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Melisa Carrasco

Researcher at University of Michigan

Publications -  27
Citations -  2312

Melisa Carrasco is an academic researcher from University of Michigan. The author has contributed to research in topics: Error-related negativity & Default mode network. The author has an hindex of 20, co-authored 26 publications receiving 2040 citations. Previous affiliations of Melisa Carrasco include University of Rochester & University of Maryland, Baltimore.

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Abnormalities of intrinsic functional connectivity in autism spectrum disorders.

TL;DR: It is indicated that ASD subjects show altered intrinsic connectivity within the default network, and connectivity between these structures is associated with specific ASD symptoms.
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Alterations of resting state functional connectivity in the default network in adolescents with autism spectrum disorders

TL;DR: The findings indicate that adolescents with ASD show weaker connectivity in the default network than previously reported in adults with ASD, and shows that weaker connectivity within thedefault network is associated with specific impairments in ASD.
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Neural circuitry of emotional face processing in autism spectrum disorders.

TL;DR: When attention bias to emotional faces was equivalent between ASD and control groups, ASD was associated with greater amygdala activation, and alterations in connectivity are consistent with emotion and face processing disturbances in ASD.
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Age-related changes in the structure and function of prefrontal cortex-amygdala circuitry in children and adolescents: a multi-modal imaging approach.

TL;DR: Results indicate that greater structural connectivity of the uncinate fasciculus predicts reduced amygdala activation to sad and happy faces and this effect is moderated by age, with younger participants exhibiting a stronger relation.
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Increased error‐related brain activity in youth with obsessive‐compulsive disorder and unaffected siblings

TL;DR: This study was done to assess the ERN as a biomarker for OCD by comparing ERN amplitudes in pediatric OCD patients, unaffected siblings of pediatric OCD Patients, and healthy controls.