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

Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex

Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680 · see citing works

Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images

Jenkinson, M., Bannister, P., Brady, M., & Smith, S. (2002) · NeuroImage · doi:10.1006/nimg.2002.1132 · Cited by 11,888 · see citing works

AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages

Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913 · see citing works

FreeSurfer

Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526 · see citing works

Neuronal Oscillations in Cortical Networks

Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576 · see citing works

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

Receptive fields and functional architecture of monkey striate cortex

Hubel, D. H., & Wiesel, T. N. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008455 · Cited by 6,520 · see citing works

Rhythms of the Brain

Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873 · see citing works

Receptive fields of single neurones in the cat's striate cortex

Hubel, D. H., & Wiesel, T. N. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006308 · Cited by 4,653 · see citing works

Borders of Multiple Visual Areas in Humans Revealed by Functional Magnetic Resonance Imaging

Sereno, M. I., Dale, A. M., Reppas, J. B., Kwong, K. K., Belliveau, J. W., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Science · doi:10.1126/science.7754376 · Cited by 2,623 · see citing works

Large-scale recording of neuronal ensembles

Buzsáki, G. (2004) · Nature Neuroscience · doi:10.1038/nn1233 · Cited by 1,875 · see citing works

Interpreting the BOLD Signal

Logothetis, N. K., & Wandell, B. A. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.082602.092845 · Cited by 1,568 · see citing works

Anticipatory Biasing of Visuospatial Attention Indexed by Retinotopically Specific α-Bank Electroencephalography Increases over Occipital Cortex

Worden, M. S., Foxe, J. J., Wang, N., & Simpson, G. V. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-j0002.2000 · Cited by 1,268 · see citing works

Visual field maps in human cortex.

Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.012 · Cited by 1,231 · cited 4× · see citing works

Population receptive field estimates in human visual cortex

Dumoulin, S. O., & Wandell, B. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.034 · Cited by 1,183 · see citing works

Untitled work

Angelucci (2002) · doi:10.1146/annurev.ne.08.030185.002203 · Cited by 1,170 · see citing works

Attention improves performance primarily by reducing interneuronal correlations

Cohen, M. R., & Maunsell, J. H. R. (2009) · Nature Neuroscience · doi:10.1038/nn.2439 · Cited by 1,126 · see citing works

The first step for neuroimaging data analysis: DICOM to NIfTI conversion

Li, X., Morgan, P. S., Ashburner, J., Smith, J., & Rorden, C. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.03.001 · Cited by 1,073 · see citing works

Neuronal responses to static texture patterns in area V1 of the alert macaque monkey

Knierim, J. J., & Essen, D. C. V. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.4.961 · Cited by 1,052 · see citing works

The Underpinnings of the BOLD Functional Magnetic Resonance Imaging Signal

Logothetis, N. K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-03963.2003 · Cited by 1,024 · 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

fMRI of human visual cortex

Engel, S. A., Rumelhart, D. E., Wandell, B. A., Lee, A. T.-J., Glover, G. H., Chichilnisky, E. J., & Shadlen, M. N. (1994) · Nature · doi:10.1038/369525a0 · Cited by 977 · see citing works

THE RESPONSE OF SINGLE OPTIC NERVE FIBERS OF THE VERTEBRATE EYE TO ILLUMINATION OF THE RETINA

Hartline, H. K. (1938) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1938.121.2.400 · Cited by 966 · 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

The visual field representation in striate cortex of the macaque monkey: Asymmetries, anisotropies, and individual variability

Essen, D. C. V., Newsome, W. T., & Maunsell, J. H. R. (1984) · Vision Research · doi:10.1016/0042-6989(84)90041-5 · Cited by 938 · see citing works

Alpha and gamma oscillations characterize feedback and feedforward processing in monkey visual cortex

van Kerkoerle, T., Self, M. W., Dagnino, B., Gariel-Mathis, M.-A., Poort, J., van der Togt, C., & Roelfsema, P. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402773111 · Cited by 918 · 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

Uniformity of monkey striate cortex: A parallel relationship between field size, scatter, and magnification factor

Hubel, D. H., & Wiesel, T. N. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901580305 · Cited by 897 · see citing works

Chronux: A platform for analyzing neural signals

Bokil, H., Andrews, P., Kulkarni, J. E., Mehta, S. B., & Mitra, P. P. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.06.020 · Cited by 872 · see citing works

Modelling and analysis of local field potentials for studying the function of cortical circuits

Einevoll, G. T., Kayser, C., Logothetis, N. K., & Panzeri, S. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3599 · Cited by 857 · see citing works

Hemodynamic Signals Correlate Tightly with Synchronized Gamma Oscillations

Niessing, J., Ebisch, B., Schmidt, K. E., Niessing, M., Singer, W., & Galuske, R. A. W. (2005) · Science · doi:10.1126/science.1110948 · Cited by 806 · see citing works

Nature and Interaction of Signals From the Receptive Field Center and Surround in Macaque V1 Neurons

Cavanaugh, J. R., Bair, W., & Movshon, J. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00692.2001 · Cited by 784 · see citing works

Visuotopic organization and extent of V3 and V4 of the macaque

Gattass, R., Sousa, A., & Gross, C. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-06-01831.1988 · Cited by 676 · see citing works

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

Rees, G. E., Friston, K. J., & Koch, C. (2000) · Nature Neuroscience · doi:10.1038/76673 · Cited by 650 · see citing works

Chronic recording capability of the Utah Intracortical Electrode Array in cat sensory cortex

Rousche, P. J., & Normann, R. A. (1998) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(98)00031-4 · Cited by 646 · 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

How Local Is the Local Field Potential?

Kajikawa, Y., & Schroeder, C. E. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.029 · Cited by 584 · see citing works

Neurophysiology of the BOLD fMRI Signal in Awake Monkeys

Goense, J. B. M., & Logothetis, N. K. (2008) · Current Biology · doi:10.1016/j.cub.2008.03.054 · Cited by 583 · see citing works

Functional properties of monkey caudate neurons. III. Activities related to expectation of target and reward

Hikosaka, O., Sakamoto, M., & Usui, S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.4.814 · Cited by 579 · see citing works

Two Retinotopic Visual Areas in Human Lateral Occipital Cortex

Larsson, J. T., & Heeger, D. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1657-06.2006 · Cited by 564 · see citing works

NeuroVault.org: a web-based repository for collecting and sharing unthresholded statistical maps of the human brain

Gorgolewski, K. J., Varoquaux, G. P., Rivera, G., Schwarz, Y., Ghosh, S., Maumet, C., Sochat, V., Nichols, T. E., Poldrack, R. A., Poline, J., et al. (2015) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2015.00008 · Cited by 554 · 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

The role of neuronal synchronization in selective attention

Womelsdorf, T., & Fries, P. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.02.002 · Cited by 511 · see citing works

Visual Motion Processing Investigated Using Contrast Agent-Enhanced fMRI in Awake Behaving Monkeys

Vanduffel, W., Fize, D., Mandeville, J. B., Nelissen, K., Hecke, P. V., Rosen, B. R., Tootell, R. B. H., & Orban, G. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00502-5 · Cited by 492 · see citing works

Visual topography of V2 in the macaque

Gattass, R., Gross, C. G., & Sandell, J. H. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902010405 · Cited by 488 · see citing works

Neuronal Synchronization along the Dorsal Visual Pathway Reflects the Focus of Spatial Attention

Siegel, M., Donner, T. H., Oostenveld, R., Fries, P., & Engel, A. K. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.010 · Cited by 487 · see citing works

Anticipatory haemodynamic signals in sensory cortex not predicted by local neuronal activity

Sirotin, Y. B., & Das, A. (2009) · Nature · doi:10.1038/nature07664 · Cited by 437 · 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

Imaging retinotopic maps in the human brain

Wandell, B. A., & Winawer, J. A. (2010) · Vision Research · doi:10.1016/j.visres.2010.08.004 · Cited by 376 · 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

Receptive field properties of neurons in area V3 of macaque monkey extrastriate cortex

Felleman, D. J., & Essen, D. C. V. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.4.889 · Cited by 375 · see citing works

The Retinotopic Organization of the Human Middle Temporal Area MT/V5 and Its Cortical Neighbors

Kolster, H., Peeters, R. R., & Orban, G. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2069-10.2010 · Cited by 363 · see citing works

Reward Encoding in the Monkey Anterior Cingulate Cortex

Amiez, C., Joseph, J., & Procyk, E. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj046 · Cited by 351 · see citing works

Visual Field Maps, Population Receptive Field Sizes, and Visual Field Coverage in the Human MT+ Complex

Amano, K., Wandell, B. A., & Dumoulin, S. O. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00102.2009 · Cited by 341 · see citing works

Compressive spatial summation in human visual cortex

Kay, K., Winawer, J. A., Mezer, A., & Wandell, B. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00105.2013 · Cited by 340 · see citing works

Default Mode of Brain Function in Monkeys

Mantini, D., Gerits, A., Nelissen, K., Durand, J., Joly, O., Simone, L., Sawamura, H., Wardak, C., Orban, G. A., Buckner, R. L., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2318-11.2011 · Cited by 337 · see citing works

How and when the fMRI BOLD signal relates to underlying neural activity: The danger in dissociation

Ekstrom, A. D. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.004 · Cited by 332 · see citing works

Bottom-Up Dependent Gating of Frontal Signals in Early Visual Cortex

Ekstrom, L. B., Roelfsema, P. R., Arsenault, J. T., Bonmassar, G., & Vanduffel, W. (2008) · Science · doi:10.1126/science.1153276 · Cited by 329 · see citing works

Functional properties of monkey caudate neurons. II. Visual and auditory responses

Hikosaka, O., Sakamoto, M., & Usui, S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.4.799 · Cited by 319 · see citing works

Object Selectivity of Local Field Potentials and Spikes in the Macaque Inferior Temporal Cortex

Kreiman, G., Hung, C. P., Kraskov, A., Quiroga, R. Q., Poggio, T., & DiCarlo, J. J. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.019 · Cited by 312 · see citing works

Observations on the scratch‐reflex in the spinal dog

Sherrington, C. (1906) · The Journal of Physiology · doi:10.1113/jphysiol.1906.sp001139 · Cited by 298 · see citing works

Toward a comparison of microelectrodes for acute and chronic recordings

Ward, M. P., Rajdev, P., Ellison, C., & Irazoqui, P. P. (2009) · Brain Research · doi:10.1016/j.brainres.2009.05.052 · Cited by 296 · see citing works

Constrained linear basis sets for HRF modelling using Variational Bayes

Woolrich, M. W., Behrens, T. E. J., & Smith, S. M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.12.024 · Cited by 295 · see citing works

Divergence of fMRI and neural signals in V1 during perceptual suppression in the awake monkey

Maier, A., Wilke, M., Aura, C. J., Zhu, C., Ye, F. Q., & Leopold, D. A. (2008) · Nature Neuroscience · doi:10.1038/nn.2173 · Cited by 291 · see citing works

Processing of color, form and disparity information in visual areas VP and V2 of ventral extrastriate cortex in the macaque monkey

Burkhalter, A., & Essen, D. C. V. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02327.1986 · Cited by 282 · see citing works

Responses of striatal neurons in the behaving monkey. 1. Head of the caudate nucleus

Rolls, E. T., Thorpe, S. J., & Maddison, S. P. (1983) · Behavioural Brain Research · doi:10.1016/0166-4328(83)90191-2 · Cited by 256 · see citing works

Shape perception via a high-channel-count neuroprosthesis in monkey visual cortex

Chen, X., Wang, F., Fernandez, E., & Roelfsema, P. R. (2020) · Science · doi:10.1126/science.abd7435 · Cited by 250 · see citing works

Early Exploration of the Visual Cortex

Hubel, D. H., & Wiesel, T. N. (1998) · Neuron · doi:10.1016/s0896-6273(00)80984-8 · Cited by 250 · see citing works

Local diversity and fine-scale organization of receptive fields in mouse visual cortex

Bonin, V., Histed, M. H., Yurgenson, S., & Reid, R. C. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2974-11.2011 · Cited by 247 · 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

Computational neuroimaging and population receptive fields

Wandell, B. A., & Winawer, J. A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.03.009 · Cited by 240 · see citing works

The Role of Attention in Figure-Ground Segregation in Areas V1 and V4 of the Visual Cortex

Poort, J., Raudies, F., Wannig, A., Lamme, V. A. F., Heiko Neumann, B., & Roelfsema, P. R. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.032 · Cited by 222 · see citing works

Visual Areas in Macaque Cortex Measured Using Functional Magnetic Resonance Imaging

Brewer, A. A., Press, W., Logothetis, N. K., & Wandell, B. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10416.2002 · Cited by 219 · see citing works

The macaque anterior cingulate cortex translates counterfactual choice value into actual behavioral change

Fouragnan, E. F., Chau, B. K. H., Folloni, D., Kolling, N., Verhagen, L., Klein-Flügge, M. C., Tankelevitch, L., Papageorgiou, G., Aubry, J., Sallet, J., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0375-6 · Cited by 215 · see citing works

A population MRI brain template and analysis tools for the macaque

Seidlitz, J., Sponheim, C., Glen, D., Ye, F. Q., Saleem, K. S., Leopold, D. A., Ungerleider, L. G., & Messinger, A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.04.063 · Cited by 211 · see citing works

Spatial Summation in the Receptive Fields of MT Neurons

Britten, K. H., & Heuer, H. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05074.1999 · Cited by 200 · see citing works

Retinotopy and Attention in Human Occipital, Temporal, Parietal, and Frontal Cortex

Saygın, A. P., & Sereno, M. I. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm242 · Cited by 193 · see citing works

Three-Dimensional Digital Template Atlas of the Macaque Brain

Reveley, C., Gruslys, A., Ye, F. Q., Glen, D., Samaha, J., Russ, B. E., Saad, Z. S., Seth, A. K., Leopold, D. A., & Saleem, K. S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw248 · Cited by 188 · see citing works

Chronic multiunit recordings in behaving animals: advantages and limitations

Supèr, H., & Roelfsema, P. R. (2004) · Progress in brain research · doi:10.1016/s0079-6123(04)47020-4 · Cited by 180 · see citing works

Retinotopic Organization and Functional Subdivisions of the Human Lateral Geniculate Nucleus: A High-Resolution Functional Magnetic Resonance Imaging Study

Schneider, K. A., Richter, M. C., & Kästner, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2413-04.2004 · Cited by 179 · see citing works

Alpha/beta power decreases track the fidelity of stimulus-specific information

Griffiths, B., Mayhew, S. D., Mullinger, K. J., Jorge, J., Charest, I., Wimber, M., & Hanslmayr, S. (2019) · eLife · doi:10.7554/elife.49562 · Cited by 178 · see citing works

Negative BOLD in the visual cortex: Evidence against blood stealing

Smith, A. T., Williams, A. L., & Singh, K. D. (2004) · Human Brain Mapping · doi:10.1002/hbm.20017 · Cited by 174 · see citing works

Topographic representations of object size and relationships with numerosity reveal generalized quantity processing in human parietal cortex

Harvey, B. M., Fracasso, A., Petridou, N., & Dumoulin, S. O. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515414112 · Cited by 174 · see citing works

Weak correlations between hemodynamic signals and ongoing neural activity during the resting state

Winder, A. T., Echagarruga, C., Zhang, Q., & Drew, P. J. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0007-y · Cited by 172 · see citing works

Pycortex: an interactive surface visualizer for fMRI

Gao, J. S., Huth, A. G., Lescroart, M. D., & Gallant, J. L. (2015) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2015.00023 · Cited by 171 · see citing works

Asynchronous Broadband Signals Are the Principal Source of the BOLD Response in Human Visual Cortex

Winawer, J. A., Kay, K., Foster, B. L., Rauschecker, A. M., Parvizi, J., & Wandell, B. A. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.001 · Cited by 169 · see citing works

Visual Field Map Clusters in Macaque Extrastriate Visual Cortex

Kolster, H., Mandeville, J. B., Arsenault, J. T., Ekstrom, L. B., Wald, L. L., & Vanduffel, W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0518-09.2009 · Cited by 168 · see citing works

Cortical visual areas in monkeys: location, topography, connections, columns, plasticity and cortical dynamics

Gattass, R., Nascimento‐Silva, S., Soares, J. G. M., Lima, B., Jansen, A. K., DIOGO, A. C. M., Farias, M. F., Marcondes, E. P. B. M., Mariani, O. S. C., Azzi, J. C. B., et al. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1629 · Cited by 155 · see citing works

Modeling center-surround configurations in population receptive fields using fMRI

Zuiderbaan, W., Harvey, B. M., & Dumoulin, S. O. (2012) · Journal of Vision · doi:10.1167/12.3.10 · Cited by 152 · see citing works

Receptive fields in human visual cortex mapped with surface electrodes

Yoshor, D., Bosking, W. H., Ghose, G. M., & Maunsell, J. H. R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl138 · Cited by 152 · see citing works

Vascular and neural basis of the BOLD signal

Drew, P. J. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.06.004 · Cited by 149 · see citing works

Visual topography of V1 in the Cebus monkey

Gattass, R., Sousa, A. P. B., & Rosa, M. G. P. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902590404 · Cited by 147 · see citing works

fMRI and its interpretations: an illustration on directional selectivity in area V5/MT

Bartels, A., Logothetis, N. K., & Moutoussis, K. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.06.004 · Cited by 146 · see citing works

Frequency Dependence of Signal Power and Spatial Reach of the Local Field Potential

Łęski, S., Lindén, H., Tetzlaff, T., Pettersen, K. H., & Einevoll, G. T. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003137 · Cited by 145 · see citing works

Larger extrastriate population receptive fields in autism spectrum disorders

Schwarzkopf, D. S., Anderson, E. J., de Haas, B., White, S. J., & Rees, G. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4416-13.2014 · Cited by 138 · see citing works

Optimal Electrode Size for Multi-Scale Extracellular-Potential Recording From Neuronal Assemblies

Viswam, V., Obien, M. E. J., Franke, F., Frey, U., & Hierlemann, A. R. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00385 · Cited by 136 · see citing works

Distinct Feedforward and Feedback Effects of Microstimulation in Visual Cortex Reveal Neural Mechanisms of Texture Segregation

Klink, P. C., Dagnino, B., Gariel-Mathis, M.-A., & Roelfsema, P. R. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.033 · Cited by 135 · see citing works

Feature selectivity of the gamma-band of the local field potential in primate primary visual cortex

Berens, P. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.037.2008 · Cited by 127 · see citing works

Linking Neuronal and Behavioral Performance in a Reaction-Time Visual Detection Task

Palmer, C., Cheng, S.-Y., & Seidemann, E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1940-07.2007 · Cited by 116 · see citing works

Visuotopic Organization of Macaque Posterior Parietal Cortex: A Functional Magnetic Resonance Imaging Study

Arcaro, M. J., Pinsk, M. A., Li, X., & Kästner, S. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3334-10.2011 · Cited by 115 · see citing works

Population encoding of spatial frequency, orientation, and color in macaque V1

Victor, J. D., Purpura, K. P., Katz, E., & Mao, B. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.5.2151 · Cited by 115 · see citing works

Topographic Maps of Visual Space in the Human Cerebellum

van Es, D. M., van der Zwaag, W., & Knapen, T. H. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.012 · Cited by 112 · see citing works

Probabilistic and Single-Subject Retinotopic Maps Reveal the Topographic Organization of Face Patches in the Macaque Cortex

Janssens, T., Zhu, Q., Popivanov, I. D., & Vanduffel, W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2914-13.2013 · Cited by 107 · see citing works

3D printing and modelling of customized implants and surgical guides for non-human primates.

Chen, X., Possel, J. K., Wacongne, C., van Ham, A. F., Klink, P. C., & Roelfsema, P. R. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.05.013 · Cited by 106 · see citing works

Representation of the visual field in the second visual area in the Cebus monkey

Rosa, M. G. P., Sousa, A. P. B., & Gattass, R. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902750303 · Cited by 103 · see citing works

Connective field modeling

Haak, K. V., Winawer, J. A., Harvey, B. M., Renken, R. J., Dumoulin, S. O., Wandell, B. A., & Cornelissen, F. W. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.037 · Cited by 102 · see citing works

Response to short-term deprivation of the human adult visual cortex measured with 7T BOLD

Binda, P., Kurzawski, J. W., Lunghi, C., Biagi, L., Tosetti, M., & Morrone, M. C. (2018) · eLife · doi:10.7554/elife.40014 · Cited by 100 · see citing works

The Retinotopic Organization of Macaque Occipitotemporal Cortex Anterior to V4 and Caudoventral to the Middle Temporal (MT) Cluster

Kolster, H., Janssens, T., Orban, G. A., & Vanduffel, W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3288-13.2014 · Cited by 99 · see citing works

Ventral posterior visual area of the macaque: Visual topography and areal boundaries

Newsome, W. T., Maunsell, J. H. R., & Essen, D. C. V. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902520202 · Cited by 97 · see citing works

Frequency specific spatial interactions in human electrocorticography: V1 alpha oscillations reflect surround suppression

Harvey, B. M., Vansteensel, M. J., Ferrier, C. H., Petridou, N., Zuiderbaan, W., Aarnoutse, E. J., Bleichner, M. G., Dijkerman, H. C., van Zandvoort, M. J. E., Leijten, F. S. S., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.020 · Cited by 92 · see citing works

Spikes, BOLD, Attention, and Awareness: A comparison of electrophysiological and fMRI signals in V1

Boynton, G. M. (2011) · Journal of Vision · doi:10.1167/11.5.12 · Cited by 91 · see citing works

Do Electrode Properties Create a Problem in Interpreting Local Field Potential Recordings?

Nelson, M. J., & Pouget, P. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00157.2010 · Cited by 77 · see citing works

A Network of Topographic Maps in Human Association Cortex Hierarchically Transforms Visual Timing-Selective Responses

Harvey, B. M., Dumoulin, S. O., Fracasso, A., & Paul, J. M. (2020) · Current Biology · doi:10.1016/j.cub.2020.01.090 · Cited by 77 · see citing works

p75NTR immunoreactivity in the rat dentate gyrus is mostly within presynaptic profiles but is also found in some astrocytic and postsynaptic profiles

Dougherty, K. D., & Milner, T. A. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990428)407:1 · Cited by 76 · see citing works

Topographic organization of macaque area LIP

Patel, G. H., Shulman, G. L., Baker, J. T., Akbudak, E., Snyder, A. Z., Snyder, L. H., & Corbetta, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908092107 · Cited by 71 · see citing works

Bayesian population receptive field modelling

Zeidman, P., Silson, E. H., Schwarzkopf, D. S., Baker, C. I., & Penny, W. D. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.008 · Cited by 70 · see citing works

Retinotopic Organization of Scene Areas in Macaque Inferior Temporal Cortex

Arcaro, M. J., & Livingstone, M. S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0569-17.2017 · Cited by 65 · see citing works

Population receptive field estimates of human auditory cortex

Thomas, J. M., Huber, E., Stecker, G. C., Boynton, G. M., Sàenz, M., & Fine, I. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.060 · Cited by 63 · see citing works

The development and use of phase-encoded functional MRI designs

Engel, S. A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.059 · Cited by 62 · see citing works

Stimulus‐induced dissociation of neuronal firing rates and local field potential gamma power and its relationship to the blood oxygen level‐dependent signal in macaque primary visual cortex

Bartolo, M. J., Gieselmann, M. A., Vuksanović, V., Hunter, D., Sun, L. Y., Chen, X., Delicato, L. S., & Thiele, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07877.x · Cited by 62 · see citing works

Advanced Brain Neuroimaging Topics in Health and Disease - Methods and Applications

Papageorgiou, T. D., Christopoulos, G. I., & Smirnakis, S. M. (2014) · InTech eBooks · doi:10.5772/58256 · Cited by 61 · see citing works

Measurement of population receptive fields in human early visual cortex using back-projection tomography

Greene, C. A., Dumoulin, S. O., Harvey, B. M., & Ress, D. B. (2014) · Journal of Vision · doi:10.1167/14.1.17 · Cited by 59 · see citing works

Mouse visual cortex contains a region of enhanced spatial resolution

van Beest, E. H., Mukherjee, S., Kirchberger, L., Schnabel, U. H., van der Togt, C., Teeuwen, R. R. M., Barsegyan, A., Meyer, A. F., Poort, J., Roelfsema, P. R., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24311-5 · Cited by 59 · see citing works

Neurovascular uncoupling: Much ado about nothing

Logothetis, N. K. (2010) · Frontiers in Neuroenergetics · doi:10.3389/fnene.2010.00002 · Cited by 56 · see citing works

How Visual Cortical Organization Is Altered by Ophthalmologic and Neurologic Disorders

Dumoulin, S. O., & Knapen, T. H. J. (2018) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091517-033948 · Cited by 56 · see citing works

Population Receptive Field Estimation Reveals New Retinotopic Maps in Human Subcortex

DeSimone, K., Viviano, J. D., & Schneider, K. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3840-14.2015 · Cited by 54 · see citing works

Contralateral Visual Hemifield Representations in the Human Pulvinar Nucleus

Cotton, P. L., & Smith, A. T. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00419.2007 · Cited by 53 · see citing works

Differential Sampling of Visual Space in Ventral and Dorsal Early Visual Cortex

Silson, E. H., Reynolds, R. C., Kravitz, D. J., & Baker, C. I. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2717-17.2018 · Cited by 52 · see citing works

The Critical Role of V2 Population Receptive Fields in Visual Orientation Crowding

He, D., Wang, Y., & Fang, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.068 · Cited by 52 · see citing works

A collaborative resource platform for non-human primate neuroimaging

Messinger, A., Sirmpilatze, N., Heuer, K., Loh, K. K., Mars, R. B., Sein, J., Xu, T., Glen, D., Jung, B., Seidlitz, J., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2020.117519 · Cited by 52 · see citing works

Visual Organization of the Default Network

Szinte, M., & Knapen, T. H. J. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz323 · Cited by 51 · see citing works

Submillimeter fMRI reveals a layout of dorsal visual cortex in macaques, remarkably similar to New World monkeys

Zhu, Q., & Vanduffel, W. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805561116 · Cited by 49 · see citing works

Estimating average single-neuron visual receptive field sizes by fMRI

Keliris, G. A., Li, Q., Papanikolaou, A., Logothetis, N. K., & Smirnakis, S. M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1809612116 · Cited by 48 · see citing works

Bayesian population receptive field modeling in human somatosensory cortex

Puckett, A. M., Bollmann, S., Junday, K., Barth, M., & Cunnington, R. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116465 · Cited by 44 · see citing works

Population receptive field (pRF) measurements of chromatic responses in human visual cortex using fMRI

Welbourne, L. E., Morland, A. B., & Wade, A. R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.022 · Cited by 42 · see citing works

Population receptive field tuning properties of visual cortex during childhood

Dekker, T. M., Schwarzkopf, D. S., de Haas, B., Marko Nardini, A., & Sereno, M. I. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.01.001 · Cited by 41 · see citing works

Third tier ventral extrastriate cortex in the New World monkey, Cebus apella

Rosa, M. G. P., Piñon, M. C., Gattass, R., & Sousa, A. P. B. (2000) · Experimental Brain Research · doi:10.1007/s002210000344 · Cited by 41 · see citing works

Stimulus-Related Neuroimaging in Task-Engaged Subjects Is Best Predicted by Concurrent Spiking

Lima, B., Cardoso, M. M. B., Sirotin, Y. B., & Das, A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1595-14.2014 · Cited by 40 · see citing works

Figure-Ground Modulation in the Human Lateral Geniculate Nucleus Is Distinguishable from Top-Down Attention

Poltoratski, S., Maier, A., Newton, A. T., & Tong, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.068 · Cited by 38 · see citing works

Spatial spread of local field potential is band-pass in the primary visual cortex

Dubey, A., & Ray, S. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00443.2016 · Cited by 35 · see citing works

Attention Shifts Recruit the Monkey Default Mode Network

Arsenault, J. T., Caspari, N., Vandenberghe, R. R., & Vanduffel, W. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1111-17.2017 · Cited by 35 · see citing works

Population Receptive Field Shapes in Early Visual Cortex Are Nearly Circular

Lerma‐Usabiaga, G., Winawer, J. A., & Wandell, B. A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3052-20.2021 · Cited by 29 · see citing works

Retinotopic patterns of functional connectivity between V1 and large-scale brain networks during resting fixation

Griffis, J. C., Elkhetali, A. S., Burge, W. K., Chen, R. H., Bowman, A. D., Szaflarski, J. P., & Visscher, K. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.035 · Cited by 28 · see citing works

Visual cortex organisation in a macaque monkey with macular degeneration

Shao, Y., Keliris, G. A., Papanikolaou, A., Fischer, M. D., Zobor, D., Jägle, H., Logothetis, N. K., & Smirnakis, S. M. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12349 · Cited by 27 · see citing works

Resolving the Spatial Profile of Figure Enhancement in Human V1 through Population Receptive Field Modeling

Poltoratski, S., & Tong, F. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2377-19.2020 · Cited by 26 · see citing works

Object Selection by Automatic Spreading of Top-Down Attentional Signals in V1

Ekman, M., Roelfsema, P. R., & de Lange, F. P. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0438-20.2020 · Cited by 25 · see citing works

Spatial elongation of population receptive field profiles revealed by model‐free f MRI back‐projection

Merkel, C., Hopf, J., & Schoenfeld, M. A. (2018) · Human Brain Mapping · doi:10.1002/hbm.24015 · Cited by 24 · see citing works

The Relationship between Subthreshold and Suprathreshold Ocular Dominance in Cat Primary Visual Cortex

Priebe, N. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2182-08.2008 · Cited by 22 · see citing works

Attention Priority Map of Face Images in Human Early Visual Cortex

Mo, C., He, D., & Fang, F. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1206-17.2017 · Cited by 20 · see citing works

Spatial summation in macaque parietal area 7a follows a winner-take-all rule

Oleksiak, A., Klink, P. C., Postma, A., van der Ham, I. J. M., Lankheet, M. J., & Wezel, R. J. A. V. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00907.2010 · Cited by 19 · see citing works

Functional MRI of Awake Behaving Macaques Using Standard Equipment

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

Topographic signatures of global object perception in human visual cortex

Stoll, S., Finlayson, N. J., & Schwarzkopf, D. S. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116926 · Cited by 17 · see citing works

Direct visualization of non-human primate subcortical nuclei with contrast-enhanced high field MRI

Tani, N., Joly, O., Iwamuro, H., Uhrig, L., Wiggins, C. J., Poupon, C., Kolster, H., Vanduffel, W., Bihan, D. L., Palfi, S., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.019 · Cited by 16 · see citing works

Role of Population Receptive Field Size in Complex Visual Dysfunctions

de Best, P. B., Raz, N., Guy, N., Ben‐Hur, T., Dumoulin, S. O., Pertzov, Y., & Levin, N. (2019) · JAMA Neurology · doi:10.1001/jamaneurol.2019.2447 · Cited by 14 · see citing works

Wide-field retinotopy reveals a new visuotopic cluster in macaque posterior parietal cortex

Rima, S., Cottereau, B. R., Héjja‐Brichard, Y., Trotter, Y., & Durand, J. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02134-2 · Cited by 13 · see citing works

Image identification from brain activity using the population receptive field model

Zuiderbaan, W., Harvey, B. M., & Dumoulin, S. O. (2017) · PLoS ONE · doi:10.1371/journal.pone.0183295 · Cited by 12 · see citing works

Apparent Motion Induces Activity Suppression in Early Visual Cortex and Impairs Visual Detection

Shen, L., Han, B., & de Lange, F. P. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0563-20.2020 · Cited by 12 · see citing works

Population receptive field estimates for motion-defined stimuli

Hughes, A. E., Greenwood, J. A., Finlayson, N. J., & Schwarzkopf, D. S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.05.068 · Cited by 12 · see citing works

Altered visual population receptive fields in human albinism

Alvarez, I., Smittenaar, R., Handley, S. E., Liasis, A. C., Sereno, M. I., Schwarzkopf, D. S., & Clark, C. A. (2020) · Cortex · doi:10.1016/j.cortex.2020.03.016 · Cited by 12 · see citing works

Triple visual hemifield maps in a case of optic chiasm hypoplasia

Ahmadi, K., Fracasso, A., Puźniak, R. J., Gouws, A. D., Yakupov, R., Speck, O., Kaufmann, J., Pestilli, F., Dumoulin, S. O., Morland, A. B., et al. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116822 · Cited by 10 · see citing works

X-Chromosome Insufficiency Alters Receptive Fields across the Human Early Visual Cortex

Green, T., Hosseini, S. M. H., Piccirilli, A. M., Ishak, A., Kalanit Grill-spector, A., & Reiss, A. L. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2745-18.2019 · Cited by 8 · see citing works

Computer-Plotted Receptive Fields

Barlow, H. B., Levick, W. R., Westheimer, G., & Spinelli, D. N. (1966) · Science · doi:10.1126/science.154.3751.920-a · Cited by 8 · see citing works

Sharing voxelwise neuroimaging results from rhesus monkeys and other species with Neurovault

Fox, A. S., Holley, D., Klink, P. C., Arbuckle, S. A., Barnes, C. A., Diedrichsen, J., Kwok, S. C., Kyle, C. T., Pruszynski, J. A., Seidlitz, J., et al. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117518 · Cited by 7 · see citing works

Combining brain perturbation and neuroimaging in non-human primates

Klink, P. C., Aubry, J., Ferrera, V. P., Fox, A. S., Froudist‐Walsh, S., Jarraya, B., Konofagou, E. E., Krauzlis, R. J., Messinger, A., Mitchell, A. S., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118017 · Cited by 86 · see citing works

Successor-like representation guides the prediction of future events in human visual cortex and hippocampus

Ekman, M., Kusch, S., & de Lange, F. P. (2023) · eLife · doi:10.7554/elife.78904 · Cited by 58 · see citing works

Long-term learning transforms prefrontal cortex representations during working memory

Miller, J. A., Tambini, A., Kiyonaga, A., & D’Esposito, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.019 · Cited by 56 · see citing works

A retinotopic code structures the interaction between perception and memory systems

Steel, A., Silson, E. H., Garcia, B. D., & Robertson, C. E. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01512-3 · Cited by 51 · see citing works

Divisive normalization unifies disparate response signatures throughout the human visual hierarchy

Aqil, M., Knapen, T. H. J., & Dumoulin, S. O. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2108713118 · Cited by 43 · see citing works

Towards biologically plausible phosphene simulation for the differentiable optimization of visual cortical prostheses

van der Grinten, M., de Ruyter van Steveninck, J., Lozano, A., Pijnacker, L., Rueckauer, B., Roelfsema, P., van Gerven, M., van Wezel, R., Güçlü, U., & Güçlütürk, Y. (2024) · eLife · doi:10.7554/elife.85812 · Cited by 39 · see citing works

Chronic stability of a neuroprosthesis comprising multiple adjacent Utah arrays in monkeys

Chen, X., Wang, F., Kooijmans, R. N., Klink, P. C., Boehler, C., Asplund, M., & Roelfsema, P. R. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/ace07e · Cited by 39 · see citing works

1024-channel electrophysiological recordings in macaque V1 and V4 during resting state

Chen, X., Morales-Gregorio, A., Sprenger, J., Kleinjohann, A., Sridhar, S., van Albada, S. J., Grün, S., & Roelfsema, P. R. (2022) · Scientific Data · doi:10.1038/s41597-022-01180-1 · Cited by 32 · see citing works

Comparing BOLD and VASO-CBV population receptive field estimates in human visual cortex

de Oliveira, I. A. F., Cai, Y., Hofstetter, S., Siero, J. C. W., van der Zwaag, W., & Dumoulin, S. O. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118868 · Cited by 16 · see citing works

Predictions enable top-down pattern separation in the macaque face-processing hierarchy

Nigam, T., & Schwiedrzik, C. M. (2024) · Nature Communications · doi:10.1038/s41467-024-51543-y · Cited by 14 · see citing works

Characterizing Spatiotemporal Population Receptive Fields in Human Visual Cortex with fMRI

Kim, I., Kupers, E. R., Lerma‐Usabiaga, G., & Kalanit Grill-spector, A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0803-23.2023 · Cited by 13 · see citing works

Local field potentials, spiking activity, and receptive fields in human visual cortex

Luo, L., Wang, X., Lu, J., Chen, G., Luan, G., Li, W., Wang, Q., & Fang, F. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2436-x · Cited by 13 · see citing works

Relating Scene Memory and Perception Activity to Functional Properties, Networks, and Landmarks of Posterior Cerebral Cortex—A Probabilistic Atlas

Steel, A., Prasad, D., Garcia, B. D., & Robertson, C. E. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0028-25.2025 · Cited by 15 · see citing works

Sensory reformatting for a working visual memory

Kiyonaga, A., & Serences, J. T. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.09.006 · Cited by 10 · see citing works

Low-level tuning biases in higher visual cortex reflect the semantic informativeness of visual features

Henderson, M. M., Tarr, M. J., & Wehbe, L. (2023) · Journal of Vision · doi:10.1167/jov.23.4.8 · Cited by 9 · see citing works

A multivariate comparison of electroencephalogram and functional magnetic resonance imaging to electrocorticogram using visual object representations in humans

Ebrahiminia, F., Cichy, R. M., & Khaligh‐Razavi, S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.983602 · Cited by 8 · see citing works

Precise spatial tuning of visually driven alpha oscillations in human visual cortex

Yuasa, K., Groen, I. I. A., Piantoni, G., Montenegro, S., Flinker, A., Devore, S., Devinsky, O., Doyle, W., Dugan, P. C., Friedman, D. J., et al. (2025) · eLife · doi:10.1101/2023.02.11.528137 · Cited by 8 · see citing works

Biologically plausible phosphene simulation for the differentiable optimization of visual cortical prostheses

van der Grinten, M., de Ruyter van Steveninck, J., Lozano, A., Pijnacker, L., Rückauer, B., Roelfsema, P., van Gerven, M., van Wezel, R., Güçlü, U., & Güçlütürk, Y. (2022) · doi:10.1101/2022.12.23.521749 · Cited by 39 · see citing works

Computational model links normalization to chemoarchitecture in the human visual system

Aqil, M., Knapen, T. H. J., & Dumoulin, S. O. (2024) · Science Advances · doi:10.1126/sciadv.adj6102 · Cited by 7 · see citing works

Probabilistic forward replay of anticipated stimulus sequences in human primary visual cortex and hippocampusPreprint

Ekman, M., Gennari, G., & de Lange, F. P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.26.477907 · Cited by 9 · see citing works

A model of thalamo-cortical interaction for incremental binding in mental contour-tracing

Schmid, D., & Heiko Neumann, B. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012835 · Cited by 7 · see citing works

Color and Spatial Frequency Provide Functional Signatures of Retinotopic Visual Areas

Loggia, S. R., Duffield, S. J., Braunlich, K., & Conway, B. R. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1673-23.2024 · Cited by 4 · see citing works

Time Course of Orientation Ensemble Representation in the Human Brain

Gong, X., He, T., Wang, Q., Lu, J., & Fang, F. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1688-23.2024 · Cited by 5 · see citing works

Modeling 2D spatio-tactile population receptive fields of the fingertip in human primary somatosensory cortex

Stoll, S., Lüesebrink, F., Schwarzkopf, D. S., Mattern, H., Liu, P., Noelle, J., & Kuehn, E. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1210 · Cited by 4 · see citing works

Spatial frequency adaptation modulates population receptive field sizes

Altan, E., Morgan, C., Dakin, S. C., & Schwarzkopf, D. S. (2025) · eLife · doi:10.7554/elife.100734.3 · Cited by 4 · see citing works

nBEST: Deep-learning-based non-human primates Brain Extraction and Segmentation Toolbox across ages, sites and species

Zhong, T., Wu, X., Liang, S., Ning, Z., Wang, L., Niu, Y., Yang, S., Kang, Z., Feng, Q., Li, G., et al. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120652 · Cited by 4 · see citing works

Mapping the visual world to the human brain

Ip, I. B., & Bridge, H. (2021) · eLife · doi:10.7554/elife.75171 · Cited by 4 · see citing works

Positive and Negative Retinotopic Codes in the Human Hippocampus

Angeli, P. A., Steel, A., & Robertson, C. E. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0309-26.2026 · Cited by 3 · see citing works

Large-scale mapping of artificial perceptions for neuroprostheses using spontaneous neuronal activity in macaque and human visual cortex

Lozano, A., Chen, X., Grouw, M. L., Li, B., Wang, F., van der Grinten, M., Soto‐Sánchez, C., Morales-Gregorio, A., Fernández, E., & Roelfsema, P. R. (2025) · Brain stimulation · doi:10.1016/j.brs.2025.103019 · Cited by 6 · see citing works

Characterizing Human Disparity Tuning Properties Using Population Receptive Field Mapping

Alvarez, I., Mancari, A., Ip, I. B., Parker, A. J., & Bridge, H. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0795-24.2025 · Cited by 3 · see citing works

Psilocybin alters visual contextual computations

Aqil, M., de Hollander, G., Vreugdenhil, N., Knapen, T. H. J., & Dumoulin, S. O. (2025) · Nature Communications · doi:10.1038/s41467-025-65150-y · Cited by 3 · see citing works

Large-scale RF mapping without visual input for neuroprostheses in macaque and human visual cortexPreprint

Lozano, A., Chen, X., Grouw, M. L., Li, B., Wang, F., van der Grinten, M., Soto‐Sánchez, C., Morales-Gregorio, A., Fernández, E., & Roelfsema, P. R. (2024) · medRxiv · doi:10.1101/2024.12.22.24319047 · Cited by 3 · see citing works

Contextual responses drive a unique laminar signature in human V1

Heij, J., Raimondo, L., Siero, J. C. W., van der Zwaag, W., Knapen, T. H. J., & Dumoulin, S. O. (2025) · iScience · doi:10.1016/j.isci.2025.112967 · Cited by 2 · see citing works

The Neural Organization of Visual Information in the Auditory Cortex of the Congenitally Deaf

Tal, Z., Sayal, J., Fang, F., Yanchao Bi, A., Almeida, J., & Fracasso, A. (2026) · Human Brain Mapping · doi:10.1002/hbm.70444 · Cited by 2 · see citing works

The contribution of default mode network areas to visual perception

Ùjhelyi, B., Korda, Ž., & Zaretskaya, N. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2026.03.009 · Cited by 3 · see citing works

Transcranial direct current stimulation elevates the baseline activity while sharpening the spatial tuning of the human visual cortex

Ahn, J., Ryu, J., Lee, S., Lee, C., Im, C., & Lee, S. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.07.052 · Cited by 2 · see citing works

Widespread, perception-related information in the human brain scales with levels of consciousness

Vigotsky, A. D., Jabakhanji, R., Branco, P., Iannetti, G. D., Baliki, M. N., & Apkarian, A. V. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00240 · Cited by 2 · see citing works

Signatures of vibration frequency tuning in human neocortexPreprint

Wang, L., & Yau, J. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.03.462923 · Cited by 2 · see citing works

Long-term learning transforms prefrontal cortex representations during working memoryPreprint

Miller, J. A., Tambini, A., Kiyonaga, A., & D’Esposito, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.22.481537 · Cited by 2 · see citing works

Precise Spatial Tuning of Visually Driven Alpha Oscillations in Human Visual CortexPreprint

Yuasa, K., Groen, I. I. A., Piantoni, G., Montenegro, S., Flinker, A., Devore, S., Devinsky, O., Doyle, W., Dugan, P. C., Friedman, D. J., et al. (2023) · eLife · doi:10.7554/elife.90387.1 · Cited by 3 · see citing works

Precise spatial tuning of visually driven alpha oscillations in human visual cortexPreprint

Yuasa, K., Groen, I. I. A., Piantoni, G., Montenegro, S., Flinker, A., Devore, S., Devinsky, O., Doyle, W., Dugan, P. C., Friedman, D. J., et al. (2023) · eLife · doi:10.7554/elife.90387 · Cited by 3 · see citing works

Training-induced changes in population receptive field properties in visual cortex: Impact of eccentric vision training on population receptive field properties and the crowding effect

Malania, M., Lin, Y.-S., Hörmandinger, C., Werner, J. S., Greenlee, M. W., & Plank, T. (2024) · Journal of Vision · doi:10.1167/jov.24.5.7 · Cited by 1 · see citing works

Compression-enabled interpretability of voxelwise encoding models

Kamali, F., Suratgar, A. A., Menhaj, M., & Abbasi-Asl, R. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012822 · Cited by 1 · see citing works

Stereotactic lesioning of cholinergic cells by injection of ME20.4 Saporin in the nucleus basalis of Meynert in a rhesus monkey ( Macaca mulatta )

Nazmuddin, M., Stammes, M. A., Klink, P. C., Vernes, M. K., Bakker, J., Langermans, J. A. M., van Laar, T., & Philippens, I. H. C. H. M. (2025) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaf081 · Cited by 1 · see citing works

Spatial Frequency Tuning Follows Scale Invariance in the Human Visual Cortex

Wiecek, E. K., Ramirez, L. D., Klímová, M., & Ling, S. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1490-25.2025 · Cited by 1 · see citing works

Linking retinal sampling in neural encoding models to temporal profiles of visual processing in humans

Müller, N., Chen, H., Wahlberg, S., Scholte, H. S., & Groen, I. I. A. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014371 · Cited by 1 · see citing works

Attentional enhancement and suppression of stimulus-synchronized BOLD oscillationsPreprint

Rafeh, R. W., Ngo, G. N., Muller, L., KHAN, A. R., Menon, R. S., Mur, M., & Schmitz, T. W. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.10.632431 · Cited by 1 · see citing works

Distributed illusory figure-ground segmentation signatures across the dorsal and ventral streamsPreprint

Arsenovic, A., Ischebeck, A. K., & Zaretskaya, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.01.565170

Multiple Loci for Foveolar Vision in Macaque MonkeyPreprint

Qian, M., Wang, J., Gao, Y., Chen, M., Liu, Y., Zhou, D., Lu, H. D., Zhang, X., Hu, J., & Roe, A. W. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.01.578387

A brain subcortical segmentation tool based on anatomy attentional fusion network for developing macaques

Zhong, T., Wang, Y., Xu, X., Wu, X., Liang, S., Ning, Z., Wang, L., Niu, Y., Li, G., & Zhang, Y. (2024) · Computerized Medical Imaging and Graphics · doi:10.1016/j.compmedimag.2024.102404

Retinotopic coding organizes the interaction between internally and externally oriented brain networks

Steel, A., Angeli, P. A., & Robertson, C. E. (2026) · eLife · doi:10.1101/2024.09.25.615084

Spatial frequency adaptation modulates population receptive field sizesPreprint

Altan, E., Morgan, C., Dakin, S. C., & Schwarzkopf, D. S. (2024) · eLife · doi:10.7554/elife.100734

Spatial frequency adaptation modulates population receptive field sizesPreprint

Altan, E., Morgan, C., Dakin, S. C., & Schwarzkopf, D. S. (2024) · eLife · doi:10.7554/elife.100734.1

Precise Spatial Tuning of Visually Driven Alpha Oscillations in Human Visual CortexPreprint

Yuasa, K., Groen, I. I. A., Piantoni, G., Montenegro, S., Flinker, A., Devore, S., Devinsky, O., Doyle, W., Dugan, P. C., Friedman, D. J., et al. (2025) · eLife · doi:10.7554/elife.90387.2

Non-invasive mapping of the temporal processing hierarchy in the human visual cortex

Eickhoff, K., Hillebrand, A., Knapen, T. H. J., de Jong, M. C., & Dumoulin, S. O. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014434

Spatial frequency adaptation modulates population receptive field sizesPreprint

Altan, E., Morgan, C., Dakin, S. C., & Schwarzkopf, D. S. (2025) · eLife · doi:10.7554/elife.100734.2

The precision of attention controls attraction of population receptive fields

Abdirashid, S. S., Knapen, T. H. J., & Dumoulin, S. O. (2025) · Journal of Vision · doi:10.1167/jov.25.11.3

Aligning machines and minds: neural encoding for high-level visual cortices based on image captioning task

Yin, X. X., Jiang, J., Ge, S., Gan, J. Q., & Wang, H. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/ae1164

Receptive fields from single-neuron recording and MRI reveal similar information coding for binocular depth

Parker, A. J., Alvarez, I., Mancari, A., Ip, I. B., Krug, K., & Bridge, H. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2409893122

The Richness of Vision in the Mammalian Brain: Neural Codes for Visual Perception and Behavior in Three Dimensions

Rosenberg, A., Bridge, H., Connor, C. E., Samonds, J. M., Tanabe, S., & Krug, K. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1316-25.2025 · Cited by 1 · see citing works

Unveiling early visual cortical mechanisms in perceptual filling-in: a parametric study of eccentricity and movement dependencePreprint

Koiso, K., Razafindrahaba, A., van de Ven, V. G., Martino, F. D., Roberts, M. J., & Weerd, P. D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.11.687787

Visuospatial coding by theta oscillations in human hippocampusPreprint

Rostowsky, K. A., Issa, N. P., Wu, S., Tao, J. X., Haider, H. A., Rose, S. L., Warnke, P. C., Satzer, D. I., Braga, R. M., Schuele, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.19.725196

High-channel-count neural recording and stimulation platform with 5376 simultaneous recording channels

Fan, Y., Ma, Y., Zolotavin, P., Topalli, G., Wang, W., Karlsson, M. P., Karlsson, M., Luan, L., Xie, C., & Chi, T. (2026) · npj Biomedical Innovations. · doi:10.1038/s44385-026-00103-8 · Cited by 1 · see citing works

From Functional Organization to Vascular Structure in the Primate Visual Cortex Using Ultrasound ImagingPreprint

DESAILLY, E., Alcala, I., Provansal, M., Arab, R., Zucker, N., Fallegger, F., Pouget, P., Tanter, M., Picaud, S. A., & Arcizet, F. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.18.745404

Population receptive field measurements in macaque visual cortex.

Smirnakis, S. M., Keliris, G. A., Shao, Y., Papanikolaou, A., & Logothetis, N. K. (2012) · Journal of Vision · doi:10.1167/12.9.1397 · Cited by 1 · see citing works

Population receptive field estimates in human visual cortex. Neuroimage

Dumoulin, S. O., & W, B. A. (2007)

Population receptive field estimates in human visual cortex

Dumoulin, S. O., & Wandell, B. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.034 · Cited by 1,183 · see citing works

Quantitative population receptive field estimates in human visual cortex

Dumoulin, S. O., Amano, K., & Wandell, B. A. (2010) · Journal of Vision · doi:10.1167/8.17.35 · Cited by 2 · see citing works

Reconstructing human population receptive field properties

Dumoulin, S. O., & Harvey, B. M. (2012) · Journal of Vision · doi:10.1167/12.9.1393 · Cited by 5 · see citing works