The limbic system
Open accessAbstract
“The hypothalamus, the anterior thalamic nucleus, the cingulate gyrus, the hippocampus and their interconnections, constitute a harmonious mechanism which may elaborate the functions of central emotion as well as participate in the emotional expression.” James Papez, 1937 The limbic system consists of the phylogenetically old limbic lobe and other subcortical structures and their connections. Although not empirically proven, the limbic system is a functional concept which may be employed to explain various brain functions.[1] HISTORY Paul Pierre Broca in 1878 spoke of ‘le grand lobe limbique’ or the great limbic lobe and applied the term “limbic” (from the Latin limbus for border) to the curved rim of the cortex which incudes the cingulate and the parahippocampal gyri. However, its putative role in emotion was elaborated by the American physician, James Papez in 1937 in the seminal paper titled ‘A proposed mechanism of emotion’. This anatomical model is referred to as the Papez circuit.[2] Yakovlev in 1948 proposed Yakovlev's circuit in the control of emotion involving the orbitofrontal, insular and anterior temporal lobe cortex, the amygdala and the dorsomedial nucleus of thalamus.[3] In 1952, Paul D. MacLean coined the term “limbic system” to describe Broca's limbic lobe and related subcortical nuclei as the collective neural substrate for emotion.[1] MacLean was also instrumental in proposing and defining the Triune concept of the brain. MacLean's evolutionary “Triune brain theory” proposed that the human brain was in reality three brains in one: the R-complex (reptilian complex), the limbic system and the neocortex.[4] The concept of the limbic system has since been further expanded and developed by Nauta, Heimer and others. COMPONENTS OF THE LIMBIC SYSTEM There is no universal agreement on the total list of structures, which comprise the limbic system. The brain regions that constitute the limbic system are: Limbic cortex Cingulate gyrus Parahippocampal gyrus Hippocampal formation The dentate gyrus Hippocampus Subicular Complex Amygdala Septal area Hypothalamus These structures form a complex network for controlling emotion.[5] Limbic lobe The limbic lobe situated at the inferomedial aspect of the cerebral hemispheres, consists of two concentric gyri surrounding the corpus callosum. Broca proposed that the larger outer gyrus be named “limbic gyrus” and the smaller inner one “the intralimbic gyrus”. The limbic gyrus (limbic lobe) consists of the isthmus of the cingulate gyrus, the parahippocampal gyrus (both of which are continuous via a bundle of white matter called “cingulum”) and the subcallosal area.[6] The cingulate gyrus (Latin = Belt ridge) dorsal to the corpus callosum is heavily interconnected with the association areas of the cerebral cortex. The parahippocampal gyrus in the medial temporal lobe contains several distinct regions, the most important being the entorhinal cortex (ERC). The ERC funnels highly processed cortical information to the hippocampal formation and serves as its major output pathway.[5] The hippocampal formation Hippocampal formation in the temporal lobe has three distinct zones: The dentate gyrus The hippocampus proper The subiculum Embryologically, the hippocampal formation is an extension of the medial edge of the temporal lobe. The entire hippocampal formation has a length of about 5 cm from its anterior end at the amygdala to its tapering posterior end near the splenium of the corpus callosum.[5] Dentate gyrus The dentate gyrus is composed of three layers: an outer acellular molecular layer, a granular middle layer and an inner polymorphic layer. Hippocampus The word hippocampus means “Sea Horse” in Greek. Hippocampus is a trilaminate structure with an outer molecular layer, a middle pyramidal layer and an inner polymorphic layer. On the basis of differences in cytoarchitecture and connectivity, the hippocampus has four fields (named by Lorente de No in 1934): CA1, CA2, CA3 and CA4 (CA: Cornu Ammonis). To embryologic enthusiasts, CA4 is not part of the Cornu Ammonis but is a separate structure—the dentate hilus. The thin layer of fibers adjacent to the polymorphic layer of the hippocampus is known as the alveus. These fibres coalesce to form the fimbria and subsequently, the crura of the fornix (main efferent pathway of the hippocampal formation). The crura of the fornix converge to form the body of the fornix, which later forms the columns of the fornix and pass through the hypothalamus into the mammillary bodies.[57] Subicular complex The subicular complex has three components: the presubiculum, the parasubiculum and subiculum. Subiculum is the transitional zone between the six-layered, entorhinal cortex and the three-layered hippocampus.[5] Amygdala Identified by Burdach in the early 19th century, amygdala, an almond-shaped structure deep within the temporal lobe, is a collection of nuclei lying beneath the uncus. Lying at the anterior end of the hippocampal formati
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When the connection between the limbic system and hypothalamus is impaired, emotional lability can occur.
“so when the connection between the two is impaired, emotional lability can occur.”
From Approach to the patient with acquired hypothalamic syndrome (2026) · cites this paper as [86]
The opening passage identifies the hypothalamus and its interconnections as involved in emotional expression, and the Emotional responses section describes hypothalamic involvement in fear and rage. Neither passage says that impaired connections between the limbic system and hypothalamus cause emotional lability; the Affective disorders section discusses dysfunction of a different network. No page numbers are available in our copy. (LLM, conf=0.77)
Experimental — accuracy not yet measuredThe limbic system affects emotional regulation and is integrally connected to the hypothalamus.
“The limbic system affects emotional regulation and is integrally connected to the hypothalamus (86), so when the connection between the two is impaired, emotional lability can occur.”
From Approach to the patient with acquired hypothalamic syndrome (2026) · cites this paper as [86]
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A PROPOSED MECHANISM OF EMOTION
PAPEZ, J. W. (1937) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1937.02260220069003 · Cited by 3,563 · see citing works
The Neural Basis of Addiction: A Pathology of Motivation and Choice
Kalivas, P. W., & Volkow, N. D. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.8.1403 · Cited by 2,757 · see citing works
The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress
Smith, S. M., & Vale, W. W. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/ssmith · Cited by 1,948 · see citing works
Cognitive neuroscience of emotional memory
LaBar, K. S., & Cabeza, R. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1825 · Cited by 1,834 · 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
The sleep switch: hypothalamic control of sleep and wakefulness
Saper, C. B., Chou, T. C., & Scammell, T. E. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02002-6 · Cited by 1,656 · see citing works
Adolphs, R., Tranel, D., Damasio, H., & Damasio, A. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-09-05879.1995 · Cited by 1,138 · see citing works
The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings
Strakowski, S. M., DelBello, M. P., & Adler, C. M. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001585 · Cited by 818 · see citing works
Frontal Cortical and Left Temporal Glutamatergic Dysfunction in Schizophrenia
Deakin, J. F. W., Slater, P., Simpson, M. D. C., Gilchrist, A., Skan, W., Royston, M. C., Reynolds, G. P., & Cross, A. J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb07257.x · Cited by 386 · see citing works
Extended Amygdala and Basal Forebrain
Alheid, G. F. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07082.x · Cited by 334 · see citing works
MOTILITY, BEHAVIOR AND THE BRAIN*
Yakovlev, P. I. (1948) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-194810740-00001 · Cited by 236 · see citing works
Neuroimaging in Alzheimer disease: an evidence-based review
Kantarci, K., & Jack, C. R. (2003) · Neuroimaging Clinics of North America · doi:10.1016/s1052-5149(03)00025-x · Cited by 227 · see citing works
Central control of penile erection: Role of the paraventricular nucleus of the hypothalamus
Argiolas, A., & Melis, M. R. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.06.002 · Cited by 227 · see citing works
Neural Circuitry of Anxiety: Evidence from Structural and Functional Neuroimaging Studies
Cannistraro, P. A., Rauch, S. L., Rauch, A. S. L., & MD (2025) · Psychopharmacology Bulletin · doi:10.64719/pb.4161 · Cited by 199 · see citing works
Getting his act together: Roles of glutamate, nitric oxide, and dopamine in the medial preoptic area
Hull, E. M., & Dominguez, J. M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.08.031 · Cited by 181 · see citing works
Paraneoplastic limbic encephalitis: clinico-pathological correlations.
Bakheit, A. M. O., Kennedy, P. G. E., & Behan, P. O. (1990) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.53.12.1084 · Cited by 96 · see citing works
Chan, S., Erickson, J. K., & Yoon, S.-D. (1997) · Radiographics · doi:10.1148/radiographics.17.5.9308104 · Cited by 64 · see citing works
Limbic Lobe of the Human Brain: Evaluation with Turbo Fluid-attenuated Inversion-Recovery MR Imaging
Hirai, T., Korogi, Y., Yoshizumi, K., Shigematsu, Y., Sugahara, T., & Takahashi, M. (2000) · Radiology · doi:10.1148/radiology.215.2.r00ma06470 · Cited by 63 · see citing works
Brain mechanisms for 'having a theory of mind'
Frith, C. (1996) · Journal of Psychopharmacology · doi:10.1177/026988119601000103 · Cited by 30 · see citing works
Mark, L. P., Daniels, D. L., Tp, N., & Hendrix, L. E. (1995) · PubMed Central · Cited by 26 · see citing works
The limbic system: An outline and brief history of its concept
Nakano, I. (1998) · Neuropathology · doi:10.1111/j.1440-1789.1998.tb00102.x · Cited by 21 · see citing works
Hippocampal anatomy and pathologic alterations on conventional MR images.
Mark, L. P., Daniels, D. L., Naidich, T. P., & Williams, A. L. (1993) · PubMed Central · Cited by 9 · see citing works
Flagged first, then by citations
2 of the 24 references couldn’t be matched to a known paper.
Research works printed but not linked: 7
- [4]Maclean PD The triune brain in evolution: Role in paleocerebral functions 1990 New York Plenum Press 17797318
- [5]Pierri JN Lewis DA Sadock BJ Sadock VA Functional neuroanatomy Kaplan and Sadock's Comprehensive textbook of psychiatry 8th ed Phildelphia Lippincott William and Wilkins 3 33
- [13]Ganong WF Smell and taste review of medical physiology 2003 21st ed McGraw Hill Companies Inc 188 91
- [14]Ganong WF Neural basis of instinctual behavior and emotions In Review of Medical Physiology 2003 21st ed McGraw Hill Companies Inc 260 9
- [15]Benca RM Cirelli C Rattenborg MC Tononi G Sadock BJ Sadock VA Basic science of sleep Kaplan and Sadock's Comprehensive textbook of psychiatry 8th ed Phildelphia Lippincott William and Wilkins 280 95
- [23]Paller KA Squire LR Sadock BJ Sadock VA Biology of memory Kaplan and Sadock's Comprehensive textbook of psychiatry 8th ed Phildelphia Lippincott William and Wilkins 553 66
- [31]Hechtman L Sadock BJ Sadock VA Attention-deficit/hyperactivity disorder Kaplan and Sadock's Comprehensive textbook of psychiatry 8th ed Phildelphia Lippincott William and Wilkins 3183 97
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Long, H., Wang, Y., Jian, F., Liao, L., Yang, X., & Lai, W. (2016) · International Journal of Oral Science · doi:10.1038/ijos.2016.24 · Cited by 169 · see citing works
Douet, V., & Chang, L. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00343 · Cited by 122 · see citing works
Kamali, A., Milosavljevic, S., Gandhi, A., Lano, K. R., Shobeiri, P., Sherbaf, F. G., Sair, H. I., Riascos, R., & Hasan, K. M. (2023) · Brain Topography · doi:10.1007/s10548-023-00955-y · Cited by 118 · see citing works
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Sengupta, A., & Holmes, A. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.029 · Cited by 113 · see citing works
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Ancona, A., Petito, C., Iavarone, I., Petito, V., Galasso, L., Leonetti, A., Turchini, L., Belella, D., Ferrarese, D., Addolorato, G., et al. (2020) · Digestive and Liver Disease · doi:10.1016/j.dld.2020.11.026 · Cited by 111 · see citing works
Hescham, S., Lim, L. W., Jahanshahi, A., Steinbusch, H. W. M., Prickaerts, J., Blokland, A., & Temel, Y. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.01.008 · Cited by 106 · see citing works
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Enatsu, R., Gonzalez-Martinez, J. A., Bulacio, J. C., Kubota, Y., Mosher, J. C., Burgess, R. C., Najm, I., & Nair, D. R. (2014) · Cortex · doi:10.1016/j.cortex.2014.06.018 · Cited by 105 · see citing works
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Saad, J. F., Griffiths, K. R., Kohn, M. R., Clarke, S. P., Williams, L. M., & Korgaonkar, M. S. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.05.016 · Cited by 62 · see citing works
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Torres-Vega, A., Pliego‐Rivero, B., Otero, G., Gómez‐Oliván, L. M., & Vieyra-Reyes, P. (2012) · Nutrition Reviews · doi:10.1111/j.1753-4887.2012.00521.x · Cited by 54 · see citing works
Fontes, K., Rohlicek, C. V., Saint‐Martin, C., Gilbert, G., Easson, K., Majnemer, A., Marelli, A. J., Chakravarty, M. M., & Brossard‐Racine, M. (2019) · Human Brain Mapping · doi:10.1002/hbm.24615 · Cited by 50 · see citing works
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Long, J., Li, H., Liu, Y., Liao, X., Tang, Z., Han, K., Chen, J., & Zhang, H. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1364858 · Cited by 43 · see citing works
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Kandilarova, S., Stoyanov, D., Paunova, R., Todeva-Radneva, A., Aryutova, K., & Maes, M. H. J. (2021) · Journal of Personalized Medicine · doi:10.3390/jpm11111110 · Cited by 34 · see citing works
Deep brain stimulation of fornix for memory improvement in Alzheimer’s disease: A critical review
Li, R., Zhang, C., Rao, Y., & Yuan, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101668 · Cited by 34 · see citing works
Abijo, T., Blum, K., & Gondré‐Lewis, M. C. (2019) · Current Neuropharmacology · doi:10.2174/1570159x17666191118125702 · Cited by 33 · see citing works
Wang, X., Yu, Y., Zhao, W., Li, Q., Li, X., Li, S., Yin, C., & Han, Y. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00342 · Cited by 31 · see citing works
Chen, S., Wang, J., Çiçek, A. E., Roeder, K., Yu, H., & Devlin, B. (2020) · Molecular Autism · doi:10.1186/s13229-020-00386-7 · Cited by 31 · see citing works
Sandini, T. M., Reis-Silva, T. M., Moreira, N. C. D. S., Bernardi, M. M., Lebrun, I., & Spinosa, H. D. S. (2018) · Nutritional Neuroscience · doi:10.1080/1028415x.2018.1447296 · Cited by 31 · see citing works
Kampaite, A., Gustafsson, R., York, E. N., Foley, P., MacDougall, N., Bastin, M. E., Chandran, S., Waldman, A. D., & Meijboom, R. (2024) · PLoS ONE · doi:10.1371/journal.pone.0299634 · Cited by 29 · see citing works
Life and death in the hippocampus: What's bad?
Santos, V. R., de Melo, I. S., Pacheco, A. L. D., & de Castro, O. W. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.106595 · Cited by 29 · see citing works
Irritability and brain volume in adolescents: cross-sectional and longitudinal associations
Dennis, E. L., Humphreys, K. L., King, L. S., Thompson, P. M., & Gotlib, I. H. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz053 · Cited by 28 · see citing works
Davies, J. E., Gander, P. E., & Hall, D. A. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00031 · Cited by 28 · see citing works
Connaughton, M., O’Hanlon, E., Silk, T. J., Paterson, J., O’Neill, A., Anderson, V. A., Whelan, R., & McGrath, J. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.10.005 · Cited by 27 · see citing works
Different levels of brain-derived neurotrophic factor and cortisol in healthy heavy smokers
Neves, C. D. C., Lacerda, A. C. R., Lima, L. P., Lage, V. K. D. S., Balthazar, C. H., Leite, H. R., & Mendonça, V. A. (2017) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x20176424 · Cited by 27 · see citing works
Structural and functional brain correlates of theory of mind impairment post-stroke
D, J. F. D., Nott, Z. E., Horne, K., Prangley, T., Adams, A. G., Henry, J. D., & Molenberghs, P. (2019) · Cortex · doi:10.1016/j.cortex.2019.09.017 · Cited by 27 · see citing works
Ke, T., Simoni, S. D., Barker, E. D., & Smith, P. A. (2022) · JCPP Advances · doi:10.1002/jcv2.12081 · Cited by 27 · see citing works
Parsaei, M., Taghavizanjani, F., Cattarinussi, G., Moghaddam, H. S., Camillo, F. D., Akhondzadeh, S., Sambataro, F., Brambilla, P., & Delvecchio, G. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.08.034 · Cited by 27 · see citing works
Belda, A. P., Díaz‐Parra, A., & Moratal, D. (2018) · Diagnostics · doi:10.3390/diagnostics8030051 · Cited by 26 · see citing works
Delvecchio, G., Mandolini, G. M., Arighi, A., Prunas, C., Mauri, C. M., Pietroboni, A. M., Marotta, G., Cinnante, C. M., Triulzi, F. M., Galimberti, D., et al. (2018) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867418815976 · Cited by 26 · see citing works
Brain network remodelling reflects tau-related pathology prior to memory deficits in Thy-Tau22 mice
Degiorgis, L., Karatas, M., Sourty, M., Faivre, É., Lamy, J., Noblet, V., Bienert, T., Reisert, M., von Elverfeldt, D., Buée, L., et al. (2020) · Brain · doi:10.1093/brain/awaa312 · Cited by 25 · see citing works
Rivera-Bonet, C. N., Hermann, B. P., Cook, C. J., Hwang, G., Dabbs, K., Nair, V. A., Forseth, C., Mathis, J. R., Allen, L., Almane, D. N., et al. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.07.025 · Cited by 24 · see citing works
Russell, A. L., Grimes, J. M., Larco, D. O., Cruthirds, D. F., Westerfield, J., Wooten, L., Keil, M. F., Weiser, M. J., Landauer, M. R., Handa, R. J., et al. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.01.011 · Cited by 24 · see citing works
Fathi, D., Abulsoud, A. I., Saad, M. A., Nassar, N. N., Maksimos, M., Rizk, S. M., & Senousy, M. A. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119904 · Cited by 23 · see citing works
Cerebral chemoarchitecture shares organizational traits with brain structure and function
Hänisch, B., Hansen, J. Y., Bernhardt, B. C., Eickhoff, S. B., Dukart, J., Mišić, B., & Valk, S. L. (2023) · eLife · doi:10.7554/elife.83843 · Cited by 23 · see citing works
Deng, R., Yang, X., Meng, Y., Tao, Y., Wang, H.-Y., Li, X., Wei, W., Yu, H., Wang, Q., Deng, W., et al. (2022) · BMC Psychiatry · doi:10.1186/s12888-022-03782-w · Cited by 22 · see citing works
Prompiengchai, S., & Dunlop, K. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01907-1 · Cited by 22 · see citing works
Training-Induced Neuroplasticity in Children with Developmental Coordination Disorder
Izadi‐Najafabadi, S., Gill, K. K., & Zwicker, J. G. (2020) · Current Developmental Disorders Reports · doi:10.1007/s40474-020-00191-0 · Cited by 22 · see citing works
Maňoušek, J., Kala, P., Lokaj, P., Ondrúš, T., Helánová, K., Miklíková, M., Brázdil, V., Tomandlová, M., Pařenica, J., Goldbergová, M. P., et al. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.732708 · Cited by 22 · see citing works
The role of sleep in aesthetic perception and empathy: A mediation analysis
Peretti, S., Tempesta, D., Socci, V., Pino, M. C., Mazza, M., Valenti, M., Gennaro, L. D., Dio, C. D., Marchetti, A., & Ferrara, M. (2018) · Journal of Sleep Research · doi:10.1111/jsr.12664 · Cited by 20 · see citing works
Differential longitudinal changes of hippocampal subfields in patients with anorexia nervosa
Bahnsen, K., Wronski, M., Keeler, J. L., King, J. A., Preusker, Q., Kolb, T., Weidner, K., Roessner, V., Bernardoni, F., & Ehrlich, S. (2023) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13626 · Cited by 20 · see citing works
The Impact of Digital Technologies on Memory and Memory Studies
Călınescu, A. (2024) · Journal of Contemporary Philosophical and Anthropological Studies · doi:10.59652/jcpas.v2i1.161 · Cited by 20 · see citing works
Hwang, S., Martins, J. S., Douglas, R. J., Choi, J. J., Sinha, R., & Seo, D. (2021) · Alcohol and Alcoholism · doi:10.1093/alcalc/agab064 · Cited by 20 · see citing works
Zhou, H., Fei, Z., Hong, Q., Sun, J., Du, S., Li, T., & Zhang, J. (2022) · IEEE Transactions on Cognitive and Developmental Systems · doi:10.1109/tcds.2022.3200470 · Cited by 20 · see citing works
Al-Tubaikh, J. A. (2023) · Springer eBooks · doi:10.1007/978-3-031-28575-2_16 · Cited by 20 · see citing works
Multimodal classification of neurons in the lateral septumPreprint
Reid, C. M., Ren, Y., Simon, R., Xie, Y., Garcίa, M. T., Tran, D., Vu, S., Liu, J., Adam, M. A., Hanson, S. M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.15.580381 · Cited by 20 · see citing works
Stocco, A., Rice, P. G., Thomson, R., Smith, B. M., Morrison, D., & Lebiere, C. J. (2023) · Computational Brain & Behavior · doi:10.1007/s42113-023-00189-y · Cited by 19 · see citing works
Gray Matter Volume Changes in Patients With Acute Eye Pain: A Voxel-Based Morphometry Study
Lan, D., Zhu, P., He, Y. Z., Xu, Q., Su, T., Li, B., Shi, W., Lin, Q., Yang, Y.-C., Yuan, Q., et al. (2019) · Translational Vision Science & Technology · doi:10.1167/tvst.8.1.1 · Cited by 19 · see citing works
Khalifeh, N., Omary, A., Cotter, D. L., Kim, M. S., Geffner, M. E., & Herting, M. M. (2022) · Journal of Child Neurology · doi:10.1177/08830738221100886 · Cited by 18 · see citing works
Shvarzman, R., Crocetti, D., Rosch, K. S., Li, X., & Mostofsky, S. H. (2022) · Experimental Brain Research · doi:10.1007/s00221-022-06484-7 · Cited by 18 · see citing works
Sahoo, S., Kharkar, P. S., Sahu, N. U., & Brijesh, S. (2020) · Phytotherapy Research · doi:10.1002/ptr.6900 · Cited by 18 · see citing works
Esrael, S. M. A. M., Hamed, A. M. M., Khedr, E. M., & Soliman, R. K. (2021) · The Egyptian Journal of Radiology and Nuclear Medicine · doi:10.1186/s43055-021-00460-x · Cited by 18 · see citing works
The role of phosphodiesterase 4 in excessive daytime sleepiness in Parkinson's disease
Wilson, H., Pagano, G., Niccolini, F., Muhlert, N., Mehta, M. A., Searle, G. E., Gunn, R. N., Rabiner, E. A., Foltynie, T., & Politis, M. (2019) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2019.02.027 · Cited by 18 · see citing works
Sex and Region-Specific Differences in Microglial Morphology and Function Across Development
Bishnoi, I. R., & Bordt, E. A. (2025) · Neuroglia · doi:10.3390/neuroglia6010002 · Cited by 17 · see citing works
Limbic and paralimbic respiratory modulation: From inhibition to enhancement
Chaitanya, G., Hampson, J. P., Tóth, E., Hupp, N. J., Hampson, J. S., Mosher, J. C., Pati, S. B. B., Lhatoo, S. D., & Lacuey, N. (2022) · Epilepsia · doi:10.1111/epi.17244 · Cited by 17 · see citing works
Miguel, J. C., Perez, S. E., Malek‐Ahmadi, M. H., & Mufson, E. J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.645334 · Cited by 17 · see citing works
A potential role of hippocampus on impulsivity and alcohol consumption through CB1R
Romero-Torres, B. M., Ramírez, Y. A. A., Duran-Alonzo, S. R., Ruiz‐Contreras, A. E., Herrera-Solís, A., Belmont, O. A., Prospero-Garcia, O. E., & Méndez‐Díaz, M. (2023) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2023.173558 · Cited by 17 · see citing works
Exploratory structural assessment in craniocervical dystonia: Global and differential analyses
Vilany, L., de Rezende, T. J. R., Piovesana, L. G., Campos, L. S., de Azevedo, P. C., Torres, F. R., França, M. C., Amato-Filho, A., Lopes‐Cendes, Í., Cendes, F., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182735 · Cited by 17 · see citing works
Chronic stress as an emerging risk factor for the development and progression of glioma
Yi, L., Lin, X., She, X., Gao, W. Q., & Wu, M. (2024) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002976 · Cited by 16 · see citing works
Exploring the Intricacies of Neurogenic Niches: Unraveling the Anatomy and Neural Microenvironments
Sánchez-Gomar, I., Geribaldi‐Doldán, N., Santos-Rosendo, C., Sanguino-Caneva, C., Carrillo-Chapman, C., Moreno, O. F., Camacho, J. L. V., Quiroz, E. N., & Verástegui, C. (2024) · Biomolecules · doi:10.3390/biom14030335 · Cited by 16 · see citing works
- Authors
- RajMohan, V, & Mohandas, E.
- Venue
- Indian Journal of Psychiatry
- Published
- 2007
- Volume
- 49
- Issue
- 2
- Pages
- 132
- ISSN
- 0019-5545 (ISSN-L)
- PMC
- PMC2917081
- OpenAlex
- W1968677514
- Cited by
- 342
- References
- 24
- Citations by year
- 2026: 18 · 2025: 38 · 2024: 45 · 2023: 55 · 2022: 41 · 2021: 31 · 2020: 31 · 2019: 33 · 2018: 14 · 2017: 12 · 2016: 9 · 2015: 5 · 2014: 3 · 2012: 3
- FWCI
- 0.50
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by-nc-sa
- Locations
- Indian Journal of Psychiatry (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- limbic system, Papez circuit, emotions, limbic lobe, cingulate gyrus, parahippocampal gyrus, hippocampus, amygdala, hypothalamus, septal area, triune brain theory, limbic cortex
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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