The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Bayesian model selection for group studies
Open accessAbstract
Bayesian model selection (BMS) is a powerful method for determining the most likely among a set of competing hypotheses about the mechanisms that generated observed data. BMS has recently found widespread application in neuroimaging, particularly in the context of dynamic causal modelling (DCM). However, so far, combining BMS results from several subjects has relied on simple (fixed effects) metrics, e.g. the group Bayes factor (GBF), that do not account for group heterogeneity or outliers. In this paper, we compare the GBF with two random effects methods for BMS at the between-subject or group level. These methods provide inference on model-space using a classical and Bayesian perspective respectively. First, a classical (frequentist) approach uses the log model evidence as a subject-specific summary statistic. This enables one to use analysis of variance to test for differences in log-evidences over models, relative to inter-subject differences. We then consider the same problem in Bayesian terms and describe a novel hierarchical model, which is optimised to furnish a probability density on the models themselves. This new variational Bayes method rests on treating the model as a random variable and estimating the parameters of a Dirichlet distribution which describes the probabilities for all models considered. These probabilities then define a multinomial distribution over model space, allowing one to compute how likely it is that a specific model generated the data of a randomly chosen subject as well as the exceedance probability of one model being more likely than any other model. Using empirical and synthetic data, we show that optimising a conditional density of the model probabilities, given the log-evidences for each model over subjects, is more informative and appropriate than both the GBF and frequentist tests of the log-evidences. In particular, we found that the hierarchical Bayesian approach is considerably more robust than either of the other approaches in the presence of outliers. We expect that this new random effects method will prove useful for a wide range of group studies, not only in the context of DCM, but also for other modelling endeavours, e.g. comparing different source reconstruction methods for EEG/MEG or selecting among competing computational models of learning and decision-making.
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?
In the citing paper
“Such hidden individual differences can be detected by formulating alternative computational models, each reflecting different cognitive strategies, and subjecting them to Bayesian model selection (62).”
From Can Bayesian Theories of Autism Spectrum Disorder Help Improve Clinical Practice? (2016) · cites this paper as [62]
In the citing paper
“As is made clear in [19] the GBF approach implicitly assumes that every subject uses the same model. It is therefore a Fixed Effects analysis.”
From Comparing families of dynamic causal models (2010) · cites this paper as [19]
In the citing paper
“The robustness and accuracy of this method was verified via simulations using data from synthetic populations with known frequencies of competing models [19].”
From Comparing families of dynamic causal models (2010) · cites this paper as [19]
In the citing paper
“Additionally, the use of Gibbs sampling allows us to relax the assumption made in VB that the posterior densities over and factorise [19].”
From Comparing families of dynamic causal models (2010) · cites this paper as [19]
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
Estimating the Dimension of a Model
Schwarz, G. (1978) · The Annals of Statistics · doi:10.1214/aos/1176344136 · Cited by 47,033
Book Review: Pattern Recognition and Machine Learning
Nasrabadi, N. M. (2007) · Journal of Electronic Imaging · doi:10.1117/1.2819119 · Cited by 22,066
On Information and Sufficiency
Kullback, S., & Leibler, R. A. (1951) · The Annals of Mathematical Statistics · doi:10.1214/aoms/1177729694 · Cited by 20,193
Kass, R. E., & Raftery, A. E. (1995) · Journal of the American Statistical Association · doi:10.1080/01621459.1995.10476572 · Cited by 12,558
Pattern Recognition and Machine Learning
(2007) · Kybernetes · doi:10.1108/03684920710743466 · Cited by 8,545
Information theory, inference, and learning algorithms
(2004) · Choice Reviews Online · doi:10.5860/choice.41-5949 · Cited by 6,536
Information Theory, Inference, and Learning Algorithms
(2004) · Kybernetes · doi:10.1108/03684920410534506 · Cited by 4,937
A Bayesian Analysis of Some Nonparametric Problems
Ferguson, T. S. (1973) · The Annals of Statistics · doi:10.1214/aos/1176342360 · Cited by 4,814
Friston, K. J., Harrison, L., & Penny, W. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00202-7 · Cited by 4,583
Self-citation
Cited by
Sorted by citations
Model-based influences on humans’ choices and striatal prediction errors
Daw, N. D., Gershman, S. J., Seymour, B., Dayan, P., & Dolan, R. J. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.027 · Cited by 1,779
Goulden, N., Khusnulina, A., Davis, N. J., Bracewell, R. M., Bokde, A. L., McNulty, J. P., & Mullins, P. G. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.052 · Cited by 810
Ten simple rules for dynamic causal modeling
Stephan, K. E., Penny, W. D., Moran, R. J., den Ouden, H. E. M., Daunizeau, J., & Friston, K. J. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.015 · Cited by 803
Self-citationNeural computations underlying arbitration between model-based and model-free learning
Lee, S. W., Shimojo, S., & O’Doherty, J. P. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.028 · Cited by 642
Comparing families of dynamic causal models
Penny, W. D., Stephan, K. E., Daunizeau, J., Rosa, M. J., Friston, K. J., Schofield, T. M., & Leff, A. P. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000709 · Cited by 688
Self-citationMapping the self in the brain's default mode network
Davey, C. G., Pujol, J., & Harrison, B. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.022 · Cited by 559
Hare, T. A., Malmaud, J., & Rangel, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6383-10.2011 · Cited by 556
Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
Huys, Q. J., Pizzagalli, D. A., Bogdan, R., & Dayan, P. (2013) · Biology of Mood & Anxiety Disorders · doi:10.1186/2045-5380-3-12 · Cited by 480
Attention reverses the effect of prediction in silencing sensory signals
Kok, P., Rahnev, D., Jehee, J. F. M., Lau, H. C., & de Lange, F. P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr310 · Cited by 430
Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
Stephan, K. E., Manjaly, Z. M., Mathys, C. D., Weber, L. A. E., Paliwal, S., Gard, T., Tittgemeyer, M., Fleming, S. M., Haker, H., Seth, A. K., et al. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00550 · Cited by 437
“The evidence represents a principled measure of the goodness of a generative model which trades-off accuracy and complexity (Stephan et al., 2009; Penny, 2012); notably, its logarithm relates to the information-theoretic concept of (Shannon) surprise, S (sometimes also referred to as surprisal or…”
BackgroundSelf-citationNeural evidence for inequality-averse social preferences
Tricomi, E., Rangel, A., Camerer, C. F., & O’Doherty, J. P. (2010) · Nature · doi:10.1038/nature08785 · Cited by 462
VBA: A Probabilistic Treatment of Nonlinear Models for Neurobiological and Behavioural Data
Daunizeau, J., Adam, V., & Rigoux, L. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003441 · Cited by 385
Hierarchical Prediction Errors in Midbrain and Basal Forebrain during Sensory Learning
Iglesias, S., Mathys, C., Brodersen, K. H., Kasper, L., Piccirelli, M., den Ouden, H. E. M., & Stephan, K. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.009 · Cited by 342
Self-citationComputations of uncertainty mediate acute stress responses in humans
de Berker, A. O., Rutledge, R. B., Mathys, C., Marshall, L., Cross, G. F., Dolan, R. J., & Bestmann, S. (2016) · Nature Communications · doi:10.1038/ncomms10996 · Cited by 330
Dynamic causal modelling: A critical review of the biophysical and statistical foundations
Daunizeau, J., David, O., & Stephan, K. E. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.062 · Cited by 331
Self-citationCortical Hierarchies Perform Bayesian Causal Inference in Multisensory Perception
Rohe, T., & Noppeney, U. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002073 · Cited by 344
Six problems for causal inference from fMRI
Ramsey, J. D., Hanson, S. J., Hanson, C., Halchenko, Y. O., Poldrack, R. A., & Glymour, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.065 · Cited by 337
Hierarchical active inference: A theory of motivated control
Pezzulo, G., Rigoli, F., & Friston, K. J. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.01.009 · Cited by 334
Self-citationMapping value based planning and extensively trained choice in the human brain
Wunderlich, K., Dayan, P., & Dolan, R. J. (2012) · Nature Neuroscience · doi:10.1038/nn.3068 · Cited by 310
Striatal Prediction Error Modulates Cortical Coupling
den Ouden, H. E. M., Daunizeau, J., Roiser, J., Friston, K. J., & Stephan, K. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4458-09.2010 · Cited by 304
Self-citationComputational psychiatry: towards a mathematically informed understanding of mental illness
Adams, R. A., Huys, Q. J. M., & Roiser, J. P. (2015) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2015-310737 · Cited by 285
Neural mechanisms underlying motivation of mental versus physical effort
Schmidt, L., Lebreton, M., Cléry-Melin, M.-L., Daunizeau, J., & Pessiglione, M. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001266 · Cited by 310
Comparing dynamic causal models using AIC, BIC and free energy
Penny, W. D. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.039 · Cited by 298
Self-citationComputational approaches to psychiatry
Stephan, K. E., & Mathys, C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.007 · Cited by 260
Self-citationNicholson, 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
Deconstructing the human algorithms for exploration
Gershman, S. J. (2018) · Cognition · doi:10.1016/j.cognition.2017.12.014 · Cited by 267
The hierarchical organization of the lateral prefrontal cortex
Nee, D. E., & D'Esposito, M. (2016) · eLife · doi:10.7554/elife.12112 · Cited by 233
A step-by-step tutorial on active inference and its application to empirical data
Smith, R., Friston, K. J., & Whyte, C. J. (2022) · Journal of Mathematical Psychology · doi:10.1016/j.jmp.2021.102632 · Cited by 246
Self-citationAttentional Enhancement of Auditory Mismatch Responses: a DCM/MEG Study
Auksztulewicz, R., & Friston, K. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu323 · Cited by 227
Self-citationDeserno, L., Huys, Q. J. M., Boehme, R., Buchert, R., Heinze, H.-J., Grace, A. A., Dolan, R. J., Heinz, A., & Schlagenhauf, F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417219112 · Cited by 233
The dopaminergic midbrain encodes the expected certainty about desired outcomes
Schwartenbeck, P., FitzGerald, T. H. B., Mathys, C., Dolan, R., & Friston, K. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu159 · Cited by 219
Self-citationActive inference on discrete state-spaces: A synthesis
Da Costa, L., Parr, T., Sajid, N., Veselic, S., Neacsu, V., & Friston, K. (2020) · Journal of Mathematical Psychology · doi:10.1016/j.jmp.2020.102447 · Cited by 226
Self-citationHauser, T. U., Iannaccone, R., Walitza, S., Brandeis, D., & Brem, S. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.018 · Cited by 203
Bifurcation in brain dynamics reveals a signature of conscious processing independent of report
Sergent, C., Corazzol, M., Labouret, G., Stockart, F., Wexler, M., King, J.-R., Meyniel, F., & Pressnitzer, D. (2021) · Nature Communications · doi:10.1038/s41467-021-21393-z · Cited by 200
Inferring on the intentions of others by hierarchical Bayesian learning
Diaconescu, A. O., Mathys, C., Weber, L. A. E., Daunizeau, J., Kasper, L., Lomakina, E. I., Fehr, E., & Stephan, K. E. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003810 · Cited by 219
Self-citationReduced prefrontal-parietal effective connectivity and working memory deficits in schizophrenia
Deserno, L., Sterzer, P., Wüstenberg, T., Heinz, A., & Schlagenhauf, F. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3405-11.2012 · Cited by 214
Neural Mechanisms of Belief Inference during Cooperative Games
Yoshida, W., Seymour, B., Friston, K. J., & Dolan, R. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5895-09.2010 · Cited by 212
Self-citationAnalyzing effective connectivity with functional magnetic resonance imaging
Stephan, K. E., & Friston, K. J. (2010) · WIREs Cognitive Science · doi:10.1002/wcs.58 · Cited by 202
Self-citationAnterior insular cortex plays a critical role in interoceptive attention
Wang, X., Wu, Q., Egan, L., Gu, X., Liu, P., Gu, H., Yang, Y., Luo, J., Wu, Y., Gao, Z., et al. (2019) · eLife · doi:10.7554/elife.42265 · Cited by 204
Dopaminergic Genes Predict Individual Differences in Susceptibility to Confirmation Bias
Doll, B. B., Hutchison, K. E., & Frank, M. J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6486-10.2011 · Cited by 184
The neural dynamics of hierarchical Bayesian causal inference in multisensory perception
Rohe, T., Ehlis, A.-C., & Noppeney, U. (2019) · Nature Communications · doi:10.1038/s41467-019-09664-2 · Cited by 187
Stratified medicine for mental disorders
Schumann, G., Binder, E. B., Holte, A., de Kloet, E. R., Oedegaard, K. J., Robbins, T. W., Walker-Tilley, T. R., Bitter, I., Brown, V. J., Buitelaar, J., et al. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.09.010 · Cited by 186
Self-citationA computational reward learning account of social media engagement
Lindström, B., Bellander, M., Schultner, D. T., Chang, A., Tobler, P. N., & Amodio, D. M. (2021) · Nature Communications · doi:10.1038/s41467-020-19607-x · Cited by 185
Skvortsova, V., Palminteri, S., & Pessiglione, M. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1350-14.2014 · Cited by 177
Cho, Y. T., Fromm, S., Guyer, A. E., Detloff, A., Pine, D. S., Fudge, J. L., & Ernst, M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.013 · Cited by 173
The brain’s functional network architecture reveals human motives
Hein, G., Morishima, Y., Leiberg, S., Sul, S., & Fehr, E. (2016) · Science · doi:10.1126/science.aac7992 · Cited by 165
Modelling trial-by-trial changes in the mismatch negativity
Lieder, F., Daunizeau, J., Garrido, M. I., Friston, K. J., & Stephan, K. E. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002911 · Cited by 168
Hauser, T. U., Iannaccone, R., Ball, J., Mathys, C., Brandeis, D., Walitza, S., & Brem, S. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1093 · Cited by 168
Nicholson, A. A., Friston, K. J., Zeidman, P., Harricharan, S., McKinnon, M. C., Densmore, M., Neufeld, R. W. J., Théberge, J., Corrigan, F., Jetly, R., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23748 · Cited by 159
Self-citationKlein-Flügge, M. C., Kennerley, S. W., Saraiva, A. C., Penny, W. D., & Bestmann, S. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004116 · Cited by 163
“BMC at the group level, also known as random effects model [101,102], has become a standard statistical test in the fields of neuroimaging and behavioral modeling ([101] cited> 250 times).”
BackgroundMethodGenerative embedding for model-based classification of fMRI data
Brodersen, K. H., Schofield, T. M., Leff, A. P., Ong, C. S., Lomakina, E. I., Buhmann, J. M., & Stephan, K. E. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002079 · Cited by 165
Self-citationTAPAS: An Open-Source Software Package for Translational Neuromodeling and Computational Psychiatry
Frässle, S., Aponte, E. A., Bollmann, S., Brodersen, K. H., Do, C. T., Harrison, O. K., Harrison, S. J., Heinzle, J., Iglesias, S., Kasper, L., et al. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.680811 · Cited by 169
Self-citationAllefeld, C., Görgen, K., & Haynes, J.-D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.07.040 · Cited by 157
Jiang, J., Beck, J., Heller, K., & Egner, T. (2015) · Nature Communications · doi:10.1038/ncomms9165 · Cited by 160
Pharmacological Fingerprints of Contextual Uncertainty
Marshall, L., Mathys, C., Ruge, D., de Berker, A. O., Dayan, P., Stephan, K. E., & Bestmann, S. (2016) · PLOS Biology · doi:10.1371/journal.pbio.1002575 · Cited by 158
Self-citationSpatial attention, precision, and Bayesian inference: a study of saccadic response speed
Vossel, S., Mathys, C., Daunizeau, J., Bauer, M., Driver, J., Friston, K. J., & Stephan, K. E. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs418 · Cited by 146
Self-citationBrain networks for confidence weighting and hierarchical inference during probabilistic learning
Meyniel, F., & Dehaene, S. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1615773114 · Cited by 138
Comparing Bayesian and non-Bayesian accounts of human confidence reports
Adler, W. T., & Ma, W. J. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006572 · Cited by 118
A hemodynamic model for layered BOLD signals
Heinzle, J., Koopmans, P. J., den Ouden, H. E. M., Raman, S., & Stephan, K. E. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.025 · Cited by 144
Self-citationCompulsivity reveals a novel dissociation between action and confidence
Vaghi, M. M., Luyckx, F., Sule, A., Fineberg, N. A., Robbins, T. W., & De Martino, B. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.006 · Cited by 145
Can Bayesian Theories of Autism Spectrum Disorder Help Improve Clinical Practice?
Haker, H., Schneebeli, M., & Stephan, K. E. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00107 · Cited by 130
Self-citationThe Control of Mimicry by Eye Contact Is Mediated by Medial Prefrontal Cortex
Wang, Y., Ramsey, R., & de C. Hamilton, A. F. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0845-11.2011 · Cited by 141
Confidence controls perceptual evidence accumulation
Balsdon, T., Wyart, V., & Mamassian, P. (2020) · Nature Communications · doi:10.1038/s41467-020-15561-w · Cited by 137
A predictive coding account of bistable perception - a model-based fMRI study
Weilnhammer, V., Stuke, H., Hesselmann, G., Sterzer, P., & Schmack, K. (2017) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005536 · Cited by 120
Doubly Bayesian Analysis of Confidence in Perceptual Decision-Making
Aitchison, L., Bang, D., Bahrami, B., & Latham, P. E. (2015) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1004519 · Cited by 131
Model averaging, optimal inference, and habit formation
FitzGerald, T. H. B., Dolan, R. J., & Friston, K. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00457 · Cited by 121
Self-citationGeneralization of value in reinforcement learning by humans
Wimmer, G. E., Daw, N. D., & Shohamy, D. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08017.x · Cited by 111
Computational nosology and precision psychiatry
Friston, K. J., Redish, A. D., & Gordon, J. A. (2017) · Computational Psychiatry · doi:10.1162/cpsy_a_00001 · Cited by 126
Self-citationChennu, S., Noreika, V., Gueorguiev, D., Shtyrov, Y., Bekinschtein, T. A., & Henson, R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1125-16.2016 · Cited by 107
Impaired top-down processes in schizophrenia: a DCM study of ERPs
Dima, D., Dietrich, D. E., Dillo, W., & Emrich, H. M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.086 · Cited by 122
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
Encoding of Stimulus Probability in Macaque Inferior Temporal Cortex
Bell, A. H., Summerfield, C., Morin, E. L., Malecek, N. J., & Ungerleider, L. G. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.007 · Cited by 118
Cross, K. A., Torrisi, S., Reynolds Losin, E. A., & Iacoboni, M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.060 · Cited by 113
Effective connectivity analysis demonstrates involvement of premotor cortex during speech perception
Osnes, B., Hugdahl, K., & Specht, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.078 · Cited by 112
Flexible combination of reward information across primates
Farashahi, S., Donahue, C. H., Hayden, B. Y., Lee, D., & Soltani, A. (2019) · Nature Human Behaviour · doi:10.1038/s41562-019-0714-3 · Cited by 112
An afferent white matter pathway from the pulvinar to the amygdala facilitates fear recognition
McFadyen, J., Mattingley, J. B., & Garrido, M. I. (2019) · eLife · doi:10.7554/elife.40766 · Cited by 115
Belief state representation in the dopamine system
Babayan, B. M., Uchida, N., & Gershman, S. J. (2018) · Nature Communications · doi:10.1038/s41467-018-04397-0 · Cited by 101
Autonomic and brain responses associated with empathy deficits in autism spectrum disorder
Gu, X., Eilam‐Stock, T., Zhou, T., Anagnostou, E., Kolevzon, A., Soorya, L., Hof, P. R., Friston, K. J., & Fan, J. (2015) · Human Brain Mapping · doi:10.1002/hbm.22840 · Cited by 110
Self-citationModeling ketamine effects on synaptic plasticity during the mismatch negativity
Schmidt, A., Diaconescu, A. O., Kometer, M., Friston, K. J., Stephan, K. E., & Vollenweider, F. X. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs238 · Cited by 109
Self-citationSchlösser, R. G. M., Wagner, G., Schachtzabel, C., Peikert, G., Koch, K., Reichenbach, J. R., & Sauer, H. (2010) · Human Brain Mapping · doi:10.1002/hbm.20980 · Cited by 111
Acerbi, L., Dokka, K., Angelaki, D. E., & Ma, W. J. (2018) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1006110 · Cited by 111
Cortical coupling reflects Bayesian belief updating in the deployment of spatial attention
Vossel, S., Mathys, C., Stephan, K. E., & Friston, K. J. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1382-15.2015 · Cited by 99
Self-citationThe impact of evidence reliability on sensitivity and bias in decision confidence.
Boldt, A., de Gardelle, V., & Yeung, N. (2017) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037/xhp0000404 · Cited by 110
Kraehenmann, R., Schmidt, A., Friston, K., Preller, K. H., Seifritz, E., & Vollenweider, F. X. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.08.009 · Cited by 104
Self-citationThe Tortoise and the Hare: Interactions between Reinforcement Learning and Working Memory
Collins, A. G. E. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01238 · Cited by 97
Evidence for surprise minimization over value maximization in choice behavior
Schwartenbeck, P., FitzGerald, T. H. B., Mathys, C., Dolan, R., Kronbichler, M., & Friston, K. (2015) · Scientific Reports · doi:10.1038/srep16575 · Cited by 96
Self-citationCooper, J. C., Dunne, S., Furey, T., & O'Doherty, J. P. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00114 · Cited by 101
Network activity underlying the illusory self‐attribution of a dummy arm
Limanowski, J., & Blankenburg, F. (2015) · Human Brain Mapping · doi:10.1002/hbm.22770 · Cited by 101
State anxiety biases estimates of uncertainty and impairs reward learning in volatile environments
Hein, T. P., de Fockert, J., & Ruiz, M. H. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2020.117424 · Cited by 99
Moran, R. J., Jung, F., Kumagai, T., Endepols, H., Graf, R., Dolan, R. J., Friston, K. J., Stephan, K. E., & Tittgemeyer, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022790 · Cited by 88
“fixed effects analysis of the models was performed using the group Bayes factor [47,50], with log-evidences averaged over hemi-”
MethodSelf-citationSchmidt, A., Smieskova, R., Aston, J., Simon, A., Allen, P., Fusar-Poli, P., McGuire, P. K., Riecher-Rössler, A., Stephan, K. E., & Borgwardt, S. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.117 · Cited by 93
Self-citationLong-lasting crossmodal cortical reorganization triggered by brief postnatal visual deprivation
Collignon, O., Dormal, G., de Heering, A., Lepore, F., Lewis, T. L., & Maurer, D. (2015) · Current Biology · doi:10.1016/j.cub.2015.07.036 · Cited by 94
Causal evidence for lateral prefrontal cortex dynamics supporting cognitive control
Nee, D. E., & D'Esposito, M. (2017) · eLife · doi:10.7554/elife.28040 · Cited by 87
Hauser, T. U., Iannaccone, R., Dolan, R. J., Ball, J., Hättenschwiler, J., Drechsler, R., Rufer, M., Brandeis, D., Walitza, S., & Brem, S. (2017) · Psychological Medicine · doi:10.1017/s0033291716003305 · Cited by 86
Blunted medial prefrontal cortico-limbic reward-related effective connectivity and depression
Rupprechter, S., Romaniuk, L., Series, P., Hirose, Y., Hawkins, E., Sandu, A.-L., Waiter, G. D., McNeil, C. J., Shen, X., Harris, M. A., et al. (2020) · Brain · doi:10.1093/brain/awaa106 · Cited by 80
The hippocampus extrapolates beyond the view in scenes: an fMRI study of boundary extension
Chadwick, M. J., Mullally, S. L., & Maguire, E. A. (2013) · Cortex · doi:10.1016/j.cortex.2012.11.010 · Cited by 80
Evidence for model-based computations in the human amygdala during Pavlovian conditioning
Prévost, C., McNamee, D., Jessup, R. K., Bossaerts, P., & O'Doherty, J. P. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002918 · Cited by 79
Attractor-like dynamics in belief updating in schizophrenia
Adams, R. A., Napier, G., Roiser, J. P., Mathys, C., & Gilleen, J. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.3163-17.2018 · Cited by 77
Consistent spectral predictors for dynamic causal models of steady-state responses
Moran, R. J., Stephan, K. E., Dolan, R. J., & Friston, K. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.012 · Cited by 75
Self-citationMulti-subject analyses with dynamic causal modeling
Kasess, C. H., Stephan, K. E., Weissenbacher, A., Pezawas, L., Moser, E., & Windischberger, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.037 · Cited by 70
Self-citation
Metadata
- Authors
- Stephan, K. E., Penny, W. D., Daunizeau, J., Moran, R. J., & Friston, K. J.
- Affiliations
- Wellcome Centre for Human Neuroimaging (GB)
- Corresponding author
- Stephan, Klaas Enno
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 46
- Issue
- 4
- Pages
- 1004-1017
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC2703732
- OpenAlex
- W2135173838
- Cited by
- 1,423
- References
- 49
- Citations by year
- 2026: 63 · 2025: 74 · 2024: 76 · 2023: 71 · 2022: 86 · 2021: 100 · 2020: 135 · 2019: 97 · 2018: 102 · 2017: 91 · 2016: 89 · 2015: 109 · 2014: 67 · 2013: 75 · 2012: 59
- FWCI
- 51.46
- Type
- journal article
- Language
- en
- Open access
- green
- www.zora.uzh.ch
- Licence
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, other-oa)
- PubMed Central (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Explore Bristol Research (submittedVersion)
- UEA Digital Repository (University of East Anglia) (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- Wellcome Trust (056750, 088130)
- Topics
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods and Bayesian Inference
- Physical Sciences › Computer Science › Artificial Intelligence › Bayesian Modeling and Causal Inference
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Keywords
- Bayesian model selection, group study, dynamic causal modeling, random effects, Bayesian hierarchical model, variational inference, outliers, exceedance probability, Dirichlet distribution, model comparison
- MeSH terms
- Algorithms, Bayes Theorem, Brain, Cognition, Diagnostic Imaging, Humans, Models, Neurological
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