Evidence for Sensory Prediction Deficits in Schizophrenia

The Brief Psychiatric Rating Scale.

Overall, J. E., & Gorham, D. R. (1962) · Psychological Reports · doi:10.2466/pr0.1962.10.3.799 · Cited by 11,090

An internal model for sensorimotor integration

Wolpert, D. M., Ghahramani, Z., & Jordan, M. I. (1995) · Science · doi:10.1126/science.7569931 · Cited by 3,553

Neural basis of the spontaneous optokinetic response produced by visual inversion

Sperry, R. W. (1950) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0055479 · Cited by 1,789

Central cancellation of self-produced tickle sensation

Blakemore, S.-J., Wolpert, D. M., & Frith, C. D. (1998) · Nature Neuroscience · doi:10.1038/2870 · Cited by 1,467

The cognitive neuroscience of action

(1997) · Choice Reviews Online · doi:10.5860/choice.34-5975 · Cited by 1,118

Relations between the central Nervous System and the peripheral organs

Holst, E. V. (1954) · The British Journal of Animal Behaviour · doi:10.1016/s0950-5601(54)80044-x · Cited by 1,104

Explaining the symptoms of schizophrenia: abnormalities in the awareness of action.

Frith, C. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00052-1 · Cited by 782

Mapping auditory hallucinations in schizophrenia using functional magnetic resonance imaging

Shergill, S. S., Brammer, M. J., Williams, S. C. R., Murray, R. M., & McGuire, P. K. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.11.1033 · Cited by 666 · cited 1×

Two Eyes for an Eye: The Neuroscience of Force Escalation

Shergill, S. S., Bays, P. M., Frith, C., & Wolpert, D. M. (2003) · Science · doi:10.1126/science.1085327 · Cited by 414

Predicting the Consequences of Our Own Actions: The Role of Sensorimotor Context Estimation

Blakemore, S., Goodbody, S. J., & Wolpert, D. M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-18-07511.1998 · Cited by 380

Aberrant Force Processing in Schizophrenia

Martinelli, C., Rigoli, F., & Shergill, S. S. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw092 · Cited by 25

Rapid Eye Movements in Sleep Furnish a Unique Probe Into Consciousness

Hong, C. C.-H., Fallon, J. H., Friston, K. J., & Harris, J. C. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02087 · Cited by 29

Disturbed Consciousness

Gennaro, R. J. (2015) · The MIT Press eBooks · doi:10.7551/mitpress/9780262029346.001.0001 · Cited by 25

A Deep Convolutional Neural Network Model for Sense of Agency and Object Permanence in Robots

Lang, C., Schillaci, G., & Hafner, V. V. (2018) · IEEE International Conference on Development and Learning (ICDL) · doi:10.1109/devlrn.2018.8761015 · Cited by 24

Consider the pons: bridging the gap on sensory prediction abnormalities in schizophrenia

Abram, S. V., Hua, J. P. Y., & Ford, J. M. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.08.008 · Cited by 22

Abnormal amygdala subregional-sensorimotor connectivity correlates with positive symptom in schizophrenia

Zhang, M., Yang, F., Fan, F., Wang, Z., Hong, X., Tan, Y., Tan, S., & Hong, L. E. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102218 · Cited by 25

Auditory processing control by the medial prefrontal cortex: A review of the rodent functional organisation

Hockley, A., & Malmierca (2024) · Hearing Research · doi:10.1016/j.heares.2024.108954 · Cited by 27

The positive dimension of schizotypy is associated with a reduced attenuation and precision of self-generated touch

Asimakidou, E., Job, X., & Kilteni, K. (2022) · Schizophrenia · doi:10.1038/s41537-022-00264-6 · Cited by 28

An EEG Study on the Effects of Induced Spiritual Experiences on Somatosensory Processing and Sensory Suppression

van Elk, M. (2015) · Journal for the Cognitive Science of Religion · doi:10.1558/jcsr.v2i2.24573 · Cited by 24

Prosthesis embodiment and attenuation of prosthetic touch in upper limb amputees – A proof-of-concept study

Fritsch, A., Lenggenhager, B., & Bekrater‐Bodmann, R. (2020) · Consciousness and Cognition · doi:10.1016/j.concog.2020.103073 · Cited by 26

The Many Roles of Precision in Action

Limanowski, J., Adams, R. A., Kilner, J. M., & Parr, T. (2024) · Entropy · doi:10.3390/e26090790 · Cited by 25

Superior size–weight illusion performance in patients with schizophrenia: Evidence for deficits in forward models

Williams, L. E., Ramachandran, V. S., Hubbard, E. M., BRAFF, D. L., & Light, G. A. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.10.021 · Cited by 24

Perisaccadic Perception of Visual Space in People with Schizophrenia

Richard, A., Churan, J., Whitford, V., O’Driscoll, G. A., Titone, D. A., & Pack, C. C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4744-13.2014 · Cited by 21

Altered processing of sensorimotor feedback in schizophrenia

Posada, A., Nicolas Franck, B., Augier, S., Georgieff, N., & Jeannerod, M. (2007) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2007.02.003 · Cited by 21

Brief Temporal Perturbations in Somatosensory Reafference Disrupt Perceptual and Neural Attenuation and Increase Supplementary Motor Area–Cerebellar Connectivity

Kilteni, K., Houborg, C., & Ehrsson, H. H. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1743-22.2023 · Cited by 24

Impaired saccadic adaptation in schizophrenic patients with high neurological soft sign scores

Picard, H., Séac’h, A. L., Amado, I., Raphaël Gaillard, B., Krebs, M., & Beauvillain, C. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.04.039 · Cited by 20

Low-level, prediction-based sensory and motor processes are unimpaired in Autism

Finnemann, J., Plaisted-Grant, K. C., Moore, J. W., Teufel, C., & Fletcher, P. C. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.107835 · Cited by 22

The cerebellum and learning of non-motor associations in individuals at clinical-high risk for psychosis

Bernard, J. A., Orr, J. M., Dean, D. J., & Mittal, V. A. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.023 · Cited by 20

GABAA and NMDA receptor density alterations and their behavioral correlates in the gestational methylazoxymethanol acetate model for schizophrenia

Kiemes, A., Gomes, F. V., Cash, D., Uliana, D. L., Simmons, C., Singh, N., Vernon, A. C., Turkheimer, F., Davies, C., Stone, J. M., et al. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01213-0 · Cited by 18

Defective Embodiment of Alien Hand Uncovers Altered Sensorimotor Integration in Schizophrenia

Rossetti, I., Romano, D., Florio, V., Doria, S., Nisticò, V., Conca, A., Mencacci, C., & Maravita, A. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sbz050 · Cited by 19

Cultural Differences in Perceiving Sounds Generated by Others: Self Matters

Cao, L., & Groß, J. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01865 · Cited by 23

Imaging auditory hallucinations in schizophrenia

Tracy, D. K., & Shergill, S. S. (2006) · Acta Neuropsychiatrica · doi:10.1111/j.1601-5215.2006.00129.x · Cited by 20

The Paradox of Delusions

Nicholas Furl, A., Coltheart, M., & McKay, R. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198872221.003.0012 · Cited by 19

Motor Planning of Vertical Arm Movements in Healthy Older Adults: Does Effort Minimization Persist With Aging?

Poirier, G., Papaxanthis, C., Mourey, F., & Gaveau, J. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00037 · Cited by 18

Thought consciousness and source monitoring depend on robotically controlled sensorimotor conflicts and illusory states

Serino, A., Pozeg, P., Bernasconi, F., Solcà, M., Hara, M., Progin, P., Stripeikyte, G., Dhanis, H., Salomon, R., Bleuler, H., et al. (2020) · iScience · doi:10.1016/j.isci.2020.101955 · Cited by 18

Prediction-Related Frontal-Temporal Network for Omission Mismatch Activity in the Macaque Monkey

Suda, Y., Tada, M., Matsuo, T., Kawasaki, K., Saigusa, T., Ishida, M., Mitsui, T., Kumano, H., Kirihara, K., Suzuki, T., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.557954 · Cited by 18

When Passive Feels Active - Delusion-Proneness Alters Self-Recognition in the Moving Rubber Hand Illusion

Louzolo, A., Kalckert, A., & Petrović, P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128549 · Cited by 19

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders

Ishizuka, K., Kimura, H., Wang, C., Xing, J., Kushima, I., Arioka, Y., Oya‐Ito, T., Uno, Y., Okada, T., Mori, D., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153224 · Cited by 19

Goal‐directed behaviors in patients with schizophrenia: Concept relevance and updated model

Rinaldi, R., & Lefèbvre, L. (2016) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12401 · Cited by 18

Computational models of the “active self” and its disturbances in schizophrenia

Möller, T. J., Georgie, Y. K., Schillaci, G., Voss, M., Hafner, V. V., & Kaltwasser, L. (2021) · Consciousness and Cognition · doi:10.1016/j.concog.2021.103155 · Cited by 19

Voluntary or involuntary? A neurophysiologic approach to functional movement disorders

Stenner, M., & Haggard, P. (2016) · Handbook of clinical neurology · doi:10.1016/b978-0-12-801772-2.00011-4 · Cited by 18

Impaired perception of temporal contiguity between action and effect is associated with disorders of agency in schizophrenia

Roth, M. J., Lindner, A., Hesse, K., Wildgruber, D., Wong, H. Y., & Buehner, M. J. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2214327120 · Cited by 18

Schizophrenia as a disorder of embodied self

Szczotka, J., & Majchrowicz, B. (2018) · Psychiatria Polska · doi:10.12740/pp/67276 · Cited by 17

Computational mechanisms underlying illusion of control in delusional individuals

Na, S., Blackmore, S., Chung, D., O’Brien, M., Banker, S. M., Heflin, M., Fiore, V. G., & Gu, X. (2022) · Schizophrenia Research · doi:10.1016/j.schres.2022.01.054 · Cited by 15

The dynamic boundaries of the Self: Serial dependence in the Sense of Agency

Stern, Y., Ben-Yehuda, I., Koren, D., Zaidel, A., & Salomon, R. (2022) · Cortex · doi:10.1016/j.cortex.2022.03.015 · Cited by 18

Growing up laughing: Laughables and pragmatic functions between 12 and 36 months

Mazzocconi, C., & Ginzburg, J. (2023) · Journal of Pragmatics · doi:10.1016/j.pragma.2023.04.015 · Cited by 16

Aging exerts a limited influence on the perception of self-generated and externally generated touch

Timar, L., Job, X., de Xivry, J. O., & Kilteni, K. (2023) · Journal of Neurophysiology · doi:10.1152/jn.00145.2023 · Cited by 17

Neuroimaging Effects of 1 Hz Right Temporoparietal rTMS on Normal Auditory Processing

Tracy, D. K., de Abreu, M. D. S., Orlov, N. D., Mao, L., Lage, C., & Shergill, S. S. (2014) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000098 · Cited by 16

The impact of using an upper-limb prosthesis on the perception of real and illusory weight differences

Buckingham, G., Parr, J. V. V., Wood, G., Vine, S. J., Dimitriou, P., & Day, S. J. (2018) · Psychonomic Bulletin & Review · doi:10.3758/s13423-017-1425-2 · Cited by 15

The neuroscience of free will: implications for psychiatry

Pierre, J. M. (2013) · Psychological Medicine · doi:10.1017/s0033291713002985 · Cited by 16

Know thy agency in predictive coding: Meta-monitoring over forward modeling

Asai, T. (2017) · Consciousness and Cognition · doi:10.1016/j.concog.2017.03.001 · Cited by 17

Paradoxical Sensitivity to Sub-threshold Asynchronies in Schizophrenia: A Behavioral and EEG Approach

da Silva, J. E. M. C., Krieg, J., Duval, C. Z., Schwitzer, T., & Giersch, A. (2021) · Schizophrenia Bulletin Open · doi:10.1093/schizbullopen/sgab011 · Cited by 16

Functional Brain Imaging of Auditory Hallucinations: From Self-Monitoring Deficits to Co-opted Neural Resources

Ford, J. M., & Hoffman, R. E. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4121-2_19 · Cited by 17

Tactile cognition in rodents

Diamond, M. E., & Toso, A. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105161 · Cited by 16

Sense of agency in schizophrenia: A reconciliation of conflicting findings through a theory-driven literature review

Rossetti, I., Mariano, M., Maravita, A., Paulesu, E., & Zapparoli, L. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105781 · Cited by 18

Continuous theta-burst stimulation to primary motor cortex reduces the overproduction of forces following removal of visual feedback

Therrien, A. S., Richardson, B. A., & Balasubramaniam, R. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.06.023 · Cited by 15

Transsaccadic Perception Deficits in Schizophrenia Reflect the Improper Internal Monitoring of Eye Movement Rather Than Abnormal Sensory Processing

Bansal, S., Bray, L. C. J., Schwartz, B. L., & Joiner, W. M. (2017) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2017.06.004 · Cited by 15

The ability to tickle oneself is associated with level of psychometric schizotypy in non-clinical individuals

Whitford, T. J., Mitchell, A., & Mannion, D. J. (2017) · Consciousness and Cognition · doi:10.1016/j.concog.2017.04.017 · Cited by 16

Contextual perception under active inference

Mirza, M. B., Cullen, M., Parr, T., Shergill, S. S., & Moran, R. (2021) · Scientific Reports · doi:10.1038/s41598-021-95510-9 · Cited by 14

Sense of external agency is sustained by multisensory functional integration in the somatosensory cortex

Piras, F., Vecchio, D., Ciullo, V., Gili, T., Banaj, N., Piras, F., & Spalletta, G. (2020) · Human Brain Mapping · doi:10.1002/hbm.25107 · Cited by 12

Illusion of control affects ERP amplitude reductions for auditory outcomes of self‐generated actions

Seidel, A., Ghio, M., Studer, B., & Bellebaum, C. (2021) · Psychophysiology · doi:10.1111/psyp.13792 · Cited by 15

N-methyl-d-aspartate receptor hypofunction causes recurrent and transient failures of perceptual inference

Weilnhammer, V. A., Rothkirch, M., Yilmaz, D., Fritsch, M., Ptasczynski, L. E., Reichenbach, K., Roediger, L., Corlett, P. R., & Sterzer, P. (2025) · Brain · doi:10.1093/brain/awaf011 · Cited by 15

Experience of action depends on intention, not body movement: An experiment on memory for mens rea

Jensen, M., Vagnoni, E., Overgaard, M. S., & Haggard, P. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.07.022 · Cited by 13

Evidence of absence: no relationship between behaviourally measured prediction error response and schizotypy

Humpston, C. S., Evans, L. H., Teufel, C., Ihssen, N., & Linden, D. E. J. (2017) · Cognitive Neuropsychiatry · doi:10.1080/13546805.2017.1348289 · Cited by 13

Predictive Modulation of Corticospinal Excitability and Implicit Encoding of Movement Probability in Schizophrenia

Dupin, L., Carment, L., Guedj, L., Cuenca, M., Krebs, M., Maier, M. A., Amado, I., & Lindberg, P. G. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sby186 · Cited by 13

Clinical, cognitive and neural correlates of self-monitoring deficits in schizophrenia: an update

Raveendran, V., & Kumari, V. (2007) · Acta Neuropsychiatrica · doi:10.1111/j.1601-5215.2007.00151.x · Cited by 13

I Predict, Therefore I Am: Perturbed Predictive Coding Under Ketamine and in Schizophrenia

Corlett, P. R. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.12.007 · Cited by 12

Reduced transfer of visuomotor adaptation is associated with aberrant sense of agency in schizophrenia

Bansal, S., Murthy, K. G., Fitzgerald, J. J., Schwartz, B. L., & Joiner, W. M. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.06.012 · Cited by 12

Aging into Perceptual Control: A Dynamic Causal Modeling for fMRI Study of Bistable Perception

Dowlati, E. P., Adams, S. E., Stiles, A. B., & Moran, R. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00141 · Cited by 11

Altered corollary discharge signaling in the auditory cortex of a mouse model of schizophrenia predisposition

Rummell, B., Bikas, S., Babl, S. S., Gogos, J. A., & Sigurdsson, T. (2023) · Nature Communications · doi:10.1038/s41467-023-42964-2 · Cited by 12

Illusions, Delusions, and Your Backwards Bayesian Brain: A Biased Visual Perspective

Born, R. T., & Bencomo, G. (2020) · Brain Behavior and Evolution · doi:10.1159/000514859 · Cited by 12

Methods of Somatosensory Attenuation

Kilteni, K. (2023) · Neuromethods · doi:10.1007/978-1-0716-3068-6_2 · Cited by 11

Bayesian Inference, Predictive Coding, and Computational Models of Psychosis

Adams, R. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809825-7.00007-9 · Cited by 16

Sequential neural changes during motor learning in schizophrenia

Rowland, L. M., Shadmehr, R., Kravitz, D. J., & Holcomb, H. H. (2008) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2007.10.006 · Cited by 11

Sensory Attenuation in Sport and Rehabilitation: Perspective from Research in Parkinson’s Disease

Kearney, J., & Brittain, J. (2021) · Brain Sciences · doi:10.3390/brainsci11050580 · Cited by 10

Predictions of bimanual self-touch determine the temporal tuning of somatosensory perception

Cemeljic, N., Job, X., & Kilteni, K. (2024) · iScience · doi:10.1016/j.isci.2024.111643 · Cited by 11

Do Cyborgs dream of Electric Limbs? Experiential Factors in Human-Computer Integration Design and Evaluation

Danry, V., Pataranutaporn, P., Horowitz, A. H., Strohmeier, P., Andrés, J., Patibanda, R., Li, Z., Nakamura, T., Nishida, J., Lopes, P., et al. (2021) · CHI Conference Extended Abstracts on Human Factors in Computing Systems (CHI EA) · doi:10.1145/3411763.3441355 · Cited by 10

Delusional thinking and action binding in healthy individuals

Cao, L., Steinborn, M. B., & Händel, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-97977-y · Cited by 8

‘Social dysmetria’ in first-episode psychosis patients

Waters, F., Rock, D. J., Dragović, M., & Jablensky, A. V. (2010) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2010.01651.x · Cited by 10

Detection of visual events along the apparent motion trace in patients with paranoid schizophrenia

Sanders, L. L. O., Muckli, L. F., de Millas, W., Lautenschlager, M. M., Heinz, A., Kathmann, N., & Sterzer, P. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.03.006 · Cited by 10

Auditory verbal hallucination in schizophrenic patients and the general population: The sense of agency in speech

Asai, T., Sugimori, E., & Tanno, Y. (2011) · Cited by 10

The Endocannabinoid System is a Major Player in Schizophrenia

Köfalvi, A., & Fritzsche, M. (2007) · Springer eBooks · doi:10.1007/978-0-387-74349-3_22 · Cited by 10

Hearing a Voice as one’s own: Two Views of Inner Speech Self-Monitoring Deficits in Schizophrenia

Langland‐Hassan, P. (2015) · Review of Philosophy and Psychology · doi:10.1007/s13164-015-0250-7 · Cited by 13

Neural correlates of an illusionary sense of agency caused by virtual reality

Cai, Y., Yang, H., Wang, X., Xiong, Z., Kühn, S., Bi, Y., & Wei, K. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad547 · Cited by 9

Predictive processing accounts of psychosis: bottom-up or top-down disruptions

Goodwin, I., Diederen, K. M. J., Hird, E., Weilnhammer, V. A., Garrido, M. I., & Knolle, F. (2026) · Nature Mental Health · doi:10.1038/s44220-025-00558-5 · Cited by 9

Elucidating multifinal and equifinal pathways to developmental disorders by constructing real-world neurorobotic models

Idei, H., & Yamashita, Y. (2023) · Neural Networks · doi:10.1016/j.neunet.2023.10.005 · Cited by 11

Schizophrenia Spectrum Disorders: Linking Motor and Process Skills, Sensory Patterns, and Psychiatric Symptoms

Halperin, L., & Falk-Kessler, J. P. (2020) · The Open Journal of Occupational Therapy · doi:10.15453/2168-6408.1659 · Cited by 9

Evaluating the Case for the Low-Level Approach to Agentive Awareness

Mylopoulos, M. I. (2012) · Philosophical Topics · doi:10.5840/philtopics201240216 · Cited by 9

The promise of layer-specific neuroimaging for testing predictive coding theories of psychosisPreprint

Haarsma, J., Kok, P., & Browning, M. D. (2020) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/5p64f · Cited by 9

Uptake, polymorphism, and the construction of networked events on Twitter

Rathnayake, C. (2020) · Telematics and Informatics · doi:10.1016/j.tele.2020.101518 · Cited by 8

Methodological considerations for the force-matching task

McNaughton, D. T., Hope, R., Gray, E. C., Xavier, F., Beath, A., & Jones, M. (2022) · Behavior Research Methods · doi:10.3758/s13428-022-01954-w · Cited by 13

Robotically-induced auditory-verbal hallucinations: combining self-monitoring and strong perceptual priors

Orepić, P., Bernasconi, F., Faggella, M., Faivre, N., & Blanke, O. (2023) · Psychological Medicine · doi:10.1017/s0033291723002222 · Cited by 7

Abnormal Oculomotor Corollary Discharge Signaling as a Trans-diagnostic Mechanism of Psychosis

Yao, B., Rolfs, M., Slate, R., Roberts, D., Fattal, J., Achtyes, E. D., Tso, I. F., Diwadkar, V. A., Kashy, D. A., Bao, J. Y., et al. (2024) · Schizophrenia Bulletin · doi:10.1093/schbul/sbad180 · Cited by 8

Course and symptom and functional correlates of passivity symptoms in schizophrenia: an 18-year multi-follow-up longitudinal study

Herbener, E. S., & Harrow, M. (2019) · Psychological Medicine · doi:10.1017/s0033291719003428 · Cited by 8

Impaired Sensorimotor Adaption in Schizophrenia in Comparison to Age-Matched and Elderly Controls

Cornelis, C., Picker, L. D., Coppens, V., Morsel, A., Timmers, M., Dumont, G., Sabbe, B., Morrens, M., & Hulstijn, W. (2021) · Neuropsychobiology · doi:10.1159/000518867 · Cited by 8

Perceptual sensory attenuation in chronic pain subjects and healthy controls

McNaughton, D. T., Beath, A., Hush, J. M., & Jones, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-13175-4 · Cited by 8

Corollary Discharge Failure in an Oculomotor Task Is Related to Delusional Ideation in Healthy Individuals

Malassis, R., Cul, A. D., & Collins, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134483 · Cited by 12

Cognition sociale et sens de l’agentivité en autisme : de l’action à l’interaction

Lafleur, A., Soulières, I., & d’Arc, B. F. (2016) · Santé mentale au Québec · doi:10.7202/1036970ar · Cited by 11

Actions Speak Louder Than Words: The Role of Action in Self‐Referential Advantage in Children With Autism

Wuyun, G., Wang, J., Zhang, L., Wang, K., Yi, L., & Wu, Y. (2020) · Autism Research · doi:10.1002/aur.2274 · Cited by 8

The Imbalanced Plasticity Hypothesis of Schizophrenia-Related Psychosis: A Predictive Perspective

Guterman, Y., Ataria, Y., & Silverstein, S. M. (2021) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-021-00911-y · Cited by 10

Predictive neural processing of self-generated hand and tool actions in patients with schizophrenia spectrum disorders and healthy individuals

Schmitter, C. V., Pazen, M., Uhlmann, L., van Kemenade, B. M., Kircher, T. T. J., & Straube, B. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03306-6 · Cited by 8

Modulation of Bodily Self-Consciousness by Self and External Touch

Hara, M., Kanayama, N., Blanke, O., & Salomon, R. (2021) · IEEE Transactions on Haptics · doi:10.1109/toh.2021.3067651 · Cited by 7

A Bayesian predictive processing account of Othello syndrome in Parkinson’s disease

Foley, J. A., Chen, C., Paget, A., & Cipolotti, L. (2023) · Cognitive Neuropsychiatry · doi:10.1080/13546805.2023.2229080 · Cited by 8

The influence of hallucination proneness and social threat on time perception

Coy, A. L., & Hutton, S. B. (2012) · Cognitive Neuropsychiatry · doi:10.1080/13546805.2012.730994 · Cited by 7

Detection of schizophrenia: A machine learning algorithm for potential early detection and prevention based on event-related potentials

Frick, J., Rieg, T., & Buettner, R. (2021) · Hawaii International Conference on System Sciences (HICSS) · doi:10.24251/hicss.2021.460 · Cited by 7

Altered processing of self-produced sensations in psychosis at cortical and spinal levels

Salamone, P., Enmalm, A., Kaldewaij, R., Åman, M., Medley, C., Pietrzak, M., Olausson, H., Capusan, A. J., & Boehme, R. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03130-w · Cited by 7

Distinguishing the voice of self from others: The self-monitoring hypothesis of auditory hallucination

Asai, T., & Tanno, Y. (2010) · The Japanese journal of psychology · doi:10.4992/jjpsy.81.247 · Cited by 6

Thalamo-cortical circuits during sensory attenuation in emerging psychosis: a combined magnetoencephalography and dynamic causal modelling study

Hua, L., Adams, R. A., Grent-‘t-Jong, T., Gajwani, R., Groß, J., Gumley, A. I., Krishnadas, R., Lawrie, S. M., Schultze‐Lutter, F., Schwannauer, M., et al. (2023) · Schizophrenia · doi:10.1038/s41537-023-00341-4 · Cited by 7

Experimentally-evidenced personality alterations following meningioma resection: A case report

Orepić, P., Iannotti, G. R., Haemmerli, J., Goga, C., Park, H.-D., Betka, S., Blanke, O., Michel, C. M., Bondolfi, G., & Schaller, K. (2023) · Cortex · doi:10.1016/j.cortex.2023.08.006 · Cited by 5

SENSORY ATTENUATION ASSESSED BY SENSORY EVOKED POTENTIALS IN FUNCTIONAL MOVEMENT DISORDERS

Macerollo, A., Chen, J., Pareés, I., Kassavetis, P., Kilner, J. M., & Edwards, M. J. (2015) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2015-311750.8 · Cited by 6

Deficits in sensory prediction are related to delusional ideation in healthy individuals

Teufel, C., Kingdon, A., Ingram, J. N., Wolpert, D. M., & Fletcher, P. C. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.10.024 · Cited by 71

Functional magnetic resonance imaging of impaired sensory prediction in schizophrenia

Shergill, S. S., White, T. P., Joyce, D. W., Bays, P. M., Wolpert, D. M., & Frith, C. D. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.2974 · Cited by 163

Psychophysiological measures of sensory attenuation to self-generated actions: a biomarker for schizophrenia?

Thomas, W. (2016) · Frontiers in Human Neuroscience · doi:10.3389/conf.fnhum.2016.221.00009

Altered awareness of action in schizophrenia: a specific deficit in predicting action consequences

Voss, M., Moore, J., Hauser, M., Gallinat, J., Heinz, A., & Haggard, P. (2010) · Brain · doi:10.1093/brain/awq152 · Cited by 366

Misattributions of agency in schizophrenia are based on imprecise predictions about the sensory consequences of one's actions

Synofzik, M., Thier, P., Leube, D. T., Schlotterbeck, P., & Lindner, A. (2010) · Brain · doi:10.1093/brain/awp291 · Cited by 321