Author

R. Torene

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Open access Aug 2026

Estimating the contribution of coding mutations to autism

It is found that damaging de novo single-nucleotide variants and frameshift indels explain 3.4% (95% CI: 2.1% - 4.7%) of autism variance on the observed scale.

A. Nadig, J. Fu, F. Satterstrom et al. · medRxiv · 0 citations

Aug 2026

Genomics-first association of pharmacogenomic risk phenotypes with adverse drug reactions in a healthcare-based population.

A portion of population ADR burden could possibly have been prevented through PGx-guided therapy and a portion of population ADR burden could possibly have been prevented through PGx-guided therapy.

R. Torene, Ryley Uber, Tracy Brandt et al. · Genetics in Medicine · 0 citations