Andrea H. Ramirez

Frequency of pharmacogenomic variation and medication exposures among All of Us Participants

The paper assesses pharmacogenomic variation and medication exposures in a diverse cohort using whole genome sequencing and EHR data, finding high prevalence of actionable variants and previously unreported alleles.

Common and Rare Variants Associated with Cardiometabolic Traits across 98,622 Whole-Genome Sequences in the All of Us Research Program

The paper analyzes whole-genome sequences from 98,622 participants to identify common and rare variants associated with cardiometabolic traits, replicating known associations and finding new loci.

A genome-wide association study of polycystic ovary syndrome identified from electronic health records

This paper identifies novel genetic variants associated with PCOS using EHR-based GWAS and validates them in independent cohorts.

Interactions between genetic variation and cellular environment in skeletal muscle gene expression

The paper identifies genetic-environment interactions in skeletal muscle gene expression using allele-specific expression and clinical traits as environmental proxies.