{"id":486,"date":"2020-01-18T16:33:02","date_gmt":"2020-01-18T16:33:02","guid":{"rendered":"http:\/\/sites.rutgers.edu\/pare-lab\/?page_id=486"},"modified":"2025-12-01T09:16:31","modified_gmt":"2025-12-01T09:16:31","slug":"publications","status":"publish","type":"page","link":"https:\/\/sites.rutgers.edu\/pare-lab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<p><strong>Publications<\/strong><\/p>\n<p>Asterisks indicate research trainees.<\/p>\n<p>*Kim IT, Huerta-Ocampo I, *Urena O, Yamamoto R, Pare\u0301 D (2025) Collateralization patterns of principal basolateral amygdala neurons delineate distinct output streams. iScience. <a href=\"https:\/\/www.cell.com\/iscience\/fulltext\/S2589-0042(25)01350-1\">doi: 10.1016\/j.isci.2025.113089<\/a><\/p>\n<p>*Badawy M, *Kim IT, *Amir A, *Herzallah MM, *Gomez-Alatorre LF, *Headley DB, Pare\u0301 D (2025) Major individual and regional variations in unit entrainment by oscillations of different frequencies. Scientific Reports. <a href=\"https:\/\/www.nature.com\/articles\/s41598-025-85914-2\">doi: 10.1038\/s41598-025-85914-2<\/a><\/p>\n<p>*Gielow MR, *Headley DB, *Herzallah MM, Pare\u0301 D (2025) Common neocortical and hippocampal correlates of performance errors in a timing task. Journal of Neuroscience. <a href=\"https:\/\/www.jneurosci.org\/content\/early\/2025\/01\/08\/JNEUROSCI.2003-23.2024\">doi: 10.1523\/JNEUROSCI.2003-23.2024<\/a><\/p>\n<p>*Amir A, *Headley DB, *Herzallah MM, *Karki A, *Kim IT, Pare\u0301 D (2024) Studying decision making in rats using a contextual visual discrimination task: Detection and prevention of alternative behavioral strategies. Journal of Neuroscience Methods, 415:110346. <a href=\"https:\/\/doi.org\/10.1016\/j.jneumeth.2024.110346\">doi: 10.1016\/j.jneumeth.2024.110346<\/a><\/p>\n<p>Chen Z, *Headley DB, *Gomez-Alatorre LF, *Kanta V, Ho KC, Pare D, Nair SS (2023) Approaches to characterizing oscillatory burst detection algorithms for electrophysiological recordings. Journal of Neuroscience Methods, 391:109865. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0165027023000845\">doi: 10.1016\/j.jneumeth.2023.109865<\/a><\/p>\n<p>Pare\u0301 D, *Headley DB (2023) The amygdala mediates the facilitating influence of emotions on memory through multiple interacting mechanisms. Neurobiology of Stress, 24:100529. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2352289523000176\">doi: 10.1016\/j.ynstr.2023.100529<\/a><\/p>\n<p>*Ahmed N, Pare D (2023) The basolateral amygdala sends a mixed (GABAergic and glutamatergic) projection to the mediodorsal thalamic nucleus. Journal of Neuroscience. <a href=\"https:\/\/www.jneurosci.org\/content\/jneuro\/early\/2023\/02\/13\/JNEUROSCI.1924-22.2022.full.pdf\">doi: 10.1523\/JNEUROSCI.1924-22.2022<\/a><\/p>\n<p>*Herzallah MM, *Amir A, Pare\u0301 D (2022) Influence of rat central thalamic neurons on foraging behavior in a hazardous environment. Journal of Neuroscience, 42(31):6053-6068. <a href=\"https:\/\/www.jneurosci.org\/content\/42\/31\/6053\">doi: 10.1523\/JNEUROSCI.0461-22.2022<\/a><\/p>\n<p>*Haufler D, Liran O, Buchanan RJ, Pare D (2022) Human anterior insula signals salience and deviations from expectations via bursts of beta oscillations. Journal of Neurophysiology. <a href=\"https:\/\/journals.physiology.org\/doi\/abs\/10.1152\/jn.00106.2022\">doi: 10.1152\/jn.00106.2022<\/a><\/p>\n<p>*Ahmed N, *Headley DB, Pare\u0301 D (2021) Optogenetic study of central medial and paraventricular thalamic projections to the basolateral amygdala. Journal of Neurophysiology. <a href=\"https:\/\/journals.physiology.org\/doi\/abs\/10.1152\/jn.00253.2021\">doi: 10.1152\/jn.00253.2021<\/a><\/p>\n<p>*Headley DB, *Kyriazi P, Feng F, Nair S, Pare D (2021) Gamma oscillations in the basolateral amygdala: localization, microcircuitry, and behavioral correlates. Journal of Neuroscience, 41(28):6087-6101. <a href=\"https:\/\/www.jneurosci.org\/content\/early\/2021\/06\/01\/JNEUROSCI.3159-20.2021\">doi: 10.1523\/JNEUROSCI.3159-20.2021.<\/a><\/p>\n<p>*Kyriazi P, *Headley DB, Pare\u0301 D (2020) Different multidimensional representations across the amygdalo-prefrontal network during an approach-avoidance task. Neuron, 107(4):717-730.e5. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627320304293?via%3Dihub\">doi: 10.1016\/j.neuron.2020.05.039<\/a><\/p>\n<p>*Yamamoto R, Furuyama T, Sugai T, Ono M, Pare\u0301 D, Kato N (2019) Serotonergic control of GABAergic inhibition in the lateral amygdala. Journal of Neurophysiology, 123(2):670-681. <a href=\"https:\/\/www.physiology.org\/doi\/abs\/10.1152\/jn.00500.2019\">doi: 10.1152\/jn.00500.2019<\/a>\u00a0 \u00a0 \u00a0<a href=\"https:\/\/rutgers.box.com\/s\/yfp55nxd0wax9htkbxfix4mj7x74ddzr\">PDF<\/a><\/p>\n<p>*Kanta V, Pare\u0301 D, *Headley D (2019) Closed-loop control of gamma oscillations in the amygdala demonstrates their role in spatial memory consolidation. Nature Communications, 10(1):3970. <a href=\"https:\/\/www.nature.com\/articles\/s41467-019-11938-8\">doi: 10.1038\/s41467-019-11938-8<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/jvkl22pe7683nst37v0ewhbq6sqeiwxj\">PDF<\/a><\/p>\n<p>*Headley DB, *Kanta V, *Kyriazi P, Par\u00e9 D (2019) Embracing complexity in defensive networks. Neuron, 103(2):189-201. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627319304775?via%3Dihub\">doi: 10.1016\/j.neuron.2019.05.024<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/fsoa6zpj4ggwwxhiozfgwxk7axdb9wlc\">PDF<\/a><\/p>\n<p>*Amir A, *Kyriazi P, *Lee SC, *Headley DB, Par\u00e9 D (2019) Basolateral amygdala neurons are activated during threat expectation. Journal of Neurophysiology, 121(5):1761-1777. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00807.2018?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00807.2018<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/3eq7wzw5x38bjohaqfx4hnvtgt53ojac\">PDF<\/a><\/p>\n<p>Feng F, *Headley DB, *Amir A, *Kanta V, Chen Z, Par\u00e9 D, Nair SS (2019) Gamma oscillations in the basolateral amygdala: Biophysical mechanisms and computational consequences. eNeuro, 6(1). <a href=\"https:\/\/www.eneuro.org\/content\/6\/1\/ENEURO.0388-18.2018.long\">doi: 10.1523\/ENEURO.0388-18.2018<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/782juafg1qmuvtc43tzg1k0g3epng094\">PDF<\/a><\/p>\n<p>*Haufler D, Par\u00e9 D (2019) Detection of multiway gamma coordination reveals how frequency mixing shapes neural dynamics. Neuron, 101(4):603-614. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627318311486?via%3Dihub\">doi: 10.1016\/j.neuron.2018.12.028<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/glkjimpuirz0bkelix6mi0wpkpfvqxnk\">PDF<\/a><\/p>\n<p>*Amir A, Par\u00e9 JF, Smith Y, Par\u00e9 D (2019) Midline thalamic inputs to the amygdala: Ultrastructure and synaptic targets. Journal of Comparative Neurology, 527(5):942-956. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/cne.24557\">doi: 10.1002\/cne.24557<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/qzuh2qp94zgiwo0wqyw2sofn7lgl718p\">PDF<\/a><\/p>\n<p>*Kyriazi P, *Headley DB, Pare\u0301 D (2018) Multi-dimensional coding by basolateral amygdala neurons. Neuron, 99(6):1315-1328. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627318306342?via%3Dihub\">doi: 10.1016\/j.neuron.2018.07.036<\/a> \u00a0 \u00a0 <a href=\"https:\/\/rutgers.box.com\/s\/p06bcow7er9l4ycsvz8rglcs9s8r8kwh\">PDF<\/a><\/p>\n<p>*Yamamoto R, *Ahmed N, Ito T, *Gungor NZ, Pare\u0301\u00a0D (2018) Optogenetic study of anterior BNST and basomedial amygdala projections to the ventromedial hypothalamus. eNeuro, 5(3). <a href=\"https:\/\/www.eneuro.org\/content\/5\/3\/ENEURO.0204-18.2018.long\">doi: 10.1523\/ENEURO.0204-18.2018<\/a><\/p>\n<p>*Gungor NZ, *Yamamoto R, Pare\u0301 D (2018) Glutamatergic and gabaergic ventral BNST neurons differ in their physiological properties and responsiveness to noradrenaline. Neuropsychopharmacology, 43(10):2126-2133. <a href=\"https:\/\/www.nature.com\/articles\/s41386-018-0070-4\">doi: 10.1038\/s41386-018-0070-4<\/a><\/p>\n<p>*Amir A, *Headley DB, *Lee SC, *Haufler D, Pare\u0301 D (2018) Vigilance-associated gamma oscillations coordinate the ensemble activity of basolateral amygdala neurons. Neuron, 97(3):656-669. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627317311832?via%3Dihub\">doi: 10.1016\/j.neuron.2017.12.035<\/a><\/p>\n<p>*Lee SC, *Amir A, *Haufler D, Pare\u0301 D (2017) Differential recruitment of competing valence-related amygdala networks during anxiety. Neuron, 96(1):81-88. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627317307900?via%3Dihub\">doi: 10.1016\/j.neuron.2017.09.002<\/a><\/p>\n<p>Par\u00e9 D, Quirk GJ (2017) When scientific paradigms lead to tunnel vision: lessons from the study of fear. npj Science of Learning. <a href=\"https:\/\/www.nature.com\/articles\/s41539-017-0007-4\">doi: https:\/\/doi.org\/10.1038\/s41539-017-0007-4<\/a><\/p>\n<p>*Headley DB, *Kanta V, Par\u00e9 D (2017) Intra- and interregional cortical interactions related to sharp-wave ripples and dentate spikes. Journal of Neurophysiology, 117:556-565. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00644.2016?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00644.2016<\/a><\/p>\n<p>Nair SS, Par\u00e9 D, Vicentic A (2016) Biologically based neural circuit modeling for the study of fear learning and extinction. npj Science of Learning, 1: 16015. <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC5846682\/pdf\/npjscilearn201615.pdf\">doi: 10.1038\/npjscilearn.2016.15<\/a><\/p>\n<p>*Headley DB, Par\u00e9 D (2016) Common oscillatory mechanisms across multiple memory systems. npj Science of Learning, 2: 1. <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6171763\/pdf\/41539_2016_Article_1.pdf\">doi: 10.1038\/s41539-016-0001-2<\/a><\/p>\n<p>*Lee SC, *Amir A, *Headley DB, *Haufler D, Par\u00e9 D (2016) Basolateral amygdala nucleus responses to appetitive conditioned stimuli correlate with variations in conditioned behavior. Nature Communications, 7:12275. <a href=\"https:\/\/www.nature.com\/articles\/ncomms12275\">doi: 10.1038\/ncomms12275<\/a><\/p>\n<p>*Rodriguez-Sierra, *Goswami S, *Turesson HK, Par\u00e9 D (2016) Altered responsiveness of BNST and amygdala neurons in trauma-induced anxiety. Translational Psychiatry, 6:e857. <a href=\"https:\/\/www.nature.com\/articles\/tp2016128\">doi: 10.1038\/tp.2016.128<\/a><\/p>\n<p>*Gungor NZ, Pare\u0301 D (2016) Functional heterogeneity in the bed nucleus of the stria terminalis. Journal of Neuroscience, 36:8038-49. <a href=\"https:\/\/www.jneurosci.org\/content\/36\/31\/8038.long\">doi: 10.1523\/JNEUROSCI.0856-16.2016<\/a><\/p>\n<p>Feng F, Samarth P, Pare\u0301 D, Nair SS (2016) Mechanisms underlying the formation of the amygdala fear memory trace: a computational perspective. Neuroscience, 322:370-376. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0306452216002086?via%3Dihub\">doi: 10.1016\/j.neuroscience.2016.02.059<\/a><\/p>\n<p>Samarth P, Ball JM, *Unal G, Pare\u0301 D, Nair SS (2016) Mechanisms of memory storage in a model perirhinal network. Brain Structure and Function, 222:183-200. <a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs00429-016-1210-4\">doi: 10.1007\/s00429-016-1210-4<\/a><\/p>\n<p>*Jhangiani-Jashanmal I, *YamamotoR, *Gungor NZ, Pare\u0301 D (2015) Electroresponsive properties of rat central medial thalamic neurons. Journal of Neurophysiology, 115:1533-1541. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00982.2015?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00982.2015<\/a><\/p>\n<p>*Gungor NZ, *Yamamoto R, Pare\u0301 D (2015) Optogenetic study of the projections from the bed nucleus of the stria terminalis to the central amygdala. Journal of Neurophysiology, 114:2903-2911. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00677.2015?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00677.2015<\/a><\/p>\n<p>*Amir A, *Lee SC, *Headley DB, *Herzallah MM, Pare\u0301 D(2015) Amygdala signaling during foraging in a hazardous environment. Journal of Neuroscience, 35:12994-3005. <a href=\"https:\/\/www.jneurosci.org\/content\/35\/38\/12994.long\">doi: 10.1523\/JNEUROSCI.0407-15.2015<\/a><\/p>\n<p>Cascardi M, *Armstrong D, *Chung L, Pare\u0301 D(2015) Pupil Response to Threat in Trauma-Exposed Individuals With or Without PTSD. Journal of Traumatic Stress, 28:370-4. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/jts.22022\">doi: 10.1002\/jts.22022<\/a><\/p>\n<p>Kim D, Samarth P, Feng F, Pare\u0301 D, Nair SS (2015) Synaptic competition in the lateral amygdala and the stimulus specificity of conditioned fear: a biophysical modeling study. Brain Structure and Function, 221(4):2163-82. <a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs00429-015-1037-4\">doi: 10.1007\/s00429-015-1037-4<\/a><\/p>\n<p>*Headley DB, *DeLucca MV, *Haufler D, Pare\u0301 D (2015) Incorporating 3D-printing technology in the design of head-caps and electrode drives for recording neurons in multiple brain regions. Journal of Neurophysiology, 113:2721-32. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00955.2014?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00955.2014<\/a><\/p>\n<p>*Unal CT, Pare\u0301 D, Zaborszky L (2015) Impact of basal forebrain cholinergic inputs on basolateral amygdala neurons. Journal of Neuroscience, 35:853-63. <a href=\"https:\/\/www.jneurosci.org\/content\/35\/2\/853.long\">doi: 10.1523\/JNEUROSCI.2706-14.2015<\/a><\/p>\n<p>Duvarci S, Par\u00e9 D (2014) Amygdala microcircuits controlling learned fear. Neuron, 82:966-80. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0896627314003572?via%3Dihub\">doi: 10.1016\/j.neuron.2014.04.042<\/a><\/p>\n<p>*Haufler D, Par\u00e9 D (2014) High frequency oscillations are prominent in the extended amygdala. Journal of Neurophysiology, 112:110-9. <a href=\"https:\/\/www.physiology.org\/doi\/full\/10.1152\/jn.00107.2014?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dpubmed\">doi: 10.1152\/jn.00107.2014<\/a><\/p>\n<p>*Gungor NZ, Par\u00e9 D (2014) CGRP inhibits neurons of the bed nucleus of the stria terminalis: implications for the regulation of fear and anxiety. Journal of Neuroscience, 34:60-65. <a href=\"https:\/\/www.jneurosci.org\/content\/34\/1\/60.long\">doi: 10.1523\/JNEUROSCI.3473-13.2014<\/a><\/p>\n<p>*Headley DB, Par\u00e9 D (2013) In sync: gamma oscillations and emotional memory. Frontiers in Behavioral Neuroscience, 7:170. <a href=\"https:\/\/www.frontiersin.org\/articles\/10.3389\/fnbeh.2013.00170\/full\">doi: 10.3389\/fnbeh.2013.00170<\/a><\/p>\n<p>*Unal G, Par\u00e9 J-F, Smith Y, Par\u00e9 D (2013) Cortical inputs innervate cabindin-immunoreactive interneurons of the basolateral amygdaloid complex. Journal of Comparative Neurology, 522:1915-28.<\/p>\n<p>*Haufler D, *Nagy FZ, Par\u00e9 D (2013) Neuronal correlates of fear conditioning in the bed nucleus of the stria terminalis. Learning &amp; Memory, 20:633-41.<\/p>\n<p>Kim D, Par\u00e9 D, Nair SS (2013) Assignment of model amygdala neurons to the fear memory trace depends on competitive synaptic interactions. Journal of Neuroscience, 33:14354-8.<\/p>\n<p>*Rodriguez-Sierra OE, *Turesson HK, Par\u00e9 D (2013) Contrasting distribution of physiological cell types in different regions of the bed nucleus of the stria terminalis. J Neurophysiol, 110:2037-49.<\/p>\n<p>*Goswami S, *Rodr\u00edguez Sierra O, Cascardi M, Par\u00e9 D (2013) Animal models of post-traumatic stress disorder. Frontiers in Behavioral Neuroscience, 7:89.<\/p>\n<p>Kim D, Par\u00e9 D, Nair S (2013) Mechanisms contributing to the induction and storage of Pavlovian fear memories in the lateral amygdala. Learning &amp; Memory, 20:421-30.<\/p>\n<p>Paz R, Par\u00e9 D (2013) Emotional modulation of memory circuits by the amygdala. Curr Opin Neurobiol, 23:381-6.<\/p>\n<p>*Turesson HK, *Rodriguez-Sierra O, Par\u00e9 D (2013) Intrinsic connectivity of the bed nucleus of the stria terminalis. J Neurophysiol, 109:2438-50.<\/p>\n<p>*Unal G, Par\u00e9 JF, Smith Y, Par\u00e9 D (2013) Differential connectivity of short- vs. long-range extrinsic and intrinsic cortical inputs to perirhinal neurons. J Comp Neurol, 521:2538-50.<\/p>\n<p>*Amano T, *Amir A, *Goswami S, Par\u00e9 D (2012) Morphology, PKC\u03b4 expression, and synaptic responsiveness of different types of rat central lateral amygdala neurons. J Neurophysiol [Epub ahead of print]<\/p>\n<p>*Goswami S, *Samuel S, *Sierra OR, *Cascardi M, Par\u00e9 D (2012) A rat model of post-traumatic stress disorder reproduces the hippocampal deficits seen in the human syndrome. Front Behav Neurosci, 6:26.<\/p>\n<p>Par\u00e9 D, *Duvarci S (2012) Amygdala microcircuits mediating fear expression and extinction. Curr Opin Neurobiol, 22:717-723.<\/p>\n<p>*Amano T, *Duvarci S, *Popa D, Par\u00e9 D (2011) The fear circuit revisited: contributions of the basal amygdala nuclei to conditioned fear. J Neurosci, 31:15481-15489.<\/p>\n<p>*Unal G, *Apergis-Schoute J, Par\u00e9 D (2011) Associative properties of the perirhinal network. Cereb Cortex, 22:1318-1332.<\/p>\n<p>*Amir A, *Amano T, Par\u00e9 D (2011) Physiological identification and infralimbic responsiveness of rat intercalated amygdala neurons. J Neurophysiol, 105:3054-3066.<\/p>\n<p>Li G, *Amano T, Par\u00e9 D, Nair SS (2011) Impact of infralimbic inputs on intercalated amygdala neurons: a biophysical modeling study. Learning and Memory, 18:226-240.<\/p>\n<p>*Duvarci S, *Popa D, Par\u00e9 D (2011) Central amygdala activity during fear conditioning. J Neurosci, 31:289-294.<\/p>\n<p>*Popescu AT, Par\u00e9 D (2011) Synaptic interactions underlying synchronized inhibition in the basal amygdala: evidence for existence of two types of projection cells. J Neurophysiol, 105:687-696.<\/p>\n<p>Quirk GJ, Par\u00e9 D, Richardson R, Herry C, Monfils MH, Schiller D, Vicentic A (2010) Erasing fear memories with extinction training. J Neurosci, 30:14993-14997.<\/p>\n<p>*Goswami S, *Cascardi M, *Rodriguez-Sierra OE, *Duvarci S, Par\u00e9 D (2010) Impact of predatory threat on fear extinction in Lewis rats. Learning and Memory, 17:494-501.<\/p>\n<p>*Popescu AT, *Saghyan AA, *Nagy FZ, Par\u00e9 D (2010) Facilitation of corticostriatal plasticity by the amygdala requires Ca2+-induced Ca2+ release in the ventral striatum. J Neurophysiol, 104:1673-1680.<\/p>\n<p>Pape HC, Par\u00e9 D (2010) Plastic synaptic networks of the amygdala for the acquisition, expression, and extinction of conditioned fear. Physiol Rev, 90:419-463.<\/p>\n<p>*Popa D, *Duvarci S, *Popescu AT, L\u00e9na C, Par\u00e9 D (2010) Coherent amygdalocortical theta promotes fear memory consolidation during paradoxical sleep. Proc Natl Acad Sci USA, 107:6516-6519.<\/p>\n<p>*Amano T, *Unal CT, Par\u00e9 D (2010) Synaptic correlates of fear extinction in the amygdala. Nature Neuroscience, 13:489-494.<\/p>\n<p>*Duvarci S, *Bauer EP, Par\u00e9 D (2009) The bed nucleus of the stria terminalis mediates inter-individual variations in anxiety and fear. J Neurosci, 29:10357-10361.<\/p>\n<p>*Popescu A, *Popa D, Par\u00e9 D (2009) Coherent gamma oscillations couple the amygdala and striatum during learning. Nature Neuroscience, 12:801-807.<\/p>\n<p>*Paz R, *Bauer EP, Par\u00e9 D (2009) A novel approach to study neuronal interactions between four simultaneously recorded brain regions. J Neurophysiol, 101:2507-15.<\/p>\n<p>*Popa D, *Popescu A, Par\u00e9 D (2009) Contrasting activity profile of two distributed cortical networks as a function of attentional demands. J Neurosci, 29:1191-201.<\/p>\n<p>*Nagy F, Par\u00e9 D (2008) Timing of impulses from the central amygdala and bed nucleus of the stria terminalis to the brainstem. J Neurophysiol, 100:3429-36.<\/p>\n<p>*Likhtik E, *Popa D, *Apergis-Schoute A, Fidacaro GA, Par\u00e9 D (2008) Amygdala intercalated neurons are required for expression of fear extinction. Nature, 454:642-645.<\/p>\n<p>*Paz R, *Bauer EP, Par\u00e9 D (2008) Theta synchronizes the activity of medial prefontal neurons during learning. Learning and Memory, 15:524-31.<\/p>\n<p>*Bauer EP, *Paz R, Par\u00e9 D (2007) Gamma oscillations coordinate amygdalo-rhinal interactions during learning. J Neurosci, 27:9369-9379.<\/p>\n<p>*Duvarci S, Par\u00e9 D, (2007) Glucocorticoids enhance the excitability of principal basolateral amygdala neurons. J Neurosci, 27:4482-4491.<\/p>\n<p>*Apergis-Schoute J, *Pinto A, Par\u00e9 D, (2007) Muscarinic control of long-range GABAergic inhibition within the rhinal cortices. J Neurosci, 27:4061-4071.<\/p>\n<p>*Paz R, *Bauer EP, Par\u00e9 D, (2007) Learning-related facilitation of rhinal interactions by medial prefrontal inputs. J Neurosci, 27:6542-6551.<\/p>\n<p>*Popescu AT, *Saghyan AA, Par\u00e9 D, (2007) NMDA-dependent facilitation of corticostriatal plasticity by the amygdala. Proc Natl Acad Sci USA, 104:341-346.<\/p>\n<p>*Likhtik E, *Pelletier JG, *Popescu AT, Par\u00e9 D, (2006) Identification of basolateral amygdala projection cells and interneurons using extracellular recordings. J Neurophysiol, 96:3257-3265.<\/p>\n<p>*Paz R, *Pelletier JG, *Bauer EP, Par\u00e9 D, (2006) Emotional enhancement of memory via amygdala-driven facilitation of rhinal interactions. Nature Neuroscience, 9:1321-1329.<\/p>\n<p>*Apergis-Schoute J, *Pinto A, Par\u00e9 D, (2006) Ultrastructural organization of medial prefrontal inputs to the rhinal cortices. Eur J Neurosci, 24:135-144.<\/p>\n<p>*Samson RD, Par\u00e9 D, Par\u00e9 D (2006) A spatially structured network of inhibitory and excitatory connections directs impulse traffic within the lateral amygdala. Neuroscience, 141:1599-1609.<\/p>\n<p>*Pinto A, *Fuentes C, Par\u00e9 D (2006) Feedforward inhibition regulates perirhinal transmission of neocortical inputs to the entorhinal cortex: ultrastructural study in guinea pigs. J Comp Neurol., 495:722-734.<\/p>\n<p>*Samson R, *Duvarci S, Par\u00e9 D (2005) Synaptic plasticity in the central nucleus of the amygdala. Reviews in the Neurosciences, 16:287-302.<\/p>\n<p>Rudolph M, *Pelletier J-G, Par\u00e9 D, Destexhe A (2005) Characterization of synaptic conductances and integrative properties during electrically-induced EEG activated states in neocortical neurons in vivo. J Neurophysiol., 94:1837-1848.<\/p>\n<p>*Likhtik E, *Pelletier J-G, *Paz R, Par\u00e9 D (2005) Prefrontal control of the amygdala. J Neurosci., 25:7429-7437.<\/p>\n<p>*Pelletier J-G, *Apergis-Schoute J, Par\u00e9 D (2005) Interaction between amygdala and neocortical inputs in the perirhinal cortex. J Neurophysiol., 94:1837-1848.<\/p>\n<p>*Pelletier J-G, *Likhtik E, *Filali M, Par\u00e9 D (2005) Lasting increases in basolateral amygdala activity after emotional arousal: implications for facilitated consolidation of emotional memories. Learning and Memory, 12:96-102.<\/p>\n<p>Berretta S, Pantazopoulos P, Pantazopoulos H, Par\u00e9 D (2005) Stimulation of the infralimbic cortex increases C-Fos expression in intercalated neurons of the amygdala. Neuroscience, 132:943-953.<\/p>\n<p>*Samson R, Par\u00e9 D (2005) Activity-dependent synaptic plasticity in the central nucleus of the amygdala. J. Neurosci., 25:1847-1855.<\/p>\n<p>De Curtis M, Par\u00e9 D (2004) The rhinal cortices: a wall of inhibition between the neocortex and hippocampus. Prog. Neurobiol., 74:101-110.<\/p>\n<p>Par\u00e9 D (2004) Presynaptic induction and expression of NMDA-dependent LTP. Trends in Neuroscience, 27:440-441.<\/p>\n<p>Par\u00e9 D, Quirk GJ, LeDoux JE (2004) New vistas on amygdala networks in conditioned fear. J. Neurophysiol., 92:1-9.<\/p>\n<p>*Pelletier JG, *Apergis J, Par\u00e9 D (2004) Low probability transmission of neocortical and entorhinal impulses through the perirhinal cortex. J. Neurophysiol., 91:2079-2089.<\/p>\n<p>Rudolph M, *Pelletier JG, Par\u00e9 D, Destexhe A (2004) Estimation of synaptic conductances and their variances from intracellular recordings of neocortical neurons in vivo. Neurocomputing, in press.<\/p>\n<p>*Pelletier JG, Par\u00e9 D (2004) Role of amygdala oscillations in the consolidation of emotional memories. Biol Psychiatry, 55: 559-562.<\/p>\n<p>Destexhe A, Rudolph M, Par\u00e9 D (2003) The high-conductance state of neocortical neurons in vivo. Nature Neurosci Rev, 4: 739-751.<\/p>\n<p>Quirk GJ, *Likhtik E, *Pelletier JG, Par\u00e9 D (2003) Stimulation of medial prefrontal cortex decreases the responsiveness of central amygdala output neurons. J Neurosci, 23: 8800-8807.<\/p>\n<p>Par\u00e9 D (2003) Role of the basolateral amygdala in memory consolidation. Prog Neurobiol, 70: 409-420.<\/p>\n<p>*Royer S, Par\u00e9 D (2003) Conservation of total synaptic weights via inverse homo- vs. heterosynaptic LTD and LTP. Nature 422: 518-522.<\/p>\n<p>*Samson R, Dumont EC, Par\u00e9 D (2003) Feedback inhibition defines transverse processing modules in the lateral amygdala. J. Neurosci. 23:1966-1973.<\/p>\n<p>*Royer S, Par\u00e9 D (2002) Bidirectional synaptic plasticity in intercalated amygdala neurons and the extinction of conditioned fear responses. Neuroscience, 115:455-462.<\/p>\n<p>Par\u00e9 D (2002) Mechanisms of Pavlovian fear conditioning: Has the engram been located? Trends in Neuroscience, 25:436-437.<\/p>\n<p>Par\u00e9 D, *Collins DR, *Pelletier, JG (2002) Amygdala oscillations and the consolidation of emotional memories. Trends in Cognitive Sciences 6:306-314.<\/p>\n<p>*Dumont \u00c9, *Martina M, *Samson R, Drolet G, Par\u00e9 D (2002) Physiological properties of central amygdala neurons: species differences. Eur. J. Neurosci. 15:545-552.<\/p>\n<p>*Pelletier JG, Par\u00e9 D (2002) Uniform range of conduction times from the lateral amygdala to distributed perirhinal sites. J. Neurophysiol. 87:1213-1221.<\/p>\n<p>*Martina M, *Royer S, Par\u00e9 D (2001) Cell-type specific GABA responses and chloride homeostasis in the cortex and amygdala. J. Neurophysiol. 86:2887-2895.<\/p>\n<p>*Martina M, *Royer S, Par\u00e9 D (2001) Propagation of neocortical inputs in the perirhinal cortex. J. Neurosci. 21:2878-2888.<\/p>\n<p>*Collins DR, *Pelletier JG, Par\u00e9 D (2001) Slow and fast (gamma) neuronal oscillations in the perirhinal cortex and lateral amygdala. J. Neurophysiol. 85:1661-1672.<\/p>\n<p>*Royer S, *Martina M, Par\u00e9 D (2000) Bistable behavior of inhibitory neurons controlling impulse traffic through the amygdala: role of a slowly deinactivating K+ current. J. Neurosci. 20:9034-9039.<\/p>\n<p>*Royer S, *Martina M, Par\u00e9 D (2000) Polarized synaptic interactions between intercalated neurons of the amygdala. J. Neurophysiol. 83:3509-3518.<\/p>\n<p>Destexhe A, Par\u00e9 D (2000) A combined computational and intracellular study of correlated synaptic bombardment in neocortical pyramidal neurons in vivo. Neurocomputing 32-33:113-119.<\/p>\n<p>*Collins DR, Par\u00e9 D (2000) Differential fear conditioning induces reciprocal changes in the sensory responses of the lateral amygdala neurons to the CS+ and CS-. Learning and Memory 7:97-103.<\/p>\n<p>Par\u00e9 D, *Collins DR (2000) Neuronal correlates of fear in the lateral amygdala: multiple extracellular recordings in conscious cats. J. Neurosci. 20:2701-2710.<\/p>\n<p>Smith Y, Par\u00e9 J-F, Par\u00e9 D (2000) Differential innervation of parvalbumin-immunoreactive interneurons of the basolateral amygdaloid complex by cortical and intrinsic inputs. J. Comp. Neurol. 416:496-508.<\/p>\n<p>*Royer S, *Martina M, Par\u00e9 D (1999) An inhibitory interface gates impulse traffic between the input and ouput stations of the amygdala. J. Neurosci. 19:10575-10583.<\/p>\n<p>*Martina M, *Royer S, Par\u00e9 D (1999) Physiological properties of central medial and central lateral amygdala neurons. J. Neurophysiol. 82:1843-1854.<\/p>\n<p>*Collins DR, Par\u00e9 D (1999) Spontaneous and evoked activity of intercalated amygdala neurons. Eur. J. Neurosci. 11:3441-3448.<\/p>\n<p>Destexhe A, Par\u00e9 D (1999) Impact of network activity on the integrative properties of neocortical pyramidal neurons. J. Neurophysiol. 81:1531-1547.<\/p>\n<p>*Collins DR, Par\u00e9 D (1999) Reciprocal changes in the firing probability of lateral and central medial amygdala neurons. J. Neurosci. 19:836-844.<\/p>\n<p>*Collins DR, *Lang EJ, Par\u00e9 D (1999) Spontaneous activity of the perirhinal cortex in behaving cats. Neuroscience 89:1025-1039.<\/p>\n<p>Par\u00e9 D, *Lang EJ (1998) Calcium electrogenesis in neocortical pyramidal neurons in vivo. Eur. J. Neurosci. 10:3164-3170.<\/p>\n<p>Par\u00e9 D, Smith Y (1998) Intrinsic circuitry of the amygdaloid complex: common principles of organization in rats and cats. Trends Neurosci. 21:240-241.<\/p>\n<p>Par\u00e9 D, *Shink E, *Gaudreau H, Destexhe A, *Lang EJ (1998) Impact of spontaneous synaptic activity on the resting properties of cat neocortical pyramidal neurons in vivo. J. Neurophysiol. 79:1450-1460.<\/p>\n<p>Smith Y, Par\u00e9 J-F, Par\u00e9 D (1998) Cat intra-amygdaloid inhibitory network: Ultrastructural organization of parvalbumin-immunoreactive elements. J. Comp. Neurol. 391:164-179.<\/p>\n<p>*Lang EJ and Par\u00e9 D (1998) Synaptic responsiveness of interneurons of the cat lateral amygdaloid nucleus. Neuroscience 83:877-889.<\/p>\n<p>Pape H-C, Par\u00e9 D, Driesang RB (1998) Two types of intrinsic oscillations in neurons of the lateral and basolateral nuclei of the amygdala. J. Neurophysiol. 79:205-216.<\/p>\n<p>Par\u00e9 D, *Lang EJ, Detexhe A (1998) Inhibitory control of somatodendritic interactions underlying action potentials in neocortical pyramidal neurons in vivo: Intracellular and computational study. Neuroscience 84:377-402.<\/p>\n<p>Par\u00e9 D, *Lebel E, *Lang EJ (1997) Differential impact of miniature synaptic potentials on the soma and dendrites of pyramidal neurons in vivo. J. Neurophysiol. 78:1735-1739.<\/p>\n<p>*Lang EJ, Par\u00e9 D (1997) Synaptic and synaptically-activated intrinsic conductances underlie inhibitory potentials in cat lateral amygdaloid projection neurons in vivo. J. Neurophysiol. 77:353-363.<\/p>\n<p>*Lang EJ, Par\u00e9 D (1997) Similar inhibitory processes dominate the responses of cat lateral amygdaloid projection neurons to their various afferents. J. Neurophysiol. 77:341-352.<\/p>\n<p>Par\u00e9 D, Smith Y (1996) Thalamic collaterals of corticostriatal axons: their termination field and synaptic targets in cats. J. Comp. Neurol. 372:1-17.<\/p>\n<p>Par\u00e9 D, *Gaudreau H (1996) Projection cells and interneurons of the basolateral amygdala: Distinct firing patterns and differential relation to theta and delta rhythms in conscious cats. J. Neurosci. 16:3334-3350.<\/p>\n<p>*Gaudreau H, Par\u00e9 D (1996) Projection neurons of the lateral nucleus are virtually silent throughout the sleep-waking cycle. J. Neurophysiol. 75:1301-1305.<\/p>\n<p>Par\u00e9 D, Smith Y (1995) Intra-amygdaloid projections of the basolateral and basomedial nuclei in the cat: PHA-L anterograde tracing at the light and electron microscopic level. Neuroscience 69:567-583.<\/p>\n<p>Par\u00e9 D, Pape H-C, *Dong J (1995) Bursting and oscillating neurons of the cat basolateral amygdaloid complex in vivo: electrophysiological properties and morphological features. J. Neurophysiol. 74:1179-1191.<\/p>\n<p>Charpak S, Par\u00e9 D, Llin\u00e1s RR (1995) The entorhinal cortex entrains fast CA1 hippocampal oscillations in the anaesthetized guinea pig: role of the monosynaptic component of the perforant path. Eur. J. Neurosci. 7:1548-1557.<\/p>\n<p>Par\u00e9 D, Llin\u00e1s RR (1995) Conscious and pre-conscious processes as seen from the standpoint of sleep-waking cycle neurophysiology. Neuropsychologia 33:1155-1168.<\/p>\n<p>Par\u00e9 D, *Dong, J, *Gaudreau, H (1995) Amygdalo-entorhinal relations and their reflection in the hippocampal formation: Genesis of sharp sleep potentials. J. Neurosci. 15:2482-2503.<\/p>\n<p>Par\u00e9 D, Llin\u00e1s RR (1995) Intracellular study of direct entorhinal inputs to field CA1 in the isolated guinea pig brain in vitro. Hippocampus 5:115-119.<\/p>\n<p>Par\u00e9 D, Llin\u00e1s RR (1994) Non-lamellar propagation of entorhinal influences in the hippocampal formation: Multiple electrode recording in the isolated guinea pig brain in vitro. Hippocampus 4:403-409.<\/p>\n<p>Smith Y, Par\u00e9 D (1994) Intra-amygdaloid projections of the lateral nucleus in the cat: PHA-L anterograde labeling combined with post-embedding GABA and glutamate immunocytochemistry. J. Comp. Neurol. 342:232-248.<\/p>\n<p>Par\u00e9 D, Smith Y (1994) GABAergic projection from the intercalated cell masses of the amygdala to the basal forebrain in cats. J. Comp. Neurol. 344:33-49.<\/p>\n<p>Par\u00e9 D, Smith Y (1993) The intercalated cell masses project to the central and medial nuclei of the amygdala in cats. Neuroscience 57:1077-1090.<\/p>\n<p>Par\u00e9 D, Smith Y (1993) Distribution of GABA immunoreactivity in the amygdaloid complex of the cat. Neuroscience 57:1961-1076.<\/p>\n<p>Par\u00e9 D, Steriade M (1993) The reticular thalamic nucleus projects to the contralateral dorsal thalamus in macaque monkey. Neurosci. Lett. 154:96-100.<\/p>\n<p>Par\u00e9 D, deCurtis M, Llin\u00e1s RR (1992) Role of the entorhinal-hippocampal loop in temporal lobe epilepsy. Extra- and intracellular study in the isolated guinea pig brain in vitro. J. Neurosci. 12:1867-1881.<\/p>\n<p>Dossi RC, Par\u00e9 D, Steriade M (1992) Various types of inhibitory postsynaptic potentials in anterior thalamic cells are differentially altered by stimulation of laterodorsal tegmental cholinergic nucleus. Neuroscience 47:279-289.<\/p>\n<p>deCurtis M, Par\u00e9 D, Llin\u00e1s RR (1991) The electrophysiology of the olfactory-hippocampal circuit in the isolated and perfused adult mammalian brain in vitro. Hippocampus 1:341-354.<\/p>\n<p>Datta S, Dossi RC, Par\u00e9 D, Oakson G, Steriade M (1991) Substantia nigra reticulata neurons during sleep-waking states: Relation with Ponto-Geniculo-Occipital waves. Brain Res. 566:344-347.<\/p>\n<p>Par\u00e9 D, Dossi RC, Steriade M (1991) Three types of inhibitory post-synaptic potentials generated by interneurons in the anterior thalamic complex of the cat. J. Neurophysiol. 66:1190-1205. <a href=\"https:\/\/doi.org\/10.1152\/jn.1991.66.4.1190\">doi: 10.1152\/jn.1991.66.4.1190<\/a>\u00a0 \u00a0 \u00a0<a href=\"https:\/\/rutgers.box.com\/s\/t73j3fitan15ajnga7sad25df8s057uz\">PDF<\/a><\/p>\n<p>Llin\u00e1s RR, Par\u00e9 D (1991) Of dreaming and wakefulness. Neuroscience 44:521-535.<\/p>\n<p>Steriade M, Dossi RC, Par\u00e9 D, Oakson G (1991) Fast oscillations (20-40 Hz) in thalamocortical systems and their potentiation by mesopontine cholinergic nuclei in the cat. Proc. Natl. Acad. Sci. USA 88:4396-4400.<\/p>\n<p>Dossi RC, Par\u00e9 D, Steriade M (1991) Short-lasting nicotinic and long-lasting muscarinic depolarizing responses of thalamocortical neurons to stimulation of mesopontine cholinergic nuclei. J. Neurophysiol. 65:393-406.<\/p>\n<p>Par\u00e9 D, Hazrati L N, Parent A, Steriade M (1990) Substantia nigra pars reticulata projects to the reticular thalamic nucleus of the cat: a morphological and electrophysiological study. Brain Res. 535:139-146.<\/p>\n<p>Par\u00e9 D, Dossi RC, Datta S, Steriade M (1990) Brainstem genesis of reserpine-induced ponto-geniculo-occipital waves: an electrophysiological and morphological investigation. Exp. Brain Res. 81:533-544.<\/p>\n<p>Steriade M, Par\u00e9 D, Datta S, Oakson G, Dossi RC (1990) Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves. J. Neurosci. 10:2546-2565.<\/p>\n<p>Steriade M, Datta S, Par\u00e9 D, Oakson G, Dossi RC (1990) Neuronal activities in brainstem cholinergic nuclei related to tonic activation processes in thalamocortical systems. J. Neurosci. 10:2527-2545.<\/p>\n<p>Par\u00e9 D, Smith Y, Parent A, Steriade M (1990) Neuronal activity of identified posterior hypothalamic neurons projecting to the brainstem peribrachial area of the cat. Neurosci. Lett. 107:145-150.<\/p>\n<p>Par\u00e9 D, Dossi RC, Steriade M (1990) Neuronal basis of the parkinsonian resting tremor: a hypothesis and its implications for treatment. Neuroscience 35:217-226.<\/p>\n<p>Par\u00e9 D, Bouhassira D, Oakson G, Datta S (1990) Spontaneous and evoked activities of anterior thalamic neurons during waking and sleep states. Exp. Brain Res. 80:54-62.<\/p>\n<p>Par\u00e9 D, Steriade M, Desch\u00eanes M, Bouhassira D (1990) Prolonged enhancement of anterior thalamic synaptic responsiveness by stimulation of a brainstem cholinergic group. J. Neurosci. 10:20-33.<\/p>\n<p>Steriade M, Par\u00e9 D, Bouhassira D, Desch\u00eanes M, Oakson G (1989) Phasic activation of lateral geniculate and perigeniculate thalamic neurons during sleep with ponto-geniculo-occipital waves. J. Neurosci. 9:2215-2229.<\/p>\n<p>Smith Y, Par\u00e9 D, Desch\u00eanes M, Parent A, Steriade M (1988) Cholinergic and non-cholinergic projections from the upper brainstem core to the visual thalamus in the cat. Exp. Brain Res. 70:166-180.<\/p>\n<p>Steriade M, Par\u00e9 D, Parent A, Smith Y (1988) Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey. Neuroscience 25:47-67.<\/p>\n<p>Parent A, Par\u00e9 D, Smith Y, Steriade M (1988) Basal forebrain cholinergic and non-cholinergic projections to the thalamus and brainstem in cats and monkeys. J. Comp. Neurol. 277:281-301.<\/p>\n<p>Par\u00e9 D, Smith Y, Parent A, Steriade M (1988) Projections of brainstem core cholinergic and non-cholinergic neurons of cat to intralaminar and reticular thalamic nuclei. Neuroscience 25:69-86.<\/p>\n<p>Steriade M, Parent A, Par\u00e9 D, Smith Y (1987) Cholinergic and non-cholinergic neurons of cat basal forebrain project to reticular and mediodorsal thalamic nuclei. Brain Res. 408:372-376.<\/p>\n<p>Par\u00e9 D, Oakson G, Desch\u00eanes M, Steriade M (1987) Physiological characteristics of anterior thalamic nuclei, a group devoid of inputs from the reticular thalamic nucleus. J. Neurophysiol. 57:1669-1685.<\/p>\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Par%C3%A9+D+Rutgers\">For all articles<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><strong>Book Chapters and Other Invited Communications<\/strong><\/p>\n<p>Bauer EP, Pare D (2016) Behavioral Neuroscience of circuits involved in fear processing. In: Neurobiology of PTSD. K Ressler and I Liberzon editors. Oxford University Press, in press.<\/p>\n<p>Par\u00e9 D (2009) The amygdala (rodents and felines). In: The New Encyclopedia of Neuroscience. LR Squire, ed. Elsevier, Oxford, UK.<\/p>\n<p>Duvarci S, Par\u00e9 D (2007 March 27) \u201cCan we control our fears?\u201d In Mind Matters, the Scientific American blog on science and mind. http:\/\/blog.sciam.com\/index.php?title=can_we_control_our_fears_1<\/p>\n<p>Par\u00e9 D, *Royer S, Smith Y, Lang EJ (2003) Contextual inhibitory gating of impulse traffic in the intra-amygdaloid network. Annals of the New York Academy of Science 985: 78-91.<\/p>\n<p>Destexhe A, Lang EJ, Par\u00e9 D (1998) Somato-dendritic interactions underlying action potential generation in neocortical pyramidal cells in vivo. In: Computational Neuroscience. Trends in Research, Plenum Press, New York, pp. 167-172.<\/p>\n<p>Llin\u00e1s RR, Par\u00e9 D (1997) Coherent oscillations in specific and nonspecific thalamocortical networks and their role in cognition. In: Thalamus. M Steriade, EG Jones and DA McCormick, eds, Pergamon, New York, pp. 501-516.<\/p>\n<p>Llin\u00e1s RR, Par\u00e9 D (1996) The brain as a closed system modulated by the senses. In: The Mind-Brain Continuum. RR Llin\u00e1s, P Churchland and A DeMolina, eds, MIT Press, Cambridge, pp.1-18.<\/p>\n<p>Llin\u00e1s RR, Par\u00e9 D (1994) The role of intrinsic neuronal oscillations and network ensembles in the genesis of normal and pathological tremors. In: Handbook of Tremor Disorders. LJ Findley and WC Koller, eds, Marcel Dekker, New York, pp. 7-36.<\/p>\n<p>DeCurtis M, Par\u00e9 D, Llin\u00e1s RR (1993) Epileptogenesis in the hippocampus of the isolated guinea pig maintained in vitro: A model for limbic seizures. In: Epileptogenic and Excitotoxic Mechanisms, pp. 79-87. G Avanzini, R Sariello, U Heinneman and R Mutani, eds, John Libbey, London.<\/p>\n<p>Steriade M, Dossi RC, Par\u00e9 D (1991) Mesopontine cholinergic systems suppress slow rhythms and induce fast oscillations in thalamocortical circuits. In: Induced Rhythms in the Brain, pp. 251-267. E Basar and TH Bullock, eds, Birkhauser, Boston.<\/p>\n<p>Steriade M, Par\u00e9 D (1990) Brainstem genesis and thalamic transfer of internal signals during dreaming sleep: cellular data and hypotheses. In: Basic Mechanisms of Sleep, pp. 148-162. J Montplaisir and R Godbout, eds, Oxford University Press, New York.<\/p>\n<p>Par\u00e9 D, Steriade M (1990) Control of the mammillothalamic axis by brainstem cholinergic laterodorsal tegmental afferents: possible involvement in mnemonic processes. In: Brain Cholinergic Systems, 337-354. M Steriade &amp; D Biesold, eds, Oxford Univ Press, New York.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Books<\/strong><\/p>\n<p>Steriade M, Par\u00e9 D (2008) Gating in Cerebral Networks. Cambridge University Press.<\/p>\n<p>Steriade M, Par\u00e9 D, Hu B, Desch\u00eanes M (1990) The visual thalamocortical system and its modulation by the brainstem core. In: Progress in Sensory Physiology, Vol. 10, pp. 1-124. D Ottosen, eds, Springer, Heideberg-New York.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Publications Asterisks indicate research trainees. *Kim IT, Huerta-Ocampo I, *Urena O, Yamamoto R, Pare\u0301 D (2025) Collateralization patterns of principal basolateral amygdala neurons delineate distinct output streams. iScience. doi: 10.1016\/j.isci.2025.113089 &hellip; <a href=\"https:\/\/sites.rutgers.edu\/pare-lab\/publications\/\" class=\"\">Read More<\/a><\/p>\n","protected":false},"author":680,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-486","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Publications - Denis Par\u00e9 lab<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sites.rutgers.edu\/pare-lab\/publications\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Denis Par\u00e9 lab\" \/>\n<meta property=\"og:description\" content=\"Publications Asterisks indicate research trainees. *Kim IT, Huerta-Ocampo I, *Urena O, Yamamoto R, Pare\u0301 D (2025) Collateralization patterns of principal basolateral amygdala neurons delineate distinct output streams. iScience. doi: 10.1016\/j.isci.2025.113089 &hellip; 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