Area of research
Molecular Biology · Cognitive Neuroscience
Research interest
Research interests include Autism Spectrum Disorder Research, Zebrafish Biomedical Research Applications, Congenital heart defects research, and Retinal Development and Disorders.
Going with the Flow: Sensorimotor Integration Along the Zebrafish GI Tract
A Frank Assessment of <scp>SHANK</scp> : Impacts of Pathogenic Variations in <scp>SHANK3</scp> on Preclinical Models of Phelan <scp>McDermid</scp> Syndrome
Context-dependent hyperactivity in syngap1a and syngap1b zebrafish models of SYNGAP1-related disorder
The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models
Restoring Shank3 in the rostral brainstem of shank3ab−/− zebrafish autism models rescues sensory deficits
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease
Tryptophan carbon dots and their ability to cross the blood-brain barrier
Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism
Zebrafish: A Pharmacogenetic Model for Anesthesia
A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure
Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study
Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish
Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy
“Dark” carbon dots specifically “light-up” calcified zebrafish bones
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Mutations in <i><scp>RIT1</scp></i> cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype
Mutation K42E in Dehydrodolichol Diphosphate Synthase (DHDDS) Causes Recessive Retinitis Pigmentosa
Zebrafish Calls for Reinterpretation for the Roles of P/Q Calcium Channels in Neuromuscular Transmission
Distinct phenotypes in zebrafish models of human startle disease
Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss