scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Alessandra Griffa | |
Martijn P Van den Heuvel | |||
P2860 | cites work | Prominence and Control: The Weighted Rich-Club Effect | Q21563728 |
Identification of a common neurobiological substrate for mental illness | Q23890289 | ||
Dwelling quietly in the rich club: brain network determinants of slow cortical fluctuations | Q27324168 | ||
The dynamic functional connectome: State-of-the-art and perspectives | Q28248600 | ||
The connectomics of brain disorders | Q28257389 | ||
Cortical hubs revealed by intrinsic functional connectivity: mapping, assessment of stability, and relation to Alzheimer's disease | Q29619733 | ||
Building the Ferretome | Q30382756 | ||
The dynamics of resting fluctuations in the brain: metastability and its dynamical cortical core | Q30572787 | ||
Structural connectomics in brain diseases | Q30620266 | ||
Comparative primate neuroimaging: insights into human brain evolution | Q30750588 | ||
Depression, neuroimaging and connectomics: a selective overview | Q30872845 | ||
Rich-club organization of the newborn human brain | Q33665539 | ||
The rich club of the C. elegans neuronal connectome | Q33923419 | ||
Time-resolved resting-state brain networks | Q33925731 | ||
The hubs of the human connectome are generally implicated in the anatomy of brain disorders | Q33937468 | ||
Structural and functional aspects relating to cost and benefit of rich club organization in the human cerebral cortex | Q34027760 | ||
Generative models of rich clubs in Hebbian neuronal networks and large-scale human brain networks | Q34113679 | ||
Cortex, cognition and the cell: new insights into the pyramidal neuron and prefrontal function | Q34272074 | ||
White matter maturation reshapes structural connectivity in the late developing human brain. | Q34278989 | ||
Evolution of the human brain: when bigger is better | Q34414755 | ||
An evolutionary theory of schizophrenia: cortical connectivity, metarepresentation, and the social brain | Q34435814 | ||
A unifying framework for measuring weighted rich clubs | Q34590213 | ||
Connectomics-based analysis of information flow in the Drosophila brain. | Q34669265 | ||
Task-based core-periphery organization of human brain dynamics | Q35004414 | ||
Comparative analysis of the macroscale structural connectivity in the macaque and human brain | Q35133647 | ||
Architecture of the cerebral cortical association connectome underlying cognition | Q35549110 | ||
Wiring cost and topological participation of the mouse brain connectome | Q35961424 | ||
High-cost, high-capacity backbone for global brain communication | Q36094436 | ||
Global workspace theory of consciousness: toward a cognitive neuroscience of human experience. | Q36268860 | ||
Generative models of the human connectome | Q36307192 | ||
Rich-Club Organization in Effective Connectivity among Cortical Neurons | Q36480227 | ||
A transcriptional signature of hub connectivity in the mouse connectome. | Q36563458 | ||
Neural synchrony in brain disorders: relevance for cognitive dysfunctions and pathophysiology | Q36610366 | ||
Prion-like propagation of protein aggregation and related therapeutic strategies | Q36983208 | ||
Mapping putative hubs in human, chimpanzee and rhesus macaque connectomes via diffusion tractography | Q37039039 | ||
Multi-task connectivity reveals flexible hubs for adaptive task control | Q37135195 | ||
Adolescence is associated with genomically patterned consolidation of the hubs of the human brain connectome | Q37181845 | ||
Gene transcription profiles associated with inter-modular hubs and connection distance in human functional magnetic resonance imaging networks | Q37214987 | ||
Functional complexity emerging from anatomical constraints in the brain: the significance of network modularity and rich-clubs | Q37472318 | ||
Resting-brain functional connectivity predicted by analytic measures of network communication | Q37495132 | ||
The economy of brain network organization | Q38002308 | ||
Network attributes for segregation and integration in the human brain | Q38072132 | ||
The evolution of distributed association networks in the human brain | Q38161191 | ||
Contributions and challenges for network models in cognitive neuroscience | Q38200899 | ||
Evolutionary and developmental changes in the lateral frontoparietal network: a little goes a long way for higher-level cognition | Q38283141 | ||
Sensitive and critical periods during neurotypical and aberrant neurodevelopment: a framework for neurodevelopmental disorders | Q38286468 | ||
Network morphospace | Q38300494 | ||
Rich club organization and intermodule communication in the cat connectome. | Q38405880 | ||
Rethinking segregation and integration: contributions of whole-brain modelling | Q38529765 | ||
Rich cell-type-specific network topology in neocortical microcircuitry. | Q38743899 | ||
Comparative Connectomics | Q38793154 | ||
Structural connectome topology relates to regional BOLD signal dynamics in the mouse brain. | Q38813059 | ||
Connectome Disconnectivity and Cortical Gene Expression in Patients With Schizophrenia | Q39309088 | ||
The Dynamics of Functional Brain Networks: Integrated Network States during Cognitive Task Performance | Q39332096 | ||
Cortical hubs form a module for multisensory integration on top of the hierarchy of cortical networks. | Q40201643 | ||
Bridging Cytoarchitectonics and Connectomics in Human Cerebral Cortex | Q40430574 | ||
Connectivity, not region-intrinsic properties, predicts regional vulnerability to progressive tau pathology in mouse models of disease | Q41395309 | ||
Nonlinear growth: an origin of hub organization in complex networks | Q42072482 | ||
Geometric explanation of the rich-club phenomenon in complex networks. | Q42266707 | ||
Linking macroscale graph analytical organization to microscale neuroarchitectonics in the macaque connectome | Q42680387 | ||
The diverse club. | Q43419091 | ||
An anatomical substrate for integration among functional networks in human cortex. | Q45150218 | ||
Evidence for expansion of the precuneus in human evolution | Q46615790 | ||
White Matter Disruptions in Schizophrenia Are Spatially Widespread and Topologically Converge on Brain Network Hubs. | Q47958113 | ||
Fluctuations between high- and low-modularity topology in time-resolved functional connectivity | Q48147663 | ||
Evolutionarily novel functional networks in the human brain? | Q48155609 | ||
Affected Anatomical Rich Club and Structural-Functional Coupling in Young Offspring of Schizophrenia and Bipolar Disorder Patients | Q48184166 | ||
Rich Club Organization and Cognitive Performance in Healthy Older Participants | Q48193164 | ||
A Spotlight on Bridging Microscale and Macroscale Human Brain Architecture. | Q48249449 | ||
Cortical rich club regions can organize state-dependent functional network formation by engaging in oscillatory behavior | Q48391530 | ||
Rich club organization supports a diverse set of functional network configurations. | Q51097405 | ||
Comorbidity was associated with neurologic and psychiatric diseases: a general practice-based controlled study. | Q51910234 | ||
Structural connectivity in schizophrenia and its impact on the dynamics of spontaneous functional networks. | Q54375012 | ||
Optimized connectome architecture for sensory-motor integration | Q56380327 | ||
Rich-Club Organization of the Human Connectome | Q57271902 | ||
Rich-club connectivity dominates assortativity and transitivity of complex networks | Q83182699 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported | Q19125045 |
P433 | issue | 2 | |
P921 | main subject | brain | Q1073 |
P304 | page(s) | 121-132 | |
P577 | publication date | 2018-06-01 | |
P1433 | published in | Dialogues in Clinical Neuroscience | Q24255736 |
P1476 | title | Rich-club neurocircuitry: function, evolution, and vulnerability | |
P478 | volume | 20 |
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