Open access
Sep 2026
Rare copy number variation in Post-traumatic stress disorder using whole genome sequencing and biobank data
S. Kramer, S. Valilou, M. Singh et al.
· medRxiv · 0 citations
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Aug 2026
Prioritizing Genes and Rare Protein-Coding Variants in Acute Myeloid Leukemia via Whole Genome Sequencing Data
These findings demonstrate that leveraging whole-genome sequencing in large-scale biobanks enables the identification of rare protein-coding variants, genes, and gene sets associated with AML.
S. Vieno, M. Singh, S. Kramer et al.
· medRxiv · 0 citations