Navya Shilpa Josyula

This study identifies 14 genome-wide significant loci for obstructive sleep apnea, including three independent of BMI, and highlights genetic pathways involving obesity, neurological, and craniofacial factors.

This study identifies novel genetic signals associated with severe obesity through GWAS and shows strong genetic overlap with BMI, highlighting shared comorbidities and lifestyle interactions.

The paper investigates the phenotypic effects of ELN gene variants using exome data and phenotyping, finding associations with connective tissue disorders beyond known conditions.

This study identifies robust gene-phenotype associations by analyzing rare loss-of-function variants in exome-wide data linked to electronic health records.

The paper identifies genetic variants associated with obstructive sleep apnea using electronic health records and links them to comorbidities.

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

The paper maps the AHR-mediated gene regulatory network in mouse liver using gene expression and TF binding data, showing distinct expression patterns and biological process enrichments among AHR-bound and unbound genes.