Area of research
Genetics · Pulmonary and Respiratory Medicine
Research interest
Research interests include Cleft Lip and Palate Research, Chronic Obstructive Pulmonary Disease (COPD) Research, Asthma and respiratory diseases, and Genetic Associations and Epidemiology.
Chronic Obstructive Pulmonary Disease Exacerbations Increase the Risk of Subsequent Cardiovascular Events: A Longitudinal Analysis of the COPDGene Study
Clonal haematopoiesis and risk of chronic liver disease
Causes of and Clinical Features Associated with Death in Tobacco Cigarette Users by Lung Function Impairment
Early Evidence of Chronic Obstructive Pulmonary Disease Obscured by Race-Specific Prediction Equations
Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
The combined finding of HPV 16, 18, or 45 and cytologic Atypical Glandular Cells (AGC) indicates a greatly elevated risk of in situ and invasive cervical adenocarcinoma
Prevalence of abnormal spirometry in individuals with a smoking history and no known obstructive lung disease
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate
Xanthine oxidoreductase gene polymorphisms are associated with high risk of sepsis and organ failure
Use of the Spirometric “Fixed-Ratio” Underdiagnoses COPD in African-Americans in a Longitudinal Cohort Study
Author Correction: Clonal haematopoiesis and risk of chronic liver disease
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios
Pulmonary Arterial Pruning and Longitudinal Change in Percent Emphysema and Lung Function
Longitudinal Association Between Muscle Loss and Mortality in Ever Smokers
Multiethnic genome-wide and HLA association study of total serum IgE level
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip
Emphysema Progression and Lung Function Decline Among Angiotensin Converting Enzyme Inhibitors and Angiotensin-Receptor Blockade Users in the COPDGene Cohort
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
Protective effect of club cell secretory protein (CC-16) on COPD risk and progression: a Mendelian randomisation study
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
COPDGene® 2019: Redefining the Diagnosis of Chronic Obstructive Pulmonary Disease
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations