A Meta-analysis of Functional Neuroimaging Studies of Self- and Other Judgments Reveals a Spatial Gradient for Mentalizing in Medial Prefrontal Cortex
Open accessAbstract
The distinction between processes used to perceive and understand the self and others has received considerable attention in psychology and neuroscience. Brain findings highlight a role for various regions, in particular the medial PFC (mPFC), in supporting judgments about both the self and others. We performed a meta-analysis of 107 neuroimaging studies of self- and other-related judgments using multilevel kernel density analysis [Kober, H., & Wager, T. D. Meta-analyses of neuroimaging data. Wiley Interdisciplinary Reviews, 1, 293–300, 2010]. We sought to determine what brain regions are reliably involved in each judgment type and, in particular, what the spatial and functional organization of mPFC is with respect to them. Relative to nonmentalizing judgments, both self- and other judgments were associated with activity in mPFC, ranging from ventral to dorsal extents, as well as common activation of the left TPJ and posterior cingulate. A direct comparison between self- and other judgments revealed that ventral mPFC as well as left ventrolateral PFC and left insula were more frequently activated by self-related judgments, whereas dorsal mPFC, in addition to bilateral TPJ and cuneus, was more frequently activated by other-related judgments. Logistic regression analyses revealed that ventral and dorsal mPFC lay at opposite ends of a functional gradient: The z coordinates reported in individual studies predicted whether the study involved self- or other-related judgments, which were associated with increasingly ventral or dorsal portions of mPFC, respectively. These results argue for a distributed rather than localizationist account of mPFC organization and support an emerging view on the functional heterogeneity of mPFC.
AI snapshot
Written from the paper’s full text.
TL;DR
This meta-analysis of 107 functional neuroimaging studies found that self- and other-related judgments share medial prefrontal cortex (mPFC), left temporoparietal junction, and posterior cingulate activity, but differ in mPFC subregions. A logistic regression showed a dorsal–ventral spatial gradient in mPFC, with increasingly ventral activation associated with self judgments and increasingly dorsal activation associated with other judgments.
Key findings
- Across 107 published reports and 307 contrasts, both Self>Baseline and Other>Baseline involved broad mPFC activation from ventral to dorsal extents, plus common activation in left temporoparietal junction, posterior cingulate, and left middle temporal gyrus/superior temporal sulcus.
- Direct Self>Other comparisons activated vmPFC, including left rostral BA 10, anterior paracingulate cortex (BA 32), left ventrolateral PFC, left anterior and mid-insula, left dorsal caudate, thalamus, and left temporal pole; Other>Self activated bilateral dmPFC, bilateral TPJ, and cuneus.
- Logistic regression within mPFC used 47 Self contrasts and 43 Other contrasts from 33 and 34 studies, respectively; z coordinate significantly predicted Self vs. Other contrast status, while x and y coordinates did not. The scatterplot relating estimated self proportions to z coordinate showed r = −0.71, p < 0.01.
- The authors interpret the results as supporting a distributed gradient rather than discrete, localizationist modules for self- and other-related processing in mPFC.
Methods
- Literature search covered January 1995–February 2008 and included healthy, unmedicated adults, PET or fMRI, image subtraction, and Talairach/MNI coordinates; this yielded 107 reports and 307 contrasts, with 74 Self, 76 Other, and 24 Baseline contrasts drawn from 48, 48, and 19 studies, respectively.
- Multilevel Kernel Density Analysis (MKDA) registered peaks to MNI space, convolved them with a 10-mm spherical kernel, created Comparison Indicator Maps, weighted by square root of sample size, and thresholded with 5,000 Monte Carlo iterations at p < .05 FWE-corrected.
- A binary logistic regression predicted self vs. other activation status from MNI x, y, and z coordinates within an independently defined mPFC boundary (|x| < 25, y > 15, z > −5).
Limitations
- Stated: the relatively small number of studies within each Self/Other × judgment-type condition meant that differences between types of mental state judgments were not the focus; future work may test whether the gradient is specific to certain judgment types.
- Stated: 29 studies were coded but did not contribute contrasts because of the conservative coding algorithm, and contrasts reflecting both Self and Other judgments were excluded.
- Evident: as a coordinate-based meta-analysis, it relies on reported significant activation foci and cannot directly assess individual-study effect sizes, within-study variability, or the full range of mentalizing task designs.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 16 cited sources checked · 0 supported · 0 flagged
- Findingown data
Estimated self proportions correlated negatively with z coordinate within the mPFC boundary (r = −0.71, p < 0.01).
“Further, to illustrate the logistic regression result for the z coordinates in particular, a scatterplot showing estimated self proportions as a function of z coordinate within the mPFC boundary is shown in Figure 5 (r=−0.71, p<0.01).”
Quote in the paperSubstantial claim - Findingown data
Self-related judgments were associated with relatively ventral mPFC (BA 10) and anterior paracingulate cortex (BA 32).
“Consistent with prior work (Gilbert et al., 2006; Mitchell, Banaji, & Macrae, 2005; Mitchell et al., 2006; Northoff et al., 2006; Qin & Northoff, 2011; van der Meer et al., 2010), we found that self-related judgments were associated with relatively ventral mPFC (BA 10) and anterior paracingulate cortex (BA 32) whereas other-related judgments were associated with relatively dorsal mPFC (BA 8 & 9).”
Quote in the paperSubstantial claim - Findingown data
There was substantial functional overlap in left temporoparietal junction, posterior cingulate, and left middle temporal gyrus and superior temporal sulcus for self- and other-related judgments.
“While the overlap in mPFC was the most striking and extensive, there was substantial functional overlap in other areas of the brain as well, including left temporoparietal junction (TPJ), posterior cingulate, and left middle temporal gyrus and superior temporal sulcus, all of which have been previously associated with mentalizing about the beliefs, desires, perceptions, or emotions of oneself and”
Quote in the paperSubstantial claim - Findingown data
In direct comparison, other-related judgments more frequently activated dorsal mPFC, bilateral TPJ, and cuneus than self-related judgments.
“whereas dorsal mPFC (dmPFC), in addition to bilateral TPJ and cuneus, were more frequently activated by other-related judgments.”
- Also stated in: § MKDA Analyses: Regions involved in Processing Self, Other, or Both · boosted
“For the Other condition relative to the Self condition, robust bilateral dmPFC activity was observed, in addition to bilateral TPJ and cuneus activity (Supplementary Figure 2 and Supplementary Table 4).”
Quote in the paperSubstantial claim- The authors state this as an assumption: The null hypothesis for the Monte Carlo simulation was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.
- Also stated in: § MKDA Analyses: Regions involved in Processing Self, Other, or Both · boosted
- Findingown data
Within medial prefrontal cortex (mPFC), the z coordinate significantly predicted Self vs. Other contrast status.
“Within mPFC, logistic regression analyses showed a significant effect of z coordinate predicting Self vs. Other contrast status, while x and y coordinates were not significantly predictive (Table 1).”
Quote in the paperSubstantial claim
- Findingown data
Broad overlap was observed in both ventral and dorsal mPFC for self- and other-related judgments.
“Broad overlap was observed in both ventral and dorsal mPFC, which is consistent with prior work indicating that mPFC is involved in attending to one’s own or another’s mental state (Gilbert et al., 2006; Legrand & Ruby, 2009; Ochsner et al., 2005; Ochsner et al., 2004; Van Overwalle, 2011; Van Overwalle & Baetens, 2009).”
Quote in the paperSubstantial claim - Findingown data
Within mPFC, the x and y coordinates were not significantly predictive of Self vs. Other contrast status.
“Within mPFC, logistic regression analyses showed a significant effect of z coordinate predicting Self vs. Other contrast status, while x and y coordinates were not significantly predictive (Table 1).”
Quote in the paperSubstantial claim - Findingown data
Other-related judgments were associated with relatively dorsal mPFC (BA 8 & 9).
“Consistent with prior work (Gilbert et al., 2006; Mitchell, Banaji, & Macrae, 2005; Mitchell et al., 2006; Northoff et al., 2006; Qin & Northoff, 2011; van der Meer et al., 2010), we found that self-related judgments were associated with relatively ventral mPFC (BA 10) and anterior paracingulate cortex (BA 32) whereas other-related judgments were associated with relatively dorsal mPFC (BA 8 & 9).”
Quote in the paperSubstantial claim - Findingown data
The meta-analysis included 107 published reports involving 307 individual contrasts.
“We performed a meta-analysis of 107 neuroimaging studies of self- and other-related judgments using Multilevel Kernel Density Analysis (MKDA; Kober & Wager, 2010).”
- Also stated in: § Identification of Studies · plain
“This process yielded 107 published reports, which involved 307 individual contrasts (summarized in Supplementary Tables 1 & 2).”
Quote in the paperSubstantial claim - Also stated in: § Identification of Studies · plain
- Findingown data
The MKDA direct comparison showed apparently discrete and separate dorsal and ventral mPFC regions associated with other- and self-related judgments, respectively.
“Recall that this comparison showed apparently discrete and separate dorsal and ventral mPFC regions associated with other- and self-related judgments, respectively.”
Quote in the paperSubstantial claim - Findingcitation
Mentalizing (attention to mental state of either self or other) was associated with medial activation within mPFC, including BA 10.
“Consistent with Gilbert and colleagues, we found that mentalizing (i.e. attention to mental state of either self or other) was associated with medial activation within mPFC, including BA 10.”
Quote in the paperSubstantial claim - Study design and conductown data
A binary logistic regression was used to draw inferences about the spatial distribution of self vs. other representations unbiased by potential smoothing artifacts.
“In order to draw direct inferences about the spatial distribution of self vs. other representations that are unbiased by potential smoothing artifacts, we performed a binary logistic regression incorporating three continuous predictors (MNI-standardized x, y, and z coordinates for each point located within an independently-defined mPFC boundary) and one binary dependent variable (activation point”
Quote in the paperSubstantial claim - Interpretationown data
The suite of regions including mPFC, left TPJ, posterior cingulate, and left middle temporal gyrus/superior temporal sulcus is essential for making judgments about mental states regardless of whose states they are.
“As such, these results confirm the idea that this suite of regions is essential for making judgments about mental states – regardless of whose states they are.”
Quote in the paperSubstantial claim - Premisenone given
None of the prior meta-analyses quantitatively assessed the spatial organization of self and other judgment processing in mPFC.
“Indeed, none of the prior meta-analyses quantitatively assessed the nature of the spatial organization of self and other judgment processing in mPFC, and making inferences about this organization was a principal aim in the current study.”
Quote in the paperSubstantial claim - Premisecitation
Some apparent double dissociations may be more accurately conceptualized as gradients.
“The notion that some apparent double dissociations may be more accurately conceptualized as gradients has been described in other domains in the physiology and neuroimaging literature (Fuster, 2003, 2006), including in an fMRI examination of the medial temporal lobe regarding response profiles to objects and scenes (Litman, Awipi, & Davachi, 2009).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Fuster, 2003, 2006
Not checked in the free run.
- cites Litman, Awipi, & Davachi, 2009
Not checked in the free run.
- Interpretationreasoning
Increasingly ventral mPFC activity is more strongly associated with self-related "default" functional activity.
“The present results suggest that increasingly ventral activity is more strongly associated with self-related “default” functional activity, given that mPFC activity is also prominently observed during rest.”
Quote in the paperSubstantial claim - Interpretationcitation
Left ventrolateral PFC activity in self-related judgments plausibly reflects retrieval of information from semantic memory, given task demands requiring recall of personally-relevant information.
“Ventrolateral PFC, and in particular left vlPFC, has been associated with retrieval of information from semantic memory (Badre & Wagner, 2007; Thompson-Schill, Bedny, & Goldberg, 2005), and this represents a plausible functional explanation in this case, given task demands that required recalling personally-relevant information.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Badre & Wagner, 2007 source
Not checked in the free run.
- cites Thompson-Schill, Bedny, & Goldberg, 2005
Not checked in the free run.
- Interpretationreasoning
The results support a distributed rather than a localizationist account of the neural mechanisms that support judgments about the self and others.
“Thus, we argue that these results support a distributed rather than a localizationist account (cf. Poldrack, 2008) of the neural mechanisms that support judgments about the self others.”
Quote in the paperSubstantial claim - Interpretationcitation
Left anterior insula activity in self-related judgments is consistent with a role for interoception in self-related awareness involving the anterior insula.
“The left anterior insula findings are consistent with the results of another recent self-other meta-analysis (Qin et al., 2011; Qin & Northoff, 2011) and are consistent with a role for interoception in self-related awareness that involves the anterior insula (Craig, 2009; Denny, Ochsner, Weber, & Wager, in prep.; Wager & Barrett, 2004).”
Quote in the paperNot a substantial claim0 of 3 sources checked
- May combine two claims. 20
- Classified as probably not a substantial claim. 14
- The quote only partly states this claim. 1
May combine two claims.
Findingown dataSelf-related judgments were associated with almost entirely left-lateralized activity, including left ventrolateral PFC, left anterior and mid-insula, and dorsal caudate.
“In addition, self-related judgments were associated with almost entirely left-lateralized activity, including left ventrolateral PFC (vlPFC), left anterior and mid-insula, and dorsal caudate.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Findingown dataThe logistic regression analysis was performed on 47 Self contrasts and 43 Other contrasts within the mPFC region, drawn from 33 and 34 studies respectively.
“The resulting analysis was performed on 47 Self contrasts and 43 Other contrasts that reported activation points within this mPFC region. These contrasts were drawn from 33 studies for Self and 34 studies for Other.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataSelf- and other-related judgments are supported by both common and distinct groups of brain regions that include many regions implicated in mentalizing in prior work.
“Using a database of 107 published neuroimaging studies we reported evidence for self- and other-related judgments being (1) supported by both common and distinct groups of regions that include many implicated in mentalizing in prior work, and (2) associated with a spatial mentalizing gradient within mPFC, with increasingly ventral activation being increasingly associated with self-related judgment”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data29 studies were coded but did not contribute contrasts to the meta-analysis due to the conservative coding algorithm.
“As detailed in Supplementary Table 1, 29 studies were coded but did not contribute contrasts to the meta-analysis due to our conservative coding algorithm, described below.”
Quote in the paperNot a substantial claimMay combine two claims. The quote only partly states this claim.
Findingown dataRelative to non-mentalizing baseline, both self and other judgments were associated with activity in mPFC ranging from ventral to dorsal extents, as well as common activation of left temporoparietal junction, posterior cingulate, and left middle temporal gyrus/superior temporal sulcus.
“Relative to non-mentalizing judgments, both self and other judgments were associated with activity in mPFC, ranging from ventral to dorsal extents, as well as common activation of the left temporoparietal junction (TPJ) and posterior cingulate.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The null hypothesis for the Monte Carlo simulation was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataAcross Self and Other conditions, the mental state judgment types varied: affectively-relevant (17 Self, 19 Other), trait (11 Self, 14 Other), intentions (9 Self, 20 Other); cognitive/ToM contrasts were more often Other (22) than Self (2).
“Across Self and Other judgment conditions the nature of the mental state judgment varied, although for each judgment a comparable number of contrasts were coded as being affectively-relevant (17 for Self, 19 for Other), relating to trait judgments (11 for Self, 14 for Other), and relating to a target’s intentions (9 for Self, 20 for Other). Contrasts coded as cognitive, such as theory-of-mind judg”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataThe total number of contrasts per condition were 74 for Self, 76 for Other, and 24 for Baseline, drawn from 48, 48, and 19 studies respectively.
“The total number of contrasts that pertained to each condition were as follows: 74 for Self, 76 for Other, and 24 for Baseline. These contrasts were drawn from 48 studies for Self, 48 studies for Other, and 19 studies for Baseline (Supplementary Tables 1 & 2).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn direct comparison, self-related judgments more frequently activated ventral mPFC (including left rostral BA 10 and anterior paracingulate cortex BA 32), left ventrolateral PFC, left anterior and mid-insula, left dorsal caudate, thalamus, and left temporal pole than other-related judgments.
“A direct comparison between self and other judgments revealed that ventral mPFC (vmPFC), as well as left ventrolateral PFC and left insula, were more frequently activated by self-related judgments”
- Also stated in: § MKDA Analyses: Regions involved in Processing Self, Other, or Both · plain
“Figure 3 shows that the Self condition, relative to the Other condition, significantly activated vmPFC, including left rostral BA 10, anterior paracingulate cortex (BA 32), left ventrolateral PFC (vlPFC), left anterior and mid-insula, left dorsal caudate, thalamus, and left temporal pole.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The null hypothesis for the Monte Carlo simulation was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.
- Also stated in: § MKDA Analyses: Regions involved in Processing Self, Other, or Both · plain
May combine two claims.
Findingown dataSelf-related judgments were reliably associated with activation along the cortical midline, including mPFC, anterior cingulate, and posterior cingulate, particularly for the self vs. baseline comparison, though activation was not exclusive to the midline.
“Specifically, like Northoff and colleagues, we found evidence for self-related judgments being reliably associated with activation along the cortical midline, including mPFC, anterior cingulate, and posterior cingulate, particularly for the self vs. baseline comparison, though activation was not exclusive to the midline.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataDirect comparisons between self and other judgments yielded a distributed set of regions more active for self judgments (vmPFC, left vlPFC, left caudate) and another set more active for other judgments (dmPFC, bilateral TPJ, cuneus).
“Direct comparisons between judgments of self and others yielded a distributed set of regions that are relatively more active for self judgments, including vmPFC, left vlPFC, and left caudate, and another set of regions that are more active for other judgments, including dmPFC, bilateral TPJ and cuneus.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataBoth ventral and dorsal mPFC were active for both self and other judgments, and self judgments were more strongly associated with ventral relative to dorsal mPFC activity across all studies.
“While this particular discrepant result could stem from multiple causes, we included the results from this study in the present meta-analysis and found that while both ventral and dorsal mPFC were active for both self and other judgments, self judgments were more strongly associated with ventral relative to dorsal mPFC activity across all studies.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataThe results support a distributed rather than localizationist account of mPFC organization and an emerging view of mPFC functional heterogeneity.
“These results argue for a distributed rather than localizationist account of mPFC organization and support an emerging view on the functional heterogeneity of mPFC.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The null hypothesis for the Monte Carlo simulation was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPrior work has associated self-related judgments with right-lateralized activity.
“This stands in contrast to prior work that has associated self-related judgments with right-lateralized activity (Keenan, Ganis, Freund, & Pascual-Leone, 2000; Keenan, Wheeler, Gallup, & Pascual-Leone, 2000).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Keenan, Ganis, Freund, & Pascual-Leone, 2000
Not checked in the free run.
- cites Keenan, Wheeler, Gallup, & Pascual-Leone, 2000
Not checked in the free run.
Classified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenContrasts were excluded if they involved patients with major psychiatric disease, participants on a therapeutic regimen, children under 18, or non-contrast analyses.
“Contrasts were excluded if they met any of the following criteria: (1) They involved patients with major psychiatric disease; (2) They involved participants on a therapeutic regimen; (3) They involved children under 18 years of age; (4) They were non-contrast analyses (e.g. parametric analyses).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based).
Premisenone givenAs of the time of the study, there was no clear model of the functional organization of mPFC with respect to processes supporting self and other judgments.
“Our ability to draw inferences about the meaning of these data is limited, however, by the fact that there is as of yet no clear model of the functional organization of mPFC with respect to processes that support judgments of self and others.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenCoordinates were verified by at least 2 independent investigators.
“Coordinates were verified by at least 2 independent investigators.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataSelf- and other-related processing in mPFC is organized as a spatial gradient, with increasingly ventral activation associated with self-related judgments and increasingly dorsal activation associated with other-related judgments.
“These results reflect a spatial processing gradient, such that increasingly ventral or dorsal mPFC activation were increasingly associated with either self- or other-related judgments, respectively.”
- Also stated in: § Discussion · plain
“Using a database of 107 published neuroimaging studies we reported evidence for self- and other-related judgments being (1) supported by both common and distinct groups of regions that include many implicated in mentalizing in prior work, and (2) associated with a spatial mentalizing gradient within mPFC, with increasingly ventral activation being increasingly associated with self-related judgment”
- Also stated in: § Discerning the Spatial and Functional Organization of mPFC · plain
“Thus, the present data argue that the representation of processes supporting judgments about the self and others in mPFC is organized as a gradient rather than discrete modules.”
Quote in the paperSubstantial claim- Also stated in: § Discussion · plain
Classified as probably not a substantial claim. May combine two claims.
Study design and conductcitationAll contrasts were coded by at least 2 trained coders, and disagreements were arbitrated after independent coding.
“All contrasts were coded by at least 2 trained coders. Any disagreements between coders were arbitrated after independent coding in order to any resolve any discrepancies (Kober et al., 2008).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Kober et al., 2008 source
Not checked in the free run.
Classified as probably not a substantial claim. May combine two claims.
Study design and conductown dataResults survived whole-brain correction if they met height-based criteria alone or cluster extent-based criteria, with all thresholds significant at p<0.05, FWE-corrected.
“Results survived whole-brain correction if they either met height-based criteria alone (i.e. sufficiently large activation proportion differential, regardless of extent), or if they met cluster extent-based criteria. Height (i.e. activation proportion) and extent thresholds varied for each MKDA, but all were significant at p<0.05, FWE-corrected.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenThe binary logistic regression analysis was independent of the MKDA and independent of any spatial smoothing.
“Using a binary logistic regression analysis that was independent of the MKDA and independent of any spatial smoothing, we found that self or other judgment status was significantly predicted by location along the dorsal-ventral axis in mPFC.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationIncreasingly ventral mPFC is more associated with processing self-relevant judgments, whereas dorsal mPFC is relatively more attuned to focusing attention on making judgments about the external world.
“Thus, increasingly ventral mPFC is more associated with processing self-relevant judgments, whereas dorsal mPFC is relatively more attuned to focusing attention on making judgments about the external world.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationCaudate body activity may reflect a connection between self-focused mentalizing and generalized reward processing.
“In addition, the caudate body activity reported here may reflect a connection between self-focused mentalizing and generalized reward processing, consistent with the notion that there are inherently rewarding aspects to the self (Enzi, de Greck, Prosch, Tempelmann, & Northoff, 2009).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Enzi, de Greck, Prosch, Tempelmann, & Northoff, 2009
Not checked in the free run.
May combine two claims.
PremisecitationConnectivity analyses within anterior mPFC have revealed a ventrally mediated viscerolimbic affective and self-relevance network and a dorsally mediated cognitive network.
“Connectivity analyses within anterior mPFC have revealed a ventrally mediated viscerolimbic affective and self-relevance network (with connections to amygdala, insula, and nucleus accumbens) and a dorsally mediated cognitive network (with connections to dorsolateral PFC and hippocampus) (Kim & Whalen, 2009; Price, Carmichael, & Drevets, 1996; Schmitz & Johnson, 2006).”
Quote in the paperSubstantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationvmPFC supports relatively stimulus-driven processes that may be important for computing the value of stimuli in a current judgment context, whereas dmPFC supports more reflective processes used for selecting higher level social and affective meanings.
“This view is also consistent with the notion, derived from a recent review of the functional neuroimaging literature, that vmPFC supports relatively stimulus-driven processes that may be important for computing the value of stimuli in a current judgment context, whereas dmPFC supports more reflective processes used for selecting higher level social and affective meanings (Olsson & Ochsner, 2008).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Olsson & Ochsner, 2008
Not checked in the free run.
May combine two claims.
PremisereasoningContrasts comparing only the categories represented at the end-points of a gradient can only show apparent double dissociations; detecting a gradient requires a finer-grained analysis that takes into account regions spanning the end points.
“In all cases, contrasts comparing only the categories represented at the end-points of a gradient can only show apparent double dissociations. In order to detect a gradient, one needs a finer-grained analysis that takes into account regions spanning the end points - as we did with the logistic regression used here.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationGusnard and colleagues (2001) found internally-directed (self-referential) attention to be more associated with dorsal mPFC activity.
“It is notable, however, that Gusnard and colleagues (2001) addressed this question with a neuroimaging task involving internally versus externally-directed attention and came to a divergent conclusion, finding internally-directed (self-referential) attention to be more associated with dorsal mPFC activity.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Gusnard et al., 2001 source
Not checked in the free run.
The authors state this as an assumption.
The null hypothesis for the Monte Carlo simulation was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.
“The null hypothesis was a uniform random distribution of peaks within each comparison in gray matter in the standard brain.”
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?
Ex-partner versus Friend was predicted by increased activity in dmPFC, right TPJ, precuneus, and other regions associated with negative emotion and its regulation.
“Ex-partner versus Friend was predicted by increased activity in dorsomedial prefrontal cortex (dmPFC), right temporal parietal junction (TPJ) and precuneus, which are reliably associated with mentalizing about others38,39, and several other regions associated with negative emotion and its regulation20,40,41, including thalamus, supplementary motor area and inferior frontal gyrus.”
From Separate neural representations for physical pain and social rejection (2014) · cites this paper as [38]
Cites
Culture and the self: Implications for cognition, emotion, and motivation.
Markus, H. R., & Kitayama, S. (1991) · Psychological Review · doi:10.1037/0033-295x.98.2.224 · Cited by 21,995 · see citing works
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · cited 2× · see citing works
“…are consistent with the results of another recent self–other meta-analysis (Qin et al., 2012; Qin & Northoff, 2011) and with a role for interoception in self-related awareness that involves the anterior insula (Denny, Ochsner, Weber, & Wager, in preparation; Craig, 2009; Wager & Barrett, 2004).”
ResultTalairach, J., Tournoux, P., & Rayport, M. (1988) · Thieme eBooks · Cited by 5,058 · see citing works
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782 · see citing works
Lewis, M., & Haviland, J. M. (1993) · Cited by 3,308 · see citing works
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997 · see citing works
Self-referential processing in our brain—A meta-analysis of imaging studies on the self
Northoff, G., Heinzel, A., de Greck, M., Bermpohl, F., Dobrowolny, H., & Panksepp, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.002 · Cited by 2,792 · see citing works
Wandering minds: the default network and stimulus-independent thought
Mason, M. F., Norton, M. I., Van Horn, J. D., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1131295 · Cited by 2,792 · see citing works
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works
Self-citationFunctional imaging of ‘theory of mind’
Gallagher, H. L., & Frith, C. D. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)00025-6 · Cited by 2,092 · see citing works
Assessing the significance of focal activations using their spatial extent
Friston, K. J., Worsley, K. J., Frackowiak, R. S. J., Mazziotta, J. C., & Evans, A. C. (1994) · Human Brain Mapping · doi:10.1002/hbm.460010306 · Cited by 1,907 · see citing works
Cognitive Reappraisal of Emotion: A Meta-Analysis of Human Neuroimaging Studies
Buhle, J. T., Silvers, J. A., Wager, T. D., Lopez, R., Onyemekwu, C., Kober, H., Weber, J., & Ochsner, K. N. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht154 · Cited by 1,896 · see citing works
Self-citationSelf-reference and the encoding of personal information.
Rogers, T. B., Kuiper, N. A., & Kirker, W. S. (1977) · Journal of Personality and Social Psychology · doi:10.1037//0022-3514.35.9.677 · Cited by 1,871 · see citing works
Social cognition and the brain: A meta-analysis
Van Overwalle, F. (2009) · Human Brain Mapping · doi:10.1002/hbm.20547 · Cited by 1,792 · cited 9× · see citing works
“In addition, our results are consistent with those of Van Overwalle (2011), who found that mPFC activation is positively associated with degree of mentalizing content, although, in the present analysis, we did not characterize the degree to which mentalizing is involved in each contrast.”
BackgroundMethodResultInfluentialFinding the self? An event-related fMRI study
Kelley, W. M., Macrae, C. N., Wyland, C. L., Caglar, S., Inati, S., & Heatherton, T. F. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260138672 · Cited by 1,606 · cited 2× · see citing works
“Across studies, numerous regions have been associated with attributions about the self or others, including the ventral and dorsal portions of the mPFC, ACC, posterior cingulate cortex (PCC), medial parietal cortex, precuneus, and the temporal poles (Mitchell, Macrae, & Banaji, 2006; Ochsner et al., 2004, 2005; Kelley…”
BackgroundLeft ventrolateral prefrontal cortex and the cognitive control of memory
Badre, D., & Wagner, A. D. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.06.015 · Cited by 1,471 · see citing works
Whitfield-Gabrieli, S., Thermenos, H. W., Milanovic, S., Tsuang, M. T., Faraone, S. V., McCarley, R. W., Shenton, M. E., Green, A. I., Nieto-Castanon, A., LaViolette, P., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809141106 · Cited by 1,435 · see citing works
Self-reference and the encoding of personal information.
Rogers, T. B., Kuiper, N. A., & Kirker, W. S. (1977) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.35.9.677 · Cited by 1,422 · see citing works
The self-reference effect in memory: A meta-analysis
Symons, C. S., & Johnson, B. T. (1997) · Psychological Bulletin · doi:10.1037/0033-2909.121.3.371 · Cited by 1,361 · cited 3× · see citing works
“…have long debated the nature of the mental representations that separate the self from others (Goldman, 1992; Stich & Nichols, 1992), and addressing this question has generated an extensive experimental literature (Symons & Johnson, 1997; Klein & Kihlstrom, 1986; Rogers, Kuiper, & Kirker, 1977).”
BackgroundUnderstanding others' actions and goals by mirror and mentalizing systems: a meta-analysis
Van Overwalle, F., & Baetens, K. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.009 · Cited by 1,329 · see citing works
Drevets, W. C. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00203-8 · Cited by 1,146 · see citing works
Kober, H., Barrett, L. F., Joseph, J., Bliss-Moreau, E., Lindquist, K., & Wager, T. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.059 · Cited by 1,144 · see citing works
Self-citationSelf-focused attention and negative affect: A meta-analysis.
Mor, N., & Winquist, J. (2002) · Psychological Bulletin · doi:10.1037/0033-2909.128.4.638 · Cited by 1,069 · see citing works
Dissociable Medial Prefrontal Contributions to Judgments of Similar and Dissimilar Others
Mitchell, J. P., Macrae, C. N., & Banaji, M. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.040 · Cited by 1,023 · see citing works
How is our self related to midline regions and the default-mode network?
Qin, P., & Northoff, G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.028 · Cited by 909 · see citing works
Social Cognition And Social Perception
Higgins, E. T., & Bargh, J. A. (1987) · Annual Review of Psychology · doi:10.1146/annurev.ps.38.020187.002101 · Cited by 907 · see citing works
Ochsner, K. N., Knierim, K., Ludlow, D. H., Hanelin, J., Ramachandran, T., Glover, G., & Mackey, S. C. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042947829 · Cited by 850 · see citing works
Self-citationThe Link between Social Cognition and Self-referential Thought in the Medial Prefrontal Cortex
Mitchell, J. P., Banaji, M. R., & Macrae, C. N. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929055002418 · Cited by 806 · see citing works
Understanding Other Minds: Linking Developmental Psychology and Functional Neuroimaging
Saxe, R., Carey, S., & Kanwisher, N. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.55.090902.142044 · Cited by 726 · see citing works
Anterior insular cortex and emotional awareness
Gu, X., Hof, P. R., Friston, K. J., & Fan, J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23368 · Cited by 712 · see citing works
Functional Specialization within Rostral Prefrontal Cortex (Area 10): A Meta-analysis
Gilbert, S. J., Spengler, S., Simons, J. S., Steele, J. D., Lawrie, S. M., Frith, C., & Burgess, P. W. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.6.932 · Cited by 681 · see citing works
Neuroimaging studies of shifting attention: a meta-analysis
Wager, T. D., Jonides, J., & Reading, S. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.052 · Cited by 654 · see citing works
Self-citationThe functional neuroanatomy of PTSD: a critical review
Liberzon, I., & Sripada, C. S. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)67011-3 · Cited by 594 · see citing works
Martino, A. D., Ross, K. V., Uddin, L. Q., Sklar, A. B., Castellanos, F. X., & Milham, M. P. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.09.022 · Cited by 574 · see citing works
The neural correlates of direct and reflected self-knowledge
Ochsner, K. N., Beer, J. S., Robertson, E. R., Cooper, J. C., Gabrieli, J. D. E., Kihsltrom, J. F., & D'Esposito, M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.069 · Cited by 562 · see citing works
Self-citationvan der Meer, L., Costafreda, S., Aleman, A., & David, A. S. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.004 · Cited by 520 · see citing works
In defense of the simulation theory.
GOLDMAN, A. I. (1992) · Mind & Language · doi:10.1111/j.1468-0017.1992.tb00200.x · Cited by 516 · see citing works
Bipolar and major depressive disorder: Neuroimaging the developmental-degenerative divide
Savitz, J., & Drevets, W. C. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.01.004 · Cited by 494 · see citing works
Cortex and Mind. Unifying Cognition
Jellinger, K. A. (2003) · European Journal of Neurology · doi:10.1046/j.1468-1331.2003.00567.x · Cited by 488 · see citing works
(2003) · Cited by 476 · see citing works
Gillihan, S. J., & Farah, M. J. (2005) · Psychological Bulletin · doi:10.1037/0033-2909.131.1.76 · Cited by 470 · see citing works
What is self-specific? Theoretical investigation and critical review of neuroimaging results
Legrand, D., & Ruby, P. (2009) · Psychological Review · doi:10.1037/a0014172 · Cited by 470 · cited 3× · see citing works
“Broad overlap was observed in both vmPFC and dmPFC, which is consistent with prior work indicating that mPFC is involved in attending to oneʼs own or anotherʼs mental state (Van Overwalle, 2011; Legrand & Ruby, 2009; Van Overwalle & Baetens, 2009; Gilbert et al., 2006; Ochsner et al., 2004, 2005).”
BackgroundResultRemembering information related to one's self
Bower, G. H., & Gilligan, S. G. (1979) · Journal of Research in Personality · doi:10.1016/0092-6566(79)90005-9 · Cited by 457 · see citing works
Meta-analysis of functional neuroimaging data: current and future directions
Wager, T. D., Lindquist, M., & Kaplan, L. (2007) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsm015 · Cited by 434 · see citing works
Self-citationThe structural integrity of an amygdala-prefrontal pathway predicts trait anxiety
Kim, M. J., & Whalen, P. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2335-09.2009 · Cited by 433 · see citing works
Encoding of personal information: Self-other differences.
Kuiper, N. A., & Rogers, T. B. (1979) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.37.4.499 · Cited by 423 · see citing works
Salimi-Khorshidi, G., Smith, S. M., Keltner, J. R., Wager, T. D., & Nichols, T. E. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.039 · Cited by 388 · see citing works
Self-citationFolk Psychology: Simulation or Tacit Theory?
Stich, S., & Nichols, S. (1992) · Mind & Language · doi:10.1111/j.1468-0017.1992.tb00196.x · Cited by 376 · see citing works
The frontal lobes and the regulation of mental activity
Thompson‐Schill, S. L., Bedny, M., & Goldberg, R. F. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.006 · Cited by 329 · see citing works
Elaboration, organization, and the self-reference effect in memory.
Klein, S. B., & Kihlstrom, J. F. (1986) · Journal of Experimental Psychology General · doi:10.1037//0096-3445.115.1.26 · Cited by 329 · see citing works
Emotion deficits in people with schizophrenia
Kring, A. M., & Elis, O. (2013) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050212-185538 · Cited by 318 · see citing works
The role of social cognition in emotion
Olsson, A., & Ochsner, K. N. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.11.010 · Cited by 289 · see citing works
Self-citationSelf-recognition and the right prefrontal cortex
Keenan, J. P., Wheeler, M. A., Gallup, G. G., & Pascual-Leone, A. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01521-7 · Cited by 285 · see citing works
fMRI reveals reciprocal inhibition between social and physical cognitive domains
Jack, A. I., Dawson, A. J., Begany, K. L., Leckie, R. L., Barry, K. P., Ciccia, A. H., & Snyder, A. Z. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.061 · Cited by 280 · see citing works
Coupling social attention to the self forms a network for personal significance
Sui, J., Rotshtein, P., & Humphreys, G. W. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221862110 · Cited by 263 · see citing works
The cognit: A network model of cortical representation
Fuster, J. M. (2006) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.12.015 · Cited by 258 · see citing works
The symbolic self in evolutionary context
Sedikides, C., & Skowronski, J. J. (1997) · Personality and Social Psychology Review · doi:10.1207/s15327957pspr0101_6 · Cited by 251 · see citing works
Elaboration, organization, and the self-reference effect in memory.
Klein, S. B., & Kihlstrom, J. F. (1986) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.115.1.26 · Cited by 242 · see citing works
The role of fMRI in Cognitive Neuroscience: where do we stand?
Poldrack, R. A. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.07.006 · Cited by 227 · see citing works
Neural correlates of nondual awareness in meditation
Josipovic, Z. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12261 · Cited by 226 · see citing works
Price, J. L., Carmichael, S. T., & Drevets, W. C. (1996) · Progress in Brain Research · doi:10.1016/s0079-6123(08)61885-3 · Cited by 222 · see citing works
A dissociation between social mentalizing and general reasoning
Overwalle, F. V. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.043 · Cited by 205 · see citing works
The representation of self and person knowledge in the medial prefrontal cortex
Wagner, D. D., Haxby, J. V., & Heatherton, T. F. (2012) · WIREs Cognitive Science · doi:10.1002/wcs.1183 · Cited by 201 · see citing works
From affect to control: Functional specialization of the insula in motivation and regulationPreprint
Wager, T. D., & Barrett, L. F. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/102368 · Cited by 200 · see citing works
Self-citationNeuroimaging studies in post-traumatic stress disorder
Bremner, J. D. (2002) · Current Psychiatry Reports · doi:10.1007/s11920-996-0044-9 · Cited by 194 · see citing works
Enzi, B., de Greck, M., Prösch, U., Tempelmann, C., & Northoff, G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008429 · Cited by 138 · see citing works
Current directions in social cognitive neuroscience
Ochsner, K. N. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.011 · Cited by 127 · see citing works
Self-citationCategory-specificity in the Human Medial Temporal Lobe Cortex
Litman, L., Awipi, T., & Davachi, L. (2009) · Hippocampus · doi:10.1002/hipo.20515 · Cited by 117 · 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
Visioning in the brain: An fMRI study of inspirational coaching and mentoring
Jack, A. I., Boyatzis, R. E., Khawaja, M., Passarelli, A. M., & Leckie, R. L. (2013) · Social Neuroscience · doi:10.1080/17470919.2013.808259 · Cited by 114 · see citing works
Qin, P.-M., Liu, Y., Shi, J., Wang, Y., Duncan, N., Gong, Q., Weng, X., & Northoff, G. (2012) · Human Brain Mapping · doi:10.1002/hbm.21201 · Cited by 111 · see citing works
Memory for personally relevant information.
Ferguson, T. J., Rule, B. G., & Carlson, D. (1983) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.44.2.251 · Cited by 106 · see citing works
Brains creating stories of selves: the neural basis of autobiographical reasoning.
D'Argembeau, A., Cassol, H., Phillips, C., Balteau, E., Salmon, É., & der Linden, M. V. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst028 · Cited by 102 · see citing works
The Default Mode of Human Brain Function Primes the Intentional Stance
Spunt, R. P., Meyer, M. L., & Lieberman, M. D. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00785 · Cited by 98 · see citing works
Reward-related neural responses are dependent on the beneficiary
Braams, B. R., Güroğlu, B., de Water, E., Meuwese, R., Koolschijn, P. C., Peper, J. S., & Crone, E. A. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst077 · Cited by 75 · see citing works
Anticipatory brain activity predicts the success or failure of subsequent emotion regulation
Denny, B. T., Ochsner, K. N., Weber, J., & Wager, T. D. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss148 · Cited by 75 · see citing works
Self-citationMeta-analysis of neuroimaging data
Kober, H., & Wager, T. D. (2010) · WIREs Cognitive Science · doi:10.1002/wcs.41 · Cited by 74 · see citing works
Self-citationThe Functional Neural Architecture of Self-Reports of Affective Experience
Satpute, A. B., Shu, J., Weber, J., Roy, M., & Ochsner, K. N. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.10.001 · Cited by 72 · see citing works
Self-citationOuthred, T., Hawkshead, B. E., Wager, T. D., Das, P., Malhi, G. S., & Kemp, A. H. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.07.010 · Cited by 67 · see citing works
Self-citationVasopressin modulates neural responses related to emotional stimuli in the right amygdala
Brunnlieb, C., Münte, T. F., Tempelmann, C., & Heldmann, M. (2013) · Brain Research · doi:10.1016/j.brainres.2013.01.009 · Cited by 63 · see citing works
Barrett, L. F., & Satpute, A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.12.012 · Cited by 58 · see citing works
Mainieri, A. G., Heim, S., Straube, B., Binkofski, F., & Kircher, T. T. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.021 · Cited by 53 · see citing works
Considerations of fairness in the adolescent brain
Crone, E. A. (2013) · Child Development Perspectives · doi:10.1111/cdep.12022 · Cited by 48 · see citing works
Outcome dependency alters the neural substrates of impression formation
Ames, D. L., & Fiske, S. T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.001 · Cited by 45 · see citing works
Satpute, A., Badre, D., & Ochsner, K. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs408 · Cited by 45 · see citing works
Self-citationAge-related differences in agenda-driven monitoring of format and task information
Mitchell, K., Ankudowich, E., Durbin, K. A., Greene, E. J., & Johnson, M. K. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.01.012 · Cited by 40 · see citing works
Impartiality in humans is predicted by brain structure of dorsomedial prefrontal cortex
Baumgärtner, T., Schiller, B., Hill, C., & Knoch, D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.047 · Cited by 39 · see citing works
Self-reflection and positive schizotypy in the adolescent brain
Debbané, M., Vrtička, P., Lazouret, M., Badoud, D., Sander, D., & Eliez, S. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.06.027 · Cited by 38 · see citing works
Green, M. F., Lee, J., & Ochsner, K. N. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt131 · Cited by 33 · see citing works
Self-citationChen, P.-H. A., Wagner, D. D., Kelley, W. M., Powers, K. E., & Heatherton, T. F. (2013) · Culture and Brain · doi:10.1007/s40167-013-0001-5 · Cited by 33 · see citing works
Self-face identification is increased with left hand responses
Keenan, J. P., Ganis, G., Freund, S., & Pascual‐Leone, Á. (2000) · Laterality Asymmetries of Body Brain and Cognition · doi:10.1080/713754382 · Cited by 30 · see citing works
The gender you are and the gender you like: sexual preference and empathic neural responses.
Perry, D., Walder, K., Hendler, T., & Shamay-Tsoory, S. (2013) · Brain Research · doi:10.1016/j.brainres.2013.08.040 · Cited by 27 · see citing works
Subclinical delusional thinking predicts lateral temporal cortex responses during social reflection
Brent, B. K., Coombs, G., Keshavan, M. S., Seidman, L. J., Moran, J. M., & Holt, D. J. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss129 · Cited by 21 · see citing works
Behavioral and neural reactions to emotions of others in the distribution of resources
Lelieveld, G., van Dijk, E., Güroğlu, B., van Beest, I., Kleef, G. A. V., Rombouts, S. A. R. B., & Crone, E. A. (2012) · Social Neuroscience · doi:10.1080/17470919.2012.735621 · Cited by 19 · see citing works
Brain activation related to the perception of minimal agency cues: The role of the mirror system
Stosic, M., Braß, M., Hoeck, N. V., Ma, N., & Overwalle, F. V. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.10.007 · Cited by 18 · see citing works
Zaki, J., & Ochsner, K. N. (2011) · Social Neuroscience · doi:10.1093/acprof:oso/9780195316872.003.0002 · Cited by 18 · see citing works
Self-citationChanging Implicit Attitudes by Contrasting the Self with Others
Perugini, M., Zogmaister, C., Richetin, J., Prestwich, A., & Hurling, R. (2013) · Social Cognition · doi:10.1521/soco_2012_1003 · Cited by 17 · see citing works
Brain systems underlying anxiety disorders: a view from neuroimaging
Etkin, A., & Wager, T. D. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511777578.019 · Cited by 10 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Andrews‐Hanna, J. R., Smallwood, J., & Spreng, R. N. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12360 · Cited by 2,102 · see citing works
Cognitive Reappraisal of Emotion: A Meta-Analysis of Human Neuroimaging Studies
Buhle, J. T., Silvers, J. A., Wager, T. D., Lopez, R., Onyemekwu, C., Kober, H., Weber, J., & Ochsner, K. N. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht154 · Cited by 1,896 · see citing works
Self-citationFractionating theory of mind: a meta-analysis of functional brain imaging studies
Schurz, M., Radua, J., Aichhorn, M., Richlan, F., & Perner, J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.01.009 · Cited by 1,656 · see citing works
Reconstructing and deconstructing the self: cognitive mechanisms in meditation practice
Dahl, C. J., Lutz, A., & Davidson, R. J. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.07.001 · Cited by 809 · see citing works
Emotion and the prefrontal cortex: an integrative review
Dixon, M. L., Thiruchselvam, R., Todd, R., & Christoff, K. (2017) · Psychological Bulletin · doi:10.1037/bul0000096 · Cited by 745 · see citing works
Anterior insular cortex and emotional awareness
Gu, X., Hof, P. R., Friston, K. J., & Fan, J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23368 · Cited by 712 · see citing works
“…that the insular cortex works closely with a network of regions, including the ACC (Critchley, 2004; Critchley et al., 2004; Medford and Critchley, 2010; Fan et al., 2011; Denny et al., 2012; Lindquist et al., 2012), somatosensory cortex (Gu et al., 2013), and amygdala (Etkin and Wager, 2007).”
BackgroundZhou, H.-X., Chen, X., Shen, Y.-Q., Li, L., Chen, N.-X., Zhu, Z.-C., Castellanos, F. X., & Yan, C.-G. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2019.116287 · Cited by 656 · see citing works
Barrett, L. F., & Satpute, A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.12.012 · Cited by 58 · see citing works
Dixon, M. L., De La Vega, A., Mills, C., Andrews-Hanna, J., Spreng, R. N., Cole, M. W., & Christoff, K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715766115 · Cited by 595 · see citing works
Johnson, M. W., Hendricks, P. S., Barrett, F. S., & Griffiths, R. R. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.11.010 · Cited by 506 · see citing works
Li, W., Mai, X., & Liu, C. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00074 · Cited by 459 · see citing works
Deconstructing and reconstructing theory of mind
Schaafsma, S. M., Pfaff, D. W., Spunt, R. P., & Adolphs, R. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.11.007 · Cited by 498 · see citing works
Mundy, P. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13720 · Cited by 376 · see citing works
Toward a brain-based componential semantic representation
Binder, J. R., Conant, L. L., Humphries, C., Fernandino, L., Simons, S. B., Aguilar, M., & Desai, R. H. (2016) · Cognitive Neuropsychology · doi:10.1080/02643294.2016.1147426 · Cited by 360 · see citing works
A Sensitive and Specific Neural Signature for Picture-Induced Negative Affect
Chang, L. J., Gianaros, P. J., Manuck, S. B., Krishnan, A., & Wager, T. D. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002180 · Cited by 336 · see citing works
Self-citationThe Neuroscience of Intergroup Relations
Cikara, M., & Bavel, J. J. V. (2014) · Perspectives on Psychological Science · doi:10.1177/1745691614527464 · Cited by 354 · see citing works
Emotion deficits in people with schizophrenia
Kring, A. M., & Elis, O. (2013) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050212-185538 · Cited by 318 · see citing works
Andrews-Hanna, J. R., Saxe, R., & Yarkoni, T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.01.032 · Cited by 313 · see citing works
Separate neural representations for physical pain and social rejection
Woo, C.-W., Koban, L., Kross, E., Lindquist, M. A., Banich, M. T., Ruzic, L., Andrews-Hanna, J. R., & Wager, T. D. (2014) · Nature Communications · doi:10.1038/ncomms6380 · Cited by 310 · see citing works
Self-citationLarge-Scale Meta-Analysis of Human Medial Frontal Cortex Reveals Tripartite Functional Organization
de la Vega, A. I., Chang, L. J., Banich, M. T., Wager, T. D., & Yarkoni, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4402-15.2016 · Cited by 288 · see citing works
Self-citationfMRI reveals reciprocal inhibition between social and physical cognitive domains
Jack, A. I., Dawson, A. J., Begany, K. L., Leckie, R. L., Barry, K. P., Ciccia, A. H., & Snyder, A. Z. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.061 · Cited by 280 · see citing works
Classic Hallucinogens and Mystical Experiences: Phenomenology and Neural Correlates
Barrett, F. S., & Griffiths, R. R. (2017) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2017_474 · Cited by 273 · see citing works
The neural and computational systems of social learning
Olsson, A., Knapska, E., & Lindström, B. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0276-4 · Cited by 267 · see citing works
Lieberman, M. D., Straccia, M. A., Meyer, M. L., Du, M., & Tan, K. M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.12.021 · Cited by 262 · see citing works
On the Role of the Ventromedial Prefrontal Cortex in Self-Processing: The Valuation Hypothesis
D’Argembeau, A. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00372 · Cited by 270 · see citing works
A Bayesian Model of Category-Specific Emotional Brain Responses
Wager, T. D., Kang, J., Johnson, T. D., Nichols, T. E., Satpute, A. B., & Barrett, L. F. (2015) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1004066 · Cited by 262 · see citing works
Self-citationCoupling social attention to the self forms a network for personal significance
Sui, J., Rotshtein, P., & Humphreys, G. W. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221862110 · Cited by 263 · see citing works
Towards a neurophysiological signature for fibromyalgia
López‐Solà, M., Woo, C., Pujol, J., Deus, J., Harrison, B. J., Monfort, J., & Wager, T. D. (2016) · Pain · doi:10.1097/j.pain.0000000000000707 · Cited by 255 · see citing works
Self-citationAdolfi, F., Couto, B., Richter, F., Decety, J., Lopez, J., Sigman, M., Manes, F., & Ibáñez, A. (2017) · Cortex · doi:10.1016/j.cortex.2016.12.019 · Cited by 238 · see citing works
Self and Others in Adolescence
Crone, E. A., & Fuligni, A. J. (2020) · Annual Review of Psychology · doi:10.1146/annurev-psych-010419-050937 · Cited by 239 · see citing works
Neural correlates of nondual awareness in meditation
Josipovic, Z. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12261 · Cited by 226 · see citing works
The self in context: brain systems linking mental and physical health
Koban, L., Gianaros, P. J., Hedy Kober, A., & Wager, T. D. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00446-8 · Cited by 241 · see citing works
Self-citationEmpathic Care and Distress: Predictive Brain Markers and Dissociable Brain Systems
Ashar, Y. K., Andrews‐Hanna, J. R., Dimidjian, S., & Wager, T. D. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.014 · Cited by 231 · see citing works
Self-citationDixon, M. L., Andrews‐Hanna, J. R., Spreng, R. N., Irving, Z. C., Mills, C., Girn, M., & Kalina Christoff, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.073 · Cited by 228 · see citing works
Definition and characterization of an extended social-affective default network
Amft, M., Bzdok, D., Laird, A. R., Fox, P. T., Schilbach, L., & Eickhoff, S. B. (2015) · Brain Structure and Function · doi:10.1007/s00429-013-0698-0 · Cited by 208 · see citing works
Qin, P., Wang, M., & Northoff, G. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.05.004 · Cited by 220 · see citing works
Self-Processing and the Default Mode Network: Interactions with the Mirror Neuron System
Molnar-Szakacs, I., & Uddin, L. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00571 · Cited by 208 · see citing works
How and where: Theory-of-mind in the brain
Mahy, C. E. V., Moses, L. J., & Pfeifer, J. H. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2014.01.002 · Cited by 213 · see citing works
Social cognition and the cerebellum: A meta‐analytic connectivity analysis
Overwalle, F. V., D’aes, T., & Mariën, P. (2015) · Human Brain Mapping · doi:10.1002/hbm.23002 · Cited by 212 · see citing works
The representation of self and person knowledge in the medial prefrontal cortex
Wagner, D. D., Haxby, J. V., & Heatherton, T. F. (2012) · WIREs Cognitive Science · doi:10.1002/wcs.1183 · Cited by 201 · see citing works
Schurz, M., Aichhorn, M., Martin, A., & Perner, J. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00712 · Cited by 201 · see citing works
Positively Biased Processing of Self-Relevant Social Feedback
Korn, C. W., Prehn, K., Park, S. Q., Walter, H., & Heekeren, H. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3016-12.2012 · Cited by 193 · see citing works
Persuasion, Influence, and Value: Perspectives from Communication and Social Neuroscience
Falk, E. B., & Scholz, C. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-122216-011821 · Cited by 192 · see citing works
Schurz, M., Tholen, M. G., Perner, J., Mars, R. B., & Sallet, J. (2017) · Human Brain Mapping · doi:10.1002/hbm.23675 · Cited by 199 · see citing works
Brain Mechanisms of the Placebo Effect: An Affective Appraisal Account
Ashar, Y. K., Chang, L. J., & Wager, T. D. (2017) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-021815-093015 · Cited by 191 · see citing works
Self-citationStawarczyk, D., & D'Argembeau, A. (2015) · Human Brain Mapping · doi:10.1002/hbm.22818 · Cited by 188 · see citing works
James, C. E., Oechslin, M. S., Van De Ville, D., Hauert, C.-A., Descloux, C., & Lazeyras, F. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0504-z · Cited by 180 · see citing works
Historical pitfalls and new directions in the neuroscience of emotion
Barrett, L. F., & Satpute, A. B. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2017.07.045 · Cited by 180 · see citing works
The computational and neural substrates of moral strategies in social decision-making
van Baar, J. M., Chang, L. J., & Sanfey, A. G. (2019) · Nature Communications · doi:10.1038/s41467-019-09161-6 · Cited by 184 · see citing works
Neuroimaging the consciousness of self: Review, and conceptual-methodological framework
Frewen, P., Schroeter, M. L., Riva, G., Cipresso, P., Fairfield, B., Padulo, C., Kemp, A. H., Palaniyappan, L. K., Owolabi, M. O., Kusi‐Mensah, K., et al. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.023 · Cited by 177 · see citing works
Powers, J. P., & LaBar, K. S. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.023 · Cited by 173 · see citing works
Tajadura-Jiménez, A., & Tsakiris, M. (2014) · Journal of Experimental Psychology: General · doi:10.1037/a0033171 · Cited by 167 · see citing works
Self-Other Mergence in the Frontal Cortex during Cooperation and Competition
Wittmann, M. K., Kolling, N., Faber, N. S., Scholl, J., Nelissen, N., & Rushworth, M. F. S. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.022 · Cited by 168 · see citing works
The neural crossroads of psychiatric illness: an emerging target for brain stimulation
Downar, J., Blumberger, D. M., & Daskalakis, Z. J. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.007 · Cited by 166 · see citing works
The Cognitive Neuroscience of Placebo Effects: Concepts, Predictions, and Physiology.
Geuter, S., Koban, L., & Wager, T. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031132 · Cited by 139 · see citing works
Self-citationKumaran, D., Banino, A., Blundell, C., Hassabis, D., & Dayan, P. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.052 · Cited by 155 · see citing works
The affective meanings of automatic social behaviors: Three mechanisms that explain priming.
Schröder, T., & Thagard, P. R. (2012) · Psychological Review · doi:10.1037/a0030972 · Cited by 155 · see citing works
Neural mechanisms tracking popularity in real-world social networks
Zerubavel, N., Bearman, P., Weber, J., & Ochsner, K. (2015) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1511477112 · Cited by 128 · see citing works
Self-citationMeta-analysis of human prediction error for incentives, perception, cognition, and action
Corlett, P. R., Mollick, J. A., & Kober, H. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01264-3 · Cited by 135 · see citing works
Wieber, F., Thürmer, J. L., & Gollwitzer, P. M. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00395 · Cited by 151 · see citing works
Sul, S., Tobler, P. N., Hein, G., Leiberg, S., Jung, D., Fehr, E., & Kim, H. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1423895112 · Cited by 147 · see citing works
Andrewes, D., & Jenkins, L. (2019) · Neuropsychology Review · doi:10.1007/s11065-019-09398-4 · Cited by 138 · see citing works
The Social Neuroscience of Prejudice
Amodio, D. M., & Cikara, M. (2020) · Annual Review of Psychology · doi:10.1146/annurev-psych-010419-050928 · Cited by 151 · see citing works
Impaired self-awareness in human addiction: deficient attribution of personal relevance
Moeller, S. J., & Goldstein, R. Z. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.09.003 · Cited by 140 · see citing works
Functional brain imaging predicts public health campaign success
Falk, E. B., O’Donnell, M. B., Tompson, S., Gonzalez, R., Cin, S. D., Strecher, V. J., Cummings, K. M., & An, L. C. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv108 · Cited by 128 · see citing works
Self as Object: Emerging Trends in Self Research
Sui, J., & Gu, X. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.09.002 · Cited by 131 · see citing works
Gratitude and Subjective Wellbeing: A Proposal of Two Causal Frameworks
Alkozei, A., Smith, R. S., & Killgore, W. D. S. (2017) · Journal of Happiness Studies · doi:10.1007/s10902-017-9870-1 · Cited by 131 · see citing works
Learning-Induced Plasticity in Medial Prefrontal Cortex Predicts Preference Malleability
Garvert, M., Moutoussis, M., Kurth-Nelson, Z., Behrens, T., & Dolan, R. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.033 · Cited by 110 · see citing works
Brains creating stories of selves: the neural basis of autobiographical reasoning.
D'Argembeau, A., Cassol, H., Phillips, C., Balteau, E., Salmon, É., & der Linden, M. V. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst028 · Cited by 102 · see citing works
Neural correlates of gratitude
Fox, G. R., Kaplan, J., Damásio, H., & Damásio, A. R. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01491 · Cited by 124 · see citing works
Schurz, M., Kronbichler, M., Weissengruber, S., Surtees, A. D. R., Samson, D., & Perner, J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.031 · Cited by 116 · see citing works
Validating the Why/How contrast for functional MRI studies of Theory of Mind
Spunt, R. P., & Adolphs, R. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.023 · Cited by 116 · see citing works
Social information is integrated into value and confidence judgments according to its reliability
De Martino, B., Bobadilla-Suarez, S., Nouguchi, T., Sharot, T., & Love, B. C. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3880-16.2017 · Cited by 118 · see citing works
The Default Network and Social Cognition
Spreng, R. N., & Andrews‐Hanna, J. R. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00173-1 · Cited by 118 · see citing works
Araujo, H. F., Kaplan, J. T., & Damásio, A. S. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00548 · Cited by 103 · see citing works
Neural Mechanisms of Social Cognition in Primates
Wittmann, M. K., Lockwood, P. L., & Rushworth, M. F. S. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080317-061450 · Cited by 113 · see citing works
Hypoactive medial prefrontal cortex functioning in adults reporting childhood emotional maltreatment
van Harmelen, A., van Tol, M., Dalgleish, T., van der Wee, N. J. A., Veltman, D. J., Aleman, A., Spinhoven, P., Penninx, B. W. J. H., & Elzinga, B. M. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu008 · Cited by 113 · see citing works
An Integrative Interdisciplinary Perspective on Social Dominance Hierarchies
Qu, C., Ligneul, R., der Henst, J. V., & Dreher, J. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.08.004 · Cited by 111 · see citing works
Visioning in the brain: An fMRI study of inspirational coaching and mentoring
Jack, A. I., Boyatzis, R. E., Khawaja, M., Passarelli, A. M., & Leckie, R. L. (2013) · Social Neuroscience · doi:10.1080/17470919.2013.808259 · Cited by 114 · see citing works
Sheldon, S., Farb, N., Palombo, D. J., & Levine, B. (2016) · Cortex · doi:10.1016/j.cortex.2015.11.005 · Cited by 104 · see citing works
Nguyen, T. T., Kovacevic, S., Dev, S. I., Lu, K., Liu, T. T., & Eyler, L. T. (2017) · Neuropsychology · doi:10.1037/neu0000317 · Cited by 109 · see citing works
Self-Other Representation in the Social Brain Reflects Social Connection
Courtney, A. L., & Meyer, M. L. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2826-19.2020 · Cited by 108 · see citing works
Implicit and explicit social mentalizing: dual processes driven by a shared neural network
Overwalle, F. V., & Vandekerckhove, M. M. P. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00560 · Cited by 110 · see citing works
Neural Basis of Strategic Decision Making
Lee, D., & Seo, H. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.11.002 · Cited by 104 · see citing works
Decoding fMRI Signatures of Real-world Autobiographical Memory Retrieval
Rissman, J., Chow, T. E., Reggente, N., & Wagner, A. D. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00920 · Cited by 100 · see citing works
The Educational Benefits of Self-Related Information Processing
Hidi, S. E., Renninger, K. A., & Northoff, G. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316823279.003 · Cited by 105 · see citing works
Silvers, J. A., Insel, C., Powers, A., Franz, P., Helion, C., Martin, R., Weber, J., Mischel, W., Casey, B. J., & Ochsner, K. N. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.06.005 · Cited by 99 · see citing works
Self-citationKubit, B. M., & Jack, A. I. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00323 · Cited by 101 · see citing works
Mentalized affectivity: A new model and assessment of emotion regulation
Greenberg, D. M., Kolasi, J., Hegsted, C. P., Berkowitz, Y., & Jurist, E. L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0185264 · Cited by 102 · see citing works
The Default Mode of Human Brain Function Primes the Intentional Stance
Spunt, R. P., Meyer, M. L., & Lieberman, M. D. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00785 · Cited by 98 · see citing works
Dynamical Representation of Dominance Relationships in the Human Rostromedial Prefrontal Cortex
Ligneul, R., Obeso, I., Ruff, C. C., & Dreher, J. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.015 · Cited by 95 · see citing works
Wang, X., Margulies, D. S., Smallwood, J., & Jefferies, E. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117074 · Cited by 95 · see citing works
Leshikar, E. D., & Duarte, A. (2013) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-013-0198-y · Cited by 96 · see citing works
Salvato, G., Richter, F., Sedeño, L., Bottini, G., & Paulesu, E. (2019) · Human Brain Mapping · doi:10.1002/hbm.24810 · Cited by 95 · see citing works
The neuroscience of moral cognition: from dual processes to dynamic systems
Van Bavel, J. J., FeldmanHall, O., & Mende-Siedlecki, P. (2015) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2015.08.009 · Cited by 95 · see citing works
Cascio, C. N., O’Donnell, M. B., Tinney, F. J., Lieberman, M. D., Taylor, S. E., Strecher, V. J., & Falk, E. B. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv136 · Cited by 101 · see citing works
Capacity and tendency: A neuroscientific framework for the study of emotion regulation
Silvers, J. A., & Moreira, J. F. G. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.017 · Cited by 93 · see citing works
The neural bases of uninstructed negative emotion modulation
Silvers, J. A., Wager, T. D., Weber, J., & Ochsner, K. N. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu016 · Cited by 90 · see citing works
Self-citationDecety, J., & Cowell, J. M. (2017) · Development and Psychopathology · doi:10.1017/s0954579417000530 · Cited by 91 · see citing works
Mentalization‐based treatment and its evidence‐base status: A systematic literature review
Malda‐Castillo, J., Browne, C., & Perez‐Algorta, G. (2019) · Psychology and Psychotherapy: Theory, Research and Practice · doi:10.1111/papt.12195 · Cited by 89 · see citing works
- Authors
- Denny, B. T., Kober, H., Wager, T. D., & Ochsner, K. N.
- Affiliations
- Columbia University (US)
- 2Yale University
- University of Colorado Boulder (US)
- Venue
- Journal of Cognitive Neuroscience
- Publisher
- MIT Press - Journals
- Published
- 2012-08-01
- Volume
- 24
- Issue
- 8
- Pages
- 1742-1752
- ISSN
- 0898-929X (ISSN-L)
- 1530-8898
- PMC
- PMC3806720
- OpenAlex
- W2121677155
- Semantic Scholar
- ed0070456b9770cbce9d09e1ff1311a2be401caa
- Cited by
- 830
- References
- 98
- Citations by year
- 2026: 49 · 2025: 45 · 2024: 53 · 2023: 55 · 2022: 57 · 2021: 85 · 2020: 66 · 2019: 63 · 2018: 64 · 2017: 73 · 2016: 66 · 2015: 59 · 2014: 43 · 2013: 43 · 2012: 9
- FWCI
- 3.90
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Journal of Cognitive Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation
- Neurosciences Foundation
- National Institutes of Health
- National Institute of Mental Health (R21 MH528021, R01MH076137, R21MH082308)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD069178)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Social Sciences › Psychology › Social Psychology › Action Observation and Synchronization
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Keywords
- self-other judgment, mentalization, medial prefrontal cortex, functional heterogeneity, anterior temporal pole, posterior cingulate cortex, insula, ventrolateral prefrontal cortex, self-referential processing
- MeSH terms
- Humans, Self Concept, Prefrontal Cortex, Theory of Mind, Functional Neuroimaging
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.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
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