Heij, J., Knapen, T. H. J., Siero, J. C. W., van der Zwaag, W., & Dumoulin, S. O. (2025) · Brain Topography · doi:10.1007/s10548-025-01107-0
Functional Neuroimaging of Electrophysiological Rhythms in Pathological and Normal Brains
Yang, L. (2012) · University of Minnesota Digital Conservancy (University of Minnesota)
Self-citationJung, D., Han, H.-B., Kim, J., Kim, J. H., Froemke, R. C., & Choi, J. H. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2603966123
Lan, X., Rodríguez-Labrada, R., Luo, C., & Dong, L. (2026) · Brain-Apparatus Communication A Journal of Bacomics · doi:10.1080/27706710.2026.2715174
- Authors
- Liu, Z., Rios, C., Zhang, N., Yang, L., Chen, W., & He, B.
- Affiliations
- University of Minnesota (US)
- Corresponding author
- He, Bin
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2010-04
- Volume
- 50
- Issue
- 3
- Pages
- 1054-1066
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC2841568
- OpenAlex
- W2148211890
- Cited by
- 88
- References
- 53
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 3 · 2023: 8 · 2022: 7 · 2021: 7 · 2020: 3 · 2019: 3 · 2018: 7 · 2017: 3 · 2016: 4 · 2015: 2 · 2014: 5 · 2013: 9 · 2012: 10
- FWCI
- 7.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship@UMassChan (submittedVersion)
- Funders
- NIH (RO1EB007920, RO1EB006433, P41RR008079, P30NS057091)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Optical Imaging and Spectroscopy Techniques
- Keywords
- neurovascular coupling, interstimulus interval, visual contrast, vascular response, visual stimulation, hemodynamic response
- MeSH terms
- Algorithms, Brain, Electroencephalography, Evoked Potentials, Visual, Female, Humans, Magnetic Resonance Imaging, Male, Oxygen, Photic Stimulation, Time Factors, Visual Perception, Linear Models, Nonlinear Dynamics, Young Adult
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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