Author

S. Kramer

h-index 0 View on Semantic Scholar

We have 2 of 2 papers

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

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

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