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Dive into the research topics where R. J. R. Blair is active.

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Featured researches published by R. J. R. Blair.


Consciousness and Cognition | 2005

Responding to the emotions of others: Dissociating forms of empathy through the study of typical and psychiatric populations

R. J. R. Blair

Empathy is a lay term that is becoming increasingly viewed as a unitary function within the field of cognitive neuroscience. In this paper, a selective review of the empathy literature is provided. It is argued from this literature that empathy is not a unitary system but rather a loose collection of partially dissociable neurocognitive systems. In particular, three main divisions can be made: cognitive empathy (or Theory of Mind), motor empathy, and emotional empathy. The two main psychiatric disorders associated with empathic dysfunction are considered: autism and psychopathy. It is argued that individuals with autism show difficulties with cognitive and motor empathy but less clear difficulties with respect to emotional empathy. In contrast, individuals with psychopathy show clear difficulties with a specific form of emotional empathy but no indications of impairment with cognitive and motor empathy.


Journal of Abnormal Child Psychology | 2001

A selective impairment in the processing of sad and fearful expressions in children with psychopathic tendencies

R. J. R. Blair; E. Colledge; L.K. Murray; Derek G.V. Mitchell

The processing of emotional expressions is fundamental for normal socialisation and interaction. Reduced responsiveness to the expressions of sadness and fear has been implicated in the development of psychopathy (R. J. R. Blair, 1995). The current study investigates the sensitivity of children with psychopathic tendencies to facial expressions. Children with psychopathic tendencies and a comparison group, as defined by the Psychopathy Screening Device (PSD; P. J. Frick & R. D. Hare, in press), were presented with a cinematic display of a standardised set of facial expressions that depicted sadness, happiness, anger, disgust, fear, and surprise. Participants observed as these facial expressions slowly evolved through 20 successive frames of increasing intensity. The children with psychopathic tendencies presented with selective impairments; they needed significantly more stages before they could successfully recognise the sad expressions and even when the fearful expressions were at full intensity were significantly more likely to mistake them for another expression. These results are interpreted with reference to an amygdala and empathy impairment explanation of psychopathy.


Neuroscience & Biobehavioral Reviews | 2008

Deficits in facial affect recognition among antisocial populations: A meta-analysis

Abigail A. Marsh; R. J. R. Blair

Individuals with disorders marked by antisocial behavior frequently show deficits in recognizing displays of facial affect. Antisociality may be associated with specific deficits in identifying fearful expressions, which would implicate dysfunction in neural structures that subserve fearful expression processing. A meta-analysis of 20 studies was conducted to assess: (a) if antisocial populations show any consistent deficits in recognizing six emotional expressions; (b) beyond any generalized impairment, whether specific fear recognition deficits are apparent; and (c) if deficits in fear recognition are a function of task difficulty. Results show a robust link between antisocial behavior and specific deficits in recognizing fearful expressions. This impairment cannot be attributed solely to task difficulty. These results suggest dysfunction among antisocial individuals in specified neural substrates, namely the amygdala, involved in processing fearful facial affect.


Personality and Individual Differences | 1999

Responsiveness to distress cues in the child with psychopathic tendencies

R. J. R. Blair

This study investigates the psychophysiological responsiveness of children with emotional and behavioral difficulties, divided according to their Psychopathy Screening Device (PSD) scores (Frick and Hare, in press) to distress cues, threatening and neutral stimuli. From this population, 16 high PSD scoring children and 16 low scoring controls were shown slides of these three types of stimuli and their electrodermal responses were recorded. An additional 16 normal developing children in mainstream education were also presented with these stimuli. The high PSD scoring children showed, relative to the controls, reduced electrodermal responses to the distress cues and threatening stimuli. In contrast, the two groups did not differ in their electrodermal responses to the neutral stimuli. The results are interpreted within the Violence Inhibition Mechanism model (Blair, 1995) of Psychopathy.


Neuropsychologia | 2002

Risky decisions and response reversal: is there evidence of orbitofrontal cortex dysfunction in psychopathic individuals?

Derek G.V. Mitchell; E. Colledge; Alan Leonard; R. J. R. Blair

This study investigates the performance of psychopathic individuals on tasks believed to be sensitive to dorsolateral prefrontal and orbitofrontal cortex (OFC) functioning. Psychopathic and non-psychopathic individuals, as defined by the Hare psychopathy checklist revised (PCL-R) [Hare, The Hare psychopathy checklist revised, Toronto, Ontario: Multi-Health Systems, 1991] completed a gambling task [Cognition 50 (1994) 7] and the intradimensional/extradimensional (ID/ED) shift task [Nature 380 (1996) 69]. On the gambling task, psychopathic participants showed a global tendency to choose disadvantageously. Specifically, they showed an impaired ability to show learning over the course of the task. On the ID/ED task, the performance of psychopathic individuals was not significantly different from incarcerated controls on attentional set-shifting, but significant impairments were found on response reversal. These results are interpreted with reference to an OFC and amygdala dysfunction explanation of psychopathy.


Neuropsychologia | 2003

Theory of mind and psychopathy: can psychopathic individuals read the ‘language of the eyes’?

R.A Richell; Derek G.V. Mitchell; C. Newman; A Leonard; Simon Baron-Cohen; R. J. R. Blair

There have been suggestions that Theory of Mind (ToM) impairment might lead to aggressive behaviour and psychopathy. Psychopathic and matched non-psychopathic individuals, as defined by the Hare Psychopathy Checklist [The Hare Psychopath Checklist-Revised, 1991] completed the Reading the Mind in the Eyes ToM Test [Journal of Child Psychology and Psychiatry, 1997;38:813]. This test requires the self-paced identification of mental states from photographs of the eye region alone. Results indicated that the psychopathic individuals did not present with any generalised impairment in ToM. The data are discussed with reference to the putative neural system mediating performance on this task and models of psychopathy.


Journal of Abnormal Child Psychology | 2001

Somatic markers and response reversal: Is there orbitofrontal cortex dysfunction in boys with psychopathic tendencies?

R. J. R. Blair; E. Colledge; Derek G.V. Mitchell

This study investigated the performance of boys with psychopathic tendencies and comparison boys, aged 9 to 17 years, on two tasks believed to be sensitive to amygdala and orbitofrontal cortex functioning. Fifty-one boys were divided into two groups according to the Psychopathy Screening Device (PSD, P. J. Frick & R. D. Hare, in press) and presented with two tasks. The tasks were the gambling task (A. Bechara, A. R. Damasio, H. Damasio, & S. W. Anderson, 1994) and the Intradimensional/Extradimensional (ID/ED) shift task (R. Dias, T. W. Robbins, & A. C. Roberts, 1996). The boys with psychopathic tendencies showed impaired performance on the gambling task. However, there were no group differences on the ID/ED task either for response reversal or extradimensional set shifting. The implications of these results for models of psychopathy are discussed.


Archives of General Psychiatry | 2008

Amygdala and Ventrolateral Prefrontal Cortex Function During Anticipated Peer Evaluation in Pediatric Social Anxiety

Amanda E. Guyer; Jennifer Y. F. Lau; Erin B. McClure-Tone; Jessica M. Parrish; Nina Shiffrin; Richard C. Reynolds; Gang Chen; R. J. R. Blair; Ellen Leibenluft; Nathan A. Fox; Monique Ernst; Daniel S. Pine; Eric E. Nelson

CONTEXTnAmygdala and ventrolateral prefrontal cortex (vlPFC) dysfunction manifests in adolescents with anxiety disorders when they view negatively valenced stimuli in threatening contexts. Such fear-circuitry dysfunction may also manifest when anticipated social evaluation leads socially anxious adolescents to misperceive peers as threatening.nnnOBJECTIVEnTo determine whether photographs of negatively evaluated smiling peers viewed during anticipated social evaluation engage the amygdala and vlPFC differentially in adolescents with and without social anxiety.nnnDESIGNnCase-control study.nnnSETTINGnGovernment clinical research institute.nnnPARTICIPANTSnFourteen adolescents with anxiety disorders associated with marked concerns of social evaluation and 14 adolescents without a psychiatric diagnosis matched on sex, age, intelligence quotient, and socioeconomic status.nnnMAIN OUTCOME MEASURESnBlood oxygenation level-dependent signal measured with event-related functional magnetic resonance imaging. Before and during neuroimaging scans, participants anticipating social evaluation completed peer- and self-appraisals. Event-related analyses were tailored to participants ratings of specific peers.nnnRESULTSnParticipants classified 40 pictures of same-age peers as ones with whom they did or did not want to engage in a social interaction. Anxious adolescents showed greater amygdala activation than healthy adolescents when anticipating evaluation from peers previously rated as undesired for an interaction. Psychophysiological interaction connectivity analyses also revealed a significant positive association between amygdala and vlPFC activation in anxious vs healthy adolescents in response to these stimuli.nnnCONCLUSIONSnAnticipating social evaluation from negatively perceived peers modulates amygdala and vlPFC engagement differentially in anxious and healthy adolescents. Amygdala and vlPFC dysfunction manifests in adolescent anxiety disorders in specific contexts of anticipated peer evaluation.


Journal of Genetic Psychology | 2001

Recognition of Emotion in Facial Expressions and Vocal Tones in Children With Psychopathic Tendencies

D Stevens; Tony Charman; R. J. R. Blair

Abstract The authors investigated the ability of children with emotional and behavioral difficulties, divided according to their Psychopathy Screening Device scores (P. J. Frick & R. D. Hare, in press), to recognize emotional facial expressions and vocal tones. The Psychopathy Screening Device indexes a behavioral syndrome with two dimensions: affective disturbance and impulsive and conduct problems. Nine children with psychopathic tendencies and 9 comparison children were presented with 2 facial expression and 2 vocal tone subtests from the Diagnostic Analysis of Nonverbal Accuracy (S. Nowicki & M. P. Duke, 1994). These subtests measure the ability to name sad, fearful, happy, and angry facial expressions and vocal affects. The children with psychopathic tendencies showed selective impairments in the recognition of both sad and fearful facial expressions and sad vocal tone. In contrast, the two groups did not differ in their recognition of happy or angry facial expressions or fearful, happy, and angry vocal tones. The results are interpreted with reference to the suggestion that the development of psychopathic tendencies may reflect early amygdala dysfunction (R. J. R. Blair, J. S. Morris, C. D. Frith, D. I. Perrett, & R. Dolan, 1999).


American Journal of Psychiatry | 2008

Response to Emotional Expressions in Generalized Social Phobia and Generalized Anxiety Disorder: Evidence for Separate Disorders

Karina S. Blair; Jonathan Shaywitz; Bruce W. Smith; Rebecca Rhodes; R.N. Marilla Geraci; B.A. Matthew Jones; B.A. Daniel McCaffrey; Meena Vythilingam; Elizabeth Finger; B.A. Krystal Mondillo; Madeline Jacobs; Dennis S. Charney; R. J. R. Blair; Wayne C. Drevets; Daniel S. Pine

OBJECTIVEnGeneralized social phobia involves fear/avoidance, specifically of social situations, whereas generalized anxiety disorder involves intrusive worry about diverse circumstances. It remains unclear the degree to which these two, often comorbid, conditions represent distinct disorders or alternative presentations of a single, core underlying pathology. Functional magnetic resonance imaging assessed the neural response to facial expressions in generalized social phobia and generalized anxiety disorder.nnnMETHODnIndividuals matched on age, IQ, and gender with generalized social phobia without generalized anxiety disorder (N=17), generalized anxiety disorder (N=17), or no psychopathology (N=17) viewed neutral, fearful, and angry expressions while ostensibly making a simple gender judgment.nnnRESULTSnThe patients with generalized social phobia without generalized anxiety disorder showed increased activation to fearful relative to neutral expressions in several regions, including the amygdala, compared to healthy individuals. This increased amygdala response related to self-reported anxiety in patients with generalized social phobia without generalized anxiety disorder. In contrast, patients with generalized anxiety disorder showed significantly less activation to fearful relative to neutral faces compared to the healthy individuals. They did show significantly increased response to angry expressions relative to healthy individuals in a lateral region of the middle frontal gyrus. This increased lateral frontal response related to self-reported anxiety in patients with generalized anxiety disorder.nnnCONCLUSIONSnThese results suggest that neural circuitry dysfunctions differ in generalized social phobia and generalized anxiety disorder.

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Daniel S. Pine

National Institutes of Health

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Karina S. Blair

National Institutes of Health

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Derek G.V. Mitchell

University of Western Ontario

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Marilla Geraci

National Institutes of Health

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Abigail A. Marsh

National Institutes of Health

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Ellen Leibenluft

National Institutes of Health

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Marcela Otero

National Institutes of Health

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Meena Vythilingam

National Institutes of Health

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Madeline Jacobs

National Institutes of Health

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Nick Hollon

National Institutes of Health

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