Neural control of social behavior: Prefrontal and anterior temporal cortex

The Frontal Granular Cortex and Behavior.

Cole, M. (1964) · Archives of Neurology · doi:10.1001/archneur.1964.00460240114017 · Cited by 468

Brain Mechanisms Underlying Speech and Language.

(1967) · Annals of Internal Medicine · doi:10.7326/0003-4819-67-3-693_2 · Cited by 265

Effects of orbital frontal lesions on aversive and aggressive behaviors in rhesus monkeys.

Butter, C. M., Snyder, D. R., & McDonald, J. A. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0029303 · Cited by 245

The effects of lesions in the cingular gyrus and adjacent areas in monkeys

Glees, P., Cole, J., Whitty, C. W. M., & Cairns, H. (1950) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.13.3.178 · Cited by 162

Loss of social group affinity following prefrontal lesions in free-ranging macaques

Myers, R. E., Swett, C., & Miller, M. (1973) · Brain Research · doi:10.1016/0006-8993(73)90182-0 · Cited by 90

OUTLINES OF CANID AND FELID BRAIN EVOLUTION*

Radinsky, L. (1969) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1969.tb20450.x · Cited by 84

HYPERACTIVITY IN MONKEYS FOLLOWING LESIONS OF THE FRONTAL LOBES

Kennard, M. A., Spencer, S., & Fountain, G. (1941) · Journal of Neurophysiology · doi:10.1152/jn.1941.4.7.512 · Cited by 58

Influence of Prefrontal Lobotomy on Social Interaction in a Monkey Group

Brody, E. B., & ROSVOLD, E. H. (1952) · Psychosomatic Medicine · doi:10.1097/00006842-195209000-00007 · Cited by 54

Effects of bilateral lesions of the frontal granular cortex on the social behavior of rhesus monkeys.

Deets, A. C., Harlow, H. F., Singh, S. D., & Blomquist, A. J. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0029729 · Cited by 51

Social behavior deficits of free-ranging monkeys after anterior temporal cortex removal: a preliminary report

Myers, R. E., & Swett, C. P. (1970) · Brain Research · doi:10.1016/0006-8993(70)90140-x · Cited by 49

Neurobiology of Affiliative Behavior in Nonhuman Primates**Partial support for this research has been obtained from the Research Council, Rutgers University; Veterans Administration Research funds; the Harry Frank Guggenheim Foundation, New York; and The Epilepsy Foundation of America. We thank Dr. M.J. Raleigh for commenting on an earlier version of this chapter and Ms. Sylva Grossman for typing the manuscript.

Steklis, H. D., & Kling, A. S. (1985) · Elsevier eBooks · doi:10.1016/b978-0-12-586780-1.50008-2 · Cited by 35

Age effects on social behavior deficits following prefrontal lesions in monkeys

Franzen, E. A., & Myers, R. E. (1973) · Brain Research · doi:10.1016/0006-8993(73)90049-8 · Cited by 35

Light affects the prefrontal cortex via intrinsically photosensitive retinal ganglion cells

Ospri, L. L., Zhan, J. J., Thomsen, M. B., Wang, H. M., Komal, R., Tang, Q., Messanvi, F., du Hoffmann, J., Cravedi, K., Chudasama, Y., et al. (2024) · Science Advances · doi:10.1126/sciadv.adh9251 · Cited by 36

Comparison of emotional responses in monkeys with rhinal cortex or amygdala lesions.

Meunier, M., & Bachevalier, J. (2002) · Emotion · doi:10.1037/1528-3542.2.2.147 · Cited by 34

Mesial prefrontal cortical lesions and timidity in rats. III. behavior in a semi-natural environment

Holson, R. R. (1986) · Physiology & Behavior · doi:10.1016/0031-9384(86)90226-x · Cited by 32

The Fiber Connections of the Temporal Lobe with Emphasis on the Rhesus Monkey

Streitfeld, B. (1980) · International Journal of Neuroscience · doi:10.3109/00207458009147579 · Cited by 30

Sniffing the human body volatile hexadecanal blocks aggression in men but triggers aggression in women

Mishor, E., Amir, D., Weiss, T., Honigstein, D. R., Weissbrod, A., Livne, E., Gorodisky, L., Karagach, S., Ravia, A., Snitz, K., et al. (2021) · Science Advances · doi:10.1126/sciadv.abg1530 · Cited by 29

Primate phonation: Anterior cingulate lesion effects on response rate and acoustical structure

Trachy, R. E., Sutton, D., & Lindeman, R. C. (1981) · American Journal of Primatology · doi:10.1002/ajp.1350010106 · Cited by 24

Reactions of patients with focal cerebral lesions to success or failure

Weddell, R. A., Trevarthen, C., & Miller, J. D. (1988) · Neuropsychologia · doi:10.1016/0028-3932(88)90092-9 · Cited by 23

Behavioral and Neurobiological Aspects of Primate Vocalization and Facial Expression

Steklis, H. D., & Raleigh, M. J. (1979) · Elsevier eBooks · doi:10.1016/b978-0-12-665650-3.50015-3 · Cited by 23

Human Brain Evolution: I. Evolution of Language Circuits

Deacon, T. W. (1988) · Springer eBooks · doi:10.1007/978-3-642-70877-0_19 · Cited by 23

Neurology of Social Behavior and Affect in Primates: A Study of Prefrontal and Anterior Temporal Cortex

Myers, R. E. (1975) · Springer eBooks · doi:10.1007/978-3-642-66204-1_13 · Cited by 19

Evidence for a social function of the anterior temporal lobes: Low-frequency rTMS reduces implicit gender stereotypes

Wong, C. L., Harris, J. A., & Gallate, J. E. (2011) · Social Neuroscience · doi:10.1080/17470919.2011.582145 · Cited by 18

The Role of Amygdala in Self-Conscious Emotions in a Patient With Acquired Bilateral Damage

Piretti, L., Pappaianni, E., Lunardelli, A., Zorzenon, I., Ukmar, M., Pesavento, V., Rumiati, R. I., Job, R., & Grecucci, A. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00677 · Cited by 17

Mnestische Blockaden als Stress- und Traumafolgen

Markowitsch, H. J. (2001) · Zeitschrift für Klinische Psychologie und Psychotherapie · doi:10.1026//16-3443.30.3.204 · Cited by 16

An example of lack of frontal inhibition: the ‘utilization behaviour’

Brazzelli, M. G., & Spinnler, H. R. (1998) · European Journal of Neurology · doi:10.1046/j.1468-1331.1998.540347.x · Cited by 15

Biology of Maternal Behavior: Recent Findings and Implications

Capitanio, J. P., Weissberg, M., & Reite, M. L. (1985) · Elsevier eBooks · doi:10.1016/b978-0-12-586780-1.50007-0 · Cited by 15

Ethanol Alters Variability, But Not Rate, of Firing in Medial Prefrontal Cortex Neurons of Awake‐Behaving Rats

Morningstar, M. D., Linsenbardt, D. N., & Lapish, C. C. (2020) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14463 · Cited by 14

From Indifference to Ardor: The Onset, Maintenance, and Meaning of the Maternal Brain

González‐Mariscal, G., & Kinsley, C. H. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00003-6 · Cited by 14

Context–specific social behavior is altered by orbitofrontal cortex lesions in adult rhesus macaques

Babineau, B. A., Bliss‐Moreau, E., Machado, C. J., Toscano, J. E., Mason, W. A., & Amaral, D. G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.01.019 · Cited by 14

The Ethological Analysis of Monkeys in a Social Setting as an Animal Model for Schizophrenia

Ellenbroek, B. A. (1991) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-6419-0_26 · Cited by 13

Neuropsychological Rehabilitation and the Problem of Altered Self-Awareness

Prigatano, G. P. (1992) · Springer eBooks · doi:10.1007/978-3-642-77067-8_6 · Cited by 13

Degenerative Dementia of the Frontal Type

Galante, E., Muggia, S., Spinnler, H. R., & Zuffi, M. (1998) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000017094 · Cited by 13

On Aggressive Behavior and Brain Disease — Some Questions and Possible Relationships Derived from the Study of Men and Monkeys

Mirsky, A. F., & Harman, N. (1974) · Advances in behavioral biology · doi:10.1007/978-1-4684-3072-1_10 · Cited by 12

Role of Reversal Learning Impairment in Social Disinhibition following Severe Traumatic Brain Injury

Osborne‐Crowley, K., McDonald, S., & Rushby, J. A. (2016) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715001277 · Cited by 13

Understanding ethanol's acute effects on medial prefrontal cortex neural activity using state-space approaches

Morningstar, M. D., Barnett, W. H., Goodlett, C. R., Kuznetsov, A. S., & Lapish, C. C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108780 · Cited by 10

Longitudinal structural MRI analysis and classification in Alzheimer's disease and mild cognitive impairment

Zhang, Y., Liu, S., & Yu, X. (2019) · International Journal of Imaging Systems and Technology · doi:10.1002/ima.22390 · Cited by 9

The role responses of expression and identity in the face-selective of neurons in the temporal visual cortex of the monkey

Hasselmo, M. E., Rolls, E. T., & Baylis, G. C. (1989) · Cited by 9

Brain and Self: Toward a Neuropsychodynamic Model of Ego Autonomy and Personality

Miller, L. (1991) · Journal of the American Academy of Psychoanalysis · doi:10.1521/jaap.1.1991.19.2.213 · Cited by 9

Disease and Illness from a Biocultural Standpoint

Fábrega, H. (1979) · Springer eBooks · doi:10.1007/978-1-4613-2991-6_2 · Cited by 8

THE ANATOMY OF AGGRESSION AND AFFILIATION

Kling, A. S. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-558703-7.50016-4 · Cited by 8

Spatial and temporal progression of neurodegeneration in confirmed and suspected TDP-43 type C pathology

Stocks, J. K., Behn, J. Q., Barbieri, E., & Mesulam, M. M. (2025) · Imaging Neuroscience · doi:10.1162/imag.a.83 · Cited by 7

Pourquoi et comment doit-on tenir compte des neurosciences en éthique ?

Racine, É. (2005) · Laval théologique et philosophique · doi:10.7202/011510ar · Cited by 7

Evolutionary Theories on Primate Social Structures and Behaviors: A Discussion on a Synthesis

Sawaguchi, T., & Kudo, H. (1987) · Primate Research · doi:10.2354/psj.3.48 · Cited by 6

Vers une neuropsychologie humaine des conduites émotionnelles?

Seron, X., & der Linden, M. V. (1979) · L’Année psychologique · doi:10.3406/psy.1979.1361 · Cited by 6

Experimental studies on the effect of early malnutrition on the norepinephrinergic system projecting to the cerebral cortex

Soto‐Moyano, R., Hernández, A., Pérez, H., Ruíz, S., & Belmar, J. (1989) · Cited by 5

EEG Characteristics of Adolescents Raised in Institutional Environments and Their Relation to Psychopathological Symptoms

Hevia-Orozco, J. C., & Sanz‐Martin, A. (2018) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2018.810032 · Cited by 4

Effects of orbitofrontal lesions on social behavior in a confined group of stump-tail macaques (Macaca speciosa)

Miller, M. H., & Levine, E. R. (1977) · Primates · doi:10.1007/bf02382939 · Cited by 4

A componential analysis of the functions of primate orbitofrontal cortex

Roberts, A., & Parkinson, J. A. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198565741.003.0009 · Cited by 4

Control of Attention in Rhesus Monkeys Measured Using a Flanker Task

Hassett, T. C., & Hampton, R. R. (2022) · Attention Perception & Psychophysics · doi:10.3758/s13414-022-02452-z · Cited by 3

Chapter 3 Cortical neuroanatomy and cognition

Rosen, H. J., & Viskontas, I. V. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88003-1 · Cited by 3

Vers un cadre neuropsychologique général pour le développement du nourrisson

Braun, C. M. J. (2003) · Enfance · doi:10.3917/enf.554.0293 · Cited by 3

The Neural Bases of Aggression and Sexual Behavior in the Rhesus Monkey

Perachio, A. A., & Alexander, M. (1975) · Elsevier eBooks · doi:10.1016/b978-0-12-119301-0.50017-2 · Cited by 3

Gamma Oscillations in the Temporal Pole in Response to Eyes

Sato, W., Kochiyama, T., Uono, S., Matsuda, K., Usui, K., Usui, N., Inoue, Y., & Toichi, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162039 · Cited by 2

Phylogenetic precursors of psychiatric illness: A theoretical inquiry

Fábrega, H. (1979) · Comprehensive Psychiatry · doi:10.1016/0010-440x(79)90021-x · Cited by 2

«Active» selection may participate in the evolution of primates

Sawaguchi, T., & Kudo, H. (1991) · Human Evolution · doi:10.1007/bf02438143 · Cited by 2

The DOPA scaffold: Tracing catechol chemistry from prebiotic earth to cognitive agency

Alachkar, A. (2025) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2025.10.004 · Cited by 1

School Success after Brain Injury: Behavioral, Social and Academic Issues

Ylvisaker, M., & Feeney, T. J. (2006) · CRC Press eBooks · doi:10.1201/b14456-10

Die Rezeption systemischer Denk- und Therapieansätze für die klinische Neuropsychologie

Nielsen, J. (2014) · Zeitschrift für Neuropsychologie · doi:10.1024/1016-264x/a000111 · Cited by 1

WITHDRAWN: Light affects the prefrontal cortex via intrinsically photosensitive retinal ganglion cellsPreprint

Ospri, L. L., Zhan, J. J., Thomsen, M. B., Wang, H., Messanvi, F., du Hoffmann, J., Cravedi, K., Komal, R., Chudasama, Y., Zhao, H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.22.556752 · Cited by 1

Das Erleben der Patienten und die Natur höherer Hirnfunktionen

Prigatano, G. P. (2004) · Springer eBooks · doi:10.1007/978-3-642-18768-1_2

Alternativ splicing i mänsklig sjukdom

Edin, E. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Autobiographical memory begins and ends with the self : autobiographical memory, consciousness, the influence of stress and neural correlates

Vandekerckhove, M. M. P. (2004) · PUB – Publications at Bielefeld University (Bielefeld University)

Employees propensity for emotional contagion as a mediating variable between job satisfaction and perceptions of customers’ mood: a comparative case study

Rueff-Lopes, R., Planella, E., & Pendleton, A. (2014) · Investigação e Intervenção em Recursos Humanos · doi:10.26537/iirh.v0i3.1776

Early onset frontotermporal dementia and alzheimers disease: diagnosis, treatment and care

Rudge, J. S. (2007) · Murdoch University Research Portal

Blushing and gaze avoidance in social anxiety disorder : a structural neuroanatomical investigation

der Merwe, V., & Thandiwe, N. (2014) · Open University of Cape Town (University of Cape Town)

Zusammenarbeit in interdisziplinären Rehabilitationsteams

Prigatano, G. P. (2004) · Springer eBooks · doi:10.1007/978-3-642-18768-1_10

Références

Feyereisen, P. (1994) · Presses Universitaires de France eBooks · doi:10.3917/puf.feyer.1994.01.0181

References

(2015) · Elsevier eBooks · doi:10.1016/b978-0-12-416040-8.16001-8

Prefrontal Cortex in Motor Control

Fuster, J. M. (1981) · Comprehensive physiology · doi:10.1002/j.2040-4603.1981.tb00863.x

Relations entre variabilités interindividuelles dans les performances de flexibilité cognitive et socialité chez le babouin de Guinée (Papio papio)

Gullstrand, J. (2023) · doi:10.70675/2cea7b3azdd0cz4eb4zb1d1zc0fd93aa611d

Loss of social group affinity following prefrontal lesions in free-ranging macaques

Myers, R. E., Swett, C., & Miller, M. (1973) · Brain Research · doi:10.1016/0006-8993(73)90182-0 · Cited by 90

Role of prefrontal and anterior temporal cortex in social behavior and affect in monkeys.

Myers, R. E. (1972) · PubMed · Cited by 56

Context–specific social behavior is altered by orbitofrontal cortex lesions in adult rhesus macaques

Babineau, B. A., Bliss‐Moreau, E., Machado, C. J., Toscano, J. E., Mason, W. A., & Amaral, D. G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.01.019 · Cited by 14

Effects of orbitofrontal lesions on social behavior in a confined group of stump-tail macaques (Macaca speciosa)

Miller, M. H., & Levine, E. R. (1977) · Primates · doi:10.1007/bf02382939 · Cited by 4

A Role for the Macaque Anterior Cingulate Gyrus in Social Valuation

Rudebeck, P. H., Buckley, M. J., Walton, M. E., & Rushworth, M. F. S. (2006) · Science · doi:10.1126/science.1128197 · Cited by 312