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J. Christopher Edgar

J. Christopher Edgar

· Ph.D.

University of Pennsylvania · Rehabilitation Medicine

Active 1987–2024

h-index59
Citations10.4k
Papers25970 last 5y
Funding$13.1M2 active
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About

J. Christopher Edgar, PhD, is a Professor of Radiology at the Children's Hospital of Philadelphia and a Senior Scientist in the Department of Radiology at the same institution. His research expertise includes brain imaging techniques such as magnetoencephalography and electroencephalography, with a focus on understanding neurodevelopmental and neuropsychiatric conditions including Autism Spectrum Disorder and Schizophrenia. His work involves studying how the brain changes throughout childhood, exemplified by projects like The Brains Change Program, which investigates the emergence of infant behavior through advanced analysis methods. Dr. Edgar's educational background includes a BA in Philosophy and English Literature from Texas Christian University, an MS in Psychology from the University of New Mexico, and a PhD in Clinical Psychology from the same university. His research and clinical interests are centered on neuropsychology, with a particular emphasis on brain development and neuroimaging techniques to better understand neurodevelopmental disorders.

Research topics

  • Biology
  • Psychiatry
  • Genetics
  • Neuroscience
  • Psychology
  • Medicine

Selected publications

  • Effects of eight neuropsychiatric copy number variants on human brain structure

    Translational Psychiatry · 2021 · 46 citations

    • Neuroscience
    • Psychology
    • Genetics

    Many copy number variants (CNVs) confer risk for the same range of neurodevelopmental symptoms and psychiatric conditions including autism and schizophrenia. Yet, to date neuroimaging studies have typically been carried out one mutation at a time, showing that CNVs have large effects on brain anatomy. Here, we aimed to characterize and quantify the distinct brain morphometry effects and latent dimensions across 8 neuropsychiatric CNVs. We analyzed T1-weighted MRI data from clinically and non-clinically ascertained CNV carriers (deletion/duplication) at the 1q21.1 (n = 39/28), 16p11.2 (n = 87/78), 22q11.2 (n = 75/30), and 15q11.2 (n = 72/76) loci as well as 1296 non-carriers (controls). Case-control contrasts of all examined genomic loci demonstrated effects on brain anatomy, with deletions and duplications showing mirror effects at the global and regional levels. Although CNVs mainly showed distinct brain patterns, principal component analysis (PCA) loaded subsets of CNVs on two latent brain dimensions, which explained 32 and 29% of the variance of the 8 Cohen's d maps. The cingulate gyrus, insula, supplementary motor cortex, and cerebellum were identified by PCA and multi-view pattern learning as top regions contributing to latent dimension shared across subsets of CNVs. The large proportion of distinct CNV effects on brain morphology may explain the small neuroimaging effect sizes reported in polygenic psychiatric conditions. Nevertheless, latent gene brain morphology dimensions will help subgroup the rapidly expanding landscape of neuropsychiatric variants and dissect the heterogeneity of idiopathic conditions.

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