The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“with amygdala dysfunction underlying psychopathology;59”
From Distinct and shared therapeutic neural mechanisms of mindfulness-based and social support stress reduction groups in adults with autism spectrum disorder (2023) · cites this paper as [59]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
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
ANew Look at the Statistical Model Identification
AKAlKE, H. (2011) · Cited by 4,177
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
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
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
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
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
Gitelman, D. R., Penny, W. D., Ashburner, J., & Friston, K. J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00058-2 · Cited by 799
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
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 1,000
Outhred, T., Das, P., Dobson‐Stone, C., Felmingham, K. L., Bryant, R. A., Nathan, P. J., Malhi, G. S., & Kemp, A. H. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.02.019 · Cited by 21
Age Differences in Hippocampal Activation during Gist-based False Recognition
Paige, L. E., Cassidy, B. S., Schacter, D., & Gutchess, A. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.06.014 · Cited by 21
Wang, G.-Y., van Eijk, J., Demirakça, T., Sack, M., Krause-Utz, A., Cackowski, S., Schmahl, C. G., & Ende, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.013 · Cited by 21
Residual effects of emotion are reflected in enhanced visual activity after sleep
Bennion, K. A., Payne, J. D., & Kensinger, E. A. (2016) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-016-0479-3 · Cited by 21
Neural processes underlying cultural differences in cognitive persistence
Telzer, E. H., Qu, Y., & Lin, L. C. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.05.034 · Cited by 23
Increased Global Interaction Across Functional Brain Modules During Cognitive Emotion Regulation
Brandl, F., Bratec, S. M., Xie, X., Wohlschläger, A. M., Riedl, V., Meng, C., & Sorg, C. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx178 · Cited by 21
The neural signatures of egocentric bias in normative decision-making
Feng, C., Feng, X., Wang, L., Wang, L., Gu, R., Ni, A., Deshpande, G., Li, Z., & Luo, Y. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-9893-1 · Cited by 21
Larabi, D. I., van der Meer, L., Pijnenborg, G. H. M., Ćurĉić‐Blake, B., & Aleman, A. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.09.009 · Cited by 21
Frontostriatal pathways gate processing of behaviorally relevant reward dimensions
Weber, S. C., Kahnt, T., Quednow, B. B., & Tobler, P. N. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005722 · Cited by 18
Linke, J. O., Jones, E. J. H., Pagliaccio, D., Swetlitz, C., Lewis, K. M., Silverman, W. K., Bar‐Haim, Y., Pine, D. S., & Brotman, M. A. (2019) · BMC Psychiatry · doi:10.1186/s12888-019-2224-2 · Cited by 24
Markett, S. A., Jawinski, P., Kirsch, P., & Gerchen, M. F. (2020) · Scientific Reports · doi:10.1038/s41598-020-61522-0 · Cited by 20
Liu, L., Margoni, F., He, Y., & Liu, H. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107721 · Cited by 26
Facilitation of emotion regulation with a single dose of escitalopram: A randomized fMRI study
Outhred, T., Das, P., Felmingham, K. L., Bryant, R. A., Nathan, P. J., Malhi, G. S., & Kemp, A. H. (2015) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2015.07.018 · Cited by 24
Neukel, C., Bertsch, K., Fuchs, A., Zietlow, A., Reck, C., Möhler, E., Brunner, R. M., Bermpohl, F., & Herpertz, S. C. (2018) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.170026 · Cited by 20
Pagni, B. A., Hill, E., Walsh, M. J. M., Delaney, S., Ogbeama, D., Monahan, L., Cook, J. R., Guerithault, N., Dixon, M. V., Ballard, L., et al. (2023) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.220159 · Cited by 20
Zhao, W., Geng, Y., Luo, L., Zhao, Z., Ma, X., Xu, L., Yao, S., & Kendrick, K. M. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00272 · Cited by 20
McDermott, T. J., Kirlić, N., Akeman, E., Touthang, J., Cosgrove, K. T., DeVille, D. C., Clausen, A. N., White, E. J., Kuplicki, R., & Aupperle, R. L. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117077 · Cited by 20
Bryant, R. A., Williamson, T., Erlinger, M., Felmingham, K. L., Malhi, G. S., Hinton, M., Williams, L. M., & Korgaonkar, M. S. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01340-8 · Cited by 21
The neural correlates of intermanual transfer
Dirren, E., Bourgeois, A., Klug, J., Kleinschmidt, A. K., van Assche, M., & Carrera, E. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118657 · Cited by 20
Li, L., Di, X., Zhang, H., Huang, G., Zhang, L., Liang, Z., & Zhang, Z. (2021) · Human Brain Mapping · doi:10.1002/hbm.25707 · Cited by 20
Kilteni, K., Houborg, C., & Ehrsson, H. H. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1743-22.2023 · Cited by 24
Zhang, Y., Zhang, Q., Wang, J., Zhou, M., Qing, Y., Zou, H., Li, J., Yang, C., Becker, B., Kendrick, K. M., et al. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120455 · Cited by 20
Kann, S. J., O’Rawe, J. F., Huang, A., Klein, D. N., & Leung, H. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx079 · Cited by 22
Lu, J., Yang, H., He, H., Jeon, S., Hou, C., Evans, A. C., & Yao, D. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00695 · Cited by 22
Kraus, J., Frick, A., Fischer, H., Howner, K., Fredrikson, M., & Furmark, T. (2018) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2018.08.012 · Cited by 22
Enhanced food-related responses in the ventral medial prefrontal cortex in narcolepsy type 1
van Holst, R. J., Janssen, L. K., van Mierlo, P., Lammers, G. J., Cools, R., Overeem, S., & Aarts, E. (2018) · Scientific Reports · doi:10.1038/s41598-018-34647-6 · Cited by 20
Pedale, T., Macaluso, E., & Santangelo, V. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01873-1 · Cited by 20
Caviezel, M. P., Reichert, C., Bahmani, D. S., Linnemann, C., Liechti, C., Bieri, O., Borgwardt, S., Leyhe, T., & Melcher, T. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.01002 · Cited by 21
Yan, Z., Schmidt, S. N. L., Frank, J., Witt, S. H., Haß, J., Kirsch, P., & Mier, D. U. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0637-8 · Cited by 19
Anxiety and amygdala connectivity during movie-watching
Kirk, P. A., Robinson, O. J., & Skipper, J. I. (2022) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108194 · Cited by 23
Saleh, S., Adamovich, S. V., & Tunik, E. (2012) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2012.6346981 · Cited by 20
Zhang, X., Zhu, Y., Lu, J., Chen, Q., Chen, F., Long, C., Xu, X., Ge, D., Bai, Y., Liu, D., et al. (2024) · Human Brain Mapping · doi:10.1002/hbm.26814 · Cited by 19
Barnaveli, I., Viganò, S., Reznik, D., Haggard, P., & Doeller, C. F. (2025) · Nature Communications · doi:10.1038/s41467-025-59153-y · Cited by 23
Facing temptation: The neural correlates of gambling availability during sports picture exposure
Brevers, D., Herremans, S. C., He, Q., Vanderhasselt, M., Petieau, M., Verdonck, D., Poppa, T., Witte, S. D., Kornreich, C., Bechara, A., et al. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-0599-z · Cited by 22
Adverse effects of GHB-induced coma on long-term memory and related brain function
Pereira, F. R., McMaster, M. T. B., Polderman, N., de Vries, Y. D. A. T., van den Brink, W., & van Wingen, G. A. (2018) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2018.05.019 · Cited by 19
Farb, N. A. S., Zuo, Z., & Price, C. J. (2023) · eNeuro · doi:10.1523/eneuro.0088-23.2023 · Cited by 19
Schumer, M. C., Bertocci, M. A., Aslam, H. A., Graur, S., Bebko, G. M., Stiffler, R. S., Skeba, A. S., Brady, T. J., Benjamin, O. E., Wang, Y., et al. (2023) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2023.4150 · Cited by 19
Kaldewaij, R., Salamone, P., Enmalm, A., Östman, L., Pietrzak, M., Karlsson, H., Löfberg, A., Gauffin, E., Samuelsson, M., Gustavson, S., et al. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01906-2 · Cited by 23
Kireev, M. V., Slioussar, N., Korotkov, A. D., Chernigovskaya, T. V., & Medvedev, S. V. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00036 · Cited by 19
Yu, Y., Yang, J., Ejima, Y., Fukuyama, H., & Wu, J. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00662 · Cited by 19
Neurocognitive decision-making processes of casual methamphetamine users
Droutman, V., Xue, F., Barkley‐Levenson, E. E., Lam, H. Y., Bechara, A., Smith, B. J., Lu, Z., Xue, G., Miller, L. C., & Read, S. J. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.101643 · Cited by 19
Disturbed retrieval network and prospective memory decline in postpartum women
Shin, N., Bak, Y., Nah, Y., Han, S., Kim, D. J., Kim, S. J., Lee, J. E., Lee, S., & Lee, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-23875-5 · Cited by 19
Re-learning to be different: Increased neural differentiation supports post-stroke language recovery
Purcell, J. J., Wiley, R. W., & Rapp, B. C. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116145 · Cited by 19
Salomon, T., Botvinik‐Nezer, R., Oren, S., & Schönberg, T. (2019) · Human Brain Mapping · doi:10.1002/hbm.24859 · Cited by 20
The brain regions supporting schema-related processing of people’s identities
Raykov, P., Keidel, J. L., Oakhill, J. V., & Bird, C. M. (2019) · Cognitive Neuropsychology · doi:10.1080/02643294.2019.1685958 · Cited by 18
Greven, I. M., & Ramsey, R. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.01.003 · Cited by 18
Functional connectivity during smooth pursuit eye movements
Schröder, R., Kasparbauer, A., Meyhöfer, I., Steffens, M., Trautner, P., & Ettinger, U. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00317.2020 · Cited by 20
Mengotti, P., Käsbauer, A.-S., Fink, G. R., & Vossel, S. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab511 · Cited by 17
Tadayonnejad, R., Majid, D. S. A., Tsolaki, E. C., Rane, R., Wang, H., Moody, T. D., Pauli, W. M., Pouratian, N., Bari, A., Murray, S. B., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.806327 · Cited by 19
The effect of hunger state on hypothalamic functional connectivity in response to food cues
Kullmann, S., Veit, R., Crabtree, D. R., Buosi, W., Androutsos, O., Johnstone, A. M., Μanios, Y., Preissl, H. T., & Smeets, P. A. M. (2022) · Human Brain Mapping · doi:10.1002/hbm.26059 · Cited by 16
Cansino, S. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1012870 · Cited by 20
Age differences in the neural processing of semantics, within and beyond the core semantic network
Wu, W., & Hoffman, P. (2023) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.07.022 · Cited by 18
Stress-induced brain responses are associated with BMI in women
Kühnel, A., Hagenberg, J., Arloth, J., Ködel, M., Czisch, M., Sämann, P. G., BeCOME working group, Brückl, T. M., Spoormaker, V. I., Erhardt, A., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05396-8 · Cited by 21
Yang, X., Zeng, Y., Jiao, G., Gan, X., Linden, D. E. J., Hernaus, D., Zhu, C., Li, K., Yao, D., Yao, S., et al. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.110968 · Cited by 17
Kayser, A. S., Vega, T. A., Weinstein, D., Peters, J., & Mitchell, J. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.12.022 · Cited by 19
Dalenberg, J. R., Hoogeveen, H. R., & Lorist, M. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-08-101743-2.00011-x · Cited by 18
Kim, J., & Kang, E. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00371 · Cited by 17
Neural response to stress and perceived stress differ in patients with left temporal lobe epilepsy
Goodman, A. M., Allendorfer, J. B., Heyse, H., Szaflarski, B. A., Eliassen, J. C., Nelson, E. B., Storrs, J. M., & Szaflarski, J. P. (2019) · Human Brain Mapping · doi:10.1002/hbm.24606 · Cited by 17
Morningstar, M. A., Grannis, C., Mattson, W. I., & Nelson, E. E. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00108 · Cited by 19
Bertocci, M. A., Chase, H. W., Graur, S., Stiffler, R. S., Edmiston, E. K., Coffman, B. A., Greenberg, B. D., & Phillips, M. L. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0567-1 · Cited by 17
Gomes, C. A., Figueiredo, P., & Mayes, A. R. (2015) · Hippocampus · doi:10.1002/hipo.22537 · Cited by 18
Guediche, S., Reilly, M., Santiago, C., Laurent, P. A., & Blumstein, S. E. (2016) · Cortex · doi:10.1016/j.cortex.2016.03.014 · Cited by 18
Tompson, S., Chua, H. F., & Kitayama, S. (2016) · Human Brain Mapping · doi:10.1002/hbm.23277 · Cited by 19
Large-Scale Network Coupling with the Fusiform Cortex Facilitates Future Social Motivation
Utevsky, A. V., Smith, D. V., Young, J. S., & Huettel, S. A. (2017) · eNeuro · doi:10.1523/eneuro.0084-17.2017 · Cited by 19
Ross, A. J., Roule, A. L., Deveney, C. M., Towbin, K. E., Brotman, M. A., Leibenluft, E., & Tseng, W. (2020) · Bipolar Disorders · doi:10.1111/bdi.12985 · Cited by 18
Aberrant Cortical Connectivity During Ambiguous Object Recognition Is Associated With Schizophrenia
Pokorny, V., Espensen-Sturges, T. D., Burton, P. C., Sponheim, S. R., & Olman, C. A. (2020) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2020.09.018 · Cited by 18
Temporal Interference Stimulation Boosts Working Memory Performance in the Frontoparietal Network
Zheng, S., Zhang, Y., Huang, K., Zhuang, J., Lü, J., & Liu, Y. (2025) · Human Brain Mapping · doi:10.1002/hbm.70160 · Cited by 19
Nicotine restores functional connectivity of the ventral attention network in schizophrenia
Smucny, J., D, A. O. M., & Tregellas, J. R. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.04.015 · Cited by 17
Vinci‐Booher, S., James, T. W., & James, K. H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117554 · Cited by 17
Chen, Y., Liu, C., Xin, F., Zou, H., Huang, Y., Wang, J., Dai, J., Zou, Z., Ferraro, S., Kendrick, K. M., et al. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110716 · Cited by 18
Edmiston, E. K., Chase, H. W., Jones, N. P., Nhan, T. J., Phillips, M. L., & Fournier, J. C. J. (2024) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsae009 · Cited by 17
Motion parallax links visual motion areas and scene regions
Schindler, A., & Bartels, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.066 · Cited by 17
Schindler, A., & Bartels, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw136 · Cited by 18
Uncertainty and expectancy deviations require cortico-subcortical cooperation
Mestres-Missé, A., Trampel, R., Turner, R., & Kotz, S. A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.069 · Cited by 17
Age and executive ability impact the neural correlates of race perception
Cassidy, B. S., Lee, E. J., & Krendl, A. C. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw081 · Cited by 17
Coccaro, E. F., Keedy, S., Gorka, S. M., King, A. C., Fanning, J. R., Lee, R., & Phan, K. L. (2016) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2016.09.001 · Cited by 17
Semantic Congruence Alters Functional Connectivity during Olfactory-Visual Perception
Sijben, R., Hoffmann-Hensel, S. M., Rodriguez‐Raecke, R., Haarmeier, T., & Freiherr, J. (2018) · Chemical Senses · doi:10.1093/chemse/bjy048 · Cited by 19
Kunas, S. L., Yang, Y., Straube, B., Kircher, T. T. J., Gerlach, A. L., Pfleiderer, B., Arolt, V., Wittmann, A., Ströhle, A., Wïttchen, H., et al. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2018.11.026 · Cited by 17
Rogers, C. R., Perino, M. T., & Telzer, E. H. (2019) · Journal of Research on Adolescence · doi:10.1111/jora.12500 · Cited by 20
Early interpersonal trauma reduces temporoparietal junction activity during spontaneous mentalising
Cracco, E., Hudson, A. R., Hamme, C. V., Maeyens, L., Braß, M., & Mueller, S. C. (2020) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaa015 · Cited by 24
Neural Systems for Memory-based Value Judgment and Decision-making
Vaidya, A. R., & Badre, D. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01595 · Cited by 16
Yamazaki, H., Kanazawa, Y., & Omori, K. (2020) · Hearing Research · doi:10.1016/j.heares.2020.108024 · Cited by 17
Herman, A. M., Palmer, C. E., Azevedo, R. T., & Manos Tsakiris, A. (2020) · Cortex · doi:10.1016/j.cortex.2020.11.019 · Cited by 19
Rai, S., Griffiths, K. R., Breukelaar, I. A., Barreiros, A. R., Chen, W., Boyce, P. M., Hazell, P., Foster, S., Malhi, G. S., Bryant, R. A., et al. (2020) · Bipolar Disorders · doi:10.1111/bdi.13042 · Cited by 17
Bara, I., Darda, K. M., Kurz, A. S., & Ramsey, R. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15479 · Cited by 17
Sakaki, M., Meliß, S., Murayama, K., Yomogida, Y., Matsumori, K., Sugiura, A., Matsumoto, M., & Matsumoto, K. (2022) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-022-01046-4 · Cited by 19
Independent circuits in basal ganglia and cortex for the processing of reward and precision feedback
Pascucci, D., Hickey, C., Jovicich, J., & Turatto, M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.08.067 · Cited by 19
Yang, Q., Shao, R., Zhang, Q., Li, C., Li, Y., Li, H., & Lee, T. (2019) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.01.020 · Cited by 18
Cardinale, E. M., Breeden, A. L., Robertson, E., Lozier, L. M., VanMeter, J. W., & Marsh, A. A. (2017) · Development and Psychopathology · doi:10.1017/s0954579417001079 · Cited by 17
Genauck, A., Matthis, C., Andrejević, M., Ballon, L., Chiarello, F., Duecker, K., Heinz, A., Kathmann, N., & Romanczuk‐Seiferth, N. (2020) · Addiction Biology · doi:10.1111/adb.12951 · Cited by 16
Yan, Y., Hulbert, J. C., Zhuang, K., Liu, W., Wei, D., Qiu, J., Anderson, M. C., & Yang, W. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac336 · Cited by 16
Sustained upregulation of widespread hippocampal–neocortical coupling following memory encoding
Folvik, L., Sneve, M. H., Ness, H. T., Dídac Vidal-piñeiro, A., Raud, L., Geier, O. M., Walhovd, K. B., & Fjell, A. M. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac384 · Cited by 17
Does prefrontal connectivity during task switching help or hinder children’s performance?
Schwarze, S. A., Laube, C., Khosravani, N., Lindenberger, U., Bunge, S. A., & Fandakova, Y. (2023) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2023.101217 · Cited by 16
Functional network reconfiguration supporting memory-guided attention
Isenburg, K., Morin, T., Rosen, M. L., Somers, D. C., & Stern, C. E. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad073 · Cited by 16
Unruh, K. E., Bartolotti, J., McKinney, W. S., Schmitt, L., Sweeney, J. A., & Mosconi, M. W. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad177 · Cited by 16
Beffara, B., Hadj‐Bouziane, F., Hamed, S. B., Boehler, C. N., Chelazzi, L., Santandrea, E., & Macaluso, E. (2023) · Human Brain Mapping · doi:10.1002/hbm.26520 · Cited by 20
Satake, T., Taki, A., Kasahara, K., Yoshimaru, D., & Tsurugizawa, T. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1337976 · Cited by 17
Targeting VMPFC‐amygdala circuit with TMS in substance use disorder: A mechanistic framework
Soleimani, G., Conelea, C. A., Kuplicki, R., Opitz, A., Lim, K. O., Paulus, M. P., & Ekhtiari, H. (2025) · Addiction Biology · doi:10.1111/adb.70011 · Cited by 18
Orbitofrontal cortex connectivity as a mechanism of adolescent behavior change
Ewing, S. W. F., Chung, T. A., Caouette, J. D., Ketcherside, A., Hudson, K. A., & Filbey, F. M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.076 · Cited by 17
Neural network integration during the perception of in-group and out-group members
Greven, I. M., & Ramsey, R. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.09.036 · Cited by 15
Metadata
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review