The role of engram cells in the systems consolidation of memory - Tonegawa, S.; Morrissey, M. D.; Kitamura, T. (Nat. Rev. Neurosci., 2018)

Modulating Human Memory via Entrainment of Brain Oscillations - Hanslmayr, S.; Axmacher, N.; Inman, C. S. (Trends Neurosci., 2019)

A network approach for modulating memory processes via direct and indirect brain stimulation: Toward a causal approach for the neural basis of memory - Kim, K.; Ekstrom, A. D.; Tandon, N. (Neurobiol. Learn. Mem., 2016)

Targeted enhancement of cortical-hippocampal brain networks and associative memory - Wang, J. X. (Science, 2014)

Frequency-specific noninvasive modulation of memory retrieval and its relationship with hippocampal network connectivity - Hermiller, M. S.; VanHaerents, S.; Raij, T.; Voss, J. L. (Hippocampus, 2019)

Transcranial electrical stimulation (tes - tdcs; trns; tacs) methods - Paulus, W. (Neuropsychol. Rehabil. An Int. J., 2011)

Entraining neurons via noninvasive electric stimulation improves cognition - Plas, M.; Hanslmayr, S. (PLoS Biol., 2020)

Neurocognitive, physiological, and biophysical effects of transcranial alternating current stimulation - Wischnewski, M.; Alekseichuk, I.; Opitz, A. (Trends Cogn. Sci., 2023)

Theta Oscillations in Human Memory - Herweg, N. A.; Solomon, E. A.; Kahana, M. J. (Trends Cogn. Sci., 2020)

Memory, navigation and theta rhythm in the hippocampal-entorhinal system - Buzsáki, G.; Moser, E. I. (Nat. Neurosci., 2013)

Expanding the Language Network: Direct Contributions from the Hippocampus - Covington, N. V.; Duff, M. C. (Trends Cogn. Sci., 2016)

The Theta-Gamma Neural Code - Lisman, J. E.; Jensen, O. (Neuron, 2013)

Behavioral state-specific changes in human hippocampal theta activity - Meador, K. J. (Neurology, 1991)

Theta rhythm of navigation: link between path integration and landmark navigation, episodic and semantic memory - Buzsáki, G. (Hippocampus, 2005)

Prediction, sequences and the hippocampus - Lisman, J.; Redish, A. D. (Philos. Trans. R. Soc. B Biol. Sci., 2009)

Oscillations Go the Distance: Low-Frequency Human Hippocampal Oscillations Code Spatial Distance in the Absence of Sensory Cues during Teleportation - Vass, L. K. (Neuron, 2016)

Functional role of gamma and theta oscillations in episodic memory - Nyhus, E.; Curran, T. (Neurosci. Biobehav. Rev., 2010)

Hippocampal theta codes for distances in semantic and temporal spaces - Solomon, E. A.; Lega, B. C.; Sperling, M. R.; Kahana, M. J. (Proc. Natl. Acad. Sci. USA., 2019)

Time cells in the human hippocampus and entorhinal cortex support episodic memory - Umbach, G. (Proc. Natl. Acad. Sci. USA., 2020)

Direct brain recordings reveal hippocampal rhythm underpinnings of language processing - Piai, V. (Proc. Natl. Acad. Sci. USA., 2016)

Hippocampus: Cognitive processes and neural representations that underlie declarative memory - Eichenbaum, H. (Neuron, 2004)

Bellmund, J. L. S., Gärdenfors, P., Moser, E. I. & Doeller, C. F. Navigating cognition: Spatial codes for human thinking. Science. 362, eaat6766 (2018).

Synchronization of medial temporal lobe and prefrontal rhythms in human decision making - Guitart-Masip, M. (J. Neurosci., 2013)

Theta oscillations index human hippocampal activation during a working memory task - Tesche, C. D.; Karhu, J. (Proc. Natl. Acad. Sci. USA., 2000)

Hippocampal-prefrontal theta oscillations support memory integration - Backus, A. R.; Schoffelen, J. M.; Szebényi, S.; Hanslmayr, S.; Doeller, C. F. (Curr. Biol., 2016)

Frequency-specific hippocampal-prefrontal interactions during associative learning - Brincat, S. L.; Miller, E. K. (Nat. Neurosci., 2015)

Hippocampal-prefrontal connectivity predicts midfrontal oscillations and long-term memory performance - Cohen, M. X. (Curr. Biol., 2011)

BOLD signal effects of transcranial alternating current stimulation (tACS) in the alpha range: A concurrent tACS–fMRI study - Vosskuhl, J.; Huster, R. J.; Herrmann, C. S. (Neuroimage, 2016)

Concurrent tACS-fMRI reveals causal influence of power synchronized neural activity on resting state fMRI connectivity - Bächinger, M. (J. Neurosci., 2017)

fMRI and transcranial electrical stimulation (tES): A systematic review of parameter space and outcomes - Ghobadi-Azbari, P. (Prog. Neuro Psychopharmacol. Biol. Psychiatry, 2021)

Transcranial alternating current stimulation entrains single-neuron activity in the primate brain - Krause, M. R.; Vieira, P. G.; Csorba, B. A.; Pilly, P. K.; Pack, C. C. (Proc. Natl. Acad. Sci. USA., 2019)

Vöröslakos, M. et al. Direct effects of transcranial electric stimulation on brain circuits in rats and humans. Nat. Commun. 9, 483 (2018).

Liu, A. et al. Immediate neurophysiological effects of transcranial electrical stimulation. Nat. Commun. 9, 5092 (2018).

Escitalopram Decreases Cross-Regional Functional Connectivity within the Default-Mode Network - Ven, V.; Wingen, M.; Kuypers, K. P. C.; Ramaekers, J. G.; Formisano, E. (PLoS One, 2013)

Coherent spontaneous activity identifies a hippocampal-parietal memory network - Vincent, J. L. (J. Neurophysiol., 2006)

Hippocampal-targeted Theta-burst Stimulation Enhances Associative Memory Formation - Tambini, A.; Nee, D. E.; D’Esposito, M. (J. Cogn. Neurosci., 2018)

Transcranial alternating current stimulation at theta frequency to left parietal cortex impairs associative, but not perceptual, memory encoding - Meng, A. (Neurobiol. Learn. Mem., 2021)

Reduced Current Spread by Concentric Electrodes in Transcranial Electrical Stimulation (tES) - Bortoletto, M.; Rodella, C.; Salvador, R.; Miranda, P. C.; Miniussi, C. (Brain Stimul., 2016)

Wang, Y., De Weerd, P., Sack, A. T. & van de Ven, V. Distinct effects of slow and fast theta tACS in enhancing temporal memory. Imaging Neurosci. 2, 1–14 (2024).

Episodic memory retrieval, parietal cortex, and the default mode network: functional and topographic analyses - Sestieri, C.; Corbetta, M.; Romani, G. L.; Shulman, G. L. (J. Neurosci., 2011)

Orienting of attention - Posner, M. I. (Q. J. Exp. Psychol., 1980)

The Spatial Orienting paradigm: How to design and interpret spatial attention experiments - Chica, A. B.; Martín-Arévalo, E.; Botta, F.; Lupiáñez, J. (Neurosci. Biobehav. Rev., 2014)

Hemifield-specific Correlations between Cue-related Blood Oxygen Level Dependent Activity in Bilateral Nodes of the Dorsal Attention Network and Attentional Benefits in a Spatial Orienting Paradigm - Mayrhofer, H. C.; Duecker, F.; Ven, V.; Jacobs, H. I. L.; Sack, A. T. (J. Cogn. Neurosci., 2019)

Left parietal tACS at alpha frequency induces a shift of visuospatial attention - Schuhmann, T. (PLoS One, 2019)

Safety, Tolerability, Blinding Efficacy and Behavioural Effects of a Novel MRI-Compatible, High-Definition tDCS Set-Up - Gbadeyan, O.; Steinhauser, M.; Mcmahon, K.; Meinzer, M. (Brain Stimul., 2016)

Accessibility of cortical regions to focal TES: Dependence on spatial position, safety, and practical constraints - Saturnino, G. B.; Siebner, H. R.; Thielscher, A.; Madsen, K. H. (Neuroimage, 2019)

Stimulus Presentation at Specific Neuronal Oscillatory Phases Experimentally Controlled with tACS: Implementation and Applications - Oever, S. (Front. Cell. Neurosci., 2016)

Conn: A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks - Whitfield-Gabrieli, S.; Nieto-Castanon, A. (Brain Connect., 2012)

Morfini, F., Whitfield-Gabrieli, S. & Nieto-Castañón, A. Functional connectivity MRI quality control procedures in CONN. Front. Neurosci. 17, 1092125 (2023).

Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion - Power, J. D.; Barnes, K. A.; Snyder, A. Z.; Schlaggar, B. L.; Petersen, S. E. (Neuroimage, 2012)

Impact of in-scanner head motion on multiple measures of functional connectivity: Relevance for studies of neurodevelopment in youth - Satterthwaite, T. D. (Neuroimage, 2012)

Freedberg, M. et al. Persistent Enhancement of Hippocampal Network Connectivity by Parietal rTMS Is Reproducible. eNeuro6, ENEURO.0129-19.2019 (2019).

Functional connectivity as revealed by spatial independent component analysis of fMRI measurements during rest - Ven, V. G.; Formisano, E.; Prvulovic, D.; Roeder, C. H.; Linden, D. E. J. (Hum. Brain Mapp., 2004)

Functional connectivity in the motor cortex of resting human brain using echo-planar MRI - Biswal, B. B.; Yetkin, F. Z.; Haughton, V. M.; Hyde, J. S. (Magn. Reson. Med., 1995)

Very slow activity fluctuations in monkey visual cortex: implications for functional brain imaging - Leopold, D. A.; Murayama, Y.; Logothetis, N. K. (Cereb. Cortex, 2003)

Frequencies contributing to functional connectivity in the cerebral cortex in ‘resting-state’ data - Cordes, D. (Am. J. Neuroradiol., 2001)

An improved approach to detection of amplitude of low-frequency fluctuation (ALFF) for resting-state fMRI: Fractional ALFF - Zou, Q. H. (J. Neurosci. Methods, 2008)

Resting-state functional connectivity reflects structural connectivity in the default mode network - Greicius, M. D.; Supekar, K.; Menon, V.; Dougherty, R. F. (Cereb. Cortex, 2009)

A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches - McLaren, D. G.; Ries, M. L.; Xu, G.; Johnson, S. C. (Neuroimage, 2012)

JASP Team. JASP. at https://jasp-stats.org/ (2018).

Default Bayes factors for ANOVA designs - Rouder, J. N.; Morey, R. D.; Speckman, P. L.; Province, J. M. (J. Math. Psychol., 2012)

Bayes factor design analysis: Planning for compelling evidence - Schönbrodt, F. D.; Wagenmakers, E. J. (Psychon. Bull. Rev., 2018)

Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging - Fox, M. D.; Raichle, M. E. (Nat. Rev. Neurosci., 2007)

The brain’s default network: Anatomy, function, and relevance to disease - Buckner, R. L.; Andrews-Hanna, J. R.; Schacter, D. L. (Ann. N. Y. Acad. Sci., 2008)

The Role of the Hippocampus in Prediction and Imagination - Buckner, R. L. (Annu. Rev. Psychol., 2010)

Krause, M. R., Vieira, P. G., Thivierge, J. P. & Pack, C. C. Brain stimulation competes with ongoing oscillations for control of spike timing in the primate brain. PLoS Biol. 20, e3001650 (2022).

Dose-dependent effects of transcranial alternating current stimulation on spike timing in awake nonhuman primates - Johnson, L. (Sci. Adv., 2020)

When zero is not zero: the problem of ambiguous baseline conditions in fMRI - Stark, C. E.; Squire, L. R. (Proc. Natl. Acad. Sci. USA, 2001)

Sequential replay of nonspatial task states in the human hippocampus - Schuck, N. W.; Niv, Y. (Science, 2019)

Where is the “where” in the brain? A meta-analysis of neuroimaging studies on spatial cognition - Cona, G.; Scarpazza, C. (Hum. Brain Mapp., 2019)

Differences and similarities for spatial and feature-based selective attentional orienting - Galashan, D.; Siemann, J. (Front. Neurosci., 2017)

Neuroimaging studies of shifting attention: A meta-analysis - Wager, T. D.; Jonides, J.; Reading, S. (Neuroimage, 2004)

tACS entrains neural activity while somatosensory input is blocked - Vieira, P. G.; Krause, M. R.; Pack, C. C. (PLoS Biol., 2020)

Competition between functional brain networks mediates behavioral variability - Clare Kelly, A. M.; Uddin, L. Q.; Biswal, B. B.; Castellanos, F. X.; Milham, M. P. (Neuroimage, 2008)

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. (Neuroimage, 2010)

Architecture and connectivity of the human angular gyrus and of its homolog region in the macaque brain - Niu, M.; Palomero-Gallagher, N. (Brain Struct. Funct., 2023)

Neurobiology of Schemas and Schema-Mediated Memory - Gilboa, A.; Marlatte, H. (Trends Cogn. Sci., 2017)

Discovering Event Structure in Continuous Narrative Perception and Memory - Baldassano, C. (Neuron, 2017)

Resting-state networks predict individual differences in common and specific aspects of executive function - Reineberg, A. E.; Andrews-Hanna, J. R.; Depue, B. E.; Friedman, N. P.; Banich, M. T. (Neuroimage, 2015)

Neuronavigation maximizes accuracy and precision in TMS positioning: Evidence from 11,230 distance, angle, and electric field modeling measurements - Caulfield, K. A. (Brain Stimul., 2022)

Frequency-specific insight into short-term memory capacity - Feurra, M.; Galli, G.; Pavone, E. F.; Rossi, A.; Rossi, S. (J. Neurophysiol., 2016)

Increasing working memory capacity with theta transcranial alternating current stimulation (tACS) - Jaušovec, N.; Jaušovec, K. (Biol. Psychol., 2014)

Transcranial alternating current stimulation: a review of the underlying mechanisms and modulation of cognitive processes - Herrmann, C. S.; Rach, S.; Neuling, T.; Strüber, D. (Front. Hum. Neurosci., 2013)

Orchestrating neuronal networks: Sustained after-effects of transcranial alternating current stimulation depend upon brain states - Neuling, T.; Rach, S.; Herrmann, C. S. (Front. Hum. Neurosci., 2013)

Alpha power increase after transcranial alternating current stimulation at alpha frequency (a-tACS) reflects plastic changes rather than entrainment - Vossen, A.; Gross, J.; Thut, G. (Brain Stimul., 2015)

Transcranial direct current stimulation and visual perception - Antal, A.; Paulus, W. (Perception, 2008)