Within‐subject reliability of concurrent TMS‐fMRI during a single session

Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS‐fMRI experiment. We leveraged an ex...

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Published inPsychophysiology Vol. 60; no. 7; pp. e14252 - n/a
Main Authors Hawco, Colin, Steeves, Jennifer K. E., Voineskos, Aristotle N., Blumberger, Daniel M., Daskalakis, Zafiris J.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.07.2023
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Abstract Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS‐fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub‐threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS‐fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS‐fMRI protocol in order to achieve reliable spatial changes in activity. Single‐subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t‐maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate‐high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS‐evoked activity. These results demonstrate concurrent TMS‐fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes. Reliability has become a central issue in fMRI research. While TMS‐fMRI can be a powerful tool to probe brain function, the reliability of the evoked signal has not yet been assessed. Within session reliability of the fMRI‐evoked response following TMS was assessed. Reliability was moderate‐high with 50 trials and moderate with 30 trials. This is higher than typical fMRI measurements, which has important implications for study design and interpretation.
AbstractList Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS‐fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub‐threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS‐fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS‐fMRI protocol in order to achieve reliable spatial changes in activity. Single‐subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations ( R ) between t ‐maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate‐high for 50 trials (mean R  = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of R s differed across participants, but regional R was correlated with the magnitude of TMS‐evoked activity. These results demonstrate concurrent TMS‐fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes. Reliability has become a central issue in fMRI research. While TMS‐fMRI can be a powerful tool to probe brain function, the reliability of the evoked signal has not yet been assessed. Within session reliability of the fMRI‐evoked response following TMS was assessed. Reliability was moderate‐high with 50 trials and moderate with 30 trials. This is higher than typical fMRI measurements, which has important implications for study design and interpretation.
Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS‐fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub‐threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS‐fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS‐fMRI protocol in order to achieve reliable spatial changes in activity. Single‐subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t‐maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate‐high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS‐evoked activity. These results demonstrate concurrent TMS‐fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes. Reliability has become a central issue in fMRI research. While TMS‐fMRI can be a powerful tool to probe brain function, the reliability of the evoked signal has not yet been assessed. Within session reliability of the fMRI‐evoked response following TMS was assessed. Reliability was moderate‐high with 50 trials and moderate with 30 trials. This is higher than typical fMRI measurements, which has important implications for study design and interpretation.
Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS-fMRI) allows real-time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS-fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub-threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS-fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS-fMRI protocol in order to achieve reliable spatial changes in activity. Single-subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t-maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate-high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS-evoked activity. These results demonstrate concurrent TMS-fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes.
Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS-fMRI) allows real-time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS-fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub-threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS-fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS-fMRI protocol in order to achieve reliable spatial changes in activity. Single-subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t-maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate-high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS-evoked activity. These results demonstrate concurrent TMS-fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes.Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS-fMRI) allows real-time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS-fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub-threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS-fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS-fMRI protocol in order to achieve reliable spatial changes in activity. Single-subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t-maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate-high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS-evoked activity. These results demonstrate concurrent TMS-fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes.
Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However, technical challenges, safety, and tolerability may limit the number of trials employed during a concurrent TMS‐fMRI experiment. We leveraged an existing data set with 100 trials of active TMS compared to a sub‐threshold control condition to assess the reliability of the evoked BOLD response during concurrent TMS‐fMRI. This data will permit an analysis of the minimum number of trials that should be employed in a concurrent TMS‐fMRI protocol in order to achieve reliable spatial changes in activity. Single‐subject maps of brain activity were created by splitting the trials within the same experimental session into groups of 50, 40, 30, 25, 20, 15, or 10 trials, correlations (R) between t‐maps derived from paired subsets of trials within the same individual were calculated as reliability. R was moderate‐high for 50 trials (mean R = .695) and decreased as the number of trials decreased. Consistent with previous findings of high individual variability in the spatial patterns of evoked neuronal changes following a TMS pulse, the spatial pattern of Rs differed across participants, but regional R was correlated with the magnitude of TMS‐evoked activity. These results demonstrate concurrent TMS‐fMRI produces a reliable pattern of activity at the individual level at higher trial numbers, particularly within localized regions. The spatial pattern of reliability is individually idiosyncratic and related to the individual pattern of evoked changes.
Author Voineskos, Aristotle N.
Hawco, Colin
Steeves, Jennifer K. E.
Blumberger, Daniel M.
Daskalakis, Zafiris J.
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Cites_doi 10.1016/j.cortex.2018.07.010
10.1097/00124509-199803000-00004
10.1017/S0033291713000512
10.1016/j.cub.2006.06.057
10.1523/JNEUROSCI.5642‐09.2010
10.1016/j.neuron.2018.03.035
10.1093/cercor/bhm159
10.1016/j.neuroimage.2005.08.010
10.1016/j.neuropsychologia.2015.10.027
10.1016/j.jns.2016.01.039
10.1002/jmri.21749
10.1038/nature18933
10.1523/JNEUROSCI.3043‐08.2008
10.1016/j.neuroimage.2019.116157
10.1016/j.neuroimage.2019.03.053
10.1016/j.neuron.2017.07.011
10.1001/jamapsychiatry.2015.3097
10.1073/pnas.1106439108
10.3389/fnsys.2013.00124
10.1371/journal.pcbi.1009279
10.1016/j.pscychresns.2018.06.004
10.1016/j.neuroimage.2016.10.020
10.1002/hbm.24307
10.1016/j.neuroimage.2019.04.078
10.1016/j.brs.2018.12.381
10.1523/ENEURO.0163‐22.2022
10.1177/0956797621989730
10.1016/s0006‐3223(01)01199‐4
10.1073/pnas.1602413113
10.1038/nn.4135
10.1093/cercor/bhm013
10.1523/JNEUROSCI.4993‐13.2014
10.1371/journal.pone.0035578
10.1093/cercor/bhq015
10.3389/fnhum.2017.00404
10.1101/136259
10.1177/0956797620916786
10.1073/pnas.1311772110
10.1016/j.neuroimage.2020.117077
10.1002/1522‐2594(200007)44:1<162::AID‐MRM23>3.0.CO;2‐E
10.1016/j.neuroimage.2017.09.022
10.1016/S0006‐3223(01)01153‐2
10.1016/j.brs.2017.12.010
10.1016/j.neuroimage.2021.117823
10.1093/cercor/bhx230
10.1152/jn.00279.2010
10.1016/j.brs.2008.11.002
10.1038/tp.2017.204
10.1126/science.1146426
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2013
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References_xml – volume: 231
  year: 2021
  article-title: Moving beyond the mean: Subgroups and dimensions of brain activity and cognitive performance across domains
  publication-title: Neuroimage
– volume: 17
  start-page: 2841
  issue: 12
  year: 2007
  end-page: 2852
  article-title: Imaging the brain activity changes underlying impaired visuospatial judgments: Simultaneous FMRI, TMS, and behavioral studies
  publication-title: Cerebral Cortex
– volume: 27
  start-page: 5415
  issue: 11
  year: 2017
  end-page: 5429
  article-title: Influences on the test‐retest reliability of functional connectivity MRI and its relationship with behavioral utility
  publication-title: Cerebral Cortex
– volume: 50
  start-page: 58
  issue: 1
  year: 2001
  end-page: 61
  article-title: Transcranial magnetic stimulation in therapy studies: Examination of the reliability of “standard” coil positioning by neuronavigation
  publication-title: Biological Psychiatry
– volume: 17
  issue: 9
  year: 2021
  article-title: Eliminating accidental deviations to minimize generalization error and maximize replicability: Applications in connectomics and genomics
  publication-title: PLoS Computational Biology
– volume: 50
  start-page: 712
  issue: 9
  year: 2001
  end-page: 720
  article-title: Unilateral left prefrontal transcranial magnetic stimulation (TMS) produces intensity‐dependent bilateral effects as measured by interleaved BOLD fMRI
  publication-title: Biological Psychiatry
– volume: 162
  start-page: 289
  year: 2017
  end-page: 296
  article-title: Towards understanding rTMS mechanism of action: Stimulation of the DLPFC causes network‐specific increase in functional connectivity
  publication-title: Neuroimage
– volume: 108
  start-page: 17510
  issue: 42
  year: 2011
  end-page: 17515
  article-title: Causal evidence for frontal involvement in memory target maintenance by posterior brain areas during distracter interference of visual working memory
  publication-title: Proceedings of the National Academy of Sciences of the United States of America
– volume: 18
  start-page: 1281
  issue: 6
  year: 2008
  end-page: 1291
  article-title: Dorsal premotor cortex exerts state‐dependent causal influences on activity in contralateral primary motor and dorsal premotor cortex
  publication-title: Cerebral Cortex
– volume: 195
  start-page: 174
  year: 2019
  end-page: 189
  article-title: Addressing the reliability fallacy in fMRI: Similar group effects may arise from unreliable individual effects
  publication-title: Neuroimage
– volume: 7
  issue: 10
  year: 2017
  article-title: Quantifying person‐level brain network functioning to facilitate clinical translation
  publication-title: Translational Psychiatry
– volume: 44
  start-page: 162
  issue: 1
  year: 2000
  end-page: 167
  article-title: Image‐based method for retrospective correction of physiological motion effects in fMRI: RETROICOR
  publication-title: Magnetic Resonance in Medicine
– volume: 317
  start-page: 1918
  issue: 5846
  year: 2007
  end-page: 1921
  article-title: Transcranial magnetic stimulation elicits coupled neural and hemodynamic consequences
  publication-title: Science
– volume: 220
  year: 2020
  article-title: Visual cortical regions show sufficient test‐retest reliability while salience regions are unreliable during emotional face processing
  publication-title: Neuroimage
– year: 2017
  article-title: How sample size influences the replicability of task‐based fMRI
  publication-title: bioRxiv
– start-page: 159
  year: 2013
  end-page: 170
– volume: 110
  start-page: 19944
  issue: 49
  year: 2013
  end-page: 19949
  article-title: Causal interactions between fronto‐parietal central executive and default‐mode networks in humans
  publication-title: Proceedings of the National Academy of Sciences of the United States of America
– volume: 146
  start-page: 959
  year: 2017
  end-page: 970
  article-title: Multisite reliability of MR‐based functional connectivity
  publication-title: Neuroimage
– volume: 12
  start-page: 425
  issue: 2
  year: 2019
  end-page: 427
  article-title: Individualizing brainstimulation through concurrent TMS/fMRI
  publication-title: Brain Stimulation
– volume: 113
  start-page: 7900
  issue: 28
  year: 2016
  end-page: 7905
  article-title: Cluster failure: Why fMRI inferences for spatial extent have inflated false‐positive rates
  publication-title: Proceedings of the National Academy of Sciences of the United States of America
– volume: 104
  start-page: 1339
  issue: 3
  year: 2010
  end-page: 1346
  article-title: Reliability of long‐interval cortical inhibition in healthy human subjects: A TMS‐EEG study
  publication-title: Journal of Neurophysiology
– volume: 9
  issue: 4
  year: 2022
  article-title: TMS does not increase BOLD activity at the site of stimulation: A review of all concurrent TMS‐fMRI studies
  publication-title: eNeuro
– volume: 108
  start-page: 160
  year: 2018
  end-page: 172
  article-title: Spread of activity following TMS is related to intrinsic resting connectivity to the salience network: A concurrent TMS‐fMRI study
  publication-title: Cortex
– volume: 197
  start-page: 818
  year: 2019
  end-page: 826
  article-title: Ciftify: A framework for surface‐based analysis of legacy MR acquisitions
  publication-title: Neuroimage
– volume: 18
  start-page: 1664
  issue: 11
  year: 2015
  end-page: 1671
  article-title: Functional connectome fingerprinting: Identifying individuals using patterns of brain connectivity
  publication-title: Nature Neuroscience
– volume: 29
  start-page: 1211
  issue: 5
  year: 2009
  end-page: 1217
  article-title: Image artifacts in concurrent transcranial magnetic stimulation (TMS) and fMRI caused by leakage currents: Modeling and compensation
  publication-title: Journal of Magnetic Resonance Imaging
– volume: 79
  start-page: 86
  year: 2015
  end-page: 96
  article-title: TMS to object cortex affects both object and scene remote networks while TMS to scene cortex only affects scene networks
  publication-title: Neuropsychologia
– volume: 73
  start-page: 337
  issue: 4
  year: 2016
  end-page: 345
  article-title: Indicators for remission of suicidal ideation following magnetic seizure therapy in patients with treatment‐resistant depression
  publication-title: JAMA Psychiatry
– volume: 20
  start-page: 2702
  issue: 11
  year: 2010
  end-page: 2711
  article-title: Studying the role of human parietal cortex in visuospatial attention with concurrent TMS–fMRI
  publication-title: Cerebral Cortex
– volume: 203
  year: 2019
  article-title: A decade of test‐retest reliability of functional connectivity: A systematic review and meta‐analysis
  publication-title: Neuroimage
– volume: 28
  start-page: 13202
  issue: 49
  year: 2008
  end-page: 13208
  article-title: Interhemispheric effect of parietal TMS on somatosensory response confirmed directly with concurrent TMS–fMRI
  publication-title: The Journal of Neuroscience
– volume: 32
  start-page: 622
  year: 2021
  end-page: 626
  article-title: Functional MRI can be highly reliable, but it depends on what you measure: A commentary on Elliott et al. (2020)
  publication-title: Psychological Science
– volume: 16
  start-page: 1479
  issue: 15
  year: 2006
  end-page: 1488
  article-title: Concurrent TMS‐fMRI and psychophysics reveal frontal influences on human retinotopic visual cortex
  publication-title: Current Biology
– volume: 536
  start-page: 171
  issue: 7615
  year: 2016
  end-page: 178
  article-title: A multi‐modal parcellation of human cerebral cortex
  publication-title: Nature
– volume: 31
  start-page: 792
  issue: 7
  year: 2020
  end-page: 806
  article-title: What is the test‐retest reliability of common task‐functional MRI measures? New empirical evidence and a meta‐analysis
  publication-title: Psychological Science
– volume: 39
  start-page: 4580
  issue: 11
  year: 2018
  end-page: 4592
  article-title: A novel concurrent TMS‐fMRI method to reveal propagation patterns of prefrontal magnetic brain stimulation
  publication-title: Human Brain Mapping
– volume: 11
  start-page: 536
  issue: 3
  year: 2018
  end-page: 544
  article-title: Test‐retest reliability of transcranial magnetic stimulation EEG evoked potentials
  publication-title: Brain Stimulation
– volume: 30
  start-page: 11926
  issue: 36
  year: 2010
  end-page: 11937
  article-title: The role of contralesional dorsal premotor cortex after stroke as studied with concurrent TMS‐fMRI
  publication-title: The Journal of Neuroscience
– volume: 14
  start-page: 25
  issue: 1
  year: 1998
  end-page: 27
  article-title: Motor threshold in transcranial magnetic stimulation: A comparison of a neurophysiological method and a visualization of movement method
  publication-title: The Journal of ECT
– volume: 29
  start-page: 1000
  issue: 3
  year: 2006
  end-page: 1006
  article-title: Long‐term test‐retest reliability of functional MRI in a classification learning task
  publication-title: Neuroimage
– volume: 98
  start-page: 439
  issue: 2
  year: 2018
  end-page: 452.e5
  article-title: Functional brain networks are dominated by stable group and individual factors, not cognitive or daily variation
  publication-title: Neuron
– volume: 2
  start-page: 58
  issue: 2
  year: 2009
  end-page: 80
  article-title: Consensus paper: Combining transcranial stimulation with neuroimaging
  publication-title: Brain Stimulation
– volume: 11
  year: 2017
  article-title: Differing time of onset of concurrent TMS‐fMRI during associative memory encoding: A measure of dynamic connectivity
  publication-title: Frontiers in Human Neuroscience
– volume: 282
  start-page: 134
  year: 2018
  end-page: 142
  article-title: A longitudinal human phantom reliability study of multi‐center T1‐weighted, DTI, and resting state fMRI data
  publication-title: Psychiatry Research. Neuroimaging
– volume: 44
  start-page: 225
  issue: 2
  year: 2014
  end-page: 239
  article-title: Response, remission and drop‐out rates following high‐frequency repetitive transcranial magnetic stimulation (rTMS) for treating major depression: A systematic review and meta‐analysis of randomized, double‐blind and sham‐controlled trials
  publication-title: Psychological Medicine
– volume: 95
  start-page: 791
  issue: 4
  year: 2017
  end-page: 807.e7
  article-title: Precision functional mapping of individual human brains
  publication-title: Neuron
– volume: 7
  year: 2013
  article-title: The effect of theta‐burst TMS on cognitive control networks measured with resting state fMRI
  publication-title: Frontiers in Systems Neuroscience
– volume: 34
  start-page: 6849
  issue: 20
  year: 2014
  end-page: 6859
  article-title: Dose‐dependent effects of theta burst rTMS on cortical excitability and resting‐state connectivity of the human motor system
  publication-title: The Journal of Neuroscience
– volume: 362
  start-page: 209
  year: 2016
  end-page: 216
  article-title: Test‐retest reliability of single and paired pulse transcranial magnetic stimulation parameters in healthy subjects
  publication-title: Journal of the Neurological Sciences
– volume: 7
  issue: 4
  year: 2012
  article-title: An iterative jackknife approach for assessing reliability and power of fMRI group analyses
  publication-title: PLoS ONE
– ident: e_1_2_9_27_1
  doi: 10.1016/j.cortex.2018.07.010
– ident: e_1_2_9_39_1
  doi: 10.1097/00124509-199803000-00004
– ident: e_1_2_9_5_1
  doi: 10.1017/S0033291713000512
– ident: e_1_2_9_42_1
  doi: 10.1016/j.cub.2006.06.057
– ident: e_1_2_9_7_1
  doi: 10.1523/JNEUROSCI.5642‐09.2010
– ident: e_1_2_9_22_1
  doi: 10.1016/j.neuron.2018.03.035
– ident: e_1_2_9_6_1
  doi: 10.1093/cercor/bhm159
– ident: e_1_2_9_3_1
  doi: 10.1016/j.neuroimage.2005.08.010
– ident: e_1_2_9_41_1
  doi: 10.1016/j.neuropsychologia.2015.10.027
– ident: e_1_2_9_28_1
  doi: 10.1016/j.jns.2016.01.039
– ident: e_1_2_9_50_1
  doi: 10.1002/jmri.21749
– ident: e_1_2_9_19_1
  doi: 10.1038/nature18933
– ident: e_1_2_9_8_1
  doi: 10.1523/JNEUROSCI.3043‐08.2008
– ident: e_1_2_9_36_1
  doi: 10.1016/j.neuroimage.2019.116157
– ident: e_1_2_9_18_1
  doi: 10.1016/j.neuroimage.2019.03.053
– ident: e_1_2_9_21_1
  doi: 10.1016/j.neuron.2017.07.011
– ident: e_1_2_9_45_1
  doi: 10.1001/jamapsychiatry.2015.3097
– ident: e_1_2_9_16_1
  doi: 10.1073/pnas.1106439108
– ident: e_1_2_9_23_1
  doi: 10.3389/fnsys.2013.00124
– ident: e_1_2_9_10_1
  doi: 10.1371/journal.pcbi.1009279
– ident: e_1_2_9_26_1
  doi: 10.1016/j.pscychresns.2018.06.004
– ident: e_1_2_9_37_1
  doi: 10.1016/j.neuroimage.2016.10.020
– ident: e_1_2_9_49_1
  doi: 10.1002/hbm.24307
– ident: e_1_2_9_12_1
  doi: 10.1016/j.neuroimage.2019.04.078
– ident: e_1_2_9_47_1
  doi: 10.1016/j.brs.2018.12.381
– ident: e_1_2_9_40_1
  doi: 10.1523/ENEURO.0163‐22.2022
– ident: e_1_2_9_32_1
  doi: 10.1177/0956797621989730
– ident: e_1_2_9_34_1
  doi: 10.1016/s0006‐3223(01)01199‐4
– ident: e_1_2_9_13_1
  doi: 10.1073/pnas.1602413113
– ident: e_1_2_9_17_1
  doi: 10.1038/nn.4135
– start-page: 159
  volume-title: Springer proceedings in mathematics & statistics
  year: 2013
  ident: e_1_2_9_31_1
– ident: e_1_2_9_43_1
  doi: 10.1093/cercor/bhm013
– ident: e_1_2_9_35_1
  doi: 10.1523/JNEUROSCI.4993‐13.2014
– ident: e_1_2_9_51_1
  doi: 10.1371/journal.pone.0035578
– ident: e_1_2_9_9_1
  doi: 10.1093/cercor/bhq015
– ident: e_1_2_9_24_1
  doi: 10.3389/fnhum.2017.00404
– ident: e_1_2_9_48_1
  doi: 10.1101/136259
– ident: e_1_2_9_14_1
  doi: 10.1177/0956797620916786
– ident: e_1_2_9_11_1
  doi: 10.1073/pnas.1311772110
– ident: e_1_2_9_33_1
  doi: 10.1016/j.neuroimage.2020.117077
– ident: e_1_2_9_20_1
  doi: 10.1002/1522‐2594(200007)44:1<162::AID‐MRM23>3.0.CO;2‐E
– ident: e_1_2_9_46_1
  doi: 10.1016/j.neuroimage.2017.09.022
– ident: e_1_2_9_29_1
  doi: 10.1016/S0006‐3223(01)01153‐2
– ident: e_1_2_9_30_1
  doi: 10.1016/j.brs.2017.12.010
– ident: e_1_2_9_25_1
  doi: 10.1016/j.neuroimage.2021.117823
– ident: e_1_2_9_38_1
  doi: 10.1093/cercor/bhx230
– ident: e_1_2_9_15_1
  doi: 10.1152/jn.00279.2010
– ident: e_1_2_9_44_1
  doi: 10.1016/j.brs.2008.11.002
– ident: e_1_2_9_4_1
  doi: 10.1038/tp.2017.204
– ident: e_1_2_9_2_1
  doi: 10.1126/science.1146426
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Snippet Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS‐fMRI) allows real‐time causative probing of brain connectivity. However,...
Concurrent transcranial magnetic stimulation with functional MRI (concurrent TMS-fMRI) allows real-time causative probing of brain connectivity. However,...
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SubjectTerms Brain - diagnostic imaging
Brain - physiology
Brain mapping
Brain Mapping - methods
concurrent TMS‐fMRI
Evoked Potentials, Motor - physiology
Functional magnetic resonance imaging
functional MRI
Humans
Magnetic fields
Magnetic Resonance Imaging - methods
Neural networks
reliability
Reproducibility of Results
Transcranial magnetic stimulation
Transcranial Magnetic Stimulation - methods
Title Within‐subject reliability of concurrent TMS‐fMRI during a single session
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fpsyp.14252
https://www.ncbi.nlm.nih.gov/pubmed/36694109
https://www.proquest.com/docview/2823465738
https://www.proquest.com/docview/2769592548
Volume 60
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