|
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 |
|
Parent-Child Interaction and Emotion Regulation in Preschoolers with Autism Spectrum Disorder |
1K23MH127420-01A1 |
|
NIMH |
2022 |
|
Neural Mechanisms of Depressive Symptoms in Youth with Autism SpectrumDisorder |
1K23MH128466-01A1 |
|
NIMH |
2022 |