Consolidating Memories

The Principles of Psychology

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Emotion circuits in the brain

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Developments of a water-maze procedure for studying spatial learning in the rat

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The organization of behavior.

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Cognitive maps in rats and men

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Memory - A century of consolidation

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The role of the amygdala in fear and anxiety

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THE AMYGDALA MODULATES THE CONSOLIDATION OF MEMORIES OF EMOTIONALLY AROUSING EXPERIENCES

McGaugh, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144157 · Cited by 2,296

Purposive Behavior in Animals and Men

Irwin, F. W. (1932) · Europe PMC (PubMed Central) · Cited by 1,867

Emotion: Clues from the Brain

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NTRK2 methylation is related to reduced PTSD risk in two African cohorts of trauma survivors

Vukojevic, V., Coynel, D., Ghaffari, N. R., Freytag, V., Elbert, T., Kolassa, I.-T., Wilker, S., McGaugh, J. L., Papassotiropoulos, A., & de Quervain, D. J.-F. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2008415117 · Cited by 19

Factors modulating the effects of waking rest on memory

Martini, M., & Sachse, P. (2019) · Cognitive Processing · doi:10.1007/s10339-019-00942-x · Cited by 19

Ketamine anesthesia enhances fear memory consolidation via noradrenergic activation in the basolateral amygdala

Morena, M., Colucci, P., Mancini, G. F., Castro, V. D., Peloso, A., Schelling, G., & Campolongo, P. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107362 · Cited by 19

Autonomous Cognitive Robots Need Emotional Modulations: Introducing the eMODUL Model

Belkaid, M., Cuperlier, N., & Gaussier, P. (2018) · IEEE Transactions on Systems Man and Cybernetics Systems · doi:10.1109/tsmc.2018.2792542 · Cited by 20

Chronic stress and emotion: Differential effects on attentional processing and recognition memory

Wirkner, J., Ventura‐Bort, C., Schwabe, L., Hamm, A. O., & Weymar, M. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.05.008 · Cited by 19

Alpha-2 Adrenoreceptor Antagonist Yohimbine Potentiates Consolidation of Conditioned Fear

Sperl, M. F. J., Panitz, C., Skoluda, N., Nater, U. M., Pizzagalli, D. A., Hermann, C., & Mueller, E. M. (2022) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyac038 · Cited by 20

Leveraging Dual Resistive Switching in Quasi-2D Perovskite Memristors for Integrated Non-volatile Memory, Synaptic Emulation, and Reservoir Computing

Luo, Z., Wang, W., Wu, J., Ma, G., Hou, Y., Yang, C., Wang, X., Zheng, F., Zhao, Z., Zhao, Z., et al. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c21159 · Cited by 18

Mechanisms underlying the effects of n-3 polyunsaturated fatty acids on fear memory processing and their hypothetical effects on fear of cancer recurrence in cancer survivors

Okubo, R., Chen, C., Sekiguchi, M., Hamazaki, K., & Matsuoka, Y. (2018) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2018.03.006 · Cited by 18

Embodiment in episodic memory through premotor-hippocampal coupling

Meyer, N. H., Gauthier, B., Stampacchia, S., Boscheron, J., Babo-Rebelo, M., Potheegadoo, J., Herbelin, B., Lance, F., Alvarez, V., Franc, E., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06757-7 · Cited by 16

Potential of microRNAs as novel targets in the alleviation of pathological fear

Murphy, C. P., & Singewald, N. (2017) · Genes Brain & Behavior · doi:10.1111/gbb.12427 · Cited by 18

Post-learning stress reduces the misinformation effect: effects of psychosocial stress on memory updating

Nitschke, J. P., Chu, S., Pruessner, J. C., Bartz, J. A., & Sheldon, S. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.12.008 · Cited by 14

Event‐related potentials of emotional and neutral memories: The role of encoding position and delayed testing

Wirkner, J., Ventura‐Bort, C., Schulz, P., Hamm, A. O., & Weymar, M. (2018) · Psychophysiology · doi:10.1111/psyp.13069 · Cited by 16

Effects of wakeful resting versus social media usage after learning on the retention of new memories

Martini, M., Heinz, A., Hinterholzer, J., Martini, C. L., & Sachse, P. (2020) · Applied Cognitive Psychology · doi:10.1002/acp.3641 · Cited by 18

Hunger Bias or Gut Instinct? Responses to Judgments of Harm Depending on Visceral State Versus Intuitive Decision-Making

Brown, H., Proulx, M. J., & Fraser, D. S. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.02261 · Cited by 18

Interactions of Noradrenergic, Glucocorticoid and Endocannabinoid Systems Intensify and Generalize Fear Memory Traces

Gazarini, L., Stern, C. A. J., Takahashi, R. N., & Bertoglio, L. J. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.09.012 · Cited by 17

The glucocorticoid response in a free-living bird predicts whether long-lasting memories fade or strengthen with time

Jones, B. C., Bebus, S. E., Ferguson, S. M., Bateman, P. W., & Schoech, S. J. (2016) · Animal Behaviour · doi:10.1016/j.anbehav.2016.10.009 · Cited by 16

Object Recognition and Object Location Recognition Memory – The Role of Dopamine and Noradrenaline

Moreno‐Castilla, P., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00028-8 · Cited by 16

PDZD8-deficient mice manifest behavioral abnormalities related to emotion, cognition, and adaptation due to dyslipidemia in the brain

Kurihara, Y., Mitsunari, K., Mukae, N., Shoji, H., Miyakawa, T., & Shirane, M. (2023) · Molecular Brain · doi:10.1186/s13041-023-01002-4 · Cited by 14

Distinct medial-temporal lobe mechanisms of encoding and amygdala-mediated memory reinstatement for disgust and fear

Riegel, M., Wierzba, M., Wypych, M., Ritchey, M., Jednoróg, K., Grabowska, A., Vuilleumier, P. O., & Marchewka, A. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.118889 · Cited by 15

Bacosides Encapsulated in Lactoferrin Conjugated PEG-PLA-PCL-OH Based Polymersomes Act as Epigenetic Modulator in Chemically Induced Amnesia

Goyal, K., Konar, A., Kumar, A., & Koul, V. (2020) · Neurochemical Research · doi:10.1007/s11064-020-02953-z · Cited by 14

The effects of acute exercise on long-term episodic memory: a systematic review and meta-analysis

Qazi, A. S., Schmid, D. G., Gridley, N., Lambourne, K., Daly-Smith, A., & Tomporowski, P. D. (2024) · Frontiers in Cognition · doi:10.3389/fcogn.2024.1367569 · Cited by 20

Enhanced mnemonic discrimination for emotional memories: the role of arousal in interference resolution

Szöllősi, Á., & Racsmány, M. (2020) · Memory & Cognition · doi:10.3758/s13421-020-01035-3 · Cited by 15

Dopamine activity on the perceptual salience for recognition memory

Osorio‐Gómez, D., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.963739 · Cited by 14

Naloxone effects on extinction of ethanol- and cocaine-induced conditioned place preference in mice

Font, L., Houck, C. A., & Cunningham, C. L. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4672-z · Cited by 13

Sex hormones and cortisol during experimental trauma memory consolidation: Prospective association with intrusive memories

Krinke, E., Held, U., Steigmiller, K., Felmingham, K. L., & Kleim, B. (2022) · European Journal of Psychotraumatology · doi:10.1080/20008198.2022.2040818 · Cited by 14

Synaptic consolidation as a temporally variable process: Uncovering the parameters modulating its time-course

Casagrande, M. A., Haubrich, J., Pedraza, L. K., Popik, B., Quillfeldt, J. A., & Alvares, L. D. O. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.03.002 · Cited by 17

Goal-relevant situations facilitate memory of neutral faces

Montagrin, A., Virginie Sterpenich, A., Brosch, T., Grandjean, D., Armony, J. L., Ceravolo, L., & Sander, D. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-0637-x · Cited by 15

Spermidine, a positive modulator of the NMDA receptor, facilitates extinction and prevents the reinstatement of morphine-induced conditioned place preference in mice

Girardi, B., Fabbrin, S. B., Wendel, A. L., Mello, C. F., & Rubin, M. A. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05403-z · Cited by 11

Episodic memory is emotionally laden memory, requiring amygdala involvement

Staniloiu, A., & Markowitsch, H. J. (2019) · Behavioral and Brain Sciences · doi:10.1017/s0140525x19001857 · Cited by 12

Effects of Isometric Hand-Grip Muscle Contraction on Young Adults' Free Recall and Recognition Memory

Tomporowski, P. D., Albrecht, C., & Pendleton, D. M. (2017) · Research Quarterly for Exercise and Sport · doi:10.1080/02701367.2016.1264567 · Cited by 12

Role of dorsal hippocampus κ opioid receptors in contextual aversive memory consolidation in rats

Vanz, F., Bicca, M. A., Linartevichi, V. F., Giachero, M., Bertoglio, L. J., & de Lima, T. C. M. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.02.029 · Cited by 12

Methods for Assessment of Memory Reactivation

Liu, S., Grosmark, A., & Chen, Z. S. (2018) · Neural Computation · doi:10.1162/neco_a_01090 · Cited by 11

Transcutaneous auricular vagus nerve stimulation in poststroke cognitive impairment: protocol for a randomised controlled trial

Li, Z.-D., Qiu, H., Wang, X., Zhang, C., & Zhang, Y.-J. (2022) · BMJ Open · doi:10.1136/bmjopen-2022-063803 · Cited by 11

Emotional metacontrol of attention: Top-down modulation of sensorimotor processes in a robotic visual search task

Belkaid, M., Cuperlier, N., & Gaussier, P. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184960 · Cited by 13

Neuroplasticidade, memória e aprendizagem

Chaves, J. M. (2023) · Revista Psicopedagogia · doi:10.51207/2179-4057.20230006 · Cited by 10

Aha! and D’oh! experiences enhance learning for incidental information—new evidence supports the insight memory advantage

Salvi, C., Keller, N. E., Cooper, S. E., Leiker, E., & Dunsmoor, J. E. (2024) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-024-01184-x · Cited by 13

Event Segmentation Promotes the Reorganization of Emotional Memory

Laing, P. A. F., & Dunsmoor, J. E. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02244 · Cited by 13

Individual differences in working memory capacity moderate effects of post-learning activity on memory consolidation over the long term

Martini, M., Marhenke, R., Martini, C. L., Rossi, S., & Sachse, P. (2020) · Scientific Reports · doi:10.1038/s41598-020-74760-z · Cited by 12

An Exploration of Collective Memory in the Tourism Context

Zhou, H., Ap, J., & Yang, H. (2023) · Journal of China Tourism Research · doi:10.1080/19388160.2023.2273275 · Cited by 12

Effects of wakeful rest on memory consolidation: A systematic review and meta-analysis

Weng, L., Yu, J., Lv, Z., Yang, S., Jülich, S. T., & Lei, X. (2025) · Psychonomic Bulletin & Review · doi:10.3758/s13423-025-02665-x · Cited by 13

Effects of acute exercise on emotional memory

Loprinzi, P. D., Olafson, D., Scavuzzo, C. J., Lovorn, A., Mather, M., Frith, E., & Fujiwara, E. (2022) · Cognition & Emotion · doi:10.1080/02699931.2022.2050890 · Cited by 10

Distinct stress‐related changes in intrinsic amygdala connectivity predict subsequent positive and negative memory performance

Ford, J. H., Kim, S. Y., Kark, S. M., Daley, R. T., Payne, J. D., & Kensinger, E. A. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15777 · Cited by 10

Inhibition of steroid receptor coactivator-1 in the hippocampus impairs the consolidation and reconsolidation of contextual fear memory in mice

Chen, X., Yiqin, T., Zhu, H., Bian, C., & Li, M. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117386 · Cited by 9

Hypothalamic–Pituitary–Adrenal Axis Activity in Childhood Predicts Emotional Memory Effects and Related Neural Circuitry in Adolescent Girls

Shields, G. S., Hostinar, C. E., Vilgis, V., Forbes, E. E., Hipwell, A. E., Keenan, K. E., & Guyer, A. E. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01687 · Cited by 9

Synaptic devices for simulating brain processes in visual-information perception to persisting memory through attention mechanisms

Kim, J., Lim, J. W., & Kim, H. S. (2023) · Materials Today Advances · doi:10.1016/j.mtadv.2023.100421 · Cited by 8

Dog–Human Play, but Not Resting Post-Learning Improve Re-Training Performance up to One Year after Initial Task Acquisition in Labrador Retriever Dogs: A Follow-On Study

Affenzeller, N. (2020) · Animals · doi:10.3390/ani10071235 · Cited by 8

Recruitment of neurons in basolateral amygdala after intense training produces a stronger memory trace

Ruiz-López, C. X., Medina, A. C., Bello-Medina, P. C., Quirarte, G. L., & Prado-Alcalá, R. A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107428 · Cited by 8

Facing stress: No effect of acute stress at encoding or retrieval on face recognition memory

Marr, C., Quaedflieg, C. W. E. M., Otgaar, H., Hope, L., & Sauerland, M. (2021) · Acta Psychologica · doi:10.1016/j.actpsy.2021.103376 · Cited by 8

Empathy reduces susceptibility to false memory

Lo, S.-Y. (2021) · Scientific Reports · doi:10.1038/s41598-021-02281-4 · Cited by 10

Blockade of intracellular Zn 2+ signaling in the basolateral amygdala affects object recognition memory via attenuation of dentate gyrus LTP

Fujise, Y., Kubota, M., Suzuki, M., Tamano, H., & Takeda, A. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.01.014 · Cited by 8

Methylprednisolone as a memory enhancer in rats: Effects on aversive memory, long-term potentiation and calcium influx

de Vargas, L. D. S., Gonçalves, R., de Lara, M. V. S., Costa‐Ferro, Z. S. M., Salamoni, S. D., Domingues, M. F., Piovesan, A. R., de Assis, D. R., Vinadé, L., Corrado, A. P., et al. (2017) · Brain Research · doi:10.1016/j.brainres.2017.06.007 · Cited by 8

Post-learning arousal enhances veridical memory and reduces false memory in the Deese-Roediger-McDermott paradigm

Nielson, K. A., & Correro, A. N. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.07.009 · Cited by 8

Analysis of memory modulation by conditioned stimuliPreprint

Lapointe, T., Wolter, M., & Leri, F. (2021) · Learning & Memory · doi:10.1101/lm.052407.120 · Cited by 7

Memory Consolidation

Roesler, R., & McGaugh, J. L. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21493-4 · Cited by 14

Ibogalogs improve spatial and recognition memory in rodents through a mechanism involving 5-HT2A receptor activation-enhanced NMDA receptor activity in hippocampal pyramidal CA1 neurons

Chagraoui, A., Santillan, L. A. H., Bocian, R., Cohen, S. J., Ruíz, Y. E. S., Knox, M., Kaźmierska, P., Zimoń, W., Stackman, R. W., Flores‐Hernández, J., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118742 · Cited by 7

Extended amygdala, conditioned withdrawal and memory consolidation

Baidoo, N., & Leri, F. (2021) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2021.110435 · Cited by 7

Hippocampal cholinergic receptors and the mTOR participation in fear-motivated inhibitory avoidance extinction memory

Rosa, J., Myskiw, J. D. C., Fiorenza, N. G., Furini, C. R. G., Sapiras, G. G., & Izquierdo, I. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114129 · Cited by 7

Wakeful Rest Benefits Recall, but Not Recognition, of Incidentally Encoded Memory Stimuli in Younger and Older Adults

Millar, P. R., & Balota, D. A. (2022) · Brain Sciences · doi:10.3390/brainsci12121609 · Cited by 7

States of epistemic curiosity interfere with memory for incidental scholastic facts

Keller, N. E., Salvi, C., Leiker, E., Gruber, M. J., & Dunsmoor, J. E. (2024) · npj Science of Learning · doi:10.1038/s41539-024-00234-w · Cited by 8

The future can shape memory for the present

Kensinger, E. A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.02.008 · Cited by 7

Facilitation of fear learning by prior and subsequent fear conditioning

Lee, J., Russo, A. S., & Parsons, R. G. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.03.008 · Cited by 7

Are episodic memory and episodic simulation different in kind?

Schwartz, A. (2025) · Philosophical Psychology · doi:10.1080/09515089.2025.2451819 · Cited by 8

Highly Superior Autobiographical Memory

Mcgaugh, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21047-x · Cited by 8

Inhibition of noradrenergic and corticotrophin-releasing factor systems: Effects on enhancement of memory consolidation by unconditioned and conditioned heroin withdrawal

Baidoo, N., & Leri, F. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109018 · Cited by 6

Interfering With Contextual Fear Memories by Post-reactivation Administration of Propranolol in Mice: A Series of Null Findings

Cox, W. R., Faliagkas, L., Besseling, A., van der Loo, R. J., Spijker, S., Kindt, M., & Rao‐Ruiz, P. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.893572 · Cited by 6

Wakeful resting and listening to music contrast their effects on verbal long-term memory in dependence on word concreteness

Martini, M., Wasmeier, J. R., Talamini, F., Huber, S. E., & Sachse, P. (2022) · Cognitive Research Principles and Implications · doi:10.1186/s41235-022-00415-4 · Cited by 8

Adrenergic β receptor activation in the basolateral amygdala, which is intracellular Zn2+-dependent, rescues amyloid β1-42-induced attenuation of dentate gyrus LTP

Tamano, H., Kubota, M., Fujise, Y., Shimaya, R., Itoh, R., Suzuki, M., Adlard, P. A., Bush, A. I., & Takeda, A. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.07.005 · Cited by 6

THE REORGANIZATION OF THE FAMILY SYSTEM AT THE TIME OF COVID-19: EDUCATIONAL RESILIENCE AND ASSISTIVE TECHNOLOGIES

Annarumma, M., Vitale, L., Sessa, F., & Tedesco, I. (2020) · Problems of Psychology in the 21st Century · doi:10.33225/ppc/20.14.18 · Cited by 6

Norepinephrine–Astrocyte Signaling Regulates Cortical State Homeostasis

Li, Y., Li, L., Wang, Y., Li, X., & Chen, Z. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01213-2 · Cited by 5

The effects of stress on working-memory-related prefrontal processing: an fNIRS study

Geissler, C. F., Frings, C., & Domes, G. (2025) · Stress · doi:10.1080/10253890.2025.2472067 · Cited by 5

The Impact of Emotional Arousal on Amygdala Activity, Memory Consolidation, and Long-Term Potentiation in the Hippocampus

Zhang, I. (2022) · Journal of Student Research · doi:10.47611/jsr.v11i2.1614 · Cited by 6

Never Forget: Cognitive Restructuring Limitations in Holocaust Related Layered Trauma

Suttenberg, L. P. (2015) · Clinical Social Work Journal · doi:10.1007/s10615-015-0563-0 · Cited by 5

Effects of an acute therapeutic or rewarding dose of amphetamine on acquisition of Pavlovian autoshaping and ventral striatal dopamine signaling

Schuweiler, D. R., Athens, J. M., Thompson, J., Vazhayil, S. T., & Garris, P. A. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.09.003 · Cited by 5

Relearning can eliminate the effect of retrieval-induced forgetting

Storm, B. C., & Soares, J. S. (2021) · Psychological Research · doi:10.1007/s00426-021-01601-7 · Cited by 5

Kognitiv-affektive Neurowissenschaft: Emotionale Modulation des Erinnerns, Entscheidens und Handelns

Goschke, T., & Dreisbach, G. (2020) · Springer eBooks · doi:10.1007/978-3-662-61814-1_5 · Cited by 6

The illusion of pure reason in science: A cautionary note

Miller, R. R. (2023) · Behavioural Processes · doi:10.1016/j.beproc.2023.104863 · Cited by 6

The reconsolidation using rewind study (RETURN): trial protocol

Wright, L. A., Barawi, K., Simon, N. A., Lewis, C., Muss, D., Roberts, N. P., Kitchiner, N., & Bisson, J. I. (2021) · European Journal of Psychotraumatology · doi:10.1080/20008198.2020.1844439 · Cited by 8

Active information sampling varies across the cardiac cyclePreprint

Kunzendorf, S., Klotzsche, F., Akbal, M., Villringer, A., Ohl, S., & Gaebler, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/283838 · Cited by 7

Trauma-predictive brain network connectivity adaptively responds to mild acute stress

Hardi, F. A., Ye, J., Zhou, I., Bai, Z., Nguyen, D. T., Loetscher, K. B., Pratt, J. G., Harris, B. B., Gee, D. G., & Goldfarb, E. V. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2505965122 · Cited by 6

Dynamic brain mechanisms supporting salient memories under cortisol

Huang, Y., O’Connor, D. A., Harris, B. B., Sinha, R., Constable, R. T., & Goldfarb, E. V. (2025) · Science Advances · doi:10.1126/sciadv.adz4143 · Cited by 5

Autobiographical memory bias in social anxiety: The role of state anxiety

Askari, F., & Zia-Tohidi, A. (2022) · Current Psychology · doi:10.1007/s12144-021-02592-9 · Cited by 4

Orally retrieved negative autobiographical events are associated with increased heart rate as compared with fabricated ones

Mangiulli, I., Battista, F., Otgaar, H., Lanciano, T., Piro, A., Grassi, D., Novielli, N., Lanubile, F., & Curci, A. (2024) · Memory & Cognition · doi:10.3758/s13421-024-01663-z · Cited by 5

Optimizing laboratory animal stress paradigms: The H-H* experimental design

McCarty, R. C. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.10.004 · Cited by 4

Working Memory and Executive Attention: Insights from Developmental Studies and Implications for Learning and Education

Kar, B. R., & Kenderla, P. K. (2017) · Journal of the Indian Institute of Science · doi:10.1007/s41745-017-0044-2 · Cited by 4

Guilty by association: Time-dependent memory consolidation facilitates the generalization of negative – but not positive – person memories to group and self-judgments

Lupo, A. K., & Zárate, M. A. (2019) · Journal of Experimental Social Psychology · doi:10.1016/j.jesp.2019.02.008 · Cited by 4

On the theory of mental representation block. a novel perspective on learning and behavior

Tobore, T. O. (2021) · Communicative & Integrative Biology · doi:10.1080/19420889.2021.1898752 · Cited by 4

Characterization of deconditioning-update on fear memory attenuation

Popik, B., Guerra, K. T. K., Luft, J. G., Fernandes, H. S., & Alvares, L. D. O. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107763 · Cited by 6

Wakeful rest benefits memory when materials can be rehearsedPreprint

Millar, P. R., & Balota, D. A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/449835 · Cited by 3

Emotional learning selectively distorts the temporal organization of memory: A quantitative synthesis

Laing, P. A. F., Hennings, A. C., Cooper, S. E., & Dunsmoor, J. E. (2025) · Cognition · doi:10.1016/j.cognition.2025.106382 · Cited by 3

Navigating challenges: coping, memory, and the interpretations of travel adversities among middle-aged and older Chinese adults

Li, T. E., Chan, E. T. H., & Wood, E. H. (2024) · Current Issues in Tourism · doi:10.1080/13683500.2024.2440616 · Cited by 3

Highly Superior Autobiographical Memory

McGaugh, J. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805159-7.02013-1 · Cited by 3

Reappraisal enhances memory formation for a stressful episode

Lin, L., Zhang, L., & Schwabe, L. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105924 · Cited by 3

On the search for a selective and retroactive strengthening of memory: repeated failure to find category-specific behavioral taggingPreprint

Kalbe, F., & Schwabe, L. (2020) · doi:10.31234/osf.io/ed3z8 · Cited by 3

Comunicación y memoria visual en escolares con discapacidad intelectual. Una relación clave para la intervención

Guerra, J. V., & Álvarez, C. D. L. P. (2016) · Indivisa Boletín de Estudios e Investigación · doi:10.37382/indivisa.vi17.237 · Cited by 2

Amygdala stimulation transforms short-term memory into remote memory by persistent activation of atypical PKC in the anterior cingulate cortex

Almaguer‐Melian, W., Mercerón‐Martínez, D., Alacán‐Ricardo, L., Pina, A. B., Hsieh, C., Bergado, J. A., & Sacktor, T. C. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2025.01.065 · Cited by 2

The effects of physical activity timing and complexity on episodic memory: A randomized controlled trial

Schmid, D. G., Qazi, A. S., Scott, N. M., & Tomporowski, P. D. (2022) · Psychology of sport and exercise · doi:10.1016/j.psychsport.2022.102332 · Cited by 2

On the boundary conditions of avoidance memory reconsolidation: An attractor network perspective

Santiago, R. M. M., & Tort, A. B. L. (2020) · Neural Networks · doi:10.1016/j.neunet.2020.04.013 · Cited by 2

Developing the social and emotional competence of adolescents through implementation of the STEPS-A curriculum

Atkiss, E., & Stringer, P. (2023) · Educational and Child Psychology · doi:10.53841/bpsecp.2023.40.3.47 · Cited by 2

Drawbacks to strengthening neural salience encoding: a link between cortisol and risky drinkingPreprint

Harris, B. B., Sinha, R., & Goldfarb, E. V. (2024) · doi:10.31234/osf.io/kht4d · Cited by 2

Stress enhances memory for previously encoded events depending on stressor recallPreprint

Lilja, A., Fernández, G., & Schwabe, L. (2024) · Learning & Memory · doi:10.1101/lm.053987.124 · Cited by 3

Emotional arousal regulation of memory consolidation

McGaugh, J. L. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.10.003 · Cited by 144

Making lasting memories: Remembering the significant

McGaugh, J. L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301209110 · Cited by 311

Crear recuerdos perdurables: acordarse de lo significativo

McGaugh, J. L. (2013) · Ludus vitalis: revista de filosofía de las ciencias de la vida = journal of philosophy of life sciences = revue de philosophie des sciences de la vie

Role of the Basolateral Amygdala in Memory Consolidation

McINTYRE, C. K., POWER, A. E., ROOZENDAAL, B., & McGAUGH, J. L. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07088.x · Cited by 147

Emotional Hormones and Memory Modulation

McGaugh, J. L., & Roozendaal, B. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00849-4 · Cited by 23