Jessica E. Schwarz

This paper introduces IMaP, a method to analyze tau proteoforms at the single-molecule level, revealing ordered phosphorylation patterns and disease-specific modifications.

This study shows that age-related blood-borne factors alter circadian gene expression in cultured fibroblasts, affecting oxidative phosphorylation and cholesterol biosynthesis pathways.

This study identifies hugin+ neurons as a key interface between the sleep homeostat and circadian clock neurons, showing they regulate sleep timing and recovery.