The anatomy of memory: an interactive overview of the parahippocampal–hippocampal network
By N. V. Strien, Natalie L. M. Cappaert, M.P. Witter. 2009
1,015 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience, Neurology
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- James L. McClelland
- Dharshan Kumaran
- Ivan Soltesz
- Menno P. Witter
- Ahmed A. Moustafa
- Hongkui Zeng
- Richard B. Buxton
- Eleonora Aronica
In Cognitive Neuroscience
- James L. McClelland
- Dharshan Kumaran
- Ivan Soltesz
- P. Kahane
- John Pluta
- Menno P. Witter
- Ahmed A. Moustafa
- Richard B. Buxton
In Neurology
Citations in the corpus
- Generalization Through the Recurrent Interaction of Episodic Memories (2012, background): “…of “big-loop” recurrency, both within the hippocampal system itself and more widely between the hippocampus and the neocortex (van Strien, Cappaert, & Witter, 2009)—an idea that contrasts with an earlier focus on the internally recurrent circuitry of the CA3 region (Burgess, 2006; Lisman, 1999;…”
- What Learning Systems do Intelligent Agents Need? Complementary Learning Systems Theory Updated. (2016, neutral): “ERC neurons give rise to projections to three subregions of the hippocampus proper, the dentate gyrus (DG), CA1, and CA3 [28,84].”
- Quantitative Assessment of CA1 Local Circuits: Knowledge Base for Interneuron-Pyramidal Cell Connectivity (2013, background): “There are also some connections from the subiculum, presubiculum, and parasubiculum as reviewed in Van Strien et al. (2009).”
- A taxonomy of transcriptomic cell types across the isocortex and hippocampal formation (2020, background): “Underlying the functions, the input and output connections across many regions both within and outside HPF are highly complex yet highly organized (Bienkowski et al., 2018; van Strien et al., 2009).”
- A computational model of pattern separation efficiency in the dentate gyrus with implications in schizophrenia (2015, background): “In the classic tri-synaptic pathway, information proceeds from the entorhinal cortex (EC) to the dentate gyrus (DG) to CA3 and then to CA1 which is known as the main hippocampal output (Van Strien et al., 2009; Newman and Hasselmo, 2014; Figure 1A ).”
- A pathophysiological framework of hippocampal dysfunction in ageing and disease (2011, background): “The subiculum and, to a lesser extent, CA1 are the hippocampal subregions that provide the dominant outflow of the hippocampal circui”
- Molecularly Defined Circuitry Reveals Input-Output Segregation in Deep Layers of the Medial Entorhinal Cortex (2015, background): “Spatial cognition and episodic memory rely on signal processing by the medial entorhinal cortex (MEC), which is believed to function both as a relay of hippocampal outputs to other brain structures and as a major source of cortical input to the hippocampus (Burwell, 2000; van Strien et al., 2009).”
- Automated Volumetry and Regional Thickness Analysis of Hippocampal Subfields and Medial Temporal Cortical Structures in Mild Cognitive Impairment (2014, background): “These cortical regions are tightly interconnected with the hippocampus as part of the medial temporal memory networks [Ranganath and Ritchey, 2012; Squire et al., 2004; van Strien et al., 2009; Yassa and Stark, 2011; Wolk et al., 2011].”
- International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods (2013, methodology): “A helpful and interactive overview of the Epilepsia, 54(7):1315–1329, 2013 doi: 10.1111/epi.12220 parahippocampal-hippocampal network is provided by van Strien et al. (2009).”
- Switching between internal and external modes: A multiscale learning principle (2017, neutral): “Computationally, both fast and slow forms of hippocampal switching reflect an alternation between epochs of “encoding,” where bottom-up activity drives CA1, and epochs of “retrieval,” where CA3 drives CA1 (Hasselmo, 1995; Hasselmo & Schnell, 1994; Meeter, Murre, & Talamini, 2004).”