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Adv."],"published-print":{"date-parts":[[2026,7,31]]},"abstract":"<jats:p>Comparative genomic studies of Marek\u2019s disease virus (MDV) conducted in the past two decades have proven powerful for identifying genomic loci driving historical shifts in virulence. However, past efforts were limited to comparing a few strains at a time, lacked access to certain regions of the MDV genome, and were restricted in their ability to characterize viral phenotypes. To address these limitations, we performed whole-genome sequencing on a collection of 65 MDV strains previously characterized using a standardized phenotyping assay. In addition to phylogenetic and recombination analyses, this approach enabled us to perform a genome-wide association study of virulence for this pathogen. In total, we identified 10 genome-wide significant loci associated with virulence, including a tandem repeat variant resulting from two alternative versions of a 132-bp repeating motif. 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