DEVELOPMENT OF STATISTICAL METHODS FOR PERINATAL DISEASE

围产期疾病统计方法的发展

基本信息

  • 批准号:
    2673722
  • 负责人:
  • 金额:
    $ 12.5万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1994
  • 资助国家:
    美国
  • 起止时间:
    1994-05-01 至 2000-04-30
  • 项目状态:
    已结题

项目摘要

Built upon two advanced nonparametric statistical techniques, Multivariate Adaptive Regression Splines and Classification and Regression Trees, tree-based methods will be developed and applied to explore the data from the Yale Pregnancy Outcome Study (YPOS), which was designed to examine the relationship between pregnancy outcome and a variety of risk factors, including prescription drug and alcohol use, tobacco smoke, caffeine consumption, and contraceptive practice. Data from about 7,000 subjects will be available from two related YPOS's. Analyses will also be extended to several other important databases including the 1988 National Health Interview Survey on Child Health. In contrast to traditional statistical methods and software, the mechanisms that we will employ and investigate have several advantages: (i) automatically finding the important variables and significant interactions among a large number of variables, making it more likely that new risk factors for pregnancy outcome study (other studies as well) will be discovered; (ii) identifying high risk individuals; (iii) efficiently using data by dealing with missing data and predictors of mixed (ordinal, nominal, and nested) types appropriately. We will study pregnancy outcomes associated with perinatal death such as intrauterine growth retardation, small for gestational age, and preterm delivery, and determine the relationship between these outcomes and putative risk factors. Although the YPOS data base has been extensively analyzed using more traditional methods, the tree-based methods will provide a deeper understanding of risk factors, and will therefore impact on the development of plans for public health programs to prevent birth defects. The emphasis of this project will be on interactive effects among risk factors in connection to the outcome of interest (e.g., miscarriage or birthweight). The methods and software developed by this study will offer researchers the opportunity to perform more flexible, realistic, and efficient analyses in epidemiologic studies.
基于两种先进的非参数统计技术,

项目成果

期刊论文数量(11)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A frailty model of segregation analysis: understanding the familial transmission of alcoholism.
隔离分析的脆弱模型:了解酗酒的家族传播。
  • DOI:
    10.1111/j.0006-341x.2000.00815.x
  • 发表时间:
    2000
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Zhang,H;Merikangas,K
  • 通讯作者:
    Merikangas,K
Tree-based, two-stage risk factor analysis for spontaneous abortion.
基于树的自然流产两阶段危险因素分析。
  • DOI:
    10.1093/oxfordjournals.aje.a008869
  • 发表时间:
    1996
  • 期刊:
  • 影响因子:
    5
  • 作者:
    Zhang,H;Bracken,MB
  • 通讯作者:
    Bracken,MB
Model for the analysis of binary time series of respiratory symptoms.
用于分析呼吸道症状二元时间序列的模型。
  • DOI:
    10.1093/oxfordjournals.aje.a010171
  • 发表时间:
    2000
  • 期刊:
  • 影响因子:
    5
  • 作者:
    Zhang,H;Triche,E;Leaderer,B
  • 通讯作者:
    Leaderer,B
Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations.
用极端不一致的同胞对绘制数量性状基因座:抽样考虑。
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes.
通过使用极端一致的同胞对来绘制人类的数量性状基因座:根据亲本表型进行选择抽样。
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HEPING ZHANG其他文献

HEPING ZHANG的其他文献

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{{ truncateString('HEPING ZHANG', 18)}}的其他基金

Analysis of Genomic and Complex Data
基因组和复杂数据分析
  • 批准号:
    9927662
  • 财政年份:
    2019
  • 资助金额:
    $ 12.5万
  • 项目类别:
Analysis of Genomic and Complex Data
基因组和复杂数据分析
  • 批准号:
    10371032
  • 财政年份:
    2019
  • 资助金额:
    $ 12.5万
  • 项目类别:
Analysis of Big Data Squared in Biomedical Studies
生物医学研究中的大数据平方分析
  • 批准号:
    10361461
  • 财政年份:
    2018
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    7935595
  • 财政年份:
    2009
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    7292273
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    9198560
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    7742645
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    8005708
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    8993908
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:
Data Coordination Center for the RMN
RMN 数据协调中心
  • 批准号:
    8204480
  • 财政年份:
    2007
  • 资助金额:
    $ 12.5万
  • 项目类别:

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ALG14-先天性糖基化障碍的发病机制。
  • 批准号:
    23K14967
  • 财政年份:
    2023
  • 资助金额:
    $ 12.5万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Identifying New Therapeutics and Molecular Mechanisms in Congenital Disorders of Glycosylation.
确定先天性糖基化疾病的新疗法和分子机制。
  • 批准号:
    10644811
  • 财政年份:
    2023
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通过人群规模分析研究具有心血管症状的先天性疾病背后的基因型-表型关系
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    10724185
  • 财政年份:
    2023
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Identifying understudied protein-related glycoproteome disruption in Congenital Disorders of Glycosylation
识别先天性糖基化障碍中尚未研究的蛋白质相关糖蛋白组破坏
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    10725869
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Pathogenic Mechanisms of Congenital Disorders of Glycosylation
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靶向醛糖还原酶:依帕司他新用途治疗先天性糖基化障碍 (PMM2-CDG) 的 IIb/III 期试验
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    10480649
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评估内源干细胞治疗先天性疾病的潜在应用
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    22K20740
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靶向醛糖还原酶:依帕司他新用途治疗先天性糖基化障碍 (PMM2-CDG) 的 IIb/III 期试验
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先天性糖基化障碍神经功能缺损的O-糖基化机制
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    10040788
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先天性糖基化障碍神经功能缺损的O-糖基化机制
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