|
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 |
|
The role of glutamatergic inputs to the paraventricular nucleus of the hypothalamus in social behavior and oxytocin neural activity |
1F31MH129025-01 |
|
NIMH |
2022 |
|
Transdiagnostic Mechanisms of Youth Externalizing Psychopathology from Childhood to Adolescence: A Longitudinal Person-Centered Approach |
1F31MH129054-01 |
|
NIMH |
2022 |
|
The role of state agencies in mental health services for individuals with co-occurring intellectual and developmental disabilities and mental illness |
1F31MH131311-01 |
|
NIMH |
2022 |
|
Defining the gene regulatory roles of non-coding variants in the pathogenesis of autism |
1F31MH131380-01 |
|
NIMH |
2022 |
|
Single-molecule Investigation of the Interaction Between MeCP2 and Chromatin |
1F31MH132306-01 |
|
NIMH |
2022 |