What is the amygdala?

Handbook of Chemical Neuroanatomy

Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,159 · see citing works

Brain Maps: Structure of the Rat Brain

Swanson, L. W. (1992) · Medical Entomology and Zoology · Cited by 1,851 · see citing works

Brain maps: structure of the rat brain

Guillery, R. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90187-q · Cited by 1,677 · see citing works

Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: An anterograde tract‐tracing study with <i>Phaseolus vulgaris</i> leucoagglutinin

Sesack, S. R., Deutch, A. Y., Roth, R. H., & Bunney, B. S. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902900205 · Cited by 1,568 · see citing works

The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.

Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536 · see citing works

Anatomical evidence of direct projections from the nucleus of the solitary tract to the hypothalamus, amygdala, and other forebrain structures in the rat

Ricardo, J. A., & Koh, E. T. (1978) · Brain Research · doi:10.1016/0006-8993(78)91125-3 · Cited by 1,362 · see citing works

Amygdaloid projections to subcortical structures within the basal forebrain and brainstem in the rat and cat

Krettek, J. E., & Price, J. L. (1978) · Journal of Comparative Neurology · doi:10.1002/cne.901780204 · Cited by 1,293 · see citing works

The amygdala: Neurobiological aspects of emotion, memory and mental dysfunction

Scheel-Krüger, J. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90037-5 · Cited by 1,277 · see citing works

New perspectives in basal forebrain organization of special relevance for neuropsychiatric disorders: The striatopallidal, amygdaloid, and corticopetal components of substantia innominata

Alheid, G. F., & Heimer, L. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90217-5 · Cited by 1,217 · see citing works

Catecholamine innervation of the basal forebrain IV. Topography of the dopamine projection to the basal forebrain and neostriatum

Fallon, J. H., & Moore, R. Y. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901800310 · Cited by 1,172 · see citing works

Columnar organization in the midbrain periaqueductal gray: modules for emotional expression?

Bandler, R., & Shipley, M. T. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90047-7 · Cited by 1,051 · see citing works

The differential projections of the olfactory bulb and accessory olfactory bulb in mammals

Scalia, F., & Winans, S. S. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901610105 · Cited by 983 · see citing works

Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala

Pitkänen, A., Savander, V., & LeDoux, J. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01125-9 · Cited by 980 · see citing works

Organization of projections from the medial nucleus of the amygdala: A PHAL study in the rat

Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903600203 · Cited by 884 · see citing works

Amygdaloid projections to the mesencephalon, pons and medulla oblongata in the cat

Hopkins, D. A., & Holstege, G. (1978) · Experimental Brain Research · doi:10.1007/bf00239551 · Cited by 866 · see citing works

Projections from the amygdaloid complex to the cerebral cortex and thalamus in the rat and cat

Krettek, J. E., & Price, J. L. (1977) · Journal of Comparative Neurology · doi:10.1002/cne.901720408 · Cited by 785 · see citing works

Efferent projections of the infralimbic cortex of the rat

Hurley, K. M., Herbert, H., Moga, M. M., & Saper, C. B. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903080210 · Cited by 777 · see citing works

Neurotransmission in the rat amygdala related to fear and anxiety

Davis, M., Rainnie, D., & Cassell, M. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90106-6 · Cited by 771 · see citing works

A description of the amygdaloid complex in the rat and cat with observations on intra‐amygdaloid axonal connections

Krettek, J. E., & Price, J. L. (1978) · Journal of Comparative Neurology · doi:10.1002/cne.901780205 · Cited by 727 · see citing works

Projections of the medial and lateral prefrontal cortices to the amygdala: a Phaseolus vulgaris leucoagglutinin study in the rat

McDonald, A. J., Mascagni, F., & Guo, L. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00417-3 · Cited by 689 · see citing works

Further contributions to the study of the evolution of the forebrain

Johnston, J. B. (1923) · The Journal of Comparative Neurology · doi:10.1002/cne.900350502 · Cited by 667 · see citing works

The topographic organization of associational fibers of the olfactory system in the rat, including centrifugal fibers to the olfactory bulb

Luskin, M. B., & Price, J. L. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902160305 · Cited by 552 · see citing works

Organization of projections from the ventromedial nucleus of the hypothalamus: A Phaseolus vulgaris ‐Leucoagglutinin study in the rat

Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903480103 · Cited by 547 · see citing works

Topographic organization of neurons in the acoustic thalamus that project to the amygdala

LeDoux, J., Farb, C. R., & Ruggiero, D. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01043.1990 · Cited by 546 · see citing works

The Human Central Nervous System: A Synopsis and Atlas

Nieuwenhuys, R., Voogd, J., & van Huijzen, C. (2012) · Medical Entomology and Zoology · Cited by 543 · see citing works

Projections of the ventral subiculum to the amygdala, septum, and hypothalamus: A PHAL anterograde tract‐tracing study in the rat

Canteras, N. S., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240204 · Cited by 541 · see citing works

Projections from the amygdaloid complex and adjacent olfactory structures to the entorhinal cortex and to the subiculum in the rat and cat

Krettek, J. E., & Price, J. L. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720409 · Cited by 535 · see citing works

An autoradiographic study of complementary laminar patterns of termination of afferent fibers to the olfactory cortex

Price, J. L. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901500105 · Cited by 530 · see citing works

Connections of the amygdala of the rat. IV: Corticoamygdaloid and intraamygdaloid connections as studied with axonal transport of horseradish peroxidase

Ottersen, O. P. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902050104 · Cited by 474 · see citing works

Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat

McDonald, A. J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90247-l · Cited by 463 · see citing works

Extrinsic projections from area CA 1 of the rat hippocampus: Olfactory, cortical, subcortical, and bilateral hippocampal formation projections

van Groen, T., & Wyss, J. M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020308 · Cited by 415 · see citing works

The organization of the efferent projections from the pontine parabrachial area to the amygdaloid complex: A phaseolus vulgaris leucoagglutinin (PHA‐L) study in the rat

Bernard, J. F., Alden, M., & Besson, J. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290205 · Cited by 411 · see citing works

Efferent projections of the paraventricular thalamic nucleus in the rat

Moga, M. M., Weis, R. P., & Moore, R. Y. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590204 · Cited by 402 · see citing works

Information Cascade from Primary Auditory Cortex to the Amygdala: Corticocortical and Corticoamygdaloid Projections of Temporal Cortex in the Rat

Romanski, L. M., & LeDoux, J. E. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.6.515 · Cited by 398 · see citing works

Topographical organization of amygdaloid projections to the caudatoputamen, nucleus accumbens, and related striatal-like areas of the rat brain

Mcdonald, A. J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90248-m · Cited by 372 · see citing works

Amygdaloid projections to the frontal cortex and the striatum in the rat

Kita, H., & Kitai, S. T. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980104 · Cited by 351 · see citing works

Intrinsic GABAergic neurons in the rat central extended amygdala

Sun, N., & Cassell, M. D. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903300308 · Cited by 351 · see citing works

The structural organization of connections between hypothalamus and cerebral cortex 1Published on the World Wide Web on 2 June 1997. 1

Risold, P., Thompson, R. H., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00007-6 · Cited by 347 · see citing works

The Human Central Nervous System: A Synopsis and Atlas

Clayman, C. Β. (1979) · JAMA · doi:10.1001/jama.1979.03300140055030 · Cited by 332 · see citing works

The organization of the thalamocortical connections of the mediodorsal thalamic nucleus in the rat, related to the ventral forebrain–prefrontal cortex topography

Ray, J. P., & Price, J. L. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903230204 · Cited by 326 · see citing works

Neuronal architecture in the rat central nucleus of the amygdala: A cytological, hodological, and immunocytochemical study

Cassell, M. D., Gray, T. S., & Kiss, J. Z. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902460406 · Cited by 297 · see citing works

Connections of the posterior nucleus of the amygdala

Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240203 · Cited by 273 · see citing works

Chemoarchitecture of the rat lateral septal nucleus 1Published on the World Wide Web on 2 June 1997. 1

Risold, P. Y., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00008-8 · Cited by 263 · see citing works

A direct projection from the central nucleus of the amygdala to the acoustic startle pathway: Anterograde and retrograde tracing studies.

Rosen, J. B., Hitchcock, J. M., Sananes, C. B., Miserendino, M. J. D., & al, E. (1991) · Behavioral Neuroscience · doi:10.1037/0735-7044.105.6.817 · Cited by 256 · see citing works

Comparative localization of mRNAs encoding two forms of glutamic acid decarboxylase with nonradioactive in situ hybridization methods

Esclapez, M., Tillakaratne, N. J. K., Tobin, A. J., & Houser, C. R. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903310305 · Cited by 251 · see citing works

Projections from the lateral part of the central amygdalar nucleus to the postulated fear conditioning circuit

Petrovich, G. D., & Swanson, L. W. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01361-3 · Cited by 234 · see citing works

Projections of the ventral premammillary nucleus

Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240205 · Cited by 222 · see citing works

Localization of GABA-like immunoreactivity in the monkey amygdala

McDonald, A. J., & Augustine, J. R. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90156-a · Cited by 216 · see citing works

The Excitable Cortex in Conscious Man

Penfield, W. G. (1958) · Medical Entomology and Zoology · Cited by 211 · see citing works

Model of forebrain regionalization based on spatiotemporal patterns of POU‐III homeobox gene expression, birthdates, and morphological features

Álvarez-Bolado, G., Rosenfeld, M. G., & Swanson, L. W. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903550207 · Cited by 205 · see citing works

Vom Baue und Leben des gehirns

Burdach, K. F. (1819) · Medical Entomology and Zoology · Cited by 189 · see citing works

Corticoamygdaloid and corticocortical projections of the rat temporal cortex: APhaseolus vulgaris leucoagglutinin study

Mascagni, F., McDonald, A. J., & Coleman, J. R. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90016-9 · Cited by 186 · see citing works

Organization of amygdaloid projections to the mediodorsal thalamus and prefrontal cortex: A fluorescence retrograde transport study in the rat

McDonald, A. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902620105 · Cited by 181 · see citing works

Calcitonin gene‐related peptide (CGRP) immunoreactive projections from the thalamus to the striatum and amygdala in the rat

Yasui, Y., Saper, C. B., & Cechetto, D. F. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903080212 · Cited by 155 · see citing works

The cortical projection of the basolateral amygdaloid nucleus in the rat: A retrograde fluorescent dye study

Sripanidkulchai, K., Sripanidkulchai, B., & Wyss, J. M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290310 · Cited by 146 · see citing works

Hormonal control of neuropeptide gene expression in sexually dimorphic olfactory pathways

Simerly, R. B. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90186-e · Cited by 115 · see citing works

Historical aspects of cerebral anatomy

Powell, T. P. S. (1972) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(72)90144-x · Cited by 94 · see citing works

Estrogen differentially regulates neuropeptide gene expression in a sexually dimorphic olfactory pathway.

Simerly, R. B., Young, B. J., Capozza, M. A., & Swanson, L. W. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.12.4766 · Cited by 94 · see citing works

Developmental brain maps : structure of the embryonic rat brain

Álvarez-Bolado, G., & Swanson, L. W. (1996) · Elsevier eBooks · Cited by 84 · see citing works

Ultrastructure of the stomatogastric ganglion neuropil of the crab, Cancer borealis

Kilman, V. L., & Marder, E. E. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961021)374:3 · Cited by 81 · see citing works

Historical Aspects of Cerebral Anatomy.

(1971) · Annals of Internal Medicine · doi:10.7326/0003-4819-75-5-825_1 · Cited by 73 · see citing works

Contributions of the amygdaloid central nucleus to the modulation of the nictitating membrane reflex in the rabbit.

Whalen, P. J., & Kapp, B. S. (1991) · Behavioral Neuroscience · doi:10.1037//0735-7044.105.1.141 · Cited by 67 · see citing works

The excitable cortex in conscious man

COBB, S. S. (1959) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(59)90070-7 · Cited by 56 · see citing works

Neurogenesis in the basal forebrain of the Chinese hamster (Cricetulus griseus)

ten Donkelaar, H. J., & Dederen, P. J. W. C. (1979) · Anatomy and Embryology · doi:10.1007/bf00299631 · Cited by 51 · see citing works

Contributions of the amygdaloid central nucleus to the modulation of the nictitating membrane reflex in the rabbit.

Whalen, P. J., & Kapp, B. S. (1991) · Behavioral Neuroscience · doi:10.1037/0735-7044.105.1.141 · Cited by 51 · see citing works

The adolescent brain and age-related behavioral manifestations

Spear, L. P. (2000) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00014-2 · Cited by 5,433 · see citing works

Neural regulation of endocrine and autonomic stress responses

Ulrich-Lai, Y. M., & Herman, J. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2647 · Cited by 3,318 · see citing works

Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex

Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129 · see citing works

Neuronal circuits for fear and anxiety

Tovote, P., Fadok, J. P., & Lüthi, A. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3945 · Cited by 1,786 · see citing works

The Amygdaloid Complex: Anatomy and Physiology

SAH, P., FABER, E. S. L., LOPEZ DE ARMENTIA, M., & POWER, J. (2003) · Physiological Reviews · doi:10.1152/physrev.00002.2003 · Cited by 1,745 · see citing works

Chronic stress induces contrasting patterns of dendritic remodeling in hippocampal and amygdaloid neurons

Vyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06810.2002 · Cited by 1,662 · see citing works

Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo–pituitary–adrenocortical responsiveness

Herman, J. P., Figueiredo, H., Mueller, N. K., Ulrich-Lai, Y., Ostrander, M. M., Choi, D. C., & Cullinan, W. E. (2003) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2003.07.001 · Cited by 1,586 · see citing works

Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis

Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322 · see citing works

A two-dimensional neuropsychology of defense: fear/anxiety and defensive distance

McNaughton, N., & Corr, P. J. (2004) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.005 · Cited by 1,308 · see citing works

Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: intersubject variability and probability maps

Amunts, K., Kedo, O., Kindler, M., Pieperhoff, P., Mohlberg, H., Shah, N. J., Habel, U., Schneider, F., & Zilles, K. (2005) · Anatomy and Embryology · doi:10.1007/s00429-005-0025-5 · Cited by 1,264 · see citing works

The amygdala

LeDoux, J. (2007) · Current Biology · doi:10.1016/j.cub.2007.08.005 · Cited by 1,281 · see citing works

The Medial Extended Amygdala in Male Reproductive Behavior A Node in the Mammalian Social Behavior Network

NEWMAN, S. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09271.x · Cited by 1,189 · see citing works

The amygdala and reward

Baxter, M. G., & Murray, E. A. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn875 · Cited by 1,200 · see citing works

Functional grouping and cortical–subcortical interactions in emotion: a meta-analysis of neuroimaging studies

Kober, H., Barrett, L. F., Joseph, J., Bliss-Moreau, E., Lindquist, K., & Wager, T. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.059 · Cited by 1,144 · see citing works

Evoked axonal oxytocin release in the central amygdala attenuates fear response

Knobloch, H. S., Charlet, A., Hoffmann, L. C., Eliava, M., Khrulev, S., Cetin, A. H., Osten, P., Schwarz, M. K., Seeburg, P. H., Stoop, R., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.030 · Cited by 1,049 · see citing works

The human amygdala and the emotional evaluation of sensory stimuli

Zald, D. H. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00248-5 · Cited by 1,062 · see citing works

The Vertebrate mesolimbic reward system and social behavior network: A comparative synthesis

O'Connell, L. A., & Hofmann, H. A. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22735 · Cited by 986 · see citing works

Amygdala inhibitory circuits and the control of fear memory

Ehrlich, I., Humeau, Y., Grenier, F., Ciocchi, S., Herry, C., & Lüthi, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.026 · Cited by 878 · see citing works

Social cognition and the human brain

Adolphs, R. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01399-6 · Cited by 895 · see citing works

What does the amygdala contribute to social cognition

Adolphs, R. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05445.x · Cited by 836 · see citing works

Mosaic evolution of brain structure in mammals

Barton, R. A., & Harvey, P. H. (2000) · Nature · doi:10.1038/35016580 · Cited by 797 · see citing works

Functional connectivity of the human amygdala using resting state fMRI

Roy, A. K., Shehzad, Z., Margulies, D. S., Kelly, A. M. C., Uddin, L. Q., Gotimer, K., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.11.030 · Cited by 749 · see citing works

Predictors of amygdala activation during the processing of emotional stimuli: A meta-analysis of 385 PET and fMRI studies

Costafreda, S. G., Brammer, M. J., David, A. S., & Fu, C. H. Y. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.012 · Cited by 772 · see citing works

Topography of projections from amygdala to bed nuclei of the stria terminalis

Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00079-0 · Cited by 714 · see citing works

Associative processes in addiction and reward. The role of amygdala-ventral striatal subsystems

EVERITT, B. J., PARKINSON, J. A., OLMSTEAD, M. C., ARROYO, M., ROBLEDO, P., & ROBBINS, T. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09280.x · Cited by 708 · see citing works

The emerging science of Interoception: sensing, integrating, interpreting, and regulating signals within the self

Chen, W. G., Schloesser, D., Arensdorf, A. M., Simmons, J. M., Cui, C., Valentino, R., Gnadt, J. W., Nielsen, L., Hillaire-Clarke, C. S., Spruance, V., et al. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.10.007 · Cited by 707 · see citing works

The Neuroscience of Mammalian Associative Learning

Fanselow, M. S., & Poulos, A. M. (2005) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070213 · Cited by 683 · see citing works

The many paths to fear

Gross, C. T., & Canteras, N. S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3301 · Cited by 596 · see citing works

Parallel incentive processing: an integrated view of amygdala function

Balleine, B. W., & Killcross, S. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.03.002 · Cited by 622 · see citing works

Limbic Regulation of Hypothalamo‐Pituitary‐Adrenocortical Function during Acute and Chronic Stress

Jankord, R., & Herman, J. P. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1410.012 · Cited by 578 · see citing works

Central nervous system control of gastrointestinal motility and secretion and modulation of gastrointestinal functions

Browning, K. N., & Travagli, R. A. (2014) · Comprehensive Physiology · doi:10.1002/cphy.c130055 · Cited by 541 · see citing works

Basic organization of projections from the oval and fusiform nuclei of the bed nuclei of the stria terminalis in adult rat brain

Dong, H., Petrovich, G. D., Watts, A. G., & Swanson, L. W. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1079 · Cited by 521 · see citing works

Neuromodulation by Oxytocin and Vasopressin

Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works

Roles for nigrostriatal—not just mesocorticolimbic—dopamine in reward and addiction

Wise, R. A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.06.004 · Cited by 500 · see citing works

Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars

Benes, F. M., Lim, B., Matzilevich, D., Walsh, J. P., Subburaju, S., & Minns, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703806104 · Cited by 483 · see citing works

Lhx6 delineates a pathway mediating innate reproductive behaviors from the amygdala to the hypothalamus

Choi, G. B., Dong, H.-W., Murphy, A. J., Valenzuela, D. M., Yancopoulos, G. D., Swanson, L. W., & Anderson, D. J. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.011 · Cited by 462 · see citing works

Contextual and Auditory Fear Conditioning are Mediated by the Lateral, Basal, and Central Amygdaloid Nuclei in Rats

Goosens, K. A., & Maren, S. (2001) · Learning &amp; Memory · doi:10.1101/lm.37601 · Cited by 451 · see citing works

Detecting Activated Cell Populations Using Single-Cell RNA-Seq

Wu, Y. E., Pan, L., Zuo, Y., Li, X., & Hong, W. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.026 · Cited by 438 · see citing works

The Hypothalamic-Pituitary-Adrenal Axis: Development, Programming Actions of Hormones, and Maternal-Fetal Interactions

Sheng, J. A., Bales, N. J., Myers, S. A., Bautista, A. I., Roueinfar, M., Hale, T. M., & Handa, R. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.601939 · Cited by 418 · see citing works

Neural and cellular mechanisms of fear and extinction memory formation

Orsini, C. A., & Maren, S. (2012) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.12.014 · Cited by 429 · see citing works

Gonadal steroid hormones and the hypothalamo–pituitary–adrenal axis

Handa, R. J., & Weiser, M. J. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.11.001 · Cited by 408 · see citing works

Sex-related difference in amygdala activity during emotionally influenced memory storage

Cahill, L., Haier, R. J., White, N. S., Fallon, J., Kilpatrick, L., Lawrence, C., Potkin, S. G., & Alkire, M. T. (2001) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2000.3999 · Cited by 413 · see citing works

Antagonistic control of social versus repetitive self-grooming behaviors by separable amygdala neuronal subsets

Hong, W., Kim, D.-W., & Anderson, D. J. (2014) · Cell · doi:10.1016/j.cell.2014.07.049 · Cited by 405 · see citing works

Amygdala and Ventral Hippocampus Contribute Differentially to Mechanisms of Fear and Anxiety.

McHugh, S. B., Deacon, R. M. J., Rawlins, J. N. P., & Bannerman, D. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.63 · Cited by 384 · see citing works

Decreased Volume of the Brain Reward System in Alcoholism

Makris, N., Oscar-Berman, M., Jaffin, S. K., Hodge, S. M., Kennedy, D. N., Caviness, V. S., Marinkovic, K., Breiter, H. C., Gasic, G. P., & Harris, G. J. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.01.018 · Cited by 372 · see citing works

Functional subsets of serotonergic neurones: implications for control of the hypothalamic-pituitary-adrenal axis

Lowry, C. A. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00861.x · Cited by 362 · see citing works

A developmental neurobiological model of motivated behavior: Anatomy, connectivity and ontogeny of the triadic nodes

Ernst, M., & Fudge, J. L. (2009) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.10.009 · Cited by 358 · see citing works

“Liking” and “wanting” in eating and food reward: Brain mechanisms and clinical implications

Morales, I., & Berridge, K. C. (2020) · Physiology &amp; Behavior · doi:10.1016/j.physbeh.2020.113152 · Cited by 346 · see citing works

Functional neuroimaging of the olfactory system in humans

Zald, D. H., & Pardo, J. V. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(99)00110-5 · Cited by 334 · see citing works

Glucocorticoid actions on synapses, circuits, and behavior: Implications for the energetics of stress

Myers, B., McKlveen, J. M., & Herman, J. P. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.12.003 · Cited by 318 · see citing works

Upregulation of voluntary alcohol intake, behavioral sensitivity to stress, and amygdala crhr1 expression following a history of dependence

Sommer, W. H., Rimondini, R., Hansson, A. C., Hipskind, P. A., Gehlert, D. R., Barr, C. S., & Heilig, M. A. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.01.010 · Cited by 309 · see citing works

The amygdala, fear, and memory

FANSELOW, M. S., & GALE, G. D. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07077.x · Cited by 299 · see citing works

Role of dopamine receptor mechanisms in the amygdaloid modulation of fear and anxiety: Structural and functional analysis

de la Mora, M. P., Gallegos-Cari, A., Arizmendi-García, Y., Marcellino, D., & Fuxe, K. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.10.010 · Cited by 296 · see citing works

Role of GABA and Glutamate Circuitry in Hypothalamo‐Pituitary‐Adrenocortical Stress Integration

HERMAN, J. P., MUELLER, N. K., & FIGUEIREDO, H. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1296.004 · Cited by 282 · see citing works

Mechanisms of rapid glucocorticoid feedback inhibition of the hypothalamic–pituitary–adrenal axis

Tasker, J. G., & Herman, J. P. (2011) · Stress · doi:10.3109/10253890.2011.586446 · Cited by 277 · see citing works

Local circuit regulation of paraventricular nucleus stress integration

Herman, J. P., Tasker, J. G., Ziegler, D. R., & Cullinan, W. E. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00681-5 · Cited by 274 · see citing works

Medial amygdalar aromatase neurons regulate aggression in both sexes

Unger, E. K., Burke, K. J., Yang, C. F., Bender, K. J., Fuller, P. M., & Shah, N. M. (2015) · Cell Reports · doi:10.1016/j.celrep.2014.12.040 · Cited by 275 · see citing works

Seeking a Spotless Mind: Extinction, Deconsolidation, and Erasure of Fear Memory

Maren, S. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.023 · Cited by 259 · see citing works

Facial-Expression and Gaze-Selective Responses in the Monkey Amygdala

Hoffman, K. L., Gothard, K. M., Schmid, M. C., & Logothetis, N. K. (2007) · Current Biology · doi:10.1016/j.cub.2007.03.040 · Cited by 258 · see citing works

Food for thought: hedonic experience beyond homeostasis in the human brain

Kringelbach, M. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.04.035 · Cited by 236 · see citing works

Something in the Air? New Insights into Mammalian Pheromones

Brennan, P. A., & Keverne, E. B. (2004) · Current Biology · doi:10.1016/j.cub.2003.12.052 · Cited by 236 · see citing works

Neurofunctional correlates of posttraumatic stress disorder: a PET symptom provocation study

Pissiota, A., Frans, Ö., Fernandez, M., von Knorring, L., Fischer, H., & Fredrikson, M. (2002) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s004060200014 · Cited by 228 · see citing works

Organization and evolution of the avian forebrain

Reiner, A., Yamamoto, K., & Karten, H. J. (2005) · The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology · doi:10.1002/ar.a.20253 · Cited by 222 · see citing works

The Neurobiology of Conditioned and Unconditioned Fear: A Neurobehavioral System Analysis of the Amygdala

Rosen, J. B. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304265945 · Cited by 219 · see citing works

A neural switch for active and passive fear

Gozzi, A., Jain, A., Giovanelli, A., Bertollini, C., Crestan, V., Schwarz, A. J., Tsetsenis, T., Ragozzino, D., Gross, C. T., & Bifone, A. (2010) · Neuron · doi:10.1016/j.neuron.2010.07.008 · Cited by 209 · see citing works

Differential Contribution of Right and Left Amygdala to Affective Information Processing

Markowitsch, H. J. (1999) · Behavioural Neurology · doi:10.1155/1999/180434 · Cited by 199 · see citing works

Thoughts on the development, structure and evolution of the mammalian and avian telencephalic pallium

Puelles, L. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2001.0973 · Cited by 196 · see citing works

Regulating anxiety with extrasynaptic inhibition

Botta, P., Demmou, L., Kasugai, Y., Markovic, M., Xu, C., Fadok, J. P., Lu, T., Poe, M. M., Xu, L., Cook, J. M., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4102 · Cited by 192 · see citing works

Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders

Schumann, C. M., Bauman, M. D., & Amaral, D. G. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.09.028 · Cited by 178 · see citing works

Functional properties and projections of neurons in the medial amygdala

Keshavarzi, S., Sullivan, R. K. P., Ianno, D. J., & Sah, P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1176-14.2014 · Cited by 176 · see citing works

Neural Regulation of the Stress Response: The Many Faces of Feedback

Myers, B., McKlveen, J. M., & Herman, J. P. (2012) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-012-9801-y · Cited by 175 · see citing works

Revisiting the global workspace orchestrating the hierarchical organization of the human brain

Deco, G., Vidaurre, D., & Kringelbach, M. L. (2021) · Nature Human Behaviour · doi:10.1038/s41562-020-01003-6 · Cited by 162 · see citing works

Sleep leads to changes in the emotional memory trace: evidence from FMRI

Payne, J. D., & Kensinger, E. A. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21526 · Cited by 169 · see citing works

The physiological control of eating: signals, neurons, and networks

Watts, A. G., Kanoski, S. E., Sanchez-Watts, G., & Langhans, W. (2022) · Physiological Reviews · doi:10.1152/physrev.00028.2020 · Cited by 168 · see citing works

Role of the paraventricular nucleus microenvironment in stress integration

Herman, J. P., Cullinan, W. E., Ziegler, D. R., & Tasker, J. G. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02133.x · Cited by 168 · see citing works

Childhood trauma history differentiates amygdala response to sad faces within MDD

Grant, M. M., Cannistraci, C., Hollon, S. D., Gore, J., & Shelton, R. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.12.004 · Cited by 166 · see citing works

A model of differential amygdala activation in psychopathy

Moul, C., Killcross, S., & Dadds, M. R. (2012) · Psychological Review · doi:10.1037/a0029342 · Cited by 159 · see citing works

Basal forebrain cholinergic signalling: development, connectivity and roles in cognition

Ananth, M. R., Rajebhosale, P., Kim, R., Talmage, D. A., & Role, L. W. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00677-x · Cited by 148 · see citing works

An oxytocin antagonist infused into the central nucleus of the amygdala increases maternal aggressive behavior

Lubin, D. A., Elliot, J. C., Black, M. C., & Johns, J. M. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.2.195 · Cited by 145 · see citing works

Prenatal bisphenol A exposure alters sex-specific estrogen receptor expression in the neonatal rat hypothalamus and amygdala

Cao, J., Rebuli, M. E., Rogers, J., Todd, K. L., Leyrer, S. M., Ferguson, S. A., & Patisaul, H. B. (2013) · Toxicological Sciences · doi:10.1093/toxsci/kft035 · Cited by 141 · see citing works

Selective processing of social stimuli in the superficial amygdala

Goossens, L., Kukolja, J., Onur, O. A., Fink, G. R., Maier, W., Griez, E., Schruers, K., & Hurlemann, R. (2009) · Human Brain Mapping · doi:10.1002/hbm.20755 · Cited by 132 · see citing works

Manipulating a “Cocaine Engram” in Mice

Hsiang, H.-L. (., Epp, J. R., van den Oever, M. C., Yan, C., Rashid, A. J., Insel, N., Ye, L., Niibori, Y., Deisseroth, K., Frankland, P. W., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3327-14.2014 · Cited by 131 · see citing works

Lateral amygdaloid nucleus expansion in adult rats is associated with exposure to prenatal stress

Salm, A. K., Pavelko, M., Krouse, E. M., Webster, W., Kraszpulski, M., & Birkle, D. L. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.11.005 · Cited by 125 · see citing works

Extraordinary diversity in vasopressin (V1a) receptor distributions among wild prairie voles (<i>Microtus ochrogaster</i>): Patterns of variation and covariation

Phelps, S. M., & Young, L. J. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10902 · Cited by 116 · see citing works

Neonatal development of projections from the basolateral amygdala to prefrontal, striatal, and thalamic structures in the rat

Bouwmeester, H., Wolterink, G., & Van Ree, J. M. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.10084 · Cited by 112 · see citing works

The central nucleus of the amygdala and the construction of defensive modes across the threat-imminence continuum

Moscarello, J. M., & Penzo, M. A. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01130-5 · Cited by 112 · see citing works

Vasopressin, oxytocin, and social odor recognition

Wacker, D. W., & Ludwig, M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.08.014 · Cited by 112 · see citing works

Neural architecture of the vertebrate brain: implications for the interaction between emotion and cognition

Pessoa, L., Medina, L., Hof, P. R., & Desfilis, E. (2019) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.021 · Cited by 105 · see citing works

Thalamic paraventricular nucleus lesions facilitate central amygdala neuronal responses to acute psychological stress

Spencer, S. J., Fox, J. C., & Day, T. A. (2004) · Brain Research · doi:10.1016/j.brainres.2003.10.054 · Cited by 99 · see citing works

Early life adversity during the infant sensitive period for attachment: Programming of behavioral neurobiology of threat processing and social behavior

Opendak, M., Gould, E., & Sullivan, R. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2017.02.002 · Cited by 94 · see citing works

Stress-induced structural plasticity of medial amygdala stellate neurons and rapid prevention by a candidate antidepressant

Lau, T., Bigio, B., Zelli, D., McEwen, B. S., & Nasca, C. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.68 · Cited by 93 · see citing works

Phasic activation of locus ceruleus neurons by the central nucleus of the amygdala

Bouret, S., Duvel, A., Onat, S., & Sara, S. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03491.2003 · Cited by 84 · see citing works

Amygdala-centred functional connectivity affects daily cortisol concentrations: a putative link with anxiety

Hakamata, Y., Komi, S., Moriguchi, Y., Izawa, S., Motomura, Y., Sato, E., Mizukami, S., Kim, Y., Hanakawa, T., Inoue, Y., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-08918-7 · Cited by 76 · see citing works

Disruptive effects of repeated stress on basolateral amygdala neurons and fear behavior across the estrous cycle in rats

Blume, S. R., Padival, M., Urban, J. H., & Rosenkranz, J. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-48683-3 · Cited by 71 · see citing works

Evidence for coordinated functional activity within the extended amygdala of non-human and human primates

Oler, J. A., Birn, R. M., Patriat, R., Fox, A. S., Shelton, S. E., Burghy, C. A., Stodola, D. E., Essex, M. J., Davidson, R. J., & Kalin, N. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.045 · Cited by 67 · see citing works

A Central Amygdala-Globus Pallidus Circuit Conveys Unconditioned Stimulus-Related Information and Controls Fear Learning

Giovanniello, J., Yu, K., Furlan, A., Nachtrab, G. T., Sharma, R., Chen, X., & Li, B. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.2090-20.2020 · Cited by 65 · see citing works

Central amygdala nucleus (Ce) gene expression linked to increased trait-like Ce metabolism and anxious temperament in young primates

Fox, A. S., Oler, J. A., Shelton, S. E., Nanda, S. A., Davidson, R. J., Roseboom, P. H., & Kalin, N. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206723109 · Cited by 57 · see citing works

The mouse Engrailed genes: A window into autism

KUEMERLE, B., GULDEN, F., CHEROSKY, N., WILLIAMS, E., & HERRUP, K. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.09.009 · Cited by 60 · see citing works

Tobacco use across the formative years: a road map to developmental vulnerabilities

Jamner, L., Whalen, C., Loughlin, S., Mermelstein, R., Audrain-McGovern, J., Krishnan-Sarin, S., Worden, J., & Leslie, F. (2003) · Nicotine &amp; Tobacco Research · doi:10.1080/14622200310001625573 · Cited by 60 · see citing works

Anterior medial temporal lobe in human cognition: Memory for fear and the unexpected

Strange, B. A., & Dolan, R. J. (2006) · Cognitive Neuropsychiatry · doi:10.1080/13546800500305096 · Cited by 60 · see citing works

Adjusting Behavior to Context: Striatal Network Functions in Learning and Memory

Graybiel, A. M., & Blázquez, P. M. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4757-3538-3_86 · Cited by 1 · see citing works

Repeated restraint stress increases basolateral amygdala neuronal activity in an age-dependent manner

Zhang, W., & Rosenkranz, J. A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.051 · Cited by 77 · see citing works

Intrinsic circuits of the striatum

Benarroch, E. E. (2016) · Neurology · doi:10.1212/wnl.0000000000002599 · Cited by 24 · see citing works

Fear, Anxiety, and the Amygdala

Sah, P. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.013 · Cited by 137 · see citing works

Behavioural Effects of Manipulation of Basal Ganglia Neurotransmitters

Iversen, S. D. (1984) · Novartis Foundation symposium · doi:10.1002/9780470720882.ch10 · Cited by 31 · see citing works