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Charles F. Gillespie

Researcher at Emory University

Publications -  76
Citations -  6714

Charles F. Gillespie is an academic researcher from Emory University. The author has contributed to research in topics: Population & Child abuse. The author has an hindex of 28, co-authored 71 publications receiving 5584 citations. Previous affiliations of Charles F. Gillespie include Georgia State University.

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Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults.

TL;DR: There were no main effects of the SNPs on PTSD symptoms and no significant genetic interactions with level of non-child abuse trauma as predictor of adult PTSD symptoms, suggesting a potential gene-childhood environment interaction for adult PTSD.
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Influence of child abuse on adult depression: moderation by the corticotropin-releasing hormone receptor gene.

TL;DR: Data support the corticotropin-releasing hormone hypothesis of depression and suggest that a gene x environment interaction is important for the expression of depressive symptoms in adults with CRHR1 risk or protective alleles who have a history of child abuse.
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Trauma exposure and stress-related disorders in inner city primary care patients

TL;DR: These data document high levels of childhood and adult trauma exposure, principally interpersonal violence, in a large sample of an inner-city primary care population and predictors of posttraumatic stress and depressive symptomatology.
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Inflammation in Fear- and Anxiety-Based Disorders: PTSD, GAD, and Beyond.

TL;DR: The available data suggest that targeting inflammation may serve as a potential therapeutic target for treating fear- and anxiety-based disorders in the future, but the field must continue to characterize the specific role pro-inflammatory signaling in the maintenance of these unique psychiatric conditions.
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Hypercortisolemia and depression.

TL;DR: The authors review the history of techniques used to assess the functions of the HPA axis, evidence for hypercortisolemia as a state rather than trait component of depression, and treatment implications.