Area of research
Genetics · Physiology
Research interest
Research interests include Genome-wide association study, Genetic association, Biology, Genetics, Disease, and Medicine.
Endovascular treatment for cerebral venous thrombosis: a multicenter study in China
Shared genetics and causal association between plasma levels of <scp>SARS</scp>‐<scp>CoV</scp>‐2 entry receptor <scp>ACE2</scp> and Alzheimer's disease
Genetic Insights into Glycine’s Protective Role Against CAD — European and East Asia, 2015 and 2020
Potential of Secondary Metabolites of Diaporthe Species Associated with Terrestrial and Marine Origins
Chemical Investigation of Endophytic Diaporthe unshiuensis YSP3 Reveals New Antibacterial and Cytotoxic Agents
Evaluation of Equisetin as an Anti-Microbial and Herbicidal Agent from Endophytic Fungus Fusarium sp. JDJR1
rs56405341 Variant Associates with Expression of <i>C4orf33</i> and <i>C4orf33</i> Was Downregulated in Alzheimer’s Disease and Progressive Supranuclear Palsy
Regional transcriptional vulnerability to basal forebrain functional dysconnectivity in mild cognitive impairment patients
Parkinson’s Disease rs117896735 Variant Regulates <i>INPP5F</i> Expression in Brain Tissues and Increases Risk of Alzheimer’s Disease
[High-density fermentation of <i>Escherichia coli</i> to express 4-hydroxyphenylacetate 3-hydroxylase and efficient biosynthesis of caffeic acid].
The Critical Role of 12-Methyl Group of Anthracycline Dutomycin to Its Antiproliferative Activity
Safety and efficacy of remote ischemic conditioning for the treatment of intracerebral hemorrhage: A proof-of-concept randomized controlled trial
Impact of serum calcium levels on total body bone mineral density: A mendelian randomization study in five age strata
Impact of Vitamin D Binding Protein Levels on Alzheimer’s Disease: A Mendelian Randomization Study
<i>SERPINA1</i> gene expression in whole blood links the rs6647 variant G allele to an increased risk of large artery atherosclerotic stroke
Metabolic engineering of Saccharomyces cerevisiae for efficient production of endocrocin and emodin
LncRNA2Target v2.0: a comprehensive database for target genes of lncRNAs in human and mouse
Interleukin-6 Receptor and Inflammatory Bowel Disease: A Mendelian Randomization Study
EWAS: epigenome-wide association study software 2.0
Autoimmune disease variants regulate <i>GSDMB</i> gene expression in human immune cells and whole blood
SORL1 Variants Show Different Association with Early-Onset and Late-Onset Alzheimer’s Disease Risk
Multiple sclerosis risk pathways differ in Caucasian and Chinese populations
Alzheimer’s Disease Variants with the Genome-Wide Significance are Significantly Enriched in Immune Pathways and Active in Immune Cells
PICALM rs3851179 Variant Confers Susceptibility to Alzheimer’s Disease in Chinese Population
Integrating genome-wide association studies and gene expression data highlights dysregulated multiple sclerosis risk pathways
Genetic Variants and Multiple Sclerosis Risk Gene SLC9A9 Expression in Distinct Human Brain Regions
The study of the relation of DNA repair pathway genes SNPs and the sensitivity to radiotherapy and chemotherapy of NSCLC
CDH1 rs9929218 variant at 16q22.1 contributes to colorectal cancer susceptibility
The framework for population epigenetic study