Martin Schneider

The paper identifies neuronal cell types in the zebrafish optic tectum and shows that transcriptionally similar neurons can have distinct functional and morphological traits based on their spatial position.

The paper investigates how RIM and RIM-binding proteins regulate synaptic transmission by localizing Cav2 channels in C. elegans neuromuscular junctions, showing differential effects on cholinergic and GABAergic transmission.

The paper investigates how retinal input affects neurogenesis and cell-type configuration in the visual forebrain of zebrafish, finding that neurogenesis slows but cell-type configuration remains intact.

This paper introduces optoSynC, an optogenetic tool that rapidly and reversibly silences synaptic transmission by clustering synaptic vesicles in C. elegans.

The paper introduces a GFP-based cGMP sensor, WincG2, for real-time imaging of cGMP dynamics in intact C. elegans, showing its sensitivity to cGMP changes and responses to NaCl and SDS.

This paper engineers Cpf1 variants with altered PAM specificities to expand their targeting range while maintaining specificity.

BLISS quantifies DNA double-strand breaks in situ with high sensitivity and efficiency, showing Cpf1 has higher specificity than Cas9.