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Perception and central coherence in autism: A family genetic eye-tracking study

Perception and central coherence in autism: A family genetic eye-tracking study
自闭症的感知和中心一致性:家庭遗传眼动追踪研究
批准号:
9234424
负责人:
Molly C Losh
金额:
$7.34万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-03-03 至 2019-02-28

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中文摘要
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英文摘要
 DESCRIPTION (provided by applicant): Autism Spectrum Disorder (ASD) is a neurogenetic disorder characterized by social-communication deficits as well as restricted and repetitive interests and behaviors. Differences in perceptual coherence, including a local perceptual bias at the expense of global processing and perseverative visual attention related to circumscribed interests, are thought to underlie key features of ASD. Local and global (i.e., selective attention to parts vs. wholes, respectively) processing abilities rely on different underlying neural correlates, which may correspond to ASD symptomatology and severity. Differences in perceptual coherence and attentional styles have also been observed in family members of individuals with ASD, along with a constellation of subclinical features believed to index genetic liability (i.e., the broad autism phenotype; BAP). Similar to what has been observed in individuals with ASD, evidence suggests that relatives may also demonstrate a preference for local features of their visual scene compared to parents of typically developing individuals. Such patterns may serve as a phenotypic marker of genetic liability to ASD. This proposal employs eye tracking to examine i) visual perception during two tasks of perceptual coherence (illusory contours and the Navon hierarchical stimuli) and attention during one task of visual perseveration (visual exploration of social and non-social arrays). Using a family-genetic design, the study will explore these visual strategies in high functioning individuals with ASD and their parents. Further, the proposal examines performance on perceptual coherence and attentional tasks in relationship to a broad battery of existing clinical, cognitive, language, and social-cognitive data available on an existing sample of probands and parents participating in a companion study. The use of eye tracking may afford insights into underlying processing strategies that give rise to perceptual biases and/or attention and perseveration, which may importantly relate to clinical phenotypes, and serve as candidate endophenotypes.
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会议论文
A Family-Genetic Study of Language in Autism
  • 批准号:
    10739167
  • 项目类别:
  • 资助金额:
    $71.14万
  • 财政年份:
    2023
  • 负责人:
    Molly C Losh
  • 依托单位:
Novel Computational Analysis of Prosody in ASD and the Broad Autism Phenotype
  • 批准号:
    10113580
  • 项目类别:
  • 资助金额:
    $7.46万
  • 财政年份:
    2020
  • 负责人:
    Molly C Losh
  • 依托单位:
Human Subject Recruitment & Management
  • 批准号:
    8416041
  • 项目类别:
  • 资助金额:
    $15.58万
  • 财政年份:
    2013
  • 负责人:
    Molly C Losh
  • 依托单位:
A Family-Genetic Study of Autism and Fragile X Syndrome
  • 批准号:
    10452587
  • 项目类别:
  • 资助金额:
    $73.64万
  • 财政年份:
    2012
  • 负责人:
    Molly C Losh
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国内基金
海外基金
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    2022
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  • 项目类别:
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  • 资助金额:
    52万元
  • 批准年份:
    2022
  • 负责人:
    陈立达
  • 依托单位: