Sandrine Schmutz

This study creates a spatial transcriptomic atlas of the developing mouse cochlea to identify gene expression gradients and cell-type specific signatures linked to cochlear function.

This study identifies L. pneumophila's LpDot1 protein as a bacterial effector that modifies SFPQ, disrupting paraspeckle organization and host splicing, leading to alternative splice variants of infection-related genes.

The paper uses single-cell and spatial transcriptomics to study hematopoietic stem and progenitor cell diversity and their niches in zebrafish development.

The paper identifies fetal liver stromal subsets using spectral cytometry and autofluorescence, finding two distinct autofluorescent signals corresponding to hepatoblasts/cholangiocytes and stellate cells.

This study uses TATTOO-seq to identify spatial and cell type-specific regulatory programs during limb development and shows how perturbations affect cell fate and spatial organization.

The paper uses whole-organism single-cell RNA-seq to analyze cell type diversity in Nematostella vectensis, identifying 35% of genes and 51% of TFs as cell type-specific.