A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches
Open accessAbstract
Functional MRI (fMRI) allows one to study task-related regional responses and task-dependent connectivity analysis using psychophysiological interaction (PPI) methods. The latter affords the additional opportunity to understand how brain regions interact in a task-dependent manner. The current implementation of PPI in Statistical Parametric Mapping (SPM8) is configured primarily to assess connectivity differences between two task conditions, when in practice fMRI tasks frequently employ more than two conditions. Here we evaluate how a generalized form of context-dependent PPI (gPPI; http://www.nitrc.org/projects/gppi), which is configured to automatically accommodate more than two task conditions in the same PPI model by spanning the entire experimental space, compares to the standard implementation in SPM8. These comparisons are made using both simulations and an empirical dataset. In the simulated dataset, we compare the interaction beta estimates to their expected values and model fit using the Akaike information criterion (AIC). We found that interaction beta estimates in gPPI were robust to different simulated data models, were not different from the expected beta value, and had better model fits than when using standard PPI (sPPI) methods. In the empirical dataset, we compare the model fit of the gPPI approach to sPPI. We found that the gPPI approach improved model fit compared to sPPI. There were several regions that became non-significant with gPPI. These regions all showed significantly better model fits with gPPI. Also, there were several regions where task-dependent connectivity was only detected using gPPI methods, also with improved model fit. Regions that were detected with all methods had more similar model fits. These results suggest that gPPI may have greater sensitivity and specificity than standard implementation in SPM. This notion is tempered slightly as there is no gold standard; however, data simulations with a known outcome support our conclusions about gPPI. In sum, the generalized form of context-dependent PPI approach has increased flexibility of statistical modeling, and potentially improves model fit, specificity to true negative findings, and sensitivity to true positive findings.
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Amygdala dysfunction underlies psychopathology.
“with amygdala dysfunction underlying psychopathology;59”
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The Introduction discusses psychophysiological interaction methods, and the Empirical Data section describes a recognition-memory study in healthy participants; neither addresses amygdala dysfunction as an underlying cause of psychopathology. Searches for “amygdala dysfunction underlying psychopathology” and “amygdala psychopathology psychiatric disorders” found no relevant passage in our copy. No page numbers were provided for these passages. (LLM, conf=0.76)
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A new look at the statistical model identification
Akaike, H. (1974) · IEEE Transactions on Automatic Control · doi:10.1109/tac.1974.1100705 · Cited by 51,879 · see citing works
Model selection and multimodel inference: a practical information-theoretic approach.
Guthery, F. S., Burnham, K. P., & Anderson, D. R. (2003) · The Journal of Wildlife Management · doi:10.2307/3802723 · Cited by 41,495 · see citing works
ANew Look at the Statistical Model Identification
AKAlKE, H. (2011) · Cited by 4,177 · see citing works
Psychophysiological and Modulatory Interactions in Neuroimaging
Friston, K. J., Buechel, C., Fink, G. R., Morris, J., Rolls, E., & Dolan, R. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0291 · Cited by 3,097 · see citing works
Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1
Boynton, G., Engel, S., Glover, G., & Heeger, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04207.1996 · Cited by 2,522 · see citing works
Analysis of fMRI Time-Series Revisited
Friston, K. J., Holmes, A. P., Poline, J., Grasby, P. M., Williams, S., Frackowiak, R. S. J., & Turner, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1007 · Cited by 2,504 · see citing works
A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex
Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151 · see citing works
Erroneous analyses of interactions in neuroscience: A problem of significance
Nieuwenhuis, S., Forstmann, B. U., & Wagenmakers, E.-J. (2011) · Nature Neuroscience · doi:10.1038/nn.2886 · Cited by 864 · see citing works
Gitelman, D. R., Penny, W. D., Ashburner, J., & Friston, K. J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00058-2 · Cited by 799 · see citing works
Characterizing evoked hemodynamics with fMRI.
Friston, K. J., Frith, C., Turner, R., & Frackowiak, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1018 · Cited by 711 · see citing works
Ludden, T. M., Beal, S. L., & Sheiner, L. B. (1994) · Journal of Pharmacokinetics and Biopharmaceutics · doi:10.1007/bf02353864 · Cited by 306 · see citing works
Mixed blocked/event-related designs separate transient and sustained activity in fMRI
Visscher, K. M., Miezin, F. M., Kelly, J. E., Buckner, R., Donaldson, D., McAvoy, M. P., Bhalodia, V. M., & Petersen, S. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00178-2 · Cited by 273 · see citing works
Distributed and causal influence of frontal operculum in task control
Higo, T., Mars, R. B., Boorman, E. D., Buch, E. R., & Rushworth, M. F. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013361108 · Cited by 164 · see citing works
Self-appraisal decisions evoke dissociated dorsal—ventral aMPFC networks
Schmitz, T. W., & Johnson, S. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.10.030 · Cited by 116 · see citing works
Self-citationThe effects of single-trial averaging upon the spatial extent of fMRI activation
Huettel, S. A., & McCarthy, G. (2001) · Neuroreport · doi:10.1097/00001756-200108080-00025 · Cited by 94 · see citing works
Sleep deprivation and its effects on object-selective attention
Chee, M. W. L., Tan, J. C., Parimal, S., & Zagorodnov, V. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.067 · Cited by 89 · see citing works
Xu, G., McLaren, D. G., Ries, M. L., Fitzgerald, M. E., Bendlin, B. B., Rowley, H. A., Sager, M. A., Atwood, C., Asthana, S., & Johnson, S. C. (2008) · Brain · doi:10.1093/brain/awn254 · Cited by 82 · see citing works
Self-citationCondition-dependent functional connectivity: syntax networks in bilinguals
Dodel, S., Golestani, N., Pallier, C., Kouby, V. E., Bihan, D. L., & Poline, J. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1653 · Cited by 77 · see citing works
A bilateral occipitotemporal network mediates face perception
Minnebusch, D. A., Boris Suchan, A., Köster, O., & Daum, I. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.041 · Cited by 61 · see citing works
Effective connectivity of cortical and subcortical regions during unification of sentence structure
Snijders, T. M., Petersson, K. M., & Peter Hagoort, A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.035 · Cited by 57 · see citing works
Kim, J., & Horwitz, B. (2008) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2007.10.011 · Cited by 56 · see citing works
Habeck, C. G., Hilton, H. J., Zarahn, E., Brown, T. R., & Stern, Y. (2006) · Brain Research · doi:10.1016/j.brainres.2005.11.102 · Cited by 22 · see citing works
den Dekker, A. J., Poot, D. H. J., Bos, R., & Sijbers, J. (2008) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2008.2004427 · Cited by 16 · see citing works
Walter (1998) · doi:10.1002/(sici)1097-0258(19980115)17:1
Flagged first, then by citations
Cited by
Sorted by citations
Multi-task connectivity reveals flexible hubs for adaptive task control
Cole, M. W., Reynolds, J. R., Power, J. D., Repovs, G., Anticevic, A., & Braver, T. S. (2013) · Nature Neuroscience · doi:10.1038/nn.3470 · Cited by 1,704 · see citing works
Causal interactions between fronto-parietal central executive and default-mode networks in humans
Chen, A. C., Oathes, D. J., Chang, C. E., Bradley, T., Zhou, Z.-W., Williams, L. M., Glover, G. H., Deisseroth, K. A., & Etkin, A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311772110 · Cited by 561 · see citing works
Hanson, J. L., Hariri, A. R., & Williamson, D. E. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.05.010 · Cited by 338 · see citing works
Kral, T. R. A., Schuyler, B. S., Mumford, J. A., Rosenkranz, M. A., Lutz, A., & Davidson, R. J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.013 · Cited by 326 · see citing works
Non-invasive temporal interference electrical stimulation of the human hippocampus
Violante, I. R., Alania, K., Cassara, A. M., Neufeld, E., Acerbo, E., Carron, R., Williamson, A., Kurtin, D. L., Rhodes, E., Hampshire, A., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01456-8 · Cited by 292 · see citing works
When Is an Adolescent an Adult? Assessing Cognitive Control in Emotional and Nonemotional Contexts
Cohen, A. O., Breiner, K., Steinberg, L., Bonnie, R. J., Scott, E. S., Taylor-Thompson, K., Rudolph, M. D., Chein, J., Richeson, J. A., Heller, A. S., et al. (2016) · Psychological Science · doi:10.1177/0956797615627625 · Cited by 272 · see citing works
Nicholson, A. A., Rabellino, D., Densmore, M., Frewen, P. A., Paret, C., Kluetsch, R., Schmahl, C., Théberge, J., Neufeld, R. W. J., McKinnon, M. C., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23402 · Cited by 273 · see citing works
A Hitchhiker's Guide to Functional Magnetic Resonance Imaging
Soares, J. M., Magalhães, R. J. D. S., Moreira, P. S., Sousa, A., Ganz, E., Sampaio, A., Alves, V., Marques, P., & Sousa, N. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00515 · Cited by 270 · see citing works
Resilience after trauma: The role of memory suppression
Mary, A., Dayan, J., Leone, G., Postel, C., Fraisse, F., Malle, C., Vallée, T., Klein-Peschanski, C., Viader, F., Sayette, V. D. L., et al. (2020) · Science · doi:10.1126/science.aay8477 · Cited by 253 · see citing works
Oxytocin facilitates protective responses to aversive social stimuli in males
Striepens, N., Scheele, D., Kendrick, K. M., Becker, B., Schäfer, L., Schwalba, K., Reul, J., Maier, W., & Hurlemann, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208852109 · Cited by 242 · see citing works
Hirsch, J., Zhang, X., Noah, J. A., & Ono, Y. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.06.018 · Cited by 236 · see citing works
Ng, T. H., Alloy, L. B., & Smith, D. V. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0644-x · Cited by 244 · see citing works
Muscatell, K. A., Dedovic, K., Slavich, G. M., Jarcho, M. R., Breen, E. C., Bower, J. E., Irwin, M. R., & Eisenberger, N. I. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.06.201 · Cited by 240 · see citing works
Impaired reward prediction error encoding and striatal-midbrain connectivity in depression
Kumar, P., Goer, F., Murray, L., Dillon, D. G., Beltzer, M. L., Cohen, A. L., Brooks, N. H., & Pizzagalli, D. A. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0032-x · Cited by 219 · see citing works
Morey, R. A., Dunsmoor, J. E., Haswell, C. C., Brown, V. M., Vora, A., Weiner, J., Stjepanovic, D., Wagner, H. R., Workgroup, V. M.-A. M., Brancu, M., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.196 · Cited by 221 · see citing works
Mindful attention to breath regulates emotions via increased amygdala–prefrontal cortex connectivity
Doll, A., Hölzel, B. K., Bratec, S. M., Boucard, C. C., Xie, X., Wohlschläger, A. M., & Sorg, C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.041 · Cited by 228 · see citing works
Identity-specific coding of future rewards in the human orbitofrontal cortex
Howard, J. D., Gottfried, J. A., Tobler, P. N., & Kahnt, T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503550112 · Cited by 222 · see citing works
Interactions between human orbitofrontal cortex and hippocampus support model-based inference
Wang, F., Schoenbaum, G. M., & Kahnt, T. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000578 · Cited by 220 · see citing works
Konishi, M., McLaren, D. G., Engen, H., & Smallwood, J. (2015) · PLOS ONE · doi:10.1371/journal.pone.0132209 · Cited by 194 · see citing works
Self-citationOxytocin facilitates the extinction of conditioned fear in humans
Eckstein, M., Becker, B., Scheele, D., Scholz, C., Preckel, K., Schlaepfer, T. E., Grinevich, V., Kendrick, K. M., Maier, W., & Hurlemann, R. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.10.015 · Cited by 210 · see citing works
Task activations produce spurious but systematic inflation of task functional connectivity estimates
Cole, M. W., Ito, T., Schultz, D. H., Mill, R. D., Chen, R. J., & Cocuzza, C. V. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.12.054 · Cited by 211 · see citing works
Neural correlates associated with suicide and nonsuicidal self-injury in youth
Auerbach, R. P., Pagliaccio, D., Allison, G. O., Alqueza, K. L., & Alonso, M. F. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.002 · Cited by 204 · see citing works
Corticostriatal Output Gating during Selection from Working Memory
Chatham, C. H., Frank, M. J., & Badre, D. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.002 · Cited by 193 · see citing works
Oxytocin, the peptide that bonds the sexes also divides them
Gao, S., Becker, B., Luo, L., Geng, Y., Zhao, W., Yin, Y., Hu, J., Gao, Z., Gong, Q., Hurlemann, R., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602620113 · Cited by 186 · see citing works
Brain Mechanisms for Processing Affective (and Nonaffective) Touch Are Atypical in Autism
Kaiser, M. D., Yang, D. Y. ‐., Voos, A. C., Bennett, R. H., Gordon, I., Pretzsch, C. M., Beam, D. E., Keifer, C. M., Eilbott, J. A., McGlone, F. P., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv125 · Cited by 204 · see citing works
A causal account of the brain network computations underlying strategic social behavior
Hill, C., Suzuki, S., Polanía, R., Moisa, M., O’Doherty, J. P., & Ruff, C. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4602 · Cited by 196 · see citing works
A comparison of statistical methods for detecting context-modulated functional connectivity in fMRI
Cisler, J. M., Bush, K., & Steele, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.018 · Cited by 194 · see citing works
How cognitive and reactive fear circuits optimize escape decisions in humans
Qi, S., Hassabis, D., Sun, J., Guo, F., Daw, N. D., & Mobbs, D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712314115 · Cited by 185 · see citing works
Hearne, L. J., Cocchi, L., Zalesky, A., & Mattingley, J. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0485-17.2017 · Cited by 178 · see citing works
CONN functional connectivity toolbox: RRID SCR_009550, release 22
Nieto-Castañón, A., & Whitfield, S. (2022) · Hilbert Press eBooks · doi:10.56441/hilbertpress.2246.5840 · Cited by 182 · see citing works
de Vries, F. E., de Wit, S. J., Cath, D. C., van der Werf, Y. D., van der Borden, V., van Rossum, T. B., van Balkom, A. J. L. M., van der Wee, N. J. A., Veltman, D. J., & van den Heuvel, O. A. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.11.021 · Cited by 177 · see citing works
Rapid stimulation of human dentate gyrus function with acute mild exercise
Suwabe, K., Byun, K., Hyodo, K., Reagh, Z. M., Roberts, J. M., Matsushita, A., Saotome, K., Ochi, G., Fukuie, T., Suzuki, K., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805668115 · Cited by 174 · see citing works
Constructing, Perceiving, and Maintaining Scenes: Hippocampal Activity and Connectivity
Zeidman, P., Mullally, S. L., & Maguire, E. A. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu266 · Cited by 169 · see citing works
Musical training sharpens and bonds ears and tongue to hear speech better
Du, Y., & Zatorre, R. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712223114 · Cited by 168 · see citing works
Cortico-hippocampal network connections support the multidimensional quality of episodic memory
Cooper, R. A., & Ritchey, M. (2019) · eLife · doi:10.7554/elife.45591 · Cited by 156 · see citing works
The hippocampus supports deliberation during value-based decisions
Bakkour, A., Palombo, D. J., Zylberberg, A. D., Kang, Y. H., Reid, A. G., Verfaellie, M. H., Shadlen, M. N., & Daphna Shohamy, A. (2019) · eLife · doi:10.7554/elife.46080 · Cited by 146 · see citing works
The visual word form area (VWFA) is part of both language and attention circuitry
Chen, L., Wassermann, D., Abrams, D. A., Kochalka, J., Gallardo, G., & Menon, V. (2019) · Nature Communications · doi:10.1038/s41467-019-13634-z · Cited by 150 · see citing works
Individual differences in self-reported self-control predict successful emotion regulation
Paschke, L. M., Dörfel, D., Steimke, R., Trempler, I., Magrabi, A., Ludwig, V. U., Schubert, T., Stelzel, C., & Walter, H. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw036 · Cited by 161 · see citing works
Neuroimaging of reward mechanisms in Gambling disorder: an integrative review
Clark, L., Boileau, I., & Zack, M. H. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0230-2 · Cited by 149 · see citing works
Li, L. M., Violante, I. R., Leech, R., Ross, E., Hampshire, A., Opitz, A., Rothwell, J. C., Carmichael, D. W., & Sharp, D. J. (2018) · Human Brain Mapping · doi:10.1002/hbm.24420 · Cited by 148 · see citing works
Diano, M., Tamietto, M., Celeghin, A., Weiskrantz, L., Tatu, K., Bagnis, A., Duca, S., Geminiani, G. C., Cauda, F., & Costa, T. (2017) · Scientific Reports · doi:10.1038/srep45260 · Cited by 147 · see citing works
Breakdown of the brain’s functional network modularity with awareness
Godwin, D., Barry, R. L., & Marois, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414466112 · Cited by 145 · see citing works
Rosenberg‐Lee, M., Ashkenazi, S., Chen, T., Young, C. B., Geary, D. C., & Menon, V. (2014) · Developmental Science · doi:10.1111/desc.12216 · Cited by 142 · see citing works
Wu, M., Kujawa, A., Lu, L. H., Fitzgerald, D. A., Klumpp, H., Fitzgerald, K. D., Monk, C. S., & Phan, K. L. (2016) · Human Brain Mapping · doi:10.1002/hbm.23129 · Cited by 130 · see citing works
Howard, J. D., & Kahnt, T. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3473-16.2017 · Cited by 131 · see citing works
Training emotion regulation through real-time fMRI neurofeedback of amygdala activity
Herwig, U., Lutz, J., Scherpiet, S., Scheerer, H., Kohlberg, J., Opialla, S., Preuss, A., Steiger, V. R., Sulzer, J. S., Weidt, S., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.068 · Cited by 134 · see citing works
Self‐other resonance, its control and prosocial inclinations: Brain–behavior relationships
Christov‐Moore, L., & Iacoboni, M. (2016) · Human Brain Mapping · doi:10.1002/hbm.23119 · Cited by 134 · see citing works
Herweg, N. A., Apitz, T., Leicht, G., Mulert, C., Fuentemilla, L., & Bunzeck, N. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3629-15.2016 · Cited by 133 · see citing works
Gorka, S. M., Fitzgerald, D. A., Labuschagne, I., Hosanagar, A., Wood, A. G., Nathan, P. J., & Phan, K. L. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.168 · Cited by 131 · see citing works
Dissociable Neural Routes to Successful Prospective Memory
McDaniel, M. A., LaMontagne, P., Beck, S. M., Scullin, M. K., & Braver, T. S. (2013) · Psychological Science · doi:10.1177/0956797613481233 · Cited by 130 · see citing works
Javanbakht, A., King, A. P. J., Evans, G. W., Swain, J. E., Angstadt, M., Phan, K. L., & Liberzon, I. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00154 · Cited by 131 · see citing works
Cogitate Consortium, Ferrante, O., Gorska-Klimowska, U., Henin, S., Hirschhorn, R., Khalaf, A., Lepauvre, A., Liu, L., Richter, D., Vidal, Y., et al. (2025) · Nature · doi:10.1038/s41586-025-08888-1 · Cited by 136 · see citing works
“For fMRI, connectivity was assessed through gPPI implemented in SPM 119 .”
InfluentialWhen Brain Beats Behavior: Neuroforecasting Crowdfunding Outcomes
Genevsky, A., Yoon, C., & Knutson, B. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1633-16.2017 · Cited by 122 · see citing works
Different brain circuitries mediating controllable and uncontrollable pain
Bräscher, A.-K., Becker, S., Hoeppli, M.-E., & Schweinhardt, P. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1954-15.2016 · Cited by 118 · see citing works
Longitudinal Changes in Prefrontal Cortex Activation Underlie Declines in Adolescent Risk Taking
Qu, Y., Galván, A., Fuligni, A. J., Lieberman, M. D., & Telzer, E. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1553-15.2015 · Cited by 124 · see citing works
Impact of Sex and Menopausal Status on Episodic Memory Circuitry in Early Midlife
Jacobs, E. G., Weiss, B. K., Makris, N., Whitfield-Gabrieli, S., Buka, S. L., Klibanski, A., & Goldstein, J. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0951-16.2016 · Cited by 124 · see citing works
Paret, C., Ruf, M., Gerchen, M. F., Kluetsch, R., Demirakca, T., Jungkunz, M., Bertsch, K., Schmahl, C., & Ende, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.027 · Cited by 113 · see citing works
Helpman, L., Marin, M.-F., Papini, S., Zhu, X., Sullivan, G. M., Schneier, F., Neria, M., Shvil, E., Malaga Aragon, M. J., Markowitz, J. C., et al. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.10.007 · Cited by 121 · see citing works
Supekar, K., Kochalka, J., Schaer, M., Wakeman, H. N., Qin, S., Padmanabhan, A., & Menon, V. (2018) · Brain · doi:10.1093/brain/awy191 · Cited by 118 · see citing works
Selective Effects of Psychotherapy on Frontopolar Cortical Function in PTSD
Fonzo, G. A., Goodkind, M. S., Oathes, D. J., Zaiko, Y. V., Harvey, M., Peng, K. K., Weiss, M. E., Thompson, A. L., Zack, S. E., Mills-Finnerty, C. E., et al. (2017) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2017.16091073 · Cited by 120 · see citing works
Sharda, M., Midha, R., Malik, S., Mukerji, S., & Singh, N. C. (2014) · Autism Research · doi:10.1002/aur.1437 · Cited by 121 · see citing works
From connectome to cognition: The search for mechanism in human functional brain networks
Mill, R. D., Ito, T., & Cole, M. W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.060 · Cited by 118 · see citing works
Alterations of amygdala-prefrontal connectivity with real-time fMRI neurofeedback in BPD patients.
Paret, C., Kluetsch, R., Zaehringer, J., Ruf, M., Demirakca, T., Bohus, M., Ende, G., & Schmahl, C. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw016 · Cited by 114 · see citing works
Mothers know best: redirecting adolescent reward sensitivity toward safe behavior during risk taking
Telzer, E. H., Ichien, N. T., & Qu, Y. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv026 · Cited by 117 · see citing works
Self-regulatory depletion increases emotional reactivity in the amygdala
Wagner, D. D., & Heatherton, T. F. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss082 · Cited by 115 · see citing works
A Latent Variable Approach to Differentiating Neural Mechanisms of Irritability and Anxiety in Youth
Kircanski, K., White, L. K., Tseng, W., Wiggins, J. L., Frank, H. R., Sequeira, S. L., Zhang, S., Abend, R., Towbin, K. E., Stringaris, A. K., et al. (2018) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2018.0468 · Cited by 111 · see citing works
Effects of Prior-Knowledge on Brain Activation and Connectivity During Associative Memory Encoding
Liu, Z., Grady, C. L., & Moscovitch, M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw047 · Cited by 114 · see citing works
Young, C. B., Chen, T., Nusslock, R., Keller, J., Schatzberg, A. F., & Menon, V (2016) · Translational Psychiatry · doi:10.1038/tp.2016.80 · Cited by 108 · see citing works
Kilteni, K., & Ehrsson, H. H. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1732-19.2019 · Cited by 107 · see citing works
Emotion regulation deficits in regular marijuana users
Zimmermann, K., Walz, C., Derckx, R. T., Kendrick, K. M., Weber, B., Doré, B., Ochsner, K. N., Hurlemann, R., & Becker, B. (2017) · Human Brain Mapping · doi:10.1002/hbm.23671 · Cited by 106 · see citing works
Sex similarities and differences in pain-related periaqueductal gray connectivity
Linnman, C., Beucke, J., Jensen, K. B., Gollub, R. L., & Kong, J. (2011) · Pain · doi:10.1016/j.pain.2011.11.006 · Cited by 101 · see citing works
Slow escape decisions are swayed by trait anxiety
Fung, B. J., Qi, S., Hassabis, D., Daw, N. D., & Mobbs, D. (2019) · Nature Human Behaviour · doi:10.1038/s41562-019-0595-5 · Cited by 102 · see citing works
Zhao, Z., Yao, S., Li, K., Sindermann, C., Zhou, F., Zhao, W., Li, J., Lührs, M., Goebel, R., Kendrick, K. M., et al. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000496057 · Cited by 102 · see citing works
Reward prospect rapidly speeds up response inhibition via reactive control
Boehler, C. N., Schevernels, H., Hopf, J., Stoppel, C. M., & Krebs, R. M. (2014) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-014-0251-5 · Cited by 103 · see citing works
Zhan, L., Guo, D., Chen, G., & Yang, J. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00277 · Cited by 106 · see citing works
Cai, W., Griffiths, K. R., Korgaonkar, M. S., Williams, L. M., & Menon, V. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0564-4 · Cited by 100 · see citing works
Non-invasive stimulation of the human striatum disrupts reinforcement learning of motor skills
Vassiliadis, P., Beanato, E., Popa, T., Windel, F., Morishita, T., Neufeld, E., Duqué, J., Derosière, G., Wessel, M. J., & Hummel, F. C. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01901-z · Cited by 97 · see citing works
White, L. K., Sequeira, S., Britton, J. C., Brotman, M. A., Gold, A. L., Berman, E., Towbin, K., Abend, R., Fox, N. A., Bar-Haim, Y., et al. (2017) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2017.16070847 · Cited by 96 · see citing works
Anticipatory Anxiety Disrupts Neural Valuation during Risky Choice
Engelmann, J. B., Meyer, F., Fehr, E., & Ruff, C. C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2880-14.2015 · Cited by 95 · see citing works
Pathomechanisms and compensatory efforts related to Parkinsonian speech
Arnold, C., Gehrig, J., Gispert, S., Seifried, C., & Kell, C. A. (2014) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.10.016 · Cited by 98 · see citing works
A central role for the retrosplenial cortex in de novo environmental learning
Auger, S. D., Zeidman, P., & Maguire, E. A. (2015) · eLife · doi:10.7554/elife.09031 · Cited by 97 · see citing works
Kearney-Ramos, T. E., Dowdle, L. T., Lench, D. H., Mithoefer, O. J., DeVries, W. H., George, M. S., Anton, R. F., & Hanlon, C. A. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.03.016 · Cited by 91 · see citing works
The neural correlates of worry in association with individual differences in neuroticism
Servaas, M. N., Riese, H., Ormel, J., & Aleman, A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22476 · Cited by 96 · see citing works
Insula response and connectivity during social and non-social attention in children with autism
Odriozola, P., Uddin, L. Q., Lynch, C. J., Kochalka, J., Chen, T., & Menon, V. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv126 · Cited by 95 · see citing works
Time-dependent memory transformation along the hippocampal anterior–posterior axis
Dandolo, L., & Schwabe, L. (2018) · Nature Communications · doi:10.1038/s41467-018-03661-7 · Cited by 97 · see citing works
Swain, J. E., Ho, S.-H. S., Rosenblum, K. L., Morelen, D. M., Dayton, C. J., & Muzik, M. (2017) · Development and Psychopathology · doi:10.1017/s0954579417000165 · Cited by 94 · see citing works
Sripada, C., Angstadt, M., Kessler, D. A., Phan, K. L., Liberzon, I., Evans, G. W., Welsh, R. C., Kim, P., & Swain, J. E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.006 · Cited by 93 · see citing works
Empathy and stress related neural responses in maternal decision making
Ho, S.-H. S., Konrath, S., Brown, S., & Swain, J. E. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00152 · Cited by 93 · see citing works
Yue, Q., Martin, R. C., Hamilton, A. C., & Rose, N. S. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy037 · Cited by 91 · see citing works
Stoddard, J., Tseng, W., Kim, P., Chen, G., Yi, J. Y., Donahue, L. M., Brotman, M. A., Towbin, K. E., Pine, D. S., & Leibenluft, E. (2016) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3282 · Cited by 92 · see citing works
Violent offenders respond to provocations with high amygdala and striatal reactivity
da Cunha‐Bang, S., Fisher, P. M., Hjordt, L. V., Perfalk, E., Skibsted, A. P., Bock, C., Baandrup, A. O., Deen, M., Thomsen, C., Sestoft, D. M., et al. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx006 · Cited by 92 · see citing works
Alterations of Functional Brain Connectivity After Long-Duration Spaceflight as Revealed by fMRI
Pechenkova, E., Nosikova, I., Rumshiskaya, A. D., Litvinova, L., Rukavishnikov, I. V., Mershina, E. A., Sinitsyn, V. E., Ombergen, A. V., Jeurissen, B., Jillings, S., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00761 · Cited by 97 · see citing works
Neural Conflict-Control Mechanisms Improve Memory for Target Stimuli
Krebs, R. M., Boehler, C. N., Belder, M. D., & Egner, T. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht283 · Cited by 92 · see citing works
Hu, J., Qi, S., Becker, B., Luo, L., Gao, S., Gong, Q., Hurlemann, R., & Kendrick, K. M. (2015) · Human Brain Mapping · doi:10.1002/hbm.22760 · Cited by 91 · see citing works
Orbitofrontal cortex mediates pain inhibition by monetary reward
Becker, S., Gandhi, W., Pomares, F. B., Wager, T. D., & Schweinhardt, P. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw173 · Cited by 92 · see citing works
Rabinak, C. A., MacNamara, A., Kennedy, A. E., Angstadt, M., Stein, M. B., Liberzon, I., & Phan, K. L. (2014) · Depression and Anxiety · doi:10.1002/da.22243 · Cited by 89 · see citing works
Le, T. M., Borghi, J., Kujawa, A., Klein, D. N., & Leung, H. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.01.004 · Cited by 91 · see citing works
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 · see citing works
CONN functional connectivity toolbox: RRID SCR_009550, release 21
Nieto-Castañón, A., & Whitfield, S. (2021) · Hilbert Press eBooks · doi:10.56441/hilbertpress.2161.7292 · Cited by 89 · see citing works
Oxytocin Modulates Attention Switching Between Interoceptive Signals and External Social Cues
Yao, S., Becker, B., Zhao, W., Zhao, Z., Kou, J., Ma, X., Geng, Y., Ren, P., & Kendrick, K. M. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.189 · Cited by 86 · see citing works
- Authors
- McLaren, D. G., Ries, M. L., Xu, G., & Johnson, S. C.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Johnson, Sterling C.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2012-07
- Volume
- 61
- Issue
- 4
- Pages
- 1277-1286
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC3376181
- OpenAlex
- W2132137022
- Cited by
- 1,445
- References
- 24
- Citations by year
- 2026: 99 · 2025: 121 · 2024: 113 · 2023: 100 · 2022: 117 · 2021: 125 · 2020: 139 · 2019: 115 · 2018: 129 · 2017: 120 · 2016: 122 · 2015: 71 · 2014: 44 · 2013: 19 · 2012: 7
- FWCI
- 23.11
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Department of Veterans Affairs Merit Review (I01CX000165)
- National Institutes of Health (AG021155, AG000213)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Keywords
- generalized psychophysiological interaction, functional MRI, statistical parametric mapping, model fit, Akaike information criterion, brain connectivity
- MeSH terms
- Brain, Brain Mapping, Female, Humans, Image Interpretation, Computer-Assisted, Magnetic Resonance Imaging, Male, Middle Aged, Models, Neurological, Psychophysiology, Sensitivity and Specificity
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