Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genomics and Rare Diseases, Genetic Mapping and Diversity in Plants and Animals, and Epigenetics and DNA Methylation.
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Principles and methods for transferring polygenic risk scores across global populations
Beyond the exome: What’s next in diagnostic testing for Mendelian conditions
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program
Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations
Protein prediction for trait mapping in diverse populations
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease risk
Genome sequencing unveils a regulatory landscape of platelet reactivity
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level
Genetic analyses of diverse populations improves discovery for complex traits
Genetic association testing using the GENESIS R/Bioconductor package
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology
Multiethnic Meta-Analysis Identifies <i>RAI1</i> as a Possible Obstructive Sleep Apnea–related Quantitative Trait Locus in Men
A meta-analysis of genome-wide association studies of asthma in Puerto Ricans