Dr. Holder is a Primary Investigator, Assistant Professor, Department of Pediatrics and Developmental Neuroscience, Baylor College of Medicine, Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital.
Research Focus: Neurodevelopmental disorders, Autism, SHANK3 mutations
The Holder lab investigates the genetic and neurobiological basis of neurodevelopmental and neuropsychiatric disorders. There are currently three main projects in the Holder Lab.
First, we use cell-based screens to identify genetic modifiers of two synaptic proteins, SHANK3 and SynGAP. Mutations in the SHANK3 and SYNGAP1 genes cause severe neurodevelopmental disorders associated with intellectual disability, autism and epilepsy. Both are typically caused by de novo mutations which result in haploinsufficiency. By identifying genetic modifiers of protein stability, we aim to identify therapeutic entry points for these disorders. Verifying a physiological role for genes identified through these screens will be performed in animal models and iPSC-derived neurons from patients.
Second, we are investigating the neuronal and circuit dysfunction responsible for the phenotypes associated with SHANK3 Duplication Syndrome. We are currently focusing on the role of striatal neurons in behavioral abnormalities of mice modeling this disorder. Our lab is using Cre-LoxP and Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to map the neurons responsible for these behavioral abnormalities.
Third, we are investigating the role of genetic variants on bipolar disorder. We use next generation sequencing to identify genetic changes that predispose to bipolar disorder in families. We then propose to use animal models of these changes to validate their role in neuropsychiatric disorders.
Strong Collaborations + SYNGAP1 Research = Accelerated Development of Better Treatments
West Bank, Sheffield, UK