CSCarl E. Schwartz

Carl E. Schwartz

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article

Previous Organizations / Institutes

The organizations / institutes from the scholar's other articles in the past ten years


Carl E. Schwartz has a total of 33 co-authors. Here are the top co-authors by number of shared publications:

  • Jerome Kagan

    Department of Psychology, Harvard University, Cambridge, MA

    2 shared publications
  • P S Kunwar

    Developmental Neuroimaging Laboratory, Psychiatric Neuroscience Program, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA

    2 shared publications
  • Scott L. Rauch

    2 shared publications
  • A Henin

    Department of Psychiatry, Harvard Medical School, Boston, MA, USA

    1 shared publication
  • Britta K. Hölzel

    Massachusetts General Hospital, 120 2nd Ave., Charlestown, MA, 02129, USA ; Bender Institute of Neuroimaging, Justus-Liebig University, Otto-Behaghel-Str. 10H, 35394 Giessen, Germany

    1 shared publication
  • Christopher I. Wright

    Developmental Psychopathology Research Group, Department of Psychiatry, Massachusetts General Hospital (MGH), Harvard Medical School, 13th Street, Building 149, CNY-9, Charlestown, MA 02129, USA

    1 shared publication

Latest Publications

  • Open Access

    Behavioral inhibition in childhood predicts smaller hippocampal volume in adolescent offspring of parents with panic disorder

    by C E Schwartz, P S Kunwar, D R Hirshfeld-Becker, A Henin, M G Vangel, S L Rauch, J Biederman, J F Rosenbaum

    Behavioral inhibition (BI) is a genetically influenced behavioral profile seen in 15–20% of 2-year-old children. Children with BI are timid with people, objects and situations that are novel or unfamiliar, and are more reactive physiologically to these challenges as evidenced by higher heart rate, pupillary dilation, vocal cord tension and higher levels of cortisol. BI predisposes to the later development of anxiety, depression and substance abuse. Reduced hippocampal volumes have been observed in anxiety disorders, depression and posttraumatic stress disorder. Animal models have demonstrated that chronic stress can damage the hippocampal formation and implicated cortisol in these effects. We, therefore, hypothesized that the hippocampi of late adolescents who had been behaviorally inhibited as children would be smaller compared with those who had not been inhibited. Hippocampal volume was measured with high-resolution structural magnetic resonance imaging in 43 females and 40 males at 17 years of age who were determined to be BI+ or BI− based on behaviors observed in the laboratory as young children. BI in childhood predicted reduced hippocampal volumes in the adolescents who were offspring of parents with panic disorder, or panic disorder with comorbid major depression. We discuss genetic and environmental factors emanating from both child and parent that may explain these findings. To the best of our knowledge, this is the first study to demonstrate a relationship between the most extensively studied form of temperamentally based human trait anxiety, BI, and hippocampal structure. The reduction in hippocampal volume, as reported by us, suggests a role for the hippocampus in human trait anxiety and anxiety disorder that warrants further investigation.


  • Open Access

    Neural mechanisms of symptom improvements in generalized anxiety disorder following mindfulness training

    by Britta K. Hölzel, Elizabeth A. Hoge, Douglas N. Greve, Tim Gard, J. David Creswell, Kirk Warren Brown, Lisa Feldman Barrett, Carl Schwartz, Dieter Vaitl, Sara W. Lazar


  • Open Access

    A phenotype of early infancy predicts reactivity of the amygdala in male adults

    by C E Schwartz, P S Kunwar, D N Greve, J Kagan, N C Snidman, R B Bloch

    One of the central questions that has occupied those disciplines concerned with human development is the nature of continuities and discontinuities from birth to maturity. The amygdala has a central role in the processing of novelty and emotion in the brain. Although there is considerable variability among individuals in the reactivity of the amygdala to novel and emotional stimuli, the origin of these individual differences is not well understood. Four-month old infants called high reactive (HR) demonstrate a distinctive pattern of vigorous motor activity and crying to specific unfamiliar visual, auditory and olfactory stimuli in the laboratory. Low-reactive infants show the complementary pattern. Here, we demonstrate that the HR infant phenotype predicts greater amygdalar reactivity to novel faces almost two decades later in adults. A prediction of individual differences in brain function at maturity can be made on the basis of a single behavioral assessment made in the laboratory at 4 months of age. This is the earliest known human behavioral phenotype that predicts individual differences in patterns of neural activity at maturity. These temperamental differences rooted in infancy may be relevant to understanding individual differences in vulnerability and resilience to clinical psychiatric disorder. Males who were HR infants showed particularly high levels of reactivity to novel faces in the amygdala that distinguished them as adults from all other sex/temperament subgroups, suggesting that their amygdala is particularly prone to engagement by unfamiliar faces. These findings underline the importance of taking gender into account when studying the developmental neurobiology of human temperament and anxiety disorders. The genetic study of behavioral and biologic intermediate phenotypes (or ‘endophenotypes’) indexing anxiety-proneness offers an important alternative to examining phenotypes based on clinically defined disorder. As the HR phenotype is characterized by specific patterns of reactivity to elemental visual, olfactory and auditory stimuli, well before complex social behaviors such as shyness or fearful interaction with strangers can be observed, it may be closer to underlying neurobiological mechanisms than behavioral profiles observed later in life. This possibility, together with the fact that environmental factors have less time to impact the 4-month phenotype, suggests that this temperamental profile may be a fruitful target for high-risk genetic studies.


  • Open Access

    Structural Differences in Adult Orbital and Ventromedial Prefrontal Cortex Predicted by Infant Temperament at 4 Months of Age

    by Carl E. Schwartz, Pratap S. Kunwar, Douglas N. Greve, Lyndsey R. Moran, Jane C. Viner, Jennifer M. Covino, Jerome Kagan, S. Evelyn Stewart, Nancy C. Snidman, Mark G. Vangel, et al.

    Temperament refers to a biologically based predilection for a distinctive pattern of emotions, cognitions, and behaviors first observed in infancy or early childhood. Approximately 20% of white 4-month-old infants demonstrate a high-reactive temperament, which is defined by vigorous limb activity, arching of their back, and crying to unfamiliar visual, olfactory, and auditory stimuli. In contrast, 40% of 4-month-olds show both low motor activity and low vocal distress to the same stimuli and are categorized as low reactive.1-3 These profiles were based on direct observations in the laboratory. As the 2 groups mature, they become toddlers who show distinctive responses to unfamiliar people, objects, and situations. High-reactive infants are biased to be timid with unfamiliar people, objects, and situations. In contrast, low-reactive infants are biased to develop into uninhibited children who spontaneously approach unfamiliar situations.1-4 This result is consistent with an account that emphasizes variation in the excitability of the amygdala and its projections to the ventral striatum, the periaqueductal gray, and anterior cingulate.3,5


  • Temperament and Its Implications for Neuroimaging of Anxiety Disorders

    by Carl E. Schwartz, Scott L. Rauch

    We review the attributes of inhibited and uninhibited infant temperaments, and their developmental trajectories into early adulthood. Inborn individual differences in infants' propensity to respond to novel people and objects are associated with persistent differences in the responsivity of the amygdala to novelty, as measured with functional magnetic resonance imaging, after more than 20 years of development. Because an inhibited temperament is a risk factor for developing later psychiatric disorders, particularly generalized social anxiety disorder, temperamental differences are confounds in neuroimaging and genetic studies. Longitudinal studies are a unique tool for understanding the developmental and temperamental risk factors for psychiatric disorder.


  • Inhibited and Uninhibited Infants "Grown Up": Adult Amygdalar Response to Novelty

    by Carl E. Schwartz, Christopher I. Wright, Lisa M. Shin, Jerome Kagan, Scott L. Rauch

    Infants with an inhibited temperament tend to develop into children who avoid people, objects, and situations that are novel or unfamiliar, whereas uninhibited children spontaneously approach novel persons, objects, and situations. Behavioral and physiological features of these two temperamental categories are moderately stable from infancy into early adolescence and have been hypothesized to be due, in part, to variation in amygdalar responses to novelty. We found that adults who had been categorized in the second year of life as inhibited, compared with those previously categorized as uninhibited, showed greater functional MRI signal response within the amygdala to novel versus familiar faces.