Cited by 9Motor Control and AdaptationNeural and Behavioral Psychology StudiesMental Health and Psychiatry

The DOI matches its Crossref record; 312 of the 313 references it cites were found in a registry or an index.

Motor actions across psychiatric disorders: A research domain criteria (RDoC) perspective

Open access

Osborne, K. Juston, Walther, Sebastian, Mittal, Vijay A.·2024·Clinical Psychology Review

DOI 10.1016/j.cpr.2024.102511

Open this paper in CoChat — free account

Abstract

The motor system is critical for understanding the pathophysiology and treatment of mental illness. Abnormalities in the processes that allow us to plan and execute movement in a goal-directed, context-appropriate manner (i.e., motor actions) are especially central to clinical motor research. Within this context, the NIMH Research Domain Criteria (RDoC) framework now includes a Motor Actions construct within the recently incorporated Sensorimotor Systems Domain, providing a useful framework for conducting research on motor action processes. However, there is limited available resources for understanding or implementing this framework. We address this gap by providing a comprehensive critical review and conceptual integration of the current clinical literature on the subconstructs comprising the Motor Actions construct. This includes a detailed discussion of each Motor Action subconstruct (e.g., action planning/execution) and its measurement across different units of analysis (e.g., molecules to behavior), the temporal and conceptual relationships among the Motor Action subconstructs (and other relevant RDoC domain constructs), and how abnormalities in these Motor Action subconstructs manifest in mental illness. Together, the review illustrates how motor system dysfunction is implicated in the pathophysiology of many psychiatric conditions and demonstrates shared and distinct mechanisms that may account for similar manifestations of motor abnormalities across disorders.

Integrity signals

Registry

Crossref · 10.1016/j.cpr.2024.102511

Cites

312 of 312 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Diagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,845
Research domain criteria (RDoC): toward a new classification framework for research on mental disorders
Insel, T., Cuthbert, B., Garvey, M., Heinssen, R., Pine, D. S., Quinn, K., Sanislow, C., & Wang, P. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09091379 · Cited by 7,067
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
Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: Basic principles and procedures for routine clinical and research application. An updated report from an I.F.C.N. Committee
Rossini, P., Burke, D. F., Chen, R., Cohen, L., Daskalakis, Z., Iorio, R. D., di Lazzaro, V., Ferreri, F., Fitzgerald, P., George, M., et al. (2015) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.02.001 · Cited by 2,729
The variable nature of cognitive control: a dual mechanisms framework
Braver, T. S. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.12.010 · Cited by 2,482
Computational principles of movement neuroscience
Wolpert, D. M., & Ghahramani, Z. (2000) · Nature Neuroscience · doi:10.1038/81497 · Cited by 2,122
Error Correction, Sensory Prediction, and Adaptation in Motor Control
Shadmehr, R., Smith, M. A., & Krakauer, J. W. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153135 · Cited by 1,869
Principles of sensorimotor learning
Wolpert, D. M., Diedrichsen, J., & Flanagan, J. R. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3112 · Cited by 1,391
The RDoC framework: facilitating transition from ICD/DSM to dimensional approaches that integrate neuroscience and psychopathology: Forum - The Research Domain Criteria Project
Cuthbert, B. N. (2014) · World Psychiatry · doi:10.1002/wps.20087 · Cited by 1,377
Motor prediction
Wolpert, D. M., & Flanagan, J. R. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00432-8 · Cited by 1,257
From Reactive to Proactive and Selective Control: Developing a Richer Model for Stopping Inappropriate Responses
Aron, A. R. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.07.024 · Cited by 1,236
Catatonia. I. Rating scale and standardized examination
Bush, G., Fink, M., Petrides, G., Dowling, F., & Francis, A. (1996) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1996.tb09814.x · Cited by 1,102
A consensus guide to capturing the ability to inhibit actions and impulsive behaviors in the stop-signal task
Verbruggen, F., Aron, A. R., Band, G. P., Beste, C., Bissett, P. G., Brockett, A. T., Brown, J. W., Chamberlain, S. R., Chambers, C. D., Colonius, H., et al. (2019) · eLife · doi:10.7554/elife.46323 · Cited by 990
Motor Learning
Krakauer, J. W., Hadjiosif, A. M., Xu, J., Wong, A. L., & Haith, A. M. (2019) · Comprehensive physiology · doi:10.1002/cphy.c170043 · Cited by 918
Explaining the Many Varieties of Working Memory Variation: Dual Mechanisms of Cognitive Control
Braver, T. S., Gray, J. R., & Burgess, G. C. (2008) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195168648.003.0004 · Cited by 886
Overlooking the Obvious: A Meta-analytic Comparison of Digit Symbol Coding Tasks and Other Cognitive Measures in Schizophrenia
Dickinson, D., Ramsey, M. E., & Gold, J. M. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.5.532 · Cited by 863
Current Concepts in Diagnosis and Treatment of Functional Neurological Disorders
Espay, A. J., Aybek, S., Carson, A., Edwards, M. J., Goldstein, L. H., Hallett, M., LaFaver, K., LaFrance, W. C., Lang, A. E., Nicholson, T., et al. (2018) · JAMA Neurology · doi:10.1001/jamaneurol.2018.1264 · Cited by 786
Computational Mechanisms of Sensorimotor Control
Franklin, D. W., & Wolpert, D. M. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.006 · Cited by 776
Explicit and implicit contributions to learning in a sensorimotor adaptation task
Taylor, J. A., Krakauer, J. W., & Ivry, R. B. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3619-13.2014 · Cited by 768
Current Perspectives on Motor Functioning in Infants, Children, and Adults With Autism Spectrum Disorders
Bhat, A. N., Landa, R. J., & Galloway, J. C. (2011) · Physical Therapy · doi:10.2522/ptj.20100294 · Cited by 678
The bliss (not the problem) of motor abundance (not redundancy)
Latash, M. L. (2012) · Experimental Brain Research · doi:10.1007/s00221-012-3000-4 · Cited by 663
Best practices in eye tracking research
Carter, B. T., & Luke, S. G. (2020) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2020.05.010 · Cited by 659
The NIMH research domain criteria initiative: Background, issues, and pragmatics
Kozak, M. J., & Cuthbert, B. N. (2016) · Psychophysiology · doi:10.1111/psyp.12518 · Cited by 655
The test–retest reliability of centre of pressure measures in bipedal static task conditions – A systematic review of the literature
Ruhe, A., Fejer, R., & Walker, B. F. (2010) · Gait & Posture · doi:10.1016/j.gaitpost.2010.09.012 · Cited by 645
The subthalamic nucleus in the context of movement disorders
Hamani, C. (2003) · Brain · doi:10.1093/brain/awh029 · Cited by 586
Developmental coordination disorder: A review and update
Zwicker, J. G., Missiuna, C. A., Harris, S. R., & Boyd, L. A. (2012) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2012.05.005 · Cited by 570
Human Postural Control
Ivanenko, Y. P., & Gurfinkel, V. S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00171 · Cited by 497
Stressful life events and maltreatment in conversion (functional neurological) disorder: Systematic review and meta-analysis of case-control studies
Ludwig, L., Pasman, J. A., Nicholson, T., Aybek, S., David, A. S., Tuck, S., Kanaan, R. A., Roelofs, K., Carson, A., & Stone, J. (2018) · The Lancet Psychiatry · doi:10.1016/s2215-0366(18)30051-8 · Cited by 495
Understanding performance deficits in developmental coordination disorder: a meta‐analysis of recent research
Wilson, P. H., Ruddock, S., Smits-Engelsman, B. C. M., Polatajko, H. J., & Blank, R. (2012) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.2012.04436.x · Cited by 494
Impairment of actions chains in autism and its possible role in intention understanding
Cattaneo, L., Fabbri‐Destro, M., Boria, S., Pieraccini, C., Monti, A., Cossu, G., & Rizzolatti, G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706273104 · Cited by 483
Motor Abilities in Autism: A Review Using a Computational Context
Gowen, E., & Hamilton, A. F. D. C. (2012) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-012-1574-0 · Cited by 453
Cognitive deficits in schizophrenia: an updated metanalysis of the scientific evidence
Fioravanti, M., Bianchi, V., & Cinti, M. E. (2012) · BMC Psychiatry · doi:10.1186/1471-244x-12-64 · Cited by 430
Psychomotor retardation in depression: Biological underpinnings, measurement, and treatment
Close, J. S., McClintock, S. M., & Croarkin, P. E. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.10.019 · Cited by 420
On the globality of motor suppression: unexpected events and their influence on behavior and cognition
Wessel, J. R., & Aron, A. R. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.013 · Cited by 409
Sensory integration for human balance control
Peterka, R. J. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63916-5.00002-1 · Cited by 399
Explicit and Implicit Processes Constitute the Fast and Slow Processes of Sensorimotor Learning
McDougle, S. D., Bond, K. M., & Taylor, J. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5061-14.2015 · Cited by 385
Motor Symptoms and Schizophrenia
Walther, S., & Strik, W. K. (2012) · Neuropsychobiology · doi:10.1159/000339456 · Cited by 381
2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)
Zheng, H., Dubitzky, W., Hu, X., Hao, J., Berrar, D., Cho, K.-H., Wang, Y., & David, G. (2021) · doi:10.1109/bibm52615.2021 · Cited by 378
Cerebellar-Prefrontal Network Connectivity and Negative Symptoms in Schizophrenia
Brady, R. O., Gonsalvez, I., Lee, I., Öngür, D., Seidman, L. J., Schmahmann, J. D., Eack, S. M., Keshavan, M. S., Pascual-Leone, A., & Halko, M. A. (2019) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2018.18040429 · Cited by 372
The uses and interpretations of the motor-evoked potential for understanding behaviour
Bestmann, S., & Krakauer, J. W. (2015) · Experimental Brain Research · doi:10.1007/s00221-014-4183-7 · Cited by 355
What catatonia can tell us about “top-down modulation”: A neuropsychiatric hypothesis
Northoff, G. (2002) · Behavioral and Brain Sciences · doi:10.1017/s0140525x02000109 · Cited by 352
A survey on sleep assessment methods
Valle, V. I.-D., Silva, J., & Cauli, O. (2018) · PeerJ · doi:10.7717/peerj.4849 · Cited by 352
Decision-making in sensorimotor control
Gallivan, J. P., Chapman, C. S., Wolpert, D. M., & Flanagan, J. R. (2018) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0045-9 · Cited by 332
Structure and neural mechanisms of catatonia
Walther, S., Stegmayer, K., Wilson, J. E., & Heckers, S. (2019) · The Lancet Psychiatry · doi:10.1016/s2215-0366(18)30474-7 · Cited by 331
Motor learning and consolidation: the case of visuomotor rotation
Krakauer, J. W. (2009) · Advances in Experimental Medicine and Biology · doi:10.1007/978-0-387-77064-2_21 · Cited by 324
Linking RDoC and HiTOP: A new interface for advancing psychiatric nosology and neuroscience
Michelini, G., Palumbo, I. M., DeYoung, C. G., Latzman, R. D., & Kotov, R. (2021) · Clinical Psychology Review · doi:10.1016/j.cpr.2021.102025 · Cited by 304
Psychomotor Retardation in Depression: A Systematic Review of Diagnostic, Pathophysiologic, and Therapeutic Implications
Bennabi, D., Vandel, P., Papaxanthis, C., Pozzo, T., & Haffen, É. (2013) · BioMed Research International · doi:10.1155/2013/158746 · Cited by 287
What, If, and When to Move: Basal Ganglia Circuits and Self-Paced Action Initiation
Klaus, A., Alves da Silva, J., & Costa, R. M. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031033 · Cited by 284
Multimodal Machine Learning Workflows for Prediction of Psychosis in Patients With Clinical High-Risk Syndromes and Recent-Onset Depression
Koutsouleris, N., Dwyer, D. B., Degenhardt, F., Maj, C., Urquijo-Castro, M. F., Sanfelici, R., Popovic, D., Oeztuerk, O., Haas, S. S., Weiske, J., et al. (2021) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2020.3604 · Cited by 275
A Functional Taxonomy of Bottom-Up Sensory Feedback Processing for Motor Actions
Scott, S. H. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.06.001 · Cited by 274
Friedreich Ataxia: Neuropathology Revised
Koeppen, A. H., & Mazurkiewicz, J. E. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31827e5762 · Cited by 273
Physiological Markers of Motor Inhibition during Human Behavior
Duqué, J., Greenhouse, I., Labruna, L., & Ivry, R. B. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.02.006 · Cited by 267
Evidence of Cortical Inhibitory Deficits in Major Depressive Disorder
Levinson, A. J., Fitzgerald, P. B., Favalli, G., Blumberger, D. M., Daigle, M., & Daskalakis, Z. J. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.025 · Cited by 261
Motor Planning
Wong, A. L., Haith, A. M., & Krakauer, J. W. (2014) · The Neuroscientist · doi:10.1177/1073858414541484 · Cited by 257
Compromised motor control in children with DCD: A deficit in the internal model?—A systematic review
Adams, I. L. J., Lust, J. M., Wilson, P. H., & Steenbergen, B. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.08.011 · Cited by 255
Catatonia and Its Treatment
Rosebush, P. I., & Mazurek, M. F. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp141 · Cited by 253
Medial frontal cortex: From self-generated action to reflection on one's own performance
Passingham, R. E., Bengtsson, S. L., & Lau, H. C. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.11.001 · Cited by 252
Activity in the lateral prefrontal cortex reflects multiple steps of future events in action plans
Mushiake, H., Saito, N., Sakamoto, K., Itoyama, Y., & Tanji, J. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.045 · Cited by 249
The Research Domain Criteria (RDoC): An analysis of methodological and conceptual challenges
Lilienfeld, S. O. (2014) · Behaviour Research and Therapy · doi:10.1016/j.brat.2014.07.019 · Cited by 248
The expanding universe of disorders of the basal ganglia
Obeso, J. A., Rodríguez-Oroz, M. C., Stamelou, M., Bhatia, K. P., & Burn, D. J. (2014) · The Lancet · doi:10.1016/s0140-6736(13)62418-6 · Cited by 240
Actions, Action Sequences and Habits: Evidence That Goal-Directed and Habitual Action Control Are Hierarchically Organized
Dezfouli, A., & Balleine, B. W. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003364 · Cited by 239
Corticospinal Circuits from the Sensory and Motor Cortices Differentially Regulate Skilled Movements through Distinct Spinal Interneurons
Ueno, M., Nakamura, Y., Li, J., Gu, Z., Niehaus, J. K., Maezawa, M., Crone, S. A., Goulding, M., Baccei, M. L., & Yoshida, Y. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.137 · Cited by 234
Real-time mobile monitoring of the dynamic associations among motor activity, energy, mood, and sleep in adults with bipolar disorder
Merikangas, K. R., Swendsen, J., Hickie, I. B., Cui, L., Shou, H., Merikangas, A. K., Zhang, J., Lamers, F., Crainiceanu, C., Volkow, N. D., et al. (2019) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2018.3546 · Cited by 231
Contrasting network and modular perspectives on inhibitory control
Hampshire, A., & Sharp, D. J. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.06.006 · Cited by 221
Postural sway as a marker of progression in Parkinson's disease: A pilot longitudinal study
Mancini, M., Carlson-Kuhta, P., Zampieri, C., Nutt, J. G., Chiari, L., & Horak, F. B. (2012) · Gait & Posture · doi:10.1016/j.gaitpost.2012.04.010 · Cited by 221
What do reflex and voluntary mean? Modern views on an ancient debate
Procházka, A., Clarac, F., Loeb, G. E., Rothwell, J. C., & Wolpaw, J. R. (2000) · Experimental Brain Research · doi:10.1007/s002219900250 · Cited by 221
The prevalence of psychiatric comorbidities in adult ADHD compared with non-ADHD populations: A systematic literature review
Choi, W.-S., Woo, Y. S., Wang, S.-M., Lim, H. K., & Bahk, W.-M. (2022) · PLOS ONE · doi:10.1371/journal.pone.0277175 · Cited by 221
Inhibition of action, thought, and emotion: A selective neurobiological review
Dillon, D. G., & Pizzagalli, D. A. (2007) · Applied and Preventive Psychology · doi:10.1016/j.appsy.2007.09.004 · Cited by 218
Biomechanics of human movement and its clinical applications
Lu, T., & Chang, C. (2012) · The Kaohsiung Journal of Medical Sciences · doi:10.1016/j.kjms.2011.08.004 · Cited by 217
Sensorimotor adaptation of saccadic eye movements
Pélisson, D., Alahyane, N., Panouillères, M., & Tilikete, C. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.010 · Cited by 213
Planning actions in autism
Fabbri‐Destro, M., Cattaneo, L., Boria, S., & Rizzolatti, G. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1578-3 · Cited by 205
The Role of Movement Analysis in Diagnosing and Monitoring Neurodegenerative Conditions: Insights from Gait and Postural Control
Buckley, C., Alcock, L., Ardle, R. M., Rehman, R. Z. U., Din, S. D., Mazzà, C., Yarnall, A. J., & Rochester, L. (2019) · Brain Sciences · doi:10.3390/brainsci9020034 · Cited by 204
All roads lead to the motor cortex: psychomotor mechanisms and their biochemical modulation in psychiatric disorders
Northoff, G., Hirjak, D., Wolf, R. C., Magioncalda, P., & Martino, M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0814-5 · Cited by 204
Neural Control of Walking in People with Parkinsonism
Peterson, D. S., & Horak, F. B. (2016) · Physiology · doi:10.1152/physiol.00034.2015 · Cited by 200
Primary motor cortex and movement prevention: Where Stop meets Go
Stinear, C. M., Coxon, J. P., & Byblow, W. D. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.08.013 · Cited by 199
Enhancing Visuomotor Adaptation by Reducing Error Signals: Single-step (Aware) versus Multiple-step (Unaware) Exposure to Wedge Prisms
Michel, C., Laure Pisella, A., Prablanc, C., Gilles Rode, A., & Rossetti, Y. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.2.341 · Cited by 193
Can delay discounting deliver on the promise of RDoC?
Lempert, K. M., STEINGLASS, J. E., Pinto, A., Kable, J. W., & Simpson, H. B. (2018) · Psychological Medicine · doi:10.1017/s0033291718001770 · Cited by 193
Postural disorders in Parkinson’s disease
Bénatru, I., Vaugoyeau, M., & Azulay, J.-P. (2008) · Neurophysiologie Clinique · doi:10.1016/j.neucli.2008.07.006 · Cited by 189
Vocal biomarkers of depression based on motor incoordination
Williamson, J. R., Quatieri, T. F., Helfer, B. S., Horwitz-Martin, R. L., Yu, B., & Mehta, D. D. (2013) · doi:10.1145/2512530.2512531 · Cited by 189
Supplementary Motor Area Exerts Proactive and Reactive Control of Arm Movements
Chen, X., Scangos, K. W., & Stuphorn, V. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2669-10.2010 · Cited by 185
What Is Wrong with Balance in Parkinson’s Disease?
Park, J., Kang, Y.-J., & Horak, F. B. (2015) · Journal of Movement Disorders · doi:10.14802/jmd.15018 · Cited by 184
The Role of Primary Motor Cortex: More Than Movement Execution
Bhattacharjee, S., Kashyap, R., Abualait, T., Chen, S. A., Yoo, W., & Bashir, S. (2020) · Journal of Motor Behavior · doi:10.1080/00222895.2020.1738992 · Cited by 184
Reaching for the unknown: Multiple target encoding and real-time decision-making in a rapid reach task
Chapman, C. S., Gallivan, J. P., Wood, D. K., Milne, J. L., Culham, J. C., & Goodale, M. A. (2010) · Cognition · doi:10.1016/j.cognition.2010.04.008 · Cited by 178
Mechanisms of saccade suppression revealed in the anti-saccade task
Coe, B. C., & Munoz, D. P. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0192 · Cited by 172
A practical introduction to using the drift diffusion model of decision-making in cognitive psychology, neuroscience, and health sciences
Myers, C. E., Interian, A., & Moustafa, A. A. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.1039172 · Cited by 172
Functional Neuroanatomy and Neurophysiology of Functional Neurological Disorders (Conversion Disorder)
Voon, V., Cavanna, A. E., Coburn, K. L., Sampson, S. M., Reeve, A., & LaFrance, W. C., Jr. (2016) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.14090217 · Cited by 169
The “What” and “When” of Self-Initiated Movements
Hoffstaedter, F., Grefkes, C., Zilles, K., & Eickhoff, S. B. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhr391 · Cited by 166
A new science of emotion: implications for functional neurological disorder
Jungilligens, J., Paredes-Echeverri, S., Popkirov, S., Barrett, L. F., & Perez, D. L. (2022) · Brain · doi:10.1093/brain/awac204 · Cited by 164
Dual-process decomposition in human sensorimotor adaptation
Huberdeau, D. M., Krakauer, J. W., & Haith, A. M. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.03.003 · Cited by 161
38th Annual International Conference of the IEEE Engineering in Medicine and Biology Society
(2015) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2015.2462411 · Cited by 160
Motor Skill Interventions in Children With Developmental Coordination Disorder: A Systematic Review and Meta-Analysis
Yu, J. J., Burnett, A., & Sit, C. H. P. (2018) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2017.12.009 · Cited by 158
Balance Dysfunction in Parkinson’s Disease
Rinalduzzi, S., Trompetto, C., Marinelli, L., Alibardi, A., Missori, P., Fattapposta, F., Pierelli, F., & Currà, A. (2015) · BioMed Research International · doi:10.1155/2015/434683 · Cited by 155
The use of force-plate posturography in the assessment of postural instability
Błaszczyk, J. W. (2015) · Gait & Posture · doi:10.1016/j.gaitpost.2015.10.014 · Cited by 155
Orbitofrontal Cortical Dysfunction in Akinetic Catatonia: A Functional Magnetic Resonance Imaging Study During Negative Emotional Stimulation
Northoff, G., Kötter, R., Baumgart, F., Dános, P., Boeker, H., Kaulisch, T., Schlagenhauf, F., Walter, H., Heinzel, A., Witzel, T., et al. (2004) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a007088 · Cited by 154
Motor learning
Wolpert, D. M., & Flanagan, J. R. (2010) · Current Biology · doi:10.1016/j.cub.2010.04.035 · Cited by 151
The role of alexithymia in the development of functional motor symptoms (conversion disorder)
Demartini, B., Petrochilos, P., Ricciardi, L., Price, G., Edwards, M. J., & Joyce, E. (2014) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-307203 · Cited by 147
Cerebellar Control of Reach Kinematics for Endpoint Precision
Becker, M. I., & Person, A. L. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.007 · Cited by 147
The dual nature of time preparation: neural activation and suppression revealed by transcranial magnetic stimulation of the motor cortex
Davranche, K., Tandonnet, C., Burle, B., Meynier, C., Vidal, F., & Hasbroucq, T. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05588.x · Cited by 143
Aberrant Hyperconnectivity in the Motor System at Rest Is Linked to Motor Abnormalities in Schizophrenia Spectrum Disorders
Walther, S., Stegmayer, K., Federspiel, A., Bohlhalter, S., Wiest, R., & Viher, P. V. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx091 · Cited by 143
Encyclopedia of Social Work
(2013) · Choice Reviews Online · doi:10.5860/choice.51-2426 · Cited by 139
A synergy-based hand control is encoded in human motor cortical areas
Leo, A., Handjaras, G., Bianchi, M., Marino, H., Gabiccini, M., Guidi, A., Scilingo, E. P., Pietrini, P., Bicchi, A., Santello, M., et al. (2016) · eLife · doi:10.7554/elife.13420 · Cited by 137
Developmental coordination disorder: core sensori-motor deficits, neurobiology and etiology
Gomez, A., & Sirigu, A. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.09.032 · Cited by 133
Motor abnormalities: from neurodevelopmental to neurodegenerative through “functional” (neuro)psychiatric disorders
Peralta, V., & Cuesta, M. J. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx089 · Cited by 133
The Catatonia Conundrum: Evidence of Psychomotor Phenomena as a Symptom Dimension in Psychotic Disorders
Ungvari, G. S., Caroff, S. N., & Gerevich, J. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp105 · Cited by 132
Dyspraxia, motor function and visual–motor integration in autism
Miller, M., Chukoskie, L., Zinni, M., Townsend, J., & Trauner, D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.04.011 · Cited by 131
Reaching and Grasping in Autism Spectrum Disorder: A Review of Recent Literature
Sacrey, L.-A. R., Germani, T., Bryson, S. E., & Zwaigenbaum, L. (2014) · Frontiers in Neurology · doi:10.3389/fneur.2014.00006 · Cited by 130
Eye movements in the wild: Oculomotor control, gaze behavior & frames of reference
Lappi, O. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.06.006 · Cited by 126
Neural and behavioral mechanisms of proactive and reactive inhibitionPreprint
Meyer, H. C., & Bucci, D. J. (2016) · Learning & Memory · doi:10.1101/lm.040501.115 · Cited by 126
What Can Different Motor Circuits Tell Us About Psychosis? An RDoC Perspective
Mittal, V. A., Bernard, J. A., & Northoff, G. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx087 · Cited by 126
The Forward Model: A Unifying Theory for the Role of the Cerebellum in Motor Control and Sense of Agency
Welniarz, Q., Worbe, Y., & Gallea, C. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.644059 · Cited by 125
Cognitive deficits in recent-onset and chronic schizophrenia
Sponheim, S. R., Jung, R. E., Seidman, L. J., Mesholam-Gately, R. I., Manoach, D. S., O’Leary, D. S., Ho, B. C., Andreasen, N. C., Lauriello, J., & Schulz, S. C. (2010) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.09.010 · Cited by 123
A competitive model for striatal action selection
Bariselli, S., Fobbs, W. C., Creed, M. C., & Kravitz, A. V. (2018) · Brain Research · doi:10.1016/j.brainres.2018.10.009 · Cited by 123
Resting-State Hyperperfusion of the Supplementary Motor Area in Catatonia
Walther, S., Schäppi, L., Federspiel, A., Bohlhalter, S., Wiest, R., Strik, W. K., & Stegmayer, K. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw140 · Cited by 122
A meta-analytic study of event rate effects on Go/No-Go performance in attention-deficit/hyperactivity disorder
Metin, B., Roeyers, H., Wiersema, J. R., van der Meere, J., & Sonuga-Barke, E. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.08.023 · Cited by 121
The Lateralized Readiness Potential
Smulders, F. T. Y., & Miller, J. O. (2011) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195374148.013.0115 · Cited by 119
The Psychology of Reaching: Action Selection, Movement Implementation, and Sensorimotor Learning
Kim, H. E., Avraham, G., & Ivry, R. B. (2020) · Annual Review of Psychology · doi:10.1146/annurev-psych-010419-051053 · Cited by 118
Catatonia
Walther, S., & Strik, W. K. (2016) · CNS Spectrums · doi:10.1017/s1092852916000274 · Cited by 118
Ocular motor disturbances in autism spectrum disorders: Systematic review and comprehensive meta-analysis
Johnson, B. P., Lum, J. A. G., Rinehart, N., & Fielding, J. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.007 · Cited by 115
Research domain criteria (RDoC) grows up: Strengthening neurodevelopment investigation within the RDoC framework
Mittal, V. A., & Wakschlag, L. S. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.12.011 · Cited by 114
The Cortical Motor Areas and the Emergence of Motor Skills: A Neuroanatomical Perspective
Strick, P. L., Dum, R. P., & Rathelot, J.-A. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050216 · Cited by 114
Cerebellar networks in individuals at ultra high‐risk of psychosis: Impact on postural sway and symptom severity
Bernard, J. A., Dean, D. J., Kent, J. S., Orr, J. M., Pelletier‐Baldelli, A., Lunsford‐Avery, J. R., Gupta, T., & Mittal, V. A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22458 · Cited by 113
The clinical and prognostic value of motor abnormalities in psychosis, and the importance of instrumental assessment
van Harten, P. N., Walther, S., Kent, J. S., Sponheim, S. R., & Mittal, V. A. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.06.007 · Cited by 107
Psychomotor symptoms of schizophrenia map on the cerebral motor circuit
Walther, S. (2015) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2015.06.010 · Cited by 106
Impaired response selection in schizophrenia: Evidence from the P3 wave and the lateralized readiness potential
Luck, S. J., Kappenman, E. S., Fuller, R. L. M., Robinson, B. M., Summerfelt, A. T., & Gold, J. M. (2009) · Psychophysiology · doi:10.1111/j.1469-8986.2009.00817.x · Cited by 106
Going Back to Kahlbaum’s Psychomotor (and GABAergic) Origins: Is Catatonia More Than Just a Motor and Dopaminergic Syndrome?
Hirjak, D., Kubera, K. M., Wolf, R. C., & Northoff, G. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sbz074 · Cited by 104
The Role of Sensorimotor Difficulties in Autism Spectrum Conditions
Hannant, P., Tavassoli, T., & Cassidy, S. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00124 · Cited by 103
Restricted and repetitive behaviors in autism spectrum disorders: The relationship of attention and motor deficits
Ravizza, S. M., Solomon, M., Ivry, R. B., & Carter, C. S. (2013) · Development and Psychopathology · doi:10.1017/s0954579413000163 · Cited by 99
Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis
Braak, H., Ludolph, A. C., Neumann, M., Ravits, J., & Tredici, K. D. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1633-2 · Cited by 99
Basal ganglia and autism – a translational perspective
Subramanian, K., Brandenburg, C., Orsati, F. T., Soghomonian, J., Hussman, J. P., & Blatt, G. J. (2017) · Autism Research · doi:10.1002/aur.1837 · Cited by 98
Catatonia
Hirjak, D., Rogers, J. P., Wolf, R. C., Kubera, K. M., Fritze, S., Wilson, J. E., Sambataro, F., Fricchione, G. L., Meyer‐Lindenberg, A., Ungvari, G. S., et al. (2024) · Nature Reviews Disease Primers · doi:10.1038/s41572-024-00534-w · Cited by 95
Brain regions and genes affecting postural control
Lalonde, R., & Strazielle, C. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.11.005 · Cited by 94
Spatial organization of cortical and spinal neurons controlling motor behavior
Levine, A. J., Lewallen, K. A., & Pfaff, S. L. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.07.002 · Cited by 93
Decreased Daytime Motor Activity Associated With Apathy in Alzheimer Disease: An Actigraphic Study
David, R., Mulin, E., Friedman, L., Duff, F. L., Cygankiewicz, E., Deschaux, O., Garcia, R., Yesavage, J. A., Robert, P. H., & Zeitzer, J. M. (2011) · American Journal of Geriatric Psychiatry · doi:10.1097/jgp.0b013e31823038af · Cited by 93
Apical dendrite degeneration, a novel cellular pathology for Betz cells in ALS
Genç, B., Jara, J. H., Lagrimas, A. K. B., Pytel, P., Roos, R. P., Mesulam, M. M., Geula, C., Bigio, E. H., & Özdi̇nler, P. H. (2017) · Scientific Reports · doi:10.1038/srep41765 · Cited by 93
45‐Hour continuous quintuple‐site actimetry: Relations between trunk and limb movements and effects of circadian sleep‐wake rhythmicity
Middelkoop, H. A. M., DAM, E. M. V., den Doel, D. A. S.-V., & DIJK, G. V. (1997) · Psychophysiology · doi:10.1111/j.1469-8986.1997.tb02132.x · Cited by 92
Age-related slowing down in the motor initiation in elderly adults
Frolov, N. S., Николаевна, П. Е., Maksimenko, V., Grubov, V., Kiselev, A. R., Wang, Z., & Hramov, A. E. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233942 · Cited by 92
Cortical Inhibition, Excitation, and Connectivity in Schizophrenia: A Review of Insights From Transcranial Magnetic Stimulation
Rogasch, N. C., Daskalakis, Z. J., & Fitzgerald, P. B. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt078 · Cited by 91
Psychomotor slowing and planning deficits in schizophrenia
Jogems-Kosterman, B. J. M., Zitman, F. G., van Hoof, J. J. M., & Hulstijn, W. (2001) · Schizophrenia Research · doi:10.1016/s0920-9964(00)00097-9 · Cited by 91
Transdiagnostic approaches to psychopathology measurement: Recommendations for measure selection, data analysis, and participant recruitment.
Stanton, K. J., McDonnell, C. G., Hayden, E. P., & Watson, D. (2019) · Journal of Abnormal Psychology · doi:10.1037/abn0000464 · Cited by 91
Motor planning flexibly optimizes performance under uncertainty about task goals
Wong, A. L., & Haith, A. M. (2017) · Nature Communications · doi:10.1038/ncomms14624 · Cited by 90
The utility of an RDoC motor domain to understand psychomotor symptoms in depression
Walther, S., Bernard, J. A., Mittal, V. A., & Shankman, S. A. (2018) · Psychological Medicine · doi:10.1017/s0033291718003033 · Cited by 90
Ocular motor abnormalities in Parkinsonian syndromes
Pinkhardt, E. H., & Kassubek, J. (2010) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2010.08.004 · Cited by 89
Movement related cortical potentials of cued versus self‐initiated movements: Double dissociated modulation by dorsal premotor cortex versus supplementary motor area rTMS
Lu, M.-K., Arai, N., Tsai, C.-H., & Ziemann, U. (2012) · Human Brain Mapping · doi:10.1002/hbm.21248 · Cited by 89
Obsessive-compulsive disorder: A “sensory-motor” problem?
Russo, M., Naro, A., Mastroeni, C., Morgante, F., Terranova, C., Muscatello, M. R., Zoccali, R., Calabrò, R. S., & Quartarone, A. (2014) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2014.02.007 · Cited by 88
Stereotypies in Rett syndrome
Temudo, T. P., Oliveira, P., Santos, M., Dias, K., Vieira, J. P., Moreira, A., Calado, E., Carrilho, I., Oliveira, G., Levy, A., et al. (2007) · Neurology · doi:10.1212/01.wnl.0000259086.34769.78 · Cited by 85
Models of human movement: Trajectory planning and inverse kinematics studies
Flash, T., Meirovitch, Y., & Barliya, A. (2012) · Robotics and Autonomous Systems · doi:10.1016/j.robot.2012.09.020 · Cited by 84
Less Structured Movement Patterns Predict Severity of Positive Syndrome, Excitement, and Disorganization
Walther, S., Ramseyer, F., Horn, H., Strik, W. K., & Tschacher, W. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt038 · Cited by 83
Volition and Action in the Human Brain: Processes, Pathologies, and Reasons
Fried, I., Haggard, P., He, B. J., & Schurger, A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2584-17.2017 · Cited by 83
Saccade eye movements as a quantitative measure of frontostriatal network in children with ADHD
Goto, Y., Hatakeyama, K., Kitama, T., Sato, Y., Kanemura, H., 青柳, 閣., Sugita, K., & Aihara, M. (2009) · Brain and Development · doi:10.1016/j.braindev.2009.04.017 · Cited by 82
Symptom-specific amygdala hyperactivity modulates motor control network in conversion disorder
Hassa, T., Sebastian, A., Liepert, J., Weiller, C., Schmidt, R., & Tüscher, O. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.04.004 · Cited by 82
Combining actigraphy, ecological momentary assessment and neuroimaging to study apathy in patients with schizophrenia
Kluge, A., Kirschner, M., Hager, O. M., Bischof, M., Habermeyer, B., Seifritz, E., Walther, S., & Kaiser, S. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.09.034 · Cited by 82
Objectively measured motor activity in schizophrenia challenges the validity of expert ratings
Walther, S., Koschorke, P., Horn, H., & Strik, W. K. (2009) · Psychiatry Research · doi:10.1016/j.psychres.2008.06.020 · Cited by 81
Precursor processes of human self-initiated action
Khalighinejad, N., Schurger, A., Desantis, A., Zmigrod, L., & Haggard, P. (2017) · bioRxiv · doi:10.1016/j.neuroimage.2017.09.057 · Cited by 79
Amount and structure of force variability during short, ramp and sustained contractions in males and females
Svendsen, J. H., & Madeleine, P. (2009) · Human Movement Science · doi:10.1016/j.humov.2009.09.001 · Cited by 78
Catatonia
Heckers, S., & Walther, S. (2023) · New England Journal of Medicine · doi:10.1056/nejmra2116304 · Cited by 78
Transcranial magnetic stimulation in ALS
Floyd, A. G., Yu, Q. P., Piboolnurak, P., Tang, M.-X., Fang, Y., Smith, W. A., Yim, J., Rowland, L. P., Mitsumoto, H., & Pullman, S. L. (2009) · Neurology · doi:10.1212/01.wnl.0000341933.97883.a4 · Cited by 77
Attentional versus motor inhibition in adults with attention-deficit/hyperactivity disorder.
Carr, L. A., Nigg, J. T., & Henderson, J. M. (2006) · Neuropsychology · doi:10.1037/0894-4105.20.4.430 · Cited by 76
Catatonia in Patients with Autism: Prevalence and Management
Mazzone, L., Postorino, V., Valeri, G., & Vicari, S. (2014) · CNS Drugs · doi:10.1007/s40263-014-0143-9 · Cited by 75
Neural Oscillations and the Initiation of Voluntary Movement
Armstrong, S. R., Sale, M. V., & Cunnington, R. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02509 · Cited by 75
Gesture imitation in schizophrenia
Matthews, N., Gold, B. J., Sekuler, R., & Park, S. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr062 · Cited by 74
Aversive stimuli exacerbate defensive motor behaviour in motor conversion disorder
Blakemore, R. L., Sinanaj, I., Galli, S., Aybek, S., & Vuilleumier, P. O. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.11.005 · Cited by 74
Movement disorder and sensorimotor abnormalities in schizophrenia and other psychoses - European consensus on assessment and perspectives
Walther, S., van Harten, P. N., Waddington, J. L., Cuesta, M. J., Peralta, V., Dupin, L., Foucher, J., Sambataro, F., Morrens, M., Kubera, K. M., et al. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.07.003 · Cited by 74
Psychological treatments in adult ADHD: a systematic review
Fullen, T., Jones, S. L., Emerson, L. M., & Adamou, M. (2020) · Journal of Psychopathology and Behavioral Assessment · doi:10.1007/s10862-020-09794-8 · Cited by 73
The neural signature of psychomotor disturbance in depression
Wüthrich, F., Lefebvre, S., Mittal, V. A., Shankman, S. A., Alexander, N., Brosch, K., Flinkenflügel, K., Goltermann, J., Grotegerd, D., Hahn, T., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02327-1 · Cited by 70
Postural sway parameters using a triaxial accelerometer: comparing elderly and young healthy adults
Martínez-Méndez, R., Sekine, M., & TAMURA, T. (2011) · Computer Methods in Biomechanics & Biomedical Engineering · doi:10.1080/10255842.2011.565753 · Cited by 69
Why We Should Take a Closer Look at Gestures
Walther, S., & Mittal, V. A. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv229 · Cited by 69
Neural correlates of conversion disorder: overview and meta-analysis of neuroimaging studies on motor conversion disorder
Boeckle, M., Liegl, G., Jank, R., & Pieh, C. (2016) · BMC Psychiatry · doi:10.1186/s12888-016-0890-x · Cited by 68
Motor timing and motor sequencing contribute differently to the preparation for voluntary movement
Bortoletto, M., & Cunnington, R. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.048 · Cited by 67
Force control in object manipulation—A model for the study of sensorimotor control strategies
Nowak, D. A., Glasauer, S., & Hermsdörfer, J. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.06.003 · Cited by 66
Neural Antecedents of Spontaneous Voluntary Movement: A New Perspective
Schurger, A., Mylopoulos, M. I., & ROSENTHAL, D. M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.11.003 · Cited by 66
Central motor conduction time
Udupa, K., & Chen, R. E. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-53497-2.00031-0 · Cited by 66
Beyond decision! Motor contribution to speed–accuracy trade-off in decision-making
Spieser, L., Servant, M., Hasbroucq, T., & Burle, B. (2016) · Psychonomic Bulletin & Review · doi:10.3758/s13423-016-1172-9 · Cited by 66
Oculomotor prediction: A window into the psychotic mind
Thakkar, K. N., Diwadkar, V. A., & Rolfs, M. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.02.001 · Cited by 66
Actigraphically measured psychomotor slowing in depression: systematic review and meta-analysis
Wüthrich, F., Nabb, C. B., Mittal, V. A., Shankman, S. A., & Walther, S. (2022) · Psychological Medicine · doi:10.1017/s0033291722000903 · Cited by 66
It's in the eyes: Planning precise manual actions before execution
Belardinelli, A., Stepper, M. Y., & Butz, M. V. (2016) · Journal of Vision · doi:10.1167/16.1.18 · Cited by 65
Stroop performance in major depression: Selective attention impairment or psychomotor slowness?
Kertzman, S., Reznik, I., Hornik-Lurie, T., Weizman, A., Kotler, M., & Amital, D. (2010) · Journal of Affective Disorders · doi:10.1016/j.jad.2009.08.009 · Cited by 62
Psychomotor slowing in Schizophrenia: Implications for endophenotype and biomarker development
Osborne, K. J., Walther, S., Shankman, S. A., & Mittal, V. A. (2020) · Biomarkers in Neuropsychiatry · doi:10.1016/j.bionps.2020.100016 · Cited by 62
Motor dysfunction as research domain across bipolar, obsessive-compulsive and neurodevelopmental disorders
Hirjak, D., Meyer-Lindenberg, A., Fritze, S., Sambataro, F., Kubera, K. M., & Wolf, R. C. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.009 · Cited by 60
Intrinsic brain activity of subcortical-cortical sensorimotor system and psychomotor alterations in schizophrenia and bipolar disorder: A preliminary study
Magioncalda, P., Martino, M., Conio, B., Lee, H., Ku, H., Chen, C.-J., Inglese, M., Amore, M., Lane, T. J., & Northoff, G. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.01.009 · Cited by 60
Assessing Inhibitory Control Deficits in Adult ADHD: A Systematic Review and Meta-analysis of the Stop-signal Task
Senkowski, D., Ziegler, T., Singh, M., Heinz, A., He, J., Silk, T., & Lorenz, R. C. (2024) · Neuropsychology Review · doi:10.1007/s11065-023-09592-5 · Cited by 59
Psychometric properties of the Dyskinesia Identification System: Condensed User Scale (DISCUS)
Rl, S., Kalachnik, J. E., Slaw, K. M., & Shaw, K. M. (1989) · PubMed · Cited by 58
Neuropsychological Deficits in Adolescent Unipolar Depression
Klimkeit, E., Tonge, B. J., Bradshaw, J. L., Melvin, G. A., & Gould, K. R. (2011) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acr051 · Cited by 57
Different patterns of cortical excitability in major depression and vascular depression: a transcranial magnetic stimulation study
Concerto, C., Lanza, G., Cantone, M., Pennisi, M., Giordano, D., Spampinato, C., Ricceri, R., Pennisi, G., Aguglia, E., & Bella, R. (2013) · BMC Psychiatry · doi:10.1186/1471-244x-13-300 · Cited by 57
Impaired gesture performance in schizophrenia: particular vulnerability of meaningless pantomimes
Walther, S., Vanbellingen, T., Müri, R., Strik, W., & Bohlhalter, S. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.08.017 · Cited by 57
Self-citation
Startle and the StartReact Effect: Physiological Mechanisms
Carlsen, A. N., & Maslovat, D. (2019) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000582 · Cited by 56
Oculomotor deficits in attention deficit hyperactivity disorder (ADHD): A systematic review and comprehensive meta-analysis
Maron, D., Bowe, S. J., Spencer‐Smith, M. M., Mellahn, O. J., Perrykkad, K., Bellgrove, M. A., & Johnson, B. P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.012 · Cited by 56
Decreased cerebral blood flow in the primary motor cortex in major depressive disorder with psychomotor retardation
Yin, Y., Wang, M., Wang, Z., Xie, C., Zhang, H., Zhang, H., Zhang, Z., & Yuan, Y. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.08.013 · Cited by 55
Postural threat influences conscious perception of postural sway
Cleworth, T. W., & Carpenter, M. G. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.03.032 · Cited by 54
Communicative effectiveness of pantomime gesture in people with aphasia
Rose, M. L., Mok, Z., & Sekine, K. (2016) · International Journal of Language & Communication Disorders · doi:10.1111/1460-6984.12268 · Cited by 54
Sensorimotor Learning: Neurocognitive Mechanisms and Individual Differences
Seidler, R. D., & Carson, R. G. (2017) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-017-0279-1 · Cited by 54
Kinematic markers dissociate error correction from sensorimotor realignment during prism adaptation
O’Shea, J., Gaveau, V., Kandel, M., Koga, K., Susami, K., Prablanc, C., & Rossetti, Y. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.09.021 · Cited by 53
Corticomotor excitability during precision motor tasks
Pearce, A. J., & Kidgell, D. J. (2009) · Journal of Science and Medicine in Sport · doi:10.1016/j.jsams.2007.12.005 · Cited by 53
Postural Stability in Older Adults With Alzheimer Disease.
Mesbah, N., Perry, M., Hill, K., Kaur, M., & Hale, L. A. (2017) · PubMed · doi:10.2522/ptj.20160115 · Cited by 52
Anterior Cingulate Cortex Signals the Need to Control Intrusive Thoughts during Motivated Forgetting
Crespo‐García, M., Wang, Y., Jiang, M., Anderson, M. C., & Lei, X. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1711-21.2022 · Cited by 52
The Effect of Dual Task on Attentional Performance in Children With ADHD
Caldani, S., Razuk, M., Septier, M., Barela, J. Â., Delorme, R., Acquaviva, É., & Bucci, M. P. (2019) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2018.00067 · Cited by 51
Increased Force Variability in Chronic Stroke: Contributions of Force Modulation below 1 Hz
Lodha, N., Misra, G., Coombes, S. A., Christou, E. A., & Cauraugh, J. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083468 · Cited by 50
Major Differences in Subjective Experience of Akinetic States in Catatonic and Parkinsonian Patients
Northoff, G., Krill, W., Wenke, J., Gille, B., Russ, M., Eckert, J., Pester, U., Bogerts, B., & Pflug, B. (1998) · Cognitive Neuropsychiatry · doi:10.1080/135468098396125 · Cited by 50
Catatonia in older adults: A systematic review
Jaimes-Albornoz, W., de Pellón-Santamaría, Á. R., Nizama‐Vía, A., Isetta, M., Albájar, I., & Mestres, J. S. (2022) · World Journal of Psychiatry · doi:10.5498/wjp.v12.i2.348 · Cited by 50
Hyperactive action monitoring during motor-initiation in conversion paralysis: An event-related potential study
Roelofs, K., de Bruijn, E. R. A., & van Galen, G. P. (2005) · Biological Psychology · doi:10.1016/j.biopsycho.2005.07.002 · Cited by 49
Motor planning under uncertainty
Alhussein, L., & Smith, M. A. (2021) · eLife · doi:10.7554/elife.67019 · Cited by 49

Flagged first, then by citations

1 of the 313 references couldn’t be matched to a known paper.

Research works printed but not linked: 8

Cressman, 2021, Proprioceptive recalibration following implicit visuomotor adaptation is preserved in Parkinson’s disease, Experimental Brain Research, 239, 1551, 10.1007/s00221-021-06075-y · DOI
Feldman, 2020, Gait, balance and posture in major mental illnesses: Depression, anxiety and schizophrenia, Austin Medical Sciences, 5, 1
Gowen, 2013, Motor abilities in autism: A review using a computational context, Journal of Autism and Developmental Disorders, 43, 323, 10.1007/s10803-012-1574-0 · DOI
Insel, 2010, 167, 748
Lefebvre, 2023, The pathobiology of psychomotor slowing in psychosis: Altered cortical excitability and connectivity, Brain, awad395
Strick, 2021, The cortical motor areas and the emergence of motor skills: A neuroanatomical perspective, Annual Review of Neuroscience, 44, 425, 10.1146/annurev-neuro-070918-050216 · DOI
Walther, 2016, Vol. 42, 259
Walther, 2022, Vol. 48, 741

Sorted by citations

Future of Sensorimotor and Psychomotor Dysfunction in Mental Disorders: Emerging Tools, Methodological Challenges, and the Road Ahead
Hirjak, D., Mittal, V. A., Meyer‐Lindenberg, A., & Northoff, G. (2025) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20250533 · Cited by 9
Advancing the sensori-/psychomotor domain in schizophrenia spectrum disorders: From clinical observation to translational innovation
Hirjak, D., Volkmer, S., Pokorny, V., & Mittal, V. A. (2025) · Schizophrenia Research · doi:10.1016/j.schres.2025.09.021 · Cited by 5
Functional organization of the primary motor cortex in psychosis and the potential role of intereffector regions in psychomotor slowing
Walther, S., Wüthrich, F., Pavlidou, A., Nadesalingam, N., Heckers, S., Nuoffer, M. G., Chapellier, V., Stegmayer, K., Maderthaner, L., Kyrou, A., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2425388122 · Cited by 4
Toward precision psychiatry in catatonia: A scoping review of its factor structure and clinical implications
Flores-Cohaila, J. A., & Huarcaya-Victoria, J. (2026) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2026.104920 · Cited by 2
Clinical and Neurobiological Characterization of Akathisia in Schizophrenia Spectrum Disorders and Mood Disorders
Altinok, D. C. A., Volkmer, S., Fritze, S., Brandt, G. A., Wölfl, L., Kukovic, J., Mittal, V. A., Meyer‐Lindenberg, A., & Hirjak, D. (2026) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2026.06.002 · Cited by 1

See all 9

Authors: Osborne, K. J., Walther, S., & Mittal, V. A.
Affiliations: Northwestern University (US)
Universitätsklinikum Würzburg (DE)
Corresponding author: Osborne, K. Juston
ORCID: Osborne, K. Juston
Walther, Sebastian
Mittal, Vijay A.
Venue: Clinical Psychology Review
Publisher: Elsevier BV
Published: 2024-12
Volume: 114
Pages: 102511
ISSN: 0272-7358 (ISSN-L)
DOI: 10.1016/j.cpr.2024.102511
OpenAlex: W4403907212
Cited by: 9
References: 313
Citations by year: 2026: 5 · 2025: 4
FWCI: 0.58
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
creativecommons.org/licenses/by-nc/4.0/ (vor)
Locations: Clinical Psychology Review (publishedVersion, cc-by-nc)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Mental Health (1F31MH123121-01A1, 5T32MH100019\u201305)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Social Sciences › Arts and Humanities › Philosophy › Mental Health and Psychiatry
Keywords: motor action, Research Domain Criteria, mental illness, action planning, motor execution, sensorimotor system
MeSH terms: Mental Disorders, Humans, Motor Activity, National Institute of Mental Health (U.S.), United States

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Motor actions across psychiatric disorders: A research domain criteria (RDoC) perspective

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks