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.
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program
Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Prosaposin is a regulator of progranulin levels and oligomerization