Preprints in BioRxiv Undergoing Peer-Review

Convergent effects of neurodevelopmental disorder-associated variants at mitochondria

Context-dependent ATP7 Interactions with Parkinson′s Disease-associated Genes Modulate Copper Homeostasis Phenotypes

Distinct signaling mechanisms and proteome phenotypes are elicited by compartment-specific genetic defects of copper homeostasis

Suppressive Genetic Interactions Between Haploinsufficient Mitochondrial Genes Encoded in the 22q11.2 Microdeletion Locus Define Brain and Cardiac Phenotypes

Brain Mecp2 Gene Dosage and Gene Therapy Shape Multi-Omic Signatures and Biomarkers in Rett Syndrome

Mitochondrially Transcribed dsRNA Mediates Manganese-induced Neuroinflammation

Temporal regulation of human reactive astrocytes reveals their capacity for antigen presentation

Meclizine rescues cardiac function and mitochondrial ultrastructure by ATP- and glycolysis-independent mechanisms in a genetic model of mitochondrial energy dysfunction

Lead (Pb) exposure alters neural cell fate in the developing human brain

Neuroinflammatory Stress Preferentially Impacts Synaptic MAPK Signaling and Mitochondria in Excitatory Neurons