Author

J. R. Coleman

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Open access Sep 2026

Rare copy number variation in Post-traumatic stress disorder using whole genome sequencing and biobank data

The role of rare copy number variants (rCNVs) from multi-ancestry whole-genome sequencing data in the All of Us Research Program is examined, using an electronic health record-defined PTSD phenotype.

S. Kramer, S. Valilou, M. Singh et al. · medRxiv · 0 citations