Christopher T. Rhodes

This study integrates MRI and genomic data from GBM patients to identify common molecular signatures and link them to tumor locations, highlighting dysregulated neurotransmitter receptors and synaptic activity.

This study shows that loss of Ezh2 in the medial ganglionic eminence (MGE) leads to changes in interneuron fate, morphology, and gene expression.

The paper characterizes the epigenomic landscape of embryonic mouse forebrain neural progenitors using snATAC-Seq and integrates multi-omics data to reveal region-specific regulatory mechanisms.

This study uses single-cell RNA sequencing to reveal transcriptional heterogeneity in ventricular zone cells of the embryonic mouse forebrain, showing spatial and temporal gene expression differences.

This study identifies Grin1 as a key regulator of subtype-specific gene expression in MGE-derived interneurons, linking NMDAR signaling to neurodevelopmental disorders like schizophrenia.

This study identifies H3K27me3 and H4K20me3 targets in baboon hippocampal NSPCs, revealing their role in repressing lineage gene activation and regulating cell cycle progression.