The generalized spatial representation in the prefrontal cortex is inherited from the hippocampus
M. Nardin, K. Käfer, J.L. Csicsvari, BioRxiv (n.d.).
LibreCat: https://research-explorer.ista.ac.at/record/10080
DOI: 10.1101/2021.09.30.462269

Nonlinear computations in spiking neural networks through multiplicative synapses
M. Nardin, J.W. Phillips, W.F. Podlaski, S.W. Keemink, Peer Community Journal 1 (2021).
LibreCat: https://research-explorer.ista.ac.at/record/10635
DOI: 10.24072/pcjournal.69
arXiv: 2009.03857

Coupling of hippocampal theta and ripples with pontogeniculooccipital waves
J.F. Ramirez Villegas, M. Besserve, Y. Murayama, H.C. Evrard, A. Oeltermann, N.K. Logothetis, Nature 589 (2021) 96–102.
LibreCat: https://research-explorer.ista.ac.at/record/8818
DOI: 10.1038/s41586-020-2914-4
WoS: 000591047800005
PMID: 33208951

The structure of hippocampal C interactions optimizes spatial coding across experience
M. Nardin, J.L. Csicsvari, G. Tkadik, C. Savin, BioRxiv (n.d.).
LibreCat: https://research-explorer.ista.ac.at/record/10077
DOI: 10.1101/2021.09.28.460602

Partial coherence and frustration in self-organizing spherical grids
F. Stella, E. Urdapilleta, Y. Luo, A. Treves, Hippocampus 30 (2020) 302–313.
LibreCat: https://research-explorer.ista.ac.at/record/6796
DOI: 10.1002/hipo.23144
WoS: 000477299600001
PMID: 31339190

Replay of behavioral sequences in the medial prefrontal cortex during rule switching
K. Käfer, M. Nardin, K. Blahna, J.L. Csicsvari, Neuron 106 (2020) 4–165.e6.
LibreCat: https://research-explorer.ista.ac.at/record/7472
DOI: 10.1016/j.neuron.2020.01.015
WoS: 000525319300016
PMID: 32032512

Assembly-specific disruption of hippocampal replay leads to selective memory deficit
I. Gridchyn, P. Schönenberger, J. O’Neill, J.L. Csicsvari, Neuron 106 (2020) 291–300.e6.
LibreCat: https://research-explorer.ista.ac.at/record/7684
DOI: 10.1016/j.neuron.2020.01.021
WoS: 000528268200013
PMID: 32070475

Optogenetic inhibition-mediated activity-dependent modification of C pyramidal-interneuron connections during behavior
I. Gridchyn, P. Schönenberger, J. O’Neill, J.L. Csicsvari, ELife 9 (2020).
LibreCat: https://research-explorer.ista.ac.at/record/8740
DOI: 10.7554/eLife.61106
WoS: 000584369000001

Optogenetic alteration of hippocampal network activity
J.L. Csicsvari, I. Gridchyn, P. Schönenberger, (2020).
LibreCat: https://research-explorer.ista.ac.at/record/8563
DOI: 10.15479/AT:ISTA:8563

Cortical actin properties controlled by Drosophila Fos aid macrophage infiltration against surrounding tissue resistance
V. Belyaeva, S. Wachner, I. Gridchyn, M. Linder, S. Emtenani, A. György, M. Sibilia, D.E. Siekhaus, BioRxiv (n.d.).
LibreCat: https://research-explorer.ista.ac.at/record/8557
DOI: 10.1101/2020.09.18.301481

Hippocampal reactivation of random trajectories resembling Brownian diffusion
F. Stella, P. Baracskay, J. O’Neill, J.L. Csicsvari, Neuron 102 (2019) 450–461.
LibreCat: https://research-explorer.ista.ac.at/record/6338
DOI: 10.1016/j.neuron.2019.01.052
WoS: 000465169700017
PMID: 30819547

Assembly responses of hippocampal C place cells predict learned behavior in goal-directed spatial tasks on the radial eight-arm maze
H. Xu, P. Baracskay, J. O’Neill, J.L. Csicsvari, Neuron 101 (2019) 119–132.e4.
LibreCat: https://research-explorer.ista.ac.at/record/5828
DOI: 10.1016/j.neuron.2018.11.015
WoS: 000454791500014

Supplementary Code and Data for the paper "The Entorhinal Cognitive Map is Attracted to Goals"
M. Nardin, (2019).
LibreCat: https://research-explorer.ista.ac.at/record/6062
DOI: 10.15479/AT:ISTA:6062

The entorhinal cognitive map is attracted to goals
C.N. Boccara, M. Nardin, F. Stella, J. O’Neill, J.L. Csicsvari, Science 363 (2019) 1443–1447.
LibreCat: https://research-explorer.ista.ac.at/record/6194
DOI: 10.1126/science.aav4837
WoS: 000462738000034

The role of CCK-interneurons in regulating hippocampal network dynamics
D.K. Rangel Guerrero, The Role of CCK-Interneurons in Regulating Hippocampal Network Dynamics, Institute of Science and Technology Austria, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6849
DOI: 10.15479/AT:ISTA:6849

Disrupted-in-schizophrenia 1 overexpression disrupts hippocampal coding and oscillatory synchronization
K. Käfer, H. Malagon-Vina, D. Dickerson, J. O’Neill, S.V. Trossbach, C. Korth, J.L. Csicsvari, Hippocampus 29 (2019) 802–816.
LibreCat: https://research-explorer.ista.ac.at/record/5949
DOI: 10.1002/hipo.23076
WoS: 000480635400003

The hippocampus and medial prefrontal cortex during flexible behavior
K. Käfer, The Hippocampus and Medial Prefrontal Cortex during Flexible Behavior, Institute of Science and Technology Austria, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6825
DOI: 10.15479/AT:ISTA:6825

Reactivation content is important for consolidation of spatial memory
I. Gridchyn, Reactivation Content Is Important for Consolidation of Spatial Memory, Institute of Science and Technology Austria, 2018.
LibreCat: https://research-explorer.ista.ac.at/record/48
DOI: 10.15479/AT:ISTA:th_1042

Tetrode recording from the hippocampus of behaving mice coupled with four-point-irradiation closed-loop optogenetics: A technique to study the contribution of Hippocampal SWR events to learning
D.K. Rangel Guerrero, J.G. Donnett, J.L. Csicsvari, K. Kovács, ENeuro 5 (2018).
LibreCat: https://research-explorer.ista.ac.at/record/5914
DOI: 10.1523/ENEURO.0087-18.2018
WoS: 000443994700007

Activity dependent feedback inhibition may maintain head direction signals in mouse presubiculum
J. Simonnet, M. Nassar, F. Stella, I. Cohen, B. Mathon, C.N. Boccara, R. Miles, D. Fricker, Nature Communications 8 (2017).
LibreCat: https://research-explorer.ista.ac.at/record/514
DOI: 10.1038/ncomms16032