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The parietal cortex and episodic memory: an attentional account

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Cabeza, Roberto, Ciaramelli, Elisa, Olson, Ingrid R., Moscovitch, Morris·2008·Nature Reviews Neuroscience

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Abstract

The contribution of the parietal cortex to episodic memory is a fascinating scientific puzzle. On the one hand, parietal lesions do not normally yield severe episodic-memory deficits; on the other hand, parietal activations are seen frequently in functional-neuroimaging studies of episodic memory. A review of these two categories of evidence suggests that the answer to the puzzle requires us to distinguish between the contributions of dorsal and ventral parietal regions and between the influence of top-down and bottom-up attention on memory.

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The attention system of the human brain
Posner, M. I., & Petersen, S. E. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.000325 · Cited by 8,070
The episodic buffer: a new component of working memory?
Baddeley, A. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01538-2 · Cited by 7,359
Working memory: Looking back and looking forward
Baddeley, A. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1201 · Cited by 5,200
Memory and consciousness.
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
The reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889
The Nature of Recollection and Familiarity: A Review of 30 Years of Research
Yonelinas, A. P. (2002) · Journal of Memory and Language · doi:10.1006/jmla.2002.2864 · Cited by 3,840
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947
Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems
Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101
Voluntary orienting is dissociated from target detection in human posterior parietal cortex
Corbetta, M., Kincade, J. M., Ollinger, J. M., McAvoy, M. P., & Shulman, G. L. (2000) · Nature Neuroscience · doi:10.1038/73009 · Cited by 1,816

Show all 22 references

The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182
The organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304
Evidence for a Frontoparietal Control System Revealed by Intrinsic Functional Connectivity
Vincent, J. L., Kahn, I., Snyder, A. Z., Raichle, M. E., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90355.2008 · Cited by 1,869
The Angular Gyrus: Multiple Functions and Multiple Subdivisions
Seghier, M. L. (2013) · The Neuroscientist · doi:10.1177/1073858412440596 · Cited by 1,585
Posterior midline and ventral parietal activity is associated with retrieval success and encoding failure
Daselaar, S. M. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.013.2009 · Cited by 1,501
A taxonomy of external and internal attention.
Chun, M. M., Golomb, J. D., & Turk-Browne, N. B. (2011) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100427 · Cited by 1,472
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377
Default network activity, coupled with the frontoparietal control network, supports goal-directed cognition
Spreng, R. N., Stevens, W. D., Chamberlain, J. P., Gilmore, A. W., & Schacter, D. L. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.016 · Cited by 1,256
The cognitive neuroscience of ageing
Grady, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3256 · Cited by 1,286
Episodic future thinking reduces reward delay discounting through an enhancement of prefrontal–mediotemporal interactions
Peters, J., & Büchel, C. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.026 · Cited by 871
Event-related fMRI studies of episodic encoding and retrieval: meta-analyses using activation likelihood estimation
Spaniol, J., Davidson, P. S. R., Kim, A. S. N., Han, H., Moscovitch, M., & Grady, C. L. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.02.028 · Cited by 791
Self-citation
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736
Self-citation
A nexus model of the temporal–parietal junction
Carter, R. M., & Huettel, S. A. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.05.007 · Cited by 489
Prefrontal Contributions to Metacognition in Perceptual Decision Making
Fleming, S. M., Huijgen, J., & Dolan, R. J. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6489-11.2012 · Cited by 391
To create or to recall? Neural mechanisms underlying the generation of creative new ideas
Benedek, M., Jauk, E., Fink, A., Koschutnig, K., Reishofer, G., Ebner, F., & Neubauer, A. C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.021 · Cited by 407
Re-evaluating the role of TPJ in attentional control: Contextual updating?
Geng, J. J., & Vossel, S. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.08.010 · Cited by 411
A unified framework for the functional organization of the medial temporal lobes and the phenomenology of episodic memory
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375
Episodic memory in normal aging and Alzheimer disease: Insights from imaging and behavioral studies
Tromp, D., Dufour, A., Lithfous, S., Pebayle, T., & Després, O. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.08.006 · Cited by 390
Cognitive contributions of the ventral parietal cortex: an integrative theoretical account
Cabeza, R., Ciaramelli, E., & Moscovitch, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.04.008 · Cited by 373
Self-citation
The inferior parietal lobule and temporoparietal junction: A network perspective
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Enhanced visual functioning in autism: An ALE meta-analysis
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Creating metaphors: the neural basis of figurative language production
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Authors: Cabeza, R., Ciaramelli, E., Olson, I. R., & Moscovitch, M.
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2008-08
Volume: 9
Issue: 8
Pages: 613-625
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn2459
OpenAlex: W2014550466
Cited by: 1,197
References: 22
FWCI: 3.62
Type: journal article
Language: en
Open access: green

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The parietal cortex and episodic memory: an attentional account

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