YT
Publications
- https://scholar.google.com/citations?user=9hVh3nQAAAAJ
- Significant sparse polygenic risk scores across 813 traits in UK Biobank
- Genetics of 35 blood and urine biomarkers in the UK Biobank
- SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPs
- Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide
- Collaborative environmental DNA sampling from petal surfaces of flowering cherry Cerasus × yedoensis ‘Somei-yoshino’ across the Japanese archipelago
- Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology
- A cross-population atlas of genetic associations for 220 human phenotypes
- Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy
- WhichTF is functionally important in your open chromatin data?
- Single-cell dissection of the obesity-exercise axis in adipose-muscle tissues implies a critical role for mesenchymal stem cells
- Fast numerical optimization for genome sequencing data in population biobanks
- Large-scale multivariate sparse regression with applications to UK Biobank
- Integration of rare expression outlier-associated variants improves polygenic risk prediction
- APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups
- Bayesian model comparison for rare-variant association studies
- Mapping the human genetic architecture of COVID-19
- Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank
- Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases
- 複数の表現型を用いた人類遺伝統計学の大規模情報解析
- Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study
- Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics
- Reported CCR5-∆32 deviation from Hardy-Weinberg equilibrium is explained by poor genotyping of rs62625034
- Medical relevance of common protein-altering variants in GPCR genes across 337,205 individuals in the UK Biobank
- Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma
- Pervasive additive and non-additive effects within the HLA region contribute to disease risk in the UK Biobank
- High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs
- LPA and APOE are associated with statin selection in the UK Biobank
- Sex-specific genetic effects across biomarkers
- A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank
- Polygenic risk modeling with latent trait-related genetic components
- Survival analysis on rare events using group-regularized multi-response Cox regression
- Bayesian mixture model for clustering rare-variant effects in human genetic studies
- Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank
- A second update on mapping the human genetic architecture of COVID-19
- Human microglial state dynamics in Alzheimer’s disease progression
- Power of inclusion: Enhancing polygenic prediction with admixed individuals
- A polygenic score method boosted by non-additive models
- LPAandAPOEare associated with statin selection in the UK Biobank
- Hypometric genetics: Improved power in genetic discovery by incorporating quality control flags
