Cited by 269Transcranial Magnetic Stimulation StudiesMotor Control and AdaptationNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 73 of the 73 references it cites were found in a registry or an index.

Modifying motor learning through gating and homeostatic metaplasticity

Ziemann, Ulf, Siebner, Hartwig R.·2008·Brain Stimulation

DOI 10.1016/j.brs.2007.08.003

Open this paper in CoChat — free account

Abstract

Synaptic plasticity in the motor cortex is involved at least in some forms of motor learning. Recent evidence showed that the extent of practice-dependent plasticity in the motor cortex can be purposefully enhanced by experimental manipulation. One way of improving motor learning is to transiently increase the excitability of the motor cortex during motor learning. This can be achieved by weakening the excitability of intracortical inhibitory circuits concurrently with practice. This principle is being referred to as "gating." Another strategy to boost learning is to decrease the threshold for induction of synaptic plasticity by lowering neuronal activity in the motor cortex before practice. This approach invokes homeostatic metaplasticity. Here we highlight how transcranial brain stimulation can exploit gating and homeostatic metaplasticity to enhance motor learning in healthy subjects and in patients after stroke.

Integrity signals

Registry

Crossref · 10.1016/j.brs.2007.08.003

Cites

73 of 73 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?

Theta Burst Stimulation of the Human Motor Cortex
Huang, Y.-Z., Edwards, M. J., Rounis, E., Bhatia, K. P., & Rothwell, J. C. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.033 · Cited by 4,158
Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Synaptic plasticity: taming the beast
Abbott, L. F., & Nelson, S. B. (2000) · Nature Neuroscience · doi:10.1038/81453 · Cited by 2,263
Depression of motor cortex excitability by low-frequency transcranial magnetic stimulation
Chen, R., Classen, J., Gerloff, C., Celnik, P., Wassermann, E. M., Hallett, M., & Cohen, L. G. (1997) · Neurology · doi:10.1212/wnl.48.5.1398 · Cited by 2,128
Molecular cloning and characterization of the rat NMDA receptor
Moriyoshi, K., Masu, M., Ishii, T., Shigemoto, R., Mizuno, N., & Nakanishi, S. (1991) · Nature · doi:10.1038/354031a0 · Cited by 1,771
Responses to rapid-rate transcranial magnetic stimulation of the human motor cortex
Pascual‐Leone, Á., Valls‐Solé, J., Wassermann, E. M., & Hallett, M. (1994) · Brain · doi:10.1093/brain/117.4.847 · Cited by 1,486
Induction of plasticity in the human motor cortex by paired associative stimulation
Stefan, K. (2000) · Brain · doi:10.1093/brain/123.3.572 · Cited by 1,484
Effects of non-invasive cortical stimulation on skilled motor function in chronic stroke
Hummel, F. C. (2005) · Brain · doi:10.1093/brain/awh369 · Cited by 1,141
Facilitation of implicit motor learning by weak transcranial direct current stimulation of the primary motor cortex in the human
Nitsche, M. A., Schauenburg, A., Lang, N., Liebetanz, D., Exner, C., Paulus, W., & Tergau, F. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321662994 · Cited by 1,032

Flagged first, then by citations

Show all 73 references

Sorted by citations

Items 101–200 of 268

Anodal transcranial direct current stimulation over premotor cortex facilitates observational learning of a motor sequence
Wade, S., & Hammond, G. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12916 · Cited by 36
Are studies of motor cortex plasticity relevant in human patients with Parkinson’s disease?
Bologna, M., Suppa, A., Conte, A., Latorre, A., Rothwell, J. C., & Berardelli, A. (2015) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.02.009 · Cited by 39
Influence of paravertebral muscles training on brain plasticity and postural control in chronic low back pain
Massé‐Alarie, H., Beaulieu, L., Preuss, R. A., & Schneider, C. (2016) · Scandinavian Journal of Pain · doi:10.1016/j.sjpain.2016.03.005 · Cited by 38
Revisiting the Corticomotor Plasticity in Low Back Pain: Challenges and Perspectives
Massé‐Alarie, H., & Schneider, C. (2016) · Healthcare · doi:10.3390/healthcare4030067 · Cited by 42
State-dependent effects of ventromedial prefrontal cortex continuous Thetaburst stimulation on cocaine Cue reactivity in chronic cocaine users
Kearney-Ramos, T. E., Dowdle, L. T., Mithoefer, O. J., Devries, W., George, M. S., & Hanlon, C. A. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00317 · Cited by 37
Noninvasive Brain Stimulation Techniques Can Modulate Cognitive Processing
Veniero, D., Strüber, D., Thut, G., & Herrmann, C. S. (2016) · Organizational Research Methods · doi:10.1177/1094428116658960 · Cited by 39
Muscle-selective disinhibition of corticomotor representations using a motor imagery-based brain-computer interface
Takemi, M., Maeda, T., Masakado, Y., Siebner, H. R., & Ushiba, J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.08.070 · Cited by 35
Self-citation
Transcranial magnetic stimulation as a tool to induce and explore plasticity in humans
Suppa, A., Asci, F., & Guerra, A. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00005-9 · Cited by 39
The effect of gamma oscillations in boosting primary motor cortex plasticity is greater in young than older adults
Guerra, A., Asci, F., Zampogna, A., D’Onofrio, V., Berardelli, A., & Suppa, A. (2021) · Clinical Neurophysiology · doi:10.1016/j.clinph.2021.01.032 · Cited by 34
Augmenting LTP-Like Plasticity in Human Motor Cortex by Spaced Paired Associative Stimulation
Müller‐Dahlhaus, F., Lücke, C., Lu, M., Arai, N., Fuhl, A., Herrmann, E. M., & Ziemann, U. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131020 · Cited by 35
Self-citation
Primary motor cortex long‐term plasticity in multiple system atrophy
Suppa, A., Marsili, L., Stasio, F. D., Latorre, A., Parvez, A., Colosimo, C., & Berardelli, A. (2013) · Movement Disorders · doi:10.1002/mds.25668 · Cited by 34
Disruption of cortical synaptic homeostasis in individuals with chronic low back pain
Thapa, T., Graven‐Nielsen, T., Chipchase, L. S., & Schabrun, S. M. (2018) · Clinical Neurophysiology · doi:10.1016/j.clinph.2018.01.060 · Cited by 34
Brain State-dependent Gain Modulation of Corticospinal Output in the Active Motor System
Naros, G., Lehnertz, T., Leão, M. T., Ziemann, U., & Gharabaghi, A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz093 · Cited by 33
Self-citation
Facilitation of corticospinal tract excitability by transcranial direct current stimulation combined with voluntary grip exercise
Kim, G.-W., & Ko, M.-H. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.05.037 · Cited by 33
D-cycloserine normalizes long-term motor plasticity after transcranial magnetic intermittent theta-burst stimulation in major depressive disorder
Cole, J., Selby, B., Ismail, Z., & McGirr, A. (2021) · Clinical Neurophysiology · doi:10.1016/j.clinph.2021.04.002 · Cited by 35
May Dual Transcranial Direct Current Stimulation Enhance the Efficacy of Robot-Assisted Therapy for Promoting Upper Limb Recovery in Chronic Stroke?
Morone, G., Capone, F., Iosa, M., Cruciani, A., Paolucci, M., Cinnera, A. M., Musumeci, G., Brunelli, N., Costa, C. M., Paolucci, S., et al. (2022) · Neurorehabilitation and neural repair · doi:10.1177/15459683221138743 · Cited by 32
Augmenting mirror visual feedback‐induced performance improvements in older adults
Hoff, M., Kaminski, E., Rjosk, V., Sehm, B., Steele, C. J., Villringer, A., & Ragert, P. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12899 · Cited by 32
Transcranial random noise stimulation combined with cognitive training for treating ADHD: a randomized, sham-controlled clinical trial
Dakwar-Kawar, O., Mairon, N., Hochman, S., Berger, I., Kadosh, R. C., & Nahum, M. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02547-7 · Cited by 37
Effects of chronic iTBS‐rTMS and enriched environment on visual cortex early critical period and visual pattern discrimination in dark‐reared rats
Castillo-Padilla, D. V., & Funke, K. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22296 · Cited by 31
Exciting recovery
Field-Fote, E. C. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2014.12.006 · Cited by 29
NPY-Y1 receptor signaling controls spatial learning and perineuronal net expression
Bertocchi, I., Mele, P., Ferrero, G., Oberto, A., Carulli, D., & Eva, C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108425 · Cited by 26
Subthreshold stimulation intensity is associated with greater clinical efficacy of intermittent theta-burst stimulation priming for Major Depressive Disorder
Lee, J. C., Corlier, J., Wilson, A. C., Tadayonnejad, R., Marder, K. G., Ngo, D., Krantz, D. E., Wilke, S. A., Levitt, J. G., Ginder, N. D., et al. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.06.008 · Cited by 31
Short-term immobilization influences use-dependent cortical plasticity and fine motor performance
Opie, G. M., Evans, A., Ridding, M. C., & Semmler, J. G. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.06.002 · Cited by 33
Effect of tDCS on Fine Motor Control of Patients in Subacute and Chronic Post-Stroke Stages
Pavlova, E. L., Semenov, R. V., & Guekht, A. B. (2019) · Journal of Motor Behavior · doi:10.1080/00222895.2019.1639608 · Cited by 27
Examining the Effect of Transcranial Electrical Stimulation and Cognitive Training on Processing Speed in Pediatric Attention Deficit Hyperactivity Disorder: A Pilot Study
Dakwar-Kawar, O., Berger, I., Barzilay, S., Grossman, E. S., Kadosh, R. C., & Nahum, M. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.791478 · Cited by 26
Repetitive Transcranial Magnetic Stimulation for Upper Extremity Motor Recovery: Does It Help?
Schambra, H. M. (2018) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-018-0913-8 · Cited by 27
Mechanisms of Nicotinic Modulation of Glutamatergic Neuroplasticity in Humans
Lugon, M. D. M. V., Batsikadze, G., Fresnoza, S. M., Grundey, J., Kuo, M., Paulus, W., Nakamura-Palacios, E. M., & Nitsche, M. A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv252 · Cited by 27
Theta-burst direct electrical stimulation remodels human brain networks
Huang, Y., Zelmann, R., Hadar, P., Peralta, J. D., Richardson, R. M., Williams, Z. M., Cash, S. S., Keller, C. J., & Paulk, A. C. (2024) · Nature Communications · doi:10.1038/s41467-024-51443-1 · Cited by 34
Electrophysiological CNS-processes related to associative learning in humans
Christoffersen, G. R. J., & Schachtman, T. R. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.09.011 · Cited by 26
Increase in flexor but not extensor corticospinal motor outputs following ischemic nerve block
Vallence, A., Hammond, G. R., & Reilly, K. T. (2012) · Journal of Neurophysiology · doi:10.1152/jn.01118.2010 · Cited by 24
Immediate effect of transcranial direct current stimulation combined with functional electrical stimulation on activity of the tibialis anterior muscle and balance of individuals with hemiparesis stemming from a stroke
Fruhauf, A. M. A., Politti, F., Corso, S. D., Costa, G. C., Teodósio, A. D. C., Silva, S. M., Corrêa, J. C. F., & Corrêa, F. I. (2017) · Journal of Physical Therapy Science · doi:10.1589/jpts.29.2138 · Cited by 24
d-cycloserine blunts motor cortex facilitation after intermittent theta burst transcranial magnetic stimulation: A double-blind randomized placebo-controlled crossover study
Selby, B., MacMaster, F. P., Kirton, A., & McGirr, A. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.03.026 · Cited by 24
Age-related changes in motor cortex plasticity assessed with non-invasive brain stimulation: an update and new perspectives
Semmler, J., Hand, B., Sasaki, R., Merkin, A., & Opie, G. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06163-z · Cited by 23
Corticospinal correlates of fast and slow adaptive processes in motor learning
Sarwary, A. M. E., Wischnewski, M., Schutter, D. J. L. G., Selen, L. P. J., & Medendorp, W. P. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00488.2018 · Cited by 23
Intermittent theta-burst stimulation with physical exercise improves poststroke motor function: A systemic review and meta-analysis
Gao, B., Wang, Y., Zhang, D., Wang, Z., & Wang, Z. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.964627 · Cited by 22
Better together: Left and right hemisphere engagement to reduce age-related memory loss
Brambilla, M., Manenti, R., Ferrari, C., & Cotelli, M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.07.037 · Cited by 22
Repetitive transcranial magnetic stimulation modulates the impact of a negative mood induction
Möbius, M., Lacomblé, L., Meyer, T., Schutter, D. J. L. G., Gielkens, T., Becker, E. S., Tendolkar, I., & van Eijndhoven, P. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw180 · Cited by 23
Increased leg muscle fatigability during 2 mA and 4 mA transcranial direct current stimulation over the left motor cortex
Workman, C. D., Kamholz, J. A., & Rudroff, T. (2020) · Experimental Brain Research · doi:10.1007/s00221-019-05721-w · Cited by 23
The association of motor imagery and kinesthetic illusion prolongs the effect of transcranial direct current stimulation on corticospinal tract excitability
Kaneko, F., Shibata, E., 速水, 達., Nagahata, K., & Aoyama, T. (2016) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-016-0143-8 · Cited by 23
The effectiveness of anodal tDCS and cognitive training on cognitive functions in multiple sclerosis; a randomized, double-blind, parallel-group study
Simani, L., Roozbeh, M., Shojaei, M., Ramezani, M., Roozbeh, M., Gharehgozli, K., & Rostami, M. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.104392 · Cited by 20
Effects of Multiple Sessions of Cathodal Priming and Anodal HD-tDCS on Visuo Motor Task Plateau Learning and Retention
Besson, P., Muthalib, M., Vassoigne, C. D., Rothwell, J. C., & Perrey, S. (2020) · Brain Sciences · doi:10.3390/brainsci10110875 · Cited by 19
Electrifying discourse: Anodal tDCS of the primary motor cortex selectively reduces action appraisal in naturalistic narratives
Birba, A., Vitale, F., Padrón, I., Dottori, M., de Vega, M., Zimerman, M., Sedeño, L., Ibáñez, A. M., & García, A. M. (2020) · Cortex · doi:10.1016/j.cortex.2020.08.005 · Cited by 16
Pressure Pain Thresholds Increase after Preconditioning 1 Hz Repetitive Transcranial Magnetic Stimulation with Transcranial Direct Current Stimulation
Moloney, T. M., & Witney, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092540 · Cited by 22
Priming the Motor Cortex With Anodal Transcranial Direct Current Stimulation Affects the Acute Inhibitory Corticospinal Responses to Strength Training
Frazer, A. K., Howatson, G., Ahtiainen, J. P., Avela, J., Rantalainen, T., & Kidgell, D. J. (2019) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000002959 · Cited by 19
Metaplasticity in the human swallowing system: clinical implications for dysphagia rehabilitation
Cheng, I., & Hamdy, S. (2021) · Neurological Sciences · doi:10.1007/s10072-021-05654-9 · Cited by 18
Non-invasive brain stimulation associated mirror therapy for upper-limb rehabilitation after stroke: Systematic review and meta-analysis of randomized clinical trials
Zhao, Q., Li, H., Liu, Y., Mei, H., Guo, L., Liu, X., Tao, X., & Ma, J. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.918956 · Cited by 18
tDCS of Medial Prefrontal Cortex Does Not Enhance Interpersonal Trust
Colzato, L. S., Sellaro, R., van den Wildenberg, W. P. M., & Hommel, B. (2015) · Journal of Psychophysiology · doi:10.1027/0269-8803/a000144 · Cited by 17
Timing of Acupuncture during LTP-Like Plasticity Induced by Paired-Associative Stimulation
He, X., Sun, Q., Liu, H.-H., Guo, X., Chen, C., & Chen, L.-D. (2019) · Behavioural Neurology · doi:10.1155/2019/9278270 · Cited by 19
Motor cortex representation of deep and superficial neck flexor muscles in individuals with and without neck pain
Cancino, E. E., Marinovic, W., Jull, G. A., & Hodges, P. W. (2019) · Human Brain Mapping · doi:10.1002/hbm.24558 · Cited by 16
Repetitive transcranial magnetic stimulation recovers cortical map plasticity induced by sensory deprivation due to deafferentiation
Kloosterboer, E., & Funke, K. (2019) · The Journal of Physiology · doi:10.1113/jp277507 · Cited by 18
Remote Effects of Non-Invasive Cerebellar Stimulation on Error Processing in Motor Re-Learning
Taubert, M., Stein, T., Kreutzberg, T., Stockinger, C., Hecker, L., Focke, A., Ragert, P., Villringer, A., & Pleger, B. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.04.007 · Cited by 20
Evidence That Brain-Controlled Functional Electrical Stimulation Could Elicit Targeted Corticospinal Facilitation of Hand Muscles in Healthy Young Adults
Suzuki, Y., Jovanovic, L. I., Fadli, R. A., Yamanouchi, Y., Márquez-Chin, C., Popović, M. R., Nomura, T., & Milosevic, M. (2022) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2021.12.007 · Cited by 16
Test-Retest Reliability of Homeostatic Plasticity in the Human Primary Motor Cortex
Thapa, T., & Schabrun, S. M. (2018) · Neural Plasticity · doi:10.1155/2018/6207508 · Cited by 16
Effects of Transcranial Direct Current Stimulation Combined With Neuromuscular Electrical Stimulation on Upper Extremity Motor Function in Patients With Stroke
Wei, Y.-Y., Koh, C., Hsu, M., Lo, S. K., Chen, C., & Lin, J. (2021) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/phm.0000000000001759 · Cited by 15
Neuronavigated Cerebellar 50 Hz tACS: Attenuation of Stimulation Effects by Motor Sequence Learning
Herzog, R., Bolte, C., Radecke, J., von Möller, K., Lencer, R., Tzvi, E., Münchau, A. M., Bäumer, T., & Weißbach, A. (2023) · Biomedicines · doi:10.3390/biomedicines11082218 · Cited by 15
Patterned Brain Stimulation, What a Framework with Rhythmic and Noisy Components Might Tell Us about Recovery Maximization
Schmidt, S. H., Scholz, M., Obermayer, K., & Brandt, S. A. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00325 · Cited by 15
Visuomotor task acquisition is reduced by priming paired associative stimulation in older adults
Opie, G. M., Hand, B. J., Coxon, J. P., Ridding, M. C., Ziemann, U., & Semmler, J. G. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.05.017 · Cited by 14
Self-citation
Effects of repetitive transcranial magnetic and deep brain stimulation on long‐range synchrony of oscillatory activity in a rat model of developmental schizophrenia
Lippmann, B., Barmashenko, G., & Funke, K. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15125 · Cited by 15
Protocols for inducing homeostatic plasticity reflected in the corticospinal excitability in healthy human participants: A systematic review and meta‐analysis
Wittkopf, P. G., Larsen, D. B., & Graven‐Nielsen, T. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15389 · Cited by 16
Failure to Improve Verbal Fluency with Transcranial Direct Current Stimulation
Klaus, J., & Hartwigsen, G. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.09.003 · Cited by 13
Evidence of the Homeostatic Regulation With the Combination of Transcranial Direct Current Stimulation and Physical Activity
Baltar, A., Nogueira, F. L. A., Marques, D., Carneiro, M. I. S., & Monte-Silva, K. K. (2018) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/phm.0000000000000956 · Cited by 13
Electrical stimulation during skill training with a therapeutic glove enhances the induction of cortical plasticity and has a positive effect on motor memory
Christova, M., Rafolt, D., Golaszewski, S. M., Nardone, R., & Gallasch, E. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.014 · Cited by 13
Neuropeptide Y as a possible homeostatic element for changes in cortical excitability induced by repetitive transcranial magnetic stimulation
Jazmati, D., Neubacher, U., & Funke, K. (2018) · Brain stimulation · doi:10.1016/j.brs.2018.02.017 · Cited by 13
Optimal Combination of Anodal Transcranial Direct Current Stimulations and Motor Imagery Interventions
Saruco, E., Rienzo, F. D., Núñez-Nagy, S., Rubio, M. A., Debarnot, U., Collet, C., Guillot, A., & Saimpont, A. (2018) · Neural Plasticity · doi:10.1155/2018/5351627 · Cited by 13
Whole-body kinematic adaptations to running on an unstable, irregular, and compliant surface
Mohr, M., Peer, L., Michiel, A. D., van Andel, S., & Federolf, P. (2023) · Sports Biomechanics · doi:10.1080/14763141.2023.2222022 · Cited by 12
Aberrant plasticity in musculoskeletal pain: a failure of homeostatic control?
Thapa, T., Graven‐Nielsen, T., & Schabrun, S. M. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06062-3 · Cited by 13
Timing-Dependent Effects of Transcranial Direct Current Stimulation on Hand Motor Function in Healthy Individuals: A Randomized Controlled Study
Jo, N.-G., Kim, G.-W., Won, Y. H., Park, S.-H., Seo, J., & Ko, M.-H. (2021) · Brain Sciences · doi:10.3390/brainsci11101325 · Cited by 11
Single session transcranial direct current stimulation to the primary motor cortex fails to enhance early motor sequence learning in Parkinson’s disease
Simpson, M. W., & Mak, K. Y. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113624 · Cited by 11
Influences of glutamine administration on response selection and sequence learning: a randomized-controlled trial
Jongkees, B. J., Immink, M. A., & Colzato, L. S. (2017) · Scientific Reports · doi:10.1038/s41598-017-02957-w · Cited by 12
Combining transcranial direct current stimulation with aerobic exercise to optimize cortical priming in stroke
Sivaramakrishnan, A., & Madhavan, S. (2020) · Applied Physiology Nutrition and Metabolism · doi:10.1139/apnm-2020-0677 · Cited by 12
Somatosensory and transcranial direct current stimulation effects on manual dexterity and motor cortex function: A metaplasticity study
Trudgen, A., Cirillo, J., & Byblow, W. D. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.02.010 · Cited by 11
Changes in Cortical Plasticity in Relation to a History of Concussion during Adolescence
Meehan, S. K., Mirdamadi, J. L., Martini, D. N., & Broglio, S. P. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00005 · Cited by 12
Simultaneous application of slow‐oscillation transcranial direct current stimulation and theta burst stimulation prolongs continuous theta burst stimulation‐induced suppression of corticomotor excitability in humans
Doeltgen, S., McAllister, S. M., & Ridding, M. C. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08181.x · Cited by 11
After-effects of repetitive transcranial magnetic stimulation with parameter dependence on long-term potentiation-like plasticity and object recognition memory in rats
Chen, S., He, X., Wei, X., Huang, J., & Zhang, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1144480 · Cited by 10
A randomized sham-controlled trial on the effects of dual-tDCS “during” physical therapy on lower limb performance in sub-acute stroke and a comparison to the previous study using a “before” stimulation protocol
Klomjai, W., & Aneksan, B. (2022) · BMC Sports Science Medicine and Rehabilitation · doi:10.1186/s13102-022-00463-9 · Cited by 10
Theta-gamma transcranial alternating current stimulation enhances ballistic motor performance in healthy young and older adults
Gamage, N. N., Liao, W., Hand, B. J., Atherton, P. J., Piasecki, M., Opie, G. M., & Semmler, J. G. (2025) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2025.04.010 · Cited by 9
Transcranial Current Stimulation as a Tool of Neuromodulation of Cognitive Functions in Parkinson’s Disease
Brak, I. V., Filimonova, E., Zakhariya, O., Khasanov, R., & Stepanyan, I. V. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.781488 · Cited by 13
Timing-Dependent Priming Effects of Anodal tDCS on Two-Hand Coordination
Azarpaikan, A., Taheri, H. R., Sohrabi, M., Boostani, R., & Ghoshoni, M. (2019) · Journal of Psychophysiology · doi:10.1027/0269-8803/a000250 · Cited by 8
Brain-State-Dependent Non-Invasive Brain Stimulation and Functional Priming: A Hypothesis
Sergeeva, E. G., Henrich‐Noack, P., Bola, M., & Sabel, B. A. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00899 · Cited by 9
A transcranial magnetic stimulation protocol for decreasing the craving of methamphetamine-dependent patients
Chen, T., Su, H., Li, R., Jiang, H., Li, X., Wu, Q., Tan, H., Zhang, J., Zhong, N., Du, J., et al. (2021) · STAR Protocols · doi:10.1016/j.xpro.2021.100944 · Cited by 9
Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms
Bradley, C., Elliott, J., Dudley, S. C., Kieseker, G. A., Mattingley, J. B., & Sale, M. V. (2022) · Experimental Brain Research · doi:10.1007/s00221-022-06462-z · Cited by 8
Transcranial Magnetic Stimulation of Rodents
Funke, K. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00020-3 · Cited by 8
Effect of Repetitive Passive Movement Before Motor Skill Training on Corticospinal Excitability and Motor Learning Depend on BDNF Polymorphisms
Pham, M. V., Miyaguchi, S., Watanabe, H., Saito, K., Otsuru, N., & Onishi, H. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.621358 · Cited by 7
Neurobiological Bases of Learning and Their Role for the Paradigm Shift in Education
Chavez-Mancilla, V., & Parodí, J. (2015) · Psychology · doi:10.4236/psych.2015.613170 · Cited by 7
Effects of iTBS-rTMS on the Behavioral Phenotype of a Rat Model of Maternal Immune Activation
Rittweger, N., Ishorst, T., Barmashenko, G., Aliane, V., Winter, C., & Funke, K. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.670699 · Cited by 7
Train duration and inter-train interval determine the direction and intensity of high-frequency rTMS after-effects
Jin, J., Wang, X., Wang, H., Li, Y., Liu, Z., & Yin, T. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1157080 · Cited by 7
Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
Mirdamadi, J. L., & Meehan, S. K. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.920526 · Cited by 7
Effect of current direction and muscle activation on motor cortex neuroplasticity induced by repetitive paired‐pulse transcranial magnetic stimulation
Sasaki, R., Liao, W., Opie, G. M., & Semmler, J. G. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16099 · Cited by 7
Motor cortical plasticity in extrinsic hand muscles is determined by the resting thresholds of overlapping representations
Mirdamadi, J. L., Suzuki, L. Y., & Meehan, S. K. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.07.015 · Cited by 7
The effect of combined transcranial direct current stimulation and peripheral nerve electrical stimulation on corticospinal excitability
Tsuiki, S., Sasaki, R., Miyaguchi, S., Kojima, S., Saito, K., Inukai, Y., Masaki, M., Otsuru, N., & Onishi, H. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214592 · Cited by 7
Transcranial Magnetic and Electric Stimulation in Perception and Cognition Research
Miniussi, C., Ambrus, G. G., Pellicciari, M. C., Walsh, V., & Antal, A. (2012) · Frontiers in neuroscience · doi:10.1201/b14174-18 · Cited by 7
Investigating the Effects of Repetitive Paired-Pulse Transcranial Magnetic Stimulation on Visuomotor Training Using TMS-EEG
Sasaki, R., Hand, B. J., Liao, W., Semmler, J. G., & Opie, G. M. (2024) · Brain Topography · doi:10.1007/s10548-024-01071-1 · Cited by 6
Anodal tDCS improves neuromuscular adaptations to short-term resistance training of the knee extensors in healthy individuals
Angius, L., Ansdell, P., Škarabot, J., Goodall, S., Thomas, K., Cowper, G., Santarnecchi, E., Kidgell, D. J., & Howatson, G. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00289.2024 · Cited by 6
The effects of intermittent theta burst stimulation over dorsal premotor cortex on primary motor cortex plasticity in young and older adults
Liao, W., Opie, G. M., Ziemann, U., & Semmler, J. G. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16395 · Cited by 6
Self-citation
Noninvasive brain stimulation can elucidate and interact with the mechanisms underlying motor learning and retention: implications for rehabilitation
Hinder, M. R., Reißig, P., & Fujiyama, H. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00766.2013 · Cited by 6
The influence of a single transcranial direct current stimulation session on physical fitness in healthy subjects: a systematic review
Marinus, N., Hoornweder, S. V., Aarts, M., Vanbilsen, J., Hansen, D., & Meesen, R. (2022) · Experimental Brain Research · doi:10.1007/s00221-022-06494-5 · Cited by 8
Erratum to “Consensus Paper: Probing Homeostatic Plasticity of Human Cortex With Non-invasive Transcranial Brain Stimulation”. Brain Stimulation 8 (2015) 442–454
Karabanov, A., Ziemann, U., Hamada, M., George, M. S., Quartarone, A., Classen, J., Massimini, M., Rothwell, J., & Siebner, H. R. (2015) · Brain Stimulation · doi:10.1016/j.brs.2015.06.016 · Cited by 5
Self-citation
Motor adaptation and internal model formation in a robot-mediated forcefield
Taga, M., Curci, A., Pizzamigglio, S., Lacal, I., Turner, D., & Fu, C. H. Y. (2021) · Psychoradiology · doi:10.1093/psyrad/kkab007 · Cited by 3
Expanding the electrotherapeutic toolkit: a perspective on transcranial pulsating electromagnetic fields (T-PEMF)
Karabanov, A. N., & Siebner, H. R. (2014) · Acta Neuropsychiatrica · doi:10.1017/neu.2014.19 · Cited by 5
Self-citation
Cortical inhibitory deficits in Huntington's disease are not influenced by gender
Philpott, A. L., Cummins, T. D. R., Bailey, N. W., Churchyard, A., Fitzgerald, P. B., & Georgiou‐Karistianis, N. (2016) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2016.04.018 · Cited by 5

Authors: Ziemann, U., & Siebner, H. R.
Affiliations: Goethe University Frankfurt (DE)
Christian-Albrechts-Universität zu Kiel (DE)
Corresponding author: Ziemann, Ulf
ORCID: Ziemann, Ulf
Siebner, Hartwig R.
Venue: Brain Stimulation
Publisher: Elsevier BV
Published: 2008-01
Volume: 1
Issue: 1
Pages: 60-66
ISSN: 1876-4754 (ISSN-L)
1935-861X
DOI: 10.1016/j.brs.2007.08.003
OpenAlex: W2031034560
Cited by: 269
References: 73
Citations by year: 2026: 5 · 2025: 13 · 2024: 13 · 2023: 12 · 2022: 15 · 2021: 24 · 2020: 19 · 2019: 19 · 2018: 21 · 2017: 12 · 2016: 19 · 2015: 26 · 2014: 16 · 2013: 19 · 2012: 15
FWCI: 0.35
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Brain stimulation (publishedVersion)
PubMed (publishedVersion)
DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Topics: Life Sciences › Neuroscience › Neurology › Transcranial Magnetic Stimulation Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: motor learning, motor cortex, synaptic plasticity, gating, intracortical inhibition, cortical excitability, transcranial brain stimulation, stroke rehabilitation
MeSH terms: Stroke Rehabilitation, Homeostasis, Humans, Learning, Motor Activity, Motor Cortex, Neuronal Plasticity, Stroke, Transcranial Magnetic Stimulation

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

Modifying motor learning through gating and homeostatic metaplasticity

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