Literature DB >> 20740065

Electrophysiological Studies of Face Perception in Humans.

Shlomo Bentin1, Truett Allison, Aina Puce, Erik Perez, Gregory McCarthy.   

Abstract

Event-related potentials (ERPs) associated with face perception were recorded with scalp electrodes from normal volunteers. Subjects performed a visual target detection task in which they mentally counted the number of occurrences of pictorial stimuli from a designated category such us butterflies. In separate experiments, target stimuli were embedded within a series of other stimuli including unfamiliar human faces and isolated face components, inverted faces, distorted faces, animal faces, and other nonface stimuli. Unman faces evoked a negative potential at 172 msec (N170), which was absent from the ERPs elicited by other animate and inanimate nonface stimuli. N170 was largest over the posterior temporal scalp and was larger over the right than the left hemisphere. N170 was delayed when faces were presented upside-down, but its amplitude did not change. When presented in isolation, eyes elicited an N170 that was significantly larger than that elicited by whole faces, while noses and lips elicited small negative ERPs about 50 msec later than N170. Distorted human faces, in which the locations of inner face components were altered, elicited an N170 similar in amplitude to that elicited by normal faces. However, faces of animals, human hands, cars, and items of furniture did not evoke N170. N170 may reflect the operation of a neural mechanism tuned to detect (as opposed to identify) human faces, similar to the "structural encoder" suggested by Bruce and Young (1986). A similar function has been proposed for the face-selective N200 ERP recorded from the middle fusiform and posterior inferior temporal gyri using subdural electrodes in humans (Allison, McCarthy, Nobre, Puce, & Belger, 1994c). However, the differential sensitivity of N170 to eyes in isolation suggests that N170 may reflect the activation of an eye-sensitive region of cortex. The voltage distribution of N170 over the scalp is consistent with a neural generator located in the occipitotemporal sulcus lateral to the fusiform/inferior temporal region that generates N200.

Entities:  

Year:  1996        PMID: 20740065      PMCID: PMC2927138          DOI: 10.1162/jocn.1996.8.6.551

Source DB:  PubMed          Journal:  J Cogn Neurosci        ISSN: 0898-929X            Impact factor:   3.225


  57 in total

1.  Organization and functions of cells responsive to faces in the temporal cortex.

Authors:  D I Perrett; J K Hietanen; M W Oram; P J Benson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1992-01-29       Impact factor: 6.237

2.  Functional neuroanatomy of face and object processing. A positron emission tomography study.

Authors:  J Sergent; S Ohta; B MacDonald
Journal:  Brain       Date:  1992-02       Impact factor: 13.501

3.  Prosopagnosia: a clinical, psychological, and anatomical study of three patients.

Authors:  A M Whiteley; E K Warrington
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-04       Impact factor: 10.154

4.  Brain potentials reveal covert facial recognition in prosopagnosia.

Authors:  B Renault; J L Signoret; B Debruille; F Breton; F Bolgert
Journal:  Neuropsychologia       Date:  1989       Impact factor: 3.139

5.  Functional subdivisions of the temporal lobe neocortex.

Authors:  G C Baylis; E T Rolls; C M Leonard
Journal:  J Neurosci       Date:  1987-02       Impact factor: 6.167

6.  Cells in temporal cortex of conscious sheep can respond preferentially to the sight of faces.

Authors:  K M Kendrick; B A Baldwin
Journal:  Science       Date:  1987-04-24       Impact factor: 47.728

7.  Integration of direction signals of image motion in the superior temporal sulcus of the macaque monkey.

Authors:  H Saito; M Yukie; K Tanaka; K Hikosaka; Y Fukada; E Iwai
Journal:  J Neurosci       Date:  1986-01       Impact factor: 6.167

8.  Prosopagnosia: anatomic basis and behavioral mechanisms.

Authors:  A R Damasio; H Damasio; G W Van Hoesen
Journal:  Neurology       Date:  1982-04       Impact factor: 9.910

9.  Face-sensitive regions in human extrastriate cortex studied by functional MRI.

Authors:  A Puce; T Allison; J C Gore; G McCarthy
Journal:  J Neurophysiol       Date:  1995-09       Impact factor: 2.714

10.  Visual neurones responsive to faces in the monkey temporal cortex.

Authors:  D I Perrett; E T Rolls; W Caan
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

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  728 in total

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2.  An electrophysiological comparison of visual categorization and recognition memory.

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5.  Beauty is in the ease of the beholding: a neurophysiological test of the averageness theory of facial attractiveness.

Authors:  Logan T Trujillo; Jessica M Jankowitsch; Judith H Langlois
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6.  A visual short-term memory advantage for objects of expertise.

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7.  Evidence that disrupted orienting to evaluative social feedback undermines error correction in rejection sensitive women.

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8.  Preference for human eyes in human infants.

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Journal:  J Exp Child Psychol       Date:  2014-02-28

Review 9.  Using Event-Related Potentials and Startle to Evaluate Time Course in Anxiety and Depression.

Authors:  Heide Klumpp; Stewart A Shankman
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2017-09-20

10.  The perception of a familiar face is no more than the sum of its parts.

Authors:  Jason M Gold; Jarrett D Barker; Shawn Barr; Jennifer L Bittner; Alexander Bratch; W Drew Bromfield; Roy A Goode; Mary Jones; Doori Lee; Aparna Srinath
Journal:  Psychon Bull Rev       Date:  2014-12
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