Amanda Everitt

The paper develops a computational method to predict structural variant impacts on genome folding and identifies ASD-associated variants disrupting neuronal regulatory interactions.

The paper shows hypoxia impairs human cortical interneuron migration and demonstrates adrenomedullin can restore this defect through the cAMP/PKA pathway.

This study benchmarks genomic footprinting algorithms for predicting transcription factor binding sites in single-cell data, finding peak-level read coverage as the strongest predictor and proposing an ensemble model to improve concordance with ChIP-seq.

This study shows that the oxytocin receptor regulates specific aspects of pair bonding and promiscuity in prairie voles by controlling gene expression and neural mechanisms.

The paper represses 87 high-confidence ASD genes in a human cortical neurogenesis model, identifying 17 genes that disrupt developmental trajectory and reveal convergence on microtubule biology and RNA-binding proteins.