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Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion
Open accessAbstract
Here, we demonstrate that subject motion produces substantial changes in the timecourses of resting state functional connectivity MRI (rs-fcMRI) data despite compensatory spatial registration and regression of motion estimates from the data. These changes cause systematic but spurious correlation structures throughout the brain. Specifically, many long-distance correlations are decreased by subject motion, whereas many short-distance correlations are increased. These changes in rs-fcMRI correlations do not arise from, nor are they adequately countered by, some common functional connectivity processing steps. Two indices of data quality are proposed, and a simple method to reduce motion-related effects in rs-fcMRI analyses is demonstrated that should be flexibly implementable across a variety of software platforms. We demonstrate how application of this technique impacts our own data, modifying previous conclusions about brain development. These results suggest the need for greater care in dealing with subject motion, and the need to critically revisit previous rs-fcMRI work that may not have adequately controlled for effects of transient subject movements.
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“Importantly, no group differences were observed in frame-wise displacement, a metric of relative head displacement between volumes (Power et al. 2012), suggesting the groups were well-matched for head motion (Table 2).”
From A novel resting-state functional magnetic resonance imaging signature of resilience to recurrent depression (2017) · cites this paper as Power et al. 2012
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“To avoid spurious correlation due to motion55,56, we choose a priori a more conservative criterion by excluding all participants with more than 1 mm FD.”
From The relationship between resting-state functional connectivity, antidepressant discontinuation and depression relapse (2020) · cites this paper as [55]
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In the citing paper
“Head motion during fMRI acquisitions was evaluated using the framewise displacement, which was calculated as the L1-norm of the realignment-derived parameters after converting angles to linear displacements (Power et al., 2012).”
From Perception is associated with the brain’s metabolic response to sensory stimulation (2022) · cites this paper as Power et al., 2012
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“Finally there were no significant effects of percent frames scrubbed using a threshold of 0.5 mm (Power et al. 2012) on group, condition, or interactions of group and condition (group:”
From Brain Activity and Functional Connectivity Associated with Hypnosis (2016) · cites this paper as Power et al. 2012
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In the citing paper
“Additionally we examined mean framewise displacement (Power et al. 2012) and found no main effect of group (F(1,40) = 0.01, P = 0.92), condition (F(3,40) = 1.01,P = 0.39), or group by condition interaction (F(3,40) = 1.49,P = 0.22).”
From Brain Activity and Functional Connectivity Associated with Hypnosis (2016) · cites this paper as Power et al. 2012
In the citing paper
“When processing techniques intended to remove motion artifact are applied, developmental effects of this type – both in terms of overall local versus distributed coupling and in terms of changing modular assignments – are substantially attenuated, though still present to a limited extent (Fair et al., 2012b; Power et al., 2012; Satterthwaite et al., 2012).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Power et al., 2012
In the citing paper
“Indeed, there are now at least 3 reports that suggest the network structure in children as defined by community detection (see Figure 3) are largely similar to the adult (Fair et al., 2012b; Marek et al., 2015; Power et al., 2012).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Power et al., 2012
In the citing paper
“it has been revealed that motion increases non-specific local coupling and decreases long-range coupling in ways that are similar to differences found between children and adults (Fair et al., 2012b; Power et al., 2012; Satterthwaite et al., 2012; Yan et al., 2013).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Power et al., 2012
In the citing paper
“head motion has become a substantial concern since 2012 when a trio of papers pointed to systematic motion-related artifacts in rs-fcMRI (Power et al., 2012; Satterthwaite et al., 2012; Van Dijk et al., 2012).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Power et al., 2012
In the citing paper
“head motion increases functional correlations between spatially proximal nodes and decreases correlations between distant nodes (Power et al., 2012).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Power et al., 2012
In the citing paper
“researchers recently discovered that some functional connectivity analyses interpreted as demonstrating developmental increases in long-range connections during rest (i.e., independent from any task) were spurious effects of greater motion in younger participants [62,63], which were eliminated with appropriate controls for motion-induced artifacts.”
From Arrested development? Reconsidering dual-systems models of brain function in adolescence and disorders (2012) · cites this paper as [62]
In the citing paper
“Recent work has suggested that small movements may have a greater impact on resting-state analyses than previously considered (Power et al, 2012).”
From Resting-state cortico-thalamic-striatal connectivity predicts response to dorsomedial prefrontal rTMS in major depressive disorder (2014) · cites this paper as Power et al, 2012
In the citing paper
“Strict motion correction procedures were applied to resting state functional maps, due to the sensitivity of RSFC data to head motion (Power et al., 2012, Satterthwaite et al., 2012, Van Dijk et al., 2012).”
From Developmental sex differences in resting state functional connectivity of amygdala sub-regions (2015) · cites this paper as Power et al., 2012
In the citing paper
“Head motion, even of submillimeter magnitude, has been identified as a nonphysiological source of spurious variance in resting-state fMRI data (Power et al. 2012; Van Dijk et al. 2012; Satterthwaite et al. 2013).”
From Joint attention and brain functional connectivity in infants and toddlers (2017) · cites this paper as Power et al. 2012
In the citing paper
“Diagnostic groups did not differ in age, sex, handedness, FSIQ, or head motion (mean framewise displacement [FD (Power et al., 2012)], translational and rotational motion, Table 2).”
From Investigating functional brain network integrity using a traditional and novel categorical scheme for neurodevelopmental disorders (2019) · cites this paper as Power et al., 2012
In the citing paper
“Given the known problems of motion for connectivity analyses (90), we used ArtRepair software to correct for excessive movement (91).”
From Adolescent impatience decreases with increased frontostriatal connectivity (2015) · cites this paper as [90]
In the citing paper
“we elected to exclude participants where for either visit, the participant had one or more of the following: movement in any dimension ≥4 mm, and/or ≥25% of volumes identified as outliers according to the DVARS metric72 such that only participants who displayed acceptable amounts of motion under both the OT and PLC visits were included in analysis.”
From Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism (2016) · cites this paper as [72]
In the citing paper
“Following standard Statistical Parametric Mapping (SPM12; https://www.fil.ion.ucl.ac.uk/spm12 ) pre-processing steps, additional motion correction was applied in the form of censoring, i.e. identifying outliers based on framewise displacement and regressing them from the fMRI timeseries ( Power et al., 2012 , Power et al., 2014 ) (see Supplementary Methods), to compensate for using fairly lenient”
From Self-blame-selective hyper-connectivity between anterior temporal and subgenual cortices predicts prognosis in major depressive disorder (2023) · cites this paper as Power et al., 2012
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Cites
Fortunato, S. (2010) · Physics Reports · doi:10.1016/j.physrep.2009.11.002 · Cited by 11,293
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Self-citationNewman, M. (2010) · doi:10.1093/acprof:oso/9780199206650.001.0001 · Cited by 6,595
Maps of random walks on complex networks reveal community structure
Rosvall, M., & Bergstrom, C. T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706851105 · Cited by 4,583
Functional Network Organization of the Human Brain
Power, J. D., Cohen, A. L., Nelson, S. M., Wig, G. S., Barnes, K. A., Church, J. A., Vogel, A. C., Laumann, T. O., Miezin, F. M., Schlaggar, B. L., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.006 · Cited by 4,124
Self-citationMovement‐Related effects in fMRI time‐series
Friston, K. J., Williams, S., Howard, R., Frackowiak, R. S. J., & Turner, R. (1996) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910350312 · Cited by 3,774
Esmark, K., Orning, H. J., & Hermanson, L. (2011) · Choice Reviews Online · doi:10.5860/choice.48-3328 · Cited by 2,950
Probabilistic Independent Component Analysis for Functional Magnetic Resonance Imaging
Beckmann, C. F., & Smith, S. M. (2004) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2003.822821 · Cited by 2,707
The influence of head motion on intrinsic functional connectivity MRI
Van Dijk, K. R. A., Sabuncu, M. R., & Buckner, R. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.044 · Cited by 2,344
Prediction of individual brain maturity using fMRI
Dosenbach, N. U. F., Nardos, B., Cohen, A. L., Fair, D. A., Power, J. D., Church, J. A., Nelson, S. M., Wig, G. S., Vogel, A. C., Lessov-Schlaggar, C. N., et al. (2010) · Science · doi:10.1126/science.1194144 · Cited by 2,183
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Items 201–300 of 372
van Duijvenvoorde, A. C. K., Westhoff, B., de Vos, F., Wierenga, L. M., & Crone, E. A. (2019) · Human Brain Mapping · doi:10.1002/hbm.24630 · Cited by 115
Brain Network Modularity Predicts Exercise-Related Executive Function Gains in Older Adults
Baniqued, P. L., Gallen, C. L., Voss, M. W., Burzynska, A. Z., Wong, C. N., Cooke, G. E., Duffy, K., Fanning, J., Ehlers, D. K., Salerno, E. A., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00426 · Cited by 112
Jacobs, R. H., Jenkins, L. M., Gabriel, L. B., Barba, A., Ryan, K. A., Weisenbach, S. L., Verges, A., Baker, A. M., Peters, A. T., Crane, N. A., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104366 · Cited by 109
Functional connectivity in the developing brain: a longitudinal study from 4 to 9months of age
Damaraju, E., Caprihan, A., Lowe, J. R., Allen, E. A., Calhoun, V. D., & Phillips, J. P. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.038 · Cited by 103
“5 in Power et al., 2012).”
BackgroundSeminowicz, D. A., Burrowes, S. A. B., Kearson, A., Zhang, J., Krimmel, S. R., Samawi, L., Furman, A. J., Keaser, M. L., Gould, N. F., Magyari, T., et al. (2020) · Pain · doi:10.1097/j.pain.0000000000001860 · Cited by 110
“Age: median years (range) 36 (18-65) 36 (21-63) 36 (18-65) NS”
Mills, K. L., Bathula, D., Dias, T. G. C., Iyer, S. P., Fenesy, M. C., Musser, E. D., Stevens, C. A., Thurlow, B. L., Carpenter, S. D., Nagel, B. J., et al. (2012) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2012.00002 · Cited by 108
Vasa, R. A., Mostofsky, S. H., & Ewen, J. B. (2016) · Biological Psychiatry: Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.02.003 · Cited by 97
Falahpour, M., Thompson, W. K., Abbott, A. E., Jahedi, A., Mulvey, M. E., Datko, M., Liu, T. T., & Müller, R.-A. (2016) · Brain Connectivity · doi:10.1089/brain.2015.0389 · Cited by 106
Francx, W., Oldehinkel, M., Oosterlaan, J., Heslenfeld, D., Hartman, C. A., Hoekstra, P. J., Franke, B., Beckmann, C. F., Buitelaar, J. K., & Mennes, M. (2015) · Cortex · doi:10.1016/j.cortex.2015.08.012 · Cited by 102
Developmental sex differences in resting state functional connectivity of amygdala sub-regions
Alarcón, G., Cservenka, A., Rudolph, M. D., Fair, D. A., & Nagel, B. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.013 · Cited by 105
MR connectomics: a conceptual framework for studying the developing brain
Hagmann, P., Grant, P. E., & Fair, D. A. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00043 · Cited by 96
Customized head molds reduce motion during resting state fMRI scans
Power, J. D., Silver, B. M., Silverman, M. R., Ajodan, E. L., Bos, D. J., & Jones, R. M. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.016 · Cited by 88
Self-citationLin, H.-Y., Tseng, W.-Y. I., Lai, M.-C., Matsuo, K., & Gau, S. S.-F. (2015) · Journal of the International Neuropsychological Society · doi:10.1017/s135561771500020x · Cited by 102
Calzà, J., Gürsel, D. A., Schmitz-Koep, B., Bremer, B., Reinholz, L., Berberich, G., & Koch, K. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00319 · Cited by 99
“In addition, excessive head motion was established with framewise displacement (FD), calculated as the sum of the absolute values of the derivatives of the six motion parameters derived from SPM12 (22).”
MethodPantelis, P. C., Byrge, L., Tyszka, J. M., Adolphs, R., & Kennedy, D. P. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv021 · Cited by 97
Koch, K., Myers, N. E., Göttler, J., Pasquini, L., Grimmer, T., Förster, S., Manoliu, A., Neitzel, J., Kurz, A., Förstl, H., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu151 · Cited by 97
Philippi, C. L., Motzkin, J. C., Pujara, M. S., & Koenigs, M. (2015) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2015.10.005 · Cited by 93
Brain differences between persistent and remitted attention deficit hyperactivity disorder
Mattfeld, A. T., Gabrieli, J. D. E., Biederman, J., Spencer, T., Brown, A., Kotte, A., Kagan, E., & Whitfield-Gabrieli, S. (2014) · Brain · doi:10.1093/brain/awu137 · Cited by 96
Igelström, K. M., Webb, T. W., & Graziano, M. S. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw079 · Cited by 93
Johnson, S. L., Elliott, M. V., & Carver, C. S. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.08.018 · Cited by 90
Suzuki, H., Luby, J. L., Botteron, K. N., Dietrich, R., McAvoy, M. P., & Barch, D. M. (2014) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2014.04.013 · Cited by 92
Cortical excitability controls the strength of mental imagery
Keogh, R., Bergmann, J., & Pearson, J. (2020) · eLife · doi:10.7554/elife.50232 · Cited by 94
Network analysis reveals disrupted functional brain circuitry in drug-naive social anxiety disorder
Yang, X., Liu, J., Meng, Y., Xia, M., Cui, Z., Wu, X., Hu, X., Zhang, W., Gong, G., Gong, Q., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.011 · Cited by 91
Learning to read alters cortico-subcortical cross-talk in the visual system of illiterates
Skeide, M. A., Kumar, U., Mishra, R. K., Tripathi, V. N., Guleria, A., Singh, J. P., Eisner, F., & Huettig, F. (2017) · Science Advances · doi:10.1126/sciadv.1602612 · Cited by 92
Strong genetic overlap between executive functions and intelligence.
Engelhardt, L. E., Mann, F. D., Briley, D. A., Church, J. A., Harden, K. P., & Tucker-Drob, E. M. (2016) · Journal of Experimental Psychology: General · doi:10.1037/xge0000195 · Cited by 91
The neural architecture of executive functions is established by middle childhood
Engelhardt, L. E., Harden, K. P., Tucker-Drob, E. M., & Church, J. A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.024 · Cited by 87
Posner, J., Song, I., Lee, S., Rodriguez, C. I., Moore, H., Marsh, R., & Blair Simpson, H. (2017) · Human Brain Mapping · doi:10.1002/hbm.23408 · Cited by 89
Dhamala, E., Yeo, B. T. T., & Holmes, A. J. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.09.024 · Cited by 91
In vivo mapping of brainstem nuclei functional connectivity disruption in Alzheimer’s disease
Serra, L., D'Amelio, M., Di Domenico, C., Dipasquale, O., Marra, C., Mercuri, N. B., Caltagirone, C., Cercignani, M., & Bozzali, M. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.08.012 · Cited by 91
Prenatal Drug Exposure Affects Neonatal Brain Functional Connectivity
Salzwedel, A. P., Grewen, K. M., Vachet, C., Gerig, G., Lin, W., & Gao, W. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4333-14.2015 · Cited by 93
Moody, T. D., Morfini, F., Cheng, G., Sheen, C., Tadayonnejad, R., Reggente, N., O'Neill, J., & Feusner, J. D. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.192 · Cited by 86
Sutherland, M. T., Carroll, A. J., Salmeron, B. J., Ross, T. J., & Stein, E. A. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3018-8 · Cited by 89
Age effects on the default mode and control networks in typically developing children
Sato, J. R., Salum, G. A., Gadelha, A., Picon, F. A., Pan, P. M., Vieira, G., Zugman, A., Hoexter, M. Q., Anés, M., Moura, L. M., et al. (2014) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2014.07.004 · Cited by 85
Head motion and correction methods in resting-state functional MRI
GOTO, M., ABE, O., MIYATI, T., YAMASUE, H., GOMI, T., & TAKEDA, T. (2016) · Magnetic Resonance in Medical Sciences · doi:10.2463/mrms.rev.2015-0060 · Cited by 82
Bauer, C. C. C., Caballero, C., Scherer, E., West, M. R., Mrazek, M. D., Phillips, D. T., Whitfield-Gabrieli, S., & Gabrieli, J. D. E. (2019) · Behavioral Neuroscience · doi:10.1037/bne0000337 · Cited by 85
Liu, P., Jia, X., Chen, Y., Yu, Y., Zhang, K., Lin, Y., Wang, B., & Peng, G. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13451 · Cited by 87
Functional properties of resting state networks in healthy full-term newborns
De Asis-Cruz, J., Bouyssi-Kobar, M., Evangelou, I., Vezina, G., & Limperopoulos, C. (2015) · Scientific Reports · doi:10.1038/srep17755 · Cited by 85
Cservenka, A., Casimo, K., Fair, D. A., & Nagel, B. J. (2014) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2013.12.004 · Cited by 86
Early life stress is associated with default system integrity and emotionality during infancy
Graham, A. M., Pfeifer, J. H., Fisher, P. A., Carpenter, S., & Fair, D. A. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12409 · Cited by 84
Oxytocin’s effect on resting-state functional connectivity varies by age and sex
Ebner, N. C., Chen, H., Porges, E., Lin, T., Fischer, H., Feifel, D., & Cohen, R. A. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.03.013 · Cited by 84
The Fine-Scale Functional Correlation of Striate Cortex in Sighted and Blind People
Butt, O. H., Benson, N. C., Datta, R., & Aguirre, G. K. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0363-13.2013 · Cited by 84
Engen, H. G., Bernhardt, B. C., Skottnik, L., Ricard, M., & Singer, T. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.08.024 · Cited by 83
Sex differences in the functional connectivity of the amygdalae in association with cortisol
Kogler, L., Müller, V. I., Seidel, E.-M., Boubela, R., Kalcher, K., Moser, E., Habel, U., Gur, R. C., Eickhoff, S. B., & Derntl, B. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.064 · Cited by 78
Kernbach, J. M., Satterthwaite, T. D., Bassett, D. S., Smallwood, J., Margulies, D., Krall, S., Shaw, P., Varoquaux, G., Thirion, B., Konrad, K., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0179-6 · Cited by 81
Starck, T., Nikkinen, J., Rahko, J., Remes, J., Hurtig, T., Haapsamo, H., Jussila, K., Kuusikko-Gauffin, S., Mattila, M.-L., Jansson-Verkasalo, E., et al. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00802 · Cited by 75
Fani, N., King, T. Z., Shin, J., Srivastava, A., Brewster, R. C., Jovanovic, T., Bradley, B., & Ressler, K. J. (2016) · Depression and Anxiety · doi:10.1002/da.22483 · Cited by 80
Adolescent brain development and contextual influences: a decade in review
Galván, A. (2021) · Journal of Research on Adolescence · doi:10.1111/jora.12687 · Cited by 77
Solomon, M., Yoon, J. H., Ragland, J. D., Niendam, T. A., Lesh, T. A., Fairbrother, W., & Carter, C. S. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.08.036 · Cited by 78
Altered resting-state cerebellar-cerebral functional connectivity in obsessive-compulsive disorder
Xu, T., Zhao, Q., Wang, P., Fan, Q., Chen, J., Zhang, H., Yang, Z., Stein, D. J., & Wang, Z. (2019) · Psychological Medicine · doi:10.1017/s0033291718001915 · Cited by 79
Wirsich, J., Perry, A., Ridley, B., Proix, T., Golos, M., Bénar, C., Ranjeva, J.-P., Bartolomei, F., Breakspear, M., Jirsa, V., et al. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.05.010 · Cited by 77
Roland, L. T., Lenze, E. J., Hardin, F. M., Kallogjeri, D., Nicklaus, J., Wineland, A. M., Fendell, G., Peelle, J. E., & Piccirillo, J. F. (2015) · Otolaryngology–Head and Neck Surgery · doi:10.1177/0194599815571556 · Cited by 77
“38 rotation, or a variance of 5 standard deviations from the mean scaled variance, which were modeled out in time-series analysis to limit the potential impact of participant motion on connectivity measures.(22) EPI images for each participant were coregistered to that participant’s structural image and normalized to…”
MethodHow to remove or control confounds in predictive models, with applications to brain biomarkers
Chyzhyk, D., Varoquaux, G., Milham, M., & Thirion, B. (2022) · GigaScience · doi:10.1093/gigascience/giac014 · Cited by 65
Wang, X., Peelen, M. V., Han, Z., He, C., Caramazza, A., & Bi, Y. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3914-14.2015 · Cited by 68
Göttlich, M., Krämer, U. M., Kordon, A., Hohagen, F., & Zurowski, B. (2015) · Biological Psychology · doi:10.1016/j.biopsycho.2015.09.004 · Cited by 73
Schreiner, M. W., Klimes‐Dougan, B., & Cullen, K. R. (2019) · Suicide and Life-Threatening Behavior · doi:10.1111/sltb.12471 · Cited by 69
Wang, Z., Xia, M., Dai, Z., Liang, X., Song, H., He, Y., & Li, K. (2015) · Brain Structure and Function · doi:10.1007/s00429-013-0681-9 · Cited by 73
Bhaumik, R., Jenkins, L. M., Gowins, J. R., Jacobs, R. H., Barba, A., Bhaumik, D. K., & Langenecker, S. A. (2017) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.02.018 · Cited by 72
Rosch, K. S., Mostofsky, S. H., & Nebel, M. B. (2018) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-018-9254-9 · Cited by 69
Andreescu, C., Sheu, L. K., Tudorascu, D., Walker, S., & Aizenstein, H. (2014) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4051 · Cited by 70
Cai, X., Xie, D., Madsen, K. H., Wang, Y., Bögemann, S. A., Cheung, E. F. C., Møller, A., & Chan, R. C. K. (2020) · Human Brain Mapping · doi:10.1002/hbm.24797 · Cited by 62
Default mode network deactivation during emotion processing predicts early antidepressant response
Spies, M., Kraus, C., Geissberger, N., Auer, B., Klöbl, M., Tik, M., Stürkat, I.-L., Hahn, A., Woletz, M., Pfabigan, D. M., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.265 · Cited by 68
Chiesa, P. A., Cavedo, E., Vergallo, A., Lista, S., Potier, M., Habert, M., Dubois, B., Thiebaut de Schotten, M., Hampel, H., and the INSIGHT‐preAD study group, et al. (2019) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2019.03.006 · Cited by 66
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Geisler, D., Borchardt, V., Lord, A. R., Boehm, I., Ritschel, F., Zwipp, J., Clas, S., King, J. A., Wolff-Stephan, S., Roessner, V., et al. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.140310 · Cited by 62
Long-term alterations in brain and behavior after postnatal Zika virus infection in infant macaques
Raper, J., Kovacs-Balint, Z., Mavigner, M., Gumber, S., Burke, M. W., Habib, J., Mattingly, C., Fair, D., Earl, E., Feczko, E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16320-7 · Cited by 67
Humphreys, K. L., Camacho, M. C., Roth, M. C., & Estes, E. C. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100877 · Cited by 67
Kumral, D., Schaare, H. L., Beyer, F., Reinelt, J., Uhlig, M., Liem, F., Lampe, L., Babayan, A., Reiter, A., Erbey, M., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.027 · Cited by 64
Sripada, R. K., Welsh, R. C., Marx, C. E., & Liberzon, I. (2014) · Human Brain Mapping · doi:10.1002/hbm.22399 · Cited by 66
Tian, L., Meng, C., Jiang, Y., Tang, Q., Wang, S., Xie, X., Fu, X., Jin, C., Zhang, F., & Wang, J. (2016) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2015.12.003 · Cited by 63
Lawrence, K. E., Hernandez, L. M., Bookheimer, S. Y., & Dapretto, M. (2019) · Autism Research · doi:10.1002/aur.1971 · Cited by 61
Bohland, J. W., Saperstein, S., Pereira, F., Rapin, J., & Grady, L. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00078 · Cited by 64
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Gaffrey, M. S., Barch, D. M., Singer, J., Shenoy, R., & Luby, J. L. (2013) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2013.04.009 · Cited by 62
Functional brain connectivity in ex utero premature infants compared to in utero fetuses
De Asis-Cruz, J., Kapse, K., Basu, S. K., Said, M., Scheinost, D., Murnick, J., Chang, T., du Plessis, A., & Limperopoulos, C. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117043 · Cited by 63
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Chen, X., Fan, X., Hu, Y., Zuo, C., Whitfield-Gabrieli, S., Holt, D., Gong, Q., Yang, Y., Pizzagalli, D. A., Du, F., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy059 · Cited by 62
Neural and behavioral correlates of negative self‐focused thought associated with depression
Philippi, C. L., Cornejo, M. D., Frost, C. P., Walsh, E. C., Hoks, R. M., Birn, R., & Abercrombie, H. C. (2018) · Human Brain Mapping · doi:10.1002/hbm.24003 · Cited by 60
Kantrowitz, J. T., Hoptman, M. J., Leitman, D. I., Silipo, G., & Javitt, D. C. (2014) · Psychological Medicine · doi:10.1017/s0033291713000834 · Cited by 56
Pruett, J. R., Kandala, S., Hoertel, S., Snyder, A. Z., Elison, J. T., Nishino, T., Feczko, E., Dosenbach, N. U. F., Nardos, B., Power, J. D., et al. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.01.003 · Cited by 57
Self-citationZhang, H., Wang, B., Li, K., Wang, X., Li, X., Zhu, J., Zhao, Q., Yang, Y., Lv, L., Zhang, M., et al. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00522 · Cited by 55
Balsters, J. H., Mantini, D., Apps, M. A. J., Eickhoff, S. B., & Wenderoth, N. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.03.016 · Cited by 50
Mooneyham, B. W., Mrazek, M. D., Mrazek, A. J., & Schooler, J. W. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13044 · Cited by 56
Zheng, L., Gao, Z., McAvan, A. S., Isham, E. A., & Ekstrom, A. D. (2021) · Nature Communications · doi:10.1038/s41467-021-26560-w · Cited by 54
Sato, J. R., Salum, G. A., Gadelha, A., Vieira, G., Zugman, A., Picon, F. A., Pan, P. M., Hoexter, M. Q., Anés, M., Moura, L. M., et al. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.063 · Cited by 54
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Hernandez, L. M., Lawrence, K. E., Padgaonkar, N. T., Inada, M., Hoekstra, J. N., Lowe, J. K., Eilbott, J., Jack, A., Aylward, E., Gaab, N., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0750-9 · Cited by 54
Chien, H., Lin, H., Lai, M., Gau, S. S., & Tseng, W. I. (2015) · Autism Research · doi:10.1002/aur.1457 · Cited by 54
Yamashita, M., Kawato, M., & Imamizu, H. (2015) · Scientific Reports · doi:10.1038/srep07622 · Cited by 53
Fusing Mobile Phone Sensing and Brain Imaging to Assess Depression in College Students
Huckins, J. F., daSilva, A. W., Wang, R., Wang, W., Hedlund, E. L., Murphy, E. I., Lopez, R. B., Rogers, C., Holtzheimer, P. E., Kelley, W. M., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00248 · Cited by 51
Li, P., Yang, X., Greenshaw, A. J., Li, S., Luo, J., Han, H., Liu, J., Zhong, Z., Guo, Z., Xiong, H., et al. (2018) · Brain and Behavior · doi:10.1002/brb3.963 · Cited by 52
Functional connectivity and cannabis use in high-risk adolescents
Houck, J. M., Bryan, A. D., & Feldstein Ewing, S. W. (2013) · The American Journal of Drug and Alcohol Abuse · doi:10.3109/00952990.2013.837914 · Cited by 50
Puberty and functional brain development in humans: convergence in findings?
Dai, J., & Scherf, K. S. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.100690 · Cited by 51
Functional disruption of cerebello-thalamo-cortical networks in obsessive-compulsive disorder
Sha, Z., Edmiston, E. K., Versace, A., Fournier, J. C., Graur, S., Greenberg, T., Lima Santos, J. P., Chase, H. W., Stiffler, R. S., Bonar, L., et al. (2020) · Biological Psychiatry: Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.12.002 · Cited by 48
Rebollo, I., & Tallon-Baudry, C. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.1285-21.2021 · Cited by 46
Quattrini, G., Pini, L., Pievani, M., Magni, L. R., Lanfredi, M., Ferrari, C., Boccardi, M., Bignotti, S., Magnaldi, S., Cobelli, M., et al. (2019) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2018.12.010 · Cited by 48
Yamada, T., Itahashi, T., Nakamura, M., Watanabe, H., Kuroda, M., Ohta, H., Kanai, C., Kato, N., & Hashimoto, R.-I. (2016) · Molecular Autism · doi:10.1186/s13229-016-0106-8 · Cited by 50
Bernstein, G. A., Mueller, B. A., Schreiner, M. W., Campbell, S. M., Regan, E. K., Nelson, P. M., Houri, A. K., Lee, S. S., Zagoloff, A. D., Lim, K. O., et al. (2016) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2015.11.002 · Cited by 49
“5 mm) but because the noise properties of our data were different, we excluded volumes with DVARS48 rather than DVARS45 used by Power et al. (2012).”
MethodInfluentialYin, D., Liu, W., Zeljic, K., Wang, Z., Lv, Q., Fan, M., Cheng, W., & Wang, Z. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1476-16.2016 · Cited by 43
Chen, Y., Juhás, M., Greenshaw, A. J., Hu, Q., Meng, X., Cui, H., Ding, Y., Kang, L., Zhang, Y., Wang, Y., et al. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.04.030 · Cited by 47
Adolescent risk-taking and resting state functional connectivity
DeWitt, S. J., Aslan, S., & Filbey, F. M. (2014) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2014.03.009 · Cited by 45
Meyer, B., Mann, C., Götz, M., Gerlicher, A., Saase, V., Yuen, K. S. L., Aedo-Jury, F., Gonzalez-Escamilla, G., Stroh, A., & Kalisch, R. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.3128-18.2019 · Cited by 43
Amorim, L., Magalhães, R., Coelho, A., Moreira, P. S., Portugal-Nunes, C., Castanho, T. C., Marques, P., Sousa, N., & Santos, N. C. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00375 · Cited by 47
Distinct functional connectivities predict clinical response with emotion regulation therapy
Fresco, D. M., Roy, A. K., Adelsberg, S., Seeley, S., García-Lesy, E., Liston, C., & Mennin, D. S. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00086 · Cited by 43
“As micromovements have been shown to potentially introduce artifactual correlations, mean framewise displacement (FD) was computed, per recently described methods (Power et al., 2012; Van Dijk et al., 2012).”
MethodFeusner, J. D., Moody, T., Lai, T. M., Sheen, C., Khalsa, S., Brown, J., Levitt, J., Alger, J., & O’Neill, J. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00074 · Cited by 46
Metadata
- Authors
- Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Power, Jonathan D.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2012-02
- Volume
- 59
- Issue
- 3
- Pages
- 2142-2154
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC3254728
- OpenAlex
- W1990134753
- Cited by
- 7,429
- References
- 42
- Citations by year
- 2026: 404 · 2025: 506 · 2024: 475 · 2023: 525 · 2022: 604 · 2021: 671 · 2020: 696 · 2019: 647 · 2018: 604 · 2017: 587 · 2016: 504 · 2015: 439 · 2014: 357 · 2013: 294 · 2012: 104
- FWCI
- 123.02
- Type
- journal article
- Language
- en
- Update notices
- erratum (2012-11-01)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5p60dk020579-35, 5u54mh091657-05)
- National Institute of Mental Health (P50MH071616, U54-MH091657, P50MH71616)
- National Institute on Deafness and Other Communication Disorders (K23DC006638)
- National Institute of Diabetes and Digestive and Kidney Diseases (P60 DK020579-31)
- National Institute of Neurological Disorders and Stroke (R01NS32979, R01NS032979, R21NS061144)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD057076)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- subject motion, resting-state functional connectivity, spurious correlations, motion correction, spatial registration, brain development
- MeSH terms
- Algorithms, Brain, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Motion, Oxygen, Software, Cohort Studies, Artifacts, Head Movements
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