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DESCRIPTION (provided by applicant): Face recognition skills are an important substrate of effective social skills. Persons with an autism spectrum disorder (ASD: autism, asperger syndrome and pervasive developmental disorder not otherwise specified) have a variety of deficits in the manner in which they recognize faces, including a reliance on individual facial features (particularly the mouth and not eyes) rather than the typical pattern of processing faces holistically. Functional magnetic resonance imaging studies (fMRI) of face perception in ASD have shown that two brain structures - the left amygdala and the lateral aspect of the right fusiform gyrus are functionally abnormal. These findings are especially significant because they are the first brain areas to be independently confirmed by multiple labs as involved in the pathobiology of ASDs. The role of these two structures in pathobiology of ASDs is further substantiated by postmortem brain studies and gross neuroanatomical studies using conventional structural MRI. However, there remain many important questions to be answered about the parameters that modulate activity in these brain regions, both in typically developing persons and in persons with an ASD. The experiments in this R01 application are designed to extend our current knowledge in this area through a systematic series of fMRI studies. These studies make use of infra red eye tracking technology to study the relationship between scan paths and regional brain activity. These studies involve systematic manipulation of parameters that are believed to modulate level of activity in these 2 brain areas and the functional connectivity between them. In total, we propose a link series of 4 fMRI studies, each involving a comparison between 18 persons with an ASD and 18 typically developing controls (TDCs). We hypothesis that the hypoactivation of the fusiform and amygdala in ASD is mediated by (1) variation in attention and focus of perception; (2) aspects of the stimulus parameters (e.g., degree of facial emotion); and (3) interactions between the fusiform and amygdala as information comes through cortical and subcortical visual pathways.
期刊论文(11)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1007/s10803-014-2233-4
发表时间: 2015-04
期刊: JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
影响因子: 3.9
作者: [Herrington, John D., Riley, Meghan E., Grupe, Daniel W., Schultz, Robert T.]
通讯作者: Schultz, Robert T.
DOI: 10.1111/ejn.13770
发表时间: 2017-12
期刊: The European journal of neuroscience
影响因子: --
作者: [Koski JE, Collins JA, Olson IR]
通讯作者: Olson IR
DOI: 10.3389/fnhum.2013.00241
发表时间: 2013
期刊: Frontiers in human neuroscience
影响因子: 2.9
作者: [Troiani V, Schultz RT]
通讯作者: Schultz RT
Evidence against the "normalization" prediction of the early brain overgrowth hypothesis of autism.
反对自闭症早期大脑过度生长假说“正常化”预测的证据。
DOI: 10.1186/s13229-020-00353-2
发表时间: 2020
期刊: Molecular autism
影响因子: 6.2
作者: [Yankowitz,LisaD, Herrington,JohnD, Yerys,BenjaminE, Pereira,JosephA, Pandey,Juhi, Schultz,RobertT]
通讯作者: Schultz,RobertT
8
    Clinical Translational Core
    • 批准号:
      10678894
    • 项目类别:
    • 资助金额:
      $16.48万
    • 财政年份:
      2021
    • 负责人:
      ROBERT Thomas SCHULTZ
    • 依托单位:
    Clinical Translational Core
    • 批准号:
      10240000
    • 项目类别:
    • 资助金额:
      $18.91万
    • 财政年份:
      2021
    • 负责人:
      ROBERT Thomas SCHULTZ
    • 依托单位:
    Predicting Autism and Social Functioning from Computer Vision Analyses of Motor Synchrony During Dyadic Interactions
    • 批准号:
      10057391
    • 项目类别:
    • 资助金额:
      $72.09万
    • 财政年份:
      2019
    • 负责人:
      ROBERT Thomas SCHULTZ
    • 依托单位:
    Predicting Autism and Social Functioning from Computer Vision Analyses of Motor Synchrony During Dyadic Interactions
    • 批准号:
      10540333
    • 项目类别:
    • 资助金额:
      $64.6万
    • 财政年份:
      2019
    • 负责人:
      ROBERT Thomas SCHULTZ
    • 依托单位:
    国内基金
    海外基金
    补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
    靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
    • 批准号:
      JCZRQN202500010
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
    • 依托单位:
    对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
    • 批准号:
      2025JJ70209
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
      雷芬芳
    • 依托单位:
    AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
    • 批准号:
      --
    • 项目类别:
      面上项目
    • 资助金额:
      --
    • 批准年份:
      2024
    • 负责人:
      万荣
    • 依托单位: