跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要使用倾向得分检验遗传关联,未明确建立因果效应识别,故不据方法名称归入因果推断。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Yuan Jiang
Ni Li
Heping Zhang

利用倾向得分调整的广义 Kendall’s Tau 识别成瘾遗传变异

研究问题
环境因素与共病影响成瘾研究时,如何检验遗传变异与多变量表型的关联?摘要关注现有协变量调整方法的不足。
方法与思路
作者用参数估计的倾向得分及逆概率加权思想调整非参数 U 统计量,形成控制协变量的半参数关联度量与检验。
材料陈述的贡献
摘要称,新度量在所设原假设下渐近无偏,模拟中较若干比较方法功效更高,并在成瘾研究数据中发现待进一步研究的变异。
阅读关注点
应核对倾向得分的建模对象、原假设及加权条件,并检查多重检验处理、基因环境交互的定义与发现结果的复现证据。
阅读边界
依据版本未注明的 OpenAlex 索引摘要;倾向得分模型条件和多重检验细节未说明,关联发现不能直接解释为因果或已复现。

原文摘要

Identifying replicable genetic variants for addiction has been extremely challenging. Besides the common difficulties with genome-wide association studies (GWAS), environmental factors are known to be critical to addiction, and comorbidity is widely observed. Despite the importance of environmental factors and comorbidity for addiction study, few GWAS analyses adequately considered them due to the limitations of the existing statistical methods. Although parametric methods have been developed to adjust for covariates in association analysis, difficulties arise when the traits are multivariate because there is no ready-to-use model for them. Recent nonparametric development includes U-statistics to measure the phenotype-genotype association weighted by a similarity score of covariates. However, it is not clear how to optimize the similarity score. Therefore, we propose a semiparametric method to measure the association adjusted by covariates. In our approach, the nonparametric U-statistic is adjusted by parametric estimates of propensity scores using the idea of inverse probability weighting. The new measurement is shown to be asymptotically unbiased under our null hypothesis while the previous non-weighted and weighted ones are not. Simulation results show that our test improves power as opposed to the non-weighted and two other weighted U-statistic methods, and it is particularly powerful for detecting gene-environment interactions. Finally, we apply our proposed test to the Study of Addiction: Genetics and Environment (SAGE) to identify genetic variants for addiction. Novel genetic variants are found from our analysis, which warrant further investigation in the future.

笔记与分组