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The development of spatiotemporal organization of episodic memory in children and its disruption in Williams Syndrome

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9781118597705.ch13openalex-snapshot
Binding Together the Elements of Episodes: Relational Memory and the Developmental Trajectory of the Hippocampus
inferredcites →https://doi.org/10.1002/dev.20527openalex-snapshot
Episodic memory in 3‐ and 4‐year‐old children
inferredcites →https://doi.org/10.1002/hipo.1087openalex-snapshot
Bilateral hippocampal pathology impairs topographical and episodic memory but not visual pattern matching
inferredcites →https://doi.org/10.1002/hipo.20193openalex-snapshot
Dynamic mapping of normal human hippocampal development
inferredcites →https://doi.org/10.1002/hipo.22750openalex-snapshot
Space, time, and episodic memory: The hippocampus is all over the cognitive map
inferredcites →https://doi.org/10.1002/wcs.1171openalex-snapshot
Development of spatial cognition
inferredcites →https://doi.org/10.1002/wcs.1258openalex-snapshot
Space and language in Williams syndrome: insights from typical development
inferredcites →https://doi.org/10.1006/brcg.2000.1232openalex-snapshot
The Williams Syndrome Cognitive Profile
inferredcites →https://doi.org/10.1007/s00221-010-2349-5openalex-snapshot
Two systems of spatial representation underlying navigation
inferredcites →https://doi.org/10.1016/0006-8993(71)90358-1openalex-snapshot
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
inferredcites →https://doi.org/10.1016/j.brainres.2014.10.069openalex-snapshot
Time and space in the hippocampus
inferredcites →https://doi.org/10.1016/j.cognition.2015.07.010openalex-snapshot
Geometric and featural systems, separable and combined: Evidence from reorientation in people with Williams syndrome
inferredcites →https://doi.org/10.1016/j.cogpsych.2012.08.001openalex-snapshot
Development of allocentric spatial memory abilities in children from 18 months to 5 years of age
inferredcites →https://doi.org/10.1016/j.cogpsych.2018.05.003openalex-snapshot
The developing role of transparent surfaces in children's spatial representation
inferredcites →https://doi.org/10.1016/j.cortex.2012.08.004openalex-snapshot
Developmental differences in hippocampal and cortical contributions to episodic retrieval
inferredcites →https://doi.org/10.1016/j.cub.2018.03.051openalex-snapshot
The Same Hippocampal CA1 Population Simultaneously Codes Temporal Information over Multiple Timescales
inferredcites →https://doi.org/10.1016/j.ijdevneu.2009.01.004openalex-snapshot
Spatial competences in Williams syndrome: a radial arm maze study
inferredcites →https://doi.org/10.1016/j.neubiorev.2012.09.014openalex-snapshot
The operation of pattern separation and pattern completion processes associated with different attributes or domains of memory
inferredcites →https://doi.org/10.1016/j.neulet.2017.07.061openalex-snapshot
Building concepts one episode at a time: The hippocampus and concept formation
inferredcites →https://doi.org/10.1016/j.neulet.2018.04.040openalex-snapshot
Semantic memory in developmental amnesia
inferredcites →https://doi.org/10.1016/j.neuroimage.2018.05.036openalex-snapshot
Multivoxel pattern similarity suggests the integration of temporal duration in hippocampal event sequence representations
inferredcites →https://doi.org/10.1016/j.neuron.2004.08.014openalex-snapshot
Neural Basis of Genetically Determined Visuospatial Construction Deficit in Williams Syndrome
inferredcites →https://doi.org/10.1016/j.neuron.2011.07.012openalex-snapshot
Hippocampal “Time Cells” Bridge the Gap in Memory for Discontiguous Events
inferredcites →https://doi.org/10.1016/j.neuron.2014.01.015openalex-snapshot
Hippocampal Activity Patterns Carry Information about Objects in Temporal Context
inferredcites →https://doi.org/10.1016/j.neuron.2014.05.019openalex-snapshot
Hippocampal Representation of Related and Opposing Memories Develop within Distinct, Hierarchically Organized Neural Schemas
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2011.09.015openalex-snapshot
Patient HC with developmental amnesia can construct future scenarios
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2013.05.026openalex-snapshot
Development of memory for spatial context: Hippocampal and cortical contributions
inferredcites →https://doi.org/10.1016/j.ridd.2011.02.001openalex-snapshot
Explorative function in Williams syndrome analyzed through a large-scale task with multiple rewards
inferredcites →https://doi.org/10.1016/j.ridd.2013.01.024openalex-snapshot
Executive functions in intellectual disabilities: A comparison between Williams syndrome and Down syndrome
inferredcites →https://doi.org/10.1016/j.tics.2007.08.001openalex-snapshot
Imaging recollection and familiarity in the medial temporal lobe: a three-component model
inferredcites →https://doi.org/10.1016/j.tics.2011.05.008openalex-snapshot
The hippocampus: hub of brain network communication for memory
inferredcites →https://doi.org/10.1016/s0010-0277(00)00120-7openalex-snapshot
Language, space, and the development of cognitive flexibility in humans: the case of two spatial memory tasks
inferredcites →https://doi.org/10.1016/s0010-9452(08)70856-6openalex-snapshot
A Case of Amnesia at an Early Age
inferredcites →https://doi.org/10.1017/s0012162205000599openalex-snapshot
Visual and spatial long-term memory: differential pattern of impairments in Williams and Down syndromes
inferredcites →https://doi.org/10.1037/0012-1649.39.5.805openalex-snapshot
Age-related changes in verbal and nonverbal memory during early childhood.
inferredcites →https://doi.org/10.1037/0278-7393.32.1.89openalex-snapshot
Binding, relational memory, and recall of naturalistic events: A developmental perspective.
inferredcites →https://doi.org/10.1037/h0061626openalex-snapshot
Cognitive maps in rats and men.
inferredcites →https://doi.org/10.1038/nature08704openalex-snapshot
Evidence for grid cells in a human memory network
inferredcites →https://doi.org/10.1038/nature11587openalex-snapshot
A map of visual space in the primate entorhinal cortex
inferredcites →https://doi.org/10.1038/nature17955openalex-snapshot
A shared neural ensemble links distinct contextual memories encoded close in time
inferredcites →https://doi.org/10.1038/nn.4284openalex-snapshot
Linking pattern completion in the hippocampus to predictive coding in visual cortex
inferredcites →https://doi.org/10.1038/nn1494openalex-snapshot
Neural correlates of genetically abnormal social cognition in Williams syndrome
inferredcites →https://doi.org/10.1038/nrn3827openalex-snapshot
Time cells in the hippocampus: a new dimension for mapping memories
inferredcites →https://doi.org/10.1038/s41586-018-0459-6openalex-snapshot
Integrating time from experience in the lateral entorhinal cortex
inferredcites →https://doi.org/10.1068/p6050openalex-snapshot
Inefficient Search of Large-Scale Space in Williams Syndrome: Further Insights on the Role of LIMK1 Deletion in Deficits of Spatial Cognition
inferredcites →https://doi.org/10.1073/pnas.0602716103openalex-snapshot
Item memory, source memory, and the medial temporal lobe: Concordant findings from fMRI and memory-impaired patients
inferredcites →https://doi.org/10.1073/pnas.070039597openalex-snapshot
Navigation-related structural change in the hippocampi of taxi drivers
inferredcites →https://doi.org/10.1073/pnas.0909155107openalex-snapshot
Impaired geometric reorientation caused by genetic defect
inferredcites →https://doi.org/10.1073/pnas.1712711114openalex-snapshot
Contributions of primate prefrontal cortex and medial temporal lobe to temporal-order memory
inferredcites →https://doi.org/10.1080/13554794.2010.532138openalex-snapshot
Impaired event memory and recollection in a case of developmental amnesia
inferredcites →https://doi.org/10.1093/cercor/bhq092openalex-snapshot
Medial Temporal Lobe Contributions to Episodic Sequence Encoding
inferredcites →https://doi.org/10.1098/rstb.2012.0510openalex-snapshot
Space in the brain: how the hippocampal formation supports spatial cognition
inferredcites →https://doi.org/10.1111/1467-9280.00271openalex-snapshot
On the Transition from Childhood Amnesia to the Recall of Personal Memories
inferredcites →https://doi.org/10.1111/j.1365-2788.2010.01278.xopenalex-snapshot
Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory
inferredcites →https://doi.org/10.1111/j.1460-9568.2009.07061.xopenalex-snapshot
Quantitative analysis of postnatal neurogenesis and neuron number in the macaque monkey dentate gyrus
inferredcites →https://doi.org/10.1111/j.1467-7687.2004.00341.xopenalex-snapshot
Changes in reality monitoring and episodic memory in early childhood
inferredcites →https://doi.org/10.1111/j.1467-7687.2007.00662.xopenalex-snapshot
Developmental trajectories for spatial frames of reference in Williams syndrome
inferredcites →https://doi.org/10.1111/j.1467-7687.2009.00894.xopenalex-snapshot
How do individuals with Williams syndrome learn a route in a real‐world environment?
inferredcites →https://doi.org/10.1111/j.1467-8624.2009.01353.xopenalex-snapshot
Memory Binding in Early Childhood: Evidence for a Retrieval Deficit
inferredcites →https://doi.org/10.1111/j.1467-8624.2012.01736.xopenalex-snapshot
How Do the Different Components of Episodic Memory Develop? Role of Executive Functions and Short-Term Feature-Binding Abilities
inferredcites →https://doi.org/10.1111/j.1469-7610.2008.01887.xopenalex-snapshot
Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype
inferredcites →https://doi.org/10.1126/science.1173215openalex-snapshot
A Functional Role for Adult Hippocampal Neurogenesis in Spatial Pattern Separation
inferredcites →https://doi.org/10.1126/science.1244056openalex-snapshot
Neural Activity in Human Hippocampal Formation Reveals the Spatial Context of Retrieved Memories
inferredcites →https://doi.org/10.1126/science.aaf0941openalex-snapshot
Organizing conceptual knowledge in humans with a gridlike code
inferredcites →https://doi.org/10.1162/08989290151137403openalex-snapshot
Preserved Recognition in a Case of Developmental Amnesia: Implications for the Acaquisition of Semantic Memory?
inferredcites →https://doi.org/10.1177/0165025415584808openalex-snapshot
Improvement of allocentric spatial memory resolution in children from 2 to 4 years of age
inferredcites →https://doi.org/10.1177/1073858413495091openalex-snapshot
Memory, Imagination, and Predicting the Future
inferredcites →https://doi.org/10.1371/journal.pbio.0040424openalex-snapshot
An Unexpected Sequence of Events: Mismatch Detection in the Human Hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.1378-09.2009openalex-snapshot
Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where
inferredcites →https://doi.org/10.1523/jneurosci.5370-08.2009openalex-snapshot
A Specific Role of the Human Hippocampus in Recall of Temporal Sequences
inferredcites →https://doi.org/10.3200/gntp.166.3.313-328openalex-snapshot
Feature Binding in Children and Young Adults
inferredcites →https://doi.org/10.3389/fncom.2018.00011openalex-snapshot
Temporal Dissociation of Neocortical and Hippocampal Contributions to Mental Time Travel Using Intracranial Recordings in Humans
inferredcites →https://doi.org/10.3389/neuro.09.015.2008openalex-snapshot
Hippocampal Amnesia Impairs All Manner of Relational Memory
inferredcites →https://doi.org/10.7554/elife.12247openalex-snapshot
Hippocampal ensemble dynamics timestamp events in long-term memory

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5934/kjhe.2021.30.3.389openalex-snapshot
Links Between the Development of the Theory of Mind and Empathy in Preschool-aged Children
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