Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Bioinformatics and Genomic Networks, Alzheimer's disease research and treatments, and Genomics and Rare Diseases.
Asian diversity in human immune cells
SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain Disorders
Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer’s disease and a cumulative effects model for risk liability
Molecular landscape of tumor-associated tissue-resident memory T cells in tumor microenvironment of hepatocellular carcinoma
Cross-ancestry genome-wide association study identifies implications of SORL1 in cerebral beta-amyloid deposition
Mosaic chromosomal alterations in blood are associated with an increased risk of Alzheimer’s disease
Protective Effects of Genetic Proxies of Cognitive Reserve in Parkinson's Disease: A Longitudinal Multi‐Cohort Study
Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk
Meta-analysis of genetic regulation of RNA editing in the human brain identifies new genes underlying neurological disease
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease
Improving polygenic prediction in ancestrally diverse populations
Author Correction: Improving polygenic prediction in ancestrally diverse populations
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Association between adiposity and cardiovascular outcomes: an umbrella review and meta-analysis of observational and Mendelian randomization studies
Comprehensive characterization of distinct genetic alterations in metastatic breast cancer across various metastatic sites
Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery Disease
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease
Analysis of protein-coding genetic variation in 60,706 humans
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Analysis of protein-coding genetic variation in 60,706 humans
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians
Correction: SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians