The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Configural association theory: The role of the hippocampal formation in learning, memory, and amnesia
Open accessAbstract
It is proposed that the hippocampal formation makes a unique contribution to memory by providing the neural basis for the initial acquisition and storage of configural associations among events. A distinction is made between two kinds of memory processes: a simple associative process, which does not depend on the hippocampal formation, and a configural associative process, which does. The simple associative system records the organism’s experiences as changes in the strength of associations between elementary stimulus events. The configural associative system combines the representations of elementary stimulus events to construct unique representations and allows for the formation of associations between these configural representations and other elementary representations. In the present paper, the results of two experiments designed to test predictions of our theory are described. We then illustrate how the theory can be applied to explain a wide range of impairments that have been observed when learning and memory tasks have been employed to assess the effect of hippocampal formation damage. These include tasks that measure place learning, recognition memory, latent inhibition, serial-compound conditioning, discrimination-reversal learning, and stimulus-selection processes. The relationship of our position to some other views of hippocampal function is discussed, and we conclude with suggestions for future research.
Overview
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
Cites
Statistics
Verification
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.
Citations
Cites
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
A learning algorithm for Boltzmann machines
Ackley, D. H., Hinton, G. E., & Sejnowski, T. J. (1985) · Cognitive Science · doi:10.1207/s15516709cog0901_7 · Cited by 3,402
A theory of attention: Variations in the associability of stimuli with reinforcement
Mackintosh, N. J. (1975) · Psychological Review · doi:10.1037/h0076778 · Cited by 2,733
Cohen, N. J., & Squire, L. R. (1980) · Science · doi:10.1126/science.7414331 · Cited by 2,296
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018
Remembrance of places passed: Spatial memory in rats.
Olton, D. S., & Samuelson, R. J. (1976) · Journal of Experimental Psychology: Animal Behavior Processes · doi:10.1037//0097-7403.2.2.97 · Cited by 1,998
Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997
Associations across time: The hippocampus as a temporary memory store
Rawlins, J. N. P. (1985) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00001291 · Cited by 561
Solomon, P. R., & Moore, J. W. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077183 · Cited by 473
Cited by
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
The Medial Temporal Lobe Memory System
Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.
Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292
Episodic memory, amnesia, and the hippocampal–anterior thalamic axis
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879
Metadata
- Authors
- Sutherland, R. J., & Rudy, J. W.
- Venue
- Psychobiology
- Published
- 1989-06
- Volume
- 17
- Issue
- 2
- Pages
- 129-144
- ISSN
- 0889-6313 (ISSN-L)
- OpenAlex
- W2099647287
- Cited by
- 954
- References
- 9
- FWCI
- 18.43
- Type
- journal article
- Language
- en
- Open access
- diamond
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.