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Spatial memory: how egocentric and allocentric combine
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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/(sici)1098-1063(1999)9:3<206::aid-hipo2>3.0.co;2-hopenalex-snapshot
Head direction cells in the primate pre-subiculum
inferredcites →https://doi.org/10.1002/hipo.10062openalex-snapshot
Representation of place by monkey hippocampal neurons in real and virtual translocation
inferredcites →https://doi.org/10.1002/hipo.450010303openalex-snapshot
An allocentric spatial model for the hippocampal cognitive map
inferredcites →https://doi.org/10.1006/cogp.1998.0713openalex-snapshot
Sources of Flexibility in Human Cognition: Dual-Task Studies of Space and Language
inferredcites →https://doi.org/10.1006/nlme.2001.4008openalex-snapshot
Multiple Parallel Memory Systems in the Brain of the Rat
inferredcites →https://doi.org/10.1007/bf00255230openalex-snapshot
Single unit activity in the rat hippocampus during a spatial memory task
inferredcites →https://doi.org/10.1016/0010-0277(86)90041-7openalex-snapshot
A purely geometric module in the rat's spatial representation
inferredcites →https://doi.org/10.1016/0166-2236(91)90036-topenalex-snapshot
The organization of learning
inferredcites →https://doi.org/10.1016/0166-2236(92)90344-8openalex-snapshot
Separate visual pathways for perception and action
inferredcites →https://doi.org/10.1016/0306-4522(79)90015-0openalex-snapshot
The hippocampus as a cognitive map
inferredcites →https://doi.org/10.1016/j.cogdev.2005.04.003openalex-snapshot
Reorientation in a rhombic environment: No evidence for an encapsulated geometric module
inferredcites →https://doi.org/10.1016/j.cognition.2003.12.001openalex-snapshot
Geometric determinants of human spatial memory
inferredcites →https://doi.org/10.1016/j.cognition.2004.01.001openalex-snapshot
Orientational manoeuvres in the dark: dissociating allocentric and egocentric influences on spatial memory
inferredcites →https://doi.org/10.1016/s0010-0277(00)00105-0openalex-snapshot
Updating egocentric representations in human navigation
inferredcites →https://doi.org/10.1016/s0010-0277(96)00714-7openalex-snapshot
Modularity and development: the case of spatial reorientation
inferredcites →https://doi.org/10.1016/s0010-0277(99)00012-8openalex-snapshot
Active and passive scene recognition across views
inferredcites →https://doi.org/10.1016/s0301-0082(98)00004-5openalex-snapshot
Head direction cells and the neurophysiological basis for a sense of direction
inferredcites →https://doi.org/10.1016/s1364-6613(02)01961-7openalex-snapshot
Human spatial representation: insights from animals
inferredcites →https://doi.org/10.1037//0096-3445.130.3.505openalex-snapshot
Rhesus monkeys use geometric and nongeometric information during a reorientation task.
inferredcites →https://doi.org/10.1037//0097-7403.15.4.366openalex-snapshot
The vector sum model of pigeon landmark use.
inferredcites →https://doi.org/10.1037//0278-7393.15.6.1157openalex-snapshot
Access to knowledge of spatial structure at novel points of observation.
inferredcites →https://doi.org/10.1037//0278-7393.23.6.1494openalex-snapshot
Orientation specificity in representations of place.
inferredcites →https://doi.org/10.1037//0278-7393.28.1.162openalex-snapshot
Intrinsic frames of reference in spatial memory.
inferredcites →https://doi.org/10.1037//0735-7036.104.3.248openalex-snapshot
Geometric modules in animals' spatial representations: A test with chicks (Gallus gallus domesticus).
inferredcites →https://doi.org/10.1037//0735-7044.113.3.475openalex-snapshot
Mechanisms of reorientation and object localization by children: A comparison with rats.
inferredcites →https://doi.org/10.1037/0033-295x.114.2.340openalex-snapshot
Remembering the past and imagining the future: A neural model of spatial memory and imagery.
inferredcites →https://doi.org/10.1037/0097-7403.31.2.254openalex-snapshot
Shape Parameters Explain Data From Spatial Transformations: Comment on Pearce et al. (2004) and Tommasi & Polli (2004).
inferredcites →https://doi.org/10.1037/0278-7393.30.1.142openalex-snapshot
Allocentric and Egocentric Updating of Spatial Memories.
inferredcites →https://doi.org/10.1037/0278-7393.31.5.1069openalex-snapshot
Allocentric Coding of Object-to-Object Relations in Overlearned and Novel Environments.
inferredcites →https://doi.org/10.1037/0278-7393.32.4.867openalex-snapshot
Transient and enduring spatial representations under disorientation and self-rotation.
inferredcites →https://doi.org/10.1037/0278-7393.32.6.1274openalex-snapshot
Roles of egocentric and allocentric spatial representations in locomotion and reorientation.
inferredcites →https://doi.org/10.1037/0735-7036.119.4.455openalex-snapshot
Goldfish (Carassius auratus) matching geometric and featural cues: A reinterpretation of some of the data of Vargas, López, Salas, and Thinus-Blanc (2004).
inferredcites →https://doi.org/10.1038/370057a0openalex-snapshot
A geometric process for spatial reorientation in young children
inferredcites →https://doi.org/10.1038/381425a0openalex-snapshot
Geometric determinants of the place fields of hippocampal neurons
inferredcites →https://doi.org/10.1038/nature01964openalex-snapshot
Cellular networks underlying human spatial navigation
inferredcites →https://doi.org/10.1038/nrn1932openalex-snapshot
Path integration and the neural basis of the 'cognitive map'
inferredcites →https://doi.org/10.1093/oso/9780198524533.001.0001openalex-snapshot
The Hippocampal and Parietal Foundations of Spatial Cognition
inferredcites →https://doi.org/10.1098/rstb.2001.0948openalex-snapshot
Memory for events and their spatial context: models and experiments
inferredcites →https://doi.org/10.1111/1467-9280.00062openalex-snapshot
Perceiving Real-World Viewpoint Changes
inferredcites →https://doi.org/10.1111/1467-9280.00461openalex-snapshot
Children's Use of Landmarks: Implications for Modularity Theory
inferredcites →https://doi.org/10.1111/j.0956-7976.2002.00461.xopenalex-snapshot
Children's Use of Landmarks: Implications for Modularity Theory
inferredcites →https://doi.org/10.1111/j.1467-9280.1997.tb00442.xopenalex-snapshot
Viewpoint Dependence in Scene Recognition
inferredcites →https://doi.org/10.1111/j.1467-9280.2006.01753.xopenalex-snapshot
Dissecting the Geometric Module
inferredcites →https://doi.org/10.1152/jn.1998.79.3.1145openalex-snapshot
Spatial View Cells in the Primate Hippocampus: Effects of Removal of View Details
inferredcites →https://doi.org/10.1242/jeb.199.1.201openalex-snapshot
Path Integration in Mammals and its Interaction With Visual Landmarks
inferredcites →https://doi.org/10.1242/jeb.199.1.219openalex-snapshot
Do Animals Have Cognitive Maps?
inferredcites →https://doi.org/10.1523/jneurosci.22-20-09035.2002openalex-snapshot
Relationships between Place Cell Firing Fields and Navigational Decisions by Rats
inferredcites →https://doi.org/10.3758/bf03196346openalex-snapshot
Is there a geometric module for spatial orientation? squaring theory and evidence
inferredcites →https://doi.org/10.3758/bf03196519openalex-snapshot
Egocentric and geocentric frames of reference in memory of large-scale space
inferredcites →https://doi.org/10.3758/bf03196562openalex-snapshot
Simultaneous spatial updating in nested environments
inferredcites →https://doi.org/10.3758/bf03196563openalex-snapshot
Inertial cues do not enhance knowledge of environmental layout
inferredcites →https://doi.org/10.3758/bf03209379openalex-snapshot
Heading in the rat: Determination by environmental shape
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Sequential egocentric strategy is acquired as early as allocentric strategy: Parallel acquisition of these two navigation strategies
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Hippocampal size predicts rapid learning of a cognitive map in humans
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Oscillations and Boundaries in My Route Through the Hippocampal Cognitive Map
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Spatial Frames of Reference and Action: A Study with Evolved Neuro-agents
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SEERBench: A Spatial Ego-Exo Reasoning Benchmark for MLLMs
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Towards Spatial Supersensing in the Wild
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Cognitive Aspects: How People Perceive, Memorize, Think and Talk About Landmarks
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A Parallel Universe: Psychological Science in the Language of Game Design
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Assessing Cognitive Improvement in People with Down Syndrome: Important Considerations for Drug-Efficacy Trials
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Electrocortical Evidence for Long-Term Incidental Spatial Learning Through Modified Navigation Instructions
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Human EEG Correlates of Spatial Navigation within Egocentric and Allocentric Reference Frames
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Putting Egocentric and Allocentric into Perspective
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An Hybrid Expert Model to Support Tutoring Services in Robotic Arm Manipulations
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Multi-paradigm Generation of Tutoring Feedback in Robotic Arm Manipulation Training
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Selective influence of prior allocentric knowledge on the kinesthetic learning of a path
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Multiple reference frames used by the human brain for spatial perception and memory
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Developmental topographical disorientation: a newly discovered cognitive disorder
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Motor transfer from map ocular exploration to locomotion during spatial navigation from memory
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Modality dependence and intermodal transfer in the Corsi Spatial Sequence Task: Screen vs. Floor
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Frames of reference and categorical/coordinate spatial relations in a “what was where” task
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Congenital blindness limits allocentric to egocentric switching ability
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The role of perception and action on the use of allocentric information in a large-scale virtual environment
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Encoding of variability of landmark-based spatial information
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Development of egocentric and allocentric spatial representations from childhood to elderly age
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The visual and haptic contributions to hand perception
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Are allocentric spatial reference frames compatible with theories of Enactivism?
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Pointing movements and visuo-spatial working memory in a joint setting: the role of motor inhibition
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The lateral intraparietal sulcus takes viewpoint changes into account during memory-guided attention in natural scenes
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Rats build and update topological representations through exploration
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An implicit spatial memory alignment effect
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A proposed attention-based model for spatial memory formation and retrieval
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Neural synchrony and cognitive map formulation in collaborative navigation: leader-follower couplings revealed by EEG hyperscanning
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The Contribution of the Cerebellum in the Hierarchial Development of the Self
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Object-spatial layout-route based hybrid map and global localization for mobile robots
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Executive functioning and spatial processing in anorexia nervosa: an experimental study and its significance for the allocentric lock theory
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The Neural Underpinnings of Spatial Memory and Navigation
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Tell Me Where to Go
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Spatial Learning and Its Neural Basis in Fish ☆
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inferred← citeshttps://doi.org/10.1016/b978-0-12-820480-1.00018-8openalex-snapshot
Navigation in individuals at risk for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-820480-1.00154-6openalex-snapshot
Neurocognitive basis of navigation in children
inferred← citeshttps://doi.org/10.1016/b978-0-12-821377-3.00009-xopenalex-snapshot
The relationship between mental and physical space and its impact on topographical disorientation
inferred← citeshttps://doi.org/10.1016/b978-0-443-15754-7.00010-9openalex-snapshot
Role of the parietal cortex in memory
inferred← citeshttps://doi.org/10.1016/b978-0-443-15754-7.00042-0openalex-snapshot
Visual memory for natural scenes
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.00288-6openalex-snapshot
Spatial Memory: Assessment in Animals
inferred← citeshttps://doi.org/10.1016/b978-008045405-4.00027-6openalex-snapshot
Orientation, Navigation, and Searching
inferred← citeshttps://doi.org/10.1016/b978-2-294-78652-5.00017-xopenalex-snapshot
Pour en savoir plus
inferred← citeshttps://doi.org/10.1016/j.actpsy.2009.07.003openalex-snapshot
Egocentric-updating during navigation facilitates episodic memory retrieval
inferred← citeshttps://doi.org/10.1016/j.actpsy.2010.01.003openalex-snapshot
Moving through imagined space: Mentally simulating locomotion during spatial description reading
inferred← citeshttps://doi.org/10.1016/j.actpsy.2013.06.015openalex-snapshot
Spatial integration of boundaries in a 3D virtual environment
inferred← citeshttps://doi.org/10.1016/j.actpsy.2025.105918openalex-snapshot
A virtual reality take on the Corsi-Block Tapping Task: Exploring VR for spatial working memory assessment
inferred← citeshttps://doi.org/10.1016/j.aei.2024.102635openalex-snapshot
NavMarkAR: A landmark-based augmented reality (AR) wayfinding system for enhancing older Adults’ spatial learning
inferred← citeshttps://doi.org/10.1016/j.anbehav.2009.01.025openalex-snapshot
Sophisticated Euclidean maps in forest chimpanzees
inferred← citeshttps://doi.org/10.1016/j.anbehav.2019.06.029openalex-snapshot
Spatial learning through active electroreception in Gnathonemus petersii
inferred← citeshttps://doi.org/10.1016/j.arr.2014.04.004openalex-snapshot
The role of egocentric and allocentric abilities in Alzheimer's disease: A systematic review
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101020openalex-snapshot
How age relates to spatial navigation performance: Functional and methodological considerations
inferred← citeshttps://doi.org/10.1016/j.bandc.2008.07.011openalex-snapshot
The egocentric reference for visual exploration and orientation
inferred← citeshttps://doi.org/10.1016/j.bandc.2010.11.010openalex-snapshot
Sexual orientation and spatial position effects on selective forms of object location memory
inferred← citeshttps://doi.org/10.1016/j.bandc.2011.08.015openalex-snapshot
Eye movement suppression interferes with construction of object-centered spatial reference frames in working memory
inferred← citeshttps://doi.org/10.1016/j.bandc.2013.07.010openalex-snapshot
Evidence for spatial navigational impairments in hydrocephalus patients without spina bifida
inferred← citeshttps://doi.org/10.1016/j.bbr.2009.05.022openalex-snapshot
Spatial memory: Theoretical basis and comparative review on experimental methods in rodents
inferred← citeshttps://doi.org/10.1016/j.bbr.2011.03.040openalex-snapshot
Geometric information is required for allothetic navigation in mice
inferred← citeshttps://doi.org/10.1016/j.bbr.2011.10.043openalex-snapshot
Impaired egocentric memory and reduced somatosensory cortex size in temporal lobe epilepsy with hippocampal sclerosis
inferred← citeshttps://doi.org/10.1016/j.bbr.2012.12.031openalex-snapshot
Selective role of lingual/parahippocampal gyrus and retrosplenial complex in spatial memory across viewpoint changes relative to the environmental reference frame
inferred← citeshttps://doi.org/10.1016/j.bbr.2015.02.021openalex-snapshot
How coordinate and categorical spatial relations combine with egocentric and allocentric reference frames in a motor task: Effects of delay and stimuli characteristics
inferred← citeshttps://doi.org/10.1016/j.bbr.2015.10.056openalex-snapshot
Changes in spatial cognition and brain activity after a single dose of testosterone in healthy women
inferred← citeshttps://doi.org/10.1016/j.bbr.2015.12.018openalex-snapshot
Allocentric coding in ventral and dorsal routes during real-time reaching: Evidence from imaging-guided multi-site brain stimulation
inferred← citeshttps://doi.org/10.1016/j.bbr.2016.10.052openalex-snapshot
Implicit coding of location and direction in a familiar, real-world “vista” space
inferred← citeshttps://doi.org/10.1016/j.bbr.2016.12.006openalex-snapshot
Deletion of the serotonin receptor type 7 disrupts the acquisition of allocentric but not egocentric navigation strategies in mice
inferred← citeshttps://doi.org/10.1016/j.bbr.2017.11.041openalex-snapshot
Hex Maze: A new virtual maze able to track acquisition and usage of three navigation strategies
inferred← citeshttps://doi.org/10.1016/j.bbr.2019.02.032openalex-snapshot
Incidental learning of allocentric and egocentric strategies by both men and women in a dual-strategy virtual Morris Water Maze
inferred← citeshttps://doi.org/10.1016/j.bbr.2019.112013openalex-snapshot
The expression of allocentric object-place recognition memory during development
inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113566openalex-snapshot
Do spatial and recognition memories have a lateralized processing by the dorsal hippocampus CA3?
inferred← citeshttps://doi.org/10.1016/j.bbr.2024.115388openalex-snapshot
Navigational object-location memory assessment in real and virtual environments: A systematic review
inferred← citeshttps://doi.org/10.1016/j.bbr.2026.116227openalex-snapshot
Sex differences in the use of spatial strategies in humans: An updated systematic review of the last decade
inferred← citeshttps://doi.org/10.1016/j.beproc.2009.03.016openalex-snapshot
Evidence for averaging of distance from landmarks in the domestic dog
inferred← citeshttps://doi.org/10.1016/j.beproc.2015.08.001openalex-snapshot
Seeing the forest before the trees–spatial orientation in freshwater stingrays (Potamotrygon motoro) in a hole-board task
inferred← citeshttps://doi.org/10.1016/j.beproc.2021.104442openalex-snapshot
Memory for surface objects in an arena by the horse (Equus ferus caballus) under saddle: Evidence for dual process theory of spatial representation
inferred← citeshttps://doi.org/10.1016/j.cccb.2022.100155openalex-snapshot
Spatial orientation – a stable marker for vascular cognitive impairment?
inferred← citeshttps://doi.org/10.1016/j.cities.2017.12.006openalex-snapshot
Spatial navigation and place imageability in sense of place
inferred← citeshttps://doi.org/10.1016/j.cities.2021.103245openalex-snapshot
Place imageability, sense of place, and spatial navigation: A community investigation
inferred← citeshttps://doi.org/10.1016/j.cobeha.2015.03.005openalex-snapshot
Spatial memory and hippocampal enhancement
inferred← citeshttps://doi.org/10.1016/j.cobeha.2017.06.005openalex-snapshot
Human spatial navigation: representations across dimensions and scales
inferred← citeshttps://doi.org/10.1016/j.cogdev.2026.101709openalex-snapshot
Children’s and adults’ performance in Simon-like tasks with multiple spatial dimensions
inferred← citeshttps://doi.org/10.1016/j.cognition.2007.10.008openalex-snapshot
Reorientation in the real world: The development of landmark use and integration in a natural environment
inferred← citeshttps://doi.org/10.1016/j.cognition.2008.03.005openalex-snapshot
Representational flexibility and specificity following spatial descriptions of real-world environments
inferred← citeshttps://doi.org/10.1016/j.cognition.2009.05.003openalex-snapshot
A viewpoint-independent process for spatial reorientation
inferred← citeshttps://doi.org/10.1016/j.cognition.2010.12.009openalex-snapshot
Plasticity of human spatial cognition: Spatial language and cognition covary across cultures
inferred← citeshttps://doi.org/10.1016/j.cognition.2011.02.012openalex-snapshot
Spatial reasoning in Tenejapan Mayans
inferred← citeshttps://doi.org/10.1016/j.cognition.2011.12.015openalex-snapshot
Navigation as a source of geometric knowledge: Young children’s use of length, angle, distance, and direction in a reorientation task
inferred← citeshttps://doi.org/10.1016/j.cognition.2012.05.006openalex-snapshot
Retrieving enduring spatial representations after disorientation
inferred← citeshttps://doi.org/10.1016/j.cognition.2012.09.018openalex-snapshot
Object location memory: Integration and competition between multiple context objects but not between observers’ body and context objects
inferred← citeshttps://doi.org/10.1016/j.cognition.2013.04.011openalex-snapshot
Ambient visual information confers a context-specific, long-term benefit on memory for haptic scenes
inferred← citeshttps://doi.org/10.1016/j.cognition.2016.04.016openalex-snapshot
Language and memory for object location
inferred← citeshttps://doi.org/10.1016/j.cognition.2017.07.014openalex-snapshot
Where you are affects what you can easily imagine: Environmental geometry elicits sensorimotor interference in remote perspective taking
inferred← citeshttps://doi.org/10.1016/j.cognition.2017.09.005openalex-snapshot
Competing perspectives on frames of reference in language and thought
inferred← citeshttps://doi.org/10.1016/j.cognition.2018.07.012openalex-snapshot
The latent structure of spatial skill: A test of the 2 × 2 typology
inferred← citeshttps://doi.org/10.1016/j.cognition.2019.05.020openalex-snapshot
Alternative spin on phylogenetically inherited spatial reference frames
inferred← citeshttps://doi.org/10.1016/j.cogpsych.2015.02.001openalex-snapshot
Human short-term spatial memory: Precision predicts capacity
inferred← citeshttps://doi.org/10.1016/j.cogpsych.2016.04.001openalex-snapshot
Thinking outside of the box: Transfer of shape-based reorientation across the boundary of an arena
inferred← citeshttps://doi.org/10.1016/j.cogpsych.2016.06.001openalex-snapshot
Frames of reference in spatial language acquisition
inferred← citeshttps://doi.org/10.1016/j.cogpsych.2018.11.001openalex-snapshot
Thinking outside of the box II: Disrupting the cognitive map
inferred← citeshttps://doi.org/10.1016/j.cogsys.2011.09.001openalex-snapshot
A computational model of the allocentric and egocentric spatial memory by means of virtual agents, or how simple virtual agents can help to build complex computational models
inferred← citeshttps://doi.org/10.1016/j.cogsys.2017.08.002openalex-snapshot
A computational cognitive framework of spatial memory in brains and robots
inferred← citeshttps://doi.org/10.1016/j.compedu.2019.04.010openalex-snapshot
Mobile virtual reality for musical genre learning in primary education
inferred← citeshttps://doi.org/10.1016/j.compenvurbsys.2013.10.003openalex-snapshot
Interactive navigation interface for Virtual Reality using the human body
inferred← citeshttps://doi.org/10.1016/j.conb.2009.02.002openalex-snapshot
Doing Socrates experiment right: controlled rearing studies of geometrical knowledge in animals
inferred← citeshttps://doi.org/10.1016/j.conb.2022.102568openalex-snapshot
What does engram encode?: Heterogeneous memory engrams for different aspects of experience
inferred← citeshttps://doi.org/10.1016/j.conb.2024.102880openalex-snapshot
Cognitive maps and the magnetic sense in vertebrates
inferred← citeshttps://doi.org/10.1016/j.concog.2012.01.018openalex-snapshot
Disowning one’s seen real body during an out-of-body illusion
inferred← citeshttps://doi.org/10.1016/j.concog.2021.103108openalex-snapshot
Influence of vestibular signals on bodily self-consciousness: Different sensory weighting strategies based on visual dependency
inferred← citeshttps://doi.org/10.1016/j.cortex.2007.06.001openalex-snapshot
Behavioral and cortical mechanisms for spatial coding and action planning
inferred← citeshttps://doi.org/10.1016/j.cortex.2015.03.016openalex-snapshot
Lost in spatial translation – A novel tool to objectively assess spatial disorientation in Alzheimer's disease and frontotemporal dementia
inferred← citeshttps://doi.org/10.1016/j.cortex.2019.04.006openalex-snapshot
‘Real-life’ hippocampal-dependent spatial memory impairments in Huntington's disease
inferred← citeshttps://doi.org/10.1016/j.cortex.2020.11.010openalex-snapshot
Egocentric and allocentric spatial representations in a patient with Bálint-like syndrome: A single-case study
inferred← citeshttps://doi.org/10.1016/j.cortex.2021.04.002openalex-snapshot
Exploring the time-course and the reference frames of adaptation to optical prisms and its aftereffects
inferred← citeshttps://doi.org/10.1016/j.cortex.2026.06.022openalex-snapshot
The neural basis of creative thought: An activation likelihood estimation meta-analysis of 787 experiments
inferred← citeshttps://doi.org/10.1016/j.cub.2009.10.041openalex-snapshot
Variation in memory for body movements across cultures
inferred← citeshttps://doi.org/10.1016/j.cub.2009.10.052openalex-snapshot
Defensive tool use in a coconut-carrying octopus
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.049openalex-snapshot
The Operation of the Visual System in Relation to Action
inferred← citeshttps://doi.org/10.1016/j.cub.2016.11.046openalex-snapshot
Environmental Geometry Aligns the Hippocampal Map during Spatial Reorientation
inferred← citeshttps://doi.org/10.1016/j.cub.2018.02.042openalex-snapshot
Cross-Situational Learning Is Supported by Propose-but-Verify Hypothesis Testing
inferred← citeshttps://doi.org/10.1016/j.destud.2022.101108openalex-snapshot
Lost in imagined space: A psychoanalysis of participatory design
inferred← citeshttps://doi.org/10.1016/j.envres.2025.120830openalex-snapshot
Developmental exposure to legacy environmental contaminants, medial temporal lobe volumes and spatial navigation memory in late adolescents
inferred← citeshttps://doi.org/10.1016/j.foar.2017.06.005openalex-snapshot
Syntactical analysis of the accessibility and sociability of a square in the Kuala Lumpur City Center
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