Keren Haroush

All Publications

• Toward a neurobiological model of human performance under pressure. Proceedings of the National Academy of Sciences of the United States of America Saikley, A., Haroush, K. 2021; 118 (36)

  View details for DOI 10.1073/pnas.2113777118

  View details for PubMedID 34470823

• Current practices in nutrition management and disease incidence of common marmosets (Callithrix jacchus). Journal of medical primatology Goodroe, A., Wachtman, L., Benedict, W., Allen-Worthington, K., Bakker, J., Burns, M., Diaz, L. L., Dick, E., Dickerson, M., Eliades, S. J., Gonzalez, O., Graf, D., Haroush, K., Inoue, T., Izzi, J., Laudano, A., Layne-Colon, D., Leblanc, M., Ludwig, B., Mejia, A., Miller, C., Sarfaty, A., Sosa, M., Vallender, E., Brown, C., Forney, L., Schultz-Darken, N., Colman, R., Power, M., Capuano, S., Ross, C., Tardif, S. 2021

  Abstract

  BACKGROUND: A survey was developed to characterize disease incidence, common pathology lesions, environmental characteristics, and nutrition programs within captive research marmoset colonies.METHODS: Seventeen research facilities completed the electronic survey.RESULTS: Nutritional management programs varied amongst research institutions housing marmosets; eight primary base diets were reported. The most common clinical syndromes reported were gastrointestinal disease (i.e. inflammatory bowel disease like disease, chronic lymphocytic enteritis, chronic malabsorption, chronic diarrhea), metabolic bone disease or fracture, infectious diarrhea, and oral disease (tooth root abscesses, gingivitis, tooth root resorption). The five most common pathology morphologic diagnoses were colitis, nephropathy/nephritis, enteritis, chronic lymphoplasmacytic enteritis, and cholecystitis. Obesity was more common (average 20% of a reporting institution's population) than thin body condition (average 5%).CONCLUSIONS: Through review of current practices, we aim to inspire development of evidence-based practices to standardize husbandry and nutrition practices for marmoset research colonies.

  View details for DOI 10.1111/jmp.12525

  View details for PubMedID 33913156

• Dorsolateral prefrontal neurons mediate subjective decisions and their variation in humans NATURE NEUROSCIENCE Jamali, M., Grannan, B., Haroush, K., Moses, Z. B., Eskandar, E. N., Herrington, T., Patel, S., Williams, Z. M. 2019; 22 (6): 1010-+

  View details for DOI 10.1038/s41593-019-0378-3

  View details for Web of Science ID 000468883100020

• Dorsolateral prefrontal neurons mediate subjective decisions and their variation in humans. Nature neuroscience Jamali, M., Grannan, B., Haroush, K., Moses, Z. B., Eskandar, E. N., Herrington, T., Patel, S., Williams, Z. M. 2019

  Abstract

  Subjective decisions play a vital role in human behavior because, while often grounded in fact, they are inherently based on personal beliefs that can vary broadly within and between individuals. While these properties set subjective decisions apart from many other sensorimotor processes and are of wide sociological impact, their single-neuronal basis in humans is unknown. Here we find cells in the dorsolateral prefrontal cortex (dlPFC) that reflect variations in the subjective decisions of humans when performing opinion-based tasks. These neurons changed their activities gradually as the participants transitioned between choice options but also reflected their unique point of conversion at equipoise. Focal disruption of the dlPFC, by contrast, diminished gradation between opposing decisions but had little effect on sensory perceptual choices or their motor report. These findings suggest that the human dlPFC plays an important role in subjective decisions and propose a mechanism for mediating their variation during opinion formation.

  View details for PubMedID 31011224

• Neuronal Prediction of Opponent's Behavior during Cooperative Social Interchange in Primates CELL Haroush, K., Williams, Z. M. 2015; 160 (6): 1233-1245

  Abstract

  A cornerstone of successful social interchange is the ability to anticipate each other's intentions or actions. While generating these internal predictions is essential for constructive social behavior, their single neuronal basis and causal underpinnings are unknown. Here, we discover specific neurons in the primate dorsal anterior cingulate that selectively predict an opponent's yet unknown decision to invest in their common good or defect and distinct neurons that encode the monkey's own current decision based on prior outcomes. Mixed population predictions of the other was remarkably near optimal compared to behavioral decoders. Moreover, disrupting cingulate activity selectively biased mutually beneficial interactions between the monkeys but, surprisingly, had no influence on their decisions when no net-positive outcome was possible. These findings identify a group of other-predictive neurons in the primate anterior cingulate essential for enacting cooperative interactions and may pave a way toward the targeted treatment of social behavioral disorders.

  View details for DOI 10.1016/j.cell.2015.01.045

  View details for Web of Science ID 000351951800021

  View details for PubMedID 25728667

• Hearing While Blinking: Multisensory Attentional Blink Revisited JOURNAL OF NEUROSCIENCE Haroush, K., Deouell, L. Y., Hochstein, S. 2011; 31 (3): 922-927

  Abstract

  It is well established that cognitive system overload is reflected in the attentional blink (AB), the failure to report a second target when it closely follows detection of a first target within a rapid series of stimuli. However, there is intense controversy concerning the effect of first-target detection in one modality on subsequent dynamics of attentional resources in other modalities. Mixed results were found using an audiovisual AB paradigm: depletion of resources in one modality either impaired performance in the other modality or had no effect. Here, we circumvent the need for task switching by measuring an event-related potential, the mismatch negativity, which reflects implicit auditory change detection without requiring task engagement and is present even for background sounds that participants ignore. Surprisingly, we find that during the visual AB, auditory processing is enhanced rather than inhibited, as would be expected by system overload. We suggest that multimodal attentional resources may be freed rather than engaged during the visual AB. Suppression of irrelevant input may require active control by a central executive, which is preoccupied during the visual AB, and/or there may be no reason to suppress other-modal input since the visual system will miss its second target anyway.

  View details for DOI 10.1523/JNEUROSCI.0420-10.2011

  View details for Web of Science ID 000286373700017

  View details for PubMedID 21248117

• Momentary Fluctuations in Allocation of Attention: Cross-modal Effects of Visual Task Load on Auditory Discrimination JOURNAL OF COGNITIVE NEUROSCIENCE Haroush, K., Hochstein, S., Deouell, L. Y. 2010; 22 (7): 1440-1451

  Abstract

  Even when our attention is dedicated to an important task, background processes monitor the environment for significant events. The mismatch negativity (MMN) event-related potential is thought to reflect such a monitoring process. Nevertheless, there is continuing debate concerning the susceptibility of the MMN to attentional manipulation. We investigated the trial-by-trial relationship between brain activity related to change detection, reflected in the MMN, and visual psychophysical performance--while varying task difficulty. We find that auditory change detection is indeed "automatic" in that MMN remains robust despite increasing (visual) task load. However, the MMN amplitude and latency are susceptible to both visual load and to momentary attentional fluctuations as reflected in success or failure to identify a following visual target. We conclude that background central auditory processing is sensitive to the demands of a visual task, and fluctuates based on moment-to-moment allocation of attentional resources to the visual task.

  View details for Web of Science ID 000279057500007

  View details for PubMedID 19580389