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Multiple determinants of lifespan memory differences
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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/hbm.20179openalex-snapshot
Age effects on diffusion tensor magnetic resonance imaging tractography measures of frontal cortex connections in schizophrenia
inferredcites →https://doi.org/10.1002/hipo.20800openalex-snapshot
Preserved hippocampal novelty responses following anterior temporal‐lobe resection that impairs familiarity but spares recollection
inferredcites →https://doi.org/10.1002/hipo.20857openalex-snapshot
Predictive, interactive multiple memory systems
inferredcites →https://doi.org/10.1006/ccog.1997.0321openalex-snapshot
Experiences of Remembering, Knowing, and Guessing
inferredcites →https://doi.org/10.1006/jmla.2002.2864openalex-snapshot
The Nature of Recollection and Familiarity: A Review of 30 Years of Research
inferredcites →https://doi.org/10.1016/0001-6918(67)90011-xopenalex-snapshot
Age differences in fluid and crystallized intelligence
inferredcites →https://doi.org/10.1016/j.neuroimage.2004.01.049openalex-snapshot
fMRI correlates of the episodic retrieval of emotional contexts
inferredcites →https://doi.org/10.1016/j.neuroimage.2007.07.007openalex-snapshot
A fast diffeomorphic image registration algorithm
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.12.086openalex-snapshot
Adjusting for global effects in voxel-based morphometry: Gray matter decline in normal aging
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.09.018openalex-snapshot
The Cambridge Centre for Ageing and Neuroscience (Cam-CAN) data repository: Structural and functional MRI, MEG, and cognitive data from a cross-sectional adult lifespan sample
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.10.085openalex-snapshot
White matter and memory in healthy adults: Coupled changes over two years
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.11.028openalex-snapshot
Regional brain shrinkage and change in cognitive performance over two years: The bidirectional influences of the brain and cognitive reserve factors
inferredcites →https://doi.org/10.1016/j.neuron.2004.09.006openalex-snapshot
Memory and Executive Function in Aging and AD
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2004.04.006openalex-snapshot
Relationship between hippocampal volume and memory ability in healthy individuals across the lifespan: review and meta-analysis
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2009.01.001openalex-snapshot
Aging white matter and cognition: Differential effects of regional variations in diffusion properties on memory, executive functions, and speed
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2014.05.011openalex-snapshot
No evidence that ‘fast-mapping’ benefits novel learning in healthy Older adults
inferredcites →https://doi.org/10.1016/j.tics.2005.08.005openalex-snapshot
Aging and motivated cognition: the positivity effect in attention and memory
inferredcites →https://doi.org/10.1016/j.tics.2011.03.005openalex-snapshot
The medial temporal lobe and the attributes of memory
inferredcites →https://doi.org/10.1016/s0001-6918(97)00043-7openalex-snapshot
On the relationship between recognition familiarity and perceptual fluency: Evidence for distinct mnemonic processes
inferredcites →https://doi.org/10.1016/s1364-6613(00)01707-1openalex-snapshot
Cognitive and neural mechanisms of emotional memory
inferredcites →https://doi.org/10.1037//0278-7393.15.1.31openalex-snapshot
How many memory systems? Evidence from aging.
inferredcites →https://doi.org/10.1037//0882-7974.10.4.527openalex-snapshot
Differential effects of aging on memory for content and context: A meta-analysis.
inferredcites →https://doi.org/10.1037//0882-7974.13.1.88openalex-snapshot
Repetition priming in normal aging and Alzheimer's disease: A review of findings and theories.
inferredcites →https://doi.org/10.1037//0882-7974.9.4.539openalex-snapshot
Adult age differences in repetition priming: A meta-analysis.
inferredcites →https://doi.org/10.1037/0033-295x.103.3.403openalex-snapshot
The processing-speed theory of adult age differences in cognition.
inferredcites →https://doi.org/10.1037/0033-295x.99.2.195openalex-snapshot
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
inferredcites →https://doi.org/10.1037/0096-3445.132.2.310openalex-snapshot
Aging and emotional memory: The forgettable nature of negative images for older adults.
inferredcites →https://doi.org/10.1037/0278-7393.34.1.97openalex-snapshot
A single-system account of the relationship between priming, recognition, and fluency.
inferredcites →https://doi.org/10.1037/0882-7974.20.1.3openalex-snapshot
Stability, Growth, and Decline in Adult Life Span Development of Declarative Memory: Cross-Sectional and Longitudinal Data From a Population-Based Study.
inferredcites →https://doi.org/10.1037/0882-7974.22.1.202openalex-snapshot
The associative memory deficit of older adults: The role of strategy utilization.
inferredcites →https://doi.org/10.1037/0882-7974.23.1.104openalex-snapshot
Differential effects of age on item and associative measures of memory: A meta-analysis.
inferredcites →https://doi.org/10.1037/0894-4105.21.6.684openalex-snapshot
Effects of global atrophy, white matter lesions, and cerebral blood flow on age-related changes in speed, memory, intelligence, vocabulary, and frontal function.
inferredcites →https://doi.org/10.1037/1528-3542.7.4.705openalex-snapshot
Aging and goal-directed emotional attention: Distraction reverses emotional biases.
inferredcites →https://doi.org/10.1037/a0019940openalex-snapshot
Differential age effects for implicit and explicit conceptual associative memory.
inferredcites →https://doi.org/10.1037/a0020525openalex-snapshot
Cross-sectional age variance extraction: What's change got to do with it?
inferredcites →https://doi.org/10.1037/a0025464openalex-snapshot
Models of recognition, repetition priming, and fluency: Exploring a new framework.
inferredcites →https://doi.org/10.1037/a0035194openalex-snapshot
Meta-analysis of the age-related positivity effect: Age differences in preferences for positive over negative information.
inferredcites →https://doi.org/10.1038/ncomms6658openalex-snapshot
Distinct aspects of frontal lobe structure mediate age-related differences in fluid intelligence and multitasking
inferredcites →https://doi.org/10.1038/nn.2149openalex-snapshot
A disproportionate role for the fornix and mammillary bodies in recall versus recognition memory
inferredcites →https://doi.org/10.1073/pnas.1511904112openalex-snapshot
Extent of hippocampal atrophy predicts degree of deficit in recall
inferredcites →https://doi.org/10.1080/09658210802222183openalex-snapshot
Adult age differences in memory for name–face associations: The effects of intentional and incidental learning
inferredcites →https://doi.org/10.1080/09658211.2014.985590openalex-snapshot
Recollection, not familiarity, decreases in healthy ageing: Converging evidence from four estimation methods
inferredcites →https://doi.org/10.1080/1047840x.2011.550181openalex-snapshot
Mind the Gap: A Psychometric Approach to the Reduction Problem
inferredcites →https://doi.org/10.1093/cercor/bhu238openalex-snapshot
Multiple Brain Markers are Linked to Age-Related Variation in Cognition
inferredcites →https://doi.org/10.1093/geronb/51b.4.p234openalex-snapshot
Age Differences in Episodic Memory, Semantic Memory, and Priming: Relationships to Demographic, Intellectual, and Biological Factors
inferredcites →https://doi.org/10.1101/lm.032409.113openalex-snapshot
Negative affect impairs associative memory but not item memory
inferredcites →https://doi.org/10.1111/1467-9280.00354openalex-snapshot
Visual Implicit Memory in the Left Hemisphere: Evidence From Patients With Callosotomies and Right Occipital Lobe Lesions
inferredcites →https://doi.org/10.1111/j.1467-9280.2007.01988.xopenalex-snapshot
Looking at the Sunny Side of Life
inferredcites →https://doi.org/10.1146/annurev.neuro.30.051606.094328openalex-snapshot
The Medial Temporal Lobe and Recognition Memory
inferredcites →https://doi.org/10.1146/annurev.ps.44.020193.002321openalex-snapshot
The Structure and Organization of Memory
inferredcites →https://doi.org/10.1146/annurev.psych.49.1.87openalex-snapshot
COGNITIVE NEUROSCIENCE OF HUMAN MEMORY
inferredcites →https://doi.org/10.1177/070674370805300603openalex-snapshot
Aging and Memory: A Cognitive Approach
inferredcites →https://doi.org/10.1177/1754073908100432openalex-snapshot
Remembering the Details: Effects of Emotion
inferredcites →https://doi.org/10.1186/s12883-014-0204-1openalex-snapshot
The Cambridge Centre for Ageing and Neuroscience (Cam-CAN) study protocol: a cross-sectional, lifespan, multidisciplinary examination of healthy cognitive ageing
inferredcites →https://doi.org/10.1523/jneurosci.2317-11.2011openalex-snapshot
Frontotemporal Connections in Episodic Memory and Aging: A Diffusion MRI Tractography Study
inferredcites →https://doi.org/10.1523/jneurosci.3456-08.2008openalex-snapshot
Activity in the Medial Temporal Lobe Predicts Memory Strength, Whereas Activity in the Prefrontal Cortex Predicts Recollection
inferredcites →https://doi.org/10.1523/jneurosci.5270-08.2009openalex-snapshot
Individual Differences in True and False Memory Retrieval Are Related to White Matter Brain Microstructure
inferredcites →https://doi.org/10.18637/jss.v048.i02openalex-snapshot
lavaan : An R Package for Structural Equation Modeling
inferredcites →https://doi.org/10.2307/1912557openalex-snapshot
Likelihood Ratio Tests for Model Selection and Non-Nested Hypotheses
inferredcites →https://doi.org/10.23668/psycharchives.12784openalex-snapshot
Evaluating the Fit of Structural Equation Models: Tests of Significance and Descriptive Goodness-of-Fit Measures
inferredcites →https://doi.org/10.3389/fpsyg.2013.00639openalex-snapshot
Age effects on explicit and implicit memory
inferredcites →https://doi.org/10.3758/bf03200930openalex-snapshot
Feature memory and binding in young and older adults
inferredcites →https://doi.org/10.3758/bf03211411openalex-snapshot
Perceptual implicit memory requires attentional encoding
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/hipo.23133openalex-snapshot
The role of hippocampal subfield volume and fornix microstructure in episodic memory across the lifespan
inferred← citeshttps://doi.org/10.1007/978-3-319-29674-6_14openalex-snapshot
Factors Influencing Opposing Effects of Emotion on Cognition: A Review of Evidence from Research on Perception and Memory
inferred← citeshttps://doi.org/10.1007/s11357-026-02096-zopenalex-snapshot
Fifteen years on: a review of the Cam-CAN study of the cognitive neuroscience of ageing
inferred← citeshttps://doi.org/10.1016/j.brat.2025.104882openalex-snapshot
‘Episodic Threat Conditioning’: a novel approach to simultaneously measure Pavlovian threat conditioning and episodic memory
inferred← citeshttps://doi.org/10.1016/j.concog.2023.103626openalex-snapshot
Age differences in priming as a function of processing at encoding
inferred← citeshttps://doi.org/10.1016/j.cortex.2017.01.001openalex-snapshot
Assumptions behind scoring source versus item memory: Effects of age, hippocampal lesions and mild memory problems
inferred← citeshttps://doi.org/10.1016/j.jbusres.2025.115356openalex-snapshot
Looking at the Stars: Status shifts after collective achievements
inferred← citeshttps://doi.org/10.1016/j.jml.2019.104039openalex-snapshot
Linking repetition priming, recognition, and source memory: A single-system signal-detection account
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.09.026openalex-snapshot
Recollection-related increases in functional connectivity across the healthy adult lifespan
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2018.10.005openalex-snapshot
Strong and specific associations between cardiovascular risk factors and white matter micro- and macrostructure in healthy aging
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2020.02.016openalex-snapshot
Age-related reduction in motor adaptation: brain structural correlates and the role of explicit memory
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2021.09.018openalex-snapshot
Evidence from theta-burst stimulation that age-related de-differentiation of the hippocampal network is functional for episodic memory
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2022.03.002openalex-snapshot
The association between control of interference and white-matter integrity: A cross-sectional and longitudinal investigation
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2024.04.005openalex-snapshot
Free Water-Corrected Fractional Anisotropy of the Fornix and Parahippocampal Cingulum Predicts Longitudinal Memory Change in Cognitively Healthy Older Adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.05.039openalex-snapshot
Independent contributions of fMRI familiarity and novelty effects to recognition memory and their stability across the adult lifespan
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.116475openalex-snapshot
The importance of the ventromedial prefrontal cortex for associative memory in older adults: A latent structural equation analysis
inferred← citeshttps://doi.org/10.1016/j.nicl.2022.103033openalex-snapshot
Episodic Past, Future, and counterfactual thinking in Relapsing-Remitting Multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.ynirp.2023.100168openalex-snapshot
Associative memory is more strongly predicted by age-related differences in the prefrontal cortex than medial temporal lobes
inferred← citeshttps://doi.org/10.1017/s0033291717001519openalex-snapshot
Symptoms of depression in a large healthy population cohort are related to subjective memory complaints and memory performance in negative contexts
inferred← citeshttps://doi.org/10.1017/s1355617721000084openalex-snapshot
Validation and Normative Data of the Spanish Version of the Face Name Associative Memory Exam (S-FNAME)
inferred← citeshttps://doi.org/10.1037/pag0000216openalex-snapshot
Hyper-binding only apparent under fully implicit test conditions.
inferred← citeshttps://doi.org/10.1037/pag0000432openalex-snapshot
Healthy ageing reduces the precision of episodic memory retrieval.
inferred← citeshttps://doi.org/10.1038/s41467-020-15410-wopenalex-snapshot
Noradrenergic-dependent functions are associated with age-related locus coeruleus signal intensity differences
inferred← citeshttps://doi.org/10.1038/s41467-025-66354-yopenalex-snapshot
Vulnerability to memory decline in aging revealed by a mega-analysis of structural brain change
inferred← citeshttps://doi.org/10.1038/s41598-020-66083-wopenalex-snapshot
Frontoparietal structural properties mediate adult life span differences in executive function
inferred← citeshttps://doi.org/10.1038/s41598-022-18543-8openalex-snapshot
Resting-state functional connectivity does not predict individual differences in the effects of emotion on memory
inferred← citeshttps://doi.org/10.1038/s41598-023-49514-2openalex-snapshot
Brain age prediction using combined deep convolutional neural network and multi-layer perceptron algorithms
inferred← citeshttps://doi.org/10.1038/s42003-024-06446-5openalex-snapshot
Functional locus coeruleus imaging to investigate an ageing noradrenergic system
inferred← citeshttps://doi.org/10.1080/02699931.2023.2279182openalex-snapshot
Are multiple types of associative memory differently impacted by emotion?
inferred← citeshttps://doi.org/10.1080/02699931.2024.2333067openalex-snapshot
The relationship between environmentally induced emotion and memory for a naturalistic virtual experience
inferred← citeshttps://doi.org/10.1080/09658211.2024.2314510openalex-snapshot
In my life: memory, self and The Beatles
inferred← citeshttps://doi.org/10.1080/13854046.2025.2592647openalex-snapshot
Validation and normative data of the Italian Face-Name Association Test (ItFNAT): A tool for cross-modal memory assessment
inferred← citeshttps://doi.org/10.1089/brain.2020.0749openalex-snapshot
Dissecting the Fornix in Basic Memory Processes and Neuropsychiatric Disease: A Review
inferred← citeshttps://doi.org/10.1093/acrefore/9780190236557.013.378openalex-snapshot
Implicit Memory and Cognitive Aging
inferred← citeshttps://doi.org/10.1093/cercor/bhaa066openalex-snapshot
Age-Related Decline in the Topological Efficiency of the Brain Structural Connectome and Cognitive Aging
inferred← citeshttps://doi.org/10.1093/cercor/bhaa287openalex-snapshot
Hippocampal and Parahippocampal Gray Matter Structural Integrity Assessed by Multimodal Imaging Is Associated with Episodic Memory in Old Age
inferred← citeshttps://doi.org/10.1093/cercor/bhz252openalex-snapshot
Hippocampal Subfields and Limbic White Matter Jointly Predict Learning Rate in Older Adults
inferred← citeshttps://doi.org/10.1093/geronb/gbz075openalex-snapshot
How Multiple Retrievals Affect Neural Reactivation in Young and Older Adults
inferred← citeshttps://doi.org/10.1093/scan/nsz036openalex-snapshot
Age-related decline in positive emotional reactivity and emotion regulation in a population-derived cohort
inferred← citeshttps://doi.org/10.1101/156935openalex-snapshot
Increased prefrontal activity with aging reflects nonspecific neural responses rather than compensation
inferred← citeshttps://doi.org/10.1101/2022.03.31.485630openalex-snapshot
Affective enhancement of episodic memory is associated with widespread patterns of intrinsic functional connectivity across the adult lifespan
inferred← citeshttps://doi.org/10.1101/353870openalex-snapshot
Motor learning decline with age is related to differences in the explicit memory system
inferred← citeshttps://doi.org/10.1136/bmjopen-2016-014920openalex-snapshot
How are age-related differences in sleep quality associated with health outcomes? An epidemiological investigation in a UK cohort of 2406 adults
inferred← citeshttps://doi.org/10.1162/netn_a_00064openalex-snapshot
Cooperative contributions of structural and functional connectivity to successful memory in aging
inferred← citeshttps://doi.org/10.1177/1747021820940300openalex-snapshot
The self-defining period in autobiographical memory: Evidence from a long-running radio show
inferred← citeshttps://doi.org/10.1177/17470218211008406openalex-snapshot
Explaining the association between repetition priming and source memory: No evidence for a contribution of recognition or fluency
inferred← citeshttps://doi.org/10.1177/17470218221090128openalex-snapshot
Age and processing effects on perceptual and conceptual priming
inferred← citeshttps://doi.org/10.1177/2515245919826527openalex-snapshot
A Practical Guide to Variable Selection in Structural Equation Modeling by Using Regularized Multiple-Indicators, Multiple-Causes Models
inferred← citeshttps://doi.org/10.1186/s12889-021-11591-1openalex-snapshot
Socio-economic inequality in functional disability and impairments with focus on instrumental activity of daily living: a study on older adults in India
inferred← citeshttps://doi.org/10.1523/jneurosci.1453-21.2022openalex-snapshot
Age-Related Enhancements in Positive Emotionality across The Life Span: Structural Equation Modeling of Brain and Behavior
inferred← citeshttps://doi.org/10.1523/jneurosci.1701-17.2018openalex-snapshot
Increased Prefrontal Activity with Aging Reflects Nonspecific Neural Responses Rather than Compensation
inferred← citeshttps://doi.org/10.17605/osf.io/bxzjfopenalex-snapshot
Variable Selection in Structural Equation Models with Regularized MIMIC Models
inferred← citeshttps://doi.org/10.17863/cam.39567openalex-snapshot
A Practical Guide to Variable Selection in Structural Equation Modeling by Using Regularized Multiple-Indicators, Multiple-Causes Models
inferred← citeshttps://doi.org/10.17863/cam.86431openalex-snapshot
Age-Related Enhancements in Positive Emotionality across The Life Span: Structural Equation Modeling of Brain and Behavior.
inferred← citeshttps://doi.org/10.31234/osf.io/2eypgopenalex-snapshot
Age-related decline in positive emotional reactivity and emotion regulation in a population-derived cohort
inferred← citeshttps://doi.org/10.31234/osf.io/73vdsopenalex-snapshot
The relationship between short- and long-term memory is preserved across the age range
inferred← citeshttps://doi.org/10.31234/osf.io/bxzjfopenalex-snapshot
Variable Selection in Structural Equation Models with Regularized MIMIC Models
inferred← citeshttps://doi.org/10.31234/osf.io/gsdvzopenalex-snapshot
Estimating Statistical Power for Structural Equation Models in Developmental Cognitive Science: A Tutorial in R
inferred← citeshttps://doi.org/10.3389/fnagi.2020.00079openalex-snapshot
Dentate Gyrus Volume Mediates the Effect of Fornix Microstructure on Memory Formation in Older Adults
inferred← citeshttps://doi.org/10.3389/fnagi.2022.771413openalex-snapshot
Effect of 3-Month Aerobic Dance on Hippocampal Volume and Cognition in Elderly People With Amnestic Mild Cognitive Impairment: A Randomized Controlled Trial
inferred← citeshttps://doi.org/10.3389/fnagi.2022.874767openalex-snapshot
A Double-Edged Sword: The Role of Prior Knowledge in Memory Aging
inferred← citeshttps://doi.org/10.3389/fnbeh.2022.910180openalex-snapshot
Affective Enhancement of Episodic Memory Is Associated With Widespread Patterns of Intrinsic Functional Connectivity in the Brain Across the Adult Lifespan
inferred← citeshttps://doi.org/10.3389/fpsyg.2017.01867openalex-snapshot
Emerging Directions in Emotional Episodic Memory
inferred← citeshttps://doi.org/10.3389/fpsyg.2021.797387openalex-snapshot
Healthy Middle-Aged Adults Have Preserved Mnemonic Discrimination and Integration, While Showing No Detectable Memory Benefits
inferred← citeshttps://doi.org/10.3389/fpsyg.2024.1459617openalex-snapshot
Disentangling emotional source memory: a mega-analysis on the effects of emotion on item-context binding in episodic long-term memory
inferred← citeshttps://doi.org/10.3390/brainsci13010106openalex-snapshot
The Relationship between Short- and Long-Term Memory Is Preserved across the Age Range
inferred← citeshttps://doi.org/10.3390/ijerph16234727openalex-snapshot
Demographic and Lifestyle Factors and Memory in European Older People
inferred← citeshttps://doi.org/10.3390/jcm9113735openalex-snapshot
Associations between Hypertension, Treatment, and Cognitive Function in the Irish Longitudinal Study on Ageing
inferred← citeshttps://doi.org/10.35946/arcr.v44.1.03openalex-snapshot
Alcohol Use Disorder and Dementia: A Review
inferred← citeshttps://doi.org/10.3758/s13415-025-01371-4openalex-snapshot
Effect of emotion on hippocampal-dependent associative binding through the lens of the weather prediction task
inferred← citeshttps://doi.org/10.3758/s13421-026-01873-7openalex-snapshot
Conceptual but not perceptual encoding leads to age differences in priming
inferred← citeshttps://doi.org/10.3758/s13428-024-02396-2openalex-snapshot
Estimating statistical power for structural equation models in developmental cognitive science: A tutorial in R
inferred← citeshttps://doi.org/10.7554/elife.55335openalex-snapshot
Hippocampal and cortical mechanisms at retrieval explain variability in episodic remembering in older adults
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