The neuroanatomical and neurochemical basis of conditioned fear

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(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010

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Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376

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Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128

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Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160

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Crowley, T. (1957) · Philosophical Studies · doi:10.5840/philstudies1957703 · Cited by 3,625

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Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292

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Bloom, F. E., & Kupfer, D. J. (1995) · Medical Entomology and Zoology · Cited by 2,985

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Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483

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Lang, P. J., Bradley, M. M., & Cuthbert, B. N. (1990) · Psychological Review · doi:10.1037/0033-295x.97.3.377 · Cited by 2,205

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KLÜVER, H. (1939) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1939.02270240017001 · Cited by 1,696

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Basolateral amygdala lesions in the rat produce an abnormally persistent latent inhibition with weak preexposure but not with context shift

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Correlation between long latency evoked potentials from amygdala and evoked cardiac response to fear conditioned stimulus in rats

Kuniecki, M., Coenen, A. M. L., & Kaiser, J. (2002) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2002-1424 · Cited by 17

Differential regulation of glutamic acid decarboxylase gene expression after extinction of a recent memory vs. intermediate memoryPreprint

Sangha, S., Ilenseer, J., Sosulina, L., Lesting, J., & Pape, H. (2012) · Learning & Memory · doi:10.1101/lm.025874.112 · Cited by 17

Effects of a Flavonoid-Rich Fraction on the Acquisition and Extinction of Fear Memory: Pharmacological and Molecular Approaches

de Oliveira, D. R., Zamberlam, C. R., Rêgo, G. M., Cavalheiro, A. J., Cerutti, J. M., & Cerutti, S. M. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00345 · Cited by 16

Conditioned Inhibition of Fear and Reward in Male and Female Rats

Krueger, J. N., Patel, N. N., Shim, K., Ng, K. H., & Sangha, S. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107881 · Cited by 15

Neurobiological and Neuroethological Perspectives on Fear and Anxiety

Rau, V., & Fanselow, M. S. (2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511500008.005 · Cited by 16

Aberrant Amygdala-dependent Fear Memory in Corticosterone-treated Mice

Inagaki, R., Moriguchi, S., & Fukunaga, K. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.08.004 · Cited by 16

Habenula kisspeptin retrieves morphine impaired fear memory in zebrafish

Sivalingam, M., Ogawa, S., & Parhar, I. S. (2020) · Scientific Reports · doi:10.1038/s41598-020-76287-9 · Cited by 16

Fear: Potentiation and Startle

Falls, W. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-045396-5.00137-8 · Cited by 1

Pharmacological and anatomical analysis of fear conditioning using the fear-potentiated startle paradigm.

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The neurobiological basis of fear : a concise review : review article

Panzer, A., Viljoen, M., & Roos, J. L. (2007) · UpSpace Institutional Repository (University of Pretoria) · Cited by 2

The neurobiological basis of fear : a concise review : review article

Panzer, A., Viljoen, M., & Roos, J. L. (2007) · South African psychiatry review

Neuroanatomy of human fear conditioning: brain activity specifically related to stimuli processing and memory formation.

Fischer, H., Andersson, J. L. R., Furmark, T., & Fredrikson, M. G. (1998) · NeuroImage · doi:10.1016/s1053-8119(18)31747-6