Found 301 images.
ID | Name | Collection(s) | Description |
---|---|---|---|
11988 | Seed ROI -- Anterior cingulate cortex (ACC) | Definition and characterization of an extended social-affective default network | Anterior cingulate cortex (ACC) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
24849 | Figure 1 | Brain structure anomalies in autism spectrum disorder-a meta-analysis of VBM studies using anatomic likelihood estimation | Significant clusters of convergence obtained by ALE-based analysis indicating locations in the lateral occipital lobe, the pericentral region, the medial temporal lobe, the basal ganglia and proximate to the right parietal operculum. Both foci indicating gray and white matter changes were included in this model. Since disturbances in brain growth trajectories were discussed as a key pathophysiological feature in ASD, we integrated both foci reporting increases and decreases of gray matter (GM) or white matter (WM) in our analysis. Thus, the depicted clusters indicate brain regions consistently altered in ASD patients. |
59076 | vmPFC MACM | Segregation of the human medial prefrontal cortex in social cognition | |
59077 | dmPFC MACM | Segregation of the human medial prefrontal cortex in social cognition | |
59078 | Figure_3_rostral_module | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | The rostral left PMd module identified by multimodal CBP. |
59079 | Figure_3_central_module | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | The central left PMd module identified by multimodal CBP |
59080 | Figure_3_caudal_module | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | The caudal left PMd module identified by multimodal CBP |
59081 | Figure_3_ventral_subregion | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | The ventral (posterior) left PMd subregion identified by multimodal CBP |
59082 | Figure_3_rostro-ventral_subregion | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | The rostro-ventral left PMd subregion identified by multimodal CBP |
59083 | Figure_4_SpecificFC_rostral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Specific functional connectivity of the rostral left PMd modules |
59084 | Figure_4_SpecificFC_central | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Specific functional connectivity of the central left PMd modules |
59085 | Figure_4_SpecificFC_caudal | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Specific functional connectivity of the caudal left PMd modules |
59086 | Figure_4_SpecificFC_ventral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Specific functional connectivity of the ventral (posterior) left PMd subregion |
59087 | Figure_4_SpecificFC_RostroVentral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Specific functional connectivity of the rostro-ventral left PMd subregion |
59088 | FigureS9_MACM_rostral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Task-based functional connectivity profile of the rostral left PMd module revealed by MACM |
59089 | FigureS9_MACM_central | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Task-based functional connectivity profile of the central left PMd module revealed by MACM |
59090 | FigureS9_MACM_caudal | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Task-based functional connectivity profile of the caudal left PMd module revealed by MACM |
59091 | FigureS9_MACM_ventral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Task-based functional connectivity profile of the (posterior) ventral left PMd module revealed by MACM |
59092 | FigureS9_MACM_RostroVentral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Task-based functional connectivity profile of the rostro-ventral left PMd module revealed by MACM |
59093 | FigureS10_RSFC_rostral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Unconstrained functional connectivity profile of the rostral left PMd module revealed by RSFC |
59094 | FigureS10_RSFC_central | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Unconstrained functional connectivity profile of the central left PMd module revealed by RSFC |
59095 | FigureS10_RSFC_caudal | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Unconstrained functional connectivity profile of the caudal left PMd module revealed by RSFC |
59096 | FigureS10_RSFC_ventral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Unconstrained functional connectivity profile of the ventral left PMd module revealed by RSFC |
59097 | FigureS10_RSFC_RostroVentral | The heterogeneity of the left dorsal premotor cortex evidenced by multimodal connectivity-based parcellation and functional characterization | Unconstrained functional connectivity profile of the rostro-ventral left PMd module revealed by RSFC |
59098 | Figure 1 | Neural networks related to dysfunctional face processing in autism spectrum disorder | A single cluster indicating convergent evidence for hypoac- tivation in ASD patients compared to healthy controls during face processing was located in the left lateral temporal lobe, in particular the fusiform gyrus (-43, -61, -10, k = 172) [p < 0.05 (cluster-level FWE corrected for multiple comparisons, cluster-forming threshold p < 0.001 at voxel level)]. There were no clusters indicating increased activation in ASD patients compared to healthy controls |
59099 | Left Cluster 1 | Co-activation based parcellation of the human frontal pole | Cluster 1 binary mask of left hemisphere 3 cluster solution shown in Fig 2 |
59100 | Left Cluster 2 | Co-activation based parcellation of the human frontal pole | Cluster 2 binary mask of left hemisphere 3 cluster solution shown in Fig 2 |
59101 | Left Cluster 3 | Co-activation based parcellation of the human frontal pole | Cluster 3 binary mask of left hemisphere 3 cluster solution shown in Fig 2 |
59102 | Right Cluster 1 | Co-activation based parcellation of the human frontal pole | Cluster 1 binary mask of right hemisphere 3 cluster solution shown in Fig 2 |
59103 | Right Cluster 2 | Co-activation based parcellation of the human frontal pole | Cluster 2 binary mask of right hemisphere 3 cluster solution shown in Fig 2 |
59104 | Right Cluster 3 | Co-activation based parcellation of the human frontal pole | Cluster 3 binary mask of right hemisphere 3 cluster solution shown in Fig 2 |
59105 | Right Cluster 1 MACM | Co-activation based parcellation of the human frontal pole | Cluster 1 MACM of right hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
59106 | Right Cluster 2 MACM | Co-activation based parcellation of the human frontal pole | Cluster 2 MACM of right hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
59107 | Right Cluster 3 MACM | Co-activation based parcellation of the human frontal pole | Cluster 3 MACM of right hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
59108 | Left Cluster 1 MACM | Co-activation based parcellation of the human frontal pole | Cluster 1 MACM of left hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
59109 | Left Cluster 2 MACM | Co-activation based parcellation of the human frontal pole | Cluster 2 MACM of left hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
59110 | Left Cluster 3 MACM | Co-activation based parcellation of the human frontal pole | Cluster 3 MACM of left hemisphere 3 cluster solution shown in Fig 3. Cluster-level corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
11989 | Seed ROI -- Dorsomedial prefrontal cortex (dmPFC) | Definition and characterization of an extended social-affective default network | Dorsomedial prefrontal cortex (dmPFC) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11990 | Seed ROI -- Precuneus (PrC) | Definition and characterization of an extended social-affective default network | Precuneus (PrC) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11991 | Seed ROI -- Subgenual cingulate cortex (SGC) | Definition and characterization of an extended social-affective default network | Subgenual cingulate cortex (SGC) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11992 | Seed ROI -- Left amygdala (Amy) | Definition and characterization of an extended social-affective default network | Left amygdala (Amy) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11993 | Seed ROI -- Right temporoparietal cortex (TPJ) | Definition and characterization of an extended social-affective default network | Right temporoparietal cortex (TPJ) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11994 | Seed ROI -- Left temporoparietal cortex (TPJ) | Definition and characterization of an extended social-affective default network | Left temporoparietal cortex (TPJ) seed region derived from the conjunction DMN ∩ (EMO ∪ SOC). |
11995 | eSAD ROIs -- Left anterior middle temporal sulcus (aMTS) | Definition and characterization of an extended social-affective default network | Left anterior middle temporal sulcus (aMTS) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
11996 | eSAD ROIs -- Anterior cingulate cortex (ACC) | Definition and characterization of an extended social-affective default network | Anterior cingulate cortex (ACC) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
11997 | eSAD ROIs -- Left amygdala/hippocampus (Amy/Hipp) | Definition and characterization of an extended social-affective default network | Left amygdala/hippocampus (Amy/Hipp) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
11998 | eSAD ROIs -- Right amygdala/hippocampus (Amy/Hipp) | Definition and characterization of an extended social-affective default network | Right amygdala/hippocampus (Amy/Hipp) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
11999 | eSAD ROIs -- Left ventral basal ganglia (BG) | Definition and characterization of an extended social-affective default network | Left ventral basal ganglia (BG) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12000 | eSAD ROIs -- Right ventral basal ganglia (BG) | Definition and characterization of an extended social-affective default network | Right ventral basal ganglia (BG) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12001 | eSAD ROIs -- Dorsomedial prefrontal cortex (dmPFC) | Definition and characterization of an extended social-affective default network | Dorsomedial prefrontal cortex (dmPFC) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12002 | eSAD ROIs -- Precuneus/posterior cingulate cortex (PrC/PCC) | Definition and characterization of an extended social-affective default network | Precuneus/posterior cingulate cortex (PrC/PCC) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12003 | eSAD ROIs -- Subgenual cingulate cortex (SGC) | Definition and characterization of an extended social-affective default network | Subgenual cingulate cortex (SGC) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12004 | eSAD ROIs -- Left temporoparietal junction (TPJ) | Definition and characterization of an extended social-affective default network | Left temporoparietal junction (TPJ) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12005 | eSAD ROIs -- Right temporoparietal junction (TPJ) | Definition and characterization of an extended social-affective default network | Right temporoparietal junction (TPJ) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12006 | eSAD ROIs -- Ventromedial prefrontal cortex (vmPFC) | Definition and characterization of an extended social-affective default network | Ventromedial prefrontal cortex (vmPFC) component of the extended social-affective default (eSAD) network. These regions were derived from a consensus across MACM and RS-fMRI connectivity maps of the seed ROIs. |
12007 | Figure 3 - Whole Left Amygdala | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the human amygdala. Union of all three clusters for the left hemisphere. |
12008 | Figure 3 - Whole Right Amygdala | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the human amygdala. Union of all three clusters for the right hemisphere. |
12009 | Figure 3 - Right Amygdala (cluster #1) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the right human amygdala. Cluster #1 (red) - centromedial nuclei group |
12010 | Figure 3 - Left Amygdala (cluster #1) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the left human amygdala. Cluster #1 (red) - centromedial nuclei group |
12011 | Figure 3 - Left Amygdala (cluster #2) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the left human amygdala. Cluster #2 (green) - superficial nuclei group |
12012 | Figure 3 - Left Amygdala (cluster #3) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the left human amygdala. Cluster #3 (blue) - laterobasal nuclei group |
12013 | Figure 3 - Right Amygdala (cluster #2) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the right human amygdala. Cluster #2 (green) - superficial nuclei group |
12014 | Figure 3 - Right Amygdala (cluster #3) | An investigation of the structural, connectional, and functional subspecialization in the human amygdala | Connectivity-based parcellation (CBP) of the right human amygdala. Cluster #3 (blue) - laterobasal nuclei group |
12015 | Figure 1 (Morality) | Parsing the neural correlates of moral cognition: ALE meta-analysis on morality, theory of mind, and empathy | Figure 1, Column 1: Morality. ALE meta-analysis of neuroimaging studies on moral cognition, theory of mind, and empathy. Significant meta-analysis results displayed on frontal, right, and left surface view as well as sagittal, coronal, and axial sections of the MNI single-subject template. Coordinates in MNI space. All results were significant at a clusterforming threshold of p\0.05 and an extent threshold of k = 10 voxels (to exclude presumably incidental results). |
12016 | Figure 1 (ToM) | Parsing the neural correlates of moral cognition: ALE meta-analysis on morality, theory of mind, and empathy | Figure 1, Column 2: Theory of Mind. ALE meta-analysis of neuroimaging studies on moral cognition, theory of mind, and empathy. Significant meta-analysis results displayed on frontal, right, and left surface view as well as sagittal, coronal, and axial sections of the MNI single-subject template. Coordinates in MNI space. All results were significant at a clusterforming threshold of p\0.05 and an extent threshold of k = 10 voxels (to exclude presumably incidental results). |
12017 | Figure 1 (Empathy) | Parsing the neural correlates of moral cognition: ALE meta-analysis on morality, theory of mind, and empathy | Figure 1, Column 3: Empathy. ALE meta-analysis of neuroimaging studies on moral cognition, theory of mind, and empathy. Significant meta-analysis results displayed on frontal, right, and left surface view as well as sagittal, coronal, and axial sections of the MNI single-subject template. Coordinates in MNI space. All results were significant at a clusterforming threshold of p\0.05 and an extent threshold of k = 10 voxels (to exclude presumably incidental results). |
12018 | Figure 1 - Anterior cluster | Characterization of the temporo-parietal junction by combining data-driven parcellation, complementary connectivity analyses, and functional decoding | Connectivity-based parcellation (CBP) of the human right temporo-parietal junction - anterior cluster (aTPJ) |
12019 | Figure 1 - Posterior cluster | Characterization of the temporo-parietal junction by combining data-driven parcellation, complementary connectivity analyses, and functional decoding | Connectivity-based parcellation (CBP) of the human right temporo-parietal junction - posterior cluster (pTPJ) |
12020 | Figure 1, third column | ALE meta-analysis on facial judgments of trustworthiness and attractiveness | All neuroimaging experiments labeled as attractiveness judgment |
12021 | Figure 1, first column | ALE meta-analysis on facial judgments of trustworthiness and attractiveness | All neuroimaging experiments labeled as trustworthiness or attractiveness judgment |
12022 | Figure 1, second column | ALE meta-analysis on facial judgments of trustworthiness and attractiveness | All neuroimaging experiments labeled as trustworthiness judgment |
12023 | Meta_Observation | ALE meta-analysis of action observation and imitation in the human brain | corresponding to Fig. 1The file contains the significant meta-analysis results (p < 0.05, cluster-level corrected) showing convergent activation of brain regions across all studies reporting action observation experiments included in the meta-analysis (cf. Table 1). |
12024 | Meta_Imitation | ALE meta-analysis of action observation and imitation in the human brain | corresponding to Fig. 5The file contains the significant meta-analysis results (p < 0.05, cluster-level corrected) showing convergent activation of brain regions across all studies reporting action imitation experiments included in the meta-analysis. |
12025 | Conjunction_Observation-Imitation | ALE meta-analysis of action observation and imitation in the human brain | corresponding to Fig. 7AThe file contains the significant results of the conjunction (p < 0.05, cluster-level corrected) between the meta-analysis results for action observation and action imitation, thus the conjunction between the files in no. 1 and 2. |
12026 | Figure 3 - Anterior > posterior connectivity | Is There "One" DLPFC in Cognitive Action Control? Evidence for Heterogeneity From Co-Activation-Based Parcellation | Regions showing significantly stronger task-dependent and task-independent connectivity of the anterior versus posterior cluster |
12027 | Figure 4 - Posterior > anterior connectivity | Is There "One" DLPFC in Cognitive Action Control? Evidence for Heterogeneity From Co-Activation-Based Parcellation | Regions showing significantly stronger task-dependent and task-independent connectivity of the posterior versus anterior cluster |
12028 | Figure 2 - Anterior cluster | Is There "One" DLPFC in Cognitive Action Control? Evidence for Heterogeneity From Co-Activation-Based Parcellation | Connectivity-based parcellation (CBP) results -- Cluster #2 (anterior) |
12029 | Figure 1 - Posterior cluster | Is There "One" DLPFC in Cognitive Action Control? Evidence for Heterogeneity From Co-Activation-Based Parcellation | Connectivity-based parcellation (CBP) results -- Cluster #1 (posterior) |
12030 | Figure 1 | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | ALE result for conflict minus that for no conflict |
12031 | Figure 2A | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | ALE result for the Stroop task |
12032 | Figure 2B | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | ALE result for Spatial Interference Tasks |
12033 | Figure 2C | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | ALE result for the Stop-Signal Task |
12034 | Figure 2D | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | ALE result for the Go/No-Go Task |
12035 | Figure 3 | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | Conjunction across all four task types |
12036 | Figure 4 | Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses | Conjunction across Stroop, Spatial Interference and Stop-Signal Tasks |
12037 | Figure 4E -- Cluster #1 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Cluster #1 for the K=5 cluster solution of cytoarchitectonic area 44. |
12038 | Figure 4E -- Cluster #2 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Cluster #2 for the K=5 cluster solution of cytoarchitectonic area 44. |
12039 | Figure 4E -- Cluster #3 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Cluster #3 for the K=5 cluster solution of cytoarchitectonic area 44. |
12040 | Figure 4E -- Cluster #4 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Cluster #4 for the K=5 cluster solution of cytoarchitectonic area 44. |
12041 | Figure 4E -- Cluster #5 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Cluster #5 for the K=5 cluster solution of cytoarchitectonic area 44. |
12042 | Figure 6B -- Cluster #1 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state functional connectivity and specific MACM co-activation, for Cluster #1. Images were thresholded at p < 0.05 (FWE-corrected at cluster level; cluster-forming threshold at voxel-level p < 0.001). |
12043 | Figure 6B -- Cluster #2 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state functional connectivity and specific MACM co-activation, for Cluster #2. Images were thresholded at p < 0.05 (FWE-corrected at cluster level; cluster-forming threshold at voxel-level p < 0.001). |
12044 | Figure 6B -- Cluster #3 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state functional connectivity and specific MACM co-activation, for Cluster #3. Images were thresholded at p < 0.05 (FWE-corrected at cluster level; cluster-forming threshold at voxel-level p < 0.001). |
12045 | Figure 6B -- Cluster #4 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state functional connectivity and specific MACM co-activation, for Cluster #4. Images were thresholded at p < 0.05 (FWE-corrected at cluster level; cluster-forming threshold at voxel-level p < 0.001). |
12046 | Figure 6B -- Cluster #5 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state functional connectivity and specific MACM co-activation, for Cluster #5. Images were thresholded at p < 0.05 (FWE-corrected at cluster level; cluster-forming threshold at voxel-level p < 0.001). |
12047 | Figure 6A -- Cluster #1 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Regions significantly more co-activated with Cluster #1 than with any of the other four clusters, determined using a MACM analysis. Results are thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12048 | Figure 6A -- Cluster #2 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Regions significantly more co-activated with Cluster #2 than with any of the other four clusters, determined using a MACM analysis. Results are thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12049 | Figure 6A -- Cluster #3 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Regions significantly more co-activated with Cluster #3 than with any of the other four clusters, determined using a MACM analysis. Results are thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12050 | Figure 6A -- Cluster #4 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Regions significantly more co-activated with Cluster #4 than with any of the other four clusters, determined using a MACM analysis. Results are thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12051 | Figure 6A -- Cluster #5 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Regions significantly more co-activated with Cluster #5 than with any of the other four clusters, determined using a MACM analysis. Results are thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12052 | Figure 5A | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific co-activations, determined by MACM, across all five clusters. |
12053 | Figure 5B | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Conjunction of specific resting-state connectivity across all five clusters. |
12054 | Figure S6 -- Cluster #1 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Specific resting-state connectivity for Cluster #1 (not masked by MACM), thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12055 | Figure S6 -- Cluster #2 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Specific resting-state connectivity for Cluster #2 (not masked by MACM), thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12056 | Figure S6 -- Cluster #3 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Specific resting-state connectivity for Cluster #3 (not masked by MACM), thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12057 | Figure S6 -- Cluster #4 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Specific resting-state connectivity for Cluster #4 (not masked by MACM), thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12058 | Figure S6 -- Cluster #5 | Tackling the multifunctional nature of Broca's region meta-analytically: Co-activation-based parcellation of area 44 | Specific resting-state connectivity for Cluster #5 (not masked by MACM), thresholded at a cluster-level FWE-corrected threshold of p < 0.05 (cluster-forming threshold at voxel-level p < 0.001). |
12059 | caudal-right cluster (cluster1) | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | |
12060 | caudal-left cluster (cluster4) | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | |
12061 | rostro-dorsal cluster (cluster3) | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | |
12062 | rostro-ventral cluster (cluster2) | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | |
12063 | MACM cluster 2 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific task-dependent connectivity with cluster 2 contrasted to connectivity patterns of all three other clusters |
12064 | MACM cluster1 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific task-dependent connectivity with cluster 1, contrasted to connectivity patterns of all three other clusters |
12065 | MACM cluster 4 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific task-dependent connectivity with cluster 4, contrasted to connectivity patterns of all three other clusters |
12066 | MACM cluster3 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific task-dependent connectivity with cluster 3, contrasted to connectivity patterns of all three other clusters |
12067 | RSFC cluster 1 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific resting-state connectivity with cluster 1, contrasted to connectivity patterns of all three other clusters |
12068 | RSFC cluster 3 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific resting-state connectivity with cluster 3, contrasted to connectivity patterns of all three other clusters |
12069 | RSFC cluster 2 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific resting-state connectivity with cluster 2, contrasted to connectivity patterns of all three other clusters |
12070 | RSFC cluster 4 vs all other clusters | Functional Segregation of the Human Dorsomedial Prefrontal Cortex | Specific resting-state connectivity with cluster 4, contrasted to connectivity patterns of all three other clusters |
12071 | Figure 1A | Meta-analytical definition and functional connectivity of the human vestibular cortex | Location of all 414 foci reported in the 28 functional neuroimaging studies on vestibular stimulation on the MNI single subject template. |
12072 | Figure 1B | Meta-analytical definition and functional connectivity of the human vestibular cortex | Meta-analysis results for all vestibular experiments following statistical comparison against a null-distribution of spatial independence across studies, ALE scores were thresholded at a cluster-level p<0.05. |
12073 | Figure 2A | Meta-analytical definition and functional connectivity of the human vestibular cortex | Significant convergence of activation reported in experiments employing caloric vestibular stimulation shown in a transversal view through the insular cortex, thresholded at a cluster-level p<0.05. |
12074 | Figure 2B | Meta-analytical definition and functional connectivity of the human vestibular cortex | Significant convergence of activation reported in experiments employing vestibular stimuli other than caloric irrigation, thresholded at a cluster-level p<0.05. |
12075 | Figure 4A | Meta-analytical definition and functional connectivity of the human vestibular cortex | Functional connectivity of the PIVC as indicated by significant (cluster-level p<0.05 corrected) correlation in resting state fMRI data. |
12076 | Figure 4B | Meta-analytical definition and functional connectivity of the human vestibular cortex | Significant convergence of activation reported in experiments that employed saccadic eye movements as retrieved through the BrainMap database. |
12077 | Figure 4C | Meta-analytical definition and functional connectivity of the human vestibular cortex | Conjunction between the functional connectivity of the PIVC and the meta-analysis on saccadic eye movements indicating regions that were significant in both analyses. |
12078 | Figure 3A | Meta-analytical definition and functional connectivity of the human vestibular cortex | Significant overlap between regions showing convergent activation following caloric and non-caloric stimulation (both thresholded at a cluster-level p<0.05) was found only in a single region on the right posterior parietal operculum. The result is shown as a projection onto the surface of the temporo-parietal cortex. |
12079 | Figure 3B | Meta-analytical definition and functional connectivity of the human vestibular cortex | Significant overlap between regions showing convergent activation following left and right unilateral cold caloric stimulation, respectively, (both thresholded at a cluster-level pb0.05) was also found only in a single region on the right posterior parietal operculum. |
12080 | All Pain Studies | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE result for all pain studies |
12081 | Experimental Pain Studies | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE result for all experimentally induced pain studies |
12082 | Experimental - Neuropathic | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE results of all experimentally induced pain studies, minus that of all neuropathic pain studies. Thresholded at uncorrected p < 0.05. |
12083 | Neuropathic ∪ Experimental | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | Conjunction of ALEs for experimentally induced and neuropathic pain. Thresholded at uncorrected p < 0.05. |
12084 | All Neuropathic Studies | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE result for all neuropathic pain studies |
12085 | All Non-thermal Pain Studies | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE result for all non-thermally induced pain studies |
12086 | Non-thermal - Thermal | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE for non-thermally induced pain studies, minus that for thermally induced pain studies. Thresholded at uncorrected p < 0.05. |
12087 | Thermal ∪ Non-thermal | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | Conjunction of ALEs for all thermally and non-thermally induced pain studies. Thresholded at uncorrected p < 0.05. |
12088 | All Thermal Studies | Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain | ALE result for all thermally induced pain studies. |
12089 | Figure 2C - Left anterior insula | Identification of a Common Neurobiological Substrate for Mental Illness | Conjunction showing common grey matter loss across diagnoses in the left anterior insula. |
12090 | Figure 2C - Right anterior insula | Identification of a Common Neurobiological Substrate for Mental Illness | Conjunction showing common grey matter loss across diagnoses in the right anterior insula. |
12091 | Figure 2C - Dorsal ACC | Identification of a Common Neurobiological Substrate for Mental Illness | Conjunction showing common grey matter loss across diagnoses in the dorsal anterior cingulate cortex (dACC). |
12092 | Conjunction of sensorimotor tasks and SRTT | A quantitative meta-analysis and review of motor learning in the human brain | Areas consistently activated across both subgroups of paradigms. Using the global analysis as a mask to provide greater specificity, a conjunction analysis was conducted across the task specific analyses of sensorimotor tasks and SRTT variants. See Table 4 and Figure 6A. |
12093 | Main effect of sensorimotor tasks | A quantitative meta-analysis and review of motor learning in the human brain | Analysis of 35 sensorimotor tasks. See Table 2 and Figure 2A. |
12094 | Main effect of SRTT | A quantitative meta-analysis and review of motor learning in the human brain | Analysis of the 35 SRTT variants. See Figure 3A and Table 3. |
12095 | Contrast analysis: implicit SRTT variants vs explicit SRTT variants | A quantitative meta-analysis and review of motor learning in the human brain | Contrast analysis comparing activations during explicit and implicit SRTT variants. See Figure 5. |
12096 | aMCC Seed | The role of anterior midcingulate cortex in cognitive motor control | The seed region was taken from a recent fMRI study which examined neural effects of self-initiated movements by letting subjects choose between left or right finger movements to be initiated at an freely chosen point in time [Hoffstaedter et al., 2013] |
12097 | MACM aMCC | The role of anterior midcingulate cortex in cognitive motor control | The VOI search in the BrainMap database revealed 656 experiments containing activation foci within the aMCC. The ALE maps reflecting the convergence of co-activations with the aMCC were family wise error (FWE) corrected at a cluster level threshold of p < 0.05 (cluster-forming threshold: p < 0.001 at voxel level; cluster extend threshold k = 211), and converted to Z-scores. |
12098 | MACM aMCC cognition | The role of anterior midcingulate cortex in cognitive motor control | 277 experiments in BrainMap featuring activation in the aMCC were attributed to the behavioral domain ‘cognition’. |
12099 | MACM aMCC action | The role of anterior midcingulate cortex in cognitive motor control | 222 experiments featuring activation in the aMCC were attributed to the behavioral domain ‘action’. |
12100 | RS aMCC | The role of anterior midcingulate cortex in cognitive motor control | The aMCC was used as seed VOI in the resting-state analysis in 100 subjects. Pearson correlation coefficients were computed between the representative time series of the VOI and those of all other grey matter voxels in the brain. Correlation coefficients were Fisher's Z transformed and tested for consistency in an ANOVA. The results of this random-effects analysis were family wise error (FWE) corrected at a threshold of p < 0.05. |
12101 | Conjunction RS and MACM aMCC | The role of anterior midcingulate cortex in cognitive motor control | Conjunction RS and MACM aMCC |
12102 | Figure 2 (hard>easy) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant Activation Likelihood Estimate (ALE) clusters for the three separate ALE analyses in standard Montreal Neurological Institute space. Red: Task > Control; blue: Hard > Easy; green: Reward > Control. Numbers indicate Z coordinates in MNI space. |
12103 | Figure 2 (reward>control) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant Activation Likelihood Estimate (ALE) clusters for the three separate ALE analyses in standard Montreal Neurological Institute space. Red: Task > Control; blue: Hard > Easy; green: Reward > Control. Numbers indicate Z coordinates in MNI space. |
12104 | Figure 2 (task>control) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant Activation Likelihood Estimate (ALE) clusters for the three separate ALE analyses in standard Montreal Neurological Institute space. Red: Task > Control; blue: Hard > Easy; green: Reward > Control. Numbers indicate Z coordinates in MNI space. |
12105 | Figure 3 (hard>easy ∩ task>control) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant conjunction and subtraction clusters in standard Montreal Neurological Institute space. Green: The significant conjunction clusters for the task-general network and the task difficulty network are located in the right pre-SMA, left pre-motor cortex, bilateral anterior insula, and right PFm. Blue: The significant conjunction cluster for the task-general and reward networks is located in right anterior insula. Red: The unique areas for the task-general network compared to the reward-based network are located in left pre-SMA cortex, right hIP2, and right anterior insula. Violet: The unique areas for the reward-based network are located in left nucleus accumbens and right frontal orbital cortex. Numbers indicate Z coordinates in MNI space. |
12106 | Figure 3 (reward>control ∩ task>control) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant conjunction and subtraction clusters in standard Montreal Neurological Institute space. Green: The significant conjunction clusters for the task-general network and the task difficulty network are located in the right pre-SMA, left pre-motor cortex, bilateral anterior insula, and right PFm. Blue: The significant conjunction cluster for the task-general and reward networks is located in right anterior insula. Red: The unique areas for the task-general network compared to the reward-based network are located in left pre-SMA cortex, right hIP2, and right anterior insula. Violet: The unique areas for the reward-based network are located in left nucleus accumbens and right frontal orbital cortex. Numbers indicate Z coordinates in MNI space. |
12107 | Figure 3 ([reward>control] > [task>control]) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant conjunction and subtraction clusters in standard Montreal Neurological Institute space. Green: The significant conjunction clusters for the task-general network and the task difficulty network are located in the right pre-SMA, left pre-motor cortex, bilateral anterior insula, and right PFm. Blue: The significant conjunction cluster for the task-general and reward networks is located in right anterior insula. Red: The unique areas for the task-general network compared to the reward-based network are located in left pre-SMA cortex, right hIP2, and right anterior insula. Violet: The unique areas for the reward-based network are located in left nucleus accumbens and right frontal orbital cortex. Numbers indicate Z coordinates in MNI space. |
12108 | Figure 3 ([task>control] > [reward>control]) | Brain networks of perceptual decision-making: an fMRI ALE meta-analysis | The significant conjunction and subtraction clusters in standard Montreal Neurological Institute space. Green: The significant conjunction clusters for the task-general network and the task difficulty network are located in the right pre-SMA, left pre-motor cortex, bilateral anterior insula, and right PFm. Blue: The significant conjunction cluster for the task-general and reward networks is located in right anterior insula. Red: The unique areas for the task-general network compared to the reward-based network are located in left pre-SMA cortex, right hIP2, and right anterior insula. Violet: The unique areas for the reward-based network are located in left nucleus accumbens and right frontal orbital cortex. Numbers indicate Z coordinates in MNI space. |
12109 | Figure 1 - Emotion Regulation | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | Displayed are significant results from the meta-analysis of emotion regulation (cFWE corrected p < 0.05) |
12110 | Figure 2A - IFG | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the inferior frontal gyrus (IFG) seed region. |
12111 | Figure 2B - DLPFC | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the dorsolateral prefrontal cortex (DLPFC) seed region. |
12112 | Figure 2C - aMCC | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the anterior medial cingulate cortex (aMCC) seed region. |
12113 | Figure 2E - STG | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the superior temporal gyrus (STG) seed region. |
12114 | Figure 2F - AG | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the angular gyrus (AG) seed region. |
12115 | Figure 2D - SMA | Neural network of cognitive emotion regulation — An ALE meta-analysis and MACM analysis | MACM result for the (pre) supplementary motor area (SMA) seed region. |
12116 | Figure 1 - Attention ∩ False belief | The role of the right temporoparietal junction in attention and social interaction as revealed by ALE meta-analysis | Cerebral region identified in Activation Likelihood Estimation (ALE) conjunction analysis across reorienting of attention and false belief studies in Montreal Neurological Institute space. Family-wise error corrected P < 0.05. |
12117 | Figure 2 - Reorienting > False belief | The role of the right temporoparietal junction in attention and social interaction as revealed by ALE meta-analysis | Neural areas identified in Activation Likelihood Estimation (ALE) difference analyses for reorienting of attention (red) and false belief (green) in Montreal Neurological Institute space. Findings are uncorrected P < 0.001. |
12118 | Figure 3 - Anterior > Posterior RTPJ | The role of the right temporoparietal junction in attention and social interaction as revealed by ALE meta-analysis | Co-activation patterns for anterior right temporoparietal junction (rTPJ) versus posterior rTPJ based on a combination of task-related meta-analytic connectivity mapping analysis and task-free resting-state functional connectivity analysis in Montreal Neurological Institute space. Family-wise error corrected P < 0.05. |
12119 | Figure 4 - Posterior > Anterior RTPJ | The role of the right temporoparietal junction in attention and social interaction as revealed by ALE meta-analysis | Co-activation patterns for posterior right temporoparietal junction (rTPJ) versus anterior rTPJ based on a combination of task-related meta-analytic connectivity mapping analysis and task-free resting-state functional connectivity analysis in Montreal Neurological Institute space. Family-wise error corrected P < 0.05. |
12120 | Figure 2A (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by emotion, specific results tested against the BrainMap database |
12121 | Figure 2A (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by emotion, conventional results |
12122 | Figure 2B (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by empathy, conventional results |
12123 | Figure 2B (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by empathy, specific results tested against the BrainMap database |
12124 | Figure 3A (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by olfaction, conventional results |
12125 | Figure 3A (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by olfaction, specific results tested against the BrainMap database |
12126 | Figure 3B (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by gustation, conventional results |
12127 | Figure 3B (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by gustation, specific results tested against the BrainMap database |
12128 | Figure 4A (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by interoception, conventional results |
12129 | Figure 4A (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by interoception, specific results tested against the BrainMap database |
12130 | Figure 4B (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by pain, conventional results |
12131 | Figure 4B (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by pain, specific results tested against the BrainMap database |
12132 | Figure 4C (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by somatosensory stimuli, conventional results |
12133 | Figure 4C (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by somatosensory stimuli, specific results tested against the BrainMap database |
12134 | Figure 4D (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by motor tasks, conventional results |
12135 | Figure 4D (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by motor tasks, specific results tested against the BrainMap database |
12136 | Figure 5A (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by attention, conventional results |
12137 | Figure 5A (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by attention, specific results tested against the BrainMap database |
12138 | Figure 5B (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by language, specific results tested against the BrainMap database |
12139 | Figure 5B (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by language, conventional results |
12140 | Figure 5C (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by speech, conventional results |
12141 | Figure 5C (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by speech, specific results tested against the BrainMap database |
12142 | Figure 5D (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by working memory, conventional results |
12143 | Figure 5D (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by working memory, specific results tested against the BrainMap database |
12144 | Figure 5E (left) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by memory, conventional results |
12145 | Figure 5E (right) | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Insular activations by memory, specific results tested against the BrainMap database |
12146 | Figure 6 | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Overlap of all functional categories except somatosensation and motion, namely the anterior-dorsal part of the insula |
12147 | Figure 7A | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Functional differentiation of the insula for the sensorimotor domain |
12148 | Figure 7B | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Functional differentiation of the insula for the cognitive domain |
12149 | Figure 7C | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Functional differentiation of the insula for the chemical sensory domain |
12150 | Figure 7D | A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis | Functional differentiation of the insula for the social-emotional domain |
12151 | Figure 1 | Sustaining attention to simple tasks: A meta-analytic review of the neural mechanisms of vigilant attention. | The Nifti file "Attention_cFWE05_001_103.nii" contains the thresholded results of the ALE main effect, as shown in Fig. 1 of the associated paper. |
12152 | Figure 1 - Multidemand Network (thres) | Interindividual differences in cognitive flexibility: influence of gray matter volume, functional connectivity and trait impulsivity | The core multiple-demand network, consisting of regions that showed significant convergence across studies in three different metaanalyses, including midcingulate cortex extending into supplementary motor area (MCC/SMA), left and right anterior insula (aINS), left and right inferior frontal junction/gyrus (IFJ/IFG), right middle frontal gyrus (MFG) as well as right inferior parietal cortex extending into intraparietal sulcus (IPC/IPS).Clusters were thresholded by excluding those with less than 50 voxels. |
12153 | Figure 1 - Multidemand Network (no thres) | Interindividual differences in cognitive flexibility: influence of gray matter volume, functional connectivity and trait impulsivity | The core multiple-demand network, consisting of regions that showed significant convergence across studies in three different metaanalyses, including midcingulate cortex extending into supplementary motor area (MCC/SMA), left and right anterior insula (aINS), left and right inferior frontal junction/gyrus (IFJ/IFG), right middle frontal gyrus (MFG) as well as right inferior parietal cortex extending into intraparietal sulcus (IPC/IPS). Clusters are unthresholded. |
12154 | Figure 1A - MCI>HC during memory encoding | Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer’s disease: a coordinate-based meta-analysis | Increased right hippocampal activation in MCI patients compared to age-matched control subjects during memory encoding of visual or verbal stimuli. |
12155 | Figure 1B - MCI<HC during imagery retrieval | Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer’s disease: a coordinate-based meta-analysis | Decreased left hippocampal activation in MCI patients compared to age-matched control subjects during retrieval of previously learned image stimuli. |
12156 | Figure 1C - AD<HC during retrieval | Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer’s disease: a coordinate-based meta-analysis | Decreased right hippocampal activation in AD patients compared to age-matched control subjects during retrieval of visual or verbal stimuli. |
12157 | Figure 2 - MCI<HC during verbal retrieval | Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer’s disease: a coordinate-based meta-analysis | Decreased right insula and inferior frontal gyrus activation in MCI patients compared to age-matched control subjects during verbal episodic-memory retrieval tasks. |
12158 | Figure 3 - AD>HC during visual retrieval | Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer’s disease: a coordinate-based meta-analysis | Stronger, bilateral (right>left) precuneus activation in AD patients compared to age-matched control subjects during image encoding. |
12159 | Figure 1A | Progressive pathology is functionally linked to the domains of language and emotion: meta-analysis of brain structure changes in schizophrenia patients | 4 clusters indicating convergent regional atrophy in schizophrenia patients. Clusters were located in the left periinsular region, the bilateral thalamus, the left medial temporal lobe (mainly laterobasal amygdala) and the left basal forebrain/ventral striatum. |
12160 | Figure 1B | Progressive pathology is functionally linked to the domains of language and emotion: meta-analysis of brain structure changes in schizophrenia patients | Cluster indicating increased grey matter volume in schizophrenia patients. The cluster was located in the left putamen. |
12161 | Figure 1A | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Anterior lateral prefrontal cortex seed region (mask image) |
12162 | Figure 1B | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Posterior lateral prefrontal cortex seed region (mask image) |
12163 | Figure 2A | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | MACM result for aLPFC |
12164 | Figure 2B | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | MACM result for pLPFC |
12165 | Figure 2E | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | VBM-based grey matter volume covariance of the aLPFC |
12166 | Figure 2F | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | VBM-based grey matter volume covariance of the aLPFC |
12167 | Figure 2C | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Resting-state functional connectivity for aLPFC |
12168 | Figure 2D | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Resting-state functional connectivity for pLPFC |
12169 | Figure 3A | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Task-set working memory network, taken from Rottschy et al. (2012) |
12170 | Figure 3D | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Task-load working memory network, taken from Rottschy et al. (2012) |
12171 | Figure 2G | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of all three modalities for the aLPFC (MACM ∩ RS-FC ∩ SC) |
12172 | Figure 2H | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of all three modalities for the pLPFC (MACM ∩ RS-FC ∩ SC) |
12173 | Figure 4A | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Contrast for resting state BOLD: aLPFC > pLPFC |
12174 | Figure 4B | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Contrast for resting state BOLD: pLPFC > aLPFC |
12175 | Figure 5A | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Default mode network (DMN), taken from Schilbach et al. (2012) |
12176 | Figure 5B | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of default mode network with emotional processing network (DMN ∩ EMO), taken from Schilbach et al. (2012) |
12177 | Figure 3C | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of task-set WM network with the pLPFC conjunction of Figure 2H (task-set ∩ MACM ∩ RS-FC ∩ SC) |
12178 | Figure 3B | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of task-set WM network with the aLPFC conjunction of Figure 2G (task-set ∩ MACM ∩ RS-FC ∩ SC) |
12179 | Figure 3E | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of task-load WM network with the aLPFC conjunction of Figure 2G (task-load ∩ MACM ∩ RS-FC ∩ SC) |
12180 | Figure 3F | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of task-load WM network with the pLPFC conjunction of Figure 2G (task-load ∩ MACM ∩ RS-FC ∩ SC) |
12181 | Figure 5C | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Resting-state BOLD anti-correlations for aLPFC |
12182 | Figure 5D | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Resting-state BOLD anti-correlations for pLPFC |
12183 | Figure 5E | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of resting-state BOLD anti-correlations for aLPFC with the DMN |
12184 | Figure 5F | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of resting-state BOLD anti-correlations for pLPFC with the DMN |
12185 | Figure 5G | Multimodal connectivity mapping of the human left anterior and posterior lateral prefrontal cortex | Conjunction of resting-state BOLD anti-correlations for aLPFC with the EMO network |
12186 | Figure 1 | Modelling neural correlates of working memory: A coordinate-based meta-analysis | Figure 1. Main effect across all 189 working memory experiments revealing consistent bilateral activation of a fronto-parietal network. |
12187 | Figure 2b | Modelling neural correlates of working memory: A coordinate-based meta-analysis | Figure 2B. A conjunction analysis of task set and load effects displayed a bilateral fronto-parietal network similar to the main effect. |
12188 | Figure 3b | Modelling neural correlates of working memory: A coordinate-based meta-analysis | Figure 3B. A conjunction analysis over verbal and non-verbal tasks revealed activation of a fronto-parietal network similar to the main effect. |
12189 | Figure 4b | Modelling neural correlates of working memory: A coordinate-based meta-analysis | Figure 4B. Conjunction analysis of object identity and object location. |
12190 | Figure 5 | Modelling neural correlates of working memory: A coordinate-based meta-analysis | Figure 5. The working memory core network. Left dominant bilateral activation of regions showing converging activations in each of the following analyses: task effects for n-back and Sternberg tasks, verbal and non-verbal tasks, load effects and all three phases (encoding, maintenance, recall). |
12191 | Figure 2 - EMO Network | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the ALE meta-analysis of emotional processing tasks (EMO). |
12192 | Figure 4 - SOC ∩ EMO | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the conjunction analysis of SOC ∩ EMO. |
12193 | Figure 5 - SOC ∩ DMN | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the conjunction analysis of SOC ∩ DMN. |
12194 | Supplemental Figure 1 - EMO ∩ DMN | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the conjunction analysis of EMO ∩ DMN. |
12195 | Supplemental Figure 2 - (SOC ∪ EMO) ∩ DMN | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the conjunction analysis of (SOC ∪ EMO) ∩ DMN. |
12196 | Figure 1 - SOC Network | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the ALE meta-analysis for social cognition tasks (SOC). |
12197 | Figure 3 - DMN network | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the ALE meta-analysis of unconstrained cognition (DMN). |
12198 | Figure 6 - SOC ∩ EMO ∩ DMN | Introspective Minds: Using ALE Meta-Analyses to Study Commonalities in the Neural Correlates of Emotional Processing, Social & Unconstrained Cognition | Significant results of the conjunction analysis of SOC ∩ EMO ∩ DMN. |
18856 | Cluster 1 | Subspecialization in the human posterior medial cortex | |
18857 | Cluster 2 | Subspecialization in the human posterior medial cortex | |
18858 | Cluster 3 | Subspecialization in the human posterior medial cortex | |
18859 | Cluster 4 | Subspecialization in the human posterior medial cortex | |
18860 | Reward prediction error | Reinforcement learning models and their neural correlates: An activation likelihood estimation meta-analysis | Reward prediction error (main effect) |
18861 | Conjunction (6 studies) | Reinforcement learning models and their neural correlates: An activation likelihood estimation meta-analysis | Conjunction of all sub-contrasts (aside from smoothing) |
18862 | Expected Value | Reinforcement learning models and their neural correlates: An activation likelihood estimation meta-analysis | Expected Value contrast. |
18863 | MACM-CBP_rostral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | MACM-CBP_rostral_cluster. Figure 2A. |
18864 | MACM_CBP_central_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | MACM-CBP_central_cluster. Figure 2A. |
18865 | MACM_CBP_caudal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | MACM-CBP_caudal_cluster. Figure 2A. |
18866 | MACM-CBP_ventral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | MACM-CBP_ventral_cluster. Figure 2A. |
18867 | MACM-CBP_dorsal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | MACM-CBP_dorsal_cluster. Figure 2A. |
18868 | PDT-CBP_rostral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | PDT-CBP_rostral_cluster. Figure 2B. |
18869 | PDT-CBP_central_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | PDT-CBP_central_cluster. Figure 2B. |
18870 | PDT-CBP_caudal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | PDT-CBP_caudal_cluster. Figure 2B. |
18871 | PDT-CBP_ventral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | PDT-CBP_ventral_cluster. Figure 2B. |
18872 | PDT-CBP_dorsal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | PDT-CBP_dorsal_cluster. Figure 2B. |
18873 | RSFC-CBP_rostral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | RSFC-CBP_rostral_cluster. Figure 2C. |
18874 | RSFC-CBP_central_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | RSFC-CBP_central_cluster. Figure 2C. |
18875 | RSFC-CBP_caudal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | RSFC-CBP_caudal_cluster. Figure 2C. |
18876 | RSFC-CBP_ventral_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | RSFC-CBP_ventral_cluster. Figure 2C. |
18877 | RSFC-CBP_dorsal_cluster | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | RSFC-CBP_dorsal_cluster. Figure 2C. |
18878 | FC_MACM_specific_rostral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Task functional connectivity rostral cluster. Figure 3A |
18879 | FC_MACM_specific_central | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Task functional connectivity central cluster. Figure 3A |
18880 | FC_MACM_specific_caudal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Task functional connectivity caudal cluster. Figure 3A |
18881 | FC_MACM_specific_ventral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Task functional connectivity ventral cluster. Figure 3A |
18882 | FC_MACM_specific_dorsal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Task functional connectivity dorsal cluster. Figure 3A |
18883 | FC_RSFC_specific_rostral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Resting state functional connectivity rostral cluster. Figure 3B |
18884 | FC_RSFC_specific_central | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Resting state functional connectivity central cluster. Figure 3B |
18885 | FC_RSFC_specific_caudal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Resting state functional connectivity caudal cluster. Figure 3B |
18886 | FC_RSFC_specific_ventral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Resting state functional connectivity ventral cluster. Figure 3B |
18887 | FC_RSFC_specific_dorsal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Resting state functional connectivity dorsal cluster. Figure 3B |
18888 | FC_MACMandRSFC_specific_rostral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Specific functional connectivity pattern (common to both task and resting state) of rostral cluster. Figure 3C. |
18889 | FC_MACMandRSFC_specific_central | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Specific functional connectivity pattern (common to both task and resting state) of central cluster. Figure 3C. |
18890 | FC_MACMandRSFC_specific_caudal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Specific functional connectivity pattern (common to both task and resting state) of caudal cluster. Figure 3C. |
18891 | FC_MACMandRSFC_specific_ventral | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Specific functional connectivity pattern (common to both task and resting state) of ventral cluster. Figure 3C. |
18892 | FC_MACMandRSFC_specific_dorsal | The Right Dorsal Premotor Mosaic: Organization, Functions, and Connectivity | Specific functional connectivity pattern (common to both task and resting state) of dorsal cluster. Figure 3C. |
18893 | ALE_results_of_self-face_recognition_unthresholded | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | output from ALE 2.3, unthresholded image |
18894 | ALE_results_of_self-reference_unthresholed | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | output from ALE 2.3, unthresholed image |
18895 | ALE-results_self-face_p_value | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | p map from ALE 2.3 |
18896 | ALE-self-reference_Cluster_FWE_05 | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | Threshold Method = Cluster-level Inference Thresholding Value = 0.05 Thresholding Permutations = 5000 (equilibrium found after 27) Cluster-Forming Method = Uncorrected P value Cluster-Forming Value = 0.001 |
18897 | ALE_self-face_Cluster-level_FWE_05 | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | Threshold Method = Cluster-level Inference Thresholding Value = 0.05 Thresholding Permutations = 5000 (equilibrium found after 26) Cluster-Forming Method = Uncorrected P value Cluster-Forming Value = 0.001 |
18898 | ALE-results_self-reference_p_value | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | p map from ALE 2.3 |
18899 | Contrast_self-reference_minus_self-face | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | Results of contrast (self-reference > self-face), from ALE 2.3, thresholded at FDR p < 0.01 |
18900 | Contrast_self-face_minus_self-reference | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | Results of contrast (self-face > self-reference), from ALE 2.3, thresholded at FDR p < 0.01 |
18901 | Conjunction_self-face_self-reference | Distinct and common aspects of physical and psychological self-representation in the brain: A meta-analysis of self-bias in facial and self-referential judgements | conjunction between z-maps of self-face and self-reference using minimum method, thresholded at p < 0.001 (uncorrected) |
18902 | L1 | Neurofunctional topography of the human hippocampus | Left hippocampus segment (L1) |
18903 | L2 | Neurofunctional topography of the human hippocampus | Left hippocampus segment (L2) |
18904 | L3 | Neurofunctional topography of the human hippocampus | Left hippocampus segment (L3) |
18905 | R1 | Neurofunctional topography of the human hippocampus | Right hippocampus segment (R1) |
18906 | R2 | Neurofunctional topography of the human hippocampus | Right hippocampus segment (R2) |
18907 | R3 | Neurofunctional topography of the human hippocampus | Right hippocampus segment (R3) |
18908 | R4 | Neurofunctional topography of the human hippocampus | Right hippocampus segment (R4) |
18909 | R5 | Neurofunctional topography of the human hippocampus | Right hippocampus segment (R5) |