Area of research
Nutrition and Dietetics · Molecular Biology
Research interest
Research interests include Trace Elements in Health, Mitochondrial Function and Pathology, Cellular transport and secretion, and Genetics and Neurodevelopmental Disorders.
APOE expression and secretion are modulated by mitochondrial dysfunction
Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus
Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory Neurons
Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content
Cdh1-APC Regulates Protein Synthesis and Stress Granules in Neurons through an FMRP-Dependent Mechanism
Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior
The IDA3 adapter, required for intraflagellar transport of I1 dynein, is regulated by ciliary length
The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors
The Proteome of BLOC-1 Genetic Defects Identifies the Arp2/3 Actin Polymerization Complex to Function Downstream of the Schizophrenia Susceptibility Factor Dysbindin at the Synapse
BLOC-1 Brings Together the Actin and Microtubule Cytoskeletons to Generate Recycling Endosomes
Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease
Mutations in the BLOC-1 Subunits Dysbindin and Muted Generate Divergent and Dosage-dependent Phenotypes
Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes
Anoctamin 1 (Tmem16A) Ca <sup>2</sup> <sup>+</sup> -activated chloride channel stoichiometrically interacts with an ezrin–radixin–moesin network
Quantitative Proteomic and Genetic Analyses of the Schizophrenia Susceptibility Factor Dysbindin Identify Novel Roles of the Biogenesis of Lysosome-Related Organelles Complex 1