Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Metabolomics and Mass Spectrometry Studies, Genomics and Rare Diseases, and Genetic Mapping and Diversity in Plants and Animals.
Polygenic prediction of body mass index and obesity through the life course and across ancestries
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number
Novel loci and biomedical consequences of iron homoeostasis variation
Systematic assessment of COVID-19 host genetics using whole genome sequencing data
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
A saturated map of common genetic variants associated with human height
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences
A catalog of genetic loci associated with kidney function from analyses of a million individuals
The GenomeAsia 100K Project enables genetic discoveries across Asia
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Associations of autozygosity with a broad range of human phenotypes
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution
Are Requirements to Deposit Data in Research Repositories Compatible With the European Union's General Data Protection Regulation?
Evaluation of the role of STAP1 in Familial Hypercholesterolemia