Cited by 278Memory Processes and InfluencesMemory and Neural MechanismsCognitive Functions and Memory

The DOI matches its Crossref record; 105 of the 105 references it cites were found in a registry or an index.

Age-related differences in the functional connectivity of the hippocampus during memory encoding

Open access

Grady, Cheryl L., McIntosh, Anthony R., Craik, Fergus I.M.·2003·Hippocampus

Open this paper in CoChat — free account Open PDF

Abstract

The purpose of the current experiment was to examine the functional connectivity of the hippocampus during encoding in young and old adults, and the way in which this connectivity was related to recognition performance. Functional connectivity was defined as the correlation between activity in the hippocampus and activity in the rest of the brain, as measured by neuroimaging. During encoding of words and pictures of objects in young adults, hippocampal activity was correlated with activity in the ventral prefrontal and extrastriate regions, and increased activity in all these regions was associated with better recognition. In contrast, older adults showed correlations between hippocampal activity and the dorsolateral prefrontal and parietal regions, and positive correlations between activity in these regions and better memory performance. This ventral/dorsal distinction suggests a shift in the cognitive resources used with age from more perceptually based processes to those involved in executive and organizational functions. The results of this study provide evidence that aging is associated with alterations in hippocampal function, including how it is functionally connected with prefrontal cortex, and that these alterations have an impact on memory performance. Hippocampus 2003;13:572–586. © 2003 Wiley‐Liss, Inc.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1002/hipo.10114

Cites

105 of 105 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

“Mini-mental state”
Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975) · Journal of Psychiatric Research · doi:10.1016/0022-3956(75)90026-6 · Cited by 88,282
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
LISREL 7 : user's reference guide
Jöreskog, K. G., & Sörbom, D. (1989) · Medical Entomology and Zoology · Cited by 6,783
Bootstrap Methods for Standard Errors, Confidence Intervals, and Other Measures of Statistical Accuracy
Efron, B., & Tibshirani, R. (1986) · Statistical Science · doi:10.1214/ss/1177013815 · Cited by 6,033
A standardized set of 260 pictures: Norms for name agreement, image agreement, familiarity, and visual complexity.
Snodgrass, J. G., & Vanderwart, M. (1980) · Journal of Experimental Psychology Human Learning & Memory · doi:10.1037//0278-7393.6.2.174 · Cited by 5,604
Untitled work
(1998) · Cited by 4,172
A standardized set of 260 pictures: Norms for name agreement, image agreement, familiarity, and visual complexity.
Snodgrass, J. G., & Vanderwart, M. (1980) · Journal of Experimental Psychology Human Learning & Memory · doi:10.1037/0278-7393.6.2.174 · Cited by 3,635
Functional and effective connectivity in neuroimaging: a synthesis
Friston, K. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020107 · Cited by 2,452
Functional Connectivity: The Principal-Component Analysis of Large (PET) Data Sets
Friston, K. J., Frith, C., Liddle, P. F., & Frackowiak, R. S. J. (1993) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1993.4 · Cited by 1,997

Flagged first, then by citations

Show all 104 references

Sorted by citations

Items 201–278 of 278

Distinct Genetic Signatures of Cortical and Subcortical Regions Associated with Human Memory
Tan, P. K., Ananyev, E., & Hsieh, P. (2019) · eNeuro · doi:10.1523/eneuro.0283-19.2019 · Cited by 9
La comprensión del cerebro: El nacimiento de una ciencia del aprendizaje
OECD (2010) · OECD eBooks · doi:10.1787/9789567947928-es · Cited by 7
Time-modulated enhancing of the fronto-parietal circuits in the very-old elders
Maestú, F., Campo, P., Fernández, S., Capilla, A., Gil‐Gregorio, P., Fernández, A., Amo, C., & Ortiz, T. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.06.002 · Cited by 6
APOE ɛ4 Allele Moderates the Association Between Basal Forebrain Nuclei Volumes and Allocentric Navigation in Older Adults Without Dementia
Lerch, O., Laczó, M., Vyhnálek, M., Nedelská, Z., Hort, J., & Laczó, J. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215034 · Cited by 5
Neuronale Plastizität bei gesundem und pathologischem Altern
Kolassa, I., Glöckner, F., Leirer, V. M., & Diener, C. (2010) · Springer eBooks · doi:10.1007/978-3-642-14353-3_4 · Cited by 5
7 Compensatory Reorganization of Brain Networks in Older Adults
Grady, C. L. (2009) · doi:10.1093/acprof:oso/9780195328875.003.0007 · Cited by 4
Self-citation
Imaging Aging: Present and Future
Hayes, S. M., & Cabeza, R. E. L. (2008) · Sage eBooks · doi:10.4135/9781412976589.n19 · Cited by 4
Fornix white matter microstructure differentially predicts false recollection rates in older and younger adults
Chamberlain, J. D., Turney, I. C., Goodman, J. T., Hakun, J. G., & Dennis, N. A. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.107848 · Cited by 4
Functional Neuroimaging Studies of Aging
Grady, C. L. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00103-0 · Cited by 5
Self-citation
Neural Mechanisms of Memory
Amer, T., & Davachi, L. (2022) · doi:10.31234/osf.io/32egy · Cited by 3
Emotional learning selectively distorts the temporal organization of memory: A quantitative synthesis
Laing, P. A. F., Hennings, A. C., Cooper, S. E., & Dunsmoor, J. E. (2025) · Cognition · doi:10.1016/j.cognition.2025.106382 · Cited by 3
Topography of hippocampal connectivity with sensorimotor cortex revealed by optimizing smoothing kernel and voxel size
Burman, D. D. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260245 · Cited by 3
Functional MRI Studies of Memory in Aging, Mild Cognitive Impairment, and Alzheimer’s Disease
Risacher, S. L., Wishart, H. A., & Saykin, A. J. (2011) · Springer eBooks · doi:10.1007/978-1-4419-0345-7_24 · Cited by 3
Neural Mechanisms of Memory
Amer, T., & Davachi, L. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190917982.013.4 · Cited by 3
Age-Related Differences According to the Associative Deficit and the Environmental Support Hypotheses: An Application of the Formal Charm Associative Memory Model
Sauzeon, H., Rodrigues, J., Corsini, M.-M., & N’Kaoua, B. (2013) · Experimental Aging Research · doi:10.1080/0361073x.2013.779192 · Cited by 4
Intrinsic Brain Activity of Cognitively Normal Older Persons Resembles More That of Patients Both with and at Risk for Alzheimer's Disease Than That of Healthy Younger Persons
Pasquini, L., Tonch, A., Plant, C., Zherdin, A., Ortner, M., Kurz, A., Förstl, H., Zimmer, C., Grimmer, T., Wohlschäger, A., et al. (2014) · Brain Connectivity · doi:10.1089/brain.2013.0213 · Cited by 2
Altered neural associations with cognitive and emotional functions in cannabis dependence
Wang, X., Zhou, H., & Hu, Y. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad153 · Cited by 2
Functional MRI Studies of Memory in Aging, Mild Cognitive Impairment, and Alzheimer’s Disease
Zhu, J. K., Risacher, S. L., Wishart, H. A., & Saykin, A. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-10909-6_30 · Cited by 2
Functional Imaging in Healthy Aging and Alzheimer's Disease
Anderson, N. D., & Grady, C. L. (2004) · KARGER eBooks · doi:10.1159/000079996 · Cited by 2
Self-citation
Neural correlates of exceptional memory ability in SuperAgers: A multimodal approach using FDG-PET, PIB-PET, and MRIPreprint
Borelli, W. V., Leal‐Conceição, E., Andrade, M. A., Esper, N. B., Feltes, P. K., Soder, R. B., Matushita, C. S., Hartmann, L. M., Radaelli, G., Schilling, L. P., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/666438 · Cited by 2
Spatial Navigation
Rusconi, M. L., Fusi, G., & Crepaldi, M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819641-0.00048-7 · Cited by 2
Cross-layer Balance of Visuo-hippocampal Functional Connectivity Is Associated With Episodic Memory Recognition AccuracyPreprint
Chang, W., Langella, S., Seo, M. S., Huynh, K. M., Yap, P., Lin, W., & Giovanello, K. S. (2022) · Research Square · doi:10.21203/rs.3.rs-1789565/v1 · Cited by 2
The Precision of Hippocampal Representations Predicts Incremental Value Learning across the Adult Lifespan
van Geen, C., Lempert, K. M., Cohen, M. S., MacNear, K. A., Reckers, F. M., Zaneski, L., Wolk, D. A., & Kable, J. W. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1459-25.2026 · Cited by 1
Episodic memory neural mechanisms: patterns, connectivity, and developmental dynamics
Qu, J., Fu, J., Liu, X., Chen, M., Yang, T., & Shen, Z. (2025) · Brain and Cognition · doi:10.1016/j.bandc.2025.106374 · Cited by 2
Inflammaging and the role of micronutrients as immunomodulators: a pathway to healthy aging
Tan, S. S. L., Garg, V., Dhiman, A., Bansal, N., & Conway, P. L. (2026) · Immunity & Ageing · doi:10.1186/s12979-026-00569-5 · Cited by 1
Dissecting Altered Functional Engagement in TBI and Other Patient Groups through Connectivity Analysis: One Goal, Many Paths (A Response to Hillary)
Turner, G. R., McIntosh, A. R., & Levine, B. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00010 · Cited by 1
Self-citation
BRAIN SENESCENCE-OMICS
Chakrabarti, A., & Mukhopadhyay, D. (2013) · Journal of Proteins and Proteomics · Cited by 1
Effects of Aging on the Neural Correlates of Successful Item and Source
Dennis, N. A., Hayes, S. M., Prince, S. E., Madden, D. J., Huettel, S. A., & Cabeza, R. E. L. (2008) · Cited by 1
Toward a more integrative cognitive neuroscience of episodic memory
Stanley, M. L., Geib, B. R., & Davis, S. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813838-0.00011-x · Cited by 1
Age-Related Changes in Episodic Processing of Scenes: A Functional Activation and Connectivity Study
Miyakoshi, M., Archer, J. A., Wu, C., Nakai, T., & Chen, S. A. (2023) · Sensors · doi:10.3390/s23084107 · Cited by 1
The development of episodic memory across the lifespan : Integrating behavioral and neural evidence
Shing, Y. L., & Lindenberger, U. (2012) · Max Planck Digital Library · Cited by 1
Brain structure and verbal function across adulthood while controlling for cerebrovascular risks
Sanfratello, L., Lundy, S. L., Qualls, C., Knoefel, J. E., Adair, J. C., Caprihan, A., Stephen, J. M., & Aine, C. J. (2017) · Human Brain Mapping · doi:10.1002/hbm.23602 · Cited by 1
Sleep, Memory, and Aging: Effects of Pre- and Post-Sleep Delays and Interference on Memory in Younger and Older Adults
Scullin, M. K. (2011) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k74t6gg3 · Cited by 1
Reply to Grady (2007), Raz (2007), and Salthouse (2007): Can age and treachery triumph over youth and skill?
Greenwood, P. M. (2007) · Neuropsychology · doi:10.1037/0894-4105.21.6.680 · Cited by 1
Processing of novelty and familiarity in the aging brain
Tóth, M. (2022) · doi:10.26481/dis.20220201mt · Cited by 1
Aging effects on neural entrainment to a musical beatPreprint
Sauvé, S. A., Bolt, E., Nozaradan, S., & Zendel, B. R. (2019) · doi:10.31219/osf.io/xfrve · Cited by 1
Volume of the posterior hippocampus mediates age-related differences in spatial context memory and is correlated with increased activity in lateral frontal, parietal and occipital regions in healthy aging
Snytte, J., Fenerci, C., Rajagopal, S., Beaudoin, C., Hooper, K., Sheldon, S., Olsen, R. K., & Rajah, M. N. (2023) · doi:10.32920/24438043.v1 · Cited by 1
Age Differences in Hippocampal Neural Timescales During Movie-ViewingPreprint
Bouffard, N. R., Delarazan, A. I., Karagoz, A. B., Zacks, J. M., & Reagh, Z. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.05.723065 · Cited by 1
MRI MEASURES OF BRAIN INTEGRITY AND THEIR RELATION TO PROCESSING SPEED IN THE ELDERLY
Venkatraman, V. K. (2010) · D-Scholarship@Pitt (University of Pittsburgh)
Binding information in short-term memory: evidence from healthy individuals, Alzheimer's Disease and other clinical populations
Parra, M. A. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)
Function and brain structure in aging with and without cognitive impairment
Solé‐Padullés, C. (2007) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Estudio de la estructura dinámica de las interacciones funcionales en el hipocampo mediante procesado de registros electrofisiológicos cerebrales en rata.
LÓPEZ, M. V. G. (2013) · doi:10.4995/thesis/10251/30777
Intérêt de la stimulation magnétique transcrânienne dans la maladie d’Alzheimer
Vandel, P., Chopard, G., Magnin, É., Nicolier, M., Monnin, J., Galmiche, J., Rumbach, L., Pazart, L., Sechter, D., & Haffen, É. (2011) · Les cahiers de l année gérontologique · doi:10.1007/s12612-011-0191-4
Quand le cerveau vieillit
Lotstra, F. (2003) · Cahiers critiques de thérapie familiale et de pratiques de réseaux · doi:10.3917/ctf.031.0111
Les maladies parasitaires des bovins
Tita, S. (2014) · Docs.school Publications
The effects of aging and cognitive performance on patterns of neural activity measured by functional magnetic resonance imaging
Johnson, J. L. (2004) · UA Campus Repository (The University of Arizona)
Accelerated long-term forgetting in aging and intra-sleep
Peigneux, P., Gaillard, V., & Gotts, S. J. (2013)
Mediação das vias dopaminérgicas meso-estriatais no comportamento de escolha de ações motoras e na formação de memórias de procedimento
Wietzikoski, E. C. (2009) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Functional neuroimaging and cognitive rehabilitation:healthy aging as a model of plasticity
Grady, C. L. (2008) · Cambridge University Press eBooks · doi:10.1017/cbo9781316529898.012
Self-citation
The Neural Processes Underpinning Visual Associative Memory: A Comparison of Young Grapheme-Colour Synaesthetes, Older Adults and Young Controls.
Pfeifer, G. (2015) · ePrints Soton (University of Southampton)
Neural correlates of episodic memory formation in children and adults
Tang, L. (2015) · Human Biology
The study on dynamics of functional brain network: Based on symbolic dynamics
Wang, M., Li, Y., Chen, X., & Li, W. (2016) · Chinese Control and Decision Conference (CCDC) · doi:10.1109/ccdc.2016.7531180
Neurocognitive Plasticity: A Longitudinal Study of Memory Training and White Matter Microstructure
de Lange, & Glasø, A.-M. D. L. (2017)
Brain Oscillations and Predictive Coding: What We Know and What We Should Learn
Scarpelli, S., D’Atri, A., Gorgoni, M., Gennaro, L. D., & Ferrara, M. (2017) · Frontiers research topics · doi:10.3389/978-2-88945-161-6
Hormonal and non-hormonal factors associated with cognition in post-menopausal women
Rodrigues, M. A. (2004) · UWA Profiles and Research Repository (UWA)
Recollection, Familiarity, and Working Memory Contributions to Math and Reading Achievement at Ages 6 and 9
Blankenship, T. L. (2017) · VTechWorks (Virginia Tech)
Functional Interplay Between Neurocognitive Decline and Risk Factors in Older Adults: A Multivariate Latent Growth Curve Model of Risk
MacAulay, R. K. (2015) · Louisiana State University · doi:10.31390/gradschool_dissertations.384
Intérêt de la stimulation magnétique transcrânienne dans la maladie d'Alzheimer Cognitive effects of repetitive transcranial magnetic stimulation (rTMS) in Alzheimer disease
Vandel, P., Chopard, G., Magnin, É., Nicolier, M., Monnin, J., Galmiche, J., Rumbach, L., Pazart, L., Sechter, D., & Haffen, É. (2011)
Cognitive and Neural Correlates of Implicit Associative Memory in Young and Older Adults
Dew, I. T. Z. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/nc90-7v32
Introduction to Estrogens and Memory
Frick, K. M. (2020) · doi:10.1093/oso/9780190645908.003.0001
Functional MRI Studies of Memory in Aging, Mild Cognitive Impairment, and Alzheimer’s Disease
Risacher, S. L., Wishart, H. A., & Saykin, A. J. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1995-6_10
Análise do movimento ocular em tarefas de memória associativa no diagnóstico precoce da Doença de Alzheimer
Camargo, M. V. Z. D. A. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2022.tde-03102022-111832
Physical activity is associated with behavioral and neural changes across the lifespan
Kumar, G., Lacey, S., & Sathian, K. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137355
Volume of the posterior hippocampus mediates age-related differences in spatial context memory and is correlated with increased activity in lateral frontal, parietal and occipital regions in healthy aging
Snytte, J., Fenerci, C., Rajagopal, S., Beaudoin, C., Hooper, K., Sheldon, S., Olsen, R. K., & Rajah, M. N. (2023) · doi:10.32920/24438043
Creatine maintains mitochondrial integrity and protects against dysfunction in molecular systems involved in early epileptiform activity and cognitive impairment in young rats submitted to traumatic brain injuryPreprint
Royes, L. F. F., Busanello, G. L., Godinho, D. B., Nascimento, A. S., Lima, G. C., Cunha, J. D. S. D. N. M., Bento‐Torres, J., Sosthenes, M. C. K., Gómez‐Pinilla, F., Krishna, G., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3635710/v1
The effects of prediction error on episodic memory
Turan, G. (2023) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.81682
Task-Aware Effective Connectivity Modeling for Cognitive Function Prediction
Zou, W., Li, Y., Hu, X., Chen, X., & Liu, A. (2025) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2025.3644481
Navigational strategy switching in ageing
Harris, M. A. (2014) · ERA
Additional file 1 of Mapping the long-term delayed recall-based cortex-hippocampus network constrained by the structural and functional connectome: a case-control multimodal MRI study
Ma, J., Zheng, M., Wu, J.-J., Xing, X.-X., Xiang, Y., Wei, D., Xue, X., Zhang, H., Hua, X.-Y., Guo, Q.-H., et al. (2023) · Figshare · doi:10.6084/m9.figshare.22620194
Impacts des entraînements cognitifs sur la cognition chez les adultes âgés : quel avantage de l'entraînement combiné ?
Joubert, C. (2018) · theses.fr (ABES) · doi:10.70675/cb7519d4z8f05z4646z8dd9ze4434288deca
Le rôle du contrôle perçu dans la relation entre l’âge et la mémoire épisodique rétrospective et prospective
Maggio, C. (2018) · theses.fr (ABES) · doi:10.70675/f4fa6d10z7061z49bdzbe51z7a35199b445d
Impact d'une supplémentation en actifs d'origine marine sur la neuroinflammation associée au déclin cognitif lié à l'âge
Chataigner, M. (2021) · theses.fr (ABES) · doi:10.70675/a4317690zc4c8z4ba6za738zd457c6bb9b74
Mécanismes cognitifs et cérébraux associés au maintien de la mémoire épisodique et de la mémoire de travail au cours du vieillissement
Sastoque, L. G. (2020) · theses.fr (ABES) · doi:10.70675/41905880z9020z4e9ez9d65zd0bc4ca82309
Activité physique, éducation et vieillissement cognitif : approche comportementale et électrophysiologique
Kachouri, H. (2023) · theses.fr (ABES) · doi:10.70675/88892f8fzab02z4a62za90bza2a1802f68fd
Age Differences in the Relationship Between Interoception and Emotional Processing
Cawkwell, S., Pauly‐Takacs, K., Kolokotroni, K. Z., & Pfeifer, G. (2026) · Behavioral Sciences · doi:10.3390/bs16050672
Category-selective functional connectivity during episodic encoding and retrieval in younger and older adultsPreprint
Monier, S. A., Srokova, S., Shahanawaz, N. S., & Rugg, M. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.29.728795
Creatine preserves mitochondrial integrity and ameliorates early epileptiform activity and cognitive impairment via regulation of Na⁺,K⁺-ATPase in adolescent rats with severe traumatic brain injury
Royes, L. F. F., Busanello, G. L., Godinho, D. B., Cassol, G., Nascimento, A. S., Lima, G. C., Cunha, J. D. S. D. N. M., Sosthenes, M. C. K., Neto, J. B. T., Gómez‐Pinilla, F., et al. (2026) · Behavioural Brain Research · doi:10.1016/j.bbr.2026.116405
Effects of age on memory-related category-selective connectivity
Monier, S. A., Srokova, S., Shahanawaz, N. S., & Rugg, M. D. (2026) · Cerebral Cortex · doi:10.1093/cercor/bhag124

Authors: Grady, C. L., McIntosh, A. R., & Craik, F. I. M.
Affiliations: University of Toronto (CA)
Corresponding author: Grady, Cheryl L.
ORCID: Grady, Cheryl L.
McIntosh, Anthony R.
Craik, Fergus I.M.
Venue: Hippocampus
Publisher: Wiley
Published: 2003-01
Volume: 13
Issue: 5
Pages: 572-586
ISSN: 1050-9631 (ISSN-L)
1098-1063
DOI: 10.1002/hipo.10114
OpenAlex: W2085791991
Cited by: 277
References: 104
Citations by year: 2026: 7 · 2025: 5 · 2024: 3 · 2023: 16 · 2022: 9 · 2021: 8 · 2020: 8 · 2019: 13 · 2018: 9 · 2017: 11 · 2016: 9 · 2015: 15 · 2014: 15 · 2013: 11 · 2012: 10
FWCI: 6.72
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 99 d)
Locations: Hippocampus (publishedVersion)
PubMed (publishedVersion)
Funders: Centre for Addiction and Mental Health
University of Toronto
Canadian Institutes of Health Research (MOP14036)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
Keywords: functional connectivity, memory encoding, aging, older adults, recognition memory, ventral prefrontal cortex, dorsolateral prefrontal cortex, parietal cortex, extrastriate cortex, executive function, perceptual processing, age differences
MeSH terms: Adult, Aged, Aging, Brain Mapping, Cognition, Female, Hippocampus, Humans, Functional Laterality, Learning, Male, Memory, Memory Disorders, Middle Aged, Neural Pathways, Pattern Recognition, Visual, Photic Stimulation, Tomography, Emission-Computed, Neocortex

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Age-related differences in the functional connectivity of the hippocampus during memory encoding

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks