Markus M. Hilscher

This study examines Slc10a4 knockout mice to assess their role in auditory processing and sensory motor gating, suggesting they may model neuropsychiatric disorders like schizophrenia.

This study uses in situ sequencing to map oligodendrocyte lineage progression across brain and spinal cord regions in juvenile and adult mice, revealing spatial and temporal heterogeneity.

This study shows that reducing activity of CaMKII+ neurons in the dorsal cochlear nucleus decreases tinnitus-like responses in mice, suggesting these neurons maintain, but do not induce, tinnitus.

This study identifies an early wave of oligodendrogenesis in the human forebrain at PCW 8 using single-cell RNA-Seq and ATAC-Seq, supported by spatial gene expression analysis.

The paper spatially maps human cortical cell types using in situ sequencing and single-nucleus RNA-sequencing to create a first spatial atlas of human cortical cells.

This paper investigates the use of genetic markers to target specific cell populations in the dorsal cochlear nucleus (DCN) for auditory research, finding that certain promoters and Cre lines can be used to manipulate DCN neurons.

This paper introduces a graph-based method for analyzing in situ sequencing data to identify spatial compartments in mouse brain tissue, linking them to known brain regions and morphology.

This paper introduces HybISS, a spatial transcriptomic method that improves detection flexibility, multiplexing, and signal-to-noise while maintaining throughput efficiency in human and mouse brain tissue.