Brady J. Gaynor

Exome Array Analysis of 9,721 ischemic stroke cases from the SiGN Consortium

The paper analyzes exome array data from 9,721 ischemic stroke cases to identify coding variants associated with stroke, finding 15 significant variants, including 13 novel associations.

Genomic Risk Scores and Oral Contraceptive-Associated Ischemic Stroke Risk

The paper evaluates whether a genomic risk score modifies the risk of ischemic stroke associated with oral contraceptive use in premenopausal women.

Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

The paper uses whole genome sequencing to identify genetic loci associated with platelet aggregation, including novel variants in RGS18, SVEP1, and PEAR1.

Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland

This study examines the association between pathogenic or likely pathogenic genetic variants in cardiomyopathy and arrhythmia genes and unexplained sudden cardiac death in adults with no gross pathological findings.

An Omics Analysis Search and Information System (OASIS) for Enabling Biological Discovery in the Old Order Amish

OASIS enables real-time biological discovery from GWAS data by providing a web-based system with analysis tools and visualizations for Old Order Amish studies.

Conditional Analysis Cakewalk

The paper introduces a tool that automates sequential conditional analysis for genomic variant-phenotype associations, streamlining the process with minimal user input.