review article | Q7318358 |
scholarly article | Q13442814 |
P8978 | DBLP publication ID | journals/neuroimage/CamachoQP20 |
P356 | DOI | 10.1016/J.NEUROIMAGE.2020.116688 |
P932 | PMC publication ID | 7190083 |
P698 | PubMed publication ID | 32114148 |
P2093 | author name string | Susan B Perlman | |
M Catalina Camacho | |||
Laura E Quiñones-Camacho | |||
P2860 | cites work | Functional brain networks develop from a "local to distributed" organization | Q21092565 |
Medial prefrontal cortex and self-referential mental activity: relation to a default mode of brain function | Q24608514 | ||
The global signal and observed anticorrelated resting state brain networks | Q24648484 | ||
The maturing architecture of the brain's default network | Q24652212 | ||
Experience sampling during fMRI reveals default network and executive system contributions to mind wandering | Q24653086 | ||
Consistent resting-state networks across healthy subjects | Q24673419 | ||
The human brain is intrinsically organized into dynamic, anticorrelated functional networks | Q27860802 | ||
Neurophysiological investigation of the basis of the fMRI signal | Q27860853 | ||
Functional connectivity in the motor cortex of resting human brain using echo-planar MRI | Q27860856 | ||
The brain's default network: anatomy, function, and relevance to disease | Q27860961 | ||
Assessment and development of executive function (EF) during childhood | Q28183597 | ||
Searching for a baseline: functional imaging and the resting human brain | Q28190070 | ||
The role of physiological noise in resting-state functional connectivity | Q28257461 | ||
Maturation of cognitive processes from late childhood to adulthood | Q28282268 | ||
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis | Q29547875 | ||
Common Blood Flow Changes across Visual Tasks: II. Decreases in Cerebral Cortex | Q29617038 | ||
Synaptic activity and the construction of cortical circuits | Q29617401 | ||
The impact of global signal regression on resting state correlations: are anti-correlated networks introduced? | Q29619522 | ||
Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion | Q29619898 | ||
Functional network organization of the human brain | Q29622931 | ||
Quantifying cortical development in typically developing toddlers and young children, 1-6 years of age | Q30354263 | ||
Organization of high-level visual cortex in human infants | Q30365172 | ||
Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth | Q30424315 | ||
Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth | Q30450642 | ||
Optical brain imaging reveals general auditory and language-specific processing in early infant development | Q30470857 | ||
Reliability of cortical activity during natural stimulation | Q30477959 | ||
High-frequency gamma activity (80-150Hz) is increased in human cortex during selective attention | Q30482586 | ||
Early cognitive and language skills are linked to resting frontal gamma power across the first 3 years | Q30484549 | ||
Longitudinal four-dimensional mapping of subcortical anatomy in human development | Q30570469 | ||
An independent components and functional connectivity analysis of resting state fMRI data points to neural network dysregulation in adult ADHD. | Q30590119 | ||
Inscapes: A movie paradigm to improve compliance in functional magnetic resonance imaging | Q30670409 | ||
How well do we understand the neural origins of the fMRI BOLD signal? | Q30670634 | ||
Coupling mechanism and significance of the BOLD signal: a status report | Q30836886 | ||
Conceptual processing during the conscious resting state. A functional MRI study | Q38450671 | ||
High-frequency cortical responses reflect lexical processing: an MEG study. | Q38531272 | ||
Real-time motion analytics during brain MRI improve data quality and reduce costs | Q38627073 | ||
Age-related functional brain changes in young children | Q38688842 | ||
Can brain state be manipulated to emphasize individual differences in functional connectivity? | Q38735545 | ||
Increased sensitivity to age-related differences in brain functional connectivity during continuous multiple object tracking compared to resting-state | Q39006700 | ||
Towards a consensus regarding global signal regression for resting state functional connectivity MRI. | Q39153172 | ||
Sources and implications of whole-brain fMRI signals in humans | Q39280131 | ||
Dynamic functional connectivity of neurocognitive networks in children | Q39480853 | ||
On the other hand: Increased cortical activation to human versus mechanical hands in infants. | Q39601230 | ||
Functional brain connectivity at rest changes after working memory training | Q39687907 | ||
Modular Segregation of Structural Brain Networks Supports the Development of Executive Function in Youth | Q40182573 | ||
Benchmarking of participant-level confound regression strategies for the control of motion artifact in studies of functional connectivity | Q40288610 | ||
Default mode network connectivity during task execution | Q40684158 | ||
Functional magnetic resonance imaging of the normal and abnormal visual system in early life | Q40768556 | ||
Development of precise maps in visual cortex requires patterned spontaneous activity in the retina | Q42144918 | ||
Frontal preparatory neural oscillations associated with cognitive control: A developmental study comparing young adults and adolescents | Q42592711 | ||
Brain connectivity during resting state and subsequent working memory task predicts behavioural performance | Q43774135 | ||
Developmental loss of synchronous spontaneous activity in the mouse retina is independent of visual experience. | Q44396254 | ||
Rhythmic spontaneous activity in the developing avian auditory system | Q45088946 | ||
Preparatory Engagement of Cognitive Control Networks Increases Late in Childhood. | Q46050007 | ||
Entrainment of Arteriole Vasomotor Fluctuations by Neural Activity Is a Basis of Blood-Oxygenation-Level-Dependent "Resting-State" Connectivity | Q46163304 | ||
EEG sleep slow-wave activity as a mirror of cortical maturation | Q46440404 | ||
A developmental fMRI study of the Stroop color-word task | Q46840950 | ||
Brain state expression and transitions are related to complex executive cognition in normative neurodevelopment | Q47359845 | ||
The neural substrates of cognitive flexibility are related to individual differences in preschool irritability: A fNIRS investigation | Q47400985 | ||
From cognitive motor preparation to visual processing: The benefits of childhood fitness to brain health. | Q47657725 | ||
Prefrontal cortical activation associated with working memory in adults and preschool children: an event-related optical topography study | Q47764476 | ||
Regional hemodynamic responses to visual stimulation in awake infants | Q47988724 | ||
Optimal experimental design for event-related fMRI. | Q48088715 | ||
Differences in induced brain activity during the performance of learning and working-memory tasks related to intelligence | Q48089952 | ||
Decoding action intentions from preparatory brain activity in human parieto-frontal networks. | Q48126681 | ||
Neural development of selective attention and response inhibition. | Q48167665 | ||
Neurodevelopmental maturation as a function of irritable temperament: Insights From a Naturalistic Emotional Video Viewing Paradigm | Q48182571 | ||
As Working Memory Grows: A Developmental Account of Neural Bases of Working Memory Capacity in 5- to 8-Year Old Children and Adults. | Q48184061 | ||
Developmental changes in brain activation and functional connectivity during response inhibition in the early childhood brain | Q48241890 | ||
Is functional integration of resting state brain networks an unspecific biomarker for working memory performance? | Q48401582 | ||
Identifying the brain's most globally connected regions. | Q48409510 | ||
Somatosensory cortical activation identified by functional MRI in preterm and term infants. | Q48425082 | ||
The development of preparation, conflict monitoring and inhibition from early childhood to young adulthood: a Go/Nogo ERP study. | Q48445637 | ||
Brain basis of developmental change in visuospatial working memory. | Q48472941 | ||
Spatial attention and memory versus motor preparation: premotor cortex involvement as revealed by fMRI. | Q48475245 | ||
Development of the EEG from 5 months to 4 years of age. | Q48533748 | ||
A rapid brain metabolic change in infants detected by fMRI. | Q48565259 | ||
Development of preparatory activity indexed by the contingent negative variation in children. | Q48584141 | ||
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository | Q30943336 | ||
A method for using blocked and event-related fMRI data to study "resting state" functional connectivity | Q31095322 | ||
Imaging brain plasticity during motor skill learning | Q33185899 | ||
Spontaneous brain activity in the default mode network is sensitive to different resting-state conditions with limited cognitive load | Q33459135 | ||
What has fMRI told us about the development of cognitive control through adolescence? | Q33504975 | ||
Two views of brain function | Q33537547 | ||
The "Task B problem" and other considerations in developmental functional neuroimaging | Q33585425 | ||
The development of human functional brain networks | Q33687941 | ||
Aberrant temporal and spatial brain activity during rest in patients with chronic pain | Q33778991 | ||
Mapping infant brain myelination with magnetic resonance imaging | Q33791700 | ||
A structural MRI study of human brain development from birth to 2 years. | Q33908988 | ||
Preparing children with a mock scanner training protocol results in high quality structural and functional MRI scans. | Q34013425 | ||
Temporal and spatial evolution of brain network topology during the first two years of life | Q34038158 | ||
The influence of physiological noise correction on test-retest reliability of resting-state functional connectivity. | Q34096675 | ||
Millisecond by millisecond, year by year: normative EEG microstates and developmental stages | Q34124930 | ||
Neural basis of protracted developmental changes in visuo-spatial working memory. | Q34150562 | ||
Extraordinary neoteny of synaptic spines in the human prefrontal cortex. | Q34203392 | ||
Development of functional and structural connectivity within the default mode network in young children | Q34291951 | ||
Neural activity during natural viewing of Sesame Street statistically predicts test scores in early childhood | Q34321642 | ||
An action perspective on motor development | Q34323248 | ||
The Laboratory Rat: Relating Its Age With Human's | Q34362927 | ||
Functional connectome fingerprinting: identifying individuals using patterns of brain connectivity | Q34497695 | ||
Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. | Q34558743 | ||
Exploring age-related changes in dynamical non-stationarity in electroencephalographic signals during early adolescence | Q34629318 | ||
Neurocognitive development of the ability to manipulate information in working memory | Q34652112 | ||
Modulation of steady state functional connectivity in the default mode and working memory networks by cognitive load. | Q35050523 | ||
Resting-state activity in development and maintenance of normal brain function | Q35105250 | ||
How does your cortex grow? | Q35168287 | ||
The cortical rhythms of chronic back pain. | Q35543899 | ||
The Contribution of Network Organization and Integration to the Development of Cognitive Control | Q35880599 | ||
Functional Network Development During the First Year: Relative Sequence and Socioeconomic Correlations | Q35956666 | ||
Reorganization and plasticity in the adult brain during learning of motor skills | Q36098552 | ||
The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth | Q36113158 | ||
Development of BOLD signal hemodynamic responses in the human brain | Q36282049 | ||
Early patterns of electrical activity in the developing cerebral cortex of humans and rodents | Q36483632 | ||
A developmental fMRI study of self-regulatory control | Q36538465 | ||
The synchronization within and interaction between the default and dorsal attention networks in early infancy | Q36584735 | ||
In vivo imaging of cerebral microvascular plasticity from birth to death | Q36684191 | ||
Resolving the transition from negative to positive blood oxygen level-dependent responses in the developing brain | Q36692966 | ||
The self and social cognition: the role of cortical midline structures and mirror neurons | Q36735896 | ||
Considerations for MRI study design and implementation in pediatric and clinical populations | Q36805600 | ||
Dynamic reconfiguration of structural and functional connectivity across core neurocognitive brain networks with development | Q36809338 | ||
Neuroimaging in child clinical populations: considerations for a successful research program | Q36838772 | ||
Development of human brain cortical network architecture during infancy. | Q36850248 | ||
Functional Near-Infrared Spectroscopy Evidence for Development of Prefrontal Engagement in Working Memory in Early Through Middle Childhood | Q36908524 | ||
Patterns of coordinated anatomical change in human cortical development: a longitudinal neuroimaging study of maturational coupling. | Q36911662 | ||
The influence of head motion on intrinsic functional connectivity MRI | Q36932627 | ||
Development of working memory maintenance | Q37086502 | ||
Multi-task connectivity reveals flexible hubs for adaptive task control | Q37135195 | ||
Evidence on the emergence of the brain's default network from 2-week-old to 2-year-old healthy pediatric subjects | Q37167813 | ||
Brain connectivity related to working memory performance | Q37181000 | ||
Influence of heart rate on the BOLD signal: the cardiac response function | Q37181399 | ||
Training Working Memory in Childhood Enhances Coupling between Frontoparietal Control Network and Task-Related Regions | Q37198441 | ||
Default-mode function and task-induced deactivation have overlapping brain substrates in children | Q37326533 | ||
Probing the early development of visual working memory capacity with functional near-infrared spectroscopy | Q37384572 | ||
Learning sculpts the spontaneous activity of the resting human brain | Q37389061 | ||
Neurovascular coupling and energy metabolism in the developing brain | Q37468048 | ||
Modeling of the hemodynamic responses in block design fMRI studies. | Q37559341 | ||
Activity-dependent synaptic plasticity of NMDA receptors. | Q37613295 | ||
Emotional reactivity and its impact on neural circuitry for attention-emotion interaction in childhood and adolescence | Q37629633 | ||
Electrophysiological changes during adolescence: a review | Q37633225 | ||
Development of the Cerebral Cortex across Adolescence: A Multisample Study of Inter-Related Longitudinal Changes in Cortical Volume, Surface Area, and Thickness. | Q37730063 | ||
Morphometric study of human cerebral cortex development | Q37951080 | ||
Longitudinal development of prefrontal function during early childhood. | Q48604050 | ||
EEG theta rhythm in infants and preschool children. | Q48628692 | ||
Introduction of a method for quantitative evaluation of spontaneous motor activity development with age in infants. | Q48663475 | ||
High-resolution EEG mapping of cortical activation related to working memory: effects of task difficulty, type of processing, and practice. | Q48699446 | ||
Synaptogenesis in human visual cortex--evidence for synapse elimination during normal development. | Q48859708 | ||
Age and sex effects in the EEG: development of the normal child. | Q48890610 | ||
Variability of the hemodynamic response in infants: Influence of experimental design and stimulus complexity. | Q49351239 | ||
Behavioral interventions for reducing head motion during MRI scans in children. | Q50032168 | ||
Prestimulus EEG amplitude determinants of ERP responses in a habituation paradigm. | Q50740867 | ||
Physiology and functioning: Parents' vagal tone, emotion socialization, and children's emotion knowledge. | Q50791223 | ||
Variability of brain signals processed locally transforms into higher connectivity with brain development. | Q50804451 | ||
Cardiac vagal tone indices of temperamental reactivity and behavioral regulation in young children. | Q51101167 | ||
Age trends and sex differences of alpha rhythms including split alpha peaks. | Q51599342 | ||
Neurodevelopmental trajectories of the human cerebral cortex. | Q51892234 | ||
Predicting success: patterns of cortical activation and deactivation prior to response inhibition. | Q51940019 | ||
Early cortical specialization for face-to-face communication in human infants. | Q51950184 | ||
Development of infant sustained attention and its relation to EEG oscillations: an EEG and cortical source analysis study. | Q52099812 | ||
Modulation of induced gamma band responses in a perceptual learning task in the human EEG. | Q52116324 | ||
Functional Brain Networks Are Dominated by Stable Group and Individual Factors, Not Cognitive or Daily Variation. | Q53406685 | ||
Development of the social brain from age three to twelve years. | Q53435772 | ||
Diminished neural network dynamics after moderate and severe traumatic brain injury. | Q55361293 | ||
First-year development of modules and hubs in infant brain functional networks | Q57478870 | ||
Minds at rest? Social cognition as the default mode of cognizing and its putative relationship to the “default system” of the brain | Q57514753 | ||
Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo | Q59053098 | ||
Age-Related Trajectories of Functional Coupling between the VTA and Nucleus Accumbens Depend on Motivational State | Q60107697 | ||
Movies in the magnet: Naturalistic paradigms in developmental functional neuroimaging | Q60643400 | ||
The Protracted Maturation of Associative Layer IIIC Pyramidal Neurons in the Human Prefrontal Cortex During Childhood: A Major Role in Cognitive Development and Selective Alteration in Autism | Q64093176 | ||
Theta oscillations in 4-year-olds are sensitive to task engagement and task demands | Q64115622 | ||
Intrinsic temporal patterning in the spontaneous movement of awake neonates | Q70477568 | ||
Normal ranges of heart rate variability during infancy and childhood | Q73398159 | ||
[Heart rate variability in healthy six- to sixteen year old children] | Q74630424 | ||
Studies of the electroencephalogram of normal children: comparison of viscal and automatic frequency analyses | Q78582931 | ||
The UNC/UMN Baby Connectome Project (BCP): An overview of the study design and protocol development | Q88171881 | ||
Development of brain networks for social functions: Confirmatory analyses in a large open source dataset | Q90314876 | ||
Neural architecture supporting active emotion processing in children: A multivariate approach | Q90407702 | ||
Irritability uniquely predicts prefrontal cortex activation during preschool inhibitory control among all temperament domains: A LASSO approach | Q91434932 | ||
Cerebral blood flow in 5- to 8-month-olds: Regional tissue maturity is associated with infant affect | Q91703244 | ||
The frontoparietal network: function, electrophysiology, and importance of individual precision mapping | Q91706103 | ||
Cognitive flexibility-related prefrontal activation in preschoolers: A biological approach to temperamental effortful control | Q92465127 | ||
The brain's default network: updated anatomy, physiology and evolving insights | Q93162758 | ||
P921 | main subject | cognitive neuroscience | Q1138951 |
developmental cognitive neuroscience | Q47149375 | ||
P304 | page(s) | 116688 | |
P577 | publication date | 2020-02-27 | |
P1433 | published in | NeuroImage | Q1981225 |
P1476 | title | Does the child brain rest?: An examination and interpretation of resting cognition in developmental cognitive neuroscience | |
P478 | volume | 212 |
Q100695008 | Consistency of EEG asymmetry patterns in infants of depressed mothers | cites work | P2860 |
Search more.