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Principal Investigator  
Principal Investigator's Name: Ji-Yuan Zhou
Institution: Southern Medical University
Department: Department of Biostatistics
Country:
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Additional Investigators  
Investigator's Name: Kai-Wen Wang
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Bin Zhu
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Yu-Xin Yuan
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Yi-Fang Wei
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Yi Zhang
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Fan-Shuo Meng
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Jing-Xuan Wang
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Shun Zhang
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.
Investigator's Name: Jing-Kai Wang
Proposed Analysis: We plan to use Alzheimer’s Disease Neuroimaging Initiative (ADNI) data to conduct data analysis to discover biomarkers which can better identify Alzheimer's Disease (AD) or the single nucleotide polymorphisms (SNPs) which are strongly associated with AD or these biomarkers. Such investigation is sorely needed to identify AD in the early stage of the patient's affection status and treat it promptly. 1. Research objectives • Discover potential biomarkers related to AD. • Identify the SNPs highly associated with AD through genome-wide association analysis (GWAS), irrespective of autosomal loci or X-chromosomal loci. 2. Analysis plan • If the SNPs are on the X chromosome, we will consider X chromosome inactivation and the measures of the skewness of X-chromosome inactivation. • Analyze the development process of AD through longitudinal research. • Conduct transcriptome-wide association study (TWAS). • Investigate the relationship between the image data and the AD through functional principal component analysis.