Mental Imagery of Faces and Places Activates Corresponding Stimulus-Specific Brain Regions

Neural Mechanisms of Selective Visual Attention

Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388

The fusiform face area: a module in human extrastriate cortex specialized for face perception

Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738

Neural mechanisms of spatial selective attention in areas V1, V2, and V4 of macaque visual cortex

Luck, S. J., Chelazzi, L., Hillyard, S. A., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.1.24 · Cited by 1,615

Conceptual Processing during the Conscious Resting State: A Functional MRI Study

Binder, J. R., Frost, J. A., Hammeke, T. A., Bellgowan, P. S. F., Rao, S. M., & Cox, R. W. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563265 · Cited by 1,066

Differential sensitivity of human visual cortex to faces, letterstrings, and textures: a functional magnetic resonance imaging study

Puce, A., Allison, T., Asgari, M., Gore, J. C., & McCarthy, G. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05205.1996 · Cited by 987 · cited 1×

A functional neuroanatomy of hallucinations in schizophrenia

Silbersweig, D. A., Stern, E., Frith, C., Cahill, C., Holmes, A., Grootoonk, S., Seaward, J., McKenna, P., Chua, S. E., Schnorr, L., et al. (1995) · Nature · doi:10.1038/378176a0 · Cited by 906 · cited 2×

Areas Involved in Encoding and Applying Directional Expectations to Moving Objects

Shulman, G. L., Ollinger, J. M., Akbudak, E., Conturo, T. E., Snyder, A. Z., Petersen, S. E., & Corbetta, M. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09480.1999 · Cited by 298

Reopening the Mental Imagery Debate: Lessons from Functional Anatomy

Mellet, E., Petit, L., Mazoyer, B., Denis, M., & Tzourio, N. (1998) · NeuroImage · doi:10.1006/nimg.1998.0355 · Cited by 237 · cited 2×

Beyond mind-reading: multi-voxel pattern analysis of fMRI data

Norman, K. A., Polyn, S. M., Detre, G. J., & Haxby, J. V. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.07.005 · Cited by 2,271

Decoding subject-driven cognitive states with whole-brain connectivity patterns

Shirer, W. R., Ryali, S., Rykhlevskaia, E., Menon, V., & Greicius, M. D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr099 · Cited by 1,843

Neural foundations of imagery

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

Function in the human connectome: task-fMRI and individual differences in behavior

Barch, D. M., Burgess, G. C., Harms, M. P., Petersen, S. E., Schlaggar, B. L., Corbetta, M., Glasser, M. F., Curtiss, S., Dixit, S., Feldt, C., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.033 · Cited by 1,529

Two cortical systems for memory-guided behaviour

Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377

Semantic memory and the brain: structure and processes

Martin, A., & Chao, L. L. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00196-3 · Cited by 1,339

Consciousness, accessibility, and the mesh between psychology and neuroscience

Block, N. (2007) · Behavioral and Brain Sciences · doi:10.1017/s0140525x07002786 · Cited by 1,146

Mental Imagery: Functional Mechanisms and Clinical Applications

Pearson, J., Naselaris, T., Holmes, E. A., & Kosslyn, S. M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.08.003 · Cited by 1,087

Conceptual Processing during the Conscious Resting State: A Functional MRI Study

Binder, J. R., Frost, J. A., Hammeke, T. A., Bellgowan, P. S. F., Rao, S. M., & Cox, R. W. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563265 · Cited by 1,066

Functional specificity in the human brain: a window into the functional architecture of the mind

Kanwisher, N. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005062107 · Cited by 929

Mental imagery in emotion and emotional disorders

Holmes, E. A., & Mathews, A. (2010) · Clinical Psychology Review · doi:10.1016/j.cpr.2010.01.001 · Cited by 976

Imaginary Relish and Exquisite Torture: The Elaborated Intrusion Theory of Desire.

Kavanagh, D. J., Andrade, J., & May, J. (2005) · Psychological Review · doi:10.1037/0033-295x.112.2.446 · Cited by 956

Multiple routes to memory: distinct medial temporal lobe processes build item and source memories

Davachi, L., Mitchell, J. P., & Wagner, A. D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337195100 · Cited by 899

The human imagination: the cognitive neuroscience of visual mental imagery

Pearson, J. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0202-9 · Cited by 820

The Well-Worn Route and the Path Less Traveled

Hartley, T., Maguire, E. A., Spiers, H. J., & Burgess, N. (2003) · Neuron · doi:10.1016/s0896-6273(03)00095-3 · Cited by 817

Brain areas underlying visual mental imagery and visual perception: an fMRI study

Ganis, G., Thompson, W. L., & Kosslyn, S. M. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.02.012 · Cited by 765

Neural correlates of consciousness in humans

Rees, G., Kreiman, G., & Koch, C. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn783 · Cited by 742

Extrastriate body area in human occipital cortex responds to the performance of motor actions

Astafiev, S. V., Stanley, C. M., Shulman, G. L., & Corbetta, M. (2004) · Nature Neuroscience · doi:10.1038/nn1241 · Cited by 629

Bookworms versus nerds: Exposure to fiction versus non-fiction, divergent associations with social ability, and the simulation of fictional social worlds

Mar, R. A., Oatley, K., Hirsh, J., dela Paz, J., & Peterson, J. B. (2006) · Journal of Research in Personality · doi:10.1016/j.jrp.2005.08.002 · Cited by 614

Distributed Neural Systems for the Generation of Visual Images

Ishai, A., Ungerleider, L. G., & Haxby, J. V. (2000) · Neuron · doi:10.1016/s0896-6273(00)00168-9 · Cited by 579

Fear fosters flight: a mechanism for fear contagion when perceiving emotion expressed by a whole body

de Gelder, B., Snyder, J., Greve, D., Gerard, G., & Hadjikhani, N. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407042101 · Cited by 511

When is early visual cortex activated during visual mental imagery?

Kosslyn, S. M., & Thompson, W. L. (2003) · Psychological Bulletin · doi:10.1037/0033-2909.129.5.723 · Cited by 515

The proactive brain: memory for predictions

Bar, M. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0310 · Cited by 498

The neuroendocrine basis of social recognition

Ferguson, J. N., Young, L. J., & Insel, T. R. (2002) · Frontiers in Neuroendocrinology · doi:10.1006/frne.2002.0229 · Cited by 494

The cognitive neuroscience of remembering

Buckner, R. L., & Wheeler, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35090048 · Cited by 462

Functional-anatomic correlates of remembering and knowing

Wheeler, M. E., & Buckner, R. L. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.001 · Cited by 434

The functional impact of mental imagery on conscious perception

Pearson, J., Clifford, C. W. G., & Tong, F. (2008) · Current Biology · doi:10.1016/j.cub.2008.05.048 · Cited by 409

Distinct neural systems subserve person and object knowledge

Mitchell, J. P., Heatherton, T. F., & Macrae, C. N. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.232395699 · Cited by 407

Decoding Patterns of Human Brain Activity

Tong, F., & Pratte, M. S. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100412 · Cited by 375

Impact of mindfulness-based stress reduction training on intrinsic brain connectivity

Kilpatrick, L. A., Suyenobu, B. Y., Smith, S. R., Bueller, J. A., Goodman, T., Creswell, J. D., Tillisch, K., Mayer, E. A., & Naliboff, B. D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.034 · Cited by 355

Functional connectivity during working memory maintenance

GAZZALEY, A., RISSMAN, J., & D'ESPOSITO, M. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.4.580 · Cited by 337

Visual inspection of independent components: defining a procedure for artifact removal from fMRI data

Kelly, R. E., Alexopoulos, G. S., Wang, Z., Gunning, F. M., Murphy, C. F., Morimoto, S. S., Kanellopoulos, D., Jia, Z., Lim, K. O., & Hoptman, M. J. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.03.028 · Cited by 345

Where am I now? Distinct roles for parahippocampal and retrosplenial cortices in place recognition

Epstein, R. A., Parker, W. E., & Feiler, A. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0799-07.2007 · Cited by 331

Distributed Representations in Memory: Insights from Functional Brain Imaging

Rissman, J., & Wagner, A. D. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100344 · Cited by 299

Top-down activation of shape-specific population codes in visual cortex during mental imagery

Stokes, M., Thompson, R., Cusack, R., & Duncan, J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4657-08.2009 · Cited by 323

The Neural Fate of Consciously Perceived and Missed Events in the Attentional Blink

Marois, R., Yi, D.-J., & Chun, M. M. (2004) · Neuron · doi:10.1016/s0896-6273(04)00012-1 · Cited by 306

Seeing fearful body expressions activates the fusiform cortex and amygdala

Hadjikhani, N., & de Gelder, B. (2003) · Current Biology · doi:10.1016/j.cub.2003.11.049 · Cited by 298

Negative BOLD differentiates visual imagery and perception

Amedi, A., Malach, R., & Pascual-Leone, A. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.032 · Cited by 271

Disentangling visual imagery and perception of real-world objects

Lee, S.-H., Kravitz, D. J., & Baker, C. I. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.055 · Cited by 263

Imagery and perception share cortical representations of content and location

Cichy, R. M., Heinzle, J., & Haynes, J.-D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr106 · Cited by 242

“I have often walked down this street before”: fMRI Studies on the hippocampus and other structures during mental navigation of an old environment

Rosenbaum, R. S., Ziegler, M., Winocur, G., Grady, C. L., & Moscovitch, M. (2004) · Hippocampus · doi:10.1002/hipo.10218 · Cited by 258

fMRI activation of the fusiform gyrus and amygdala to cartoon characters but not to faces in a boy with autism

Grelotti, D. J., Klin, A. J., Gauthier, I., Skudlarski, P., Cohen, D. J., Gore, J. C., Volkmar, F. R., & Schultz, R. T. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.06.015 · Cited by 254

Brain–Computer Interface Technologies in the Coming Decades

Lance, B. J., Kerick, S. E., Ries, A. J., Oie, K. S., & McDowell, K. (2012) · Proceedings of the IEEE · doi:10.1109/jproc.2012.2184830 · Cited by 231

A cry in the dark: depressed mothers show reduced neural activation to their own infant’s cry

Laurent, H. K., & Ablow, J. C. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq091 · Cited by 224

Sleep imaging and the neuro-psychological assessment of dreams

Schwartz, S., & Maquet, P. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01818-0 · Cited by 218

The neural correlates of visual imagery vividness – An fMRI study and literature review

Fulford, J., Milton, F., Salas, D., Smith, A., Simler, A., Winlove, C., & Zeman, A. (2018) · Cortex · doi:10.1016/j.cortex.2017.09.014 · Cited by 211

Data-driven clustering reveals a fundamental subdivision of the human cortex into two global systems

Golland, Y., Golland, P., Bentin, S., & Malach, R. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.10.003 · Cited by 190

Memory: Enduring Traces of Perceptual and Reflective Attention

Chun, M. M., & Johnson, M. K. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.026 · Cited by 199

Quantifying aphantasia through drawing: Those without visual imagery show deficits in object but not spatial memory

Bainbridge, W. A., Pounder, Z., Eardley, A. F., & Baker, C. I. (2021) · Cortex · doi:10.1016/j.cortex.2020.11.014 · Cited by 195

Involvement of rostral prefrontal cortex in selection between stimulus‐oriented and stimulus‐independent thought

Gilbert, S. J., Frith, C. D., & Burgess, P. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03981.x · Cited by 193

Mental imagery of speech implicates two mechanisms of perceptual reactivation.

Tian, X., Zarate, J. M., & Poeppel, D. (2016) · Cortex · doi:10.1016/j.cortex.2016.01.002 · Cited by 178

Targeting the affective brain—a randomized controlled trial of real-time fMRI neurofeedback in patients with depression

Mehler, D. M. A., Sokunbi, M. O., Habes, I., Barawi, K., Subramanian, L., Range, M., Evans, J., Hood, K., Lührs, M., Keedwell, P., et al. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0126-5 · Cited by 175

Reinstatement of individual past events revealed by the similarity of distributed activation patterns during encoding and retrieval

Wing, E. A., Ritchey, M., & Cabeza, R. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00740 · Cited by 174

Cortical reinstatement mediates the relationship between content-specific encoding activity and subsequent recollection decisions

Gordon, A. M., Rissman, J., Kiani, R., & Wagner, A. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht194 · Cited by 173

Mental imagery of speech: linking motor and perceptual systems through internal simulation and estimation.

Tian, X., & Poeppel, D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00314 · Cited by 161

Two distinct scene processing networks connecting vision and memory

Baldassano, C., Esteva, A., Fei-Fei, L., & Beck, D. M. (2016) · eneuro · doi:10.1523/eneuro.0178-16.2016 · Cited by 144

Visual Scene Processing in Familiar and Unfamiliar Environments

Epstein, R. A., Higgins, J. S., Jablonski, K., & Feiler, A. M. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00003.2007 · Cited by 153

Visualizing minimal ingroup and outgroup faces: Implications for impressions, attitudes, and behavior.

Ratner, K. G., Dotsch, R., Wigboldus, D. H. J., van Knippenberg, A., & Amodio, D. M. (2014) · Journal of Personality and Social Psychology · doi:10.1037/a0036498 · Cited by 144

Visual Imagery and Perception Share Neural Representations in the Alpha Frequency Band

Xie, S., Kaiser, D., & Cichy, R. M. (2020) · Current Biology · doi:10.1016/j.cub.2020.04.074 · Cited by 139

Modality-independent coding of spatial layout in the human brain

Wolbers, T., Klatzky, R. L., Loomis, J. M., Wutte, M. G., & Giudice, N. A. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.038 · Cited by 143

Visual memory and visual perception recruit common neural substrates

Slotnick, S. D. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304274070 · Cited by 130

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

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

Mistaking a house for a face: neural correlates of misperception in healthy humans

Summerfield, C., Egner, T., Mangels, J., & Hirsch, J. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhi129 · Cited by 120

Neurological disorders and the structure of human consciousness

Cooney, J. W., & Gazzaniga, M. S. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(03)00058-5 · Cited by 113

The default network and the combination of cognitive processes that mediate self-generated thought

Axelrod, V., Rees, G., & Bar, M. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0244-9 · Cited by 111

Riding the Lexical Speedway: A Critical Review on the Time Course of Lexical Selection in Speech Production

Strijkers, K., & Costa, A. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00356 · Cited by 106

Reading about the actions of others: Biological motion imagery and action congruency influence brain activity

Deen, B., & McCarthy, G. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.01.028 · Cited by 101

Disentangling the neural mechanisms involved in Hinduism- and Buddhism-related meditations

Tomasino, B., Chiesa, A., & Fabbro, F. (2014) · Brain and Cognition · doi:10.1016/j.bandc.2014.03.013 · Cited by 94

Visual mental imagery in congenital prosopagnosia

Grüter, T., Grüter, M., Bell, V., & Carbon, C.-C. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.02.021 · Cited by 92

The sensory consequences of speaking: parametric neural cancellation during speech in auditory cortex

Christoffels, I. K., van de Ven, V., Waldorp, L. J., Formisano, E., & Schiller, N. O. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018307 · Cited by 72

Conditioning and cognition

Pickens, C. L., & Holland, P. C. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.003 · Cited by 69

Corticomotor Excitability during Observation and Imagination of a Work of Art

Battaglia, F., Lisanby, S. H., & Freedberg, D. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00079 · Cited by 66

Stimulus-free thoughts induce differential activation in the human default network

Preminger, S., Harmelech, T., & Malach, R. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.036 · Cited by 59

A model of egocentric to allocentric understanding in mammalian brains

Uria, B., Ibarz, B., Banino, A., Zambaldi, V., Kumaran, D., Hassabis, D., Barry, C., & Blundell, C. (2020) · doi:10.1101/2020.11.11.378141 · Cited by 48

Neural substrates of animal mental imagery: calcarine sulcus and dorsal pathway involvement—an fMRI study

Lambert, S., Sampaio, E., Scheiber, C., & Mauss, Y. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03232-2 · Cited by 50

How does the brain encode epistemic reliability? Perceptual presence, phenomenal transparency, and counterfactual richness.

Metzinger, T. (2014) · Cognitive Neuroscience · doi:10.1080/17588928.2014.905519 · Cited by 37

Different types of laughter modulate connectivity within distinct parts of the laughter perception network

Wildgruber, D., Szameitat, D. P., Ethofer, T., Brück, C., Alter, K., Grodd, W., & Kreifelts, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063441 · Cited by 33

Visual mental imagery engages the left fusiform gyrus, but not the early visual cortex: A meta-analysis of neuroimaging evidence

Spagna, A., Hajhajate, D., Liu, J., & Bartolomeo, P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.029 · Cited by 33

Prior probability modulates anticipatory activity in category-specific areas

Trapp, S., Lepsien, J., Kotz, S. A., & Bar, M. (2016) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-015-0373-4 · Cited by 24

Evidence for similar patterns of neural activity elicited by picture- and word-based representations of natural scenes

Kumar, M., Federmeier, K. D., Fei-Fei, L., & Beck, D. M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.03.037 · Cited by 20

Adolescent-specific memory effects: evidence from working memory, immediate and long-term recognition memory performance in 8–30 yr olds

Skalaban, L. J., Cohen, A. O., Conley, M. I., Lin, Q., Schwartz, G. N., Ruiz-Huidobro, N. A. M., Cannonier, T., Martinez, S. A., & Casey, B. J. (2022) · Learning & Memory · doi:10.1101/lm.053539.121 · Cited by 14

The Left Hemisphere Does Not Miss the Right Hemisphere

Gazzaniga, M. S., & Miller, M. B. (2009) · The Neurology of Consciousness · doi:10.1016/b978-0-12-374168-4.00020-4 · Cited by 13

Common and distinct neural representations of imagined and perceived speech

Lu, L., Han, M., Zou, G., Zheng, L., & Gao, J.-H. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhac519 · Cited by 11

The brain as image processor and generator: towards function-restoring brain-computer-interfaces

van Hoof, R. (2022) · doi:10.26481/dis.20220603rh · Cited by 1