Julia E. Dallman
Publications by Year
Research Areas
Autism Spectrum Disorder Research, Zebrafish Biomedical Research Applications, Congenital heart defects research, Retinal Development and Disorders, Neuroscience and Neuropharmacology Research
Most-Cited Works
- → CoREST: A functional corepressor required for regulation of neural-specific gene expression(1999)488 cited
- → Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder(2015)204 cited
- → Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes(2020)172 cited
- → Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa(2011)172 cited
- → Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study(2016)138 cited
- → Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss(2012)127 cited
- → Tryptophan carbon dots and their ability to cross the blood-brain barrier(2019)115 cited
- → Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish(2016)108 cited
- → Translocation of CaM kinase II to synaptic sites in vivo(2003)90 cited
- → Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis(2015)87 cited