|
|
Identification of optimum spectacle prescriptions for patients with Down syndrome |
| 5R01EY024590-08 |
|
NEI |
2022 |
|
|
Applications of high resolution fMRI in ultra-high field (7T) in revealing developmental disorders underlying amblyopia |
| 5R01EY030434-03 |
|
NEI |
2022 |
|
|
Investigating a novel mechanism underlying prefrontal cortex dysfunction in autism and intellectual disability |
| 1F30MH127800-01A1 |
|
NIMH |
2022 |
|
|
The molecular roles of RFX3 in neurodevelopment and Autism Spectrum disorder |
| 1F30MH128995-01A1 |
|
NIMH |
2022 |
|
|
Integrating common and rare genetic variation in autism spectrum disorder |
| 1F30MH129009-01 |
|
NIMH |
2022 |
|
|
The Role of the ASD Risk Gene CHD8 in Neural Development |
| 1F30MH132282-01 |
|
NIMH |
2022 |
|
|
Mechanisms underlying impaired hippocampal physiology in Fragile X Syndrome |
| 1F31MH127933-01A1 |
|
NIMH |
2022 |
|
|
Defining the gene regulatory roles of non-coding variants in the pathogenesis of autism |
| 1F31MH131380-01 |
|
NIMH |
2022 |
|
|
Machine Learning Methods to Develop and Deploy Real-Time Risk Surveillance for Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder from the Electronic Health Record |
| 1K01MH127309-01A1 |
|
NIMH |
2022 |
|
|
Discovery of genetic modifiers of PTEN-ASD severity in a library of genetically diverse iPSC lines |
| 1K01MH131856-01 |
|
NIMH |
2022 |