Area of research
Genetics · Immunology
Research interest
Research focused on Genetics and Genome-wide association study, with related work in Colorectal cancer, Exome, Exome sequencing. Notable publications include 'Genetic analyses of diverse populations improves discovery for complex traits', 'Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction', and 'Discovery of common and rare genetic risk variants for colorectal cancer'.
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer’s disease
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Polygenic risk score for type 2 diabetes shows context-dependent effects across populations
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study
Genetic analyses of diverse populations improves discovery for complex traits
Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer
Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer
Discovery of common and rare genetic risk variants for colorectal cancer
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk
Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants
Association of Aspirin and NSAID Use With Risk of Colorectal Cancer According to Genetic Variants
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
Detection of Minimal Residual Disease in B Lymphoblastic Leukemia by High-Throughput Sequencing of <i>IGH</i>
Estimating the heritability of colorectal cancer
Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A
Meta-analysis of loci associated with age at natural menopause in African-American women
Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci
Association of exome sequences with plasma C-reactive protein levels in >9000 participants
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans
No Evidence of Gene–Calcium Interactions from Genome-Wide Analysis of Colorectal Cancer Risk
Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study