Citations
1824 | Bayes factors
- Kass, Raftery
- 1995
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Citation Context ...he accuracy with the number of modes (left bar graph) but in the context of increasing model complexity (right bar graph). The complexity is just the difference between the free energy and accuracy. (=-=Kass and Raftery, 1995-=-)), one could consider Bayesian averaging over models (Penny et al., 2010); such that the posterior expectations are weighted by the respective evidence for their model. However, in our case, the winn... |
627 |
A default mode of brain function
- Raichle, MacLeod, et al.
- 2001
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Citation Context ...tersen, 1998; Price, 2000). The second contrast was “fixation>all tasks” and identified four task-induced deactivations that are part of the well-known default mode network (Greicius and Menon, 2004; =-=Raichle et al., 2001-=-)—including bilateral inferior parietal lobule, posterior cingulate cortex and medial prefrontal cortex (Fig. 1). Our rationale – of selecting nodes with both task-induced activations and deactivation... |
609 |
Complex brain networks: graph theoretical analysis of structural and functional systems.
- Bullmore, Sporns
- 2009
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Citation Context ...or random fluctuations (Valdes-Sosa et al., 2011). Recently, there has been growing interest in the modelling of larger networks or graphs, which we take to imply graphs with sixteen or more regions (=-=Bullmore and Sporns, 2009-=-; Guye et al., 2010; He and Evans, 2010). These analyses are usually required to contextualise the activity in subgraphs, within the setting of a larger distributed network—or to provide estimates of ... |
416 |
Dynamic causal modelling.
- Friston
- 2003
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Citation Context ...vity beyond the subgraphs normally examined in DCM. © 2012 Elsevier Inc. All rights reserved. Introduction Usually, analyses of directed (effective) connectivity using dynamic causal modelling (DCM) (=-=Friston et al., 2003-=-) on fMRI data consider a small number of regions (e.g., less than 10 regions), typically excited by carefully designed experimental manipulations (for a review see (Friston, 2011b; Seghier et al., 20... |
307 | Complex network measures of brain connectivity: uses and interpretations,”
- Rubinov, Sporns
- 2010
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Citation Context ...network—or to provide estimates of effective connectivity for subsequent characterisation with graph theory measures such as characteristic path length, modularity, centrality and network resilience (=-=Rubinov and Sporns, 2010-=-). However, increasing the number of regions or nodes in a DCM presents some problems. Clearly, the number of extrinsic (between-node) connections or edges increases with the square of the number of n... |
173 | Classical and Bayesian inference in neuroimaging: Theory.
- Friston, Penny, et al.
- 2002
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Citation Context ...ctor θ. The posterior probabilities of the model parameters θ=(A,B,C,H) are assessed with Bayesian inversion using standard variational techniques based upon the Laplace approximation (Friston, 2002; =-=Friston et al., 2002-=-, 2007a). In this Bayesian inversion framework, two quantities are estimated (e.g. (Daunizeau et al., 2011)): (i) the posterior distribution over model parameters p(θ|M,Y), which can be used to ð1Þ ma... |
169 |
Consistent resting-state networks across healthy subjects.
- Damoiseaux, Rombouts, et al.
- 2006
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Citation Context ...uted brain responses are mediated by coupling among spatial patterns or modes (Friston, 2009), of the sort seen in resting state functional connectivity studies; see for example (Biswal et al., 2010; =-=Damoiseaux et al., 2006-=-; Smith et al., 2009; Yeo et al., 2011). This means that the connections among individual regions can be replaced by connections among modes. Because we can control the number of modes, one can place ... |
126 |
Correspondence of the brain’s functional architecture during activation and rest.
- Smith, Fox, et al.
- 2009
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Citation Context ...mediated by coupling among spatial patterns or modes (Friston, 2009), of the sort seen in resting state functional connectivity studies; see for example (Biswal et al., 2010; Damoiseaux et al., 2006; =-=Smith et al., 2009-=-; Yeo et al., 2011). This means that the connections among individual regions can be replaced by connections among modes. Because we can control the number of modes, one can place an upper bound on th... |
123 |
Toward discovery science of human brain function,”
- Biswal, Mennes, et al.
- 2010
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Citation Context ...pothesis that distributed brain responses are mediated by coupling among spatial patterns or modes (Friston, 2009), of the sort seen in resting state functional connectivity studies; see for example (=-=Biswal et al., 2010-=-; Damoiseaux et al., 2006; Smith et al., 2009; Yeo et al., 2011). This means that the connections among individual regions can be replaced by connections among modes. Because we can control the number... |
114 | Comparing dynamic causal models.
- Penny, Stephan, et al.
- 2004
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Citation Context ...ution is based on plausible priors that effectively constrain the number of extrinsic coupling parameters. Crucially, the plausibility of these priors can be established by Bayesian model comparison (=-=Penny et al., 2004-=-, 2010). This approach is based upon the hypothesis that distributed brain responses are mediated by coupling among spatial patterns or modes (Friston, 2009), of the sort seen in resting state functio... |
109 | Variational free energy and the Laplace approximation.
- Friston, Mattout, et al.
- 2007
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Citation Context ... region can still have its own hemodynamic response function. It is also worth noting that priors on the noise precision at each node remain independent (for more details see (Daunizeau et al., 2009; =-=Friston et al., 2007a-=-; Li et al., 2011)). Note that the use of modes – as prior constraints on coupling among nodes – is similar to but formally distinct from modelling the coupling among modes per se; e.g. (Stevens et al... |
89 |
Neuroimaging studies of word reading.
- Fiez, Petersen
- 1998
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Citation Context ... cortex and anterior cingulate (BA 10/24) −2 40 −10 activations during reading aloud relative to fixation – including a large bilateral set of visual, auditory, phonological and articulatory regions (=-=Fiez and Petersen, 1998-=-; Price, 2000). The second contrast was “fixation>all tasks” and identified four task-induced deactivations that are part of the well-known default mode network (Greicius and Menon, 2004; Raichle et a... |
72 |
Functional–anatomic fractionation of the brain’s default network.
- Andrews-Hanna, Reidler, et al.
- 2010
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Citation Context ...mbedding as detailed in Friston et al., 2011). This revealed for instance a difference in the strength of bidirectional coupling between the core midline regions of the default mode network (as hubs (=-=Andrews-Hanna et al., 2010-=-)), with the other nodes of the reading system (see nodes 19 and 20 of Fig. 6C). We will not comment further on this connectivity graph; however, many readers will note that the underlying weighted ad... |
67 | Bayesian estimation of dynamical systems: an application to fMRI.
- Friston
- 2002
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Citation Context ...are noted as vector θ. The posterior probabilities of the model parameters θ=(A,B,C,H) are assessed with Bayesian inversion using standard variational techniques based upon the Laplace approximation (=-=Friston, 2002-=-; Friston et al., 2002, 2007a). In this Bayesian inversion framework, two quantities are estimated (e.g. (Daunizeau et al., 2011)): (i) the posterior distribution over model parameters p(θ|M,Y), which... |
61 | Default-mode activity during a passive sensory task: Uncoupled from deactivation but impacting activation. - Greicius, Menon - 2004 |
55 |
Graph theoretical modeling of brain connectivity,”
- He, Evans
- 2010
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Citation Context ...11). Recently, there has been growing interest in the modelling of larger networks or graphs, which we take to imply graphs with sixteen or more regions (Bullmore and Sporns, 2009; Guye et al., 2010; =-=He and Evans, 2010-=-). These analyses are usually required to contextualise the activity in subgraphs, within the setting of a larger distributed network—or to provide estimates of effective connectivity for subsequent c... |
38 | Functional and effective connectivity: a review,”
- Friston
- 2011
(Show Context)
Citation Context ...elling (DCM) (Friston et al., 2003) on fMRI data consider a small number of regions (e.g., less than 10 regions), typically excited by carefully designed experimental manipulations (for a review see (=-=Friston, 2011b-=-; Seghier et al., 2010b)). In terms of graph theory, this corresponds to a characterisation of subgraphs that are exposed to exogenous input—where these inputs can be experimental (stimulus) functions... |
33 |
The identification of interacting networks in the brain using fMRI: model selection, causality and deconvolution,”
- Roebroeck, Formisano, et al.
- 2009
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Citation Context ...distributed processing. The selection of candidate nodes for subsequent DCM analysis is generally motivated by one of two aims: network discovery through structural model selection (see discussion in =-=Roebroeck et al., 2011-=-) or testing hypotheses about specific connections. In the latter context,190 M.L. Seghier, K.J. Friston / NeuroImage 68 (2013) 181–191 inferences on models with a small number of nodes are generally... |
31 |
Dynamic causal modelling: A critical review of the biophysical and statistical foundations,
- Daunizeau, David, et al.
- 2011
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Citation Context ...Fax: +44 20 7813 1420. E-mail address: m.seghier@ucl.ac.uk (M.L. Seghier). This can lead to models with enormous numbers of free parameters and profound conditional dependencies among the parameters (=-=Daunizeau et al., 2011-=-). Furthermore, the computational time required to invert these models grows exponentially with the number of free parameters. In this paper, we present a simple solution to the inversion of large DCM... |
28 |
Effective connectivity: influence, causality and biophysical modeling. Neuroimage 58, 339–361. doi: 10.1016/j.neuroimage.2011.03.058
- Valdes-Sosa, Roebroeck, et al.
- 2011
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Citation Context .... In terms of graph theory, this corresponds to a characterisation of subgraphs that are exposed to exogenous input—where these inputs can be experimental (stimulus) functions or random fluctuations (=-=Valdes-Sosa et al., 2011-=-). Recently, there has been growing interest in the modelling of larger networks or graphs, which we take to imply graphs with sixteen or more regions (Bullmore and Sporns, 2009; Guye et al., 2010; He... |
27 | Comparing families of dynamic causal models.
- Penny, Stephan, et al.
- 2010
(Show Context)
Citation Context ...ncreasing model complexity (right bar graph). The complexity is just the difference between the free energy and accuracy. (Kass and Raftery, 1995)), one could consider Bayesian averaging over models (=-=Penny et al., 2010-=-); such that the posterior expectations are weighted by the respective evidence for their model. However, in our case, the winning model had a sufficiently high log evidence to make this Bayesian para... |
26 |
Variational Bayesian identification and prediction of stochastic nonlinear dynamic causal models
- Daunizeau, Friston, et al.
- 2009
(Show Context)
Citation Context ... unchanged and thus each region can still have its own hemodynamic response function. It is also worth noting that priors on the noise precision at each node remain independent (for more details see (=-=Daunizeau et al., 2009-=-; Friston et al., 2007a; Li et al., 2011)). Note that the use of modes – as prior constraints on coupling among nodes – is similar to but formally distinct from modelling the coupling among modes per ... |
25 |
Modalities, modes, and models in functional neuroimaging”.
- Friston
- 2009
(Show Context)
Citation Context ...ablished by Bayesian model comparison (Penny et al., 2004, 2010). This approach is based upon the hypothesis that distributed brain responses are mediated by coupling among spatial patterns or modes (=-=Friston, 2009-=-), of the sort seen in resting state functional connectivity studies; see for example (Biswal et al., 2010; Damoiseaux et al., 2006; Smith et al., 2009; Yeo et al., 2011). This means that the connecti... |
24 |
Investigating the functional heterogeneity of the default mode network using coordinate-based meta-analytic modeling
- Laird, Eickhoff, et al.
- 2009
(Show Context)
Citation Context ...ive and negative posterior estimates of the coupling parameters and to explicitly model interactions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; Graves et al., 2010; =-=Laird et al., 2009-=-; Richardson et al., 2011; Seghier and Price, 2009; Seghier et al., 2010a; Wirth et al., 2011)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e., summary time seri... |
20 |
Dynamic causal modeling and Granger causality. Comments on: The identification of interacting networks in the brain using fMRI: Model selection, causality and deconvolution. Neuroimage 2009; doi:10.1016/j.neuroimage.2009.09.031
- Friston
(Show Context)
Citation Context ...s on models with a small number of nodes are generally sufficient, given that conditional estimates of effective connectivity from a full graph are often consistent with estimates based on subgraphs (=-=Friston, 2011a-=-). In the setting of network discovery, our approach enables the inversion of large DCMs that can then be submitted to graph theory and related analyses. In principle, the analyses described in this p... |
19 |
Graph theoretical analysis of structural and functional connectivity MRI in normal and pathological brain networks.
- Guye, Bettus, et al.
- 2010
(Show Context)
Citation Context ...des-Sosa et al., 2011). Recently, there has been growing interest in the modelling of larger networks or graphs, which we take to imply graphs with sixteen or more regions (Bullmore and Sporns, 2009; =-=Guye et al., 2010-=-; He and Evans, 2010). These analyses are usually required to contextualise the activity in subgraphs, within the setting of a larger distributed network—or to provide estimates of effective connectiv... |
18 |
Functional subdivisions in the left angular gyrus where the semantic system meets and diverges from the default network,”
- Seghier, Fagan, et al.
- 2010
(Show Context)
Citation Context ... explicitly model interactions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; Graves et al., 2010; Laird et al., 2009; Richardson et al., 2011; Seghier and Price, 2009; =-=Seghier et al., 2010a-=-; Wirth et al., 2011)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e., summary time series) were extracted from each subject (using voxels in subject-specific SP... |
17 |
Functional neural networks underlying response inhibition in adolescents and adults.
- Stevens, Kiehl, et al.
- 2007
(Show Context)
Citation Context ...et al., 2007a; Li et al., 2011)). Note that the use of modes – as prior constraints on coupling among nodes – is similar to but formally distinct from modelling the coupling among modes per se; e.g. (=-=Stevens et al., 2007-=-)). In other words, the DCM is still trying to explain region-specific activity in each node (as opposed to the activity of modes). This concludes our description of how functionally informed modes of... |
16 | Comparing dynamic causal models using AIC, BIC and free energy.
- Penny
- 2012
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Citation Context ...model p(Y|M), known as the model evidence or marginal likelihood. The log evidence is approximated by a negative (variational) free energy that is used for Bayesian model comparison or scoring (e.g. (=-=Penny, 2012-=-)). Further details about DCM for fMRI responses can be found elsewhere (Friston, 2011b; Seghier et al., 2010b). Priors on the parameters of DCM for fMRI In this work, we used the latest release of DC... |
15 |
Generalised filtering and stochastic DCM for fMRI
- Li, Daunizeau, et al.
- 2011
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Citation Context ...its own hemodynamic response function. It is also worth noting that priors on the noise precision at each node remain independent (for more details see (Daunizeau et al., 2009; Friston et al., 2007a; =-=Li et al., 2011-=-)). Note that the use of modes – as prior constraints on coupling among nodes – is similar to but formally distinct from modelling the coupling among modes per se; e.g. (Stevens et al., 2007)). In oth... |
12 |
Network discovery with DCM
- Friston, Li, et al.
- 2011
(Show Context)
Citation Context ...ber of a priori modes) could be applied to any fMRI time series using DCMs with full extrinsic connectivity. The model with the greatest evidence can then be pruned using post-hoc model optimisation (=-=Friston et al., 2011-=-) to provide posterior estimates for subsequent characterisation of the resulting directed graphs. We will illustrate these procedures using empirical data. This paper comprises three sections. In the... |
12 |
Identifying abnormal connectivity in patients using dynamic causal modeling of fMRI responses. Front Syst Neurosci
- Seghier, Zeidman, et al.
- 2010
(Show Context)
Citation Context ...iston et al., 2003) on fMRI data consider a small number of regions (e.g., less than 10 regions), typically excited by carefully designed experimental manipulations (for a review see (Friston, 2011b; =-=Seghier et al., 2010b-=-)). In terms of graph theory, this corresponds to a characterisation of subgraphs that are exposed to exogenous input—where these inputs can be experimental (stimulus) functions or random fluctuations... |
12 | Tractography-based priors for dynamic causal models. Neuroimage 47, 1628–1638. doi: 10.1016/j.neuroimage.2009.05.096
- Stephan, Weiskopf, et al.
- 2009
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Citation Context .... Interestingly, this is exactly the same as the use of (undirected probabilistic) anatomical connectivity, when using diffusion weighted imaging or tractography data to inform dynamic causal models (=-=Stephan et al., 2009-=-). The use of such informative constraints ensures that each node still has its own intrinsic connectivity and haemodynamic parameters, while enabling DCM to provide unbiased and more efficient estima... |
11 | Post hoc Bayesian model selection
- Friston, Penny
- 2011
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Citation Context ... intensive. This means the search for the optimal number of prior covariance (functional connectivity) modes may become prohibitive. However, this problem can be finessed using post-hoc optimisation (=-=Friston and Penny, 2011-=-). In other words, one would invert a full model (with no covariance constraints) and then evaluate the post-hoc model evidence (free energy) of reduced models, whose prior covariances have progressiv... |
11 | Neural systems for reading aloud: a multiparametric approach
- WW, Desai, et al.
- 2010
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Citation Context ...– was to ensure positive and negative posterior estimates of the coupling parameters and to explicitly model interactions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; =-=Graves et al., 2010-=-; Laird et al., 2009; Richardson et al., 2011; Seghier and Price, 2009; Seghier et al., 2010a; Wirth et al., 2011)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e... |
11 |
Dissociating functional brain networks by decoding the between-subject variability.
- Seghier, Price
- 2009
(Show Context)
Citation Context ...oupling parameters and to explicitly model interactions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; Graves et al., 2010; Laird et al., 2009; Richardson et al., 2011; =-=Seghier and Price, 2009-=-; Seghier et al., 2010a; Wirth et al., 2011)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e., summary time series) were extracted from each subject (using voxels... |
11 |
Inter-subject variability in the use of two different neuronal networks for reading aloud familiar words
- Seghier, Lee, et al.
- 2008
(Show Context)
Citation Context ...the selection of regions or nodes and the ensuing dynamic causal model. The empirical data came from a block-design fMRI activation study of 10 healthy subjects described in (Seghier and Price, 2010; =-=Seghier et al., 2008-=-). During two separate scanning sessions, subjects were asked to (i) read aloud 96 three to six letter object names with consistent spelling-to-sound relationships (e.g. hat, tent, horse, carrot); (ii... |
8 |
Multiple routes from occipital to temporal cortices during reading
- Richardson, Seghier, et al.
- 2011
(Show Context)
Citation Context ...terior estimates of the coupling parameters and to explicitly model interactions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; Graves et al., 2010; Laird et al., 2009; =-=Richardson et al., 2011-=-; Seghier and Price, 2009; Seghier et al., 2010a; Wirth et al., 2011)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e., summary time series) were extracted from e... |
7 |
The main sources of intersubject variability in neuronal activation for reading aloud
- Kherif, Josse, et al.
- 2009
(Show Context)
Citation Context ... projector, a front-projection screen and a system of mirrors attached to a head coil. Additional details about the paradigm and stimuli can be found in our previous descriptions of this study (c.f. (=-=Kherif et al., 2009-=-; Seghier and Price, 2010; Seghier et al., 2008)). fMRI data acquisition and analysis Data were acquired on a 1.5 T scanner (Siemens Medical Systems, Erlangen, Germany). Functional imaging consisted o... |
6 |
Distributed processing; distributed functions
- Fox, Friston
- 2012
(Show Context)
Citation Context ...ecent trends of using informed or tailored priors based on prior beliefs forwarded by models of anatomical connectivity—or on the basis of meta-analytic functional connectivity (see recent review in (=-=Fox and Friston, 2012-=-)). Future work needs to explore how our findings generalise to other DCM schemes, including stochastic DCM (Daunizeau et al., 2009; Li et al., 2011). Acknowledgments This work was funded by the Welco... |
6 | Reading aloud boosts connectivity through the putamen
- Seghier, Price
- 2010
(Show Context)
Citation Context ...the experimental design, the selection of regions or nodes and the ensuing dynamic causal model. The empirical data came from a block-design fMRI activation study of 10 healthy subjects described in (=-=Seghier and Price, 2010-=-; Seghier et al., 2008). During two separate scanning sessions, subjects were asked to (i) read aloud 96 three to six letter object names with consistent spelling-to-sound relationships (e.g. hat, ten... |
4 |
Semantic memory involvement in the default mode network: a functional neuroimaging study using independent component analysis. Neuroimage 54(4):3057–66
- Wirth, Jann, et al.
- 2011
(Show Context)
Citation Context ...actions between functionally heterogeneous networks (e.g. (AndrewsHanna et al., 2010; Graves et al., 2010; Laird et al., 2009; Richardson et al., 2011; Seghier and Price, 2009; Seghier et al., 2010a; =-=Wirth et al., 2011-=-)). After defining our 20 regions from the group analysis, principal eigenvariates (i.e., summary time series) were extracted from each subject (using voxels in subject-specific SPMs that survived a c... |
1 | Variational Bayes under the Laplace approximation - Friston, Mattout, et al. |